Lung infections Flashcards

(35 cards)

1
Q

Acute bronchitis usually due to ___? It’s clinical course is ___? Post infectious cough occurs ___? CXR appears ___?

A

viruses
self resolving
3-8 weeks after infection resolves
normal

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2
Q

In chronic bronchitis you have ____ mucus production and change of ___? Why? How is air flow reduced? CXR?

A

increased
character of sputum

increased mucus production/decreased clearance

increased mucus production and inflammation

unchanged/normal

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3
Q

Mucus production and chronic inflammation in chronic bronchitis may lead to ___?

A

permanent lung damage

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4
Q

chronic bronchitis management

A

bronchodilators
corticosteroids
antibiotics

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5
Q

What PFTs are decreased in chronic bronchitis?

A

FEV1 and VC

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6
Q

What do you see on a lung exam for chronic bronchitis?

A

crackles, ronchi, wheezing

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7
Q

describe the common infection in chronic bronchitis. What are the most common organisms?

A

bacterial colonization of tracheobronchial tree

H influenza
S pneumonia
M catarrhalis

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8
Q

when is the flu considered infectious?

A

one day before -> 7 days after illness onset

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9
Q

When do you treat the flu empirically ASAP?

What are the two medications used to treat and what is their effect?

A
  • underlying chronic conditions
  • pregnancy
  • very young (65)

Tamiflu (oseltamivir)(pill) and Relenza (Zanamivir)(inhaled)
Most effective if given within 2 days after onset
Reduce severity of symptoms and length of illness by 1 day

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10
Q

Pneumonia CXR

A

Filling of airways with pus and inflammation

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11
Q

What are the clinical features of pneumonia and when do they present?

A
Acute presentation: within 2 weeks
Fever, chills
Dyspnea
Purulent sputum
Hemoptysis (possible)
Pleuritic chest pain 
Tachypnea/tachycardia
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12
Q

Pneumonia lung exam findings

A

Rales

Occasional pleural rub

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13
Q

How do the clinical features of pneumonia differe in elderly patients

A

Fever occurs mainly in younger pop
Confusion
Cough and sputum production may be absent

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14
Q

What is CAP? Which organisms are most common? Which present atypically?

A

Community acquired pneumonia
S. Pneumonia
H influenza

Atypically:
M pneumonia
C pneumonia
L pneumophilia

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15
Q

How do you decide whether to hospitalize or not?

A

CURB-65

Confusion
Uremia (BUN> 20)
Respiratory (RR>/30)
Blood pressure (systolic // old age

Get a point for each one
0- low risk
1- consider Rx at home

Consider hospitalization 2 points (or close out pt)
Hospitalize
3- hospitalize
4,5- hospitalize, ICU

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16
Q

Pneumonia APs. what are the nosocomial ones? Define them.

A

CAP

Nosocomial:
HCAP- occurs 48 hours or more after admission
->hospitalized for at least 2 days within 90 days of the infection
->received IV, chemo or wound care 30 days prior to infection

VAP- occurs 48 - 72 hours after ventilation

17
Q

HCAP most common microbio

A

S aureus
Pseudomonas
Klebsiella
Enterobacter

18
Q

VAP

A

‘ESKAPE’

Enterobacter
S aureus
Klebsiella
Acinetobacter
Pseudomonas 
Enterococcus
19
Q

Pneumonia treatment. Follow up CXR after how long?

A

Find out what type of pneumonia you are dealing with and treat accordingly ASAP
-> prognosis influenced by how fast antibiotics are started

Outpatient CAP:

  • most commonly, azithromycin and levaquin
  • doxy given less often, not effective against atypical so

In patient:

  • for CAP: ceftriaxone+azithromycin or levaquin even alone
  • Nosocomial: vancomycin + coverage for pseudomonas

Follow up CXR 6 - 8 weeks after initial to make sure pneumonia is clearing

20
Q

Note the possible source of pneumonia: GI sxs, bradycardia, confusion, liver and renal manifestations

21
Q

Note the possible source of pneumonia: Post-influenza

22
Q

Note the possible source of pneumonia: Aspiration

A

Mouth anaerobes

23
Q

Note the possible source of pneumonia: Alcoholism

A

Aspiration (mouth anaerobes), gram -

24
Q

Note the possible source of pneumonia: Sickle cell disease

A

Encapsulated organisms

25
Note the possible source of pneumonia: HIV+
Pneumocystis, tb, 'typicals'
26
Note the possible source of pneumonia: Recent immigrant, incarcerated
TB
27
Note the possible source of pneumonia: cystic fibrosis
Most often pseudomonas, S aureus
28
Bronchiectasis. How is a diagnosis established?
Abnormal dilatation and desctruction of the bronchial walls | Clinically and radiographically
29
Clinical features of bronchiectasis. PE/Lung exam findings
Similar features with COPD: - dyspnea - cough with sputum, hemoptysis Crackles>Ronchi>wheezing Clubbing
30
Bronchiectasis microbio; Lady Windermere syndrome microbio
gram negs more often isolated in sputum S aureus less common Lady windermere syndrome: middle lobe bronchiectasis and mycobacterium avium complex infection due to voluntary cough suppression
31
Cystic fibrosis
Autosomal recessive Abnormal CFTR gene on long arm of chromosome 7 - gene codes for CL- channel on epithelial cells Defect: decreased Cl- permeability -> dehydration of secretions
32
CF diagnostic criteria
Family history Positive sweat test (Cl- >60 mEq/L) Chronic obstruction to airflow Exocrine pancreatic insufficiency
33
Acute bronchitis microbio
H flu Strep pneumonia M pneumonia
34
CF manifestations
``` Pulmonary disease Nasal polyps Pancreatic insufficiency Glycosuria Intestinal symptoms Cirrhosis Heat prostration ```
35
CF treatment
``` Mucolytics Postural drainage physiotherapy Anti inflammatory Bronchodilators When needed - antibiotics Gene therapy on the rise ```