Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig disease, involves progressive loss of motor neurons (a type of nerve cell controlling muscle movements) in the brain and spinal cord. ALS is a progressive, disabling, and ultimately fatal disease of unknown cause. Walking, speaking, swallowing, breathing, and other basic functions become impaired with time. About 30 000 Americans currently have ALS. The yearly incidence rate is 1 to 2 new cases per 100 000 individuals. The disease is commonly discovered during middle age and affects more men than women. The July 11, 2007, issue of JAMA includes an article discussing the diagnosis of ALS and recommendations for palliative (supportive) care.
SYMPTOMS
It is estimated that more than 50% of motor neurons are lost before symptoms such as muscle weakness become apparent.
Gradual muscle weakness and wasting in arms and legs
Muscle fasciculations (twitches visible in muscles)
Difficulty with swallowing, speaking, and breathing
Muscle stiffness, bodily pains, and cramps, especially at night
Respiratory failure is the usual cause of death in ALS. Other causes include pneumonia. In most cases, death occurs within 3 to 6 years after symptoms begin, although some individuals with ALS live for many years, even decades.
DIAGNOSIS
Diagnosis is based on a careful medical history, physical examination, and laboratory tests. Electromyograms (EMGs)—nerve conduction studies that evaluate nerve and muscle function—are the key tests. Other tests may include blood tests and neuroimaging studies such as CT or MRI scans of the brain and spinal cord. Molecular testing, cerebrospinal fluid tests, or muscle biopsy may be necessary.
TREATMENT
Physical, occupational, and speech therapies can assist in daily functioning.
Riluzole is the only medication approved for the treatment of ALS. It may prolong survival by a few months.
Other medications may relieve symptoms such as muscle pain, cramping, drooling, spasms, and fatigue.
SUPPORTIVE CARE
Appropriate exercises to help maintain mobility, strength, and energy
Changes in diet to minimize episodes of choking and ensure adequate nutrition
Effective use of assistive devices and braces such as neck collar, foot brace, cane, walker, or wheelchair
Ramps, handrails, raised toilet seat, shower seat
Erasable writing tablets or voice amplifiers and computers to help communication
A noninvasive ventilator (breathing machine) may be important to support breathing
The progressive, disabling nature of ALS and the fact that there is no cure make it a difficult disease to manage. In addition to medical care, patients need emotional support from family, friends, doctors, and caregivers.
FOR MORE INFORMATION
Muscular Dystrophy Association ALS Division (MDA) http://www.als.mdausa.org/
Amyotrophic Lateral Sclerosis Association (ALSA) http://www.alsa.org/
SYMPTOMS
It is estimated that more than 50% of motor neurons are lost before symptoms such as muscle weakness become apparent.
Gradual muscle weakness and wasting in arms and legs
Muscle fasciculations (twitches visible in muscles)
Difficulty with swallowing, speaking, and breathing
Muscle stiffness, bodily pains, and cramps, especially at night
Respiratory failure is the usual cause of death in ALS. Other causes include pneumonia. In most cases, death occurs within 3 to 6 years after symptoms begin, although some individuals with ALS live for many years, even decades.
DIAGNOSIS
Diagnosis is based on a careful medical history, physical examination, and laboratory tests. Electromyograms (EMGs)—nerve conduction studies that evaluate nerve and muscle function—are the key tests. Other tests may include blood tests and neuroimaging studies such as CT or MRI scans of the brain and spinal cord. Molecular testing, cerebrospinal fluid tests, or muscle biopsy may be necessary.
TREATMENT
Physical, occupational, and speech therapies can assist in daily functioning.
Riluzole is the only medication approved for the treatment of ALS. It may prolong survival by a few months.
Other medications may relieve symptoms such as muscle pain, cramping, drooling, spasms, and fatigue.
SUPPORTIVE CARE
Appropriate exercises to help maintain mobility, strength, and energy
Changes in diet to minimize episodes of choking and ensure adequate nutrition
Effective use of assistive devices and braces such as neck collar, foot brace, cane, walker, or wheelchair
Ramps, handrails, raised toilet seat, shower seat
Erasable writing tablets or voice amplifiers and computers to help communication
A noninvasive ventilator (breathing machine) may be important to support breathing
The progressive, disabling nature of ALS and the fact that there is no cure make it a difficult disease to manage. In addition to medical care, patients need emotional support from family, friends, doctors, and caregivers.
FOR MORE INFORMATION
Muscular Dystrophy Association ALS Division (MDA) http://www.als.mdausa.org/
Amyotrophic Lateral Sclerosis Association (ALSA) http://www.alsa.org/
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