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城市重症监护病房中家庭对临终关怀的看法。

Family perceptions of end-of-life care in an urban ICU.

作者信息

Kjerulf Maria, Regehr Cheryl, Popova Svelana R, Baker Andrew J

机构信息

Faculty of Nursing, McMaster University.

出版信息

Dynamics. 2005 Fall;16(3):22-5.

Abstract

OBJECTIVES

As most Canadians die in hospital, the final contact of family members with their loved ones is frequently in an unknown and uncomfortable environment. Family members are integral to the end-of-life decision-making process and are vital contributors to the comfort of dying patients. A quantitative study was conducted in three critical care areas where the stated goals were to provide not only quality care to patients, but also support to families. The researchers sought to determine levels of satisfaction with care, visitation, support, comfort and pain measures.

METHOD

Three hundred surveys were mailed to next of kin who had a loved one die in the critical care areas of an urban tertiary care centre within the prior three years. Survey questions covered such issues as perceptions regarding the decision to stop life supports, access to the patient, access to physicians and nurses and information regarding the patient's status, support provided by the hospital, and organ donation attitudes.

FINDINGS

Multiple regression analysis revealed that three factors predicted perceptions of overall quality of care: 1) being informed by nurses and physicians of any changes, 2) having the same group of nurses provide care, and 3) having one individual act as the family contact. Together these factors accounted for 52% of the variance in perceptions of care. Two factors accounted for 59% of the variance in dissatisfaction with the information received: 1) the perception that physicians did not spend enough time answering family questions, and 2) that the family was not present when the patient died.

IMPLICATIONS

Consistency in nursing care and provision of information to family members may be difficult in the fast pace of an ICU, but are reasonable program objectives considering the positive influence this has on perceptions of care. Further, flexible visitation policies which maximize access between family members and both their dying loved one and health care professionals appear to have a beneficial effect on satisfaction.

摘要

目标

由于大多数加拿大人在医院去世,家庭成员与亲人的最后接触往往是在一个陌生且不舒适的环境中。家庭成员是临终决策过程中不可或缺的一部分,也是临终患者舒适度的重要贡献者。在三个重症监护领域进行了一项定量研究,其既定目标不仅是为患者提供优质护理,还要为家属提供支持。研究人员试图确定对护理、探视、支持、舒适度和疼痛处理措施的满意度水平。

方法

向在过去三年中亲人在城市三级护理中心重症监护区去世的近亲邮寄了300份调查问卷。调查问题涵盖了诸如对停止生命支持决策的看法、与患者接触的机会、与医生和护士接触的机会以及患者状况信息、医院提供的支持以及器官捐赠态度等问题。

结果

多元回归分析表明,有三个因素可预测对整体护理质量的看法:1)护士和医生告知任何变化;2)由同一组护士提供护理;3)有一人作为家属联系人。这些因素共同解释了护理看法差异的52%。有两个因素解释了对所获信息不满差异的59%:1)认为医生没有花足够时间回答家属问题;2)患者去世时家属不在场。

启示

在重症监护病房的快节奏环境中,护理的一致性以及向家属提供信息可能具有挑战性,但考虑到这对护理看法的积极影响,这是合理的项目目标。此外,灵活的探视政策可最大限度增加家庭成员与临终亲人及医护人员之间的接触机会,这似乎对满意度有有益影响。

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