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晚期恶性肿瘤外科肿瘤患者的姑息治疗结局:混合方法研究。

Palliative care outcomes in surgical oncology patients with advanced malignancies: a mixed methods approach.

机构信息

National Institutes of Health Clinical Center, Building 10, Room 2B14, 10 Center Drive, Bethesda, MD 20892, USA.

出版信息

Qual Life Res. 2012 Apr;21(3):405-15. doi: 10.1007/s11136-011-0065-7. Epub 2011 Nov 19.

Abstract

PURPOSE

To prospectively compare outcomes and processes of hospital-based early palliative care with standard care in surgical oncology patients (N = 152).

METHODS

A randomized, mixed methods, longitudinal study evaluated the effectiveness of a hospital-based Pain and Palliative Care Service (PPCS). Interviews were conducted presurgically and at follow-up visits up to 1 year. Primary outcome measures included the Gracely Pain Intensity and Unpleasantness Scales and the Symptom Distress Scale. Qualitative interviews assessed social support, satisfaction with care, and communication with providers. Survival analysis methods explored factors related to treatment crossover and study discontinuation. Models for repeated measures within subjects over time explored treatment and covariate effects on patient-reported pain and symptom distress.

RESULTS

None of the estimated differences achieved statistical significance; however, for those who remained on study for 12 months, the PPCS group performed better than their standard of care counterparts. Patients identified consistent communication, emotional support, and pain and symptom management as positive contributions delivered by the PPCS.

CONCLUSIONS

It is unclear whether lower pain perceptions despite greater symptom distress were clinically meaningful; however, when coupled with the patients' perceptions of their increased resources and alternatives for pain control, one begins to see the value of an integrated PPCS.

摘要

目的

前瞻性比较基于医院的姑息治疗与外科肿瘤患者标准治疗的结果和过程(N=152)。

方法

一项随机、混合方法、纵向研究评估了基于医院的疼痛和姑息治疗服务(PPCS)的有效性。在术前和随访期间进行了访谈,随访时间长达 1 年。主要结局测量包括 Gracely 疼痛强度和不适量表以及症状困扰量表。定性访谈评估了社会支持、对护理的满意度以及与提供者的沟通。生存分析方法探讨了与治疗交叉和研究中止相关的因素。针对受试者随时间进行的重复测量模型探讨了治疗和协变量对患者报告的疼痛和症状困扰的影响。

结果

尽管存在症状困扰,但没有一项估计差异达到统计学意义;然而,对于那些在 12 个月内仍留在研究中的患者,PPCS 组的表现优于其标准护理对照组。患者认为 PPCS 提供了一致的沟通、情感支持以及疼痛和症状管理,这是积极的贡献。

结论

尽管症状困扰增加,但疼痛感知降低是否具有临床意义尚不清楚;然而,当将患者对其增加的资源和疼痛控制替代方案的感知与疼痛感知结合起来时,就开始看到综合 PPCS 的价值。

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