作为姑息治疗有效性标准的不治之症患者的生活质量

Q4 Medicine
N. Petrova, Viktoria A. Yarovaya
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引用次数: 0

摘要

介绍。由于老年人比例的增加和患有不治之症的患者数量的增加,姑息治疗的发展问题是现实的。姑息治疗的任务是改善不治之症患者的生活质量。为了选择解决该问题的最佳方法,分析QL的所有组成部分以及评估所采取措施的有效性非常重要。本研究的目的是评估姑息治疗病房患者的生活质量及其趋势。材料和方法。研究基地——姑息治疗科。采用EORTIC - QLQ30和MSAS - SF问卷。患者样本包括82人。非肿瘤疾病患者占54.9%,癌症患者占45.1%。这项研究每隔一个月进行一次。结果。生活质量趋势分析显示不可靠(p > 0.05), QL下降:31.5 - 25.4分(最高为100分)。部分分量的变化趋势是多向的。功能量表、症状量表各指标由34.7分降至29.8分,由30.3分降至29.9分。经济幸福指数从35.0上升到38.6,社会幸福指数从14.0上升到17.1。从表征患者心理情绪状态的量表来看,患者情绪幸福感的平均得分从68.1分上升到74.4分;认知-从44.7到53.2。MSAS-SF量表上的总体GDI窘迫指数从2.3点上升到2.4点(最高4点)。的局限性。接受姑息治疗的病人;令人满意的条件;随访间隔-至少一个月。结论。应对姑息治疗患者的生活质量进行趋势评估,以全面了解患者治疗的迫切问题,纠正治疗和护理措施,并可能表明其有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quality of life in incurable patients as a criterion of effectiveness of palliative care
Introduction. The problem of palliative care developing is actual due to the increasing the proportion of older people and the number of patients with incurable diseases. The task of palliative care is to improve the quality of life in the incurable patient. To choose the best ways for solving this problem it is important to analyze all components of QL and it’s important for the evaluating the effectiveness of the measures taken. The aim of this study was to assess the quality of life in patients in the palliative care unit and its trend. Material and methods. The base of study — palliative care department. The EORTIC — QLQ30 and MSAS — SF questionnaires were used. The sample of patients included 82 people. The share of people with non-oncological diseases was 54.9%, with cancer — 45.1%. The study was conducted with an interval of one month. Results. The analysis of the trend in the quality of life showed unreliable (p > 0.05) decrease in the QL: 31.5 — 25.4 points (the maximum is 100 points). The trend in the partial components were multidirectional. The indicators of the functional scale and the symptom scale decreased from 34.7 to 29.8 points and from 30.3 to 29.9 points. The indicator of financial well-being increased: 35.0 and 38.6 points, social well–being — from 14.0 to 17.1. According to the scales characterizing the psycho-emotional status of patients, there is a positive trend: the average score of emotional well-being increased from 68.1 to 74.4; cognitive — from 44.7 to 53.2. The overall GDI distress index on the MSAS-SF scale increased from 2.3 to 2.4 points (with a maximum of 4 points). Limitations. patients receiving palliative care; satisfactory condition; follow-up interval — at least a month. Conclusion. Trend assessment in the quality of life in patients receiving palliative care should be carried out to obtain a comprehensive understanding of the urgent problems of the patient treatment, correction of therapeutic and care measures and may indicate their effectiveness.
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