Gentamicin therapy in preterms

A comparison of two dosage regimens

Lalitha Krishnan, S. A. George

Research output: Contribution to journalArticle

26 Citations (Scopus)

Abstract

Objective: To compare the pharmacokinetic profile of gentamicin given as a once daily dose as against the conventional twelve hourly dose in preterm neonates. Design: Randomized double blind study. Setting: Tertiary level Neonatal Intensive Care Unit. Subjects: Eighteen preterms admitted during the period January 1994 to May 1994. Methods: The babies were randomly assigned to receive either the once daily (plan O, 4 mg/kg Q 24 h) or the conventional (plan C, 2.5 mg/kg Q 12 h) gentamicin dosage regimen. Blood was collected for the first peak level one hour after the first dose of gentamicin. Trough the peak-2 levels were collected before and one hour after the dose due at 48 hours, respectively. Assays were done using fluorescence immunoassay and the pharmacokinetic estimations were calculated using the three measured levels on a simplified one-compartment open model. Serum concentration time curves were plotted using the computerized Bayesian forecasting. Student 't' and Mann-Whitney U tests were applied as required. Main outcome measures: Initial peak level and steady state trough and peak levels in both groups. Results: Optimum, therapeutic peak level after the first dose was achieved only with the once daily gentamicin regimen (mean level 5.88 vs 3.88 μg/ml p = 0.000). Mean trough levels remained over 2 μg/ml in the conventional regimen (2.76 vs 1.96 μg/ml p = 0.019) group. Mean peak level at the steady state were not significantly different in either regimen (6.65 vs 5.45 μg/ml in conventional p = 0.177). None of the neonates showed nephrotoxicity. Conclusion: Once daily dose (4 mg/kg) of gentamicin has logistic and monetary benefits in addition to the obvious pharmacokinetic advantage.

Original languageEnglish
Pages (from-to)1075-1080
Number of pages6
JournalIndian Pediatrics
Volume34
Issue number12
Publication statusPublished - 01-12-1997
Externally publishedYes

Fingerprint

Gentamicins
Pharmacokinetics
Newborn Infant
Therapeutics
Neonatal Intensive Care Units
Nonparametric Statistics
Immunoassay
Double-Blind Method
Fluorescence
Outcome Assessment (Health Care)
Students
Serum

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health

Cite this

Krishnan, L., & George, S. A. (1997). Gentamicin therapy in preterms: A comparison of two dosage regimens. Indian Pediatrics, 34(12), 1075-1080.
Krishnan, Lalitha ; George, S. A. / Gentamicin therapy in preterms : A comparison of two dosage regimens. In: Indian Pediatrics. 1997 ; Vol. 34, No. 12. pp. 1075-1080.
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Krishnan, L & George, SA 1997, 'Gentamicin therapy in preterms: A comparison of two dosage regimens', Indian Pediatrics, vol. 34, no. 12, pp. 1075-1080.

Gentamicin therapy in preterms : A comparison of two dosage regimens. / Krishnan, Lalitha; George, S. A.

In: Indian Pediatrics, Vol. 34, No. 12, 01.12.1997, p. 1075-1080.

Research output: Contribution to journalArticle

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T1 - Gentamicin therapy in preterms

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AU - Krishnan, Lalitha

AU - George, S. A.

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N2 - Objective: To compare the pharmacokinetic profile of gentamicin given as a once daily dose as against the conventional twelve hourly dose in preterm neonates. Design: Randomized double blind study. Setting: Tertiary level Neonatal Intensive Care Unit. Subjects: Eighteen preterms admitted during the period January 1994 to May 1994. Methods: The babies were randomly assigned to receive either the once daily (plan O, 4 mg/kg Q 24 h) or the conventional (plan C, 2.5 mg/kg Q 12 h) gentamicin dosage regimen. Blood was collected for the first peak level one hour after the first dose of gentamicin. Trough the peak-2 levels were collected before and one hour after the dose due at 48 hours, respectively. Assays were done using fluorescence immunoassay and the pharmacokinetic estimations were calculated using the three measured levels on a simplified one-compartment open model. Serum concentration time curves were plotted using the computerized Bayesian forecasting. Student 't' and Mann-Whitney U tests were applied as required. Main outcome measures: Initial peak level and steady state trough and peak levels in both groups. Results: Optimum, therapeutic peak level after the first dose was achieved only with the once daily gentamicin regimen (mean level 5.88 vs 3.88 μg/ml p = 0.000). Mean trough levels remained over 2 μg/ml in the conventional regimen (2.76 vs 1.96 μg/ml p = 0.019) group. Mean peak level at the steady state were not significantly different in either regimen (6.65 vs 5.45 μg/ml in conventional p = 0.177). None of the neonates showed nephrotoxicity. Conclusion: Once daily dose (4 mg/kg) of gentamicin has logistic and monetary benefits in addition to the obvious pharmacokinetic advantage.

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M3 - Article

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