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决策模型对自我感知生活质量的影响:一项针对脑癌患者的研究。

The impact of decision models on self-perceived quality of life: a study on brain cancer patients.

作者信息

Lucchiari C, Botturi A, Pravettoni G

机构信息

Dipartimento di Studi Sociali e Politici, Università degli studi di Milano, Via Conservatorio 7, 20122 Milano, Italy.

出版信息

Ecancermedicalscience. 2010;4:187. doi: 10.3332/ecancer.2010.187. Epub 2010 Aug 20.

Abstract

Quality of life (QoL) is an increasingly important outcome measure in medicine. Health, in fact, is not only based on functional status but also on psychological and social well being. Since QoL is related to the patient's perception of their position in life in relation to their goals, expectations, standards and concerns, the way in which the medical context is experienced may be critical. We then hypothesised that self-perceived QoL may be linked to unmet needs in information management and decision involvement. To analyse this hypothesis, we conducted a quantitative study on 84 consecutive patients with a diagnosis of primary high-grade glioma. The functional assessment of cancer therapy-Brain (FACT-Br) scales, the hospital anxiety and depression (HAD) scale and the need evaluation questionnaire (NEQ) questionnaire were used, in order to measure quality-of-life dimension, mood and unmet needs. Patients were classified as having no need (cluster 1), a moderate need (cluster 2) or a high need (cluster 3) to be more involved in the clinical process.Our data confirmed previous studies in other clinical areas, showing that shared decision might contribute to a better adaptation process to the illness [1]. In fact, patients in cluster 1 showed a significant better self-perceived QoL, despite the lack of clinical differences between clusters. The study showed that patients satisfied with respect to decisional involvement seem to be able to better cope with their disease. Finally, the study suggests the need for a more attuned decision-making process in approaching clinical decisions. Physicians need to better understand patient preferences related to information and decision sharing.

摘要

生活质量(QoL)在医学中是一种日益重要的结果衡量指标。事实上,健康不仅基于功能状态,还基于心理和社会幸福感。由于生活质量与患者对自身在生活中相对于其目标、期望、标准和关切的位置的认知相关,所以体验医疗环境的方式可能至关重要。于是我们推测,自我感知的生活质量可能与信息管理和决策参与方面未满足的需求有关。为了分析这一推测,我们对84例连续诊断为原发性高级别胶质瘤的患者进行了一项定量研究。使用癌症治疗-脑功能评估(FACT-Br)量表、医院焦虑抑郁(HAD)量表和需求评估问卷(NEQ),以测量生活质量维度、情绪和未满足的需求。患者被分为在临床过程中参与需求低(第1组)、中度需求(第2组)或高度需求(第3组)。我们的数据证实了之前在其他临床领域的研究,表明共同决策可能有助于更好地适应疾病过程[1]。事实上,第1组患者自我感知的生活质量显著更好,尽管各组之间在临床方面并无差异。该研究表明,对决策参与感到满意的患者似乎能够更好地应对疾病。最后,该研究表明在临床决策过程中需要一个更协调的决策过程。医生需要更好地理解患者在信息和决策共享方面的偏好。

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