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首页> 外文期刊>Pharmacoepidemiology and drug safety >Impact of EMA regulatory label changes on hydroxyzine initiation, discontinuation and switching to other medicines in Denmark, Scotland, England and the Netherlands: An interrupted time series regression analysis
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Impact of EMA regulatory label changes on hydroxyzine initiation, discontinuation and switching to other medicines in Denmark, Scotland, England and the Netherlands: An interrupted time series regression analysis

机译:EMA调节标志物变化对丹麦,苏格兰,英格兰和荷兰其他药物的羟基启动,停止和切换的影响:中断时间序列回归分析

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摘要

Background: Hydroxyzine is indicated for the management of anxiety, skin and sleep disorders. In 2015, the European Medicines Agency (EMA) concluded that hydroxyzine was pro-arrhythmogenic and changes to the product information were implemented in Europe. This study aimed to evaluate their impact in Denmark, Scotland, England and the Netherlands. Method: Quarterly time series analyses measuring hydroxyzine initiation, discontinuation, and switching to other antihistamines, benzodiazepines and antidepressants in Denmark, England, Scotland and the Netherlands from 2009 to 2018. Data were analysed using interrupted time series regression. Results: Hydroxyzine initiation in quarter one 2010 in Denmark, Scotland, England and the Netherlands per 100 000 was: 23.5, 91.5, 35.9 and 34.4 respectively. Regulatory action was associated with a significant: immediate fall in hydroxyzine initiation per 100 000 in England (-12.05, 95%CI -18.47 to -5.63) and Scotland (-19.01, 95%CI -26.99 to -11.02); change to a negative trend in hydroxyzine initiation per 100 000/quarter in England (-1.72, 95%CI -2.69 to -0.75) and Scotland (-2.38, 95%CI -3.32 to -1.44). Regulatory action was associated with a significant: immediate rise in hydroxyzine discontinuation per 100 000 in England (3850, 95%CI 440-7240). No consistent changes were observed in the Netherlands or Denmark. Regulatory action was associated with no switching to other antihistamines, benzodiazepines or antidepressants following hydroxyzine discontinuation in any country. Conclusion: The 2015 EMA regulatory action was associated with heterogeneous impact with reductions in hydroxyzine initiation varying by country. There was limited impact on discontinuation with no strong evidence suggesting unintended consequences of major switching to other antihistamines, benzodiazepines or antidepressants.
机译:背景:羟嗪用于治疗焦虑、皮肤和睡眠障碍。2015年,欧洲药品管理局(EMA)得出结论,羟嗪具有促心律失常作用,欧洲对产品信息进行了更改。这项研究旨在评估它们在丹麦、苏格兰、英格兰和荷兰的影响。方法:对2009年至2018年丹麦、英格兰、苏格兰和荷兰的羟嗪起效、停药和改用其他抗组胺药、苯二氮卓类和抗抑郁药进行季度时间序列分析。使用中断时间序列回归分析数据。结果:2010年第一季度,丹麦、苏格兰、英格兰和荷兰每10万人中羟嗪起始浓度分别为:23.5、91.5、35.9和34.4。监管措施与一个显著相关:英格兰(12.05,95%可信区间-18.47至-5.63)和苏格兰(19.01,95%可信区间-26.99至-11.02)每10万人中羟嗪起始浓度立即下降;英格兰(1.72,95%置信区间-2.69至-0.75)和苏格兰(2.38,95%置信区间-3.32至-1.44)每10万/季度羟嗪起始值呈负趋势。监管措施与一个显著相关:在英格兰,每10万人中立即停用羟嗪的人数增加(3850,95%可信区间440-7240)。在荷兰或丹麦没有观察到持续的变化。在任何国家,在羟嗪停药后,监管行动都与不改用其他抗组胺药、苯二氮卓类或抗抑郁药有关。结论:2015年EMA监管行动与异质性影响有关,羟嗪起始的减少因国家而异。对停药的影响有限,没有强有力的证据表明主要改用其他抗组胺药、苯二氮卓类或抗抑郁药会产生意外后果。

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