Amyotrophic lateral sclerosis: A guide to collaborative care

被引：0

作者：

Nold, Carrie Smith ^{[1
]}

机构：

[1] Philadelphia Coll Osteopath Med, PA Program, Georgia Campus, Suwanee, GA 30024 USA

来源：

JAAPA-JOURNAL OF THE AMERICAN ACADEMY OF PHYSICIAN ASSISTANTS | 2018年 / 31卷 / 09期

关键词：

amyotrophic lateral sclerosis; motor neuron disease; familial; generic; myasthenia gravis; myopathy; QUALITY STANDARDS SUBCOMMITTEE; PRACTICE PARAMETER UPDATE; AMERICAN ACADEMY; CONTROLLED-TRIAL; UNITED-STATES; DOUBLE-BLIND; ALS; EDARAVONE; EPIDEMIOLOGY; DIAGNOSIS;

D O I：

10.1097/01.JAA.0000544311.25116.de

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

With the incidence of amyotrophic lateral sclerosis (ALS) increasing over recent decades, wide variability in disease presentation, and a median survival of only 2 to 4 years from disease onset, timely referral is key for patients with suspected ALS. This article discusses primary care providers' roles in recognizing ALS and managing symptoms in patients whose travel to specialists can become restricted in the later stages of the disease.

引用

页码：15 / 20

页数：6

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