112114 clinical and path Flashcards

1
Q

rusty sputum

A

classic for pneumococcal pneumonia

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2
Q

causes of CAP-what organisms most often?

A

strep
myco
chlam
leg

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3
Q

atypical pneumonia findings

A

moderate to no sputum
no physical findings of lung consolidation (like E/A sounds)
moderate to no elevation in WBCs
lack of alveolar exudate

in actuality, these do not help differentiate

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4
Q

what antibiotics are used for atypical pneumonia

A

macrolides

quinolones

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5
Q

PCN resistant and drug resistant pneumococci develop in whom with CAP?

A
modifying risk factors--
age over 65
beta lactam in past 3 months
alcoholism
immunosuppression
multiple medical comorbidities
exposure to child at day care center
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6
Q

enteric gram negatives develop in whom with CAP?

A

nursing home resident
cardiopulm dis
multiple medical comorbities
recent antibiotic therapy

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7
Q

p aeruginosa develops in whom?

A

bronchiectasis
steroids more than 10 mg/day
malnutrition

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8
Q

how long should you wait for resolution of CAP?

A

72 hours

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9
Q

clearing of opacities on CXR will occur in 75% at what time point for CAP?

A

6 weeks

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10
Q

what if pt, after antibiotics, fails to improve?

A
maybe inadequate antimicrobial selection
unusual pathogens (blasto, non-bac)
non-infectious illnesses (PE, CHF, neoplasm)
metastatic infections (pleural space, joints, etc)
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11
Q

what is the first question we ask for a pleural effusion?

A

transudate vs exudate

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12
Q

how do you determine if it’s an exudate?

A

LIght’s criteria

PF-LDH > 2/3 upper limit of serum normal
PF/S-LDH >0.6
PF/S-protein >0.5

any one of the above three means it’s exudate

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13
Q

parapneumonic effusion

A

pleural effusion

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14
Q

should we use a chest tube?

A

see slide 33

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15
Q

approach to dyspnea

A
chest wall
pleural space
parenchyma (alveolar, interstitial)
airways
nerve
cardiac (1/3 of pts)
blood (anemia)
psychogenic
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