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23rd Annual Meeting February 7-10, 2007 New Orleans, LA |
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Two individuals entered the study that fit our inclusionary and exclusionary criteria: documented arachnoiditis with symptoms present in the lower extremities without risk factors for intolerance to thalidomide. Part of the consent involved an adherence to the STEPS program. The following were assessed in these patients before, during and after treatment: VAS, CBC, metabolic panel, EKG, NCS, SF-36, concomitant medication, concurrent opioid use, Roland-Morris Low Back Pain Questionnaire.
The cohorts who entered the study gradually titrated thalidomide to a tolerable level: 150 mg in one and 200 mg in another. Both patients reported subjective improvement in the management of their pain though the study testing parameters did not reveal significant differences. Both patients stopped the therapy in time secondary to side effects.
Though thalidomide represents a novel means of treating arachnoiditis, our study cohort was limited in size and the individuals who did enter the study could not tolerate this medication for a sufficient period of time in order to fully assess its benefits.
Sommer C, Marziniak M, Myers RR: The effect of thalidomide treatment on vascular pathology and hyperalgesia caused by chronic constriction injury of rat nerve. Pain. 1998; 74: 83-91
Schwartzman R, Bengtson K, Chevlen E, Thalidomide Has Activity in Treating Complex Regional Pain Syndrome, Arch Intern Med. 2003;163:1487-1488.
Funding: Celgene provided partial funding for study.