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美国太平洋西北地区癌症护理和姑息治疗医师的丧亲实践调查。

Survey of bereavement practices of cancer care and palliative care physicians in the Pacific Northwest United States.

机构信息

University of Washington School of Medicine, Seattle, WA 98195, USA.

出版信息

J Oncol Pract. 2012 Sep;8(5):275-81. doi: 10.1200/JOP.2011.000512. Epub 2012 Jun 5.

Abstract

PURPOSE

Physicians caring for patients with cancer frequently encounter individuals who will die as a result of their disease. The primary aim of this study was to examine the frequency and nature of bereavement practices among cancer care and palliative care physicians in the Pacific Northwest United States. Secondary aims included identification of factors and barriers associated with bereavement follow-up.

METHODS

An institutional review board (IRB) -approved, anonymous online survey of cancer specialists and palliative care physicians in Alaska, Washington, Oregon, Idaho, Montana, and Wyoming was performed in fall 2010. Potential participants were identified through membership in national professional organizations. Summary statistics and logistic regression methods were used to examine frequency and predictors of bereavement practices.

RESULTS

A total of 194 (22.7%) of 856 physicians participated in the online survey, with 164 (19.1%) meeting study inclusion criteria. Overall, 70% of respondents reported always or usually making a telephone call to families, sending a condolence letter, or attending a funeral service after a patient's death. The most common perceived barriers to bereavement follow-up were lack of time and uncertainty of which family member to contact. Sixty-nine percent of respondents did not feel that they had received adequate training on bereavement follow-up during postgraduate training.

CONCLUSION

Although a significant portion of respondents engaged in some form of bereavement follow-up, the majority felt inadequately trained in these activities. Efforts to identify available resources and address bereavement activities in postgraduate training may contribute to improved multidisciplinary treatment of patients with cancer and their families.

摘要

目的

治疗癌症患者的医生经常会遇到因疾病而死亡的患者。本研究的主要目的是调查美国太平洋西北地区癌症护理和姑息治疗医生的丧亲实践的频率和性质。次要目的包括确定与丧亲后随访相关的因素和障碍。

方法

2010 年秋季,对阿拉斯加、华盛顿、俄勒冈、爱达荷、蒙大拿和怀俄明州的癌症专家和姑息治疗医生进行了机构审查委员会 (IRB) 批准的匿名在线调查。潜在参与者通过加入国家专业组织来确定。使用描述性统计和逻辑回归方法检查丧亲实践的频率和预测因素。

结果

共有 856 名医生中的 194 名(22.7%)参加了在线调查,其中 164 名(19.1%)符合研究纳入标准。总体而言,70%的受访者表示,在患者去世后,他们通常会打电话给家属、寄唁函或参加葬礼。丧亲后随访的最常见感知障碍是缺乏时间和不确定要联系哪个家属。69%的受访者表示,他们在研究生培训期间没有感到接受过足够的丧亲后随访培训。

结论

尽管相当一部分受访者采取了某种形式的丧亲后随访,但大多数人认为自己在这些活动中接受的培训不足。努力确定可用资源并在研究生培训中解决丧亲问题,可能有助于改善癌症患者及其家属的多学科治疗。

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