首页> 外文期刊>Clinical therapeutics >One-year treatment persistence and potential adverse events among patients with atrial fibrillation treated with amiodarone or sotalol: a retrospective claims database analysis.
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One-year treatment persistence and potential adverse events among patients with atrial fibrillation treated with amiodarone or sotalol: a retrospective claims database analysis.

机译:胺碘酮或索他洛尔治疗房颤患者的一年治疗持续性和潜在不良事件:回顾性索赔数据库分析。

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BACKGROUND: The risk-benefit profile of antiarrhythmic drugs (AADs) affects the choice of pharmacotherapy for maintenance of sinus rhythm. Adverse events (AEs) associated with AADs may influence patient compliance and compromise the management of atrial fibrillation (AF). There are limited data on the incidence of AEs or persistence with AADs outside the clinical trial environment. OBJECTIVE: This study provides treatment persistence and AE data for patients with AF receiving treatment with amiodarone or sotalol, 2 of the most widely used AADs in the United States. METHODS: In this retrospective cohort study, patients satisfying the following criteria were identified from the US MarketScan claims databases: (1) age >/=18 years with a pharmacy claim for oral amiodarone or sotalol between 2004 and 2007; (2) >/=1 inpatient/outpatient medical claim with an AF diagnosis <90 days before the earliest (index) pharmacy claim; and (3) >/=12 months' continuous enrollment before and after the index pharmacy claim. Prespecified AE rates were compared between treatment cohorts during active treatment. RESULTS: Among 77,093 AF patients with >/=1 claim for amiodarone or sotalol, 3459 met all inclusion criteria (mean age, 70.8 years; 61.6% male; mean Charlson Comorbidity Index [CCI], 1.58), of whom 2392 received amiodarone (mean age, 72.2 years; 62.5% male; mean CCI, 1.8) and 1067 received sotalol (mean age, 67.5 years; 59.7% male; mean CCI, 1.1). Persistence was higher among the sotalol cohort than the amiodarone cohort (53.2% vs 30.6% at 12 months; P < 0.001). Postindex versus preindex comparisons revealed increases in cardiovascular AE rates in both cohorts. Intercohort comparisons showed higher rates of cardiovascular AEs (594 vs 339 patients/1000 patient-years; P < 0.001) and pulmonary AEs (128 vs 61 patients/1000 patient-years; P < 0.001) during active amiodarone treatment. CONCLUSIONS: Among the population analyzed, patients with AF receiving amiodarone versus sotalol therapy had differing clinical characteristics. Patients experienced frequent AEs (particularly cardiovascular events) with amiodarone and sotalol, and many discontinued treatment during the first year.
机译:背景:抗心律失常药物(AADs)的风险收益特征影响维持窦性心律的药物治疗的选择。与AAD相关的不良事件(AE)可能会影响患者的依从性并危及房颤(AF)的管理。在临床试验环境之外,关于不良事件的发生率或不良事件持续存在的数据有限。目的:本研究为接受胺碘酮或索他洛尔(美国最广泛使用的两种AAD)治疗的AF患者提供了治疗持久性和AE数据。方法:在这项回顾性队列研究中,从美国MarketScan索赔数据库中识别出满足以下标准的患者:(1)年龄≥18岁,在2004年至2007年间有口服胺碘酮或索他洛尔的药理要求; (2)在最早(指数)药房索赔发生前90天以内的AF诊断为> / = 1的住院/门诊医疗索赔; (3)在索引药房声明之前和之后连续12个月的连续注册。在积极治疗期间,比较各治疗队列之间的预定AE率。结果:在77,093名胺碘酮或索他洛尔的AF患者中,> / = 1的AF患者中,有3459名符合所有纳入标准(平均年龄70.8岁;男性为61.6%;平均Charlson合并症指数[CCI]为1.58),其中2392名接受胺碘酮(平均年龄为72.2岁;男性为62.5%;平均CCI为1.8)和1067接受索他洛尔治疗(平均年龄为67.5岁;男性为59.7%;平均CCI为1.1)。索他洛尔组的持久性高于胺碘酮组(12个月时为53.2%vs 30.6%; P <0.001)。索引后与索引前的比较显示,两个队列中的心血管AE率均增加。队列间比较显示,在积极的胺碘酮治疗期间,心血管事件的不良事件发生率较高(594比339患者/ 1000患者-年; P <0.001)和肺部不良事件发生率(128对61的患者/ 1000患者-年; P <0.001)。结论:在接受分析的人群中,接受胺碘酮和索他洛尔治疗的房颤患者具有不同的临床特征。患者使用胺碘酮和索他洛尔经历频繁的AEs(尤其是心血管事件),并且在第一年中许多患者停药。

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