Evidence map›Paper›PMID 39821850›Full record

SynthesisJournal of medical toxicology : official journal of the American College of Medical Toxicology2025

Variations in Octreotide Dosing in Published Reports of Sulfonylurea Toxicity: A Systematic Review, 1988-Present.

Erin Ryan, William Rushton

Abstract readSystematic Review
In one paragraph

Synthesis in Journal of medical toxicology : official journal of the American College of Medical Toxicology, 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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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

2 authors.

Erin RyanBanner Poison and Drug Information Center, Banner University Medical Center Phoenix, Phoenix, AZ, USA. erin.ryan@bannerhealth.com.ORCID http://orcid.org/0009-0001-4591-8136
William RushtonOffice of Medical Toxicology, University of Alabama Birmingham, Birmingham, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOctreotide is commonly used to treat hypoglycemia due to sulfonylurea toxicity, but optimal dosing for this indication is not well defined.

methodsWe performed a systematic review to identify cases in the medical literature of octreotide use for sulfonylurea poisoning. Literature published on octreotide and sulfonylureas between octreotide's FDA approval on 10/21/1988 and 8/15/2024 was reviewed.

resultsEighty unique patient cases (66 adults/adolescents and 14 pediatric patients) from 61 sources were included in the final analysis. These included 41 octreotide dosing strategies that differed in dose, frequency, and/or route of administration. Subcutaneous dosing, primarily within the range of 50-100 mcg per dose at a frequency of every 6-8 h, was the most common regimen in adults while intravenous dosing of 1 mcg/kg was most prevalent in pediatrics. There were no significant differences in duration of therapy or total dose of octreotide in adults with intermittent subcutaneous vs intravenous dosing. Treatment of hypoglycemia and maintenance of euglycemia was similar among all routes of administration. Infusions had similar durations but higher total doses of octreotide. Higher intermittent bolus doses were associated with shorter durations of therapy. Intentional exposures were associated with higher doses and longer duration of treatment with octreotide. Three adverse reactions to octreotide were reported. Except for 2 cases, all patients survived without any long-term complications.

conclusionDespite widespread variation in octreotide dosing and administration, our report showed similar efficacy and safety with various octreotide dosing practices.

Indexed as

AntidotesHypoglycemiaHypoglycemic AgentsOctreotideSulfonylurea CompoundsAdultChildDose-Response Relationship, DrugHumansInjections, SubcutaneousTreatment OutcomeAntidotesHypoglycemic AgentsOctreotideSulfonylurea CompoundsAntidotesOctreotidePharmacokineticsSulfonylurea

Identifiers

PMID39821850
PMCPMC11933575

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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.