Ryan Erin, Rushton William
Banner Poison and Drug Information Center, Banner University Medical Center Phoenix, Phoenix, AZ, USA.
Office of Medical Toxicology, University of Alabama Birmingham, Birmingham, USA.
J Med Toxicol. 2025 Apr;21(2):260-275. doi: 10.1007/s13181-024-01054-5. Epub 2025 Jan 16.
Octreotide is commonly used to treat hypoglycemia due to sulfonylurea toxicity, but optimal dosing for this indication is not well defined.
We 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.
Eighty 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.
Despite widespread variation in octreotide dosing and administration, our report showed similar efficacy and safety with various octreotide dosing practices.
奥曲肽常用于治疗因磺脲类药物毒性导致的低血糖,但该适应症的最佳剂量尚未明确界定。
我们进行了一项系统评价,以确定医学文献中使用奥曲肽治疗磺脲类药物中毒的病例。回顾了1988年10月21日奥曲肽获得美国食品药品监督管理局(FDA)批准至2024年8月15日期间发表的有关奥曲肽和磺脲类药物的文献。
最终分析纳入了来自61个来源的80例独特患者病例(66例成人/青少年和14例儿科患者)。其中包括41种奥曲肽给药策略,这些策略在剂量、频率和/或给药途径上有所不同。皮下给药是成人中最常见的方案,主要剂量范围为每剂50 - 100微克,频率为每6 - 8小时一次,而儿科中最普遍的是静脉注射剂量为1微克/千克。成人间歇性皮下给药与静脉给药在治疗持续时间或奥曲肽总剂量方面无显著差异。所有给药途径在低血糖治疗和血糖正常维持方面相似。静脉输注的持续时间相似,但奥曲肽总剂量更高。更高的间歇性推注剂量与较短的治疗持续时间相关。故意暴露与奥曲肽更高的剂量和更长的治疗持续时间相关。报告了3例奥曲肽不良反应。除2例患者外,所有患者均存活且无任何长期并发症。
尽管奥曲肽给药方式存在广泛差异,但我们的报告显示不同奥曲肽给药方法具有相似的疗效和安全性。