What is the recommended management and antibiotic regimen for a typical adult with community‑acquired pneumonia, including severity assessment and outpatient versus inpatient treatment?

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Management of Community-Acquired Pneumonia in Adults

Severity Assessment and Site-of-Care Decision

Use the Pneumonia Severity Index (PSI) or CURB-65 score to determine whether outpatient or inpatient treatment is appropriate, as these validated tools predict 30-day mortality and guide initial management decisions. 1

  • PSI Classes I–III: Treat as outpatient 1, 2
  • PSI Classes IV–V: Consider hospitalization 1, 3
  • CURB-65 score ≥2: Hospitalize the patient 1, 4
  • ICU admission criteria: Presence of septic shock requiring vasopressors, respiratory failure requiring mechanical ventilation, or ≥3 minor criteria (confusion, respiratory rate ≥30/min, hypotension, multilobar infiltrates, hypothermia, leukopenia, thrombocytopenia, uremia, hypoxemia) 1

The modified BTS severity score performs best across multiple outcomes including mortality and ICU admission, while PSI Classes IV+V and CURB demonstrate similar predictive accuracy 4. However, PSI is significantly better than CURB-65 for predicting 30-day mortality (94% vs 62% sensitivity) and ICU admission (86% vs 61% sensitivity) 3.

Outpatient Antibiotic Regimens

Previously Healthy Adults Without Comorbidities

Amoxicillin 1 g orally three times daily for 5–7 days is the preferred first-line therapy, providing superior pneumococcal coverage including drug-resistant strains. 1

  • Alternative: Doxycycline 100 mg orally twice daily for 5–7 days 1
  • Macrolides (azithromycin 500 mg day 1, then 250 mg daily; or clarithromycin 500 mg twice daily) should only be used in areas where pneumococcal macrolide resistance is documented <25% 1, 5

Adults With Comorbidities or Recent Antibiotic Use

Combination therapy is required for patients with COPD, diabetes, chronic heart/liver/renal disease, malignancy, or antibiotic use within 90 days. 1

  • Option 1: β-lactam (amoxicillin-clavulanate 875/125 mg twice daily, cefpodoxime, or cefuroxime) plus macrolide (azithromycin or clarithromycin) or doxycycline 100 mg twice daily 1
  • Option 2: Respiratory fluoroquinolone monotherapy (levofloxacin 750 mg daily or moxifloxacin 400 mg daily) 1

Inpatient Antibiotic Regimens (Non-ICU)

For hospitalized patients not requiring ICU admission, use either β-lactam plus macrolide combination or respiratory fluoroquinolone monotherapy—both regimens have equivalent efficacy with strong evidence. 1

  • Preferred regimen: Ceftriaxone 1–2 g IV daily plus azithromycin 500 mg IV or oral daily 1
  • Alternative β-lactams: Cefotaxime 1–2 g IV every 8 hours or ampicillin-sulbactam 3 g IV every 6 hours, always combined with azithromycin 1
  • Alternative monotherapy: Levofloxacin 750 mg IV daily or moxifloxacin 400 mg IV daily 1
  • Penicillin-allergic patients: Use respiratory fluoroquinolone 1

Administer the first antibiotic dose in the emergency department immediately upon diagnosis, as delays beyond 8 hours increase 30-day mortality by 20–30%. 1

Severe CAP Requiring ICU Admission

Combination therapy is mandatory for all ICU patients; β-lactam monotherapy is associated with higher mortality. 1

  • Preferred ICU regimen: Ceftriaxone 2 g IV daily (or cefotaxime 1–2 g IV every 8 hours or ampicillin-sulbactam 3 g IV every 6 hours) plus azithromycin 500 mg IV daily or respiratory fluoroquinolone (levofloxacin 750 mg IV daily or moxifloxacin 400 mg IV daily) 1

Special Pathogen Coverage (Add Only When Risk Factors Present)

Antipseudomonal coverage: Add only if structural lung disease (bronchiectasis, cystic fibrosis), recent hospitalization with IV antibiotics within 90 days, or prior Pseudomonas aeruginosa isolation 1

  • Regimen: Piperacillin-tazobactam 4.5 g IV every 6 hours or cefepime 2 g IV every 8 hours plus ciprofloxacin 400 mg IV every 8 hours or levofloxacin 750 mg IV daily plus aminoglycoside (gentamicin or tobramycin 5–7 mg/kg IV daily) 1

MRSA coverage: Add only if prior MRSA infection/colonization, recent hospitalization with IV antibiotics, post-influenza pneumonia, or cavitary infiltrates on imaging 1

  • Regimen: Vancomycin 15 mg/kg IV every 8–12 hours (target trough 15–20 mg/L) or linezolid 600 mg IV every 12 hours 1

Duration of Therapy

Treat for a minimum of 5 days and continue until the patient is afebrile for 48–72 hours with no more than one sign of clinical instability. 1, 5

  • Typical duration for uncomplicated CAP: 5–7 days 1, 5
  • Extended duration (14–21 days): Required for Legionella pneumophila, Staphylococcus aureus, or Gram-negative enteric bacilli 1, 5
  • Severe microbiologically undefined pneumonia: 10 days 5

Transition from IV to Oral Therapy

Switch from IV to oral antibiotics when the patient is hemodynamically stable (systolic BP ≥90 mmHg, heart rate ≤100 bpm), clinically improving, afebrile for 48–72 hours, respiratory rate ≤24 breaths/min, oxygen saturation ≥90% on room air, able to take oral medications, and has normal GI function—typically by hospital day 2–3. 1, 5

  • Oral step-down options: Amoxicillin 1 g three times daily plus azithromycin 500 mg daily, or continue respiratory fluoroquinolone 1

Supportive Care and Monitoring

All hospitalized patients require appropriate oxygen therapy targeting PaO₂ >8 kPa (60 mmHg) and SaO₂ >92%. 5

  • High-flow oxygen is safe in uncomplicated pneumonia 5
  • For COPD patients with ventilatory failure, guide oxygen therapy by repeated arterial blood gases to avoid CO₂ retention 5
  • Monitor temperature, respiratory rate, pulse, blood pressure, mental status, oxygen saturation, and inspired oxygen concentration at least twice daily 5
  • Assess for volume depletion and provide IV fluids as needed 5

Follow-Up and Treatment Failure

Review outpatients at 48 hours or sooner if clinically indicated to assess treatment response. 5, 1

If no clinical improvement by day 2–3, obtain repeat chest radiograph, CRP, white cell count, and additional microbiological specimens. 5

  • For non-severe pneumonia on amoxicillin monotherapy: Add or substitute a macrolide 5
  • For non-severe pneumonia on combination therapy: Switch to respiratory fluoroquinolone 5
  • For severe pneumonia not responding to combination therapy: Consider adding rifampicin 5

Schedule clinical review at 6 weeks for all hospitalized patients; chest radiograph is only required for those with persistent symptoms, physical signs, or high risk for underlying malignancy (smokers >50 years). 5, 1

Critical Pitfalls to Avoid

  • Never use macrolide monotherapy in hospitalized patients—it provides inadequate coverage for typical bacterial pathogens like S. pneumoniae 1
  • Never use macrolide monotherapy in areas where pneumococcal macrolide resistance exceeds 25%—this leads to treatment failure and breakthrough bacteremia 1
  • Never delay antibiotic administration beyond 8 hours—this increases 30-day mortality by 20–30% 1
  • Obtain blood and sputum cultures before initiating antibiotics in all hospitalized patients to enable pathogen-directed therapy and de-escalation 1
  • Avoid indiscriminate use of antipseudomonal or MRSA coverage—add only when documented risk factors are present 1
  • Do not extend therapy beyond 7–8 days in responding patients without specific indications—longer courses increase antimicrobial resistance risk without improving outcomes 1

Prevention

  • Administer pneumococcal polysaccharide vaccine to all patients ≥65 years and those with high-risk conditions 5, 1
  • Offer annual influenza vaccination to all patients, especially those with chronic medical illnesses 5, 1
  • Make smoking cessation a goal for all patients hospitalized with CAP who smoke 5, 1

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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