Haem Flashcards

(30 cards)

1
Q

Blood results of Beta thalassaemia trait Vs Beta thalassaemia major

A
  • trait presents with disproportionate MCV to anaemia - i.e MCV will be very low whilst Hb is only mildy low.
  • major presents with low MCV AND severe anaemia [v low Hb] [similar pattern is seen in alpha thalassaemia]
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2
Q

1st line imaging for suspected multiple myeloma

A

whole body MRI to assess for bony involvement.

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3
Q

multiple myeloma CFs

A
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4
Q

multiple myeloma Dx criteria

A

Both criteria must be met:
1. Clonal bone marrow plasma cells* ≥10% or biopsy-proven plasmacytoma.
2. One or more myeloma-defining events

  • [S] ≥60% plasma cells in marrow
  • [LI] Involved:uninvolved light chain ratio ≥100 (provided the involved light chain is >100 mg/l)
  • [M] 2 or more focal lesions on MRI (>5 mm in size)
  • [C] Hypercalcaemia: (>2·75 mmol/l or >0·25 mmol/l higher than upper limit of normal)
  • [R] Renal insufficiency: (serum creatinine >177 µmol/l or creatinine clearance <40 ml/min)
  • [A] Anaemia: Hb <100 g/l or 20 g/l below lower limit of normal
  • [B] 1 or more lytic bone lesion on X-ray, CT or PET/CT (>5 mm in size)
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5
Q

CLL summary

A
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6
Q

CML summary

A
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7
Q

ALL summary

A
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8
Q

AML summary

A
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9
Q

reversal agent for DOACs

A
  • dabigatran = Idarucizumab
  • apixaban + rivaroxiban = Andexanet alfa
  • edoxaban = nothing licenced
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10
Q

superior vena cava obstruction:
1. - Mc associated with
1. - CFs
1. - Mx

A
  1. lung cancer [MC] also lymphoma
  2. dyspnoea [MC], facial, neck and arm swelling, pappiloedema, visual disturbance, headache[ worse in the morning] pulseless jugular venous distension.
  3. IV dexamethasone - reduces inflammation to increase venous flow
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11
Q

hyposplenism blood film

A
  • target cells
  • Howell-Jolly bodies
  • Pappenheimer bodies
  • siderotic granules
  • acanthocytes
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12
Q

DVT investigation: if the scan is negative, but the D-dimer is positive →

A

stop anticoagulation and repeat scan in 1 week

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13
Q

how is vaso-occlusive crisis diagnosed in sickle cell

A

clinical Dx in pts with known hx of sickle cell

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14
Q

types of Sickle-cell crises

A

thrombotic, ‘vaso-occlusive’, ‘painful crises’
acute chest syndrome
anaemic
aplastic
sequestration
infection

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15
Q

key side effect of chemo

NOT complication

A

tumour lysis syndrome

  • presents with diarrhoea, paraesthesia, decreased urine output due to AKI

U+E findings = PUKE Calcium

  • Phosphate, Uric acid, potassium (K) Elevated
  • Calcium low
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16
Q

causes of microcytic anaemia

17
Q

causes of normocytic anaemia

18
Q

potential causes of neutrophilia

A
  • bacterial infection
  • meds - steroids + lithium esp.
  • inflammation
  • stress
  • malignancy
19
Q

causes of macrocytic anaemia

20
Q

key complication of chemo

  • when does it occur
  • what causes it
  • Mx
A

neutropenic sepsis

  • MC occurs 7-14 days after chemotherapy
  • defined as a neutrophil count of < 0.5 * 109 in a patient who is having anticancer treatment and has one of the following:
    • a temperature higher than 38ºC or
    • other signs or symptoms consistent with clinically significant sepsis

MC causative organism = Staphylococcus epidermidis

  • prophylaxis = fluoroquinolone. given when neutropenia is anticipated

MX

  • IMMEDIATE Abx - never wait for blood results
    • piperacillin with tazobactam (Tazocin)
  • if patients are not responding after 4-6 days the Christie guidelines suggest ordering investigations for fungal infections
21
Q

causes of B12 deficiency

A
  • diet changes - veganism
  • nitroous oxide use
  • pernicious anaemia - autoantibodies against parietal cells in the stomach, destroying the ability to produce intrinsic factor (IF), a protein necessary for B12 absorption in ileum
22
Q

neutropenic sepsis

  • definition
  • cause
  • Ix
  • Mx
A

Definition

  • MC occurs 7-14 days after chemotherapy
  • defined as a neutrophil count of < 0.5 * 109 in a patient who is having anticancer treatment and has one of the following:
    • a temperature higher than 38ºC or
    • other signs or symptoms consistent with clinically significant sepsis

Cause

MC causative organism = Staphylococcus epidermidis

Ix

  • Bloods: FBC - neutropenia [always present regardless of WCC], low or normal WCC

MX

  • IMMEDIATE Abx - never wait for blood results
    • piperacillin with tazobactam (Tazocin)
  • prophylaxis = fluoroquinolone. given when neutropenia is anticipated

//
- if patients are not responding after 4-6 days the Christie guidelines suggest ordering investigations for fungal infections

23
Q

lymphoma staging

A

lugano staging

24
Q

DIC typical blood picture:

A

↓ platelets
↓ fibrinogen
↑ PT & APTT
↑ fibrinogen degradation products

25
a 20 yr old sees you at the GP with 2 weeks of unexplained fatigue and petechiae on her arms and legs and hepatomegaly on examination. how do you proceed?
- urgent referral to haematology within hours because when either hepatosplenomegaly or unexplained petichiae are present, the patient should be referred for immediate assessment where blood tests will be performed more quickly than from general practice. - if the pt just had symptoms of new onset fatigue/ general sx of leukaemia [not listed above] then a 48 hour urgent blood test would be appropriate
26
what sx would warrant an urgen 48 hour blood test to assess possible leukaemia
* Pallor * Persistent fatigue * Unexplained fever * Unexplained persistent infections * Generalised lymphadenopathy * Persistent or unexplained bone pain * Unexplained bruising * Unexplained bleeding
27
TTP - sx - how bad is it
FATHeR - Fever - Altered mental state - Thrombocytopenia - Haemolyrtic anaemia - Reduced renal function BAD BAD
28
ITP bloods
- low platelets - TTP
29
non-pharmacological Mx/ advice for sickle cell pts
* Avoid dehydration/cold/exhaustion , * avoid alcohol (due to dehydrating effects), * avoid smoking (may cause acute sickle chest)
30
Give one immediate treatment for the hyponatraemia, and an alternative oral medication that can achieve and maintain a normal sodium.
- Fluid restriction; - demeclocycline or tolvaptan