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肺癌患者的抑郁:基于生活质量数据得出的患病率及风险因素

Depression in patients with lung cancer: prevalence and risk factors derived from quality-of-life data.

作者信息

Hopwood P, Stephens R J

机构信息

Cancer Research Campaign Psychological Medicine Group, Christie Hospital National Health Service Trust, Withington, Manchester, UK.

出版信息

J Clin Oncol. 2000 Feb;18(4):893-903. doi: 10.1200/JCO.2000.18.4.893.

Abstract

PURPOSE

To evaluate self-reported depression rates in patients with inoperable lung cancer and to explore demographic, clinical, and quality-of-life (QOL) factors associated with depression and thus identify patients at risk.

PATIENTS AND METHODS

Nine hundred eighty-seven patients from three palliative treatment trials conducted by the Medical Research Council Lung Cancer Working Party formed the study sample. 526 patients (53%) had poor prognosis small-cell lung cancer (SCLC) and 461 patients (47%) had good prognosis non-small-cell lung cancer (NSCLC). Hospital Anxiety and Depression Scale data and QOL items from the Rotterdam Symptom Checklist were analyzed, together with relevant demographic and clinical factors.

RESULTS

Depression was self-rated in 322 patients (33%) before treatment and persisted in more than 50% of patients. SCLC patients had a three-fold greater prevalence of case depression than those with NSCLC (25% v 9%; P <.0001). An increased rate for women was found for good performance status (PS) patients (PS of 0 or 1) but the sex difference reduced for poor PS patients (PS of 3 or 4) because of increased depression rates for men (chi(2) for trend, P <.0001). Multivariate analysis showed that functional impairment was the most important risk factor; depression increased by 41% for each increment on the impairment scale. Pretreatment physical symptom burden, fatigue, and clinician-rated PS were also independent predictors, but cell type was not.

CONCLUSION

Depression is common and persistent in lung cancer patients, especially those with more severe symptoms or functional limitations. Psychologic screening and appropriate intervention is an essential part of palliative care.

摘要

目的

评估无法手术的肺癌患者自我报告的抑郁率,并探讨与抑郁相关的人口统计学、临床和生活质量(QOL)因素,从而识别有风险的患者。

患者与方法

医学研究理事会肺癌工作组进行的三项姑息治疗试验中的987名患者构成了研究样本。526名患者(53%)患有预后较差的小细胞肺癌(SCLC),461名患者(47%)患有预后较好的非小细胞肺癌(NSCLC)。分析了医院焦虑抑郁量表数据和鹿特丹症状清单中的生活质量项目,以及相关的人口统计学和临床因素。

结果

322名患者(33%)在治疗前自我评定为抑郁,超过半数患者的抑郁持续存在。SCLC患者的抑郁患病率是NSCLC患者的三倍(25%对9%;P<.0001)。在功能状态(PS)良好(PS为0或1)的患者中,女性的抑郁率有所上升,但在PS较差(PS为3或4)的患者中,性别差异减小,因为男性的抑郁率增加(趋势χ²检验,P<.0001)。多变量分析表明,功能损害是最重要的危险因素;在损害量表上每增加一级,抑郁增加41%。治疗前的身体症状负担、疲劳和临床医生评定的PS也是独立的预测因素,但细胞类型不是。

结论

抑郁在肺癌患者中很常见且持续存在,尤其是那些症状更严重或功能受限的患者。心理筛查和适当干预是姑息治疗的重要组成部分。

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