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Validity, reliability and responsiveness to change of the Italian palliative care outcome scale: a multicenter study of advanced cancer patients

机译:改变意大利姑息治疗结果规模的有效性,可靠性和响应性:晚期癌症患者的多中心研究

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Background There is an increasing requirement to assess outcomes, but few measures have been tested for advanced medical illness. We aimed to test the validity, reliability and responsiveness of the Palliative care Outcome Scale (POS), and to analyse predictors of change after the transition to palliative care. Methods Phase 1: multicentre, mixed method study comprising cognitive and qualitative interviews with patients and staff, cultural refinement and adaption. Phase 2: consecutive cancer patients on admission to 8 inpatient hospices and 7 home-based teams were asked to complete the POS, the EORTC QLQ-C15-PAL and the FACIT-Sp (T0), to assess internal consistency, convergent and divergent validity. After 6 days (T1) patients and staff completed the POS to assess responsiveness to change (T1-T0), and agreement between self-assessed POS and POS completed by the staff. Finally, we asked hospices an assessment 24–48 h after T1 to assess its reliability (test re-test analysis). Results Phase I: 209 completed POS questionnaires and 29 cognitive interviews were assessed, revisions made and one item substituted. Phase II: 295 consecutive patients admitted to 15 PCTs were approached, 175 (59.3 %) were eligible, and 150 (85.7 %) consented. Consent was limited by the severity of illness in 40 % patients. We found good convergent validity, with strong and moderate correlations (r ranged 0.5–0.8) between similar items from the POS, the QLQ-C15-PAL and the FACIT-Sp. As hypothesised, the physical function subscale of QLQ-C15-PAL was not correlated with any POS item (r ranged -0.16–0.02). We found acceptable to good test re-test reliability in both versions for 6 items. We found significant clinical improvements during the first week of palliative care in 7/10 items assessed-pain, other symptoms, patient and family anxiety, information, feeling at peace and wasted time. Conclusions Both the patient self-assessed and professional POS versions are valid and with an acceptable internal consistency. POS detected significant clinical improvements during palliative care, at a time when patients are usually expected to deteriorate. These results suggest that there is room for substantial improvement in the management of patients with advanced disease, across all key domains-symptoms, psychological, information, social and spiritual.
机译:背景技术评估结果日益增长的要求,但对先进的医疗疾病进行了措施少数措施。我们旨在测试姑息治疗结果规模(POS)的有效性,可靠性和响应能力,并在过渡到姑息治疗后的变化预测因素。方法第1阶段:多期,混合方法研究,包括与患者和员工,文化改进和适应的认知和定性访谈。第2阶段:患有8阶段的癌症患者入院患者和7名住院病的患者和7个家庭基团队被要求完成POS,EORTC QLQ-C15-PAL和Facit-SP(T0),以评估内部一致性,收敛和发散的有效性。经过6天(T1)患者和工作人员完成了POS,以评估改变(T1-T0)的响应,并在工作人员完成的自我评估POS和POS之间的协议。最后,我们在T1之后向宾尼派徒提供了24-48小时的评估,以评估其可靠性(测试重新测试分析)。结果阶段I:209完成的POS问卷和29个认知访谈得到评估,修订并替代一项。第II期:295分次接受15%PCTS的连续患者,175名(59.3%)符合条件,同意150(85.7%)。同意受到40%患者疾病严重程度的限制。我们发现了良好的会聚有效性,在POS,QLQ-C15-PAL和Facit-SP的类似物品之间具有强烈和中等的相关性(R范围为0.5-0.8)。如假设,QLQ-C15-PAL的物理函数子等与任何POS项目都不相关(R范围-0.16-0.02)。我们发现在两个版本中获得了6项的良好测试重新测试可靠性。我们在7/10项中的姑息治疗的第一周内发现了显着的临床改善,评估了疼痛,其他症状,患者和家庭焦虑,信息,在和平和浪费时间。结论患者自我评估和专业POS版本都有效,内部一致性是有效的。在患者通常预期恶化时,POS检测到姑息治疗期间的显着临床改善。这些结果表明,在所有关键领域的症状,心理,信息,社会和精神上,存在高级疾病患者的实质性改善的余地。

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