Kanji Salmaan, Stewart Robert, Fergusson Dean A, McIntyre Lauralyn, Turgeon Alexis F, Hébert Paul C
Ottawa Hospital, Canada.
Crit Care Med. 2008 May;36(5):1620-4. doi: 10.1097/CCM.0b013e3181709e43.
Atrial fibrillation is a common problem associated with morbidity and mortality in critically ill patients; however, evidence-based treatment recommendations are lacking. The objective of this systematic review was to evaluate the efficacy of pharmacologic rhythm control of new-onset atrial fibrillation in noncardiac, critically ill adults.
Citations identified from an electronic search of Medline, the Cochrane register of controlled trials, and Embase databases (1966 to August 2006) were independently reviewed by two investigators.
All prospective randomized controlled trials evaluating pharmacologic rhythm conversion regimens for new-onset atrial fibrillation in (noncardiac surgery) critically ill adult patients were included. The primary end point was atrial fibrillation resolution.
Using a standardized data extraction form, data related to study design, population characteristics, pharmacologic intervention, and outcome measures were collected.
Four trials met inclusion criteria from 1995 citations screened. Of the 143 evaluable patients in these trials 89 (76%) had atrial fibrillation while the remaining ones had other atrial tachyarrhythmias. Drugs evaluated for rhythm conversion included amiodarone (n = 26), procainamide (n = 14), magnesium (n = 18), flecainide (n = 15), esmolol (n = 28), verapamil (n = 15), and diltiazem (n = 27). The definition of treatment success ranged from conversion within 1 hr to conversion within 24 hrs. No study evaluated maintenance of conversion, and one study included hemodynamically unstable patients. Lack of methodologic homogeneity prevented any pooled analysis.
Using the current published literature, we cannot recommend a standard treatment for atrial fibrillation in noncardiac critically ill adult patients. Clinical trials evaluating rhythm conversion in critically ill populations outside of cardiac surgery are lacking. Further trials that address goals of care in hemodynamically stable and unstable patients and utilize standardized definitions of successful cardioversion are required.
心房颤动是危重症患者常见的并发症,与发病率和死亡率相关;然而,缺乏基于证据的治疗建议。本系统评价的目的是评估非心脏危重症成年患者新发心房颤动药物节律控制的疗效。
两名研究者独立检索了Medline、Cochrane对照试验注册库和Embase数据库(1966年至2006年8月),对检索到的文献进行回顾。
纳入所有评估非心脏手术危重症成年患者新发心房颤动药物节律转复方案的前瞻性随机对照试验。主要终点是心房颤动转复。
使用标准化的数据提取表,收集与研究设计、人群特征、药物干预和结局指标相关的数据。
在筛选的1995篇文献中,有4项试验符合纳入标准。在这些试验的143例可评估患者中,89例(76%)为心房颤动,其余为其他房性快速心律失常。评估用于节律转复的药物包括胺碘酮(n = 26)、普鲁卡因胺(n = 14)、镁剂(n = 18)、氟卡尼(n = 15)、艾司洛尔(n = 28)、维拉帕米(n = 15)和地尔硫䓬(n = 27)。治疗成功的定义从1小时内转复到24小时内转复不等。没有研究评估转复后的维持情况,且有一项研究纳入了血流动力学不稳定的患者。方法学异质性使得无法进行任何汇总分析。
根据目前已发表的文献,我们无法推荐非心脏危重症成年患者心房颤动的标准治疗方法。缺乏评估心脏手术以外危重症人群节律转复的临床试验。需要进一步开展试验,明确血流动力学稳定和不稳定患者的治疗目标,并采用标准化的成功复律定义。