胰高血糖素样肽-1受体激动剂(GLP-1 RA)暴露在近期体重管理需求中的变化:加利福尼亚中毒控制系统数据的回顾性回顾

IF 1.1 Q4 PHARMACOLOGY & PHARMACY
Raymond Y Ho, Hsiaoting Regelman, Anita Ma, Shu Yi Lee, Saveena Sandhu, Sarah Shapiro, Justin Lewis, Ben Tsutaoka, Dorie E Apollonio
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引用次数: 0

摘要

背景:涉及暴露于胰高血糖素样肽-1受体激动剂(GLP-1 RA)的中毒中心的电话增加了。分析了2017年至2023年全州毒物控制系统的数据,以评估GLP-1 RA暴露频率的变化和报告的临床效果。方法:回顾性分析2017年12月1日至2023年12月31日向全国中毒中心报告的所有GLP-1 RA人类暴露病例。收集的数据输入REDCap(研究电子数据采集)。用中断时间序列分析(ITSA)评估暴露频率随时间的变化;干预措施是FDA于2021年6月批准semaglutide (Wegovy)用于慢性体重管理。使用Stata v17或OpenEpi (v3.01)完成统计分析。结果:纳入1447例病例。中断时间序列分析发现,报告的GLP-1 RA暴露每月增加1.16例([CI = 0.570, 1.802];P < 0.001),每月暴露导致医院使用率增加0.351 ([CI = 0.159, 0.544];P = 0.001)。常见不良反应为恶心(295例,28.0%)、呕吐(267例,25.5%)、头晕(63例,6.0%)、腹痛(54例,5.1%)和其他胃肠道症状(60例,5.7%)。大多数病例在家中进行管理(n = 696, 66.5%)。220例(21.0%)患者在急诊科就诊,46例(4.4%)患者入院。最常见的暴露原因是无意的治疗错误(n = 838, 80.0%)。报告了5例重度(0.5%)和72例中度(6.9%)的医疗结果。40例(3.8%)患者发生低血糖。确定了36例涉及复合GLP-1 RA的暴露;用药错误是该亚组暴露的主要原因(n = 33, 91.7%)。结论:胰高血糖素样肽-1受体激动剂的暴露和暴露后的医院使用率在Wegovy批准体重管理后增加。低血糖虽然不常见,但也有报道;使用GLP-1 RA的非糖尿病患者应接受低血糖识别教育。有必要对患者进行GLP-1 RA给药方面的额外教育,并进一步研究复合GLP-1 RA产品的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Changes in Glucagon-Like Peptide-1 Receptor Agonist (GLP-1 RA) Exposures Following Recent Demand for Weight Management: A Retrospective Review of California Poison Control System Data.

Background: Calls to poison centers involving exposure to glucagon-like peptide-1 receptor agonists (GLP-1 RA) have increased. Data from a statewide poison control system from 2017 to 2023 was analyzed to assess changes in GLP-1 RA exposure frequencies and reported clinical effects. Methods: Retrospective records review of all human exposure cases to GLP-1 RA reported to a statewide poison center from December 1, 2017 to December 31, 2023. Collected data were entered into REDCap (Research Electronic Data Capture). Changes in exposure frequency over time assessed with interrupted time series analysis (ITSA); the intervention was FDA approval of semaglutide (Wegovy) for chronic weight management in June 2021. Statistical analyses completed using Stata v17 or OpenEpi (v3.01). Results: One thousand forty-seven cases were included. Interrupted time series analysis identified an increase in reported GLP-1 RA exposures of 1.16 per month ([CI = 0.570, 1.802]; P < 0.001) and an increase in hospital utilization from exposures of 0.351 per month ([CI = 0.159, 0.544]; P = 0.001) following Wegovy approval. Common adverse effects were nausea (n = 295, 28.0%), vomiting (n = 267, 25.5%), dizziness (n = 63, 6.0%), abdominal pain (n = 54, 5.1%), and other gastrointestinal symptoms (n = 60, 5.7%). Most cases were managed at home (n = 696, 66.5%). Two hundred twenty (21.0%) patients were treated in the emergency department, and 46 (4.4%) were admitted. The most common reason for exposure was unintentional therapeutic error (n = 838, 80.0%). Five major (0.5%) and 72 moderate (6.9%) medical outcomes were reported. Hypoglycemia occurred in 40 (3.8%) patients. Thirty-six exposures involving compounded GLP-1 RA were identified; administration errors were the main reason for exposures among this subgroup (n = 33, 91.7%). Conclusion: Glucagon-like peptide-1 receptor agonist exposures and hospital utilization after exposure increased following Wegovy approval for weight management. Hypoglycemia, while infrequent, was reported; nondiabetic patients using GLP-1 RA should be educated on recognizing hypoglycemia. Additional patient education on GLP-1 RA administration and further study on the impact of compounded GLP-1 RA products are warranted.

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来源期刊
Journal of Pharmacy Technology
Journal of Pharmacy Technology PHARMACOLOGY & PHARMACY-
CiteScore
1.50
自引率
0.00%
发文量
49
期刊介绍: For both pharmacists and technicians, jPT provides valuable information for those interested in the entire body of pharmacy practice. jPT covers new drugs, products, and equipment; therapeutic trends; organizational, legal, and educational activities; drug distribution and administration; and includes continuing education articles.
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