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1971年以及1973 - 1978年美国的运动神经元病:死亡时的死亡率模式及相关病症

Motor neuron disease in the United States, 1971 and 1973-1978: patterns of mortality and associated conditions at the time of death.

作者信息

Leone M, Chandra V, Schoenberg B S

出版信息

Neurology. 1987 Aug;37(8):1339-43. doi: 10.1212/wnl.37.8.1339.

Abstract

Mortality rates for deaths "due to" and "with" motor neuron disease are presented for the first time. Age-specific mortality rates increase with age until 70 to 74 years and then decline. There appear to be no major differences by race in the age-adjusted mortality rates, but these rates are higher for males both white and nonwhite. A case-control study of all deaths with amyotrophic lateral sclerosis (ALS) was conducted for deaths due to ALS in the year 1971. Conditions associated with ALS at the time of death include pneumonia and bronchopneumonia, symptoms referable to respiratory system, superficial injury to shoulder and upper arm, essential benign hypertension, chronic skin ulcer, and malnutrition. No association was found between ALS and malignancies, Parkinson's disease, or dementia.

摘要

首次呈现了因运动神经元病“导致”死亡和“伴有”运动神经元病死亡的死亡率。年龄别死亡率随年龄增长至70至74岁,然后下降。年龄调整后的死亡率在种族方面似乎没有重大差异,但白人和非白人男性的这些死亡率都更高。针对1971年因肌萎缩侧索硬化症(ALS)死亡的情况进行了一项关于所有伴有ALS死亡的病例对照研究。死亡时与ALS相关的情况包括肺炎和支气管肺炎、呼吸系统相关症状、肩部和上臂的浅表损伤、原发性良性高血压、慢性皮肤溃疡和营养不良。未发现ALS与恶性肿瘤、帕金森病或痴呆之间存在关联。

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