Read e-book online Amyotrophic Lateral Sclerosis: A Guide for Patients and PDF

By Hiroshi, MD Mitsumoto

ISBN-10: 1932603727

ISBN-13: 9781932603729

This significant ebook covers each element of dwelling with ALS, from medical good points of the ailment to an summary of symptom administration to knowing its prognosis. significant sections take care of overseeing treatment and rehabilitation, residing with ALS, the disease’s complex part, end-of-life concerns, and assets. commonly revised and rewritten, this version comprises new chapters at the most modern methods to treating ALS indicators, using noninvasive ventilators, multidisciplinary staff care, new guidance being constructed by way of the yank Academy of Neurology for sufferers with ALS, using riluzole (Rilutek), and extra.

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Additional resources for Amyotrophic Lateral Sclerosis: A Guide for Patients and Families, Third Edition

Example text

It is the progression of disease to involve multiple body regions that allows for a diagnosis of definite ALS. 3) (71). Diagnostic criteria for each category have been established and refined to increase the degree of likelihood that the disease is really ALS and serve to alert the physician to search for disorders that may mimic ALS, particularly in its early stages. Although the use of these terms is sometimes distressing to patients because they are uncertain of the diagnosis when told they have “possible” or “probable” ALS, the criteria are in place to protect the patient from an improper diagnosis.

When spasticity exists, passively stretching or actively shortening a muscle spontaneously elicits a reflex that increases muscle tension. This reflex occurs because the motor neurons are more excitable. Thus, muscle relaxation is delayed, making smooth contraction difficult because the antagonist muscles—the opposite muscles that normally relax and elongate when the other muscles contract—also increase their muscle tone. The Clinical Features and Prognosis of Amyotrophic Lateral Sclerosis 29 Passive movement becomes nearly impossible when muscles are severely spastic.

Food and Drug Administration for the treatment of ALS. But riluzole is not the last word in ALS treatment. More effective therapies are necessary, and every suggestion for a potential treatment is considered seriously. The ease of electronic communication is impacting ALS treatment. Online forums and chat rooms permit rapid sharing of information and data, much of it anecdotal, about both drug and nondrug therapies. A clinical trial of gabapentin, which was developed as an antiepileptic agent, was initiated in part because of a patient’s report of beneficial response to this medication on an electronic bulletin board (69).

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Amyotrophic Lateral Sclerosis: A Guide for Patients and Families, Third Edition by Hiroshi, MD Mitsumoto


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