The Effect of Anti-Shock Garments on Prehospital Survival: The Need for Controlled Clinical Trials

P. Pepe, W. H. Bickell, K. Mattox
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引用次数: 6

Abstract

Abstract There exists strong sentiment, among emergency medical personnel and physicians alike, that the pneumatic anti-shock garment (PASG) “saves lives.” As a result, controlled studies have been criticized as the “withholding of important therapy.” The purpose of this presentation is to confirm the need for controlled clinical trials of the PASG. Despite an early report that the PASG offered no advantage in terms of the presenting emergency center Trauma Score (TS), similar disparagements have continued, particularly because survival data were not discussed. The present report is a pilot analysis of the effect of the PASG on the prehospital survival of patients arriving at an urban trauma center in the United States. In the study, sixty-eight patients were assigned randomly to control and PASG groups in a prospective investigation involving injured patients with systemic hypotension. The 32 control patients, whose mean initial systolic blood pressure (BP) was 59 ± 32 mm Hg, and the 36 PASG-treated patients, whose mean initial BP was 55 ± 31 mm Hg, were found to be well matched for age, sex, type and location of injuries, initial field TS; response, field management, and transport times; and the total amount of intravenous crystalloid infused. The results demonstrated no significant difference between the control and PASG-treated groups in terms of those pronounced dead on arrival at the trauma center (9/32 vs. 10/36). Further studies are therefore justified to determine how the PASG affects the long-term morbidity and mortality of injury victims, particularly those within certain sub-groups such as penetrating abdominal versus those with penetrating thoracic injuries. This report reaffirms the need for early responsible, scientific scrutiny of prehospital interventions.
防震服对院前生存的影响:需要对照临床试验
在急救医务人员和医生中都存在着一种强烈的情绪,即气动防震服(PASG)可以“挽救生命”。因此,对照研究被批评为“隐瞒重要治疗”。本报告的目的是确认PASG的对照临床试验的必要性。尽管早期有报道称PASG在呈现急救中心创伤评分(TS)方面没有优势,但类似的贬低仍在继续,特别是因为生存数据未被讨论。本报告是对PASG对到达美国城市创伤中心的患者院前生存影响的试点分析。在这项研究中,68名患者被随机分为对照组和PASG组,这是一项涉及全身性低血压的受伤患者的前瞻性调查。对照组32例,平均初始收缩压(BP)为59±32 mm Hg, pasg组36例,平均初始收缩压(BP)为55±31 mm Hg,年龄、性别、损伤类型和部位、初始野区TS;响应、现场管理和运输时间;以及静脉注射晶体药物的总量。结果显示,在到达创伤中心时宣布死亡的人数方面,对照组和pasg治疗组之间没有显著差异(9/32 vs 10/36)。因此,进一步的研究是有理由的,以确定PASG如何影响损伤受害者的长期发病率和死亡率,特别是在某些亚组中,如穿透性腹部损伤与穿透性胸部损伤。本报告重申需要对院前干预措施进行早期负责任的科学审查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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