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find Keyword "普罗帕酮" 2 results
  • Effectiveness and Safety of Ibutilide in Treating Atrial Fibrillation and Atrial Flutter: A Systematic Review

    Objective To assess the effectiveness and safety of ibutilide and propafenone in the treatment of atrial fibrillation (AF) and atrial flutter (AFL). Methods All randomized controlled trials (RCTs) on ibutilide and propafenone for AF and AFL were retrieved from databases including CBM (1978 to October 2011), VIP (1989 to October 2011), CNKI (1994 to October 2011) and WanFang Data (1998 to October 2011). The quality of included RCTs was assessed according to the Cochrane Handbook for Systematic Reviews of Interventions Version 4.2.6, and the Cochrane Collaboration’s software RevMan 5.0 was used for meta-analysis. Results 16 RCTs involving 1 196 patients were included. Results of meta-analysis showed that: a) About effectiveness: compare with propafenone applied as routine therapy, ibutilide was more effective in the total conversion rate of AF and AFL with regards to the time of 0~90 min, 0~4 hour and 0~24 hour with significant differences (OR=3.32, OR=2.69, OR=3.08, respectively, Plt;0.000 1); In subgroup analysis, a significant difference was found in the conversion rate of AF or AFL in the time of 0~90min. In the time duration for conversion, there was a significant difference (MD=–25.12, 95%CI –30.43 to –19.82, Plt;0.000 01); and b) About the safety: there was a significant difference between the two groups in the incidence of cardiac arrhythmia (OR=3.15, 95%CI 1.97 to 5.05, Plt;0.000 01) and other adverse effects (OR=0.16, 95%CI 0.08 to 0.33, Plt;0.000 01). Conclusion Current evidence shows that ibutilide is more effective than propafenone in converting AF or AFL, with a higher incidence of cardiac arrhythmia than propafenone. However, more high-quality, large-scale RCTs are still needed to confirm the effectiveness and safety of ibutilide and propafenone for AF/AFL because of the limitation of the methodological quality and sample size of the included studies.

    Release date:2016-09-07 11:00 Export PDF Favorites Scan
  • 口服普罗帕酮与胺碘酮联合电复律转复持续性房颤的随机对照试验

    目的 比较普罗帕酮与胺碘酮联合电复律转复持续性心房颤动及维持窦性心律的疗效与安全性。方法 将60例基础疾病治疗良好的持续性房颤患者随机分为两组,每组各30例。普罗帕酮组:普罗帕酮600 mg顿服后观察6 h,未转复者予电复律,并以最低有效量口服维持窦律;胺碘酮组:胺碘酮600 mg分3次口服,连服7天,未转复者电复律,以最低有效量维持窦律。结果 单纯药物复律,普罗帕酮组4例,胺电酮组3例,联合电复律两组分别转复25例和22例,两组早期有效率分别为90.0%和80.0%,晚期有效率分别为73.3%和70.0%,两组比较差异无统计学意义。住院时间普罗帕酮组短于胺碘酮组(Plt;0.001)。普罗帕酮组1例服药后出现一过性低血压,放弃复律,经对症治疗后好转;胺碘酮组4例服药后恶心、呕吐,未能坚持负荷量连服7天;但两组副反应发生率差异无统计学意义。结论 普罗帕酮与胺碘酮联合电复律治疗持续心房颤动安全而有效,但普罗帕酮起效快,可相对减少患者的住院时间。

    Release date:2016-09-07 02:15 Export PDF Favorites Scan
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