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Pneumonia: Dosage Regimens and Treatment Guidelines
This guide covers Community-Acquired Pneumonia (CAP), Hospital-Acquired / Ventilator-Associated Pneumonia (HAP/VAP), Pneumocystis Pneumonia (PCP), and special pathogens. Based on ATS/IDSA guidelines and multiple major textbooks.
1. Severity Assessment Before Treatment
CURB-65 Score (Practical Bedside Tool)
| Criterion | Points |
|---|
| Confusion (new-onset) | 1 |
| Urea > 19 mg/dL (7 mmol/L) | 1 |
| Respiratory rate >= 30/min | 1 |
| Blood pressure < 90 systolic or <= 60 diastolic | 1 |
| 65 years or older | 1 |
- Score 0-1: Outpatient treatment likely safe (low mortality)
- Score 2: Consider inpatient admission
- Score >= 3: ICU-level care warranted; score >3 suggests intermediate or intensive care unit admission
The Pneumonia Severity Index (PSI) uses 20 variables; scores <=90 points (classes I-III) support outpatient management. Scores >130 warrant ICU consideration.
2. Community-Acquired Pneumonia (CAP)
Antibiotics should be started as soon as CAP is diagnosed, ideally within 4 hours of hospital arrival, as delays increase mortality. Therapy should be narrowed once a microbiologic etiology is confirmed.
Outpatient Regimens
No comorbidities, no MRSA/Pseudomonas risk:
| Drug | Dose | Duration |
|---|
| Amoxicillin | 1000 mg PO q8h | >= 5 days |
| Doxycycline | 100 mg PO q12h | >= 5 days |
| Azithromycin | 500 mg PO day 1, then 250 mg qday days 2-5 | 5 days |
With comorbidities (chronic heart/lung/liver/renal disease, diabetes, alcoholism, malignancy, asplenia):
Combination therapy - choose one beta-lactam PLUS one atypical agent:
| Beta-lactam (choose one) | Dose |
|---|
| Amoxicillin/clavulanate | 875/125 mg PO q12h |
| Cefpodoxime | 200 mg PO q12h |
| Cefuroxime | 500 mg PO q12h |
PLUS doxycycline 100 mg PO q12h OR azithromycin
OR Monotherapy with a respiratory fluoroquinolone:
- Levofloxacin 750 mg PO qday
- Moxifloxacin 400 mg PO qday
Inpatient Non-Severe CAP
| Regimen | Agents |
|---|
| Beta-lactam + macrolide | Ampicillin-sulbactam 1.5-3 g IV q6h, OR ceftriaxone 1-2 g IV qday, OR cefotaxime 1-2 g IV q8h, OR ceftaroline 600 mg IV q12h PLUS azithromycin |
| Monotherapy | Levofloxacin or moxifloxacin (respiratory fluoroquinolone) |
Note: In clinically stable patients, 3 days of IV beta-lactam therapy may be sufficient without oral step-down.
Inpatient Severe CAP (ICU Admission)
Dual therapy is mandatory:
- Beta-lactam PLUS macrolide
- Beta-lactam PLUS fluoroquinolone
Duration: Minimum 5 days for most; 7 days if MRSA or Pseudomonas suspected.
CAP with Special Resistance Risks
Prior MRSA Isolation / High-Risk MRSA
Add one of:
| Drug | Dose |
|---|
| Vancomycin | 15 mg/kg IV q12h (adjusted for renal function/levels) |
| Linezolid | 600 mg IV/PO q12h |
A rapid nasal MRSA PCR test can help guide decision - negative PCR has high negative predictive value.
Prior Pseudomonas Isolation / High-Risk P. aeruginosa
Add one of (anti-pseudomonal beta-lactam):
| Drug | Dose |
|---|
| Piperacillin-tazobactam | 4.5 g IV q6h |
| Cefepime | 2 g IV q8h |
| Ceftazidime | 2 g IV q8h |
| Imipenem | 500 mg IV q6h |
| Meropenem | 1 g IV q8h |
| Aztreonam | 2 g IV q8h |
3. Hospital-Acquired Pneumonia (HAP) and Ventilator-Associated Pneumonia (VAP)
Common MDR pathogens: MRSA, Pseudomonas aeruginosa, gram-negative bacilli (Klebsiella, Acinetobacter, Enterobacteriaceae).
Risk Factors for MDR Organisms
| Category | Risk Factors |
|---|
| MDR VAP | Prior IV antibiotics within 90 days; septic shock at VAP onset; ARDS preceding VAP; >=5 days in hospital before VAP; acute renal replacement therapy |
| MDR HAP | Prior IV antibiotics within 90 days |
| MRSA VAP/HAP | See local antibiogram (>10-20% prevalence = cover empirically) |
Empiric Therapy for HAP/VAP
| Risk Category | Recommended Regimen |
|---|
| Not high mortality risk; low MRSA risk | Piperacillin-tazobactam OR Cefepime OR Imipenem/Meropenem OR Levofloxacin (monotherapy) |
| Not high mortality risk; MRSA risk present | Above anti-pseudomonal beta-lactam/FQ PLUS Vancomycin or Linezolid |
| High mortality risk (septic shock / mechanical ventilation) | Anti-pseudomonal agent from 2 different classes PLUS Vancomycin or Linezolid |
- If local gram-negative resistance >10% or rates unknown: use 2 anti-pseudomonal agents from different classes
- MSSA confirmed: De-escalate to oxacillin, nafcillin, or cefazolin
- MRSA confirmed: Vancomycin or linezolid
- Avoid aminoglycosides as monotherapy (poor lung penetration, nephrotoxicity/ototoxicity risk)
- Acinetobacter: Ampicillin-sulbactam or carbapenem (imipenem/meropenem; ertapenem has no Pseudomonas coverage)
- De-escalate to monotherapy once septic shock resolves and cultures are available
4. Pneumocystis Pneumonia (PCP) - HIV/Immunocompromised Patients
(From Goldman-Cecil Medicine)
Mild PCP (PaO2 >= 70 mmHg or A-a gradient < 35 mmHg)
| Preference | Drug | Route | Dose |
|---|
| Preferred | TMP-SMX | PO | 2 DS tablets (160/800 mg) TID |
| Alternative | Trimethoprim + Dapsone | PO | TMP 5 mg/kg TID + Dapsone 100 mg qday |
| Alternative | Clindamycin + Primaquine | PO | Clindamycin 450 mg qday or 600 mg TID + Primaquine 30 mg (base) qday |
| Alternative | Atovaquone | PO | 750 mg BID with food |
Test for G6PD deficiency before using dapsone or primaquine.
Moderate-to-Severe PCP (PaO2 < 70 mmHg or A-a gradient >= 35 mmHg)
| Preference | Drug | Route | Dose |
|---|
| Preferred | TMP-SMX | IV | TMP 5 mg/kg q8h + SMX 25 mg/kg q8h (= TMP 15 mg/kg/day + SMX 75 mg/kg/day); may switch to oral when improving |
| Alternative | Pentamidine | IV | 3-4 mg/kg qday (infuse over >60 min) |
| Alternative | Clindamycin + Primaquine | IV/PO | Clindamycin 600 mg q6h or 900 mg q8h IV; Primaquine 30 mg (base) qday PO |
Adjuvant Corticosteroids (Moderate-to-Severe, PaO2 < 70 mmHg)
Start within 72 hours (efficacy not demonstrated if started later):
| Drug | Route | Dose/Schedule |
|---|
| Prednisone | PO | 40 mg BID days 1-5; 40 mg qday days 6-10; 20 mg qday days 11-21 |
| Methylprednisolone | IV | 30 mg BID days 1-5; 30 mg qday days 6-10; 15 mg qday days 11-21 |
5. Newer/Reserve Antibiotics for Pneumonia
(From Fishman's Pulmonary Diseases)
| Drug | Class | Coverage | Dose |
|---|
| Omadacycline | Aminocycline | MRSA, DRSP, atypicals | 100 mg IV once daily |
| Lefamulin | Pleuromutilin | MRSA, MSSA, VRE, DRSP, Legionella, Mycoplasma, Chlamydia | 450 mg PO q12h x 5 days |
| Delafloxacin | Non-fluorinated quinolone | MRSA, Enterococcus, Mycoplasma, Legionella | 300 mg IV q12h, then 450 mg PO q12h x 5-10 days |
| Nemonoxacin | Novel quinolone | Gram-positive, gram-negative, atypicals, MRSA, VRE | 500 mg once daily x 7 days |
| Telavancin | Lipoglycopeptide | Gram-positive including MRSA/VRE | 10 mg/kg q24h |
| Ceftobiprole | 5th-gen cephalosporin | MSSA, H. influenzae, K. pneumoniae, P. aeruginosa | 600 mg PO BID |
Key considerations:
- Lefamulin and fluoroquinolones are contraindicated in prolonged QT interval
- Lefamulin is also contraindicated in moderate-to-severe liver disease
- Fluoroquinolones carry risk of C. difficile, tendinopathy, peripheral neuropathy, and QT prolongation
6. Aspiration Pneumonia
Common organisms: Oral anaerobes (Prevotella, Peptostreptococcus, Fusobacterium, Bacteroides, Actinomyces), MRSA, Klebsiella.
- Routine anaerobic coverage (e.g., clindamycin) is not recommended unless lung abscess or empyema is suspected
- Empiric regimens otherwise follow CAP or HAP guidelines based on setting
7. Duration of Therapy Summary
| Setting | Duration |
|---|
| Outpatient CAP (uncomplicated) | 5 days |
| Inpatient non-severe CAP (stable) | 3-5 days IV, then oral if clinically stable |
| Inpatient severe CAP | Minimum 5 days |
| Suspected MRSA or Pseudomonas | 7 days |
| HAP/VAP | Based on clinical response; de-escalate once culture data available |
| PCP (mild) | 21 days total |
| PCP (moderate-severe) | 21 days total |
8. Adjunctive and Supportive Measures
- Corticosteroids in CAP: Not recommended routinely; reserved for refractory septic shock (hydrocortisone 200 mg for 4-8 days may be considered)
- Thoracentesis: Perform on pleural effusions (analyze pH, cell count, Gram stain, culture, protein, LDH); drain empyemas
- Influenza co-infection: Add antiviral therapy (oseltamivir) plus antibiotics for bacterial co-infection; treat all hospitalized influenza-positive patients regardless of symptom duration
- SARS-CoV-2: Do NOT give antibiotics unless bacterial co-infection is suspected; use antivirals/antibody treatments in high-risk patients
- Procalcitonin: Professional societies recommend against using procalcitonin alone to decide whether to start antibiotics
- De-escalation: Always narrow therapy once culture/susceptibility data are available
Sources: The Washington Manual of Medical Therapeutics; Goldman-Cecil Medicine; Fishman's Pulmonary Diseases and Disorders; Current Surgical Therapy 14e - based on ATS/IDSA 2019 CAP Guidelines and IDSA/ATS 2016 HAP/VAP Guidelines.