What are the IDSA (Infectious Diseases Society of America)/ATS (American Thoracic Society) guidelines for the management of community-acquired pneumonia (CAP)?

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IDSA/ATS Guidelines for Community-Acquired Pneumonia

Severity Assessment and Site of Care

Use a systematic approach to determine treatment location: assess for conditions compromising home safety, calculate the Pneumonia Severity Index (PSI) or CURB-65 score, then apply clinical judgment. 1, 2

  • PSI risk classes I-III can be treated at home 2
  • CURB-65 score of 0-1 without hypoxemia indicates outpatient candidacy 1, 3
  • Patients requiring ICU admission should meet criteria for severe CAP (septic shock requiring vasopressors or respiratory failure requiring mechanical ventilation) 1

Empiric Antibiotic Therapy

Outpatient Treatment (Previously Healthy, No Recent Antibiotics)

For outpatient CAP, use amoxicillin 1g three times daily OR doxycycline 100mg twice daily as first-line therapy. 1, 2

  • Alternative: macrolide monotherapy (azithromycin or clarithromycin) in regions with <25% high-level macrolide-resistant S. pneumoniae 1
  • In regions with ≥25% macrolide resistance, avoid macrolide monotherapy 1

Outpatient Treatment (With Comorbidities or Recent Antibiotic Use)

Use a respiratory fluoroquinolone (moxifloxacin, gemifloxacin, or levofloxacin 750mg) OR combination therapy with high-dose amoxicillin (1g three times daily) or amoxicillin-clavulanate (2g twice daily) plus a macrolide. 1

  • Alternative β-lactams: ceftriaxone, cefpodoxime, or cefuroxime 500mg twice daily 1
  • Doxycycline is an acceptable alternative to macrolides 1

Inpatient Non-ICU Treatment

Hospitalized patients should receive either a respiratory fluoroquinolone alone OR a β-lactam (cefotaxime, ceftriaxone, or ampicillin) plus a macrolide. 1, 2

  • Ertapenem is acceptable for patients with risk factors for gram-negative pathogens (excluding Pseudomonas) 1
  • Doxycycline is an alternative to macrolides 1
  • For penicillin-allergic patients, use a respiratory fluoroquinolone 1

Inpatient ICU Treatment

Severe CAP requires combination therapy with a β-lactam (cefotaxime, ceftriaxone, or ampicillin-sulbactam) PLUS either azithromycin OR a respiratory fluoroquinolone. 1, 2

For Pseudomonas risk factors (structural lung disease, severe COPD, recent broad-spectrum antibiotics), use an antipseudomonal β-lactam (piperacillin-tazobactam, cefepime, imipenem, or meropenem) plus either ciprofloxacin or levofloxacin 750mg. 1, 4

  • Alternative for Pseudomonas coverage: antipseudomonal β-lactam plus aminoglycoside plus either azithromycin or antipneumococcal fluoroquinolone 1
  • For suspected community-acquired MRSA, add vancomycin or linezolid 1, 2
  • For penicillin allergy with Pseudomonas risk, substitute aztreonam for β-lactam 1

Timing and Administration

Administer the first antibiotic dose while the patient is still in the emergency department. 1, 2

  • Initiate empiric therapy regardless of initial procalcitonin level 2
  • Early treatment within 48 hours of symptom onset improves outcomes 1, 2

Transition to Oral Therapy

Switch from IV to oral antibiotics when the patient is hemodynamically stable, clinically improving, afebrile, able to ingest medications, and has normal GI function. 1

  • Inpatient observation while receiving oral therapy is unnecessary 1
  • Discharge as soon as clinically stable with no other active medical problems 1

Duration of Therapy

Treat for a minimum of 5 days, ensuring the patient is afebrile for 48-72 hours and has no more than one sign of clinical instability before stopping antibiotics. 1, 2, 5

  • Longer duration (14-21 days) required for Legionella, S. aureus, or gram-negative enteric bacilli 5
  • Extended therapy needed if initial antibiotics were inactive against the identified pathogen or if extrapulmonary complications exist (meningitis, endocarditis) 1

Pathogen-Directed Therapy

Once a pathogen is identified by reliable microbiological methods, narrow therapy to target that specific organism. 1, 2

Management of Treatment Failure

Reassess patients who fail to improve at 48-72 hours using a systematic classification based on timing and type of failure. 1

  • Up to 15% of CAP patients do not respond appropriately to initial therapy 1
  • Review clinical history, examination, prescription records, and all investigations 5

Supportive Care for Severe CAP

Use noninvasive ventilation for hypoxemia or respiratory distress unless immediate intubation is required (PaO₂/FiO₂ <150 with bilateral infiltrates). 1, 2

For mechanically ventilated patients with diffuse bilateral pneumonia or ARDS, use low-tidal-volume ventilation (6 mL/kg ideal body weight). 1, 2

  • Screen hypotensive, fluid-resuscitated patients for occult adrenal insufficiency 1

Follow-Up

Arrange clinical review at 6 weeks with either the general practitioner or hospital clinic. 2, 5

  • Obtain chest radiograph at follow-up for patients with persistent symptoms, physical signs, or higher malignancy risk (smokers, age >50 years) 2

Prevention

Administer pneumococcal polysaccharide vaccine to persons ≥65 years and those with high-risk conditions per ACIP guidelines. 1

Healthcare workers should receive annual influenza immunization. 1

  • Assess vaccination status at hospital admission for all patients 1
  • Vaccinate at discharge or during outpatient treatment 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Community-Acquired Pneumonia Treatment Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Guidelines for severe community-acquired pneumonia in the western world.

The Netherlands journal of medicine, 1999

Guideline

Community-Acquired Pneumonia Treatment Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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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