中国循证心血管医学杂志
中國循證心血管醫學雜誌
중국순증심혈관의학잡지
CHINESE JOURNAL OF EVIDENCE-BASES CARDIOVASCULAR MEDICINE
2014年
1期
6-9
,共4页
张波%付潇%程小成%胡光欣%陈竹%张眉%陈少杰%殷跃辉
張波%付瀟%程小成%鬍光訢%陳竹%張眉%陳少傑%慇躍輝
장파%부소%정소성%호광흔%진죽%장미%진소걸%은약휘
维纳卡兰%心房颤动%系统评价
維納卡蘭%心房顫動%繫統評價
유납잡란%심방전동%계통평개
Vernakalant%Atrial fibrillation%Systemic reviewing
目的:系统评价维纳卡兰转复心房颤动(房颤)的有效性及安全性。方法检索PubMed、Cochrane Library、中国生物医学文献数据库,收集2000年1月至2013年6月公开发表的关于维纳卡兰治疗房颤[或心房扑动(房扑)]的前瞻性对照研究。按照预先设定的纳入和排除标准选择文献,采用Jadad评分量表对纳入的文献进行质量评价。由两位研究者独立提取纳入文献的资料,使用Revman5.0统计软件进行Meta分析。结果有7篇前瞻性临床研究满足纳入标准。总共1133例房颤(房扑)患者纳入研究(其中维纳卡兰组668例,对照组465例)。Meta分析显示:维纳卡兰组房颤转复率明显高于对照组(38.3%vs.14.1%;OR=5.73;P<0.0001),尤其是在新发房颤患者当中其转复率可达52.2%(95%CI:46.9%~57.4%),中位转复时间为11 min。对于持续房颤维纳卡兰的转复率为8.3%(95%CI:3.1%~13.6%)。房扑终止率为2.6%。尽管维纳卡兰延长QRS波时限和QT间期,但在观察期内未增加主要不良心血管事件风险。结论现有循证医学证据显示维纳卡兰可以安全、有效、快速地转复新发房颤,维纳卡兰对房扑转复效果不显著。
目的:繫統評價維納卡蘭轉複心房顫動(房顫)的有效性及安全性。方法檢索PubMed、Cochrane Library、中國生物醫學文獻數據庫,收集2000年1月至2013年6月公開髮錶的關于維納卡蘭治療房顫[或心房撲動(房撲)]的前瞻性對照研究。按照預先設定的納入和排除標準選擇文獻,採用Jadad評分量錶對納入的文獻進行質量評價。由兩位研究者獨立提取納入文獻的資料,使用Revman5.0統計軟件進行Meta分析。結果有7篇前瞻性臨床研究滿足納入標準。總共1133例房顫(房撲)患者納入研究(其中維納卡蘭組668例,對照組465例)。Meta分析顯示:維納卡蘭組房顫轉複率明顯高于對照組(38.3%vs.14.1%;OR=5.73;P<0.0001),尤其是在新髮房顫患者噹中其轉複率可達52.2%(95%CI:46.9%~57.4%),中位轉複時間為11 min。對于持續房顫維納卡蘭的轉複率為8.3%(95%CI:3.1%~13.6%)。房撲終止率為2.6%。儘管維納卡蘭延長QRS波時限和QT間期,但在觀察期內未增加主要不良心血管事件風險。結論現有循證醫學證據顯示維納卡蘭可以安全、有效、快速地轉複新髮房顫,維納卡蘭對房撲轉複效果不顯著。
목적:계통평개유납잡란전복심방전동(방전)적유효성급안전성。방법검색PubMed、Cochrane Library、중국생물의학문헌수거고,수집2000년1월지2013년6월공개발표적관우유납잡란치료방전[혹심방복동(방복)]적전첨성대조연구。안조예선설정적납입화배제표준선택문헌,채용Jadad평분량표대납입적문헌진행질량평개。유량위연구자독립제취납입문헌적자료,사용Revman5.0통계연건진행Meta분석。결과유7편전첨성림상연구만족납입표준。총공1133례방전(방복)환자납입연구(기중유납잡란조668례,대조조465례)。Meta분석현시:유납잡란조방전전복솔명현고우대조조(38.3%vs.14.1%;OR=5.73;P<0.0001),우기시재신발방전환자당중기전복솔가체52.2%(95%CI:46.9%~57.4%),중위전복시간위11 min。대우지속방전유납잡란적전복솔위8.3%(95%CI:3.1%~13.6%)。방복종지솔위2.6%。진관유납잡란연장QRS파시한화QT간기,단재관찰기내미증가주요불양심혈관사건풍험。결론현유순증의학증거현시유납잡란가이안전、유효、쾌속지전복신발방전,유납잡란대방복전복효과불현저。
Objective To review systematically the effectiveness and safety of vernakalant in converting atrial fibrillation (AF). Methods The databases of PubMed, Cochrane Library and CBM were retrieved for collecting perspective control studies about treatment of AF (or atrial flutter) were retrieved from Jan. 2000 to Jun. 2013. The studies were selected according to pre-set inclusion and exclusion criteria and then given quality reviews by using Jadad rating scale. The data was extracted by two independent researches from included studies and then given Meta-analysis by using Revman5.0 software. Results There were 7 trials met the inclusion criterion involving 1133 patients (668 in vernakalant group and 465 in control group). The results of Meta-analysis showed that conversion rate was higher in vernakalant group than that in control group (38.3% vs. 14.1%; OR=5.73; P<0.0001). The conversion rate reached 52.2%(95%CI:46.9%~57.4%) in the patients with new-onset AF and median conversion time was 11 min. The conversion rate was 8.3% (95%CI: 3.1%~13.6%) in the patients with persistent AF. Vernakalant had not significant effect on atrial flutter and the terminating rate was 2.6%only. Although it prolonged QRS duration and QT interval, vernakalant did not increase the risk of major cardiovascular adverse events during observation period. Conclusion The current evidence of evidence-based medicine shows that vernakalant is safe, effective and quick in converting AF.