Schwab T M, Callaham M L, Madsen C D, Utecht T A
Department of Emergency Medicine, University of California, San Francisco, USA.
JAMA. 1995 Apr 26;273(16):1261-8.
To compare the effectiveness of active compression-decompression (ACD) cardiopulmonary resuscitation (CPR) with a handheld suction device vs standard manual CPR in victims of out-of-hospital cardiopulmonary arrest.
Prospective randomized clinical trial with crossover group design.
Emergency medical services (EMS) of a large (San Francisco) and medium-sized (Fresno) city in California.
All normothermic adult victims of out-of-hospital, nontraumatic cardiac arrest on whom CPR was performed by first responders.
Patients were randomized to receive either standard manual CPR according to American Heart Association guidelines or ACD CPR, on first-responder contact.
Return of spontaneous circulation, admission to the intensive care unit, survival to hospital discharge, and neurological function at hospital discharge.
The ACD group (n = 117 in Fresno; n = 297 in San Francisco) and standard group (n = 136 in Fresno; n = 310 in San Francisco) were similar with regard to demographic and prognostic variables, such as age, witnessed arrest and bystander CPR frequency, and initial cardiac rhythm. Average interval from 911 call activation to EMS responder arrival was 6.4 minutes in Fresno and 4.0 minutes in San Francisco. In Fresno, there was no difference between the ACD group and standard CPR group in return of spontaneous circulation (17% vs 20%; P = .68), hospital admission (16% vs 20%; P = .56), hospital discharge (5% vs 7%; P = .64), or cerebral performance category score at discharge (1.5 vs 1.6; P = .90). Similarly, in San Francisco there was no difference between the ACD group and standard CPR group in return of spontaneous circulation (19% vs 21%; P = .65), hospital admission (13.5% vs 14.5%; P = .79), hospital discharge (4.7% vs 5.5%; P = .80), or cerebral performance category score at discharge (2.2 vs 2.6; P = .31). There was no increase in significant complications associated with the use of ACD CPR.
There was no improvement in outcome with ACD CPR in out-of-hospital cardiac arrest in these two cities. Differences in study design, demographics, EMS systems, response intervals, training, and technique performance may contribute to the lack of improvement in initial resuscitation with ACD CPR compared with previous studies. Future research needs to control these variables to determine the reason for these differences in outcome.
比较使用手持式吸引装置的主动按压-减压(ACD)心肺复苏(CPR)与标准徒手CPR对院外心脏骤停患者的效果。
采用交叉组设计的前瞻性随机临床试验。
加利福尼亚州一个大城市(旧金山)和一个中等城市(弗雷斯诺)的紧急医疗服务(EMS)机构。
所有由急救人员进行CPR的院外非创伤性心脏骤停的正常体温成年患者。
患者在急救人员接触时被随机分配接受根据美国心脏协会指南进行的标准徒手CPR或ACD CPR。
自主循环恢复、入住重症监护病房、存活至出院以及出院时的神经功能。
ACD组(弗雷斯诺117例;旧金山297例)和标准组(弗雷斯诺136例;旧金山310例)在人口统计学和预后变量方面相似,如年龄、目击心脏骤停情况、旁观者进行CPR的频率以及初始心律。从拨打911到EMS急救人员到达的平均间隔时间在弗雷斯诺为6.4分钟,在旧金山为4.0分钟。在弗雷斯诺,ACD组和标准CPR组在自主循环恢复(17%对20%;P = 0.68)、入院率(16%对20%;P = 0.56)、出院率(5%对7%;P = 0.64)或出院时的脑功能分类评分(1.5对1.6;P = 0.90)方面无差异。同样,在旧金山,ACD组和标准CPR组在自主循环恢复(19%对21%;P = 0.65)、入院率(13.5%对14.5%;P = 0.79)、出院率(4.7%对5.5%;P = 0.80)或出院时的脑功能分类评分(2.2对2.6;P = 0.31)方面也无差异。使用ACD CPR未增加严重并发症。
在这两个城市的院外心脏骤停患者中,ACD CPR并未改善预后。研究设计、人口统计学、EMS系统、反应间隔、培训和技术操作方面的差异可能导致与先前研究相比,ACD CPR在初始复苏方面缺乏改善。未来的研究需要控制这些变量以确定这些预后差异的原因。