What is the recommended dosage of Ceftazidime (Ceftazidime) and Avibactam (Avibactam) for treating complicated infections?

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Ceftazidime-Avibactam Dosage for Complicated Infections

The recommended dosage of ceftazidime-avibactam for treating complicated infections is 2.5 grams (2 grams ceftazidime and 0.5 grams avibactam) administered intravenously every 8 hours as a 2-hour infusion. 1

Standard Dosing Regimens by Infection Type

Adult Patients (≥18 years) with Normal Renal Function (CrCl >50 mL/min)

  • Complicated Intra-abdominal Infections (cIAI):

    • Ceftazidime-avibactam: 2.5 g IV q8h as 2-hour infusion
    • Must be used with metronidazole 500 mg IV q6h 2, 1
    • Duration: 5-14 days
  • Complicated Urinary Tract Infections (cUTI) including Pyelonephritis:

    • Ceftazidime-avibactam: 2.5 g IV q8h as 2-hour infusion 2, 1
    • Duration: 7-14 days
  • Hospital-acquired/Ventilator-associated Bacterial Pneumonia (HABP/VABP):

    • Ceftazidime-avibactam: 2.5 g IV q8h as 2-hour infusion 1
    • Duration: 7-14 days
  • Bloodstream Infections due to Carbapenem-resistant Enterobacterales (CRE):

    • Ceftazidime-avibactam: 2.5 g IV q8h infused over 3 hours 2
    • Duration: 7-14 days

Dosage Adjustments for Renal Impairment in Adults

Creatinine Clearance (CrCl) Recommended Dose
>50 mL/min 2.5 g (2 g ceftazidime + 0.5 g avibactam) IV q8h
31-50 mL/min 1.25 g (1 g ceftazidime + 0.25 g avibactam) IV q8h
16-30 mL/min 0.94 g (0.75 g ceftazidime + 0.19 g avibactam) IV q12h
6-15 mL/min 0.94 g (0.75 g ceftazidime + 0.19 g avibactam) IV q24h
≤5 mL/min 0.94 g (0.75 g ceftazidime + 0.19 g avibactam) IV q48h

Pediatric Dosing

Pediatric Patients (2 years to <18 years) with eGFR >50 mL/min/1.73 m²

  • Ceftazidime-avibactam: 62.5 mg/kg to maximum of 2.5 g IV q8h as 2-hour infusion 1

Pediatric Patients (6 months to <2 years) without Renal Impairment

  • Ceftazidime-avibactam: 62.5 mg/kg IV q8h as 2-hour infusion 1

Pediatric Patients (3 months to <6 months) without Renal Impairment

  • Ceftazidime-avibactam: 50 mg/kg IV q8h as 2-hour infusion 1

Pediatric Patients (>28 days to <3 months) without Renal Impairment

  • Ceftazidime-avibactam: 37.5 mg/kg IV q8h as 2-hour infusion 1

Neonates (≤28 days with GA ≥31 weeks) without Renal Impairment

  • Ceftazidime-avibactam: 25 mg/kg IV q8h as 2-hour infusion 1

Clinical Considerations

Pharmacokinetic/Pharmacodynamic Properties

  • Both ceftazidime and avibactam have complementary PK profiles with half-lives of approximately 2 hours 3
  • The fixed-dose combination ratio of 4:1 (ceftazidime:avibactam) was established based on pharmacokinetic modeling 3
  • Primary elimination pathway for both drugs is renal clearance 3
  • Target attainment is based on:
    • 50% time above MIC for free ceftazidime
    • 50% time above threshold concentration of 1 mg/L for free avibactam 3, 4

Efficacy in Clinical Trials

  • Ceftazidime-avibactam demonstrated non-inferiority to carbapenems in phase III studies for cIAI, cUTI, and nosocomial pneumonia 3, 5, 6
  • In the REPRISE trial, clinical cure rates were similar between ceftazidime-avibactam (91%) and best available therapy (91%) for ceftazidime-resistant Enterobacteriaceae and Pseudomonas aeruginosa infections 5

Special Populations

  • Critically ill patients: Standard dosing is appropriate as pharmacokinetic modeling accounts for this population 4, 6
  • Patients on continuous renal replacement therapy: Limited data suggests dosing may need adjustment; consider monitoring drug levels if available 7

Key Clinical Pearls

  1. Always adjust dosing based on renal function and monitor renal function during treatment
  2. For cIAI, always administer with metronidazole for anaerobic coverage
  3. The 2-hour infusion time is critical for achieving optimal pharmacokinetic/pharmacodynamic targets
  4. For CRE bloodstream infections, a 3-hour infusion is recommended to optimize drug exposure
  5. Monitor for emerging resistance during therapy, particularly in settings with high prevalence of multidrug-resistant organisms

Ceftazidime-avibactam represents an important treatment option for complicated infections caused by resistant gram-negative pathogens, particularly as a carbapenem-sparing alternative when appropriate.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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