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# Gentamicin (IV)
## Overview
Gentamicin is an aminoglycoside antibiotic that inhibits bacterial protein synthesis by binding to the 30S ribosomal subunit. It is concentration-dependent, bactericidal, and primarily active against Gram-negative bacilli, including *Pseudomonas aeruginosa*.
## Primary Indications
* Serious Gram-negative infections (e.g., sepsis, pneumonia, intra-abdominal infections).
* Synergistic treatment for Gram-positive endocarditis (e.g., *Staphylococcus*, *Enterococcus*).
* Prophylaxis or treatment of neonatal sepsis.
## Adult Dosing
* **Traditional Dosing:** 1–2.5 mg/kg every 8–12 hours.
* **Extended-Interval (Once-Daily) Dosing:** 5–7 mg/kg IV every 24 hours.
* **Synergy for Endocarditis:** 1 mg/kg every 8–12 hours (typically capped at 80 mg per dose).
* *Note: Dosing must be based on Ideal Body Weight (IBW) or Adjusted Body Weight if obese.*
## Pediatric Dosing
* **Neonates (0–7 days):** 4–5 mg/kg every 24–48 hours (based on gestational age).
* **Infants/Children:** 2.5 mg/kg every 8 hours.
* *Consult local protocols (e.g., Neofax or hospital-specific guidelines) as pediatric dosing is highly dependent on weight, gestational age, and postnatal age.*
## Dose Adjustments
* **Renal Impairment:** Dosing frequency must be extended based on creatinine clearance (CrCl).
* **Obesity:** Use IBW for dosing; if actual body weight is >20% above IBW, use adjusted body weight.
* **Hepatic Impairment:** No standard adjustment required, but use with caution.
## Contraindications
* Known hypersensitivity to gentamicin or other aminoglycosides.
* Use with extreme caution in patients with myasthenia gravis or pre-existing renal impairment.
## Adverse Effects
* **Nephrotoxicity:** Usually reversible; associated with accumulation of drug in proximal tubule cells.
* **Ototoxicity:** Auditory (tinnitus, hearing loss) and vestibular (vertigo, ataxia) damage; often permanent.
* **Neuromuscular Blockade:** Rare, but can occur, especially with rapid IV infusion or in predisposed patients.
## Key Drug Interactions
* **Nephrotoxic Agents:** Increased risk of renal failure (e.g., vancomycin, amphotericin B, cisplatin, NSAIDs, loop diuretics).
* **Neuromuscular Blocking Agents:** Potentiation of blockade (e.g., succinylcholine, rocuronium).
## Monitoring
* **Renal Function:** Serum creatinine and urine output.
* **Therapeutic Drug Monitoring (TDM):**
* **Traditional:** Obtain troughs 30 minutes before the 3rd or 4th dose; peaks obtained 30 minutes post-infusion.
* **Extended-Interval:** Use Hartford Nomogram or similar; measure a "random level" 6–14 hours post-infusion.
* **Signs of Toxicity:** Auditory testing if therapy is prolonged (>14 days).
## Clinical Pearls
* **Infusion Time:** Always infuse over 30–60 minutes to prevent infusion-related neuromuscular blockade.
* **Synergy:** When used for synergy (e.g., endocarditis), serum levels are not typically required unless the patient has renal impairment.
* **Local Protocols:** Always verify institutional antibiograms and dosing nomograms before initiation.
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**Educational Disclaimer:** This information is for educational purposes only. Clinical settings vary significantly. Always verify current prescribing information, institutional protocols, and patient-specific factors with a pharmacist or physician before administering medication.