Treatment Overview
Although there is no cure for
amyotrophic lateral sclerosis (ALS), treatment can
help you maintain strength and independence, manage symptoms, and avoid
complications for as long as possible. Treatment also focuses on providing
emotional support as your disability increases.
Physical therapy and occupational therapy may help you maintain
strength and function and make the most of your remaining abilities. Speech
therapy can help you maintain your ability to communicate after speaking problems
begin.
Medicines may be used to relieve symptoms and make you more
comfortable. These include:
- Baclofen (Lioresal), tizanidine (Zanaflex),
dantrolene (Dantrium), or benzodiazepines such as diazepam (Valium), to relieve
muscle stiffness, spasms, and twitching.
- Quinine, phenytoin sodium
(Dilantin), benzodiazepines, or gabapentin to relieve muscle
cramps.
- Morphine, to help with breathing problems (dyspnea).
Antianxiety medicines such as diazepam or lorazepam may be helpful in
relieving anxiety caused by breathing problems. The American Academy of
Neurology also considers
acupuncture a useful option for breathing problems
when used in addition to medicine or breathing devices.5
- Antidepressant medicines, to help with
depression, sleeplessness, poor appetite, or fatigue, and to decrease the
production of saliva (which may be helpful if you have trouble with the muscles
that control swallowing).
- Pain relievers, to reduce muscle pain,
which sometimes develops late in the course of the disease.
If you are having problems getting enough food or taking medicine, a tube can be inserted through the skin into the stomach
(percutaneous endoscopic gastrostomy, or PEG). The tube provides an easier way
to get adequate nutrition and take medicines.
Breathing devices (ventilators) may be needed as the muscles of the
chest become affected. Initially, extra oxygen can be given through a
nasal cannula, a flexible plastic tube that is placed
in the nostrils. For people who have mild breathing problems, nonsurgical forms
of ventilation may be used. These include bilevel positive airway pressure
(BiPAP) and noninvasive positive pressure ventilation (NPPV), which deliver air
or extra oxygen through a face mask. However, in some cases, an opening in the
neck leading to the windpipe (tracheostomy) may have to be created and oxygen
delivered through a tube in the opening.
At first, breathing devices may be needed only part of the time,
such as when you are sleeping. As the disease and breathing problems
get worse, you may need to be on a breathing machine all the time.
Riluzole
A medicine called riluzole (Rilutek) may prolong survival by about 2 months.4 It is not known exactly how the
medicine works, but it may slow the release of certain brain chemicals
(neurotransmitters) that are believed to play a role in ALS. Riluzole is the
only medicine approved for the treatment of ALS.
There are some disadvantages to taking riluzole. Although it has
been shown to prolong survival for about 2 months, it does not improve symptoms
or quality of life in ways that people with ALS, their caregivers, or their
doctors have been able to detect. Most people tolerate riluzole very well, but
it can cause side effects, including nausea, vomiting, weakness, dizziness, and
coughing. Because riluzole can cause liver problems, people taking the drug
need to have their liver checked on a regular basis. Treatment with
riluzole is also expensive, and it may not help some people who have certain
forms of ALS.