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晚期生命受限疾病预后讨论中的如实告知:一项系统综述

Truth-telling in discussing prognosis in advanced life-limiting illnesses: a systematic review.

作者信息

Hancock Karen, Clayton Josephine M, Parker Sharon M, Wal der Sharon, Butow Phyllis N, Carrick Sue, Currow David, Ghersi Davina, Glare Paul, Hagerty Rebecca, Tattersall Martin H N

机构信息

Medical Psychology Research Unit, University of Sydney, New South Wales, Australia.

出版信息

Palliat Med. 2007 Sep;21(6):507-17. doi: 10.1177/0269216307080823.

Abstract

Many health professionals (HPs) express discomfort at having to broach the topic of prognosis, including limited life expectancy, and may withhold information or not disclose prognosis. A systematic review was conducted of 46 studies relating to truth-telling in discussing prognosis with patients with progressive, advanced life-limiting illnesses and their caregivers. Relevant studies meeting the inclusion criteria were identified by searching computerized databases (MEDLINE, EMBASE, CINAHL, PsychINFO and Cochrane Register of Controlled Trials) up to November 2004, with handsearching of studies, as well as inclusion of studies satisfying selection criteria reported in 2005 by the authors. The reference lists of identified studies were hand-searched for further relevant studies. Inclusion criteria were studies of any design evaluating communication of prognostic information that included adult patients with an advanced, life-limiting illness; their caregivers; and qualified HPs. Results showed that although the majority of HPs believed that patients and caregivers should be told the truth about the prognosis, in practice, many either avoid discussing the topic or withhold information. Reasons include perceived lack of training, stress, no time to attend to the patient's emotional needs, fear of a negative impact on the patient, uncertainty about prognostication, requests from family members to withhold information and a feeling of inadequacy or hopelessness regarding the unavailability of further curative treatment. Studies suggest that patients can discuss the topic without it having a negative impact on them. Differences and similarities in findings from different cultures are explored.

摘要

许多医疗专业人员在不得不提及预后问题(包括有限的预期寿命)时会表现出不适,可能会隐瞒信息或不透露预后情况。我们对46项关于与患有进行性、晚期危及生命疾病的患者及其护理人员讨论预后时如实告知情况的研究进行了系统综述。通过检索截至2004年11月的计算机化数据库(MEDLINE、EMBASE、CINAHL、PsychINFO和Cochrane对照试验注册库),并手工检索相关研究,同时纳入作者在2005年报告的符合选择标准的研究,确定了符合纳入标准的相关研究。对已确定研究的参考文献列表进行手工检索,以查找更多相关研究。纳入标准为对评估预后信息沟通情况的任何设计的研究,这些研究包括患有晚期、危及生命疾病的成年患者;他们的护理人员;以及合格的医疗专业人员。结果显示,尽管大多数医疗专业人员认为应该将预后的真实情况告知患者和护理人员,但在实际操作中,许多人要么回避讨论这个话题,要么隐瞒信息。原因包括感觉缺乏培训、压力大、没有时间关注患者的情感需求、担心对患者产生负面影响、预后判断存在不确定性、家庭成员要求隐瞒信息以及对无法获得进一步的治愈性治疗感到无能为力或绝望。研究表明,患者可以讨论这个话题而不会对他们产生负面影响。我们还探讨了不同文化背景下研究结果的差异和相似之处。

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