Evidence map›Paper›PMID 41462146›Full record

ArticleBMC infectious diseases2025

Remdesivir safety and clinical outcomes in pediatric COVID-19: a retrospective study.

Leila Barati, Narges Lashkarbolouk, Somayeh Ghorbani, Lobat Shahkar

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Article in BMC infectious diseases, 2025. 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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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Leila BaratiPediatrician, Neonatal and Children's Health Research Center, Pediatrics department, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran.
Narges LashkarboloukNeonatal and Children's Health Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
Somayeh GhorbaniBiostatistics, Cancer Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
Lobat ShahkarPediatric Pulmonologist, Neonatal and Children's Health Research Center, School of Medicine, Golestan University of Medical Sciences, Gorgan, Iran. lobatshahkar@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study evaluated clinical features of pediatric and adolescent patients with COVID-19 who received Remdesivir and assessed the adverse effects of Remdesivir in this population.

methodsIn a retrospective cross-sectional study, the documents of all patients under 18 years old were admitted due to severely respiratory distress and suspicious to COVID-19 in Taleghani hospital and according to Iranian COVID-19 treatment protocol received Remdesivir between February 2021 and September 2022, were studied.

resultsThe study included children aged 25 days to 17 years with a median age of 10 years and 50%being female. Fifteen patients were admitted to the ICU. 50% of ICU admissions were failure to thrive (FTT). BMI was significantly higher in patients over 10 years of age compared to others. Abnormal CT finding were observed in 90% of obese patients. Forty-one cases tested positive for PCR. The odds of PCR positivity were 2.87 times higher in patients over 10 years of age. Remdesivir was generally well tolerated, with no adverse events leading to drug discontinuation and no statistically significant difference in laboratory parameters before and after treatment. There were no significant hepatic or renal toxicity. Mild, transient elevations in liver transaminases (AST and ALT) were observed but did not require discontinuation of therapy. Transient bradycardia was not observed in our study.

conclusionRemdesivir appears to be a safe therapeutic option for pediatric COVID-19 patients, with minimal adverse effects and good tolerability. Nutritional status, particularly obesity and FTT, may influence disease severity. Further prospective studies are needed to better define Remdesivir’s role and its impact on viral clearance and clinical outcomes in children. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Adenosine MonophosphateAlanineAntiviral AgentsCOVID-19COVID-19 Drug TreatmentAdolescentChildChild, PreschoolCross-Sectional StudiesFemaleHumansInfantInfant, NewbornIranMaleRetrospective StudiesAdenosine MonophosphateAlanineAntiviral AgentsremdesivirAdolescentChildCOVID-19PediatricsRemdesivir

Identifiers

PMID41462146
PMCPMC12750813

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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.