What is the recommended dosage of Amikacin (an aminoglycoside antibiotic) for adults?

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Adult Dosage of Amikacin

For adults with normal renal function, administer amikacin 15 mg/kg/day intravenously or intramuscularly, divided into 2 or 3 equal doses (7.5 mg/kg every 12 hours or 5 mg/kg every 8 hours), with a maximum total daily dose not exceeding 15 mg/kg/day or 1.5 grams/day. 1

Standard Dosing Regimens

Once-Daily Dosing (Preferred for Most Infections)

  • Administer 15 mg/kg as a single daily dose for severe infections, which provides optimal concentration-dependent bactericidal activity and may reduce nephrotoxicity compared to divided dosing 2, 3, 4
  • This regimen achieves peak concentrations of 40-45 mg/L and trough concentrations of 1-2 mg/L 5
  • Clinical cure rates of 83% have been demonstrated with once-daily dosing, superior to twice-daily regimens (66% cure rate) 4
  • Once-daily dosing results in significantly less nephrotoxicity (21% vs 35% with twice-daily dosing) 4

Divided Dosing (Alternative Approach)

  • 7.5 mg/kg every 12 hours or 5 mg/kg every 8 hours for standard infections 1
  • This achieves average peak concentrations of 28 mg/L and trough concentrations of 5 mg/L 5
  • Only 48% of adult patients achieve therapeutic peak concentrations with twice-daily dosing, compared to 100% with once-daily dosing 6

Special Infection-Specific Dosing

  • For plague treatment: 15-20 mg/kg every 24 hours IV or IM 2
  • For complicated intra-abdominal infections: 15-20 mg/kg every 24 hours 2
  • For uncomplicated urinary tract infections: 250 mg twice daily may be sufficient 1

Age-Related Dose Adjustments

Elderly Patients (>59 Years)

  • Reduce dose to 10-11 mg/kg/day when using once-daily dosing 7, 8
  • Elderly patients have prolonged elimination half-lives (mean 4.8 hours vs 2 hours in younger adults) 8
  • Creatinine clearance correlates better with amikacin clearance (r=0.89) than with half-life (r=0.71) in this population 8

Renal Impairment Dosing

Dosing Interval Extension Method

  • Calculate dosing interval by multiplying serum creatinine (mg/dL) by 9 1
  • Example: If serum creatinine is 2 mg/dL, administer 7.5 mg/kg every 18 hours 1

Dose Reduction Method

  • Administer loading dose of 7.5 mg/kg, then reduce maintenance doses proportionally 1
  • Maintenance dose = (observed creatinine clearance / normal creatinine clearance) × loading dose 1
  • For severe renal impairment: reduce frequency to every 2-3 days at 12-15 mg/kg 7

Hemodialysis Patients

  • Administer after dialysis to facilitate directly observed therapy and prevent premature drug removal 7, 1

Obese Patients

  • Calculate dose using: ideal body weight + 40% of excess weight 7
  • Standard weight-based dosing may lead to underdosing in obese patients 9

Administration Guidelines

Intravenous Administration

  • Infuse over 30-60 minutes in adults 1, 3
  • Add 500 mg vial to 100-200 mL of compatible diluent (0.9% sodium chloride or 5% dextrose) 1
  • Solutions stable for 24 hours at room temperature at concentrations of 0.25-5 mg/mL 1

Intramuscular Administration

  • Same dosing as IV route 1
  • Administer as deep intramuscular injection 1

Therapeutic Drug Monitoring

Target Concentrations

  • Peak levels (once-daily): 65-80 mg/L for intermittent dosing or 25-35 mg/L for daily dosing 7, 9
  • Trough levels: <5 mg/L to prevent toxicity 7, 9
  • Peak levels >35 mg/L should be avoided to reduce toxicity risk 1

Monitoring Schedule

  • Measure peak levels within the first week of therapy 7, 9
  • Measure trough levels weekly for 4 weeks, then every 2 weeks when stable 7, 9
  • Monitor renal function monthly during treatment 9
  • Perform baseline audiometry and intermittent monitoring to detect ototoxicity (defined as 20 dB loss at one frequency or 10 dB loss at two adjacent frequencies) 9

Duration of Therapy

  • Standard duration: 7-10 days 1
  • For complicated infections: 4-7 days when adequate source control is achieved 2
  • If treatment beyond 10 days is required, re-evaluate necessity and monitor serum levels, renal function, and auditory/vestibular function closely 1

Critical Warnings

Nephrotoxicity Risk

  • Occurs in approximately 8.7% of patients receiving standard amikacin dosing 10
  • Risk increases with trough levels >5 mg/L 7, 9
  • Once-daily dosing reduces nephrotoxicity compared to divided dosing 4

Ototoxicity Risk

  • Both auditory and vestibular toxicity can occur 5
  • Requires baseline and periodic audiometric monitoring 9
  • Risk increases with prolonged therapy and elevated trough concentrations 5

Pregnancy Contraindication

  • Amikacin is contraindicated in pregnancy due to risk of fetal nephrotoxicity and congenital hearing loss 7, 10

Common Pitfalls to Avoid

  • Do not use fixed 500 mg doses regardless of patient weight, as this ignores weight-based dosing principles and risks treatment failure 9
  • Do not use every-other-day dosing for IV amikacin in most clinical scenarios, as this may lead to inadequate drug exposure 9
  • Do not exceed 15 mg/kg/day total daily dose by all routes of administration 1
  • Do not physically premix amikacin with other drugs; administer separately 1
  • Do not continue therapy without clinical response after 3-5 days; recheck antibiotic susceptibility 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Amikacin Dosage and Administration

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Amikacin once daily: a new dosing regimen based on drug pharmacokinetics.

Scandinavian journal of infectious diseases, 1990

Guideline

Amikacin Dosing and Monitoring Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Alternative Antibiotics to Amikacin in Renal Impairment

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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