pulmonology Flashcards

(43 cards)

1
Q

epiglottitis- epi and etiology

A

2-7yr
HIB
GABHS, Strep pneumonia and Staph

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2
Q

clinical epiglottitis

A

abrupt onset- high fever, toxic, muffled speech, dysphagia with drool, sitting forward in tripod

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3
Q

diagnosis epiglotitis

A

cherry red swollen epiglottis

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4
Q

epiglottitis on xray

A

thumbprint on lateral

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5
Q

antibiotic for epiglottitis

A

2nd or 3rd gen. cephalosporin IV

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6
Q

if HIB infection and ppx

A

rifampin

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7
Q

laryngotrachealbronchitis (croup)

A

inflamm. and edema of the subglottic larynx, trachea, and bronchi
viral croup –> stridor - 3 months to 3 yrs - M2:1F
spasmodic - preschool age

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8
Q

viral croup can be caused by:

A
parainfluenza
RSV
rhino
adeno
influenza A and B
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9
Q

clinical pres. of viral croup

A

URI 2-3 days followed by stridor and cough
barky cough, stridor, fever –> 3-7 days
stridor worse at night with agitation

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10
Q

xray of viral croup

A

steeple sign

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11
Q

management of croup

A

supportive
cool mist
systemic corticosteroid -
racemic epinephrine if resp. distress

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12
Q

bacterial tracheitis

A

acute inflammation of the trachea - causes stridor

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13
Q

causes of bacterial tracheitis -

A

staph, strep, nontypeable H. flu

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14
Q

bronchiolitis

A

inflammation of the bronchioles - viral infection that causes inflammatory bronchiolar obstrucion
most common in

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15
Q

bronchiolitis etiology

A

RSV

less common: para, adeno, rhino, influenza

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16
Q

clinical of bronchiolitis

A
onset is gradual
tachypnea, fine rales, wheezing 
spleen and liver might enlarge
hypoxia
apnea
CXR hyperinflation - patchy infiltrates and atelectasis
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17
Q

typical causes of pneumonia in 0-3 month

A
syphilis, toxo, CMV, rubella, herpes, tb
GBS
gram - rods 
listeria 
rsv
 (afebrile) chlamydi, CMV, PCP
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18
Q

typical pneumonia in 3 months - 5 yrs causes

A

adenovirus, influenza A and B, para , RSV,

bacterial: strep pneumoniae, staph and HIB

19
Q

age >6 pneumonia cuase

A

mycoplasma pneumoniae and chlamydia pneumoniae
viruses - adenovirus, influenza A and B, parainflue
bacterial - strep. pneumoniae

20
Q

viral pneumonia presentation

A

URI - nasal congestion and rhinorrhea - then fever, cough, dyspnea

21
Q

bacterial pneumonia presentation

A

rapid onset and greater severity - fever, cough, dyspnea, without preceding URI

22
Q

viral pneumonia xray

A

interstitial infiltrates

23
Q

bacterial pneumonia xray

A

lobar consolidation

24
Q

chlamydia trachomatis - pnemonia

presentation, diagnosis

A

most common is afebrile - 1-3 months of age
stoccato-type cough
history of conjunctivitis after birth - >50%
eosinophilia and cxr with interstitial infiltrates - definitive diagnosis by culture

25
how to manage chlamydia trachomatis pneumonia
erythromycin or azithromycin
26
mycoplasma pneumoniae
most common in older children low-grade fever, chills, nonproductive cough, HA, pharyngitis, malaise cough 3-4 wks widespread rales
27
diagnosis of mycoplasma pneumonia
positive cold agglutinins - cxr - bilateral diffuse infiltrates IgM titer for mycoplasma
28
manage of mycoplasma pnemonia
erythromycin
29
who is at risk for pertussis?
30
stages of pertussis
``` incubation 7-10 days catarrhal stage (1-2 wks) URI + low grade fever paroxysmal stage (2-4wks) forceful coughing and whoop - inspiatory gasp heard at the very end of a coughing fit -- might vomit post cough attack - otherwise well and afebrile convalescent phase - (weeks to months) - paroxysmal cough continues but become less frequent and less severe over time ```
31
diagnosis of pertussis
lymphocytosis
32
when to give antibiotics to alter course in pertussis?
during the catarrhal stage or earlier
33
isolation and pertussis
need to be on isolation until 5 days of abx
34
IgE release?
eosinophils, histamine, mast cells, basophils
35
asthma pathophys
smooth muscle bronchoconstriction, airway mucosal edema, increased secretions with mucous plugging, eventual airway wall remodeling and production of inflammatory mediators IgE
36
cxr of asthma
hyperinflation peribronchial thickening patchy atelectasis
37
CF etiology
AR - ch. 7
38
pathophys for CF
abnormal ion-channel regulator protein - causes sodium and choride transport dysfunction in epithelial cells abnormal mucus produced in airways helps create airwy obstruction inflammation and infection
39
clinical present of CF
``` chronic progressive pulmonary insuff. pancreatic insuff. high sweat electrolyte meconium ileus at birth(20%) FTT - recurrent chronic resp. symptoms respiratory signs PFTs decreased respiratory flow rates and decrease lung volumes pneumonia- staph and then pseudomonas nasal polyps and precurrent pneumonia ```
40
diagnosis of CF
one or more phenotypic feature OR positive fam. history OR increased immunoreactive trypsinogen on newborn screen - sweat chloride test 2 CF mtn characteristic ion transport abnormality across the nasal epithelium
41
management of CF
``` antibiotics pul. toilet bronchodilator pancreatic enzyme replacement - fat soluable vitamine (A, D, E, K) anti-inflammatory and immunosuppressive lung transplant psychological help ```
42
CF and mutation
CFTR gene ch. 7
43
ddx of ALTE
``` seizure GERD upper airway obstruction intracranial mass lesion sepsis metabolic abnormalities including electrolyte imbalance and hypoglycemia inborn errors of metabolism arrhythimia abnormal central control munchausen by proxy nonaccidental trauma ```