Carter Emily J R, Rine Natalie I, Kistamgari Sandhya, Hays Hannah L, Spiller Henry A, Yang Jingzhen, Zhu Motao, Smith Gary A
Center for Injury Research and Policy, The Abigail Wexner Research Institute at Nationwide Children's Hospital, 700 Children's Drive, Columbus, OH, 43205, USA.
Kirk Kerkorian School of Medicine, Las Vegas, NV, USA.
Inj Epidemiol. 2024 Nov 1;11(1):59. doi: 10.1186/s40621-024-00547-9.
Gabapentin and pregabalin were originally introduced as anticonvulsant medications but are now also prescribed on- and off-label for multiple medical disorders, especially for pain management. The national opioid crisis has led to increased use of non-opioid pain medications, including gabapentinoids, which has been associated with changing patterns of adverse events associated with these medications. This study investigated the characteristics and trends of gabapentin and pregabalin exposures reported to US poison centers from 2012 to 2022.
National Poison Data System data involving gabapentin and pregabalin exposures for 2012 to 2022 were analyzed.
There were 124,161 exposures involving gabapentin and pregabalin as the primary substance reported to US poison centers during the study period. Most exposures involved gabapentin (85.9%), females (59.4%), single-substance exposures (62.9%), or occurred at a residence (97.2%). Suspected suicides accounted for 45.2% of exposures. Most exposures were associated with a minor effect (27.4%) or no effect (34.0%), while 22.1% experienced a serious medical outcome, including 96 fatalities. The rate of gabapentin and pregabalin exposures per one million US population increased by 236.1% from 22.7 in 2012 to 76.5 in 2019 (P < 0.001), followed by a non-significant decrease to 68.5 in 2022 (P = 0.068).
The rate of gabapentin and pregabalin exposures reported to US poison centers increased by more than 230% from 2012 to 2019 before plateauing from 2019 to 2022. The observed rate trend was driven primarily by gabapentin exposures and by cases associated with suspected suicide. Although most exposures were associated with a minor or no effect, 22% of individuals experienced a serious medical outcome, including 96 fatalities. These findings contribute to the discussion of rescheduling gabapentin as a federally controlled substance, which is the current status of pregabalin. Prevention of suicide associated with gabapentin and pregabalin merits special attention.
加巴喷丁和普瑞巴林最初作为抗惊厥药物引入,但现在也被用于多种医学病症的标签内和标签外处方,尤其是用于疼痛管理。全国性的阿片类药物危机导致包括加巴喷丁类药物在内的非阿片类止痛药物的使用增加,这与这些药物相关不良事件模式的变化有关。本研究调查了2012年至2022年向美国毒物中心报告 的加巴喷丁和普瑞巴林暴露的特征和趋势。
分析了2012年至2022年美国毒物数据系统中涉及加巴喷丁和普瑞巴林暴露的数据。
在研究期间,有124,161次暴露被报告给美国毒物中心,其中加巴喷丁和普瑞巴林为主要物质。大多数暴露涉及加巴喷丁(85.9%)、女性(59.4%)、单一物质暴露(62.9%),或发生在住所(97.2%)。疑似自杀占暴露事件的45.2%。大多数暴露与轻微影响(27.4%)或无影响(34.0%)相关,而22.1%的人经历了严重的医疗后果,包括96例死亡。每百万美国人口中加巴喷丁和普瑞巴林的暴露率从2012年的22.7增加到2019年的76.5,增长了236.1%(P < 0.001),随后在2022年非显著下降至68.5(P = 0.068)。
2012年至2019年期间,向美国毒物中心报告的加巴喷丁和普瑞巴林暴露率增加了230%以上,然后在2019年至2022年趋于平稳。观察到的率趋势主要由加巴喷丁暴露和与疑似自杀相关的病例驱动。虽然大多数暴露与轻微影响或无影响相关,但22%的人经历了严重的医疗后果,包括96例死亡。这些发现有助于讨论将加巴喷丁重新分类为联邦管制物质,普瑞巴林目前就是这种情况。预防与加巴喷丁和普瑞巴林相关的自杀值得特别关注。