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Multiple Sclerosis
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Desferrioxamine in chronic progressive Multiple Sclerosis: a pilot study

Sharon G Lynch

Departments of Neurology

Kathy Peters

Departments of Neurology

Steven M LeVine

Physiology, University of Kansas Medical Center, 3901 Rainbow Boulevard, Kansas City, Kansas, 66160, USA

Chronic progressive Multiple Sclerosis is refractory to many conventional treatments. We performed a pilot study testing desferoxamine (DFO) as a candidate in the treatment of chronic progressive Multiple Sclerosis. DFO was given daily by 8 h subcutaneous infusions at a dose of 2 grams daily for 7 days, followed by 1 gram daily for 7 days. Eighteen of 19 individuals completed the full dose of 21 grams. One patient was unable to complete the course due to nausea. No acute deterioration of neurological status was seen during the administration of DFO. No worsening of vision or hearing was noted except that the one patient who was unable to tolerate the medication had a transient reduction in hearing. All patients had a local redness at the injection site. None of the patients had any sudden worsening during or shortly after the treatment This pilot study suggests that DFO is relatively well tolerated by Multiple Sclerosis patients when given in a short course of therapy.

Key Words: Multiple Sclerosis • desferoxamine • free radicals • iron • chelation

Multiple Sclerosis, Vol. 2, No. 3, 157-160 (1996)
DOI: 10.1177/135245859600200306


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