Evidence map›Paper›PMID 42658230›Full record

ArticlePediatric cardiology2026

Supratherapeutic Digoxin Levels in Children with Cardiac Disease.

Valerie Bailey, Dylan Knox, Michael Iocco, Vickren Pillay, Jessica A Barreto, Stuart Lipsitz, Katie Moynihan

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Article in Pediatric cardiology, 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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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.

Valerie Bailey *Department of Cardiology, Cardiovascular Critical Care, Boston Children's Hospital, Boston, MA, USA.
Dylan Knox *Department of Pharmacy, Boston Children's Hospital, 300 Longwood Avenue, Boston, MA, 02115, USA. dylan.knox@childrens.harvard.edu.
Michael IoccoMedical Toxicology, Boston Children's Hospital, Boston, MA, USA.
Vickren PillayDepartment of Pediatric Critical Care, University of Alberta, Edmonton, AB, Canada.
Jessica A BarretoDepartment of Cardiology, Cardiovascular Critical Care, Boston Children's Hospital, Boston, MA, USA.
Stuart LipsitzDepartment of Cardiology, Boston Children's Hospital, Boston, MA, USA.
Katie MoynihanDepartment of Cardiology, Cardiovascular Critical Care, Boston Children's Hospital, Boston, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We characterized our institution's experience with supratherapeutic digoxin levels (> 2.0 mcg/L) which is reported to occur in 0.8-4% of treated patients. Children < 18 years with a measured digoxin level between January 2014 and December 2024 were included. Data were obtained from the electronic health record including digoxin dose, indication, renal function, and clinical interventions. Descriptive patient-level analyses were performed in children with supratherapeutic levels. Laboratory sample-level analyses were performed using all measured digoxin levels comparing high (> 2.0mcg/L) verses low accounting for repeated measurements within patients. Multivariable models report adjusted odds ratios (aOR) and 95% confidence intervals (95%CI). Overall, 604 digoxin levels were obtained in 283 patients, of which 63 levels (10.4%) were > 2.0 mcg/L in 42 (14.8%) patients. Among patients with elevated levels, median age was 16-months (interquartile range [IQR]: 4-37) and 42% had documented clinical symptoms. Digoxin indications included heart failure (38%), interstage management (38%), and arrhythmia (17%). Median elevated digoxin level was 2.5mcg/L (IQR: 2.2-3.1) and dose was 7.9 mcg/kg/day (IQR: 6.1-9.9). Most patients (76%) were on interacting medications, 25% had moderate/severe renal dysfunction and clinical interventions occurred in 93%. At the sample-level, independent associations with higher odds of supratherapeutic levels included renal dysfunction (severe aOR 6.1, 95%CI 1.4-26.2]; moderate 4.3 [1.2-15.6], mild 2.9 [1.0-8.0] versus normal) and higher daily dose (1.2 mg/kg [1.0-1.3]). Outpatient samples were associated with lower odds of supratherapeutic levels. Supratherapeutic digoxin levels were common, frequently prompting clinical intervention, and associated with renal dysfunction and higher doses, supporting closer monitoring and dose adjustment in high-risk patients.

Indexed as

ChildDigoxinDrug toxicityKidney diseasesPediatric drug dosing

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