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Abstract Details

Neurogenic Pain in Multiple Sclerosis: A Single Center Comprehensive Pain Assessment
Multiple Sclerosis
MS and CNS Inflammatory Disease Posters (7:00 AM-5:00 PM)
189

Objective: Our focus was the development of a new pain assessment form to facilitate patient communication, quantify the location and types of pain, identify pain medications and track patient outcomes. 

Background: Robust literature shows 29-86% of Multiple Sclerosis (MS) patients have reported subtypes of neurogenic pain often accompanied by non-neurogenic pain such as muscle aches, spasms and joint issues.

Methods: This is a single center prospective survey project to characterize MS-related pain. We developed a new assessment that allows patients to differentiate neurogenic from non-neurogenic pain, identify the type of pain they experience, and indicate specific locations and intensity of their pain. The new form utilizes both traditional 1-10 scales and pictographic representation for both neurogenic and non-neurogenic pain. Demographics, therapeutics and management are also recorded. 

Results: We collected data from May, 2017 to December, 2019 on 70 MS patients (average age 57, 80% female) experiencing neurogenic pain. Of the 70 patients, average pain score is 7.6±1.8 (range of 2-10), with all showing frequent pain and 3 to 4 types of neurogenic pain along with non-neurogenic pain. Severity of neurogenic pain types ranged from 6.0 to 7.6 with burning and electric pain the most intense. Overall, opioid use is low (n=18) with the AEDs, gabapentin, pregabalin and oxcarbazepine utilized in the majority of patients (n=52). The pharmaco-economics were assessed and found to be generally favorable. This information is utilized to facilitate further management and as a baseline for longitudinal assessments. 

Conclusions: The design and utilization of this form in the clinical setting has definitively facilitated a meaningful patient/physician discussion of pain. It also highlights the high levels of pain, use of AEDs, and that pain control is often suboptimal. Utilization of this form in follow up visits and tracking the data longitudinally creates a potential to optimize therapies for individuals.

Authors/Disclosures
John W. Rose, MD, FAAN (Imaging and Neurosciences Center)
PRESENTER
The institution of Dr. Rose has received research support from National Multiple Sclerosis Society. The institution of Dr. Rose has received research support from Guthy Jackson Charitable Foundation. The institution of Dr. Rose has received research support from NIH . The institution of Dr. Rose has received research support from VA. The institution of Dr. Rose has received research support from Biogen. The institution of Dr. Rose has received research support from Friends of MS. Dr. Rose has received intellectual property interests from a discovery or technology relating to health care.
M. M. Paz Soldan, MD, PhD (Mayo Clinic) Dr. Paz Soldan has received personal compensation in the range of $500-$4,999 for serving as a Consultant for TG Therapeutics. The institution of Dr. Paz Soldan has received research support from National Institutes of Health. The institution of Dr. Paz Soldan has received research support from National Multiple Sclerosis Society. The institution of Dr. Paz Soldan has received research support from Western Institute for Biomedical Research. The institution of Dr. Paz Soldan has received research support from Biogen. The institution of Dr. Paz Soldan has received research support from Novartis. The institution of Dr. Paz Soldan has received research support from Clene Nanomedicine.
Ka-Ho Wong (U of U Neurology Clinic) The institution of Mr. Wong has received research support from The Sumaira Foundation . The institution of Mr. Wong has received research support from The Siegel Rare Neuroimmune Association.
No disclosure on file
No disclosure on file