What is the recommended dose of Ceftazidime (Ceftazidime) for adults with normal renal function and for pediatric patients, and how should it be adjusted in cases of impaired renal function?

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Ceftazidime Dosing Recommendations

Standard Adult Dosing with Normal Renal Function

For adults with normal renal function, the usual recommended dose of ceftazidime is 1 gram IV or IM every 8 to 12 hours, with higher doses of 2 grams every 8 hours reserved for severe infections including meningitis, serious gynecologic and intra-abdominal infections, and very severe life-threatening infections in immunocompromised patients. 1

Infection-Specific Dosing for Adults:

  • Uncomplicated urinary tract infections: 250 mg every 12 hours 1
  • Complicated urinary tract infections: 500 mg every 8 to 12 hours 1
  • Uncomplicated pneumonia and mild skin/soft tissue infections: 500 mg to 1 gram every 8 hours 1
  • Bone and joint infections: 2 grams every 12 hours 1
  • Serious gynecologic and intra-abdominal infections: 2 grams every 8 hours 1
  • Meningitis: 2 grams every 8 hours 1
  • Very severe life-threatening infections (especially immunocompromised): 2 grams every 8 hours 1
  • Pseudomonas lung infections in cystic fibrosis (normal renal function): 30 to 50 mg/kg (maximum 6 grams/day) every 8 hours 1

Special Considerations for Severe Infections:

  • For carbapenem-resistant Pseudomonas aeruginosa susceptible to ceftazidime: Use 2 grams IV every 8 hours for 5-14 days (longer courses of 10-14 days for pneumonia and bloodstream infections) 2
  • For severe infections in patients with normal renal function and augmented renal clearance: Extended infusion duration of 3-4 hours may be necessary to achieve optimal pharmacodynamic targets 3

Pediatric Dosing with Normal Renal Function

For pediatric patients (1 month to 12 years), the recommended dose is 30 to 50 mg/kg IV every 8 hours, with a maximum of 6 grams per day. 1

Age-Specific Pediatric Dosing:

  • Neonates (0-4 weeks): 30 mg/kg IV every 12 hours 1
  • Infants and children (1 month-12 years): 30 to 50 mg/kg IV every 8 hours (maximum 6 grams/day) 1
  • Higher doses (50 mg/kg) should be reserved for immunocompromised pediatric patients, those with cystic fibrosis, or meningitis 1

Renal Impairment Dosing Adjustments

Ceftazidime is excreted almost exclusively by glomerular filtration, requiring dose reduction in patients with impaired renal function (GFR <50 mL/min). 1

Initial Loading Dose:

  • Give 1 gram loading dose in patients with suspected renal insufficiency before adjusting to maintenance dosing 1

Maintenance Dosing Based on Creatinine Clearance:

Creatinine Clearance (mL/min) Recommended Dose Frequency
50-31 1 gram Every 12 hours
30-16 1 gram Every 24 hours
15-6 500 mg Every 24 hours
<5 500 mg Every 48 hours

1

Critical Dosing Principles for Renal Impairment:

  • If the dose recommended for the specific infection is lower than the renal adjustment dose, use the lower dose 1
  • For severe infections requiring 6 grams daily in normal renal function: Increase the unit dose by 50% or increase dosing frequency appropriately, guided by therapeutic monitoring 1
  • Dosing intervals should be extended rather than reducing individual doses to maintain adequate peak concentrations 4, 5

Alternative Renal Function-Based Recommendations:

Research supports the following intervals based on creatinine clearance 4:

  • ClCr >50 mL/min: Every 8 hours
  • ClCr 30-50 mL/min: Every 12 hours
  • ClCr 15-30 mL/min: Every 24 hours
  • ClCr <15 mL/min: Every 36-48 hours

Hemodialysis Dosing

For patients undergoing hemodialysis, give a 1 gram loading dose followed by 1 gram after each hemodialysis session. 1

Key Hemodialysis Considerations:

  • Ceftazidime is significantly removed by hemodialysis with a mean elimination half-life of 4.7 hours during dialysis 5
  • Post-dialysis dosing of 1 gram is effective and safe for achieving pharmacodynamic targets over 48- and 72-hour interdialytic intervals for pathogens with MICs ≤8 mg/L 6
  • The 2 gram post-dialysis dose is equally effective but may not be necessary for most patients 6
  • Administer the dose after dialysis to avoid premature drug removal 1

Peritoneal Dialysis Dosing

For patients on intraperitoneal dialysis or continuous ambulatory peritoneal dialysis (CAPD), give a 1 gram loading dose followed by 500 mg every 24 hours. 1

Alternative Administration:

  • Ceftazidime can be incorporated into dialysis fluid at a concentration of 250 mg per 2 liters of dialysis fluid 1
  • For chronic peritoneal dialysis: Loading dose of 10 mg/kg followed by continuous administration of 5 mg/kg into each dialysis cavity 7

Monitoring and Safety Considerations

Neurotoxicity Monitoring:

  • Monitor for neurotoxicity including seizures, encephalopathy, and confusion, particularly in patients with renal impairment where drug accumulation can occur 2
  • Risk increases with accumulation in renal failure patients 4, 7, 5

Duration of Therapy:

  • Continue ceftazidime for 2 days after signs and symptoms of infection have disappeared, but complicated infections may require longer therapy 1
  • For pneumonia and bloodstream infections caused by resistant organisms: Use 10-14 day courses 2

Common Pitfalls to Avoid:

  • Do not reduce individual doses below recommended levels in renal impairment; instead extend the dosing interval to maintain concentration-dependent killing 4, 5
  • Do not administer before hemodialysis as this leads to premature drug removal and subtherapeutic levels 6
  • Do not use standard dosing in patients with creatinine clearance <50 mL/min without adjustment 1, 4

No Hepatic Adjustment Required

No dosage adjustment is necessary for patients with hepatic dysfunction alone. 1

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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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