1
Q
What is the common clinical presentation of bronchiectasis
A
Commonly seen in older adults where they have a chronic cough and recurrently lung infections
2
Q
Is bronchiectasis Reversible
A
No it is irreversible
3
Q
What do Lung With Bronchiectasis Look Like
A
- Lungs with bronchiectasis usually will have an excess of puss and mucous, the bronchi and bronchioles will have a permanent dilation and thinning of the airways
- The lungs will retain inflammatory secretions and microbes that will damage the airway and cause recurrent infections and airway wall degradation
4
Q
What Part of the Lungs is Bronchiectasis Commonly Seen In
A
- One or both lungs may be involved
- Found generally in the lower lobes
- Commonly limited to lobe or segment
5
Q
How is Bronchiectasis Classified
A
- Bronchiectasis is normally based on anatomical pattern
- Remember that the bacterial infection usually affects the segmental and subsegmental bronchi
6
Q
Why are distal areas obstructed?
A
It is due to secretions, inflammation and fibrosis.
7
Q
Definition of Bronchiectasis
A
- Bronchiectasis is a chronic disease characterized of the bronchi and bronchioles characterized by the abnormal, irreversible dilation, and destruction of their walls
- It basically makes it difficult to clear mucous from your lungs due to damaged airways
8
Q
Etiology of Bronchiectasis
A
May be acquired or congenital
9
Q
Acquired Bronchiectasis-Pulmonary Infection
A
Significant lung infection in childhood can cause anatomical alterations in the developing lungs which lead to more infections and ultimately bronchiectasis
10
Q
Acquired Bronchiectasis-Bronchial Obstruction
A
Caused by a tumor enlarged by lymph nodes leading to impaired mucocilary clearance and bacterial infection ultimately leading to bronchiectasis distal to the obstruction
11
Q
Acquired Bronchiectasis-Pulmonary Tuberclosis
A
Inflammatory changes and bronchial wall destruction will lead to bronchiectasis as a secondary complication
12
Q
Types of Acquired Bronchiectasis
A
Pulmonary infection
Bronchial obstruction
Pulmonary Tuberclosis
13
Q
Types of Congenital Bronchiectasis-Cystic Fibrosis
A
Abundance of thick, stagnant mucus
Impaired mucocillary clearance
Bronchial obstruction
Necrotizing inflammation and infection
All the above lead to secondary bronchiectasis
14
Q
Types of Congenital Bronchiectasis-Hypogammaglobulinemia
A
Inherited/acquired immune deficiency disorders
High risk for respiratory infections
15
Q
Types of Congenital Bronchiectasis-Kartageners Syndrome
A
Accounts for 20% of congenital bronchiectasis
Triad consisting of bronchiectasis, dextrocardia (hart on right side of the body) and paranasal sinusitis
16
Q
Types of Congenital Bronchiectasis
A
Kartageners Syndrome
Hypogammaglobulinemia
Cystic fibrosis
17
Q
Pathophysiology of Bronchiectasis
A
- Bronchial Wall Destruction
- Impaired Mucocillary Mechanism
- Copious Amount of Foul Smelling Sputums
- Distal Bronchioles Obstruction with Secretions
- Hyperinflation of Distal Aveoli/Atelectasis Consolidation and Parachymal Fibrosis
- V/Q Mismatch, Hypoxemia, Increased WOB, Cor Pulmonale
18
Q
Cylindrical Classification
A
Regular pattern with the airway wall of the bronchioles uniformly dilated in a cylinderical shape
Occurs for 6-10 generations and appears to end squarely on bronchogram due to mucus obstruction
Increased bronchial markings
Emphysema
19
Q
Varicose Classification
A
- Irregular pattern with areas of constriction and dilation
- Distorted bulbous shape
- Bronchi dilated and constricted in irregular pattern
- End in distorted bulbous shape
20
Q
Cystic/Saccular Classification
A
A progressive increase in diameter with distal enlargement of airways resulting in sac like structures in lung parenchyma
Causes most damage to tracheobronchial tree
Loss of cartilage, elastic tissue and smooth muscle with fibrous tissue forming bronchial walls
Fibrotic markings
Atelectasis
Emphysema
21
Q
Hgh Resolution CT Scan
A
Has known mostly replaced bronchoscopy for classifying bronchiectasis
22
Q
Severe bronchiectasis is associated with:
i. Vesicular breath sounds
ii. Cor pulmonale
iii. JVD
iv. Polycythemia
A
ii. Cor pulmonale
iii. JVD
iv. Polycythemia
23
Q
The clinical manifestations are a result from the pathophysiologic mechanisms caused (or activated) by
A
Atelectasis
Consolidation
Excessive Bronchial Secretions
24
Q
Clinical Manifestations
A
Cough, sputum production, and hemoptysis
A chronic cough will produce large quantities of foul smelling sputum which is a hallmark of bronchiectasis
25
Sputum Examination
Streptococcus pneumonia
Haemophilus influenza
Pseudomonas aeruginosa
Anaerobic organisms
26
General Treatment Includes
Controlling Pulmonary Infections
Controlling Airway Secretions
Preventing Complications
27
Other Treatment Options Include
Bronchopulmonary Hygiene
Supplemental Oxygen Therapy
Mechanical Ventilation
Surgical Resection of Localized Area
Lung Transplant
28
Respiratory Care Treatment Protocols
Oxygen therapy protocol
Bronchopulmonary hygiene therapy protocol
Hyperinflation therapy protocol
Aerosolized medication protocol
Mechanical ventilation protocol
29
Medications
Antibiotics
Mucolytic agents
Bronchodilators/anticholinergics/ xanthines
Expectorants
30
What are some signs, symptoms, and observations of bronchiectasis?
A continuous cough with a large amount of sputum, recurrent local pneumonia, occasional hemoptysis, and increasing dyspnea.
31
What is the latest method used to diagnose bronchiectasis?
CT scan and HRCT.
32
What happens in the lungs of patients suffering from bronchiectasis?
Bronchial walls are destroyed, mucosa atrophied and cilia destroyed. The elastic area is filled with pus. Distal areas become obstructed.
33
What are some problems associated with bronchiectasis?
Clubbing, atelectasis, consolidation, increased thickness of the A-C membrane, bronchospasm, and excessive bronchial secretions
34
How does the pulmonary function test of a patient with bronchiectasis show?
It can show obstructive patterns. Remember “CBABE”. Bronchiectasis is a part of CBABE.
35
What does the ABG show on a patient with mild to moderate bronchiectasis?
The ABG will show respiratory alkalosis with hypoxemia
36
What does the ABG show on a patient with severe bronchiectasis?
It will show compensated respiratory acidosis with hypoxemia.
37
What are some common infections associated with bronchiectasis?
Haemophilus influenzae, streptococcus, staphylococcus, pneumonia, moraxella catarrhalis, and pseudomonas in cystic fibrosis patients.
38
What are some available management and treatment of bronchiectasis?
Removing secretions and patients’ infections, P&PD, bronchial hygiene, mucomyst, bronchodilators, antibiotics, oxygen, and surgical removal.
39
What is the prognosis of bronchiectasis?
The prognosis is extremely variable and depends on the extent of the damage. Good management is very important.
40
What will be the result of a high power bronchiectasis histology slide?
The airway wall will be full of neutrophils and there will be puss in the lumen that is mostly neutrophils too.
41
**What ethnicity does bronchiectasis common in?**
Bronchiectasis is more common in Asians and Pacific Islanders, and less common in African Americans
42
What age does bronchiectasis more common in older patients?
Bronchiectasis is more common among people ages 50-70s.
43
Who is most likely to have this disease?
Bronchiectasis is more common in women.
44
What other lung condition is bronchiectasis often misdiagnosed as?
Asthma, chronic obstructive pulmonary disease, and chronic cough.
45
How do you diagnose bronchiectasis?
CT scan and a history of a chronic cough with sputum.
46
How does cystic fibrosis cause bronchiectasis?
Cystic fibrosis has a defective gene called cystic fibrosis transmembrane conductance regulator, that causes thick sticky mucous which clogs the lungs leading to recurrent infections and damage to airways. The CFTR defect can be found at chromosome 7q31. Cystic fibrosis has allelic heterogeneity.
47
What is the laboratory results of hemoglobin and hematocrit for patients with bronchiectasis?
The results will show increased values.
48
The alpha 1 antitrypsin deficiency can lead to focal bronchiectasis. How will the left lung pocket looks like after a patient with alpha 1 antitrypsin deficiency 1 and 2 undergoes a CT scan?
The left lung’s pocket will show an abnormally large bronchi branch.
49
Tuberculosis causes bronchiectasis as it damages the airways. How will the CT scan look like for a patient post-tuberculosis bronchiectasis?
The lower left lung will show evidence of a very local damage. It is important to note that it is just a coincidence that all of these occurrences happen in the lower left lung.
50
What is a primary ciliary dyskinesia?
Primary ciliary dyskinesia is an autosomal recessive disorder. The cilia, the tiny hair-like structures that line the airways, in the primary ciliary dyskinesia are defective. This defect causes the bacteria to develop in the lungs and leads to recurrent infections and other disorders.
51
What are the complications of primary ciliary dyskinesia?
Neonatal respiratory distress, daily wet cough from birth, chronic airway disease with age-dependent bronchiectasis, recurrent otitis media and reduced fertility.
52
What are the clinical signs of bronchiectasis?
Audible secretions, severe sputum, finger clubbing, crackles, wheezes and skeletal abnormalities (tall, thin, pectus scoliosis), coarse inspiratory crackles over infected areas usually bi-basal and low body habits due to high energy demands. Situs inversus, a condition wherein all of the major chest organs are flipped like heart positioned on the right, cyanosis and cor pulmonale, an abnormal enlargement of the right side of the heart.
53
What are the clinical symptoms associated with bronchiectasis?
The symptoms include neonatal respiratory problems, recurrent otitis media, recurrent sinusitis, recurrent pancreatitis, gastrointestinal disease, infertility in men and finger clubbing. In addition, patients will have recurring cough with lots of infected sputum, intermittent hemoptysis, persistent halitosis or bad breath, dyspnea and recurrent febrile episodes commonly called as pneumonia.
54
How do you treat chronic bronchiectasis with Pseudomonas?
Azithromycin
55
How do you treat bronchiectasis?
There is no cure for this disease. Treatment and management of the symptoms of this disease are very important. Available management for bronchiectasis includes airway clearance, targeted antibiotics, airway hydration, bronchodilators, macrolides, and surgery to fix and contain the localized disease.
56
Why does airway clearance important in bronchiectasis treatment and management?
Airway clearance improves quality of life drastically and decreases the risk of infections.
57
What are macrolides in treating bronchiectasis?
Macrolides are helpful in bronchiectasis because they are both anti- inflammatory and anti-microbial. Macrolides reduce bronchiectasis exacerbations, improve quality of life, and decrease inflammation. Macrolides = 50s inhibitors = azithromycin and erythromycin.
58
**When do you use IV antibiotics in bronchiectasis?**
Use IV antibiotics during a bronchiectasis exacerbation, where symptoms are worse and a person is clearly infected. In cases of hemoptysis, starting IV antibiotics is a must.
59
What are the ABG results for patients with bronchiectasis?
For mild to moderate cases, it shows acute alveolar hyperventilation with hypoxemia. In severe cases, the result will show chronic ventilatory failure with hypoxemia.
60
What will the spirometry results show for patients with bronchiectasis?
Decreased Flow Rates (FEV1, FEV1/FVC, FEF25-75).
61
What will show on the CBC for patients with bronchiectasis?
Increased RBC/Hb/Hct.
62
What observation is seen in the sputum of bronchiectasis patients?
It may indicate that an infection is present.
63
What will be the result of the special diagnostic tests of patients with bronchiectasis?
On CT scan, an increased bronchial wall opacity with a characteristic appearance of end-on signet ring opacity.
64
What will chronic dilation of the airways in bronchiectasis patients lead to?
It leads to chronic infection and inflammation.
65
What is the difference between other chronic obstructive pulmonary diseases to bronchiectasis?
Some COPD diseases do not manifest clubbing, whereas, in bronchiectasis, clubbing is common. Sputum in COPD is not of the same quantity as with bronchiectasis
66
What is the pathology of bronchiectasis?
Pathology includes any bronchi involved most commonly lung bases. Airways dilate, purulent secretion, chronic inflammation in the wall with inflammatory granulation tissue and exacerbations leading to scarring that results in respiratory failure.
67
What four main organisms present in patients with bronchiectasis that is isolated?
These are haemophilus influenza, streptococcus pneumoniae, staphylococcus aureus and pseudomonas aeruginosa
68
What percentage of bronchiectasis is a result of idiopathic causes?
50%
69
What are four congenital causes of bronchiectasis?
Cystic fibrosis, primary ciliary dyskinesia, Kartagener’s syndrome and Young’s syndrome.
70
What are five post-infectious causes of bronchiectasis?
Measles, pertussis, pneumonia, tuberculosis and bronchiolitis.
71
What type of immunodeficiency is associated with bronchiectasis?
Hypogammaglobulinaemia.
72
What are five other causes of bronchiectasis?
Bronchial obstruction (tumor, foreign body), allergic bronchopulmonary aspergillosis, rheumatoid arthritis, ulcerative colitis and yellow nail syndrome.
73
What is the typical history of a patient that presents with bronchiectasis?
Usually, there is a history of chronic productive cough and recurrent chest infections.
74
What are the main symptoms associated with bronchiectasis?
A persistent cough with purulent sputum, hemoptysis (may be massive), fever, and weight loss.
75
What are the main signs associated with bronchiectasis?
Clubbing, coarse inspiratory crepitations, wheezes, and purulent sputum.
76
What are seven complications of bronchiectasis?
Pneumonia, pleural effusion, pneumothorax, pulmonary hypertension, massive hemoptysis, cerebral abscess, and amyloidosis.
77
What investigations would you perform in a patient presenting with suspected bronchiectasis?
Sputum: microscopy, culture and sensitivity; blood: serum Ig, aspergillus precipitins test, rheumatoid factor, α1-antitrypsin level, test Ig response to pneumococcal vaccine and spirometry: Obstructive pattern.
78
What tests are performed in patients with suspected bronchiectasis?
Test will involve sputum, blood, spirometry, and chest x-ray, high-resolution CT of the chest, bronchoscopy and cystic fibrosis sweat test.
79
What specific blood tests are ordered in patients with bronchiectasis?
Serum Ig, aspergillus precipitins test, rheumatoid factor, α1-antitrypsin level, assessment of Ig response to pneumococcal vaccine.
80
What pattern might spirometry show in a patient with bronchiectasis?
Obstructive.
81
What is the characteristic of the chest X-ray appearance of bronchiectasis?
Dilated bronchi with thickened walls (tramlines and rings) and multiple cysts containing fluid showing cystic bronchiectasis.
82
What test is the gold-standard for diagnosing bronchiectasis?
HRCT of the chest is used for diagnosing bronchiectasis. HRCT shows cystic bronchiectasis.
83
Why would you conduct a bronchoscopy in patients with suspected bronchiectasis?
To locate the site of hemoptysis, exclude obstruction, and obtain samples for culture.
84
How would you manage a patient with bronchiectasis?
Patient management includes expectorants, early childhood immunization,
lung resection, airway clearance techniques and mucolytics, and administration of antibiotics for indications of exacerbations. If ≥ 3 exacerbations/year, long-term antibiotics is necessary (may be nebulized). Patients who culture pseudomonas, oral ciprofloxacin or other suitable IV antibiotic should be given. Use of bronchodilators with nebulized B2-agonists (e.g. salbutamol) in asthmatics, corticosteroids: (e.g. prednisolone) and itraconazole for ABPA (allergic bronchopulmonary aspergillosis) and surgery for severe localized disease or severe haemoptysis.
85
What anatomic alterations are included in patients with bronchiectasis?
Hyperinflation and consolidation.
86
What are the key anatomic alterations of rigid and dilated bronchi?
Cylindrical bronchiectasis.
87
What are the key anatomic alterations of irregularly dilated and constricted bronchi?
Varicose bronchiectasis.
88
What is the greatest damaged tracheobronchial tree that can cause bronchiectasis?
Cystic Bronchiectasis.
89
What is the congenital cause of bronchiectasis?
Cystic fibrosis.
90
What will be a possible condition of a child if parents don’t give the usual childhood immunizations and the child has been repeatedly hospitalized with pulmonary infections?
Bronchiectasis.
91
What should be done to prevent bronchiectasis from worsening?
Avoid air pollution, get an influenza vaccination and avoid smoking.
92
What other conditions are associated with severe bronchiectasis?
Cor pulmonale, distended neck veins, and polycythemia.
93
What will be the hematology test results of patients with bronchiectasis?
It will show an elevated WBC count with increased hemoglobin and hematocrit.
94
What are the hallmark sypmtoms of bronchiectasis?
A chronic cough with production of large quantities of foul-smelling sputum.
95
What is the usual characteristic of the sputum of patients with bronchiectasis?
It is usually voluminous and tends to settle into several different layers.
96
What signs do patients with severe bronchiectasis may have?
Distended neck veins, pitting edema, enlarged and tender liver.
97
What lobe of the lung is bronchiectasis frequently found in?
The lower lobes.
98
What part of the airway does bronchiectasis usually affect?
Smaller bronchi.
99
**What type of organism makes the mucus very smelly?**
Anaerobic.
100
What are the three forms of bronchiectasis?
Varicose, cylindrical, and cystic.
101
What form of bronchiectasis has irregular dilations and constrictions and appear distorted and bulbous?
Varicose.
102
What is the other name for varicose bronchiectasis?
Fusiform.
103
What form of bronchiectasis has a tube-like dilation, where they lose their natural taper for 6-20 generations and appear to end squarely?
Cylindrical.
104
What is the other name for cylindrical bronchiectasis?
Tubular.
105
How many generations or divisions of the airway are there?
23
106
What shape on a CT scan do bronchial walls may have?
Signet ring-shaped or flame-shaped.
107
What is the other name for cystic bronchiectasis?
Saccular.
108
What are two types of Bronchiectasis?
Acquired and congenital.
109
What are the two types of acquired bronchiectasis?
Pulmonary infection and bronchial obstruction.
110
What is an acquired form of bronchiectasis that is in repeated and prolonged respiratory tract infections?
If children have frequent bronchopneumonia from measles, chickenpox, pertussis, or flu, this may cause bronchiectasis later and pulmonary infection.
111
What is an acquired form of bronchiectasis that occurs by tumors, big lymph nodes, or aspirated foreign bodies?
Mucus clearance is affected and can cause necrotizing bacterial infections resulting in bronchial obstruction.
112
What type of congenital bronchiectasis is dextrocardia and paranasal sinusitis?
Kartagener’s Syndrome.
113
What percentage of congenital bronchiectasis does Kartagener’s Syndrome make up?
20%.
114
What kind of disorder is caused by congenital bronchiectasis that includes rheumatoid issues, inflammatory bowel disease, and AIDS?
Systemic Disorder
115
What kind of congenital bronchiectasis causes problems with mucus clearance and thick, stagnant secretions that leads to obstruction and frequent infections?
Cystic Fibrosis.
116
What is stimulated when the PO2 drops below 60 mmHg?
Pheripheral Chemoreceptors
117
What happens to the fingers due to chronic hypoxemia?
Digital Clubbing
118
What are the three potential bacteria in bronchiectasis sputum?
Haemophilus influenzae, pseudomonas aeruginosa and anaerobic organisms.
119
What happens to the obstructive areas in tactile and vocal fremitus?
It causes a decrease in tactile and vocal fremitus.
120
What happens to the restrictive areas cause in tactile and vocal fremitus?
It causes an increase in tactile and vocal fremitus.
121
What type of disease is bronchiectasis?
It is both obstructive and restrictive.
122
What kind of flows and volumes do the obstructive areas have?
Decreased flows and increased volumes.
123
What type of flows and volumes do the restrictive areas have?
Normal flows and decreased volumes.
124
What type of ventilator acid-base assessment does a mild to moderate bronchiectasis has?
Acute alveolar hyperventilation with hypoxemia.
125
What type of ventilatory acid-base assessment does a severe bronchiectasis have?
Chronic ventilatory failure with hypoxemia.
126
What is performed by injecting an opaque contrast material into the airway to show the extent of the bronchiectasis disease?
Bronchogram. It is important to note that this method is not done very often anymore as it is very invasive.
127
What has been done in place of bronchograms?
CT scan.
128
What type of bronchiectasis has increased opacity (white) due to tissue density?
Restrictive.
129
**What type of bronchiectasis has translucent (dark) lung fields?**
Obstructive
Respiratory Therapy
flashcards
Decks in class (17)
# Cards
-
History of Respiratory Care57
-
Basics of Pulmonary Diagnostic Tests79
-
Spirometry64
-
Bronchiectasis129
-
Circulatory System24
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Cardiovascular System29
-
Neurological Assessment of Critically Ill26
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Acid Base Balance19
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Nervous System29
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Regulation of Breathing17
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Cardiac Assessment for Critically Ill10
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Congestive Heart Failure7
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Diuretic Agents11
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Extracorporeal Life Support11
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Cardiac Pharmacology128
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Aerosol Therapy79
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Speciatly Gases27
