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Antimicrobials
Clinical Criteria
Radiographic infiltrate, AND
2 of 3 clinical features:
Type of Pneumonia
CAP: Symptom onset occurring in the community setting or <48hrs after hospital admission
HCAP: Use of this term is no longer recommended due to poor predictive performance for drug resistance
Diagnostics to Consider
CXR
Vitals
ABG/O₂ sat
CBC
Respiratory GS and culture
Blood culture x 2 sites
S. pneumoniae and Legionella urinary antigens
MRSA nasal swab for PCR
Influenza A & B PCR
Empiric Treatment Notes
All dosages provided assume normal renal and hepatic function
Use of clinical judgment is encouraged when selecting empiric therapy for a patient, including consideration of severity of illness, prior microbiology, and prior antimicrobial history (duration ≥48hrs, excludes one-time doses and/or most surgical prophylaxis)
Revise antimicrobial regimen based on microorganism identification (e.g. culture, PCR) and antimicrobial susceptibility testing results
Abbreviations
APBL: Antipseudomonal beta-lactam
AMC: Amoxicillin-clavulanate
FEP: Cefepime
CRO: Ceftriaxone
CAZ: Ceftazidime
TZP: Piperacillin-tazobactam
No Pathogen-Specific Risk Factors
Risk Factors for Antipseudomonal Beta-lactam (APBL)-Susceptible Pseudomonas aeruginosa
Risk factors include:
Interstitial lung disease (e.g. severe pulmonary fibrosis, but excluding COPD or asthma)
Prior use (duration ≥48 hrs, excludes one-time doses and/or most surgical prophylaxis) of non-APBL within last 3-30 days (e.g. AMC, CRO)
Prior airway colonization with P. aeruginosa susceptible to APBL (e.g. TZP, FEP, CAZ) within the last 12 months
Severe immune compromise:
Risk Factors for Antipseudomonal Beta-lactam (APBL)-Resistant Pseudomonas aeruginosa
Cystic fibrosis or bronchiectasis
Prior APBL use for ≥48hrs within 3-30 days (e.g. TZP, FEP, CAZ). Excludes most surgical prophylaxis.
Prior airways colonization with P. aeruginosa resistant to APBL (e.g. TZP, FEP, CAZ) within the last 12 months
Aspiration Pneumonia
Beta-Lactam Allergy
Empiric Levofloxacin Use
Given the importance of fluoroquinolones in the management of serious infections and their relative toxicity (e.g. dysglycemias, CNS side effects, muscle injury, tendonitis) compared to alternative agents, it is recommended to reserve fluoroquinolones for select patient cases where benefit outweighs the risk (e.g. severe beta-lactam allergy, oral antipseudomonal coverage)
Avoid levofloxacin for gram-negative bacterial coverage if patient had prior fluoroquinolone use particularly within the past 3 months (risk of infections due to fluoroquinolone-resistant bacteria may persist for up to 12 months from fluoroquinolone use)
Renal Impairment
If tobramycin is recommended, consider replacing this agent with an antipseudomonal fluoroquinolone (i.e. ciprofloxacin or levofloxacin) in the absence of recent fluoroquinolone use within the past 3 months
Inhaled tobramycin may be considered in patients with renal impairment who received fluoroquinolones recently
MRSA Nasal Swab PCR
This test demonstrates a negative predictive value of >95% for ruling out MRSA as a causative pathogen for pneumonia
This is a useful diagnostic in patients at increased risk of MRSA pneumonia at baseline (e.g. residence in a long-term care facility, wound care in the last 30 days, prior MRSA infection/colonization within 90 days)
Respiratory Viral PCR Panel
This test, which is designed for upper respiratory tract infections, includes both viral and atypical bacterial targets for community-acquired pneumonia
If the patient is unlikely to have polymicrobial pneumonia, consider streamlining to appropriate viral pneumonia management (e.g. oseltamivir for influenza A or B virus, supportive care for rhinovirus) or atypical bacterial pneumonia management (e.g. azithromycin)
Additional Risk Factors for Antimicrobial Resistance
Extended-spectrum beta-lactamase producing organisms (ESBL):
Carbapenems are preferred in patients with high risk of pneumonia due to ESBL-producing bacteria, including:
Consult PHASST during business hours or an infectious diseases specialist for assistance determining optimal empirical antimicrobial therapy