Evidence map›Paper›PMID 41675470›Full record

ArticleThe journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG2026

Concomitant Enalapril and Spironolactone-Induced Hyperkalemia in a Pediatric Patient.

Sarah Mae Rogado, Jamie M Pinto, Liliana Cruz Hernandez, Stephanie Chin, Anita Siu

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Article in The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG, 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Sarah Mae RogadoK. Hovnanian Children's Hospital at Jersey Shore University Medical Center (SMR, JMP, LCH, SC, AS), Neptune, NJ.
Jamie M PintoK. Hovnanian Children's Hospital at Jersey Shore University Medical Center (SMR, JMP, LCH, SC, AS), Neptune, NJ.
Liliana Cruz HernandezK. Hovnanian Children's Hospital at Jersey Shore University Medical Center (SMR, JMP, LCH, SC, AS), Neptune, NJ.
Stephanie ChinK. Hovnanian Children's Hospital at Jersey Shore University Medical Center (SMR, JMP, LCH, SC, AS), Neptune, NJ.
Anita SiuK. Hovnanian Children's Hospital at Jersey Shore University Medical Center (SMR, JMP, LCH, SC, AS), Neptune, NJ.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spironolactone is a mineralocorticoid receptor antagonist with potassium-sparing effects used in the management of heart failure to minimize morbidity and mortality. It is typically given in combination with an angiotensin-converting enzyme inhibitor (ACEI) as part of standard management of pediatric heart failure but has limited literature regarding safety and efficacy in this population. We report a case of probable concomitant enalapril and spironolactone-induced hyperkalemia in a 2-month old female. The patient presented with Class III congestive heart failure and was initiated on enalapril and spironolactone. New hyperkalemia (serum potassium concentration 8.9 mEq/L) developed on day 7 after initiation and persisted despite decreases in the spironolactone dose. Persistent hyperkalemia and hyponatremia with a metabolic acidosis led to the discontinuation of spironolactone by day 12 of admission. The hyperkalemia resolved within 72 hours of discontinuation without further interventions. Based on our patient's course, hyperkalemia in a pediatric patient may occur when spironolactone and an ACEI are given concomitantly and resolve upon discontinuation of spironolactone.

Indexed as

adverse drug eventangiotensin-converting enzyme inhibitorsdrug interactionsenalaprilhyperkalemiapediatricspironolactone

Identifiers

PMID41675470
PMCPMC12889005

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