Evidence map›Paper›PMID 42277183›Full record

ArticlePediatric research2026

Pharmacokinetic analysis of conventional tobramycin dosing for infants in the cardiac intensive care unit.

Elise N Malehorn, Max Blumenthal, Jamie L Miller, Katy S Stephens, Teresa V Lewis, Sin Yin Lim, Peter N Johnson

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Article in Pediatric research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Elise N Malehorn *Department of Pharmacy, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Max Blumenthal *Pharmacy Practice and Translational Research Division, University of Wisconsin-Madison School of Pharmacy, Madison, WI, USA.
Jamie L MillerDepartment of Clinical and Administrative Sciences, University of Oklahoma College of Pharmacy, Oklahoma City, OK, USA.
Katy S StephensDepartment of Pharmacy, Oklahoma Children's Hospital at OU Health, Oklahoma City, OK, USA.
Teresa V LewisDepartment of Clinical and Administrative Sciences, University of Oklahoma College of Pharmacy, Oklahoma City, OK, USA.
Sin Yin LimPharmacy Practice and Translational Research Division, University of Wisconsin-Madison School of Pharmacy, Madison, WI, USA. Sinyin.lim@wisc.edu.ORCID http://orcid.org/0000-0003-0070-0798
Peter N JohnsonDepartment of Clinical and Administrative Sciences, University of Oklahoma College of Pharmacy, Oklahoma City, OK, USA. Peter-johnson@ou.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAminoglycoside pharmacokinetic data are limited in infants with congenital heart disease (CHD). This study aimed to characterize tobramycin pharmacokinetics and determine optimal intravenous dosing for infants in the cardiac intensive care unit (CICU).

methodsA population pharmacokinetic analysis was performed in infants >1 month to <12 months of age initiated on intravenous conventional dosing tobramycin in the CICU from January 1, 2020, through December 31, 2024. Simulations were performed to determine dosage regimens achieving the desired peak (8-12 mg/L) and trough (<1 mg/L) concentrations. Regimens were also evaluated in achieving secondary targets based on the area under the concentration-time curve (AUC).

resultsFifty-five infants, with a median age of 3.5 months and a weight of 5.1 kg, were included. Twenty (36.4%) patients were premature. A two-compartment model best described the pharmacokinetic data, with weight and eGFR identified as significant covariates for clearance. A 3.5 mg/kg/dose every-12-hour regimen optimally obtained target peak and trough concentration, and AUC targets. Infants with eGFRs <90 mL/min/1.73 m

conclusionTobramycin pharmacokinetics in CHD infants were comparable to published data on non-CHD infants. A 3.5 mg/kg/dose every-12-hour regimen was optimal, with dose adjustments needed for eGFR <90 mL/min/1.73 m IMPACT: Tobramycin pharmacokinetic data are limited in infants with congenital heart disease (CHD). A dosing regimen of 3.5 mg/kg/dose every 12 hours for intravenous tobramycin achieves therapeutic targets in infants aged 1 month to 1 year with CHD in the cardiac intensive care unit (CICU). Infants with estimated glomerular filtration rates <90 mL/min/1.73 m

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.