| Table 3: | ||
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Symptom
Management in Multiple Sclerosis
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Medication
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Dose
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Comments
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| Spasticity | ||
| baclofen | 5-20 mg BID-QID | High doses may exacerbate weakness or ataxia; can be administered by intrathecal pump |
| tizanidine | 4-8 mg TID-QID | Less tendency to produce weakness compared to baclofen but more sedating |
| gabapentin | 300-900 mg TID-QID | Useful as adjunct therapy for spasticity when there is concomitant neuropathic pain |
| diazepam | 2-10 mg QD-TID | Useful for nocturnal spasms |
| clonazepam | 0.5-5 mg QD-TID | Useful for nocturnal spasms |
| dantrolene | 25-100 mg BID-QID | Least cerebral side effects but produces obligate weakness; possible severe liver dysfunction limits use; Medication should be combined with a regular stretching program |
| Neuropathic Pain | ||
| gabapentin | 300-900 TID-QID | Well-tolerated but may require high doses; titrate to avoid sedation |
| amitriptyline | 25-150 mg QHS | Sedation and anticholinergic effects may be useful for dose-limiting |
| nortriptyline | 25-150 mg QHS | Less prominent sedation and anticholinergic effects compared to amitriptyline |
| topiramate | 25-200 BID | Slow titration (weekly) to minimize sedation |
| lamotrigine | 25-400 QD | Slow titration (weekly) to minimize sedation |
| carbamazepine | 200-400 mg TID | Seating and may exacerbate ataxiad |
| phenytoin | 300-600 mg QD | |
| Fatigue | ||
| amantadine | 100 mg BID | Watch for livedo reticularis |
| mondafinil | 100-200 mg QD | Also improves sleep |
| pemoline | 18.75-75 mg QD | Second-line drug; hepatotoxicity probably rare but must be monitored |
| fluoxetine | 20-40 mg QD | Useful
when there is concomitant depression Methylphenidate and dextroamphetamine/amphetamine are used by some clinicians, but there are no published studies to support its use Medication should be combined with a regular exercise program. Need to rule out poor sleep, other medical conditions, and medication side effects |
| Depression | ||
| SSRI | "Energizing" effect of SSRIs may be helpful with fatigue, although any anti-depressant may be useful | |
| Tricyclics |
Useful when there is concomitant pain, detrusor hyperactivity or sleep disturbance Psychotherapy should be considered in patients with depression or emotional distress. |
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| Vertigo | ||
| meclizine | 25 mg Q6H | Sedating |
| diazepam | 2-10 mg TID/QID | Sedating |
| isoniazid | 800-1200 mg/d | Supplement with pyridoxine 25-50 mg/d |
| scopolamine
patch |
Q3D | |
| ondanestron | 8 mg BID | |
| Ataxic Tremor | ||
| gabapentin | 300-900 TID | Medications usually not effective |
| clonazepam | 0.5-5 mg QD-TID | Sedating |
| carbamazepine | 200-400 mg TID | Sedating |
| ondansetron | 8 mg BID | |
| isoniazid | 800-1200 mg/d | Supplement with pyridoxine 25-50 mg/D |
| primidone | 100-250 mg TID-QID | Sedating |
| Detrusor Hyperactivity | ||
| oxybutynin | 2.5-5
mg TID or XL 5-30 mg QD |
Extended-release formulation is useful |
| tolteridine | 1-2
mg BID or LA, 2-4 mg QD |
Less sytemic anticholinergic side effects than oxybutynin but may not be as potent; Patients on anticholinergic therapy need to be monitored for incomplete bladder emptying. Fluid restriction in the evening or low-dose DDAVP may be useful for nocturia but patients need to avoid restricting fluids during the day |
| Flaccid Bladder | ||
| bethanechol | 10-50 mg BID-QID | Intermittenet catheterization or urinary diviersion often are superior |
| Detrusor-sphincter Dyssynergia | ||
| terazocin | 5-10 mg QHS | Often detrusor-sphincter dyssynergua occurs with detrusor hyperactivity. In that setting terazocin or intermittenet catheterization can be combined with anticholinergic medication. |
| Constipation | ||
|
bulk-forming agents lactulose |
Needs to be combined with adequate fluid, dietary fiber, and regular exercise | |
| Bowel Urgency | ||
| bulk-forming agents | Needs to be combined with scheduled voiding; biofeedback is sometimes useful | |
| Impotence | ||
| sildenafil | 50-100 mg PRN | Largely has supplanted other approaches. Need to rule out emotional factors, other medical conditions or medication side effects |
| Adapted from Fox RJ, Cohen JA. Cleve Clinic J of Med 2001;68:157-71. | ||
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Copyright
2002 The Cleveland Clinic Foundation
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