转载:与华法林相比,阿哌沙班治疗血液透析终末期肾病患者非瓣膜性心房颤动的有效性和安全性。

IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Journal of the American Pharmacists Association Pub Date : 2024-07-01 DOI:10.1016/j.japh.2024.102160
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引用次数: 0

摘要

研究背景本研究比较了阿哌沙班和华法林在非瓣膜性心房颤动(NVAF)和终末期肾病(ESRD)血液透析(HD)患者中的疗效和安全性。在排除了严重肾功能障碍患者的主要临床试验中,阿哌沙班与华法林相比降低了中风和出血的发生率。根据药代动力学研究,阿哌沙班不再是接受血液透析的 ESRD 患者 NVAF 的禁忌。关于接受 HD 治疗的 ESRD 患者使用阿哌沙班的临床数据有限:对 2018 年至 2019 年期间诊断为 NVAF 和接受 HD 治疗的 ESRD 患者进行了回顾性病历审查,这些患者被处方阿哌沙班或华法林来预防卒中。对患者的病历进行了长达 2 年的审查。排除了接受 HD 以外的肾脏替代治疗的患者、因 NVAF 以外的原因使用抗凝治疗的患者、Child-Pugh C 级肝硬化患者以及患有严重二尖瓣狭窄的患者。主要结果是因缺血性中风或短暂性脑缺血发作到急诊科就诊或住院。次要结果包括大出血或小出血以及不良反应:共筛选了 181 名患者,其中 110 名患者符合资格标准并纳入分析。阿哌沙班组和华法林组分别有 4 名患者(7.5%)和 6 名患者(10.5%)达到了中风住院或急诊就诊的主要结局(P = 0.742)。阿哌沙班组和华法林组分别有 39.6% 和 36.8% 的患者出现症状性出血(P = 0.918)。华法林组大出血发生率呈上升趋势,分别为52.4%和49.2%(P = 0.758):在我们研究的意向治疗分析中,阿哌沙班和华法林对接受 HD 治疗的 NVAF 和 ESRD 患者的疗效和安全性结果没有统计学意义上的显著差异。需要更大规模的试验来进一步分析这一患者群体。
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Reprint of: Efficacy and safety of apixaban compared to warfarin for nonvalvular atrial fibrillation in end-stage renal disease on hemodialysis

Background

This study compared the efficacy and safety of apixaban and warfarin in patients with nonvalvular atrial fibrillation (NVAF) and end-stage renal disease (ESRD) on hemodialysis (HD). Apixaban decreased incidence of stroke and bleeding compared with warfarin in major clinical trials that excluded patients with severe renal dysfunction. Apixaban is no longer contraindicated in patients with ESRD on HD with NVAF based on pharmacokinetic studies. Limited clinical data exist for patients with ESRD on HD on apixaban.

Methods

A retrospective chart review was performed on patients with a diagnosis of NVAF and ESRD on HD who were prescribed apixaban or warfarin for stroke prevention in the years 2018 through 2019. Patients’ charts were reviewed for up to a 2-year period. Patients on renal replacement therapy other than HD, those using anticoagulation for reasons other than NVAF, patients with Child-Pugh Class C cirrhosis, and those with severe mitral valve stenosis were excluded. The primary outcome was emergency department visits or hospital admissions for ischemic stroke or transient ischemic attack. Secondary outcomes included major or minor bleeding and adverse effects.

Results

A total of 181 patients were screened; 110 patients met eligibility criteria and were included in the analysis. Four patients (7.5%) in the apixaban group and 6 patients (10.5%) in the warfarin group met the primary outcome of hospitalization or emergency department visit for stroke (P = 0.742). Symptomatic bleeding occurred in 39.6% of patients in the apixaban group and 36.8% in the warfarin group (P = 0.918). A trend in major bleeding occurred more often in the warfarin group, 52.4% versus 49.2% (P = 0.758).

Conclusions

There were no statistically significant differences in efficacy and safety outcomes between apixaban and warfarin in patients with NVAF and ESRD on HD in the intention-to-treat analysis of our study. Larger trials are needed to further analyze this patient population.
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来源期刊
CiteScore
3.30
自引率
14.30%
发文量
336
审稿时长
46 days
期刊介绍: The Journal of the American Pharmacists Association is the official peer-reviewed journal of the American Pharmacists Association (APhA), providing information on pharmaceutical care, drug therapy, diseases and other health issues, trends in pharmacy practice and therapeutics, informed opinion, and original research. JAPhA publishes original research, reviews, experiences, and opinion articles that link science to contemporary pharmacy practice to improve patient care.
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