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创伤后应激障碍干预中筛选合适创伤患者的可行性。

Feasibility of identifying eligible trauma patients for posttraumatic stress disorder intervention.

机构信息

Emory University, Atlanta, GA.

出版信息

West J Emerg Med. 2010 Aug;11(3):274-8.

PMID:20882149
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2941366/
Abstract

OBJECTIVE

This research report examines the feasibility of identifying eligible trauma patients for a study providing an early therapeutic intervention for the prevention of posttraumatic stress disorder (PTSD), and identifies reasons around participation.

METHODS

This prospective observational study used a convenience sample of acute trauma victims presenting to a university-affiliated Level One trauma center in a large southeastern city. Patients eligible to participate in the early intervention study were adults (18- 65) who experienced a traumatic event within 72 hours of presentation, feared that they might be killed or seriously injured during the event, and were able to return for follow-up appointments. Patients were excluded if they were non-English speaking; experienced a loss of consciousness greater than five minutes; had a history of a serious mental illness or were currently suicidal; or endorsed current substance dependence. Descriptive statistics were conducted to determine differences in ineligible, eligible, and consenting trauma patients who enrolled in the intervention study.

RESULTS

Over a six-month period, n =1961 patients presented for treatment of a traumatic injury during study hours. Results showed that eligible patients were significantly younger than ineligible patients. Survivors of assaults (physical and sexual), younger patients, and women were generally more likely to participate in a study offering a psychological intervention in the immediate aftermath of a traumatic event.

CONCLUSION

Fourteen percent of trauma patients were eligible and entered a study offering an early psychological intervention for the prevention of PTSD. Trauma type, age and gender may play a role in determining preference for receiving psychological services immediately after experiencing a traumatic event.

摘要

目的

本研究报告探讨了识别有资格参加研究的创伤患者的可行性,该研究为预防创伤后应激障碍(PTSD)提供早期治疗干预,并确定了参与的原因。

方法

本前瞻性观察性研究使用了方便样本,包括在东南部大城市一所大学附属一级创伤中心就诊的急性创伤患者。有资格参加早期干预研究的患者为成年人(18-65 岁),在就诊后 72 小时内经历了创伤事件,担心在事件中可能会死亡或重伤,并且能够返回接受随访预约。如果患者是非英语使用者;意识丧失超过五分钟;有严重精神疾病史或目前有自杀倾向;或目前有物质依赖,则将其排除在外。进行描述性统计以确定参与干预研究的不合格、合格和同意的创伤患者之间的差异。

结果

在六个月的时间里,有 1961 名患者在研究时间内因创伤性损伤接受治疗。结果表明,合格患者明显比不合格患者年轻。攻击(身体和性)幸存者、年轻患者和女性通常更愿意在创伤事件发生后立即接受提供心理干预的研究。

结论

14%的创伤患者有资格参加提供早期心理干预以预防 PTSD 的研究。创伤类型、年龄和性别可能在决定创伤后立即接受心理服务的偏好方面发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f8/2941366/aeef234fbfee/wjem11_3p274f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f8/2941366/06134c25c4a1/wjem11_3p274f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f8/2941366/aeef234fbfee/wjem11_3p274f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f8/2941366/06134c25c4a1/wjem11_3p274f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f8/2941366/aeef234fbfee/wjem11_3p274f2.jpg

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