Averill Alyssa J, Kasarskis Edward J, Segerstrom Suzanne C
Department of Psychology, University of Kentucky, Lexington, Kentucky 40506, USA.
Amyotroph Lateral Scler. 2007 Aug;8(4):243-54. doi: 10.1080/17482960701374643.
Amyotrophic lateral sclerosis (ALS) is a progressive and fatal neurodegenerative disease with no known effective treatment or cure. Clinicians often expect that ALS patients will experience depression following the diagnosis because ALS is a terminal disease. The objective of the current study was to examine the evidence from the literature on psychological health in ALS patients in order to determine the prevalence and severity of depression in this population. Twenty-eight studies of ALS patients, conducted over the past 20 years, were reviewed and evaluated. The cumulative evidence suggests that clinically significant depression is neither as prevalent nor as severe as might be expected. Methodological limitations that are inherent to the measurement of depression in ALS, including the lack of appropriate instruments, small sample sizes, and reliance on cross-sectional data, have contributed to the wide range of reported results. We conclude that ALS patients are more likely to present with hopelessness and end-of-life concerns than clinically significant depression. It is important to assess a broad range of potential psychological distress early in the course of ALS, rather than focus specifically on depression, because the manner in which patients cope with their disease can affect their longevity.
肌萎缩侧索硬化症(ALS)是一种进行性致命性神经退行性疾病,目前尚无已知的有效治疗方法或治愈手段。临床医生通常认为,ALS患者在确诊后会出现抑郁情绪,因为ALS是一种绝症。本研究的目的是审查文献中有关ALS患者心理健康的证据,以确定该人群中抑郁症的患病率和严重程度。我们对过去20年进行的28项关于ALS患者的研究进行了回顾和评估。累积证据表明,具有临床意义的抑郁症的患病率和严重程度并不像预期的那么高。ALS患者抑郁症测量中固有的方法学局限性,包括缺乏合适的工具、样本量小以及依赖横断面数据,导致了报告结果的广泛差异。我们得出结论,与具有临床意义的抑郁症相比,ALS患者更有可能表现出绝望和临终担忧。在ALS病程早期评估广泛的潜在心理困扰很重要,而不是特别关注抑郁症,因为患者应对疾病的方式会影响他们的寿命。