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肢带型肌营养不良症:以肌无力和疾病持续时间作为功能障碍的预测指标

Limb girdle muscular dystrophy: weakness and disease duration as predictors of functional impairment.

作者信息

Stübgen J P, Lahouter A

机构信息

Department of Neurology, University of Pretoria, South Africa.

出版信息

Muscle Nerve. 1994 Aug;17(8):873-80. doi: 10.1002/mus.880170806.

Abstract

This cross-sectional study compared progressive weakness to functional disability in 20 patients with limb girdle muscular dystrophy. Weakness (assessed by manual muscle testing) determined disability (assessed by functional grades, timed functional tests, and an activities of daily living scale). For any functional grade the degree of weakness varied between patients. Yet, at a certain "threshold" weakness the functional level predictably deteriorated. Change in functional grade did not reflect a parallel increase in weakness nor disease progression. Functional "milestones" were reached at varying durations of disease. Only guidelines were offered to individual patients as to the time course of progression in disability. Serial timed tests should be a sensitive, objective method to follow the rate of disease progression. Timely referral of patients to establish physical needs should delay functional deterioration and minimize handicap despite progressive weakness.

摘要

这项横断面研究比较了20例肢带型肌营养不良患者的进行性肌无力与功能残疾情况。肌无力(通过徒手肌力测试评估)决定了残疾程度(通过功能分级、定时功能测试和日常生活活动量表评估)。对于任何功能分级,患者之间的肌无力程度各不相同。然而,在一定的“阈值”肌无力水平时,功能水平会可预测地恶化。功能分级的变化并未反映肌无力的平行增加或疾病进展情况。在疾病的不同阶段达到了功能“里程碑”。仅为个体患者提供了关于残疾进展时间进程的指导原则。连续定时测试应是一种跟踪疾病进展速度的敏感、客观方法。尽管存在进行性肌无力,但及时转诊患者以确定身体需求应可延缓功能恶化并将残疾程度降至最低。

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