Symptomatic Treatment of MS - European Multiple Sclerosis Platform
Symptomatic Treatment of MS - European Multiple Sclerosis Platform
Symptomatic Treatment of MS - European Multiple Sclerosis Platform
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Antiepileptics:<br />
Primidone may be effective in essential tremor but sedative side effects limit its use. Gabapentin will<br />
ameliorate essential and orthostatic tremor and carbamazepine [Sechi 1989] as well as topiramate [Sechi<br />
2003] may positively influence cerebellar tremor.<br />
Other drugs:<br />
Clonazepam (3-6 mg/d) may be <strong>of</strong> some benefit in cerebellar tremor, too [Trelles 1984]. The effect <strong>of</strong><br />
Oxitriptan (5-hydroxytryptophane) on ataxia <strong>of</strong> the trunk and legs usually occurs only after treatment<br />
with 3x300 mg/d over about 6 weeks [Trouillas 1988]. Up to now, ondansetron, a 5-hydroxytryptophan-<br />
(HT-3)-antagonist, showed conflicting results. Using 8 mg <strong>of</strong> oral Ondansetron no significant reduction<br />
<strong>of</strong> cerebellar symptoms could be demonstrated [Gbadamosi 2001; Bier 2003], whereas intravenous<br />
ondansetron (8 mg/d) caused a clear short lasting amelioration <strong>of</strong> writing ataxia and <strong>of</strong> the patients´<br />
subjective impression [Rice 1997]. Isoniazid has been used in patients with cerebellar tremor with<br />
conflicting results [Koller 1984; Hallett 1985]. Adverse effects may limit treatment. Physostigmine has no<br />
significant effect on cerebellar tremor [Duquette 1985; Wessel 1997].<br />
SURGICAL TREATMENT<br />
With stereotactic operations, e.g. VIM thalamotomy and VIM (deep brain-) stimulation, reduction <strong>of</strong><br />
tremor could be demonstrated though [Bittar 2005] VIM thalamotomy is not as effective in <strong>MS</strong> patients<br />
as in those with Parkinson´s disease. Chronic VIM stimulation will produce better results but stimulation<br />
parameters probably have to be optimized repeatedly. In some smaller studies and case series amelioration<br />
<strong>of</strong> tremor could be achieved in 87.7 % and <strong>of</strong> activities <strong>of</strong> daily life in 76 % <strong>of</strong> operated patients<br />
[Wishart 2003]. Simultaneously the level <strong>of</strong> disability and SF-36 subscales remained largely unchanged<br />
[Hooper 2002; Berk 2002]. Fortunately peri- and postoperative complications are rare. Best treatment<br />
results may be achieved in patients with stable tremor, e.g. marked axial and proximal arm tremor, and<br />
trunk ataxia [Alusi 2001]. If stereotactic treatment is considered, the patients’ disease course should be<br />
stabilized by effective immunotherapy for at least one year.<br />
RECOMMENDATIONS<br />
� Regular physiotherapy and occupational therapy, cooling.<br />
� In patients with predominant tremor: additional drug treatment (monotherapy) with a beta blocker<br />
(rapid assessment <strong>of</strong> efficacy) and, if not successful, monotherapy with carbamazepine, primidone<br />
or clonazepam. If escalation is necessary combination therapy with a beta blocker and an<br />
antiepileptic drug. Efficacy <strong>of</strong> these drugs is <strong>of</strong>ten limited by their extensive adverse effects.<br />
� If tremor is unresponsive to combination therapy: oxitriptan<br />
� Only in patients with considerable tremor unresponsive to drug treatment or with severe side effects<br />
electrical stimulation <strong>of</strong> the thalamus should be considered.<br />
25 E<strong>MS</strong>P, <strong>Symptomatic</strong> <strong>Treatment</strong> <strong>of</strong> <strong>Multiple</strong> <strong>Sclerosis</strong>, December 2006 - revised in April 2008