Meropenem Dosing for Pneumonia
For adults with normal renal function and pneumonia, administer meropenem 1 g IV every 8 hours.
Community-Acquired Pneumonia (CAP)
For empiric treatment of severe CAP requiring coverage for Pseudomonas aeruginosa, meropenem is an appropriate antipseudomonal β-lactam option at 1 g IV every 8 hours 1. This dosing applies when:
- Patient has locally validated risk factors for P. aeruginosa 1
- Severe CAP requiring ICU admission 1
- Structural lung disease (bronchiectasis, cystic fibrosis) 1
Important caveat: Meropenem should not be used as routine first-line therapy for CAP. The 2019 ATS/IDSA guidelines recommend β-lactam plus macrolide or β-lactam plus respiratory fluoroquinolone for severe CAP without specific risk factors for resistant pathogens 1.
Hospital-Acquired Pneumonia (HAP) and Ventilator-Associated Pneumonia (VAP)
Standard Dosing for HAP/VAP
Meropenem 1 g IV every 8 hours is the recommended dose for empiric treatment of HAP/VAP 1. This applies to:
- Patients with low risk of multidrug-resistant organisms (MDROs) 1
- Patients not at high risk of mortality 1
- Standard empiric coverage for gram-negative pathogens including P. aeruginosa 1
Alternative Dosing Considerations
- Imipenem 500 mg IV every 6 hours is an equivalent carbapenem alternative 1
- For severe infections or high MDRO risk, meropenem may be combined with a second antipseudomonal agent (aminoglycoside or fluoroquinolone) 1
Extended Infusion Strategy
For carbapenem-resistant Enterobacterales (CRE) infections, meropenem 1 g IV every 8 hours by extended infusion (3-hour infusion) is recommended when the MIC is ≥8 mg/L 1. This pharmacokinetic optimization may improve outcomes in difficult-to-treat infections 1.
Pathogen-Specific Dosing
When P. aeruginosa is confirmed as the causative pathogen:
- Stable hemodynamics: Meropenem 1 g IV every 8 hours as monotherapy 1
- Unstable hemodynamics: Meropenem 1 g IV every 8 hours plus aminoglycoside (gentamicin 5-7 mg/kg IV daily or amikacin 15-20 mg/kg IV daily) 1
Clinical Evidence Supporting Dosing
A prospective randomized trial in VAP demonstrated that meropenem 1 g IV every 8 hours as monotherapy achieved 82.5% satisfactory clinical response, superior to ceftazidime/amikacin combination therapy 2. Pharmacokinetic studies confirm that this dosing regimen achieves adequate drug concentrations with peak levels of approximately 30-33 mg/L and maintains therapeutic levels throughout the dosing interval 3, 4.
Renal Dose Adjustments
The standard 1 g every 8 hours dose applies only to patients with normal renal function 1. Meropenem is predominantly renally excreted, and dosage adjustments are mandatory in renal insufficiency 5, 4:
- CrCl 40-60 mL/min: 500 mg IV every 8 hours 3
- CrCl 10-39 mL/min: 500 mg IV every 12 hours 3
- Hemodialysis: Approximately 50% removed by dialysis; supplemental dosing required 5
Key Clinical Pitfalls
- Do not use meropenem routinely for CAP without documented risk factors for resistant pathogens, as this promotes carbapenem resistance 1
- Always verify renal function before prescribing standard doses, as accumulation occurs rapidly in renal impairment 5, 4
- Consider combination therapy for high-risk patients (septic shock, ARDS, prior MDRO colonization) rather than relying on monotherapy 1
- Avoid empiric carbapenem use based solely on prior "healthcare-associated pneumonia" (HCAP) criteria, which have been abandoned due to poor predictive value for resistant pathogens 1