Acute Kidney Injury During Treatment with Intravenous Acyclovir for Suspected or Confirmed Neonatal Herpes Simplex Virus Infection.


Journal

The Journal of pediatrics
ISSN: 1097-6833
Titre abrégé: J Pediatr
Pays: United States
ID NLM: 0375410

Informations de publication

Date de publication:
04 2020
Historique:
received: 25 10 2019
revised: 22 11 2019
accepted: 26 12 2019
pubmed: 11 2 2020
medline: 12 9 2020
entrez: 11 2 2020
Statut: ppublish

Résumé

To describe the epidemiology of and risk factors associated with acute kidney injury (AKI) during acyclovir treatment in neonates and infants. We conducted a multicenter (n = 4), retrospective cohort study of all hospitalized infants age <60 days treated with intravenous acyclovir (≥1 dose) for suspected or confirmed neonatal herpes simplex virus disease from January 2011 to December 2015. Infants with serum creatinine measured both before acyclovir (baseline) and during treatment were included. We classified AKI based on changes in creatinine according to published neonatal AKI criteria and performed Cox regression analysis to evaluate risk factors for AKI during acyclovir treatment. We included 1017 infants. The majority received short courses of acyclovir (median, 5 doses). Fifty-seven infants (5.6%) developed AKI during acyclovir treatment, with an incidence rate of AKI at 11.6 per 1000 acyclovir days. Cox regression analysis identified having confirmed herpes simplex virus disease (OR, 4.35; P = .002), receipt of ≥2 concomitant nephrotoxic medications (OR, 3.07; P = .004), receipt of mechanical ventilation (OR, 5.97; P = .001), and admission to an intensive care unit (OR, 6.02; P = .006) as risk factors for AKI during acyclovir treatment. Among our cohort of infants exposed to acyclovir, the rate of AKI was low. Sicker infants and those exposed to additional nephrotoxic medications seem to be at greater risk for acyclovir-induced toxicity and warrant closer monitoring.

Identifiants

pubmed: 32037154
pii: S0022-3476(19)31735-4
doi: 10.1016/j.jpeds.2019.12.056
pmc: PMC7096264
mid: NIHMS1557999
pii:
doi:

Substances chimiques

Acyclovir X4HES1O11F

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

126-132.e2

Subventions

Organisme : NICHD NIH HHS
ID : K23 HD091365
Pays : United States

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

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Auteurs

Kevin J Downes (KJ)

Division of Infectious Disease, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA; Center for Pediatric Clinical Effectiveness, Children's Hospital of Philadelphia, Research Institute, Philadelphia, PA; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA. Electronic address: downeskj@email.chop.edu.

Craig L K Boge (CLK)

Center for Pediatric Clinical Effectiveness, Children's Hospital of Philadelphia, Research Institute, Philadelphia, PA.

Elande Baro (E)

Office of Biostatistics, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, MD.

Gerold T Wharton (GT)

Office of Pediatric Therapeutics, US Food and Drug Administration, Silver Spring, MD.

Kellie M Liston (KM)

Center for Pediatric Clinical Effectiveness, Children's Hospital of Philadelphia, Research Institute, Philadelphia, PA.

Brittany L Haltzman (BL)

Center for Pediatric Clinical Effectiveness, Children's Hospital of Philadelphia, Research Institute, Philadelphia, PA.

Hannah M Emerson (HM)

Center for Pediatric Clinical Effectiveness, Children's Hospital of Philadelphia, Research Institute, Philadelphia, PA.

Edwin Doe (E)

Neonatal Intensive Care, Inova Children's Hospital, Falls Church, VA.

Rosanna Fulchiero (R)

Neonatal Intensive Care, Inova Children's Hospital, Falls Church, VA.

Van Tran (V)

Neonatal Intensive Care, Inova Children's Hospital, Falls Church, VA.

Lilly Yen (L)

Department of Pharmacy, Children's Hospital Los Angeles, Los Angeles, CA.

Phuong Lieu (P)

Department of Pharmacy, Children's Hospital Los Angeles, Los Angeles, CA.

Sara L Van Driest (SL)

Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN.

Alison G Grisso (AG)

Department of Pharmaceutical Services, Vanderbilt University Medical Center, Nashville, TN.

Ida T Aka (IT)

Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN.

Jennifer Hale (J)

Department of Pharmaceutical Services, Vanderbilt University Medical Center, Nashville, TN.

Jessica Gillon (J)

Department of Pharmaceutical Services, Vanderbilt University Medical Center, Nashville, TN.

Julie S Pingel (JS)

Department of Pharmaceutical Services, Vanderbilt University Medical Center, Nashville, TN.

Susan E Coffin (SE)

Division of Infectious Disease, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA; Center for Pediatric Clinical Effectiveness, Children's Hospital of Philadelphia, Research Institute, Philadelphia, PA; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA.

Ann W McMahon (AW)

Office of Pediatric Therapeutics, US Food and Drug Administration, Silver Spring, MD.

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