Initial Approach for Community-Acquired Pneumonia Requiring Hospital Admission
For patients with community-acquired pneumonia requiring hospital admission, immediately assess severity, initiate oxygen therapy to maintain SpO2 >92%, obtain diagnostic studies without delaying antibiotics, and start empiric combination antibiotic therapy within the first hour of presentation. 1
Immediate Assessment and Stabilization
Severity Assessment
- Evaluate adverse prognostic features immediately upon presentation to determine appropriate level of care (general ward vs. ICU) 1
- Assess for hypoxemia (SpO2 <92% or PaO2 <8 kPa), bilateral or multilobar involvement on chest radiograph, respiratory rate, systolic and diastolic blood pressure, mental status changes, and signs of volume depletion 1
- Delayed oxygenation assessment beyond 3 hours is an independent risk factor for death (hazard ratio 2.06), so oxygen saturation must be measured immediately 1
- Patients requiring ICU admission should be transferred directly from the emergency department rather than after a period on the medical ward, as delayed ICU admission (>2 days) increases mortality from 46.3% to 57.6% 1
Oxygen and Supportive Care
- Initiate appropriate oxygen therapy immediately with continuous monitoring of oxygen saturations and FiO2, targeting PaO2 >8 kPa and SpO2 >92% 1
- High concentrations of oxygen can be safely administered in uncomplicated pneumonia 1
- For patients with pre-existing COPD complicated by ventilatory failure, guide oxygen therapy by repeated arterial blood gas measurements 1
- Assess for volume depletion and initiate intravenous fluid resuscitation promptly—the choice of crystalloids (saline, Ringer's solution) versus colloids is less important than timely initiation 1
Diagnostic Studies
Essential Initial Testing
- Obtain chest radiograph, complete blood count with differential, serum electrolytes, glucose, liver and renal function tests immediately 1
- Measure oxygen saturation by pulse oximetry in all patients 1
- Obtain arterial blood gas in patients with severe illness or chronic lung disease to assess both oxygenation and carbon dioxide retention 1
- Test for COVID-19 and influenza when these viruses are common in the community, as their diagnosis affects treatment and infection prevention strategies 2
Microbiological Studies
- Collect sputum for Gram stain and culture before antibiotic administration if a drug-resistant pathogen or organism not covered by usual empiric therapy is suspected 1
- Blood cultures should be obtained, though only 38% of hospitalized CAP patients have a pathogen identified 2
- Consider legionella urinary antigen testing in severe CAP or when epidemiologically suspected 1
- Do not delay antibiotic therapy to obtain diagnostic studies in clinically unstable patients—delays in appropriate antibiotic therapy increase mortality 1
Antibiotic Therapy
Timing and Selection
- Initiate empiric antibiotic therapy within 1 hour of presentation—postponing oxygenation assessment beyond 1 hour delays antibiotic administration by 6.13 hours on average 1
- Inappropriate initial antimicrobial treatment is associated with significantly increased hospital mortality (24.7% vs 16.2%) 1
Empiric Antibiotic Regimens for Non-ICU Hospitalized Patients
- For hospitalized patients without risk factors for resistant bacteria, use β-lactam/macrolide combination therapy (e.g., ceftriaxone combined with azithromycin) for a minimum of 3 days 2
- Alternative regimen: fluoroquinolone monotherapy (e.g., levofloxacin or moxifloxacin) 2, 3
- β-lactam monotherapy was shown to be noninferior to combination therapy in non-ICU patients in a large cluster-randomized trial, though combination therapy remains standard in most guidelines 3
Empiric Antibiotic Regimens for Severe CAP/ICU Patients
- For patients with severe CAP requiring ICU admission, use combination antibiotic therapy—this is crucial when treating patients with shock 1
- Combination therapy improved outcomes in patients with shock compared to monotherapy in the CAPUCI study 1
- Consider coverage for multidrug-resistant pathogens in patients with healthcare-associated risk factors (prior hospitalization, dialysis, nursing home residence, immunocompromised state) 4
Drug Administration
- Administer antibiotics by intravenous infusion initially 5, 6, 5
- Azithromycin should be followed by oral azithromycin as required after initial IV therapy 6
Monitoring and Reassessment
Vital Signs and Clinical Parameters
- Monitor and record temperature, respiratory rate, pulse, blood pressure, mental status, oxygen saturation, and inspired oxygen concentration at least twice daily, more frequently in severe pneumonia or those requiring regular oxygen therapy 1
- Regular reassessment of severity during the illness is mandatory to adjust management appropriately 1
Laboratory and Radiographic Follow-up
- Remeasure CRP level in patients not progressing satisfactorily 1
- Repeat chest radiograph if clinical improvement is not occurring 1
- In patients improving clinically without concerning features, further investigations are not necessary just because radiological improvement lags behind clinical recovery 1
Adjunctive Therapy
Corticosteroids
- Systemic corticosteroid administration within 24 hours of development of severe CAP may reduce 28-day mortality 2
- This is particularly relevant for patients with severe disease requiring ICU admission 7
Nutritional Support
- Consider nutritional support in prolonged illness 1
Common Pitfalls to Avoid
- Delaying oxygenation assessment and antibiotic administration—organizational issues, incorrect diagnosis, and lack of physician confidence are common reasons for delays that increase mortality 1
- Failing to differentiate healthcare-associated pneumonia from community-acquired pneumonia—HCAP patients are more likely to receive inappropriate initial therapy (28.3% vs 13.0%) and have higher mortality 4
- Admitting high-risk patients to general wards initially rather than directly to ICU—delayed ICU admission significantly increases mortality 1
- Using monotherapy in patients with septic shock—combination therapy is essential in this population 1