Pulmonary Infections – VASP, Evan Schwartz
Acute Bronchitis
Background
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- 1-3 wks productive cough, often preceded by URI, may have wheezing/rhonchi
- Distinct from chronic bronchitis (>3 mos of consecutive cough x 2 consecutive yrs)
- Distinct from PNA (parenchymal consolidation, fever >100.4F, hypoxia, tachypnea)
- DDx: COVID19, post-nasal drip, GERD, undertreated/new asthma, ACE-i induced bradykinin cough, undertreated CHF, acute PE, or new lung cancer
- Typically clinical dx; CXR/labs not necessary unless PNA suspected
Management
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- Supportive: lozenges, cough suppressants (guaifenesin or dextromethorphan), smoking cessation. Consider albuterol inhaler for wheezing
- No indication for antibiotics
Influenza
Background
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- Dx often clinical w/cough, sore throat, #sputum/nasal discharge, HA, fever, myalgias, and malaise; ± N/V/D. Exam with increased flushing, rarely with lower respiratory symptoms
Evaluation
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- During flu season: Obtain RPP or dedicated Influenza PCR in pts w/immunocompromise, acute hypoxic respiratory failure, respiratory distress, worsening of COPD, asthma, CAD/CHF; testing more accurate if obtained within 96 hour of symptom onset
- CXR if concerned for bacterial superinfection
Management
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- Antivirals most effective when given <48 hours from symptom onset; however, recommended to be given if symptomatic despite duration
- Oseltamivir 75mg BID x 5 days or peramivir 600mg IV x 1 (needs renal adjustment)
- Pain and fever: high-dose acetaminophen 1g TID are most effective; avoid aspirin, especially in children due to risk of Reye syndrome
- There is emerging resistance to amantadine and rimantadine, and are no longer employed
Community Acquired Pneumonia (CAP)
Background
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- All PNA that does not otherwise meet criteria for Hospital Acquired Pneumonia (PNA that develops ≥48 hours after hospital admission), Ventilator Associated Pneumonia (PNA that develops ≥48-72 hours after endotracheal intubation), or aspiration PNA
- Healthcare-associated pneumonia is no longer a clinical entity per 2016 IDSA guidelines
- MRSA Risk Factors: recent history, cavitary lesion, post-influenza bacterial PNA, pts with IDU, severe hypoxemia requiring intubation
- Pseudomonas: Double coverage is not indicated in general population; LQ has 82% sensitivity so not recommended unless isolate proven susceptible
Evaluation
- Resting pulse oximetry, ± ambulatory pulse oximetry
- Sputum cultures prior to abx, BCx prior to abx in select groups (severe pneumonia, ICU admission, cavitary disease, immunosuppression).
- Rule out flu if the right season, COVID-19, consider RVP if it will change management
- CURB-65 or PSI can aid in decision between outpatient vs inpatient therapy
- CURB65: Confusion, Uremia (BUN >=19 mg/dL), RR (>30/min), BP(<90/60 mmHg), Age ≥ 65 If ≥ 2, hospitalization is recommended.
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- Consider urine pneumococcal Ag, urine Legionella Ag in severe CAP and in certain pts (e.g., neutropenia, asplenia, obstructive lung disease, hyponatremia, diarrhea, or heavy alcohol use); these are performed at reference labs and will take several days to return.
- CRP, ESR, and pro-calcitonin have not been shown to reliably improve outcomes; however, pro-calcitonin < 0.25 suggests against bacterial respiratory infection and antibiotic discontinuation is encouraged
- PA/ lateral CXR to evaluate for and localize infiltrate. If immunocompromised, consider CT chest w/o contrast (does not improve outcomes)
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- Lobar Consolidation - likely bacterial
- Interstitial Infiltrate - likely atypical vs. viral vs. non-infectious
- Cavitation - concerning for fungal vs. necrotizing vs. mycobacterial
- CURB65: Confusion, Uremia (BUN >=19 mg/dL), RR (>30/min), BP(<90/60 mmHg), Age ≥ 65 If ≥ 2, hospitalization is recommended.
Management
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- Duration: 5-7 days (at least 5 days and improvement with clinical stability)
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Outpatient |
Inpatient (Non- ICU & ICU) |
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No MRSA or Pseudomonas suspected |
Low Risk*: Amoxicillin 1g TID High Risk: - Amoxicillin-clavulanate 875/125 BID OR Cefdinir 300 BID + Macrolide - Amoxicillin 1g TID + Macrolide - Levofloxacin 750 daily |
CTX 2g q24 + Azithromycin 500 daily OR Levofloxacin 750 daily |
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MRSA or Pseudomonas suspected |
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MRSA: Vancomycin OR Linezolid (if no bacteremia) Pseudomonas: Cefepime 2g q8h |
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*No chronic heart, lung, liver, renal disease, DM, alcoholism, immunocompromise
Additional Information
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- CTX is generally adequate coverage for aspiration PNA without evidence of abscess, empyema, or cavitary lesion on imaging
- There is low sensitivity of S. pneumoniae to azithromycin (42%) and doxycycline (72%), so these should not be used as monotherapy
- Check for DDI with Linezolid (e.g., SSRI)
Hospital Acquired Pneumonia (HAP) and Ventilator Associated Pneumonia (VAP)
Background
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- HAP: Pneumonia that develops >48 hours after admission
- VAP: Pneumonia that develops >48 hours after endotracheal intubation
Evaluation
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- Cultures of blood, sputum, endotracheal aspirate and/or bronchoscopy specimen
- Consider MRSA nares to help with de-escalation
- If there is concern for respiratory viruses, influenza, COVID send RVP
Management
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- Duration: 7 days in uncomplicated cases, although specific pathogens (e.g., Pseudomonas) may require longer duration and ID guidance
- Consider ID consultation if the patient is not clinically improving on empiric therapy or if an MDR pathogen grows from culture
- If no MRSA isolated and pt is improving, consider stopping vancomycin ASAP
- Some concern for nephrotoxicity with combination Vancomycin and piperacillin-tazobactam, but data controversial
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MRSA Coverage |
Pseudomonas Coverage |
First Line |
Vancomycin (PMCY dosing) |
Cefepime 2g q8h OR Piperacillin-tazobactam 3.375 q8h extended infusion OR Ceftazidime 2g q8h |
Alternative |
Vancomycin allergy: Linezolid 600 mg PO q12h |
PCN allergy*: Aztreonam 2g q8h |