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2010年至2022年向美国毒物控制中心报告的洛哌丁胺病例。

Loperamide cases reported to United States poison centers, 2010-2022.

作者信息

Patel Aaditya, Rine Natalie I, Spiller Henry A, Hays Hannah, Badeti Jaahnavi, Zhu Motao, Ding Kele, Smith Gary A

机构信息

Center for Injury Research and Policy, The Abigail Wexner Research Institute at Nationwide Children's Hospital, 700 Children's Drive, Columbus, OH, 43205, USA.

Kansas City University College of Osteopathic Medicine, Kansas City, MO, USA.

出版信息

Inj Epidemiol. 2023 Nov 24;10(1):61. doi: 10.1186/s40621-023-00473-2.

Abstract

BACKGROUND

Intentional use of high doses of loperamide has been linked to serious cardiac toxicity. The objective of this study is to investigate the characteristics and trends of loperamide cases reported to United States (US) poison centers and to evaluate the changes in reported loperamide cases following US Food and Drug Administration (FDA) warnings, labeling requirements, and packaging restrictions for loperamide starting in 2016, with an emphasis on intentional exposures.

METHODS

Data from the National Poison Data System were analyzed.

RESULTS

There were 12,987 cases reported to US poison centers from 2010 to 2022, for which, loperamide was the most likely substance responsible for observed clinical effects. Although 46.1% of these cases were associated with minor or no effect, 13.4% resulted in a serious medical outcome, including 59 deaths (0.5%). Eight percent (8.1%) of cases were admitted to a critical care unit and 5.0% were admitted to a non-critical care unit. Among cases with a serious medical outcome, most were associated with loperamide abuse (38.0%), intentional-misuse (15.7%), or suspected suicide (27.5%). The majority (60.0%; n = 33) of fatalities were related to abuse, followed by suspected suicide (20.0%; n = 11) and intentional-misuse (5.5%, n = 3). The rate of loperamide cases per 100,000 US population reported to US PCs decreased from 0.44 in 2010 to 0.36 in 2015 (p = 0.0290), followed by an increase to 0.46 in 2017 (p = 0.0013), and then a trend reversal with a decrease to 0.28 in 2022 (p < 0.0001). The rate of serious medical outcomes related to loperamide increased from 0.03 in 2010 to 0.05 in 2015 (p = 0.0109), which subsequently increased rapidly to 0.11 in 2017 (p < 0.0001), and then demonstrated a trend reversal and decreased to 0.04 in 2022 (p < 0.0001).

CONCLUSIONS

FDA warnings, labeling requirements, and packaging restrictions may have contributed to the observed trend reversal and decrease in reports to US poison centers of loperamide cases related to intentional misuse, abuse, and suspected suicide. This demonstrates the potential positive effect that regulatory actions may have on public health. These findings contribute to the evidence supporting the application of similar prevention efforts to reduce poisoning from other medications associated with intentional misuse, abuse, and suicide.

摘要

背景

故意使用高剂量洛哌丁胺与严重心脏毒性有关。本研究的目的是调查向美国毒物控制中心报告的洛哌丁胺病例的特征和趋势,并评估自2016年起美国食品药品监督管理局(FDA)对洛哌丁胺发出警告、提出标签要求和实施包装限制后报告的洛哌丁胺病例的变化情况,重点关注故意暴露情况。

方法

对国家毒物数据系统的数据进行了分析。

结果

2010年至2022年期间,美国毒物控制中心共报告了12987例病例,其中洛哌丁胺最有可能是观察到的临床效应的致病物质。虽然这些病例中有46.1%与轻微或无影响相关,但13.4%导致了严重的医疗后果,包括59例死亡(0.5%)。8.1%的病例被收入重症监护病房,5.0%的病例被收入非重症监护病房。在有严重医疗后果的病例中,大多数与洛哌丁胺滥用(38.0%)、故意误用(15.7%)或疑似自杀(27.5%)有关。大多数死亡病例(60.0%;n = 33)与滥用有关,其次是疑似自杀(20.0%;n = 11)和故意误用(5.5%,n = 3)。向美国毒物控制中心报告的每10万美国人口中洛哌丁胺病例数从2010年的0.44降至2015年的0.36(p = 0.0290),随后在2017年增至0.46(p = 0.0013),然后趋势逆转,在2022年降至0.28(p < 0.0001)。与洛哌丁胺相关的严重医疗后果发生率从2010年的0.03增至2015年的0.05(p = 0.0109),随后在2017年迅速增至0.11(p < 0.0001),然后趋势逆转,在2022年降至0.04(p < 0.0001)。

结论

FDA的警告、标签要求和包装限制可能促成了观察到的趋势逆转以及向美国毒物控制中心报告的与故意误用、滥用和疑似自杀相关的洛哌丁胺病例数的减少。这证明了监管行动可能对公众健康产生的潜在积极影响。这些发现为支持采取类似预防措施以减少与故意误用、滥用和自杀相关的其他药物中毒提供了证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1010/10668506/ed81134b0f23/40621_2023_473_Fig1_HTML.jpg

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