1PSI Risk Classes, Mortality & Admission Setting
| Risk Class | PORT Score Range | 30-Day Mortality | Recommended Triage Setting |
|---|---|---|---|
| Class I | Age ≤50 + No Comorbidities + Normal Exam | 0.1% | Outpatient |
| Class II | ≤ 70 points | 0.6% | Outpatient |
| Class III | 71–90 points | 2.8% | Outpatient or Short Stay Observation |
| Class IV | 91–130 points | 8.2% | Inpatient Medical Ward |
| Class V | > 130 points | 29.2% | Inpatient / Immediate ICU Triage |
2Empiric Antibiotic Selection (ATS / IDSA 2019)
- First-Line: Amoxicillin 1 g PO TID × 5 days.
- Alternative / Atypical coverage: Doxycycline 100 mg PO BID × 5 days.
- Macrolides (Azithromycin 500 mg Day 1, then 250 mg daily) only in regions with pneumococcal macrolide resistance <25%.
- Combination Therapy: Amoxicillin-clavulanate (875/125 mg PO BID or 2000/125 mg PO BID) plus Azithromycin 500 mg Day 1 then 250 mg daily, OR Doxycycline 100 mg BID.
- Monotherapy: Respiratory fluoroquinolone (Levofloxacin 750 mg PO daily or Moxifloxacin 400 mg PO daily) × 5 days.
- Non-ICU Inpatient: IV Beta-lactam (Ceftriaxone 1–2 g IV daily or Ampicillin-sulbactam 1.5–3 g IV q6h) plus IV/PO Azithromycin 500 mg daily, OR Respiratory fluoroquinolone monotherapy.
- Severe CAP / ICU (Class V): IV Beta-lactam (Ceftriaxone or Cefotaxime) plus IV Azithromycin or IV Levofloxacin.
- Add MRSA coverage (Vancomycin or Linezolid) and antipseudomonal coverage (Piperacillin-tazobactam, Cefepime, or Meropenem) if prior isolation or specific hospital validation exists.
3PSI / PORT vs. CURB-65 Comparison
| Clinical Attribute | Pneumonia Severity Index (PSI) | CURB-65 Score |
|---|---|---|
| Total Criteria Evaluated | 20 variables across 4 tiers | 5 variables |
| Primary Strength | Superior for identifying low-risk patients safe for outpatient therapy; reduces unnecessary hospitalizations. | Rapid bedside triage; excellent for identifying patients who will deteriorate. |
| Laboratory Requirements | Requires ABG, electrolytes, BUN, glucose, hematocrit, and CXR. | Requires only Serum Urea / BUN. |
| Guideline Endorsement | Preferred by ATS / IDSA 2019 | Preferred by British Thoracic Society (BTS) |
4Clinical Utility & Two-Step Triage
The Pneumonia Severity Index was developed from the Pneumonia Patient Outcomes Research Team (PORT) cohort of over 14,000 inpatients and validated in >38,000 individuals across North America. The model employs a validated two-step decision rule:
Step 1 (Risk Class I Assessment): Identifies patients aged ≤50 years who have zero comorbid illnesses (cancer, liver failure, heart failure, stroke, renal disease) and completely normal vital signs. These patients have a 30-day mortality of 0.1% and do not require laboratory blood sampling or chest radiography for severity calculation.