Chronic Pulmonary Infection Flashcards

1
Q

Immunoglobulin deficiency

A

IgA Deficiency
Hypogammaglobulinaemia
CVID
Specific Polysaccharide Antibody Deficiency

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2
Q

Other immunodeficiencies

A

Hypo-splenism
Immune paresis (Myeloma, lymphoma etc)
HIV

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3
Q

Therapies causing immuosuppression

A
Steroids
Azathioprine
Methotrexate
Cyclophosphamide
Monoclonal antibodies 
 Infliximab, etanercept, rituximab, leflunamide
Chemotherapy
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4
Q

Defective innate host defences

A

Damaged bronchial mucosa
Abnormal cilia
Abnormal secretions

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5
Q

Causes of damaged bronchial mucosa

A

Smoking
Recent pneumonia, or viral infection
Malignancy

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6
Q

Causes of abnormal cilia

A

Kartenager’s Syndrome

Youngs Syndrome

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7
Q

Causes of abnormal secretions

A

Cystic Fibrosis

Channelopathies

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8
Q

Risk factors for developing chronic pulmonary infection

A

Immunodeficiency
Immunosuppression
Abnormal host defences
Repeated insult

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9
Q

Forms of chronic infection

A
Intrapulmonary abscess
Empyema
Chronic bronchial sepsis
Bronchiectasis
Cystic fibrosis
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10
Q

Features of intrapulmonary abscess

A
Indolent presentation
Weight loss
Lethargy
Cough
High mortality if untreated
Usually a preceding illness
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11
Q

Pathogens that cause abscesses (from pneumonia)

A
Streptococcus
Staphylococcus
E-coli
Gram negatives
Aspergillus
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12
Q

Septic emboli in injecting drug users

A

Inject into groin
DVT
Infection
PE + abscesses

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13
Q

Empyema

A

Pus in the pleural space

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14
Q

Simple parapneumonic effusion

A

Clear fluid
pH>7.2
LDH < 1000
Glucose >2.2

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15
Q

Complicated parapneumonic effusion

A

pH <7.2
LDH > 1000
Glucose <2.2
Requires chest tube drainage or becomes empyema

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16
Q

Bacteriology of empyema

A
Aerobic organisms most frequently
Gram Positive (Strep Milleri, Staph Aureus)
Gram Negatives (E-Coli, Pseudomonas, Haemophilus Influenzae, Kelbsiellae)
17
Q

Bronchiectasis

A

Localised, irreversible dilation of the bronchial tree
Involved bronchi are dilated, inflamed and easily collapsible
Airflow obstruction
Impaired clearance of secretions

18
Q

Presentation of bronchiectasis

A

Recurrent “chest infections”
Recurrent antibiotics
No response/ short lived response to antibiotics
Persistent sputum production

19
Q

Clinical bronchiectasis

A

Cough with sputum production
Chest pain
Recurrent LRTIs

20
Q

Radiological bronchiectasis

A

High resolution CT scan

21
Q

Pathophysiology of bronchiectasis

A
Bronchial obstruction
Cystic fibrosis
Young's syndrome
Kartanager's syndrom
ABPA
Immunodeficiency
Rheumatoid arthritis
Bronchopulmonary sequestration
Mounier-Khun Syndrome
Yellow nail syndrome
Traction bronchiectasis associated with pulmonary fibrosis
Idiopathic >50%
22
Q

Chronic bronchial sepsis

A

All the hallmarks of bronchiectasis but none on the HRCT

Positive sputum results

23
Q

Treatment of bronchiectasis

A
Stop smoking
Flu vaccine
Pneumococcal vaccine
Reactive antibiotics
Prophylactic antibiotics
 Nebulised gentamicin, colomycin, pulsed IV abx, 
 alternating antibiotics
Low dose macrolide antibiotics
 Clarithromycin, azithromycin
24
Q

Mortality rate from abscess

A

10%

25
Q

Mortality rate from empyema

A

20%