MSK Flashcards

(1022 cards)

1
Q

What are antihistone antibodies associated with?

A

Drug-induced lupus

Antihistone antibodies are often found in patients with drug-induced lupus erythematosus, which is a condition triggered by certain medications.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the features of drug induced lupus?

A

arthralgia
myalgia
skin (e.g. malar rash) and pulmonary involvement (e.g. pleurisy) are common
ANA positive in 100%, dsDNA negative
anti-histone antibodies are found in 80-90%
anti-Ro, anti-Smith positive in around 5%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are bisphosphonates?

A

Analogues of pyrophosphate that decrease demineralisation in bone and inhibit osteoclasts.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

How do bisphosphonates inhibit osteoclasts?

A

By reducing recruitment and promoting apoptosis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

List the clinical uses of bisphosphonates.

A
  • Prevention and treatment of osteoporosis
  • Hypercalcaemia
  • Paget’s disease
  • Pain from bone metastases
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are common adverse effects of bisphosphonates?

A
  • Oesophageal reactions (oesophagitis, oesophageal ulcers)
  • Osteonecrosis of the jaw
  • Increased risk of atypical stress fractures
  • Acute phase response (fever, myalgia, arthralgia)
  • Hypocalcaemia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Which bisphosphonate is especially associated with oesophageal ulcers?

A

Alendronate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

True or False: The risk of osteonecrosis of the jaw is greater for patients receiving IV bisphosphonates than for those receiving oral bisphosphonates.

A

True

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What factors are risk factors for osteonecrosis of the jaw in bisphosphonate patients?

A
  • Poor dental hygiene
  • Prior dental procedures
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What does the BNF advise regarding dental check-ups for bisphosphonate patients?

A

All patients with cancer and patients with poor dental status should have a dental check-up before bisphosphonate treatment.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What should patients do when taking oral bisphosphonates?

A

Tablets should be swallowed whole with plenty of water while sitting or standing.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

When should bisphosphonates be taken?

A

On an empty stomach at least 30 minutes before breakfast or another oral medication.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What should be corrected before giving bisphosphonates?

A

Hypocalcemia/vitamin D deficiency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

When might calcium be prescribed with bisphosphonates?

A

Only if dietary intake is inadequate.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is typically given alongside bisphosphonates?

A

Vitamin D supplements

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is the recommended duration for bisphosphonate treatment for certain low-risk patients?

A

Some authorities recommend stopping bisphosphonates at 5 years.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What are the criteria for stopping bisphosphonates after 5 years?

A
  • Patient is < 75 years old
  • Femoral neck T-score of > -2.5
  • Low risk according to FRAX/NOGG
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What is dermatomyositis?

A

An inflammatory disorder causing symmetrical, proximal muscle weakness and characteristic skin lesions

May be idiopathic or associated with connective tissue disorders or underlying malignancy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

What percentage of dermatomyositis patients may have an underlying malignancy?

A

20-25%

More if the patient is older

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

What is polymyositis?

A

A variant of dermatomyositis where skin manifestations are not prominent

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

What are the skin features of dermatomyositis?

A
  • Photosensitive
  • Macular rash over back and shoulder
  • Heliotrope rash in the periorbital region
  • Gottron’s papules
  • Mechanic’s hands
  • Nail fold capillary dilatation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

What are Gottron’s papules?

A

Roughened red papules over extensor surfaces of fingers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

What characterizes ‘mechanic’s hands’ in dermatomyositis?

A

Extremely dry and scaly hands with linear ‘cracks’ on the palmar and lateral aspects of the fingers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

What are some other features of dermatomyositis?

A
  • Proximal muscle weakness +/- tenderness
  • Raynaud’s
  • Respiratory muscle weakness
  • Interstitial lung disease
  • Dysphagia
  • Dysphonia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
What is the typical muscle weakness presentation in dermatomyositis?
Proximal muscle weakness +/- tenderness
26
What is the prevalence of ANA positivity in dermatomyositis patients?
Around 80%
27
What percentage of dermatomyositis patients have anti-synthetase antibodies?
Around 30%
28
Name two types of anti-synthetase antibodies associated with dermatomyositis.
* Antibodies against histidine-tRNA ligase (Jo-1) * Antibodies to signal recognition particle (SRP) * Anti-Mi-2 antibodies
29
What is an arthus reaction?
A localized type III hypersensitivity reaction caused by the deposition of immune complexes in the walls of small blood vessels at the site of antigen exposure. ## Footnote Immune complexes are formed from antigen–IgG antibody complexes.
30
What is the main cause of an arthus reaction?
Deposition of immune complexes in small blood vessels. ## Footnote This occurs particularly in individuals with high circulating antibody levels, usually IgG.
31
What happens upon re-exposure to the antigen in an arthus reaction?
Immune complexes form locally, activating complement, attracting neutrophils, and causing tissue damage. ## Footnote This process leads to vasculitis, edema, and tissue necrosis.
32
How long after antigen exposure do symptoms of an arthus reaction typically develop?
Within 4–12 hours. ## Footnote Symptoms may occur after vaccinations or injections of antigens for which the patient has high antibody levels.
33
List some clinical features of an arthus reaction.
* Localized pain * Swelling * Erythema * Warmth * Induration ## Footnote Severe cases may progress to blistering, ulceration, or tissue necrosis.
34
What are common examples of situations where an arthus reaction may occur?
* After booster vaccinations (tetanus, diphtheria, pneumococcal) * After therapeutic protein/antitoxin injections (e.g., antivenom, monoclonal antibodies) * In experimental immunology (skin testing with foreign proteins) ## Footnote These examples highlight instances of re-exposure to antigens.
35
What is the general management approach for an arthus reaction?
Generally self-limiting with supportive care. ## Footnote Supportive care includes analgesia, cool compresses, and elevation.
36
Fill in the blank: An arthus reaction is a type _______ hypersensitivity reaction.
III
37
True or False: An arthus reaction may require immediate medical intervention.
False ## Footnote The reaction is generally self-limiting.
38
What should be avoided until antibody levels fall in the case of an arthus reaction?
Unnecessary repeat antigen exposure. ## Footnote This is to prevent further complications from the hypersensitivity reaction.
39
What is antiphospholipid syndrome?
An acquired disorder characterised by a predisposition to both venous and arterial thromboses, recurrent fetal loss, and thrombocytopenia ## Footnote It may occur as a primary disorder or secondary to conditions like systemic lupus erythematosus (SLE).
40
What percentage of patients with systemic lupus erythematosus (SLE) have positive antiphospholipid antibodies?
Around 30% ## Footnote This indicates a significant association between SLE and antiphospholipid syndrome.
41
What is a key laboratory finding in antiphospholipid syndrome?
Paradoxical rise in the APTT due to lupus anticoagulant autoantibodies reacting with phospholipids ## Footnote This is an important point for understanding the coagulation cascade in these patients.
42
Name some associations of antiphospholipid syndrome aside from SLE.
* Other autoimmune disorders * Lymphoproliferative disorders * Phenothiazines (rare) ## Footnote These associations highlight the diverse clinical contexts in which antiphospholipid syndrome may occur.
43
List the features of antiphospholipid syndrome.
* Venous/arterial thrombosis * Recurrent miscarriages * Livedo reticularis * Other features: pre-eclampsia, pulmonary hypertension ## Footnote Recognition of these features is crucial for diagnosis.
44
What antibodies are investigated in antiphospholipid syndrome?
* Anticardiolipin antibodies * Anti-beta2 glycoprotein I (anti-beta2GPI) antibodies * Lupus anticoagulant ## Footnote These laboratory tests are essential for confirming the diagnosis.
45
What are the clinical criteria for diagnosing antiphospholipid syndrome?
* ≥1 clinical episode of arterial, venous, or small-vessel thrombosis * Pregnancy morbidity: three or more consecutive unexplained spontaneous abortions <10 weeks, or ≥1 unexplained fetal loss ≥10 weeks, or ≥1 preterm birth <34 weeks due to placental insufficiency ## Footnote At least one of these criteria must be met.
46
What laboratory criteria must be met for diagnosing antiphospholipid syndrome?
* Lupus anticoagulant (LA) * Anticardiolipin (aCL) antibodies * Anti-beta2 glycoprotein I (anti-β2GP1) antibodies ## Footnote At least one must be confirmed on ≥2 occasions at least 12 weeks apart.
47
What is the initial management for thromboprophylaxis in antiphospholipid syndrome?
Low-dose aspirin ## Footnote This is recommended based on EULAR guidelines.
48
What is recommended for pregnant women with antiphospholipid syndrome?
Low-dose aspirin plus LMWH for thromboprophylaxis ## Footnote This is according to RCOG guidance.
49
What is the standard treatment for initial venous thromboembolic events in antiphospholipid syndrome?
Lifelong warfarin with a target INR of 2-3 ## Footnote This is a critical aspect of secondary thromboprophylaxis.
50
True or False: DOAC therapy is routinely recommended for high-risk antiphospholipid syndrome patients.
False ## Footnote According to NICE/EULAR guidance, warfarin remains the standard of care for most patients who are not pregnant.
51
Fill in the blank: Antiphospholipid syndrome may cause _______ in pregnant women.
Recurrent miscarriages ## Footnote This highlights the impact of the syndrome on pregnancy outcomes.
52
What is carpal tunnel syndrome?
Compression of the median nerve in the carpal tunnel ## Footnote It leads to symptoms like pain and numbness in the hand.
53
What are common symptoms of carpal tunnel syndrome?
Pain and pins and needles in thumb, index, middle finger ## Footnote Symptoms may ascend proximally and are often relieved by shaking the hand.
54
What is a classic time for symptoms of carpal tunnel syndrome to occur?
At night
55
What physical examination signs indicate carpal tunnel syndrome?
Weakness of thumb abduction, wasting of thenar eminence, Tinel's sign, Phalen's sign ## Footnote Tinel's sign involves tapping causing paraesthesia, and Phalen's sign involves wrist flexion causing symptoms.
56
What does Tinel's sign indicate?
Tapping causes paraesthesia
57
What does Phalen's sign indicate?
Flexion of wrist causes symptoms
58
What are some causes of carpal tunnel syndrome?
Idiopathic, pregnancy, oedema, lunate fracture, rheumatoid arthritis ## Footnote Oedema can be due to heart failure.
59
What electrophysiological change is noted in carpal tunnel syndrome?
Prolongation of the action potential
60
What does NICE recommend for mild-moderate symptoms of carpal tunnel syndrome?
A 6-week trial of conservative treatments
61
What treatments are recommended for carpal tunnel syndrome?
Corticosteroid injection, wrist splints at night, surgical decompression ## Footnote Surgical decompression involves flexor retinaculum division.
62
True or False: Wasting occurs in the hypothenar eminence in carpal tunnel syndrome.
False
63
Fill in the blank: Carpal tunnel syndrome is caused by compression of the _______.
median nerve
64
What is temporal arteritis also known as?
Giant cell arteritis (GCA) ## Footnote Temporal arteritis is a type of vasculitis affecting medium and large-sized vessels.
65
What age group is most commonly affected by temporal arteritis?
> 50 years old, peak in 70s ## Footnote Temporal arteritis primarily occurs in older adults.
66
Why is early recognition and treatment of temporal arteritis crucial?
To minimize the risk of complications such as permanent loss of vision ## Footnote Prompt treatment is essential to prevent serious complications.
67
What is the first-line treatment for suspected temporal arteritis?
High-dose prednisolone ## Footnote Treatment should start promptly along with referral to a specialist.
68
What percentage of patients with temporal arteritis also exhibit features of polymyalgia rheumatica (PMR)?
Around 50% ## Footnote There is significant overlap between the two conditions.
69
What are common features of temporal arteritis?
* Patient typically > 60 years old * Rapid onset (e.g. < 1 month) * Headache (85%) * Jaw claudication (65%) * Tender, palpable temporal artery ## Footnote These features help in the clinical diagnosis of temporal arteritis.
70
What ocular complication is most commonly associated with temporal arteritis?
Anterior ischemic optic neuropathy ## Footnote It results from occlusion of the posterior ciliary artery.
71
What is a key investigation in all patients suspected of having temporal arteritis?
Vision testing ## Footnote Essential for assessing potential ocular complications.
72
What is the gold standard diagnostic test for giant cell arteritis (GCA)?
Temporal artery biopsy ## Footnote It confirms the presence of granulomatous inflammation with multinucleated giant cells.
73
What should be considered if a temporal artery biopsy is negative?
GCA cannot be ruled out due to skip lesions; treatment should continue if pre-test probability is high ## Footnote Clinical judgement is important in these cases.
74
What alternative diagnostic method can be used for temporal arteritis?
Temporal artery colour Doppler ultrasound ## Footnote It serves as a non-invasive option for diagnosis.
75
What is the recommended treatment if there is evolving visual loss?
IV methylprednisolone ## Footnote This is given prior to starting high-dose prednisolone.
76
What is a dramatic response to treatment indicative of?
The diagnosis may be reconsidered if there is no dramatic response ## Footnote This helps confirm the diagnosis of temporal arteritis.
77
What additional treatment is required for bone protection during long-term steroid use?
Bisphosphonates ## Footnote Necessary due to the risks associated with long-term glucocorticoid therapy.
78
Is low-dose aspirin routinely given to patients with temporal arteritis?
Yes, but the evidence base supporting this is weak ## Footnote It may help in some patients, but more research is needed.
79
What drugs cause drug induced Lupus?
Most common causes procainamide hydralazine Less common causes isoniazid minocycline phenytoin
80
What is the sensitivity of ANA in systemic lupus erythematosus?
99% ## Footnote This high sensitivity makes ANA a useful rule out test.
81
What is the specificity of ANA in systemic lupus erythematosus?
Low ## Footnote Despite its high sensitivity, ANA has low specificity.
82
What percentage of systemic lupus erythematosus patients are rheumatoid factor positive?
20% ## Footnote This indicates some overlap with rheumatoid arthritis.
83
What is the specificity and sensitivity of anti-dsDNA antibodies?
Highly specific (> 99%), sensitivity (70%) ## Footnote Anti-dsDNA is a key marker in systemic lupus erythematosus.
84
What is the specificity and sensitivity of anti-Smith antibodies?
Highly specific (> 99%), sensitivity (30%) ## Footnote Anti-Smith antibodies are another important marker for the disease.
85
List other antibodies associated with systemic lupus erythematosus.
* anti-U1 RNP * SS-A (anti-Ro) * SS-B (anti-La) ## Footnote These antibodies can also be present in systemic lupus erythematosus.
86
What full blood count findings may be present in systemic lupus erythematosus?
* Anaemia (of chronic disease or haemolytic) * Lymphopenia (common) * Thrombocytopenia due to immune-mediated destruction ## Footnote These findings are often seen in lupus patients.
87
What inflammatory marker is generally used to monitor systemic lupus erythematosus?
ESR ## Footnote ESR is a common test for monitoring inflammation.
88
What does a raised CRP indicate during active disease in systemic lupus erythematosus?
Underlying infection ## Footnote During active disease, CRP may be normal despite inflammation.
89
What complement levels are low during active disease in systemic lupus erythematosus?
C3, C4 ## Footnote Low complement levels occur due to consumption from complex formation.
90
What can anti-dsDNA titres be used for in systemic lupus erythematosus?
Disease monitoring ## Footnote Not all patients will have anti-dsDNA titres present.
91
What has revolutionized the management of rheumatoid arthritis (RA) in the past decade?
The introduction of disease-modifying therapies (DMARDs) ## Footnote DMARDs help modify the disease course and improve patient outcomes.
92
When should patients with evidence of joint inflammation start treatment?
As soon as possible with a combination of disease-modifying drugs (DMARDs) ## Footnote Early intervention is crucial for better management of RA.
93
What does NICE recommend for initial therapy in RA management?
DMARD monotherapy +/- a short-course of bridging prednisolone ## Footnote Previously, dual DMARD therapy was advocated as the initial step.
94
What is the most widely used DMARD?
Methotrexate ## Footnote Methotrexate requires careful monitoring due to potential side effects.
95
What monitoring is essential when using methotrexate?
FBC (full blood count) & LFTs (liver function tests) ## Footnote This is due to the risk of myelosuppression and liver cirrhosis.
96
Name two other important DMARDs besides methotrexate.
* Sulfasalazine * Leflunomide ## Footnote Hydroxychloroquine is considered only for mild or palindromic disease.
97
How does NICE recommend monitoring response to treatment?
Using a combination of CRP and disease activity (e.g., DAS28 score) ## Footnote This helps in assessing the efficacy of the treatment.
98
What is a common management strategy for flares of RA?
Corticosteroids - oral or intramuscular ## Footnote Corticosteroids help reduce inflammation during flares.
99
What is the current indication for a TNF-inhibitor?
An inadequate response to at least two DMARDs including methotrexate ## Footnote TNF-inhibitors are used when initial treatments are insufficient.
100
What is etanercept and how is it administered?
A recombinant human protein acting as a decoy receptor for TNF-α, administered subcutaneously ## Footnote Risks include demyelination and reactivation of tuberculosis.
101
What is infliximab and its route of administration?
A monoclonal antibody that binds to TNF-α, administered intravenously ## Footnote It prevents TNF-α from binding with TNF receptors.
102
What is adalimumab and how is it administered?
A monoclonal antibody administered subcutaneously ## Footnote It is used for patients who do not respond adequately to DMARDs.
103
What is the mechanism of action of rituximab?
Anti-CD20 monoclonal antibody resulting in B-cell depletion ## Footnote It is given as two 1g intravenous infusions two weeks apart.
104
What are common reactions associated with rituximab infusions?
Infusion reactions ## Footnote Monitoring during administration is essential due to these reactions.
105
What is abatacept and how does it affect T lymphocytes?
A fusion protein that modulates a key signal for T lymphocyte activation, decreasing T-cell proliferation and cytokine production ## Footnote It is given as an infusion but is not currently recommended by NICE.
106
What is psoriatic arthropathy?
An inflammatory arthritis associated with psoriasis, classed as a seronegative spondyloarthropathy.
107
How does psoriatic arthropathy correlate with cutaneous psoriasis?
It correlates poorly and often precedes the development of skin lesions.
108
What percentage of patients with skin lesions develop an arthropathy?
Around 10-20%.
109
Are males and females equally affected by psoriatic arthropathy?
Yes.
110
What are the patterns of presentation in psoriatic arthropathy?
* Symmetric polyarthritis (30-40% of cases) * Asymmetrical oligoarthritis (20-30%) * Sacroiliitis * DIP joint disease (around 10%) * Arthritis mutilans.
111
What is symmetric polyarthritis in psoriatic arthropathy similar to?
Rheumatoid arthritis.
112
What is arthritis mutilans?
A severe deforming form of psoriatic arthropathy characterized by 'telescoping fingers'.
113
What are some other signs of psoriatic arthropathy?
* Psoriatic skin lesions * Periarticular disease * Enthesitis * Tenosynovitis * Dactylitis * Nail changes (pitting, onycholysis).
114
What is enthesitis?
Inflammation at the site of tendon and ligament insertion.
115
What are the typical blood test results in psoriatic arthropathy?
* Elevated CRP/ESR * Negative rheumatoid factor (RF) * Negative anti-cyclic citrullinated peptide antibodies (anti-CCP) * HLA-B27 may be positive.
116
What can X-rays reveal in psoriatic arthropathy?
* Erosions * New bone formation * Periostitis * 'Pencil-in-cup' appearance in advanced disease.
117
Who should manage psoriatic arthropathy?
A rheumatologist.
118
What is the initial management for mild peripheral arthritis or mild axial disease?
NSAIDs alone.
119
What is commonly used for moderate to severe psoriatic arthropathy?
Methotrexate.
120
What types of biologics may be required for resistant or extensive disease?
* Ustekinumab (targets IL-12 and IL-23) * Secukinumab (targets IL-17) * Ixekizumab (targets IL-17) * Adalimumab (anti-TNF).
121
What is apremilast?
An oral phosphodiesterase type-4 (PDE4) inhibitor that modulates inflammatory mediators.
122
What is the prognosis of psoriatic arthropathy compared to rheumatoid arthritis?
Generally better, though some may develop progressive joint damage and disability.
123
What is pseudogout?
A form of microcrystal synovitis caused by the deposition of calcium pyrophosphate dihydrate crystals in the synovium. ## Footnote Pseudogout is now more correctly termed acute calcium pyrophosphate crystal deposition disease.
124
What age group is strongly associated with pseudogout?
Increasing age ## Footnote Patients who develop pseudogout at a younger age (< 60 years) usually have underlying risk factors.
125
List some underlying risk factors for developing pseudogout at a younger age.
* Haemochromatosis * Hyperparathyroidism * Low magnesium * Low phosphate * Acromegaly * Wilson's disease
126
Which joints are most commonly affected by pseudogout?
* Knee * Wrist * Shoulders
127
What type of crystals are found in joint aspiration for pseudogout?
Weakly-positively birefringent rhomboid-shaped crystals ## Footnote These crystals are indicative of calcium pyrophosphate dihydrate deposition.
128
What x-ray finding is associated with pseudogout?
Chondrocalcinosis ## Footnote In the knee, this can appear as linear calcifications of the meniscus and articular cartilage.
129
What is the first step in the management of pseudogout?
Aspiration of joint fluid to exclude septic arthritis.
130
What medications are used for managing pseudogout?
* NSAIDs * Intra-articular steroids * Intra-muscular steroids * Oral steroids ## Footnote These treatments are similar to those used for gout.
131
What is systemic sclerosis?
A condition of unknown aetiology characterised by hardened, sclerotic skin and other connective tissues. ## Footnote Systemic sclerosis is four times more common in females.
132
What are the three patterns of systemic sclerosis?
1. Limited cutaneous systemic sclerosis 2. Diffuse cutaneous systemic sclerosis 3. Scleroderma (without internal organ involvement) ## Footnote Each pattern has distinct characteristics and associated antibodies.
133
What is a notable first sign of limited cutaneous systemic sclerosis?
Raynaud's phenomenon ## Footnote This may occur before other symptoms.
134
Which parts of the body are predominantly affected in limited cutaneous systemic sclerosis?
Face and distal limbs ## Footnote It is associated with anti-centromere antibodies.
135
What is CREST syndrome?
A subtype of limited systemic sclerosis characterised by: * Calcinosis * Raynaud's phenomenon * Esophageal dysmotility * Sclerodactyly * Telangiectasia ## Footnote CREST syndrome is associated with limited cutaneous systemic sclerosis.
136
Which parts of the body are predominantly affected in diffuse cutaneous systemic sclerosis?
Trunk and proximal limbs ## Footnote It is associated with anti-scl-70 antibodies.
137
What is the most common cause of death in diffuse cutaneous systemic sclerosis?
Respiratory involvement ## Footnote Seen in around 80% of patients, including interstitial lung disease (ILD) and pulmonary arterial hypertension (PAH).
138
What are some complications of diffuse cutaneous systemic sclerosis?
1. Renal disease 2. Hypertension ## Footnote Patients with renal disease should be started on an ACE inhibitor.
139
Which ACE inhibitor is typically used for renal disease in systemic sclerosis patients?
Captopril ## Footnote It is chosen for its rapid onset and short half-life, allowing for dose titration.
140
How do ACE inhibitors help in systemic sclerosis?
By reducing efferent arteriolar vasoconstriction and limiting renin-angiotensin system activation. ## Footnote This addresses the underlying mechanism of renal disease.
141
What is the prognosis for patients with diffuse cutaneous systemic sclerosis?
Poor prognosis ## Footnote Due to severe complications like respiratory involvement.
142
What is a characteristic feature of scleroderma without internal organ involvement?
Tightening and fibrosis of skin ## Footnote It may manifest as plaques (morphoea) or linear.
143
What percentage of patients with systemic sclerosis test positive for ANA?
90% ## Footnote ANA positivity indicates autoimmune activity.
144
What percentage of patients with systemic sclerosis test positive for RF?
30% ## Footnote RF positivity can indicate other autoimmune conditions.
145
Which antibodies are associated with diffuse cutaneous systemic sclerosis?
Anti-scl-70 antibodies ## Footnote They are linked to a higher risk of severe interstitial lung disease.
146
Which antibodies are associated with limited cutaneous systemic sclerosis?
Anti-centromere antibodies ## Footnote They are a marker for the limited form of the disease.
147
What chromosome are HLA antigens encoded for?
Chromosome 6 ## Footnote HLA antigens are crucial for immune system function.
148
What are the class I HLA antigens?
HLA A, B, C ## Footnote Class I antigens present peptides to CD8+ T cells.
149
What are the class II HLA antigens?
DP, DQ, DR ## Footnote Class II antigens present peptides to CD4+ T cells.
150
What disease is associated with HLA-A3?
Haemochromatosis ## Footnote Haemochromatosis is a condition of iron overload.
151
What disease is associated with HLA-B51?
Behcet's disease ## Footnote Behcet's disease is a systemic vasculitis.
152
What diseases are associated with HLA-B27? (List them)
* Ankylosing spondylitis * Reactive arthritis * Acute anterior uveitis * Psoriatic arthritis ## Footnote HLA-B27 is linked to several inflammatory diseases.
153
What is the association of HLA-DQ2/DQ8?
Coeliac disease ## Footnote Coeliac disease is an autoimmune disorder triggered by gluten.
154
What diseases are associated with HLA-DR2? (List them)
* Narcolepsy * Goodpasture's ## Footnote HLA-DR2 is linked to autoimmune conditions.
155
What diseases are associated with HLA-DR3? (List them)
* Dermatitis herpetiformis * Sjogren's syndrome * Primary biliary cirrhosis ## Footnote HLA-DR3 is associated with several autoimmune disorders.
156
What diseases are associated with HLA-DR4? (List them)
* Type 1 diabetes mellitus * Rheumatoid arthritis ## Footnote Type 1 diabetes is also associated with HLA-DR3 but more strongly with HLA-DR4.
157
True or False: Type 1 diabetes mellitus is more strongly associated with HLA-DR3 than HLA-DR4.
False ## Footnote Type 1 diabetes mellitus is primarily associated with HLA-DR4.
158
What is reactive arthritis?
An arthritis that develops following an infection where the organism cannot be recovered from the joint ## Footnote It is associated with HLA-B27 and includes post-STI and post-dysenteric forms.
159
What was formerly known as Reiter's syndrome?
A term that described a classic triad of urethritis, conjunctivitis, and arthritis following a dysenteric illness ## Footnote This term has been largely replaced by the concept of reactive arthritis.
160
What is the classic triad associated with reactive arthritis?
Urethritis, conjunctivitis, arthritis ## Footnote This triad was identified in patients following dysenteric illnesses.
161
How is sexually acquired reactive arthritis sometimes referred to?
Post-STI reactive arthritis (SARA) ## Footnote This form is identified in patients following sexually transmitted infections.
162
What mnemonic describes the symptoms of reactive arthritis?
Can't see, pee or climb a tree ## Footnote This phrase summarizes the classic symptoms of reactive arthritis.
163
What is the epidemiology of post-STI reactive arthritis?
Much more common in men, approximately 10:1 ratio ## Footnote The post-dysenteric form has equal sex incidence.
164
List the organisms most commonly associated with post-dysenteric reactive arthritis.
* Shigella flexneri * Salmonella typhimurium * Salmonella enteritidis * Yersinia enterocolitica * Campylobacter ## Footnote These organisms are linked to the post-dysenteric form of reactive arthritis.
165
What organism is most commonly associated with post-STI reactive arthritis?
Chlamydia trachomatis ## Footnote This organism is linked specifically to sexually transmitted infections.
166
What is the management strategy for reactive arthritis?
* Symptomatic treatment * Analgesia * NSAIDs * Intra-articular steroids ## Footnote Sulfasalazine and methotrexate may be used for persistent disease.
167
What is the typical duration of symptoms in reactive arthritis?
Symptoms rarely last more than 12 months ## Footnote This duration varies among individuals but is generally limited.
168
What is adhesive capsulitis commonly known as?
Frozen shoulder
169
What is the most common demographic affected by adhesive capsulitis?
Middle-aged females
170
What is the aetiology of frozen shoulder?
Not fully understood
171
What percentage of diabetics may experience an episode of frozen shoulder?
Up to 20%
172
What features typically develop in adhesive capsulitis?
Over days
173
Which shoulder movement is affected more in adhesive capsulitis?
External rotation
174
What types of movement are affected in adhesive capsulitis?
Both active and passive movement
175
What are the three phases of adhesive capsulitis?
Painful freezing phase, adhesive phase, recovery phase
176
What percentage of patients may experience bilateral adhesive capsulitis?
Up to 20%
177
How long does an episode of adhesive capsulitis typically last?
Between 6 months and 2 years
178
How is adhesive capsulitis typically diagnosed?
Clinically
179
What imaging may be required for adhesive capsulitis?
For atypical or persistent symptoms
180
What single intervention has been shown to improve long-term outcomes in adhesive capsulitis?
None
181
Name two treatment options for adhesive capsulitis.
* NSAIDs * Physiotherapy * Oral corticosteroids * Intra-articular corticosteroids
182
What other medical history has been associated with adhesive capsulitis?
History of myocardial infarction, lung disease, or neck disease
183
What age group is commonly affected by adhesive capsulitis?
Females aged 40-60 years
184
Where do patients often experience symptoms in adhesive capsulitis?
In the non-dominant hand
185
What can trigger adhesive capsulitis following disuse?
Prolonged immobilisation of the arm or pain
186
Is there a known association between adhesive capsulitis and activity?
No
187
What is cauda equina syndrome (CES)?
A rare but serious condition where the lumbosacral nerve roots below the spinal cord are compressed.
188
What is the most common cause of cauda equina syndrome?
Central disc prolapse.
189
At which spinal levels does central disc prolapse typically occur in CES?
L4/5 or L5/S1.
190
List other possible causes of cauda equina syndrome.
* Tumours: primary or metastatic * Infection: abscess, discitis * Trauma * Haematoma
191
What symptom is commonly associated with cauda equina syndrome?
Low back pain.
192
What percentage of cauda equina syndrome cases present with bilateral sciatica?
Around 50%.
193
What are some features of cauda equina syndrome?
* Reduced sensation/pins-and-needles in the perianal area * Decreased anal tone * Urinary dysfunction
194
Why is it good practice to check anal tone in patients with new-onset back pain?
It may indicate cauda equina syndrome.
195
What do studies show about the sensitivity and specificity of checking anal tone for CES?
It has poor sensitivity and specificity.
196
What are some examples of urinary dysfunction in cauda equina syndrome?
* Incontinence * Reduced awareness of bladder filling * Loss of urge to void
197
What is a late sign of cauda equina syndrome that may indicate irreversible damage?
Incontinence.
198
What is the urgent investigation recommended for cauda equina syndrome?
MRI.
199
What is the management for cauda equina syndrome?
Surgical decompression.
200
What is gout?
A form of microcrystal synovitis caused by the deposition of monosodium urate monohydrate in the synovium.
201
What causes gout?
Chronic hyperuricaemia (uric acid > 450 µmol/l).
202
What are the first-line treatments for acute gout management?
* NSAIDs * Colchicine
203
How long should the maximum dose of NSAID be prescribed after gout symptoms settle?
1-2 days.
204
What may be indicated for gastroprotection during gout treatment?
A proton pump inhibitor.
205
What is the mechanism of action of colchicine?
* Inhibits microtubule polymerization by binding to tubulin * Interferes with mitosis * Inhibits neutrophil motility and activity.
206
What is a key side effect of colchicine?
Diarrhoea.
207
What is the usual dose of prednisolone for gout management?
15 mg/day.
208
When should urate-lowering therapy (ULT) be offered to gout patients?
After their first attack of gout.
209
What are the indications for urate-lowering therapy (ULT)?
* >= 2 attacks in 12 months * Tophi * Renal disease * Uric acid renal stones * Prophylaxis if on cytotoxics or diuretics.
210
Why was it traditionally advised to delay starting urate-lowering therapy after an acute attack?
To avoid precipitating a further attack.
211
What is the first-line urate-lowering therapy?
Allopurinol.
212
What is the initial dose of allopurinol?
100 mg od.
213
What is the target serum uric acid level for gout management?
< 360 µmol/l.
214
What lower target uric acid level may be considered for patients with tophi?
< 300 µmol/L.
215
What should be considered when starting allopurinol?
Colchicine cover.
216
What is the second-line agent when allopurinol is not tolerated or ineffective?
Febuxostat.
217
What is uricase?
An enzyme that catalyzes the conversion of urate to allantoin.
218
What is pegloticase used for?
To achieve rapid control of hyperuricemia in refractory cases.
219
What lifestyle modifications are recommended for gout management?
* Reduce alcohol intake * Lose weight if obese * Avoid food high in purines.
220
What are examples of foods high in purines to avoid?
* Liver * Kidneys * Seafood * Oily fish (mackerel, sardines) * Yeast products.
221
What should be considered regarding precipitating drugs in gout management?
Stopping drugs such as thiazides.
222
What is the specific uricosuric action of losartan?
It may be particularly suitable for patients with coexistent hypertension.
223
How may increased vitamin C intake affect serum uric acid levels?
It may decrease serum uric acid levels.
224
A 43-year-old woman who has rheumatoid arthritis is reviewed in clinic. She has responded poorly to methotrexate and consideration is being given to starting sulfasalazine. An existing allergy to which one of the following drugs may be a contradiction to the prescription?
The correct answer is Aspirin. Sulfasalazine is a sulfonamide drug, and patients with a known allergy to aspirin (a salicylate) may have cross-reactivity with sulfonamides due to their similar chemical structures. As a result, it is generally contraindicated to prescribe sulfasalazine in patients with an existing aspirin allergy.
225
A 59-year-old man presents to the Emergency Department with severe pain in his right 1st metatarsophalangeal joint as well as his right ankle. The pain began during the night and has become worse since the morning after he took his morning furosemide. He also takes omeprazole for a recent peptic ulcer. Which of the following medications should be commenced to treat his symptoms?
This patient is suffering from acute gout and therefore normally he would be commenced on a high-dose NSAID such as aspirin or a coxib. However, as he has recently had a peptic ulcer, the two aforementioned are contraindicated. Thus, the next step would be to treat with colchicine.
226
The following groups should be advised to take vitamin D supplementation:
all pregnant and breastfeeding women should take a daily supplement containing 10µg of vitamin D all children aged 6 months - 5 years. Babies fed with formula milk do not need to take a supplement if they are taking more than 500ml of milk a day, as formula milk is fortified with vitamin D adults > 65 years 'people who are not exposed to much sun should also take a daily supplement' e.g. housebound patients
227
Testing for vitamin D deficiency
patients with bone diseases that may be improved with vitamin D treatment e.g. known osteomalacia or Paget's disease patients with bone diseases, prior to specific treatment where correcting vitamin deficiency is appropriate e,g, prior to intravenous zolendronate or denosumab patients with musculoskeletal symptoms that could be attributed to vitamin D deficiency e.g. bone pain ?osteomalacia
228
What is polymyalgia rheumatica (PMR)?
A relatively common condition in older people characterised by muscle stiffness and raised inflammatory markers ## Footnote PMR appears to be closely related to temporal arteritis, but the underlying cause is not fully understood and it is not a vasculitic process.
229
What age group is typically affected by polymyalgia rheumatica?
Patients are usually > 60 years old
230
What is the typical onset duration for polymyalgia rheumatica?
Usually rapid onset (e.g. < 1 month)
231
What are common symptoms of polymyalgia rheumatica?
Aching, morning stiffness in proximal limb muscles ## Footnote Weakness is not considered a symptom of polymyalgia rheumatica.
232
What are additional features associated with polymyalgia rheumatica?
Mild polyarthralgia, lethargy, depression, low-grade fever, anorexia, night sweats
233
What laboratory findings are indicative of polymyalgia rheumatica?
Raised inflammatory markers e.g. ESR > 40 mm/hr
234
What results are expected from creatine kinase and EMG tests in polymyalgia rheumatica?
Normal
235
What is the first-line treatment for polymyalgia rheumatica?
Prednisolone e.g. 15mg/od
236
How do patients typically respond to steroid treatment in polymyalgia rheumatica?
Patients typically respond dramatically to steroids
237
What should be considered if a patient with polymyalgia rheumatica fails to respond to steroids?
Consideration of an alternative diagnosis
238
What are the rotator cuff muscles and their roles, innervation?
Use the mnemonic "SITS" to remember them: Supraspinatus Action: Abduction of the arm (first 15°) Innervation: Suprascapular nerve Infraspinatus Action: External (lateral) rotation of the arm Innervation: Suprascapular nerve Teres minor Action: External rotation and adduction of the arm Innervation: Axillary nerve Subscapularis Action: Internal (medial) rotation of the arm Innervation: Upper and lower subscapular nerves
239
What is a common cause of acromioclavicular joint injury?
Collision sports such as rugby, falls onto the shoulder, or FOOSH (falls on outstretched hand) ## Footnote Injuries often occur in high-impact scenarios.
240
How are AC joint injuries classified?
Graded I to VI depending on the degree of separation ## Footnote Each grade reflects the severity and type of injury.
241
What is the typical management for Grade I and II AC joint injuries?
Conservative management including resting the joint and using a sling ## Footnote These grades are common and often heal well with non-surgical treatment.
242
What grades of AC joint injuries require surgical intervention?
Grade IV, V, and VI ## Footnote These grades are rare and typically involve more severe injuries.
243
What is the management approach for Grade III AC joint injuries?
Debate exists; often depends on individual circumstances ## Footnote Treatment can vary based on specific patient needs and injury characteristics.
244
Red flags for lower back pain:
age < 20 years or > 50 years history of previous malignancy night pain history of trauma systemically unwell e.g. weight loss, fever thoracic back pain
245
A 73-year-old comes to see you asking if she can stop her alendronic acid. She has been taking it for six years having had a distal radial fracture at this time, after she tripped over on an uneven kerb. There have been no further fractures, nor any preceding this injury. Six years ago, her DEXA scan showed a T-score of -2.4. Her past medical history is otherwise unremarkable and she has no recent history of falls. She has never smoked. What is the appropriate action to discuss with the patient?
Bisphosphonate 'holidays' is a recent hot topic, addressed by recent evidence from the National Osteoporosis Guideline Group (NOGG) in January 2016. After a five year period for oral bisphosphonates (three years for IV zoledronate), treatment should be re-assessed for ongoing treatment, with an updated FRAX score and DEXA scan. This guidance separates patients into high and low risk groups. To fall into the high risk group, one of the following must be true: Age >75 Glucocorticoid therapy Previous hip/vertebral fractures Further fractures on treatment High risk on FRAX scoring T score <-2.5 after treatment If any of the high risk criteria apply, treatment should be continued indefinitely, or until the criteria no longer apply. If they are in the low risk group however, treatment may be discontinued and re-assessed after two years, or if a further fracture occurs. In the case of this patient, she has no risk factors which put her into the high risk group, but we do not have a recent DEXA scan. The best option would therefore be to re-scan her now, and consider a two year break if her T score is >-2.5
246
Systemic lupus erythematosus: management
Basics NSAIDs sun-block Hydroxychloroquine the treatment of choice for SLE If internal organ involvement e.g. renal, neuro, eye then consider prednisolone, cyclophosphamide
247
What are the most common causes of posterior heel pain?
Achilles tendon disorders ## Footnote Includes tendinopathy, partial tear, and complete rupture of the Achilles tendon.
248
What is associated with tendon disorders?
Quinolone use (e.g. ciprofloxacin) ## Footnote Quinolones are antibiotics that can increase the risk of tendon problems.
249
What predisposes to tendon xanthomata?
Hypercholesterolaemia ## Footnote High cholesterol levels can lead to the formation of fatty deposits in tendons.
250
What are the features of Achilles tendinopathy?
Gradual onset of posterior heel pain, morning pain and stiffness ## Footnote Pain worsens following activity.
251
What is the typical management for Achilles tendinopathy?
Supportive management including: * Simple analgesia * Reduction in precipitating activities * Calf muscle eccentric exercises ## Footnote Exercises may be self-directed or guided by physiotherapy.
252
What symptoms suggest an Achilles tendon rupture?
Audible 'pop', sudden significant pain in calf or ankle, inability to walk or continue sport ## Footnote These symptoms often occur during sports or running.
253
What is Simmond's triad used for?
To help exclude Achilles tendon rupture ## Footnote Involves examining angle of declination, feeling for a gap in the tendon, and calf muscle squeeze.
254
What examination technique is used to assess for Achilles tendon rupture?
Ask the patient to lie prone with feet over the edge of the bed and observe for abnormal angle of declination ## Footnote Also involves feeling for a gap in the tendon.
255
What will happen to the injured foot during a calf squeeze if there is an acute rupture?
The injured foot will stay in the neutral position ## Footnote This indicates a lack of function in the Achilles tendon.
256
What is the initial imaging modality of choice for suspected Achilles tendon rupture?
Ultrasound ## Footnote Provides an effective assessment of the tendon.
257
What should be done following a suspected Achilles tendon rupture?
Acute referral to an orthopaedic specialist ## Footnote Timely intervention is crucial for proper management.
258
Reactive arthritis: features
Features time course typically develops within 4 weeks of initial infection - symptoms generally last around 4-6 months around 25% of patients have recurrent episodes whilst 10% of patients develop chronic disease arthritis is typically an asymmetrical oligoarthritis of lower limbs dactylitis symptoms of urethritis eye conjunctivitis (seen in 10-30%) anterior uveitis skin circinate balanitis (painless vesicles on the coronal margin of the prepuce) keratoderma blenorrhagica (waxy yellow/brown papules on palms and soles)
259
What is a common site of fracture in elderly females?
Hip ## Footnote The hip is particularly vulnerable in osteoporotic patients.
260
What is a risk associated with displaced hip fractures?
Avascular necrosis ## Footnote This occurs due to disruption of blood supply to the femoral head.
261
What are the classic signs of a hip fracture?
Pain, shortened leg, externally rotated leg ## Footnote These signs help in the clinical diagnosis of hip fractures.
262
Can patients with non-displaced neck of femur fractures weight bear?
Yes ## Footnote Non-displaced or incomplete fractures may allow for weight bearing.
263
What are the two main classifications of hip fractures based on location?
Intracapsular, Extracapsular ## Footnote Intracapsular fractures are further divided into subcapital, while extracapsular includes trochanteric and subtrochanteric.
264
What is the dividing line for trochanteric and subtrochanteric fractures?
Lesser trochanter ## Footnote This anatomical landmark helps classify extracapsular fractures.
265
What does the Garden classification system categorize?
Hip fractures ## Footnote It includes types based on stability and displacement.
266
What characterizes a Type I Garden fracture?
Stable fracture with impaction in valgus ## Footnote This type indicates stability and a specific angulation.
267
What is a Type II Garden fracture?
Complete fracture but undisplaced ## Footnote This type involves a complete break without displacement.
268
Describe a Type III Garden fracture.
Displaced fracture, rotated and angulated but with boney contact ## Footnote This type indicates some contact between fracture fragments.
269
What is a Type IV Garden fracture?
Complete boney disruption ## Footnote This type indicates a complete break with no contact between fragments.
270
Which types of Garden fractures are most likely to disrupt blood supply?
Types III and IV ## Footnote These types are associated with increased risk of avascular necrosis.
271
What is the recommended management for an undisplaced intracapsular hip fracture?
Internal fixation or hemiarthroplasty if unfit ## Footnote Treatment options depend on the patient's overall health.
272
What does NICE recommend for displaced intracapsular hip fractures?
Replacement arthroplasty (total hip replacement or hemiarthroplasty) ## Footnote This recommendation is based on the patient's fitness and ability to walk.
273
When is total hip replacement favored over hemiarthroplasty?
If patients can walk independently outdoors, are not cognitively impaired, and are medically fit for anesthesia and the procedure ## Footnote This guideline ensures better outcomes for eligible patients.
274
What is the management for stable intertrochanteric fractures?
Dynamic hip screw ## Footnote This device helps stabilize the fracture effectively.
275
What is the recommended treatment for reverse oblique, transverse, or subtrochanteric fractures?
Intramedullary device ## Footnote This method provides adequate stabilization for complex fracture patterns.
276
What organization updated their guidelines on osteoporosis management in 2021?
The National Osteoporosis Guideline Group (NOGG) ## Footnote NICE guidelines are also based on the NOGG guidelines.
277
What is usually the symptom of osteoporosis until a fracture occurs?
Asymptomatic
278
What factors are considered when assessing osteoporosis management?
* High risk of fragility fracture based on QFracture or FRAX score * Starting treatment that increases the risk of osteoporosis * Recent fragility fracture
279
What lifestyle changes should be advised for patients at risk of osteoporosis?
* Healthy, balanced diet * Moderation of alcohol consumption * Avoidance of smoking
280
What dietary supplements should be offered to women at risk of osteoporosis?
Calcium and vitamin D
281
What is the first-line drug treatment for patients at risk of fragility fractures?
Bisphosphonates
282
What are the typical first-line oral bisphosphonates?
* Alendronate * Risedronate
283
What is the recommended first-line treatment following a hip fracture according to NOGG?
IV zoledronate
284
What is denosumab generally used as in osteoporosis treatment?
Second-line treatment
285
List other possible treatment options for osteoporosis.
* Strontium ranelate * Raloxifene * Teriparatide * Romosozumab
286
What is the BMD threshold for defining osteoporosis?
T-score of -2.5 SD or below
287
What should be done for high-risk patients based on QFracture or FRAX score?
Perform a DEXA scan to assess bone mineral density (BMD)
288
What should be started concurrently with oral glucocorticoids at ≥7.5 mg/day for 3 months?
Bone protective treatment
289
When should treatment for a symptomatic osteoporotic vertebral fracture be started?
Straight away
290
What is a hip fracture considered in older adults?
A manifestation of osteoporosis
291
Is a DEXA scan necessary to diagnose osteoporosis after a fragility fracture in women ≥ 75 years?
No
292
What is the recommended duration for prescribing oral bisphosphonates?
At least 5 years
293
What is the recommended duration for intravenous bisphosphonates?
At least 3 years
294
What should be done after the initial treatment period of bisphosphonates?
Re-assess fracture risk
295
What year did NICE update its guidelines on the management of osteoarthritis?
2022
296
What initial support should all patients with osteoarthritis receive?
Help with weight loss, advice about local muscle strengthening exercises, and general aerobic fitness
297
What are the first-line analgesics recommended for osteoarthritis?
Topical NSAIDs
298
For which conditions may topical NSAIDs be particularly beneficial?
OA of the knee or hand
299
What is the second-line treatment for osteoarthritis?
Oral NSAIDs
300
What should be co-prescribed with NSAIDs?
A proton pump inhibitor
301
What should be avoided when a patient takes aspirin?
NSAIDs
302
When should paracetamol or weak opioids be offered to osteoarthritis patients?
Only if used infrequently for short-term pain relief and all other pharmacological treatments are contraindicated, not tolerated, or ineffective
303
Are glucosamine and strong opioids recommended for osteoarthritis?
No
304
What non-pharmacological treatment options are suggested for knee and hip OA?
Walking aids
305
What may be tried if standard pharmacological treatment for osteoarthritis is ineffective?
Intra-articular steroid injections
306
How long do intra-articular steroid injections provide relief?
2-10 weeks
307
What should be considered if conservative methods fail for osteoarthritis?
Joint replacement
308
What type of drug is sulfasalazine?
Disease modifying anti-rheumatic drug (DMARD) ## Footnote Used in the management of inflammatory arthritis and inflammatory bowel disease.
309
What is the primary use of sulfasalazine?
Management of inflammatory arthritis, especially rheumatoid arthritis ## Footnote Also used in inflammatory bowel disease.
310
What is the mechanism of action of sulfasalazine?
Decreases neutrophil chemotaxis, suppresses proliferation of lymphocytes and pro-inflammatory cytokines ## Footnote It is a prodrug for 5-ASA.
311
What is a caution for using sulfasalazine?
G6PD deficiency ## Footnote Also caution for allergy to aspirin or sulphonamides due to cross-sensitivity.
312
List some adverse effects of sulfasalazine.
* Oligospermia * Stevens-Johnson syndrome * Pneumonitis / lung fibrosis * Myelosuppression * Heinz body anaemia * Megaloblastic anaemia * May colour tears, staining contact lenses ## Footnote These effects can vary in severity and frequency.
313
Is sulfasalazine safe to use during pregnancy?
Yes ## Footnote Considered safe to use in both pregnancy and breastfeeding.
314
What is the relationship between sulfasalazine and 5-ASA?
Sulfasalazine is a prodrug for 5-ASA ## Footnote 5-ASA is an active metabolite that contributes to its therapeutic effects.
315
What is lateral epicondylitis commonly referred to as?
'Tennis elbow' ## Footnote It typically follows activities such as house painting or playing tennis.
316
What age group is most commonly affected by lateral epicondylitis?
People aged 45-55 years ## Footnote This condition typically affects the dominant arm.
317
What are the key features of lateral epicondylitis?
* Pain and tenderness localized to the lateral epicondyle * Pain worse on wrist extension against resistance with the elbow extended * Pain worse with supination of the forearm with the elbow extended * Episodes typically last between 6 months and 2 years * Acute pain for 6-12 weeks
318
What is the typical duration of acute pain in lateral epicondylitis?
6-12 weeks ## Footnote Episodes of pain can last longer, from 6 months to 2 years.
319
Fill in the blank: Lateral epicondylitis typically follows _______ activity.
[unaccustomed]
320
What are some management options for lateral epicondylitis?
* Advice on avoiding muscle overload * Simple analgesia * Steroid injection * Physiotherapy
321
A 24-year-old male presents to the emergency department with a painful right knee associated with lethargy and feverish symptoms. His past medical history includes a Chlamydia trachomatis infection two weeks previously. Observations show: Respiratory rate 17 breath/min Heart rate 84 beats/min Blood pressure 122/76mmHg Temp 37.3ºC Oxygen saturations 97% on room air Which of the following would most likely be observed in a sample of synovial fluid taken from this patient's knee?
The correct answer is sterile synovial fluid with a high white blood cell count. The patient's presentation is suggestive of reactive arthritis, a seronegative spondyloarthritis classically associated with oligoarthritis of the lower limbs following a gastrointestinal or urogenital infection 1-4 weeks previously. The pathological process is aseptic, does not involve salt crystal formation, but is likely to cause increased white blood cells in the fluid (mostly polymorphonuclear leukocytes).
322
What is one of the most common haematological manifestations of SLE?
Lymphopenia is one of the most common haematological manifestations of SLE, occurring in 50-80% of patients. The mechanism is thought to be multifactorial, including increased apoptosis of lymphocytes, anti-lymphocyte antibodies, and bone marrow suppression. Lymphopenia is so characteristic of SLE that it is included in both the American College of Rheumatology (ACR) and the Systemic Lupus International Collaborating Clinics (SLICC) classification criteria for SLE. It is often one of the earliest haematological abnormalities detected and can fluctuate with disease activity. A lymphocyte count below 1.5 × 10^9/L is considered lymphopenia in adults and is a useful diagnostic clue in patients with suspected SLE.
323
What is discoid lupus erythematosus?
A benign disorder generally seen in younger females
324
What percentage of discoid lupus erythematosus cases progress to systemic lupus erythematosus?
Less than 5%
325
What are the characteristic features of discoid lupus erythematosus?
Erythematous, raised rash; sometimes scaly
326
What is the suspected aetiology of discoid lupus erythematosus?
Autoimmune
327
Where are lesions from discoid lupus erythematosus more commonly found?
Face, neck, ears, and scalp
328
What are the healing outcomes of lesions from discoid lupus erythematosus?
Atrophy, scarring, pigmentation
329
What management options are available for discoid lupus erythematosus?
Topical steroid cream; oral antimalarials (e.g., hydroxychloroquine) as second-line
330
What should be avoided to manage discoid lupus erythematosus?
Sun exposure
331
True or False: Discoid lupus erythematosus is commonly seen in older males.
False
332
Fill in the blank: Discoid lupus erythematosus is characterized by _______ keratin plugs.
Follicular
333
What may be a consequence of scarring from discoid lupus erythematosus?
Scarring alopecia
334
24-year-old comes to see you in the GP surgery. Over the last 24 hours, his left knee has become increasingly red, swollen, and painful. He has no medical history but does admit to what he describes as a 'chaotic weekend lifestyle' comprising multiple sexual partners and recreational cocaine use. This had been the norm for him, on and off, for the last two years. He has a mild fever but vitals are otherwise stable. You refer him to the Emergency Department for further investigations. What is the most likely morphology to be found in the analysis of his knee aspirate?
Gram negative diplococci is the correct answer. The most likely organism to cause septic arthritis in young adults who are sexually active is Neisseria gonorrhoeae, subsequent to disseminated infection. This bacterium appears as Gram-negative diplococci. A single hot, swollen, painful knee joint, with accompanying systemic upset (e.g. fever), is likely to be septic arthritis.
335
Disseminated gonococcal infection typically presents with a classic triad:
tenosynovitis, dermatitis (characterised by pustular skin lesions), and migratory polyarthritis,
336
The risk factors for congenital hip dislocation include:
Female gender Breech presentation Family history Firstborn Oligohydramnios
337
Which hip is most common for congenital hip dislocation include and how is it tested?
It is more common on the left side and is tested for using the Barlow and Ortolani tests which form part of the baby check. For babies who are at risk of congenital hip dislocation an ultrasound examination can be conducted to screen for the condition.
338
What is the primary motor function of the femoral nerve?
Knee extension, thigh flexion
339
What areas does the femoral nerve provide sensory innervation to?
Anterior and medial aspect of the thigh and lower leg
340
What are typical mechanisms of injury for the femoral nerve?
Hip and pelvic fractures, stab/gunshot wounds
341
What is the primary motor function of the obturator nerve?
Thigh adduction
342
What area does the obturator nerve provide sensory innervation to?
Medial thigh
343
What is a common mechanism of injury for the obturator nerve?
Anterior hip dislocation
344
What is the primary motor function of the lateral cutaneous nerve of the thigh?
None
345
What areas does the lateral cutaneous nerve of the thigh provide sensory innervation to?
Lateral and posterior surfaces of the thigh
346
What condition can result from compression of the lateral cutaneous nerve near the ASIS?
Meralgia paraesthetica
347
What are the symptoms of meralgia paraesthetica?
Pain, tingling and numbness in the distribution of the lateral cutaneous nerve
348
What is the primary motor function of the tibial nerve?
Foot plantarflexion and inversion
349
What area does the tibial nerve provide sensory innervation to?
Sole of foot
350
What are common mechanisms of injury for the tibial nerve?
Popliteal lacerations, posterior knee dislocation
351
What is the primary motor function of the common peroneal nerve?
Foot dorsiflexion and eversion
352
What muscle does the common peroneal nerve innervate?
Extensor hallucis longus
353
What area does the common peroneal nerve provide sensory innervation to?
Dorsum of the foot and the lower lateral part of the leg
354
Where does injury often occur for the common peroneal nerve?
At the neck of the fibula
355
What can result from a tightly applied lower limb plaster cast on the common peroneal nerve?
Foot drop
356
What is the primary motor function of the superior gluteal nerve?
Hip abduction
357
What is the sensory function of the superior gluteal nerve?
None
358
What are common mechanisms of injury for the superior gluteal nerve?
Misplaced intramuscular injection, hip surgery, pelvic fracture, posterior hip dislocation
359
What clinical sign results from injury to the superior gluteal nerve?
Positive Trendelenburg sign
360
What is the primary motor function of the inferior gluteal nerve?
Hip extension and lateral rotation
361
What is the sensory function of the inferior gluteal nerve?
None
362
How is the inferior gluteal nerve typically injured?
In association with the sciatic nerve
363
What are symptoms of injury to the inferior gluteal nerve?
Difficulty rising from seated position, can't jump, can't climb stairs
364
What has revolutionized the management of rheumatoid arthritis (RA) in the past decade?
The introduction of disease-modifying therapies ## Footnote Disease-modifying therapies (DMARDs) are crucial in altering the course of RA.
365
When should patients with evidence of joint inflammation start treatment?
As soon as possible with a combination of disease-modifying drugs (DMARD) ## Footnote Early intervention is key to managing RA effectively.
366
What does NICE recommend for initial therapy of RA?
DMARD monotherapy +/- a short-course of bridging prednisolone ## Footnote Dual DMARD therapy was previously advocated but is no longer the initial recommendation.
367
What is the most widely used DMARD?
Methotrexate ## Footnote Methotrexate requires monitoring of FBC & LFTs due to potential side effects.
368
What are the essential monitoring parameters for methotrexate?
FBC & LFTs ## Footnote Monitoring is critical because of the risks of myelosuppression and liver cirrhosis.
369
List three other DMARD options besides methotrexate.
* Sulfasalazine * Leflunomide * Hydroxychloroquine ## Footnote Hydroxychloroquine is only considered for mild or palindromic disease.
370
How does NICE recommend assessing response to treatment in RA?
Using a combination of CRP and disease activity scores such as DAS28 ## Footnote This helps in evaluating the effectiveness of the treatment.
371
What is a common management strategy for flares of RA?
Corticosteroids - oral or intramuscular ## Footnote Corticosteroids help reduce inflammation during flares.
372
What is the current indication for starting a TNF-inhibitor?
An inadequate response to at least two DMARDs including methotrexate ## Footnote TNF-inhibitors are used when standard DMARD therapy is insufficient.
373
What type of drug is etanercept?
Recombinant human protein, acts as a decoy receptor for TNF-α ## Footnote It is administered subcutaneously and has risks including demyelination.
374
How does infliximab function?
Monoclonal antibody that binds to TNF-α and prevents it from binding with TNF receptors ## Footnote Administered intravenously, it also carries risks like reactivation of tuberculosis.
375
What is adalimumab?
A monoclonal antibody administered subcutaneously ## Footnote It is used to inhibit TNF-α similar to infliximab.
376
What is the mechanism of action of rituximab?
Anti-CD20 monoclonal antibody resulting in B-cell depletion ## Footnote Rituximab is given as two 1g intravenous infusions two weeks apart.
377
What is the infusion reaction rate for rituximab?
Common ## Footnote Patients receiving rituximab often experience infusion reactions.
378
What is the function of abatacept?
A fusion protein that modulates a key signal for T lymphocyte activation ## Footnote This leads to decreased T-cell proliferation and cytokine production.
379
Is abatacept currently recommended by NICE?
No ## Footnote Despite its mechanism, abatacept is not currently recommended for use in RA treatment.
380
What is a common site of fracture in elderly females?
Hip fracture ## Footnote Particularly in those with osteoporosis
381
What is a major risk in displaced hip fractures?
Avascular necrosis ## Footnote Due to disruption of blood supply to the femoral head
382
What are the classic signs of a hip fracture?
Pain, shortened leg, externally rotated leg ## Footnote These symptoms are indicative of a hip fracture
383
Can patients with non-displaced neck of femur fractures weight bear?
Yes ## Footnote They may be able to weight bear despite the fracture
384
What are the two main classifications of hip fractures based on location?
Intracapsular and extracapsular ## Footnote Intracapsular fractures are further divided into subcapital
385
What is the dividing line for extracapsular hip fractures?
The lesser trochanter ## Footnote This line differentiates between trochanteric and subtrochanteric fractures
386
What is the Garden classification system used for?
Classifying hip fractures ## Footnote It includes types I to IV based on stability and displacement
387
What characterizes a Type I Garden fracture?
Stable fracture with impaction in valgus ## Footnote It is a non-displaced fracture
388
What characterizes a Type II Garden fracture?
Complete fracture but undisplaced ## Footnote The bone remains in its normal position
389
What characterizes a Type III Garden fracture?
Displaced fracture with boney contact ## Footnote Usually rotated and angulated
390
What characterizes a Type IV Garden fracture?
Complete boney disruption ## Footnote There is no boney contact
391
Which types of fractures most commonly disrupt blood supply?
Types III and IV ## Footnote They are associated with higher risk of avascular necrosis
392
What is the recommended treatment for an undisplaced intracapsular hip fracture?
Internal fixation or hemiarthroplasty if unfit ## Footnote Treatment options depend on the patient's fitness
393
What does NICE recommend for displaced intracapsular hip fractures?
Replacement arthroplasty (total hip replacement or hemiarthroplasty) ## Footnote Total hip replacement is preferred if patients meet certain criteria
394
What are the criteria for preferring total hip replacement over hemiarthroplasty?
* Able to walk independently outdoors with a stick * Not cognitively impaired * Medically fit for anaesthesia ## Footnote Patients should be assessed against these criteria
395
What is the management for stable intertrochanteric fractures?
Dynamic hip screw ## Footnote This is a common surgical intervention
396
What is the management for reverse oblique, transverse or subtrochanteric fractures?
Intramedullary device ## Footnote This is used to stabilize the fracture
397
What is osteogenesis imperfecta commonly known as?
Brittle bone disease
398
What type of disorders does osteogenesis imperfecta represent?
Disorders of collagen metabolism
399
What is the most common and milder form of osteogenesis imperfecta?
Type 1
400
What inheritance pattern does osteogenesis imperfecta type 1 follow?
Autosomal dominant
401
What is the primary abnormality in osteogenesis imperfecta type 1?
Abnormality in type 1 collagen due to decreased synthesis of pro-alpha 1 or pro-alpha 2 collagen polypeptides
402
At what age does osteogenesis imperfecta typically present?
Childhood
403
What is a common symptom of osteogenesis imperfecta related to fractures?
Fractures following minor trauma
404
What eye feature is often associated with osteogenesis imperfecta?
Blue sclera
405
What type of hearing issue can occur due to osteogenesis imperfecta?
Deafness secondary to otosclerosis
406
What dental issue is common in patients with osteogenesis imperfecta?
Dental imperfections
407
What are the typical results for calcium, phosphate, parathyroid hormone, and ALP in osteogenesis imperfecta?
Usually normal
408
What is Raynaud's phenomenon?
An exaggerated vasoconstrictive response of the digital arteries and cutaneous arterioles to cold or emotional stress ## Footnote It may be classified as primary (Raynaud's disease) or secondary (Raynaud's phenomenon).
409
What age group is most commonly affected by Raynaud's disease?
Typically presents in young women around 30 years old
410
What are some secondary causes of Raynaud's phenomenon?
* Connective tissue disorders * Scleroderma (most common) * Rheumatoid arthritis * Systemic lupus erythematosus * Leukaemia * Type I cryoglobulinaemia * Cold agglutinins * Use of vibrating tools * Drugs: oral contraceptive pill, ergot * Cervical rib
411
What factors suggest an underlying connective tissue disease in Raynaud's phenomenon?
* Onset after 40 years * Unilateral symptoms * Rashes * Presence of autoantibodies * Features suggesting rheumatoid arthritis or SLE (e.g., arthritis, recurrent miscarriages) * Digital ulcers * Calcinosis * Very rarely: chilblains
412
What is the management recommendation for patients with suspected secondary Raynaud's phenomenon?
All patients should be referred to secondary care
413
What is the first-line treatment for Raynaud's phenomenon?
Calcium channel blockers, e.g., nifedipine
414
What is the effect duration of IV prostacyclin (epoprostenol) infusions in Raynaud's phenomenon?
Effects may last several weeks to months
415
True or False: Raynaud's disease is more common in men than women.
False
416
Fill in the blank: Scleroderma is the _______ cause of secondary Raynaud's phenomenon.
most common
417
What is Azathioprine metabolised to?
Mercaptopurine ## Footnote Mercaptopurine is a purine analogue that inhibits purine synthesis.
418
What test may be needed for individuals prone to azathioprine toxicity?
Thiopurine methyltransferase (TPMT) test ## Footnote This test helps identify individuals who may experience adverse reactions to azathioprine.
419
List three adverse effects of Azathioprine.
* Bone marrow depression * Nausea/vomiting * Pancreatitis ## Footnote Additional risks include increased risk of non-melanoma skin cancer.
420
What should be done if infection or bleeding occurs while on Azathioprine?
Consider a full blood count ## Footnote This helps monitor for bone marrow depression.
421
What significant interaction may occur with Azathioprine?
Allopurinol ## Footnote Lower doses of azathioprine should be used if taken with allopurinol.
422
Is Azathioprine considered safe to use in pregnancy?
Yes ## Footnote Data show no increased risk of congenital malformations at standard doses.
423
How does Azathioprine compare to mycophenolate, methotrexate, and cyclophosphamide in pregnancy?
Azathioprine is considered safer ## Footnote Mycophenolate, methotrexate, and cyclophosphamide are contraindicated in pregnancy.
424
What is a greater risk to both mother and fetus than azathioprine therapy during pregnancy?
Uncontrolled SLE ## Footnote Systemic lupus erythematosus (SLE) can pose significant risks if not managed.
425
Fill in the blank: Azathioprine is a _______ that inhibits purine synthesis.
purine analogue
426
What classification divides hypersensitivity reactions into 4 types?
The Gell and Coombs classification ## Footnote This classification helps in understanding the mechanisms and examples of different hypersensitivity reactions.
427
What is the mechanism of Type I hypersensitivity?
Antigen reacts with IgE bound to mast cells ## Footnote Type I hypersensitivity is often associated with allergic reactions.
428
Give two examples of Type I hypersensitivity reactions.
• Anaphylaxis • Atopy (e.g. asthma, eczema, and hayfever) ## Footnote These conditions are characterized by immediate allergic responses.
429
What is the mechanism of Type II hypersensitivity?
IgG or IgM binds to antigen on cell surface ## Footnote This type of hypersensitivity involves antibodies reacting with cells.
430
List three examples of Type II hypersensitivity.
• Autoimmune haemolytic anaemia • ITP • Goodpasture's syndrome ## Footnote These conditions involve immune responses against the body's own cells.
431
What is the mechanism of Type III hypersensitivity?
Free antigen and antibody (IgG, IgA) combine ## Footnote This type is associated with immune complex formation.
432
Name two examples of Type III hypersensitivity.
• Serum sickness • Systemic lupus erythematosus ## Footnote These conditions result from immune complexes causing tissue damage.
433
What is the mechanism of Type IV hypersensitivity?
T-cell mediated ## Footnote This type involves delayed immune responses and does not involve antibodies.
434
Give two examples of Type IV hypersensitivity reactions.
• Tuberculosis / tuberculin skin reaction • Graft versus host disease ## Footnote These reactions typically manifest after a delay, unlike Types I-III.
435
What is the newly added Type V hypersensitivity characterized by?
Antibodies that recognise and bind to the cell surface receptors ## Footnote This type can either stimulate or block ligand binding.
436
List two examples of Type V hypersensitivity.
• Graves' disease • Myasthenia gravis ## Footnote These conditions involve antibodies affecting receptor function.
437
What type of pain is characteristic of osteoarthritis?
Pain exacerbated by exercise and relieved by rest ## Footnote Reduction in internal rotation is often the first sign
438
What are the risk factors for osteoarthritis?
Age, obesity and previous joint problems ## Footnote These factors increase the likelihood of developing osteoarthritis
439
What is a common symptom of inflammatory arthritis?
Pain in the morning ## Footnote This type of arthritis is often associated with systemic features and raised inflammatory markers
440
What may cause referred lumbar spine pain?
Femoral nerve compression may cause referred pain in the hip ## Footnote The femoral nerve stretch test may be positive if it is trapped
441
How is the femoral nerve stretch test performed?
Lie the patient prone, extend the hip joint with a straight leg, then bend the knee ## Footnote This stretches the femoral nerve and will cause pain if it is trapped
442
What condition is associated with greater trochanteric pain syndrome?
Trochanteric bursitis ## Footnote Caused by repeated movement of the fibroelastic iliotibial band
443
What are the symptoms of greater trochanteric pain syndrome?
Pain and tenderness over the lateral side of thigh ## Footnote Most common in women aged 50-70 years
444
What causes meralgia paraesthetica?
Compression of lateral cutaneous nerve of thigh ## Footnote Typically presents as burning sensation over antero-lateral aspect of thigh
445
What are the onset symptoms of avascular necrosis?
Symptoms may be of gradual or sudden onset ## Footnote May follow high dose steroid therapy or previous hip fracture or dislocation
446
What condition is common in pregnancy related to pubic symphysis?
Pubic symphysis dysfunction ## Footnote Ligament laxity increases in response to hormonal changes of pregnancy
447
What are the symptoms of pubic symphysis dysfunction?
Pain over the pubic symphysis with radiation to the groins and medial aspects of the thighs ## Footnote A waddling gait may be seen
448
What is transient idiopathic osteoporosis?
An uncommon condition sometimes seen in the third trimester of pregnancy ## Footnote Associated with groin pain and limited range of movement in the hip
449
What may be elevated in patients with transient idiopathic osteoporosis?
ESR may be elevated ## Footnote Patients may be unable to weight bear
450
What classification system is used for growth plate fractures?
Salter-Harris system ## Footnote The Salter-Harris system categorizes growth plate fractures based on their injury pattern.
451
What is a Type I Salter-Harris fracture?
Fracture through the physis only (x-ray often normal) ## Footnote Type I fractures may not show any obvious signs on an x-ray.
452
What characterizes a Type II Salter-Harris fracture?
Fracture through the physis and metaphysis ## Footnote This type of fracture is more common and usually identifiable on x-rays.
453
What is a Type III Salter-Harris fracture?
Fracture through the physis and epiphysis to include the joint ## Footnote Type III fractures can affect joint function and may require careful management.
454
What defines a Type IV Salter-Harris fracture?
Fracture involving the physis, metaphysis and epiphysis ## Footnote These fractures are complex and can have significant implications for growth.
455
What is a Type V Salter-Harris fracture?
Crush injury involving the physis (x-ray may resemble type I, and appear normal) ## Footnote Type V fractures can be subtle and may require clinical assessment beyond x-rays.
456
Why is it important to perform a chest X-ray before starting biologics for rheumatoid arthritis?
To look for TB prior to starting treatment as biologics can cause reactivation. ## Footnote Reactivation of tuberculosis is a significant risk when using immunosuppressive therapies.
457
What is a scaphoid fracture?
A type of wrist fracture typically arising from a fall onto an outstretched hand (FOOSH)
458
What causes a scaphoid fracture?
Falling onto an outstretched hand (FOOSH) and contact sports such as football or rugby
459
What percentage of blood supply to the scaphoid is derived from the dorsal carpal branch?
Around 80%
460
What is the risk associated with the interruption of blood supply to the scaphoid?
Avascular necrosis of the scaphoid
461
What are common symptoms of a scaphoid fracture?
* Pain along the radial aspect of the wrist, at the base of the thumb * Loss of grip / pinch strength
462
What is the point of maximal tenderness in a scaphoid fracture?
Over the anatomical snuffbox
463
What is the sensitivity and specificity of the anatomical snuffbox test?
Sensitivity around 90-95%, specificity <40%
464
What signs may indicate a scaphoid fracture?
* Wrist joint effusion * Pain elicited by telescoping of the thumb * Tenderness of the scaphoid tubercle * Pain on ulnar deviation of the wrist
465
What is the diagnostic probability of clinical examination when specific signs are positive?
Sensitivity 100%; specificity 74%
466
What imaging should be requested for a suspected scaphoid fracture?
Plain film radiographs of the wrist in anterior-posterior and lateral view
467
What are the 'scaphoid views' in radiography?
* Posterioranterior (PA) * Lateral * Oblique (wrist pronated at 45º) * Ziter view (PA with wrist in ulnar deviation and beam angulated at 20º)
468
What is the sensitivity of plain film radiographs in the first week of injury?
Only 80%
469
What is the superior imaging method compared to plain film radiographs?
CT scan
470
What is considered the definite investigation to confirm or exclude a scaphoid fracture diagnosis?
MRI
471
What did NICE guidance from 2016 suggest regarding MRI use for scaphoid fractures?
MRI should be considered the first-line imaging following clinical examination
472
What is the initial management of a suspected scaphoid fracture?
* Immobilisation with a Futuro splint or standard below-elbow backslab * Referral to orthopaedics * Clinical review with further imaging in 7-10 days if initial radiographs are inconclusive
473
What is the management for undisplaced fractures of the scaphoid waist?
Cast for 6-8 weeks, with union achieved in > 95%
474
What is required for displaced scaphoid waist fractures?
Surgical fixation
475
What is the complication of non-union in scaphoid fractures?
Pain and early osteoarthritis
476
What is another complication associated with scaphoid fractures?
Avascular necrosis
477
What is Dupuytren's contracture?
Fixed flexion contracture of the hand where the fingers bend towards the palm and cannot be fully extended. ## Footnote Caused by underlying contractures of the palmar aponeurosis.
478
Which fingers are most commonly affected by Dupuytren's contracture?
The ring finger and little finger. ## Footnote The middle finger may be affected in advanced cases, but the index finger and thumb are nearly always spared.
479
What is a common age demographic for Dupuytren's contracture?
Males over 40 years of age.
480
What are the associations with Dupuytren's contracture?
* Liver cirrhosis * Alcoholism * Many cases are idiopathic.
481
What is the treatment for Dupuytren's contracture?
Surgical fasciectomy. ## Footnote The condition may recur, and many surgical therapies are associated with risk of neurovascular damage.
482
What characterizes carpal tunnel syndrome?
Idiopathic median neuropathy at the carpal tunnel.
483
Which fingers exhibit altered sensation in carpal tunnel syndrome?
The lateral 3 fingers.
484
Which demographic is more commonly affected by carpal tunnel syndrome?
Females.
485
What are common symptoms of carpal tunnel syndrome?
Symptoms occur mainly at night in early stages. ## Footnote May include altered sensation and muscle wasting.
486
What is a diagnostic method for carpal tunnel syndrome?
Electrophysiological studies.
487
What is the surgical treatment for carpal tunnel syndrome?
Surgical decompression of the carpal tunnel by division of the flexor retinaculum.
488
What are Osler's nodes?
Painful, red, raised lesions found on the hands and feet due to deposition of immune complexes.
489
What are Bouchard's nodes?
Hard, bony outgrowths or gelatinous cysts on the proximal interphalangeal joints caused by osteoarthritis.
490
What are Heberden's nodes?
Permanent bony outgrowths at the fingertip resulting from chronic inflammation and pain.
491
What is a ganglion in the context of hand lumps?
Swelling in association with a tendon sheath, commonly near a joint, usually asymptomatic.
492
How is the fluid in a ganglion described?
Similar to synovial fluid but slightly more viscous.
493
What is the treatment for troublesome ganglions?
They may be excised.
494
List the four Kanavel's signs of flexor tendon sheath infection.
* Fixed flexion * Fusiform swelling * Tenderness * Pain on passive extension ## Footnote These signs are critical for identifying tendon sheath infections.
495
True or False: One of Kanavel's signs is pain on active extension.
False ## Footnote The correct sign is pain on passive extension, not active.
496
What is the initial respiratory feature of fat embolism?
Early persistent tachycardia ## Footnote Tachycardia is often one of the first signs presented in fat embolism cases.
497
What respiratory symptoms typically occur within 72 hours following injury in fat embolism?
Tachypnoea, dyspnoea, hypoxia ## Footnote These symptoms indicate respiratory distress as a result of fat embolism.
498
What dermatological feature is observed in fat embolism?
Red/brown impalpable petechial rash (usually only in 25-50%) ## Footnote This rash is a common but not universal symptom of fat embolism.
499
What other dermatological signs may be present in fat embolism?
Subconjunctival and oral haemorrhage/petechiae ## Footnote These signs can indicate systemic involvement of fat globules.
500
What central nervous system features are associated with fat embolism?
Confusion and agitation Retinal haemorrhages and intra-arterial fat globules on fundoscopy ## Footnote CNS symptoms can indicate severe cases of fat embolism.
501
What is a common finding in imaging for fat embolism?
May be normal ## Footnote Fat emboli often lodge distally, leading to normal imaging results.
502
What appearance may be seen on imaging at the periphery in cases of fat embolism?
Ground glass appearance ## Footnote This appearance can suggest the presence of fat emboli despite no vascular occlusion being visible.
503
What is the primary treatment for fat embolism?
Prompt fixation of long bone fractures ## Footnote Fixing fractures promptly can help reduce the risk of fat embolism.
504
What is the debate regarding medullary reaming in femoral shaft/tibial fractures?
Benefit vs. risk of increasing fat embolism risk (probably does not) ## Footnote The potential risks associated with medullary reaming are still under discussion.
505
What prophylaxis is recommended in the management of fat embolism?
DVT prophylaxis ## Footnote Deep vein thrombosis prophylaxis is important in managing patients at risk for embolism.
506
What type of care is generally provided to patients with fat embolism?
General supportive care ## Footnote Supportive care is crucial to manage symptoms and improve outcomes.
507
What is iliotibial band syndrome?
A common cause of lateral knee pain in runners, occurring in around 1 in 10 people who run regularly. ## Footnote Iliotibial band syndrome is often associated with overuse injuries in athletes.
508
What is a key feature of iliotibial band syndrome?
Tenderness 2-3cm above the lateral joint line. ## Footnote This tenderness is a significant indicator of the syndrome.
509
What are two management strategies for iliotibial band syndrome?
* Activity modification * Iliotibial band stretches ## Footnote These strategies aim to reduce pain and improve flexibility.
510
What should be done if iliotibial band syndrome is not improving?
Physiotherapy referral. ## Footnote Physiotherapy can provide tailored exercises and treatments to address the condition.
511
What is Behcet's syndrome?
A complex multisystem disorder associated with presumed autoimmune-mediated inflammation of the arteries and veins.
512
What are the classic triad of symptoms in Behcet's syndrome?
* Oral ulcers * Genital ulcers * Anterior uveitis
513
Where is Behcet's syndrome more common?
Eastern Mediterranean (e.g. Turkey)
514
In which gender is Behcet's syndrome more prevalent?
More common in men.
515
What age group is primarily affected by Behcet's syndrome?
Young adults (e.g. 20 - 40 years old)
516
Which human leukocyte antigen is associated with Behcet's syndrome?
HLA B51
517
What percentage of Behcet's syndrome patients have a positive family history?
Around 30%.
518
What are some additional features of Behcet's syndrome?
* Thrombophlebitis and deep vein thrombosis * Arthritis * Neurological involvement (e.g. aseptic meningitis) * GI symptoms (abdominal pain, diarrhea, colitis) * Erythema nodosum
519
Is there a definitive test for diagnosing Behcet's syndrome?
No definitive test.
520
How is the diagnosis of Behcet's syndrome primarily made?
Based on clinical findings.
521
What does a positive pathergy test indicate?
Suggestive of Behcet's syndrome (puncture site inflames and forms a small pustule).
522
What is a more specific detail about HLA B51?
It is a split antigen of HLA B5.
523
What are the significant risk factors for osteoporosis?
Advancing age and female sex ## Footnote The prevalence of osteoporosis increases from 2% at 50 years to more than 25% at 80 years in women.
524
List the main risk factors for osteoporosis used by major risk assessment tools such as FRAX.
* History of glucocorticoid use * Rheumatoid arthritis * Alcohol excess * History of parental hip fracture * Low body mass index * Current smoking
525
What are some other risk factors for osteoporosis?
* Sedentary lifestyle * Premature menopause * Caucasians and Asians * Endocrine disorders * Multiple myeloma, lymphoma * Gastrointestinal disorders * Chronic kidney disease * Osteogenesis imperfecta, homocystinuria
526
Name the endocrine disorders associated with osteoporosis.
* Hyperthyroidism * Hypogonadism * Growth hormone deficiency * Hyperparathyroidism * Diabetes mellitus
527
Which medications may worsen osteoporosis?
* SSRIs * Antiepileptics * Proton pump inhibitors * Glitazones * Long term heparin therapy * Aromatase inhibitors
528
What investigations are recommended for a patient diagnosed with osteoporosis?
* History and physical examination * Blood cell count * Sedimentation rate or C-reactive protein * Serum calcium * Albumin * Creatinine * Phosphate * Alkaline phosphatase * Liver transaminases * Thyroid function tests * Bone densitometry (DXA)
529
What are the reasons for further investigations in osteoporosis?
* Exclude diseases that mimic osteoporosis * Identify the cause of osteoporosis and contributory factors * Assess the risk of subsequent fractures * Select the most appropriate form of treatment
530
Fill in the blank: The minimum blood tests recommended for all patients with osteoporosis include _______.
full blood count, urea and electrolytes, liver function tests, bone profile, CRP, thyroid function tests
531
True or False: Osteoporosis is more prevalent in men than in women.
False
532
What is the prevalence of osteoporosis in women at age 50?
2%
533
What is the prevalence of osteoporosis in women at age 80?
More than 25%
534
List some gastrointestinal disorders that are risk factors for osteoporosis.
* Inflammatory bowel disease * Malabsorption (e.g. coeliac's) * Gastrectomy * Liver disease
535
What types of imaging are indicated for osteoporosis investigations?
* Lateral radiographs of lumbar and thoracic spine * DXA-based vertebral imaging
536
What tests are included in the investigation of secondary causes of osteoporosis?
* Protein immunoelectrophoresis * Urinary Bence-Jones proteins * 25OHD * PTH * Serum testosterone, SHBG, FSH, LH (in men) * Serum prolactin * 24 hour urinary cortisol/dexamethasone suppression test * Endomysial and/or tissue transglutaminase antibodies (coeliac disease) * Isotope bone scan * Markers of bone turnover * Urinary calcium excretion
537
What is plantar fasciitis?
The most common cause of heel pain seen in adults.
538
Where is the pain or tenderness usually worse in plantar fasciitis?
Around the medial calcaneal tuberosity.
539
What is one recommended management strategy for plantar fasciitis?
Rest the feet where possible.
540
What type of shoes should be worn to help manage plantar fasciitis?
Shoes with good arch support and cushioned heels.
541
Fill in the blank: Insoles and _______ may be helpful in managing plantar fasciitis.
heel pads
542
What is thoracic back pain considered?
A red flag that warrants further intervention
543
What are some serious underlying causes of thoracic back pain? List them.
* Degenerative disc disease (a prolapsed disc) * Skeletal disorders * Traumatic or spontaneous vertebral fractures * Vascular malformations * Metastasis
544
What are Anti-neutrophil cytoplasmic antibodies (ANCA) associated with?
They are associated with small-vessel vasculitides including: * granulomatosis with polyangiitis * eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome) * microscopic polyangiitis
545
What is the relationship between age and ANCA associated vasculitis?
ANCA associated vasculitis is more common with increasing age.
546
What are common findings in ANCA associated vasculitis?
Common findings include: * renal impairment * respiratory symptoms * systemic symptoms * vasculitic rash * ear, nose, and throat symptoms
547
What causes renal impairment in ANCA associated vasculitis?
It is caused by immune complex glomerulonephritis, leading to raised creatinine, haematuria, and proteinuria.
548
What respiratory symptoms are associated with ANCA associated vasculitis?
Respiratory symptoms include: * dyspnoea * haemoptysis
549
What systemic symptoms are seen in ANCA associated vasculitis?
Systemic symptoms include: * fatigue * weight loss * fever
550
What is a key characteristic of vasculitic rash in ANCA associated vasculitis?
The vasculitic rash is present only in a minority of patients.
551
What ear, nose, and throat symptom is commonly associated with ANCA associated vasculitis?
Sinusitis
552
What is the general approach to first-line investigations for ANCA associated vasculitis?
The approach includes: * urinalysis for haematuria and proteinuria * blood tests (urea, creatinine, full blood count, CRP) * ANCA testing * chest x-ray
553
What findings in blood tests are indicative of renal impairment?
Urea and creatinine levels are tested for renal impairment.
554
What may be seen in a full blood count for ANCA associated vasculitis?
Normocytic anaemia and thrombocytosis may be seen.
555
What chest x-ray findings may be present in ANCA associated vasculitis?
Nodular, fibrotic, or infiltrative lesions may be seen.
556
What are the two main types of ANCA?
The two main types are: * cytoplasmic (cANCA) * perinuclear (pANCA)
557
Which ANCA type is typically associated with granulomatosis with polyangiitis?
cANCA
558
Which ANCA type is typically associated with eosinophilic granulomatosis with polyangiitis?
pANCA
559
What is the target for cANCA?
Serine proteinase 3 (PR3)
560
What is the target for pANCA?
Myeloperoxidase (MPO)
561
What percentage of patients with granulomatosis with polyangiitis test positive for cANCA?
90%
562
What percentage of patients with eosinophilic granulomatosis with polyangiitis test positive for pANCA?
50%
563
What is the correlation between cANCA levels and disease activity?
There is some correlation between cANCA levels and disease activity.
564
Can pANCA levels be used to monitor disease activity?
No, pANCA levels cannot be used to monitor disease activity.
565
What is the mainstay of management for ANCA associated vasculitis?
Immunosuppressive therapy.
566
What specialist teams should manage suspected ANCA associated vasculitis?
Specialist teams such as: * renal * rheumatology * respiratory
567
What diagnostic procedure may be taken to aid the diagnosis of ANCA associated vasculitis?
Kidney or lung biopsies may be taken.
568
What chromosome encodes HLA antigens?
Chromosome 6 ## Footnote HLA antigens are crucial for the immune response.
569
Which HLA antigens are classified as class I?
HLA A, B, C ## Footnote Class I antigens present to CD8+ T cells.
570
Which HLA antigens are classified as class II?
DP, DQ, DR ## Footnote Class II antigens present to CD4+ T cells.
571
What disease is associated with HLA-A3?
Haemochromatosis ## Footnote Haemochromatosis involves iron overload in the body.
572
What disease is associated with HLA-B51?
Behcet's disease ## Footnote Behcet's disease is characterized by recurrent oral ulcers.
573
List diseases associated with HLA-B27.
* Ankylosing spondylitis * Reactive arthritis * Acute anterior uveitis * Psoriatic arthritis ## Footnote HLA-B27 is linked to several inflammatory diseases.
574
What disease is associated with HLA-DQ2/DQ8?
Coeliac disease ## Footnote Coeliac disease is an autoimmune disorder triggered by gluten.
575
List diseases associated with HLA-DR2.
* Narcolepsy * Goodpasture's ## Footnote Goodpasture's syndrome involves lung and kidney damage.
576
List diseases associated with HLA-DR3.
* Dermatitis herpetiformis * Sjogren's syndrome * Primary biliary cirrhosis ## Footnote HLA-DR3 is linked to autoimmune conditions.
577
What diseases are associated with HLA-DR4?
* Type 1 diabetes mellitus * Rheumatoid arthritis ## Footnote HLA-DR4 is particularly associated with the DRB1 gene variants.
578
True or False: Type 1 diabetes mellitus is more strongly associated with HLA-DR3 than HLA-DR4.
False ## Footnote Type 1 diabetes mellitus is associated with both but more strongly with HLA-DR4.
579
What is rheumatoid factor (RF)?
A circulating antibody (usually IgM) that reacts with the Fc portion of the patient's own IgG ## Footnote RF is recommended as the first-line antibody test for patients with suspected rheumatoid arthritis.
580
What tests can detect rheumatoid factor (RF)?
* Rose-Waaler test: sheep red cell agglutination * Latex agglutination test (less specific) ## Footnote These tests are used to identify the presence of RF in patients.
581
In what percentage of patients with rheumatoid arthritis is RF positive?
70-80% ## Footnote High titre levels of RF are associated with severe progressive disease but are not a marker of disease activity.
582
Which conditions are associated with a positive RF?
* Felty's syndrome (around 100%) * Sjogren's syndrome (around 50%) * Infective endocarditis (around 50%) * SLE (20-30%) * Systemic sclerosis (30%) * General population (5%) * Rarely: TB, HBV, EBV, leprosy ## Footnote These conditions can show a positive RF test result, complicating the diagnosis of rheumatoid arthritis.
583
What is the significance of anti-cyclic citrullinated peptide antibody in rheumatoid arthritis?
It may be detectable up to 10 years before the development of rheumatoid arthritis and allows for early detection suitable for aggressive anti-TNF therapy ## Footnote Anti-CCP has a sensitivity similar to RF (around 70%) but a higher specificity of 90-95%.
584
What does NICE recommend for patients suspected of having rheumatoid arthritis who are RF negative?
They should be tested for anti-CCP antibodies ## Footnote This recommendation aims to identify patients who may still have rheumatoid arthritis despite a negative RF test.
585
What imaging is recommended by NICE for patients with suspected rheumatoid arthritis?
X-rays of the hands and feet ## Footnote This imaging helps in assessing joint damage or changes associated with rheumatoid arthritis.
586
What are the bony components of the ankle joint?
Distal tibia, distal fibula, superior aspect of the talus
587
What structure forms the mortise of the ankle joint?
The configuration of the distal tibia and fibula with the body of the talus
588
What is the syndesmosis?
A binding structure that connects the distal tibia and fibula
589
Which ligaments compose the syndesmosis?
* Anterior inferior tibiofibular ligament (AITFL) * Posterior inferior tibiofibular ligament (PITFL) * Interosseous ligament (IOL) * Interosseous membrane
590
What ligaments secure the distal fibula to the talus?
* Anterior talofibular ligament (ATFL) * Posterior talofibular ligament (PTFL) * Calcaneofibular ligament
591
What is a sprain?
A stretching, partial or complete tear of a ligament
592
How are ankle sprains classified?
* High ankle sprains (involving syndesmosis) * Low ankle sprains (involving lateral collateral ligaments)
593
What is the most common mechanism of injury for low ankle sprains?
Inversion injury
594
What percentage of ankle sprains are classified as low ankle sprains?
>90%
595
What are the symptoms of low ankle sprains?
* Pain * Swelling * Tenderness over affected ligaments * Sometimes bruising
596
What are the classifications of low ankle sprains?
* Grade I (mild): Stretch or micro tear * Grade II (moderate): Partial tear * Grade III (severe): Complete tear
597
What is the pain and swelling presentation for Grade I low ankle sprains?
* Bruising and swelling: Minimal * Pain on weight bearing: Normal
598
What is the pain and swelling presentation for Grade II low ankle sprains?
* Bruising and swelling: Moderate * Pain on weight bearing: Minimal
599
What is the pain and swelling presentation for Grade III low ankle sprains?
* Bruising and swelling: Severe * Pain on weight bearing: Severe
600
What should be done according to the Ottawa ankle rules?
Radiographs should be performed as 15% of sprains are associated with a fracture
601
What is the RICE protocol for treating low ankle sprains?
* Rest * Ice * Compression * Elevation
602
What should be considered if symptoms of a low ankle sprain fail to settle?
MRI and possible surgical intervention
603
What is the mechanism of injury for high ankle sprains?
External rotation of the foot causing lateral push of the fibula
604
What percentage of ankle sprains are classified as high ankle sprains?
About 0.5%
605
What test is used to assess pain in high ankle sprains?
Hopkin's squeeze test
606
What might radiographs show in cases of high ankle sprains?
Widening of the tibiofibular joint (diastasis) or ankle mortise
607
What is the treatment for high ankle sprains without diastasis?
Non-weight-bearing orthosis or cast until pain subsides
608
What is warranted if there is diastasis in high ankle sprains?
Operative fixation
609
Isolated injuries to which ligament are rare?
Deltoid ligament
610
What should be checked for in cases of isolated deltoid ligament injuries?
Maisonneuve fracture of the proximal fibula
611
What is the treatment approach for isolated deltoid ligament injuries if the ankle mortise is anatomically reduced?
Treatment can be as per a low ankle sprain
612
What is the treatment approach if the ankle mortise is not anatomically reduced in deltoid ligament injuries?
Reduction and fixation may be warranted
613
What are features associated with ankylosing spondylitis?
Ankylosing spondylitis features - the 'A's Apical fibrosis Anterior uveitis Aortic regurgitation Achilles tendonitis AV node block Amyloidosis
614
What is ankylosing spondylitis associated with?
HLA-B27 associated spondyloarthropathy
615
In which demographic does ankylosing spondylitis typically present?
Males aged 20-30 years old
616
What is the typical sex ratio of ankylosing spondylitis?
3:1
617
What symptom commonly presents in young men with ankylosing spondylitis?
Lower back pain and stiffness of insidious onset
618
When is the stiffness in ankylosing spondylitis usually worse?
In the morning
619
What activity typically improves stiffness in ankylosing spondylitis?
Exercise
620
What nighttime symptom may patients with ankylosing spondylitis experience?
Pain at night which improves on getting up
621
What physical examination finding is associated with reduced lateral flexion?
Reduced lateral flexion
622
What test is used to assess forward flexion in ankylosing spondylitis?
Schober's test
623
In Schober's test, what is the distance between the two lines drawn?
10 cm above and 5 cm below the back dimples
624
How much should the distance increase during Schober's test for a positive result?
More than 5 cm
625
What is another clinical examination finding in ankylosing spondylitis?
Reduced chest expansion
626
What is a prolapsed lumbar disc usually associated with?
Clear dermatomal leg pain associated with neurological deficits.
627
What is a common characteristic of leg pain due to a prolapsed disc?
Leg pain usually worse than back pain.
628
When is pain often worse in cases of a prolapsed disc?
When sitting.
629
What sensory loss is associated with L3 nerve root compression?
Sensory loss over anterior thigh.
630
What are the features of L3 nerve root compression? (List 3)
* Weak hip flexion * Weak knee extension * Weak hip adduction
631
What reflex is reduced in L3 nerve root compression?
Knee reflex.
632
What test may be positive in L3 nerve root compression?
Positive femoral stretch test.
633
What sensory loss is associated with L4 nerve root compression?
Sensory loss anterior aspect of knee and medial malleolus.
634
What are the features of L4 nerve root compression? (List 3)
* Weak knee extension * Weak hip adduction * Reduced knee reflex
635
What test may be positive in L4 nerve root compression?
Positive femoral stretch test.
636
What sensory loss is associated with L5 nerve root compression?
Sensory loss dorsum of foot.
637
What weakness is observed in L5 nerve root compression?
Weakness in foot and big toe dorsiflexion.
638
What is the status of reflexes in L5 nerve root compression?
Reflexes intact.
639
What test may be positive in L5 nerve root compression?
Positive sciatic nerve stretch test.
640
What sensory loss is associated with S1 nerve root compression?
Sensory loss posterolateral aspect of leg and lateral aspect of foot.
641
What weakness is observed in S1 nerve root compression?
Weakness in plantar flexion of foot.
642
What reflex is reduced in S1 nerve root compression?
Reduced ankle reflex.
643
What test may be positive in S1 nerve root compression?
Positive sciatic nerve stretch test.
644
What is the management for a prolapsed disc similar to?
Management of other musculoskeletal lower back pain.
645
What is the first-line medication recommended by NICE for lower back pain without sciatica symptoms?
NSAIDs +/- proton pump inhibitors.
646
What should be considered if symptoms persist after 4-6 weeks?
Referral for consideration of MRI.
647
What is psoriatic arthropathy?
An inflammatory arthritis associated with psoriasis, classified as one of the seronegative spondyloarthropathies.
648
How does psoriatic arthropathy correlate with cutaneous psoriasis?
It correlates poorly and often precedes the development of skin lesions.
649
What percentage of patients with skin lesions develop psoriatic arthropathy?
10-20%.
650
Are males and females equally affected by psoriatic arthropathy?
Yes.
651
What are the common patterns of presentation for psoriatic arthropathy?
* Symmetric polyarthritis * Asymmetrical oligoarthritis * Sacroiliitis * DIP joint disease * Arthritis mutilans
652
Which type of arthritis is most common in psoriatic arthropathy?
Symmetric polyarthritis, seen in 30-40% of cases.
653
What is a historical belief regarding the most common type of psoriatic arthropathy?
Asymmetrical oligoarthritis was historically thought to be the most common type.
654
What are some other signs of psoriatic arthropathy?
* Psoriatic skin lesions * Enthesitis * Tenosynovitis * Dactylitis * Nail changes (pitting, onycholysis)
655
What is enthesitis?
Inflammation at the site of tendon and ligament insertion.
656
What may blood tests reveal in a patient with psoriatic arthropathy?
* Elevated CRP/ESR * Negative rheumatoid factor (RF) and anti-CCP antibodies * Positive HLA-B27 in some cases
657
What might X-ray findings show in psoriatic arthropathy?
* Erosions and new bone formation * Periostitis * 'Pencil-in-cup' appearance in advanced disease
658
How should psoriatic arthropathy be managed?
It should be managed by a rheumatologist.
659
What is the initial treatment for mild peripheral arthritis or mild axial disease?
NSAIDs alone.
660
What medication is commonly used for moderate to severe psoriatic arthropathy?
Methotrexate.
661
What are some biologics used in the treatment of psoriatic arthropathy?
* Ustekinumab (targets IL-12 and IL-23) * Secukinumab and ixekizumab (target IL-17) * Adalimumab (anti-TNF)
662
What is apremilast?
An oral phosphodiesterase type-4 (PDE4) inhibitor that modulates inflammatory mediators.
663
How does the prognosis of psoriatic arthropathy compare to rheumatoid arthritis?
Prognosis is generally better than in RA.
664
Can a subset of patients with psoriatic arthropathy develop progressive joint damage?
Yes, some may develop progressive joint damage and disability.
665
What is systemic sclerosis?
A condition of unknown aetiology characterised by hardened, sclerotic skin and other connective tissues. ## Footnote Systemic sclerosis is four times more common in females.
666
What are the three patterns of systemic sclerosis?
* Limited cutaneous systemic sclerosis * Diffuse cutaneous systemic sclerosis * Scleroderma (without internal organ involvement) ## Footnote Each pattern has distinct characteristics and associated antibodies.
667
What is a characteristic sign of limited cutaneous systemic sclerosis?
Raynaud's may be the first sign ## Footnote In this type, scleroderma predominantly affects the face and distal limbs.
668
What antibodies are associated with limited cutaneous systemic sclerosis?
Anti-centromere antibodies ## Footnote A subtype of this condition is CREST syndrome.
669
What does CREST syndrome stand for?
* Calcinosis * Raynaud's phenomenon * Esophageal dysmotility * Sclerodactyly * Telangiectasia ## Footnote CREST syndrome is a subtype of limited systemic sclerosis.
670
What is characterized by diffuse cutaneous systemic sclerosis?
Scleroderma affects trunk and proximal limbs predominantly ## Footnote It is associated with anti-scl-70 antibodies.
671
What is the most common cause of death in diffuse cutaneous systemic sclerosis?
Respiratory involvement ## Footnote This is seen in around 80% of cases, including interstitial lung disease (ILD) and pulmonary arterial hypertension (PAH).
672
What complications are associated with diffuse cutaneous systemic sclerosis?
* Renal disease * Hypertension ## Footnote Patients with renal disease should be started on an ACE inhibitor.
673
Which ACE inhibitor is typically used for renal disease in systemic sclerosis patients?
Captopril ## Footnote It is chosen due to its rapid onset and short half-life, allowing for dose titration.
674
What is the role of ACE inhibitors in systemic sclerosis?
They target the underlying mechanism by reducing efferent arteriolar vasoconstriction and limiting renin-angiotensin system activation ## Footnote This helps manage renal disease in affected patients.
675
What is the nature of scleroderma without internal organ involvement?
Tightening and fibrosis of skin ## Footnote It may manifest as plaques (morphoea) or linear.
676
What percentage of systemic sclerosis patients test positive for ANA?
90% ## Footnote This is a common laboratory finding in this condition.
677
What percentage of systemic sclerosis patients test positive for RF?
30% ## Footnote Rheumatoid factor (RF) positivity can occur in systemic sclerosis.
678
What is the association of anti-scl-70 antibodies?
Associated with diffuse cutaneous systemic sclerosis and a higher risk of severe interstitial lung disease ## Footnote This antibody is significant for prognosis.
679
What is the association of anti-centromere antibodies?
Associated with limited cutaneous systemic sclerosis ## Footnote This antibody indicates a different disease pattern than anti-scl-70.
680
What is lumbar spondylolisthesis?
A condition where a bone in the lower back (lumbar vertebra) slips forward out of alignment.
681
What can cause lumbar spondylolisthesis?
Caused by wear and tear, a stress fracture (spondylolysis), or trauma.
682
What are common symptoms of lumbar spondylolisthesis?
Lower back pain, numbness, or weakness that radiates down the legs.
683
How do symptoms of lumbar spondylolisthesis vary?
Symptoms can range from mild to severe.
684
What are the treatment options for lumbar spondylolisthesis?
Range from conservative measures like rest and physical therapy to surgical intervention.
685
Fill in the blank: Lumbar spondylolisthesis can result in _______.
[lower back pain, numbness, weakness]
686
True or False: Lumbar spondylolisthesis always requires surgical intervention.
False
687
What is lumbar spinal stenosis?
A condition in which the central canal is narrowed by tumour, disk prolapse or other degenerative changes ## Footnote It can lead to various symptoms including back pain and neuropathic pain.
688
What are common symptoms of lumbar spinal stenosis?
A combination of back pain, neuropathic pain, and symptoms mimicking claudication ## Footnote Symptoms may include difficulty walking, with positional elements affecting pain.
689
How does lumbar spinal stenosis differ from true claudication?
The positional element to the pain; sitting is better than standing ## Footnote Patients may also find it easier to walk uphill rather than downhill.
690
What is the most common underlying cause of lumbar spinal stenosis?
Degenerative disease ## Footnote This typically begins in the intervertebral disk.
691
What biochemical changes occur in the intervertebral disk during degeneration?
Cell death and loss of proteoglycan and water content ## Footnote These changes lead to progressive disk bulging and collapse.
692
What effect does disk degeneration have on the posterior facet joints?
Increased stress transfer leading to cartilaginous degeneration, hypertrophy, and osteophyte formation ## Footnote This is associated with thickening and distortion of the ligamentum flavum.
693
What are the components that contribute to the narrowing of the spinal canal in lumbar spinal stenosis?
Ventral disk bulging, osteophyte formation at the dorsal facet, and ligamentum flavum hypertrophy ## Footnote These factors combine to narrow the space available for neural elements.
694
What leads to the characteristic clinical signs and symptoms of lumbar spinal stenosis?
Compression of the nerve roots of the cauda equina ## Footnote This compression results in various neurological symptoms.
695
What imaging modality is best for diagnosing lumbar spinal stenosis?
MRI scanning ## Footnote MRI is effective in demonstrating canal narrowing.
696
What historical test was used to differentiate vascular claudicants from lumbar spinal stenosis?
Bicycle test ## Footnote True vascular claudicants were unable to complete this test.
697
What is a common surgical treatment for lumbar spinal stenosis?
Laminectomy ## Footnote This procedure involves removing the lamina to relieve pressure on the spinal canal.
698
What type of genetic disorder is Marfan's syndrome?
Marfan's syndrome is an autosomal dominant connective tissue disorder.
699
What gene is defective in Marfan's syndrome?
The defect is in the FBN1 gene on chromosome 15.
700
What protein does the FBN1 gene code for?
The FBN1 gene codes for the protein fibrillin-1.
701
What is the prevalence of Marfan's syndrome?
It affects around 1 in 3,000 people.
702
What is the arm span to height ratio indicative of Marfan's syndrome?
The arm span to height ratio is > 1.05.
703
List three skeletal features of Marfan's syndrome.
* Tall stature * High-arched palate * Arachnodactyly
704
What cardiovascular issues are associated with Marfan's syndrome?
* Dilation of the aortic sinuses * Aortic aneurysm * Aortic dissection * Aortic regurgitation * Mitral valve prolapse
705
What percentage of Marfan's syndrome patients experience mitral valve prolapse?
75%.
706
What are the lung-related complications of Marfan's syndrome?
Repeated pneumothoraces.
707
What eye condition is associated with Marfan's syndrome?
Upwards lens dislocation (superotemporal ectopia lentis).
708
What is a common ocular issue in Marfan's syndrome patients?
Myopia.
709
What is dural ectasia?
Ballooning of the dural sac at the lumbosacral level.
710
What was the life expectancy of patients with Marfan's syndrome in the past?
Around 40-50 years.
711
How has the life expectancy of Marfan's syndrome patients improved?
Through regular echocardiography monitoring and beta-blocker/ACE-inhibitor therapy.
712
What remains the leading cause of death in Marfan's syndrome patients?
Aortic dissection and other cardiovascular problems.
713
What condition can cause a raised ANCA?
Ulcerative colitis ## Footnote ANCA stands for anti-neutrophil cytoplasmic antibodies, and pANCA refers to perinuclear anti-neutrophil cytoplasmic antibodies, which are commonly associated with ulcerative colitis.
714
A normally fit and well 46-year-old woman is admitted to hospital with T11/12 discitis complicated by a T4 to L1 epidural abscess and a left psoas abscess. Surgery to drain them is carried out and intra-operative samples are cultured in the laboratory and grow Staphylococcus aureus. Additionally blood cultures on admission grow Staphylococcus aureus after 72 hours. Which of the following investigations is most appropriate in the first instance to look for a source of the infection given the pathogenic organism found?
Echocardiogram
715
What are some respiratory complications of rheumatoid arthritis?
* pulmonary fibrosis * pleural effusion * pulmonary nodules * bronchiolitis obliterans * methotrexate pneumonitis * pleurisy ## Footnote These complications can affect lung function and overall health in patients with RA.
716
What is the most common ocular complication associated with rheumatoid arthritis?
keratoconjunctivitis sicca ## Footnote This condition is characterized by dry eyes and can lead to discomfort and vision problems.
717
List some ocular complications of rheumatoid arthritis.
* keratoconjunctivitis sicca * episcleritis * scleritis * corneal ulceration * keratitis * steroid-induced cataracts * chloroquine retinopathy ## Footnote These conditions can significantly impact vision and eye health.
718
What is a common complication of rheumatoid arthritis that affects bone health?
osteoporosis ## Footnote Osteoporosis increases the risk of fractures in patients with RA.
719
How does rheumatoid arthritis relate to ischaemic heart disease?
RA carries a similar risk to type 2 diabetes mellitus ## Footnote This highlights the cardiovascular risks associated with chronic inflammatory conditions like RA.
720
What complications can rheumatoid arthritis increase the risk of?
* infections * depression ## Footnote These complications can worsen overall patient outcomes and quality of life.
721
What is Felty's syndrome?
RA + splenomegaly + low white cell count ## Footnote This syndrome is a rare complication of RA that can lead to additional health issues.
722
Name a less common complication of rheumatoid arthritis that involves protein deposits.
amyloidosis ## Footnote Amyloidosis can result in organ dysfunction due to the accumulation of amyloid proteins.
723
What does pANCA stand for?
Perinuclear anti-neutrophil cytoplasmic antibodies
724
In which condition is pANCA likely to be positive?
Ulcerative Colitis (UC)
725
In which condition is pANCA likely to be negative?
Crohn's Disease
726
True or False: pANCA is always positive in Crohn's Disease.
False
727
Fill in the blank: pANCA may be positive in _____ but likely negative in Crohn's.
Ulcerative Colitis
728
What are the Ottawa ankle rules used for?
To minimize unnecessary use of x-rays for ankle injuries ## Footnote The rules help determine if x-rays are needed based on specific criteria related to pain and tenderness.
729
When are x-rays necessary according to the Ottawa ankle rules?
If there is pain in the malleolar zone and: * Inability to weight bear for 4 steps * Tenderness over the distal tibia * Bone tenderness over the distal fibula ## Footnote These criteria help identify significant injuries that require imaging.
730
What classification systems exist for describing ankle fractures?
Potts, Weber, and AO systems ## Footnote These systems categorize fractures based on different anatomical and clinical criteria.
731
What is the Weber classification based on?
The level of the fibular fracture ## Footnote This classification helps in understanding the severity and implications of the fracture.
732
Describe Type A fractures in the Weber classification.
Fractures below the syndesmosis ## Footnote These are typically less severe and may have different management strategies.
733
What characterizes Type B fractures in the Weber classification?
Fractures starting at the level of the tibial plafond and may extend proximally to involve the syndesmosis ## Footnote These fractures can be more complex and may require careful evaluation.
734
What defines Type C fractures in the Weber classification?
Fractures above the syndesmosis which may damage the syndesmosis ## Footnote These fractures are often more serious and may necessitate surgical intervention.
735
What is a Maisonneuve fracture?
A spiral fibular fracture that leads to disruption of the syndesmosis and widening of the ankle joint ## Footnote This type of fracture often requires surgical repair due to its complexity.
736
What factors influence the management of ankle fractures?
Stability of the ankle joint and patient co-morbidities ## Footnote Different management strategies are applied based on these factors.
737
What is the initial management for all ankle fractures?
Prompt reduction to remove pressure on the overlying skin and prevent necrosis ## Footnote This step is crucial to avoid complications associated with skin integrity.
738
What is the typical management for young patients with unstable, high velocity, or proximal ankle injuries?
Usually require surgical repair, often using a compression plate ## Footnote Surgical intervention is more common in younger patients due to better bone quality.
739
How do elderly patients with ankle fractures typically fare?
Usually fare better with attempts at conservative management ## Footnote Their thin bone structure does not hold metalwork well, making surgery less favorable.
740
What is adhesive capsulitis commonly known as?
Frozen shoulder
741
Who is most commonly affected by adhesive capsulitis?
Middle-aged females
742
What is the aetiology of frozen shoulder?
Not fully understood
743
What percentage of diabetics may experience an episode of frozen shoulder?
Up to 20%
744
What feature of movement is more affected in adhesive capsulitis?
External rotation
745
In addition to external rotation, what other movements are affected in adhesive capsulitis?
Internal rotation and abduction
746
What types of movement are affected in patients with adhesive capsulitis?
Both active and passive movement
747
What are the three phases experienced by patients with adhesive capsulitis?
* Painful freezing phase * Adhesive phase * Recovery phase
748
What percentage of patients may experience bilateral adhesive capsulitis?
Up to 20%
749
How long does an episode of adhesive capsulitis typically last?
Between 6 months and 2 years
750
What is the usual method for diagnosing adhesive capsulitis?
Clinical diagnosis
751
When might imaging be required in the diagnosis of adhesive capsulitis?
For atypical or persistent symptoms
752
What has been shown to improve outcomes in the long-term for adhesive capsulitis?
No single intervention
753
What are some treatment options for adhesive capsulitis?
* NSAIDs * Physiotherapy * Oral corticosteroids * Intra-articular corticosteroids
754
What does osteomalacia describe?
Softening of the bones secondary to low vitamin D levels.
755
What is the term used for osteomalacia in growing children?
Rickets.
756
What are the main causes of osteomalacia?
* Vitamin D deficiency * Malabsorption * Lack of sunlight * Diet * Chronic kidney disease * Drug induced (e.g. anticonvulsants) * Inherited (e.g. hypophosphatemic rickets) * Liver disease (e.g. cirrhosis) * Coeliac disease
757
What are common features of osteomalacia?
* Bone pain * Bone/muscle tenderness * Fractures (especially femoral neck) * Proximal myopathy (may lead to a waddling gait)
758
What blood test results are indicative of osteomalacia?
* Low vitamin D levels * Low calcium and phosphate (in around 30%) * Raised alkaline phosphatase (in 95-100% of patients)
759
What imaging findings may indicate osteomalacia?
Translucent bands (Looser's zones or pseudofractures).
760
What is the primary treatment for osteomalacia?
Vitamin D supplementation.
761
What may be required initially in the treatment of osteomalacia?
A loading dose of vitamin D.
762
What additional supplementation may be needed if dietary calcium is inadequate?
Calcium supplementation.
763
True or False: Osteomalacia can be caused by chronic kidney disease.
True.
764
Fill in the blank: Osteomalacia is characterized by decreased _______ mineral content.
bone.
765
What is the most common organism causing septic arthritis overall?
Staphylococcus aureus ## Footnote This organism is prevalent in general cases of septic arthritis.
766
Which organism is most common in young adults who are sexually active with septic arthritis?
Neisseria gonorrhoeae ## Footnote This is associated with disseminated gonococcal infection.
767
What is the most common cause of septic arthritis?
Hematogenous spread ## Footnote This can occur from distant bacterial infections such as abscesses.
768
In adults, what is the most common location for septic arthritis?
Knee ## Footnote The knee joint is frequently affected in adult cases.
769
What are the key features of septic arthritis?
Acute, swollen joint; restricted movement in 80% of patients; warm to touch/fluctuant; fever present in the majority ## Footnote These features assist in the clinical diagnosis of septic arthritis.
770
What is obligatory for the investigation of septic arthritis?
Synovial fluid sampling ## Footnote This should be performed prior to antibiotic administration if necessary.
771
What is the typical finding in synovial fluid in septic arthritis?
Leucocytosis with neutrophil predominance ## Footnote This indicates an inflammatory response in the joint.
772
What percentage of cases show negative gram staining in septic arthritis?
30-50% ## Footnote This highlights the limitations of gram staining in detecting organisms.
773
What is the recommendation for intravenous antibiotics in septic arthritis management?
Flucloxacillin or clindamycin if penicillin allergic ## Footnote These antibiotics cover Gram-positive cocci.
774
For how long is antibiotic treatment typically given for septic arthritis?
4-6 weeks ## Footnote This duration is suggested by the BNF.
775
After how many weeks are patients typically switched to oral antibiotics?
2 weeks ## Footnote This transition occurs after initial intravenous treatment.
776
What procedure is used to decompress the joint in septic arthritis?
Needle aspiration ## Footnote This helps relieve pressure and may assist in diagnosis.
777
What may be required if needle aspiration is insufficient?
Arthroscopic lavage ## Footnote This procedure may be necessary for thorough cleaning of the joint.
778
What are the three main causes of bony injury resulting in a fracture?
* Trauma (excessive forces applied to bone) * Stress related (repetitive low velocity injury) * Pathological (abnormal bone which fractures during minimal trauma) ## Footnote These causes highlight the various mechanisms leading to fractures.
779
What factors should be evaluated in the diagnosis of a fracture?
* Site and type of injury * Associated injuries * Distal neurovascular deficits ## Footnote Diagnosis may require clinical examination and radiographs of proximal and distal joints.
780
When assessing x-rays, what should be evaluated?
* Changes in length of the bone * Angulation of the distal bone * Rotational effects * Presence of foreign material (e.g., glass) ## Footnote These evaluations help in understanding the fracture's characteristics.
781
Define oblique fracture.
Fracture lies obliquely to long axis of bone ## Footnote This type of fracture may occur due to twisting forces.
782
What is a comminuted fracture?
> 2 fragments ## Footnote This indicates a severe fracture with multiple pieces of bone.
783
What characterizes a segmental fracture?
More than one fracture along a bone ## Footnote Typically indicates significant trauma.
784
Describe a transverse fracture.
Perpendicular to long axis of bone ## Footnote This type of fracture is often caused by direct impact.
785
What is a spiral fracture?
Severe oblique fracture with rotation along long axis of bone ## Footnote Often seen in twisting injuries.
786
What distinguishes an open fracture from a closed fracture?
An open fracture involves a wound that communicates with the fracture ## Footnote Closed fractures do not have an external wound.
787
What is the Gustilo and Anderson classification system used for?
Classifying open fractures ## Footnote This system helps in determining the severity and treatment needed.
788
What are the grades in the Gustilo and Anderson classification system?
* Grade 1: Low energy wound <1cm * Grade 2: >1cm wound with moderate soft tissue damage * Grade 3: High energy wound >1cm with extensive soft tissue damage * Grade 3A: Adequate soft tissue coverage * Grade 3B: Inadequate soft tissue coverage * Grade 3C: Associated arterial injury ## Footnote Each grade indicates increasing severity and complexity of treatment.
789
What are key points in the management of fractures?
* Immobilise the fracture including proximal and distal joints * Monitor and document neurovascular status * Manage infection including tetanus prophylaxis * IV broad spectrum antibiotics for open injuries * Thoroughly debride all open fractures * Open fractures should be debrided and lavaged within 6 hours ## Footnote Effective management is crucial to prevent complications.
790
What is the most common type of shoulder dislocation?
Anterior dislocation ## Footnote It may follow a fall on arm or shoulder.
791
What should always be checked in cases of shoulder dislocation?
Pulses and nerves, particularly AXILLARY ## Footnote The axillary nerve is commonly injured in shoulder dislocations.
792
What imaging study should always be performed for shoulder dislocation?
Radiograph ## Footnote This is essential for diagnosis.
793
What are the components of treatment for anterior shoulder dislocation?
Reduction, analgesia, and sling ## Footnote Reduction can be achieved by many methods.
794
What is the cause of posterior shoulder dislocation?
Seizure or electrocution ## Footnote This type of dislocation is rare.
795
What sign is associated with posterior shoulder dislocation on x-ray?
Lightbulb sign ## Footnote This sign is indicative of posterior dislocation.
796
To whom should a posterior shoulder dislocation be referred?
Orthopaedic surgeons ## Footnote Specialized care is often needed for this type of dislocation.
797
What is a Charcot joint also known as?
A neuropathic joint
798
What causes a Charcot joint?
Loss of sensation leading to joint disruption and damage
799
Historically, what was the most common cause of Charcot joints?
Neuropathy secondary to syphilis (tabes dorsalis)
800
In modern times, which patient population most commonly presents with Charcot joints?
Diabetics
801
How painful are Charcot joints typically compared to the degree of joint disruption?
They are typically a lot less painful than expected
802
What percentage of patients report some degree of pain in Charcot joints?
75%
803
What are common features of a Charcot joint?
* Swollen * Red * Warm
804
What happens to the affected joint as Charcot joint disease progresses?
The joint becomes unstable, leading to abnormal movements and increased risk of fractures and dislocations
805
What can progressive joint destruction in Charcot joints lead to?
Significant deformities
806
What is a common deformity associated with Charcot joints in the foot?
Collapsed arch, commonly referred to as 'rocker-bottom' foot
807
What secondary complications can arise from Charcot joints?
* Skin ulceration * Infection due to repeated trauma and poor wound healing
808
What is Froment's sign used to assess?
Ulnar nerve palsy ## Footnote It tests the function of the adductor pollicis muscle.
809
How is Froment's sign tested?
Hold a piece of paper between the thumb and index finger; if unable to hold it, flex the flexor pollicis longus compensates. ## Footnote This indicates ulnar nerve palsy.
810
What condition does Phalen's test assess?
Carpal tunnel syndrome ## Footnote It is more sensitive than Tinel's sign.
811
What is the procedure for Phalen's test?
Hold wrist in maximum flexion; positive if numbness in median nerve distribution occurs.
812
What does Tinel's sign assess?
Carpal tunnel syndrome ## Footnote It evaluates the median nerve.
813
How is Tinel's sign performed?
Tap the median nerve at the wrist; positive if tingling or electric-like sensations occur over median nerve distribution.
814
True or False: Phalen's test is less sensitive than Tinel's sign.
False
815
816
What is a rib fracture?
A break in the bony segment of any rib, often due to blunt trauma to the chest wall.
817
What are common causes of rib fractures?
Most rib fractures are caused by blunt trauma to the chest wall.
818
In major trauma cases, what percentage typically presents with chest injuries?
25% of major trauma cases.
819
What can cause spontaneous rib fractures?
Coughing or sneezing, usually in patients with osteoporosis, steroid use, or chronic obstructive pulmonary disease.
820
What are pathological rib fractures often associated with?
Cancer metastases, commonly from prostate cancer in men and breast cancer in women.
821
What is the most common symptom of a rib fracture?
Severe, sharp chest wall pain.
822
What exacerbates the pain associated with rib fractures?
Deep breaths or coughing.
823
What physical examination findings are common with rib fractures?
Significant chest wall tenderness and possible visible bruising.
824
What might auscultation reveal in cases of rib fractures?
Crackles or reduced breath sounds if there is an underlying lung injury.
825
What serious complication can arise from a rib fracture?
Pneumothorax.
826
What is flail chest?
A serious consequence of multiple rib fractures where two or more ribs are fractured along three or more consecutive ribs.
827
What happens to the flail segment during respiration?
It moves paradoxically, impairing ventilation of the lung on the side of injury.
828
What may be required for the treatment of flail chest?
Invasive ventilation and surgical fixation.
829
What is the best diagnostic test for rib fractures?
CT scan of the chest.
830
What is a limitation of chest x-rays in diagnosing rib fractures?
They provide suboptimal views and do not show surrounding soft tissue injury.
831
What should be done if rib fractures fail to heal after 12 weeks of conservative management?
Consider surgical fixation.
832
What is a key consideration for managing flail chest segments?
Urgently discuss with cardiothoracic surgery.
833
What is the primary management approach for most rib fractures?
Conservative management with good analgesia.
834
What can inadequate ventilation from rib fractures lead to?
Chest infections.
835
Fill in the blank: Rib fractures can occur ______ along the length of a rib.
singly or in multiple places.
836
True or False: Rib fractures can only occur due to blunt trauma.
False.
837
What is Perthes disease?
A childhood hip condition where the blood supply to the head of the femur is interrupted
838
What happens to the bone in Perthes disease?
The bone softens and becomes deformed
839
What are common symptoms of Perthes disease?
A limp, pain in the groin, thigh, or knee, and limited hip movement
840
At what ages does Perthes disease typically start?
Between ages 4 and 10
841
Is Perthes disease more common in boys or girls?
More common in boys
842
What occurs over several months to years in Perthes disease?
The blood supply returns, and the bone regrows and reshapes
843
What can be a long-term consequence of Perthes disease?
A poorly fitting joint and an increased risk of hip arthritis in adulthood
844
True or False: Perthes disease only affects adults.
False
845
Fill in the blank: Perthes disease affects the _______ of the hip joint.
head of the femur
846
What is usually seen in xray of perthes disease?
x-ray: early changes include widening of joint space, later changes include decreased femoral head size/flattening
847
What is the most common primary malignant bone tumour?
Osteosarcoma ## Footnote It is primarily seen in children and adolescents.
848
In which region of long bones does osteosarcoma most frequently occur?
Metaphyseal region ## Footnote This occurs prior to epiphyseal closure.
849
What percentage of osteosarcoma cases occur in the femur?
40% ## Footnote 20% occur in the tibia and 10% in the humerus.
850
What x-ray findings are characteristic of osteosarcoma?
Codman triangle and 'sunburst' pattern ## Footnote Codman triangle is due to periosteal elevation.
851
Which gene mutation significantly increases the risk of osteosarcoma?
Rb gene mutation ## Footnote There is a notable association with retinoblastoma.
852
Name two other predisposing factors for osteosarcoma.
* Paget's disease of the bone * Radiotherapy
853
What type of tumour is Ewing's sarcoma?
Small round blue cell tumour ## Footnote It is also seen mainly in children and adolescents.
854
Where does Ewing's sarcoma most frequently occur?
Pelvis and long bones ## Footnote It tends to cause severe pain.
855
What genetic alteration is associated with Ewing's sarcoma?
t(11;22) translocation ## Footnote This results in an EWS-FLI1 gene product.
856
What x-ray appearance is characteristic of Ewing's sarcoma?
'Onion skin' appearance
857
What is chondrosarcoma?
Malignant tumour of cartilage ## Footnote It most commonly affects the axial skeleton.
858
In which age group is chondrosarcoma more common?
Middle-age
859
What is the Kocher technique used for?
Shoulder reduction in patients with a recent anterior dislocation ## Footnote The Kocher technique is one of several methods for reducing shoulder dislocations without analgesia or sedation.
860
What type of shoulder dislocation is the Kocher technique specifically for?
Anterior shoulder dislocation ## Footnote In an anterior dislocation, the humeral head dislodges from the glenoid cavity of the scapula.
861
What occurs during an anterior shoulder dislocation?
The humeral head dislodges from the glenoid cavity of the scapula ## Footnote This dislocation causes significant pain and immobility in the affected shoulder.
862
What is a key characteristic of the Kocher technique?
The affected arm is bent at the elbow, pressed against the body, and rotated outwards until resistance is felt ## Footnote This technique is effective without the use of medication for pain relief.
863
What is the final step in the Kocher technique?
Turn the affected arm inwards slowly after lifting it forwards ## Footnote This motion is crucial for successful reduction of the dislocated shoulder.
864
What is a challenge in shoulder reduction techniques?
There is currently no established consensus on which technique is the most effective ## Footnote Different techniques may work better for different patients or circumstances.
865
Fill in the blank: The Kocher technique involves rotating the affected arm _______ until resistance is felt.
outwards ## Footnote This rotation is part of the process to realign the dislocated shoulder.
866
True or False: The Kocher technique requires sedation for the patient.
False ## Footnote The technique can be performed without the use of analgesia or sedation in selected patients.
867
What is one reason why the Kocher technique might be preferred?
It can be performed without medication for pain relief ## Footnote This can be beneficial in certain patient populations or settings.
868
What is atlantoaxial subluxation?
A rare complication of rheumatoid arthritis that can lead to cervical cord compression ## Footnote Atlantoaxial subluxation involves misalignment of the first two cervical vertebrae.
869
Why is atlantoaxial subluxation important?
It can lead to cervical cord compression ## Footnote Cervical cord compression can result in neurological deficits.
870
What imaging techniques are used to screen for atlantoaxial subluxation?
Anteroposterior and lateral cervical spine radiographs ## Footnote These radiographs help identify any misalignment before surgery.
871
What precautions should be taken before surgery for patients with atlantoaxial subluxation?
The patient should go to surgery in a C-spine collar and the neck should not be hyperextended on intubation ## Footnote These precautions help prevent further injury to the cervical spine during the surgical process.
872
What is facet joint pain?
A common type of back or neck pain caused by wear and tear, injury, or overuse of the small facet joints that connect your vertebrae. ## Footnote Facet joints are small stabilizing joints located between and behind adjacent vertebrae.
873
What are common symptoms of facet joint pain?
Localized tenderness, stiffness, muscle spasms, and pain that can spread to other areas such as the buttocks and legs for low back pain. ## Footnote Symptoms may vary in intensity and location depending on the affected area.
874
What is the primary focus of treatment for facet joint pain?
Conservative methods such as rest, physical therapy, exercise, medication, and sometimes steroid or anesthetic injections. ## Footnote These treatments aim to reduce pain and inflammation without invasive procedures.
875
Fill in the blank: Facet joint pain is caused by _______ changes, injury, or overuse.
degenerative
876
True or False: Facet joint pain can only occur in the lower back.
False
877
What types of injections might be used in the treatment of facet joint pain?
Steroid or anesthetic injections. ## Footnote These injections are used to help reduce inflammation and manage pain.
878
What type of pain is often associated with facet joint pain?
Dull ache localized to the spine.
879
What actions worsen facet joint pain?
Bending backward or standing for long periods.
880
What action relieves facet joint pain?
Bending forward.
881
How is disc prolapse pain typically described?
Sharp pain that can radiate to the limbs.
882
What conditions can disc prolapse pain resemble?
Sciatica.
883
What actions worsen disc prolapse pain?
Sitting, bending forward, or coughing.
884
What symptoms may accompany disc prolapse pain?
Numbness or weakness.
885
True or False: Symptoms of facet joint pain and disc prolapse pain do not overlap.
False.
886
Why is a professional diagnosis essential?
For proper treatment.
887
What is pseudogout?
A form of microcrystal synovitis caused by the deposition of calcium pyrophosphate dihydrate crystals in the synovium ## Footnote Also known as acute calcium pyrophosphate crystal deposition disease.
888
What age group is pseudogout strongly associated with?
Increasing age
889
What are some underlying risk factors for developing pseudogout at a younger age (< 60 years)?
* Haemochromatosis * Hyperparathyroidism * Low magnesium * Low phosphate * Acromegaly * Wilson's disease
890
Which joints are most commonly affected by pseudogout?
* Knee * Wrist * Shoulders
891
What type of crystals are found in joint aspiration for pseudogout?
Weakly-positively birefringent rhomboid-shaped crystals
892
What is a key x-ray finding in pseudogout?
Chondrocalcinosis
893
In the knee, how can chondrocalcinosis be observed on x-ray?
As linear calcifications of the meniscus and articular cartilage
894
What is the first step in managing pseudogout?
Aspiration of joint fluid to exclude septic arthritis
895
What medications are used in the management of pseudogout?
* NSAIDs * Intra-articular steroids * Intra-muscular steroids * Oral steroids
896
What is the primary diagnostic criterion for Chronic Fatigue Syndrome (CFS)?
Disabling fatigue affecting mental and physical function more than 50% of the time for at least 3 months in the absence of other diseases.
897
Which demographic is more commonly affected by Chronic Fatigue Syndrome?
Females
898
True or False: A past psychiatric history is a risk factor for Chronic Fatigue Syndrome.
False
899
List some recognized features of Chronic Fatigue Syndrome.
* Sleep problems (insomnia, hypersomnia, unrefreshing sleep) * Muscle and/or joint pains * Headaches * Painful lymph nodes without enlargement * Sore throat * Cognitive dysfunction (difficulty thinking, inability to concentrate, impairment of short-term memory) * Physical or mental exertion worsens symptoms * General malaise or 'flu-like' symptoms * Dizziness * Nausea * Palpitations
900
What do NICE guidelines recommend for the investigation of Chronic Fatigue Syndrome?
A large number of screening blood tests to exclude other pathologies.
901
What is included in the screening blood tests recommended by NICE for CFS?
* FBC * U&E * LFT * Glucose * TFT * ESR * CRP * Calcium * CK * Ferritin * Coeliac screening * Urinalysis
902
When is a diagnosis of Chronic Fatigue Syndrome typically made?
If symptoms persist for 3 months.
903
What should be done if the diagnostic criteria for Chronic Fatigue Syndrome are met?
Refer to a specialist CFS service.
904
What is energy management in the context of Chronic Fatigue Syndrome?
A self-management strategy for individuals to manage their activities within their energy limits, with healthcare professional support.
905
Why should exercise for people with ME/CFS be overseen by a specialist team?
To ensure safety and appropriateness of physical activity.
906
What does NICE say about graded exercise therapy for Chronic Fatigue Syndrome?
It is specifically not recommended.
907
What type of therapy does NICE recommend for Chronic Fatigue Syndrome?
Cognitive behavioural therapy, described as 'supportive' rather than curative.
908
How does the prognosis of Chronic Fatigue Syndrome differ in children?
CFS has a better prognosis in children.
909
What is the bimodal age distribution for Still's disease in adults?
15-25 years and 35-46 years
910
List three clinical features of Still's disease in adults.
* Arthralgia * Elevated serum ferritin * Rash: salmon-pink, maculopapular
911
What pattern does pyrexia typically follow in Still's disease?
Rises in the late afternoon/early evening
912
What accompanies the worsening of joint symptoms and rash in Still's disease?
Pyrexia
913
What is a common laboratory finding in Still's disease regarding rheumatoid factor and anti-nuclear antibody?
Both are negative
914
What is the sensitivity of the Yamaguchi criteria for diagnosing Still's disease?
93.5%
915
What is the first-line management for fever, joint pain, and serositis in Still's disease?
NSAIDs
916
How long should NSAIDs be trialed before adding steroids in the management of Still's disease?
At least a week
917
What is the role of steroids in the management of Still's disease?
They may control symptoms but won't improve prognosis
918
If symptoms persist in Still's disease, which therapies can be considered?
* Methotrexate * IL-1 therapy * Anti-TNF therapy
919
What is Ewing sarcoma?
A group of rare cancerous tumors in bones or soft tissues
920
What age group is typically affected by Ewing sarcoma?
People age 10 to 20
921
What are common symptoms of Ewing sarcoma?
Bone pain, swollen areas on bones, lumps that feel warm to the touch
922
What is the primary treatment for Ewing sarcoma?
Chemotherapy followed by surgery to remove the tumors
923
What is Ewing's sarcoma?
A small round blue cell tumour seen mainly in children and adolescents
924
In which areas of the body does Ewing's sarcoma occur most frequently?
Pelvis and long bones
925
What symptom is commonly associated with Ewing's sarcoma?
Severe pain
926
What genetic translocation is associated with Ewing's sarcoma?
t(11;22) translocation
927
What is the result of the t(11;22) translocation in Ewing's sarcoma?
EWS-FLI1 gene product
928
What characteristic appearance is seen on x-ray for Ewing's sarcoma?
'Onion skin' appearance
929
What does osteomalacia describe?
Softening of the bones secondary to low vitamin D levels leading to decreased bone mineral content
930
What term is used for osteomalacia occurring in growing children?
Rickets
931
What are the primary causes of osteomalacia?
* Vitamin D deficiency * Malabsorption * Lack of sunlight * Diet * Chronic kidney disease * Drug induced (e.g. anticonvulsants) * Inherited (e.g. hypophosphatemic rickets) * Liver disease (e.g. cirrhosis) * Coeliac disease
932
What are common features of osteomalacia?
* Bone pain * Bone/muscle tenderness * Fractures (especially femoral neck) * Proximal myopathy (may lead to a waddling gait)
933
What blood test findings are indicative of osteomalacia?
* Low vitamin D levels * Low calcium * Low phosphate (in around 30%) * Raised alkaline phosphatase (in 95-100% of patients)
934
What radiological finding is associated with osteomalacia?
Translucent bands (Looser's zones or pseudofractures)
935
What is the initial treatment for osteomalacia?
Vitamin D supplementation
936
In osteomalacia treatment, what may be needed initially?
A loading dose
937
What additional supplementation may be required if dietary intake is inadequate in osteomalacia?
Calcium supplementation
938
What is discitis?
Discitis is an infection in the intervertebral disc space. ## Footnote It can lead to serious complications such as sepsis or an epidural abscess.
939
What are common features of discitis?
* Back pain * Pyrexia * Rigors * Sepsis * Neurological features (e.g. changing lower limb neurology if an epidural abscess develops) ## Footnote Neurological features may indicate complications such as an epidural abscess.
940
What is the most common bacterial cause of discitis?
Staphylococcus aureus ## Footnote Other causes include viral infections and TB.
941
What imaging technique has the highest sensitivity for diagnosing discitis?
MRI ## Footnote CT-guided biopsy may be required to guide antimicrobial treatment.
942
What is the standard therapy duration for discitis?
Six to eight weeks of intravenous antibiotic therapy. ## Footnote The choice of antibiotic depends on identifying the organism with a positive culture.
943
What assessments should be made in patients with discitis?
Assess for endocarditis using transthoracic echo or transesophageal echo. ## Footnote Discitis is usually due to haematogenous seeding of the vertebrae.
944
What are the potential complications of discitis?
* Sepsis * Epidural abscess ## Footnote These complications can arise if discitis is not properly treated.
945
Fill in the blank: The most important factor in choosing an antibiotic for discitis is to identify the organism with a __________.
positive culture ## Footnote This can be obtained from blood culture or CT-guided biopsy.
946
True or False: Discitis can lead to neurological changes if an epidural abscess develops.
True ## Footnote Neurological changes may include alterations in lower limb function.
947
Why are testosterone blood tests important?
They are important when suspecting osteoporosis in a man.
948
What is a common cause of osteoporosis in men?
Hypogonadism.
949
How is hypogonadism classified?
It is classified as either hypergonadotropic or hypogonadotropic.
950
What characterizes hypergonadotropic hypogonadism?
Primary gonadal failure.
951
What characterizes hypogonadotropic hypogonadism?
Secondary to a defect in the hypothalamic-pituitary axis.
952
What are the two roles of androgens on male bone metabolism?
They stimulate bone formation during puberty and prevent bone resorption during and after puberty.
953
Fill in the blank: _______ is a common cause of osteoporosis in men.
[Hypogonadism]
954
True or False: Androgens only stimulate bone formation during puberty.
False.
955
True or False: Androgens have a role in preventing bone resorption.
True.
956
What is the primary presentation of adhesive capsulitis?
A painful stiff shoulder with restriction of active and passive range of motion in abduction, internal and external rotation ## Footnote External rotation shows the most marked restriction and is the first movement to show impairment.
957
What are common difficulties reported by patients with adhesive capsulitis?
Difficulty dressing and doing up her bra, weakness of external rotation, difficulty sleeping on the affected side ## Footnote These symptoms suggest a globally impaired range of motion.
958
What demographic factors are often associated with adhesive capsulitis?
Coexisting diabetes, female gender, symptoms in the non-dominant hand ## Footnote These are common findings in this condition.
959
What symptoms are associated with acromioclavicular degeneration?
Popping, swelling, clicking, grinding, and a positive scarf test ## Footnote The scarf test was not reported in the stem.
960
What is a common complaint of patients with subacromial impingement?
Pain on overhead activities ## Footnote Patients demonstrate a painful arc of abduction, worse between 90 and 120 degrees.
961
What additional symptoms may be present in patients with subacromial impingement?
Popping, snapping, or grinding ## Footnote These symptoms are often noted during examination.
962
What causes rotator cuff tears?
Specific trauma or chronic impingement ## Footnote Patients typically describe weakness and pain.
963
What are signs of rotator cuff tears during examination?
Muscle wasting, tenderness on palpation, painful arc of movement, weakness of the affected muscle ## Footnote These signs help in diagnosing rotator cuff tears.
964
What is a typical presentation of calcific tendinopathy?
Tenderness on palpation of the affected area and reluctance to move the arm ## Footnote Symptoms may overlap with impingement syndrome, making it a less likely diagnosis.
965
What is the age of the female patient presenting to A&E?
82 years old
966
What event caused the female patient to present to A&E?
Tripping on a step
967
What is the main complaint of the patient?
Shoulder pain
968
At what degree of abduction does the patient experience pain?
90 degrees
969
What is the most common type of rotator cuff tear?
Supraspinatus tear
970
What is a common cause of a supraspinatus tear?
Degeneration
971
Is a supraspinatus tear common in younger adults?
No, it is rare
972
What is a Hill-Sachs lesion?
A Hill-Sachs lesion is when the cartilage surface of the humerus is in contact with the rim of the glenoid. ## Footnote This condition often occurs due to trauma during shoulder dislocation.
973
What percentage of anterior glenohumeral dislocations are associated with Hill-Sachs lesions?
About 50% of anterior glenohumeral dislocations are associated with this lesion. ## Footnote This statistic highlights the commonality of this injury in shoulder dislocations.
974
What is the primary cause of acromioclavicular joint (ACJ) dislocation?
Direct injury to the superior aspect of the acromion
975
What are key features of an acromioclavicular joint dislocation?
Loss of shoulder contour and prominent clavicle
976
At what age do rotator cuff tears rarely occur?
In the second decade
977
What characterizes a flail chest?
Paradoxical movement of the flail segment of the chest when breathing ## Footnote A flail chest requires immediate surgical management and invasive ventilation.
978
How are stable rib fractures generally managed?
Conservatively with good analgesia ## Footnote Effective analgesia is crucial to prevent complications.
979
What complications can arise if analgesia for rib fractures is not sufficient?
Chest infections and atelectasis ## Footnote Poor breathing due to inadequate pain control can lead to these complications.
980
What may be considered if normal analgesia does not control pain from a rib fracture?
Nerve blocks ## Footnote Nerve blocks can provide additional pain relief.
981
What is the immediate treatment required for a flail chest?
Surgical management and invasive ventilation ## Footnote Flail chest presents a critical condition that needs urgent intervention.
982
What is a rib fracture?
A break in the bony segment of any rib, often caused by blunt trauma to the chest wall ## Footnote Rib fractures can also occur due to underlying diseases that weaken the bone structure.
983
What are the common causes of rib fractures?
* Blunt trauma to the chest wall * Spontaneous fractures due to coughing or sneezing * Pathological fractures due to cancer metastases ## Footnote Common cancers that predispose to rib fractures are prostate cancer in men and breast cancer in women.
984
What is the most common symptom of a rib fracture?
Severe, sharp chest wall pain ## Footnote Pain worsens with deep breaths or coughing.
985
What physical signs may indicate a rib fracture?
* Significant chest wall tenderness * Visible bruising of the skin * Crackles or reduced breath sounds on auscultation ## Footnote These signs may indicate an underlying lung injury.
986
What is pneumothorax in relation to rib fractures?
A serious complication presenting with reduced chest expansion, reduced breath sounds, and hyper-resonant percussion on the affected side ## Footnote Pneumothorax can occur due to a rib fracture.
987
What defines a flail chest?
Two or more rib fractures along three or more consecutive ribs, leading to paradoxical movement during respiration ## Footnote Flail chest can impair ventilation and cause serious lung injury.
988
What is the best diagnostic test for rib fractures?
CT scan of the chest ## Footnote CT scans show fractures in 3D and associated soft tissue injuries.
989
What is the role of chest x-rays in diagnosing rib fractures?
They may demonstrate fractures but provide suboptimal views and no information about surrounding soft tissue injuries.
990
What is the primary management approach for rib fractures?
Conservative management with good analgesia ## Footnote This ensures breathing is not affected by pain.
991
When should surgical fixation be considered for rib fractures?
If pain is not controlled by normal analgesia and fractures have failed to heal after 12 weeks ## Footnote Flail chest segments should be urgently discussed with cardiothoracic surgery.
992
What complications should be managed in rib fractures?
* Pneumothorax * Haemothorax ## Footnote These lung complications should be addressed as necessary.
993
What is the function of the femoral nerve?
Knee extension, thigh flexion ## Footnote The femoral nerve innervates the anterior compartment of the thigh.
994
What areas does the femoral nerve provide sensation to?
Anterior and medial aspect of the thigh and lower leg ## Footnote This includes the skin over these regions.
995
What are typical mechanisms of injury for the femoral nerve?
Hip and pelvic fractures, stab/gunshot wounds ## Footnote These injuries can lead to damage of the femoral nerve.
996
What is the function of the obturator nerve?
Thigh adduction ## Footnote The obturator nerve innervates the adductor muscles of the thigh.
997
What areas does the obturator nerve provide sensation to?
Medial thigh ## Footnote This includes the skin covering the medial aspect of the thigh.
998
What is a typical mechanism of injury for the obturator nerve?
Anterior hip dislocation ## Footnote This can lead to damage of the obturator nerve.
999
What is the function of the lateral cutaneous nerve of the thigh?
None ## Footnote This nerve does not have motor functions.
1000
What areas does the lateral cutaneous nerve of the thigh provide sensation to?
Lateral and posterior surfaces of the thigh ## Footnote This nerve supplies sensation to the skin in these areas.
1001
What condition is caused by compression of the lateral cutaneous nerve near the ASIS?
Meralgia paraesthetica ## Footnote Characterized by pain, tingling, and numbness in the distribution of the nerve.
1002
What is the function of the tibial nerve?
Foot plantarflexion and inversion ## Footnote It innervates muscles in the posterior compartment of the leg.
1003
What areas does the tibial nerve provide sensation to?
Sole of foot ## Footnote This includes the skin on the plantar aspect of the foot.
1004
What are typical mechanisms of injury for the tibial nerve?
Popliteal lacerations, posterior knee dislocation ## Footnote These injuries can damage the tibial nerve.
1005
What is the function of the common peroneal nerve?
Foot dorsiflexion and eversion ## Footnote It innervates muscles in the anterior and lateral compartments of the leg.
1006
What areas does the common peroneal nerve provide sensation to?
Dorsum of the foot and the lower lateral part of the leg ## Footnote This includes the skin over these regions.
1007
Where does injury often occur for the common peroneal nerve?
At the neck of the fibula ## Footnote This is a common site for nerve injury.
1008
What can tightly applied lower limb plaster cast cause?
Injury to the common peroneal nerve leading to foot drop ## Footnote Foot drop is characterized by inability to dorsiflex the foot.
1009
What is the function of the superior gluteal nerve?
Hip abduction ## Footnote It innervates the gluteus medius and minimus muscles.
1010
What is a typical mechanism of injury for the superior gluteal nerve?
Misplaced intramuscular injection, hip surgery, pelvic fracture, posterior hip dislocation ## Footnote These can lead to damage of the superior gluteal nerve.
1011
What clinical sign results from injury to the superior gluteal nerve?
Positive Trendelenburg sign ## Footnote This sign indicates weakness in hip abduction.
1012
What is the function of the inferior gluteal nerve?
Hip extension and lateral rotation ## Footnote It innervates the gluteus maximus muscle.
1013
What is a typical mechanism of injury for the inferior gluteal nerve?
Generally injured in association with the sciatic nerve ## Footnote This can occur in various traumatic situations.
1014
What symptoms result from injury to the inferior gluteal nerve?
Difficulty rising from seated position, can't jump, can't climb stairs ## Footnote These symptoms are due to weakness in hip extension.
1015
What is Leriche syndrome?
Atherosclerotic occlusive disease involving the abdominal aorta and/or both iliac arteries.
1016
What are the classic symptoms of Leriche syndrome in male patients?
A triad of symptoms: * Claudication of the buttocks and thighs * Atrophy of the musculature of the legs * Impotence (due to paralysis of the L1 nerve)
1017
What is the main consequence of Leriche syndrome?
Compromised blood flow to the pelvic viscera.
1018
What is the management approach for Leriche syndrome?
Correcting underlying risk factors such as hypercholesterolaemia and stopping smoking.
1019
What is the common investigation method for Leriche syndrome?
Angiography.
1020
How are iliac occlusions typically treated in Leriche syndrome?
Endovascular angioplasty and stent insertion.
1021
Fill in the blank: Leriche syndrome is characterized by _______.
[a triad of symptoms including claudication, atrophy, and impotence]
1022
True or False: Leriche syndrome can occur in female patients.
False.