Monitoring of Gentamicin Serum Concentrations Among Newborns in the Neonatal Ward at Hospital Sultan Ismail Petra, Malaysia

preprint OA: closed CC-BY-4.0

Abstract

INTRODUCTION: Gentamicin is the empirical therapy of choice for sepsis in newborns, with dosing of 4mg/kg every 24 – 36 hours, depending on premenstrual age. The objective of this study was to investigate the therapeutic drug monitoring (TDM) outcomes (within therapeutic ranges or toxic) of the current IV Gentamicin regimen in treating infections among neonates. MATERIALS AND METHODS: This retrospective cohort study was conducted in Hospital Sultan Ismail Petra (HSIP). Data were abstracted and collected for neonates treated with gentamicin that were admitted to the neonatal ward from January 2020 – December 2022. Trough and peak levels were measured on the third dose where the therapeutic ranges were 5.0 mg/L, respectively. Elevated serum creatinine was defined as serum creatinine level (SCr) >71 μmol/L. Multivariable logistic regression was performed to identify the risk factors of acquiring toxic trough levels. RESULTS: A total of 227 patients were included. The total number of patients achieving the targeted peak level was 74.90%. More than half of the patients (52.0%) experienced toxic trough levels. The mean serum trough and peak levels (standard deviation) were 1.23 (1.11) mg/L and 7.31 (3.93) mg/L respectively. The risk factor associated with toxic trough level was elevated SCr (odd ratio 2.55, 95% confidence interval [1.19,5.46], p=0.016). CONCLUSION: The current gentamicin regimen resulted in an alarming proportion of patients having toxic trough levels, particularly with elevated SCr. The study findings underscore the need to refine the dosing regimen to optimise efficacy and minimise toxicity in neonates.
Full text 621 characters · extracted from oa-doi-fallback · click to expand
There is a newer version available for this {{ publicationType }}. View latest version {{ publication.field_name }} {{ publication.subfield_name }} Copyright: © {{ publicationYear }} {{ publication.presentation_authors[0].full_name + (publication.presentation_authors.length > 1 ? ' et al' : '') }}. This is an open access publication distributed under the terms of the CC BY 4.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Check the {{ publicationType | capitalize }} Source for copyright and license information. Listen on

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. This is a recent paper (2025) — citers typically take a year or two to land, and the OpenAlex reference graph may still be filling in.

Source provenance

europepmc
last seen: 2026-05-20T01:45:00.602351+00:00
unpaywall
last seen: 2026-05-22T02:00:06.705733+00:00
License: CC-BY-4.0