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运动神经元病——患病率与残疾情况研究

Motor neurone disease--a study of prevalence and disability.

作者信息

James C M, Harper P S, Wiles C M

机构信息

Department of Medicine (Neurology), University of Wales College of Medicine, Cardiff, UK.

出版信息

QJM. 1994 Nov;87(11):693-9.

PMID:7820544
Abstract

We conducted a point prevalence study of motor neurone disease in the counties of South Glamorgan, Mid Glamorgan and Gwent, whose combined population is estimated at 1,394,400. A total of 56 patients were identified, giving a point prevalence for motor neurone disease in this area of 4.02/100,000 on 22/06/92. These cases were reclassified according to the World Federation of Neurology criteria for amyotrophic lateral sclerosis following a further clinical assessment, when disability was also evaluated (in 49 cases). Seven patients were reclassified on review of their medical records alone. Overall, 38 were classified as either definite or probable cases, which gave a point prevalence of 2.73/100,000. Of these patients, 94% (46/49) were living at home, 43% (21/49) scored 15 or less on the Barthel index, 65% (32/49) had some degree of mobility impairment, and 20% (10/49) were wheelchair-dependent. Swallowing speed was reduced (< 10 ml/s) in 67% (33/49), with three requiring feeding through a percutaneous gastrostomy tube. Vital capacity was < 70% of predicted value for age, sex and height in 67% (29/43). One patient was receiving domiciliary ventilation. These results give a quantitative indication of the dependency in a population of patients with motor neurone disease.

摘要

我们在南格拉摩根郡、中格拉摩根郡和格温特郡开展了一项运动神经元病的时点患病率研究,这几个郡的总人口估计为1394400人。共识别出56例患者,1992年6月22日该地区运动神经元病的时点患病率为4.02/10万。在进一步临床评估后,根据世界神经病学联合会肌萎缩侧索硬化症标准对这些病例进行了重新分类,同时还评估了残疾情况(49例)。仅通过查阅病历就对7例患者进行了重新分类。总体而言,38例被分类为确诊或疑似病例,时点患病率为2.73/10万。在这些患者中,94%(46/49)居家生活,43%(21/49)巴氏指数得分在15分及以下,65%(32/49)有一定程度的活动障碍,20%(10/49)依赖轮椅。67%(33/49)的患者吞咽速度减慢(<10 ml/s),3例需要通过经皮胃造瘘管进食。67%(29/43)的患者肺活量低于根据年龄、性别和身高预测值的70%。1例患者接受家庭通气治疗。这些结果定量显示了运动神经元病患者群体的依赖程度。

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