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Table 1 Empirical antibiotic therapy protocol for HAP-VAP in ARC patients (CLCR > 150 ml/min)

From: Increased β-Lactams dosing regimens improve clinical outcome in critically ill patients with augmented renal clearance treated for a first episode of hospital or ventilator-acquired pneumonia: a before and after study

 

Control period (June 2016 to November 2017)

Conventional dosing regimen

Treatment period (November 2017 to January 2019)

Increased dosing regimen

Early HAP-VAP (< 5 days of hospitalization) without risk factors for NF-GNB or multidrug-resistant pathogens

• Amoxicillin-clavulanic acid (2 g IV q 8 h)

• Amoxicillin-clavulanic acid (2 g IV q 6 h)

• Cefotaxime (2 g IV q 8 h)

• Cefotaxime (2 g IV q 6 h)

• Ceftriaxone (2 g IV once/day)

• Ceftriaxone (2 g IV q 12 h)

Late HAP-VAP (≥ 5 days of hospitalization) and/or risk factors for NF-GNB or multidrug-resistant pathogens and/or immunosuppressive disease or therapy

Broad-spectrum β-lactam:

Broad-spectrum β-lactam:

• Piperacillin-tazobactam (16 g/day continuously after a loading dose of 4 g)

• Piperacillin-tazobactam (20 g/day continuously after a loading dose of 4 g)

• Cefepime (6 g/day continuously after a loading dose of 2 g over 30 min)

• Cefepime (6 g/day continuously after a loading dose of 2 g over 30 mins)

• Ceftazidime (6 g/day continuously after a loading dose of 2 g over 30 min)

• Ceftazidime (6 g/day continuously after a loading dose of 2 g over 30 min)

• Meropenem (6 g/day continuously or 2 g q 8 h over 240 min)

• Meropenem (6 g/day continuously or 2 g q 8 h over 240 min)

If risk factors for MRSA

Gram-positive antibiotics with MRSA activity: glycopeptides (vancomycin 15 mg/kg/day continuously after a loading dose of 25 mg/kg*) or oxazolidinones (linezolid 600 mg IV twice/day)

If septic shock or ARDS at time of HAP-VAP

Aminoglycosides or fluoroquinolones: amikacine (20–30 mg/kg*), gentamycin (7–10 mg/kg*), or levofloxacin (500 mg twice/day)

  1. *Glycopeptides (vancomycin) and aminoglycosides (gentamycin, amikacin) were subsequently dosed by therapeutic monitoring