pneumonia drugs

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45 Terms

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uncommon non-infectious causes

lung infarction

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common non-infectious causes

pulmonary edema

ARDS

lung cancer

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common infectious causes

streptococcus pneumoniae

Haemophilus influenzae

staphylococcus aureus

influenza and other viruses

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uncommon infectious causes

pseudomonas aeruginosa

Pneumocystis jiroveci

Moraxella catarrhalis

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typical CAP

Sudden onset of fever, chills, pleuritic chest pain, productive cough

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typical CAP organisms

• Streptococcus pneumoniae

-Haemophilus influenzae

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Atypical CAP

often preceded by mild respiratory illness

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Atypical CAP caused by

• Legionella spp.

• Mycoplasma pneumoniae (walking pneumonia)

• Chlamydophila pneumoniae

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Basics of pneumonia pharmacotherapy

• Start empiric therapy with a broad spectrum antibiotic

• Revise therapy once the causative organism is identified

• Revise therapy based on disease progression (and potential development of drug resistance)

• For hospitalized patients, once stabilized, move from IV to oral therapy prior to discharge

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Streptococcus pneumoniae: CAP typical treatment

Usually susceptible to penicillin

give:

• Penicillin G (high doses)

• Aminopenicillins: Ampicillin (high doses)

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Treatment of Penicillin-resistant Streptococcus pneumoniae

• Second Generation Cephalosoporins: Cefuroxime

• Third Generation Cephalosporins: Cefotaxime, Ceftriaxone

• Quinolones: Moxifloxacin, Levofloxacin

• Vancomycin

• Macrolides/ketolines: Telithromycin

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what cephalosporin can treat MRSA

5th generation cephalosporins differ from ALL other betalactam antibiotics by being active against Methicillin-resistant Staphylococcus aureus (MRSA)

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H.infleunzae treatment

Quinolone

macrolide

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Legionella treatment

macrolide

quinolone

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mycoplasma pneumoniae treatment

quinolone

macrolide

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aerobic gram neg bacteria treatment

quinolone

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chlamydophilia pneumoniae

quinolone

macrolide

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staphylococcus aureus

quinolone

macrolide

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outpatient with no comorbidities or MRSA risk in community more than 25%

either:

-amoxicillin

-doxycycline

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outpatient with no comorbidities or MRSA risk in community less than 25%

either:

-amoxicillin

-doxycycline

-Clarithromycin

-Azithromycin

<p>either:</p><p>-amoxicillin</p><p>-doxycycline</p><p>-Clarithromycin</p><p>-Azithromycin</p>
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outpatient with co-morbidities

either:

-monotherapy of fluoroquinolone (levifloxacin/moxifloxacin/gemifloxacin)

-beta-lactam + macrolide

-beta-lactam + doxycycline

<p>either:</p><p>-monotherapy of fluoroquinolone (levifloxacin/moxifloxacin/gemifloxacin)</p><p>-beta-lactam + macrolide</p><p>-beta-lactam + doxycycline</p>
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in-patient nonsevere

-monotherapy of fluoroquinolone (levifloxacin/moxifloxacin/gemifloxacin)

-beta-lactam + doxycyline

-beta-lactam + macrolide

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MRSA in nonsevere and severe in patient

add vancomycin or linezolid

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P.areguinosa consideration

switch the b-lactam to an antipsuedomonal beta lactam

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antipseudomonal b-lactams

-piperacillin-tazobactam

-cefepime

-ceftazidime

-imipenem

-meropenem

-aztreonam

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in-patient severe

-b lactam + macrolide

-b lactam + fluroquinolone

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HAP is divided into two classes:

Early onset HAP

Late onset HAP

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Early onset HAP

occurs within first five days of hospitalization

• Usually after 48 hrs from admission

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Late onset HAP

occurs after 5 days of hospitalization

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Bacterial Causes of Early Onset HAP

• Methicillin-sensitive Staphylococcus aureus (most)

• Haemophilus influenzae

• Enterobacteriaceae

• Streptococcus pneumoniae

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Early Onset HAP treatment

ceftriaxone

Quinolone

ampicillin/sulbactam

Ertapenem

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Bacterial Causes of Late Onset HAP

• Pseudomonas aeruginosa

• Acinetobacter spp.

• Enterobacteriaceae

• Methicillin-resistant S. aureus

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Methicillin-resistant S. aureus treatment

either:

-antipsuedomonal b-lactam

-carbapenem

with:

quinolone

or

aminoglycoside (tobramycin/gentamycin)

if MRSA suspected:

add vancomycin or linezolid

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b lactam adverse

diarrhea

nausea

vomiting

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Doxycycline adverse

inhibits bone growth

teeth discoloration

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Azithromycin and clarithromycin adverse

QT interval prolongation

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fluoroquinolones adverse

Qt interval prolongation

torsades de pointes

vaginal candida

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what should be separated from doxycycline and fluroquinolones

Calcium

Magnesium

Iron

-reduce drug absorption take several hours before or after

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what drugs shouldnt be taken with QT interval prolonging drugs

azithromycin

clarithromycin

fluoroquinolones

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what shouldnt be taken with hypoglycemic drugs

fluroquinolones

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Clarithromycin inhibits

CYP3A4

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dont give what with clarithromycin

CCB are metabolized by CYP3A4

-can lead to death, acute kidney injury, hypotension

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pregnancy aviod

• Doxycycline: inhibition of bone growth.

• Clarithromycin: teratogenic in animals.

• Fluoroquinolones: arthropathy in animal studies, but observational data in pregnant women suggest that teratogenic effects are unlikely to occur at therapeutic doses.

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pregnancy take

Amoxicillin or amoxicillin/clavulanate plus azithromycin can be used for outpatient treatment of pregnant women with CAP.