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Abstract Details

Disparities in Geographic Access to Infusion Centers Does not Impact the Use of High Efficacy Infusion Disease Modifying Therapies in Multiple Sclerosis
Multiple Sclerosis
P6 - Poster Session 6 (5:00 PM-6:00 PM)
18-007
To characterize geographic access to infusion center locations and the impact on the use of infusion high efficacy disease modifying therapies (DMTs) in multiple sclerosis (MS).  

Access to infusion centers is critical for the administration of many highly effective DMTs in MS.

In this retrospective cohort study, adult MS patients who completed a visit at a single MS center from 1/1/2015-6/30/25 were included. Infusion center locations (n=4,041) were used to compute spatial accessibility to infusions for all US census tracts. A multivariable logistic regression model was used to evaluate the association between geographic access to infusion centers and the use of infusion DMTs (CD20 monoclonal antibodies, natalizumab, alemtuzumab, cyclophosphamide) adjusting for age, sex, race, ethnicity, education, MS disease duration, MS course, patient determined disease steps (PDDS), area deprivation index (ADI), and rural-urban commuting code (RUCA). 

7,805 patients (mean [SD] age of 54.5 years [13.1], 73% female, 82% white, 96% non-Hispanic, 86% metropolitan, 55% relapsing remitting MS, 30% no disability, disease duration 17.1 years [10.5], 49% high efficacy DMT) were included. Greater access to infusion centers was not associated with receiving an infusion DMT (OR 1.00, p>0.05). Higher access to infusion centers was seen for Black compared to White (14.4%) and Hispanic compared to non-Hispanic (11.1%) patients (p<0.01). Lower access was seen for patients residing in the more disadvantaged neighborhoods (-6.5% ADI 20-40, -17.4% ADI 40-60, -21.0% ADI 60-80, -10.0% ADI 80-100), micropolitan (-35.4%), and rural areas (-43.7%) (p<0.01 for all).

Disparities to geographic access to infusion centers exist but distance did not impact the use of high efficacy infusion DMTs for patients. These results suggest that geographic barriers to resources can be mitigated to deliver highly effective treatments. 

Authors/Disclosures
Marisa P. McGinley, DO (Cleveland Clinic)
PRESENTER
Dr. McGinley has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Genentech. Dr. McGinley has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for EMD Serono. The institution of Dr. McGinley has received research support from Biogen. The institution of Dr. McGinley has received research support from Genentech. The institution of Dr. McGinley has received research support from NIH. The institution of Dr. McGinley has received research support from AHRQ. The institution of Dr. McGinley has received research support from EMD Serono.
Mengke Du (Cleveland Clinic) Mengke Du has nothing to disclose.
Daniel Ontaneda, MD, PhD, FAAN (Cleveland Clinic) Dr. Ontaneda has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Novartis. Dr. Ontaneda has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Genentech/Roche. Dr. Ontaneda has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Biogen Idec. Dr. Ontaneda has received personal compensation in the range of $500-$4,999 for serving as a Consultant for BMS. Dr. Ontaneda has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Sanofi. The institution of Dr. Ontaneda has received research support from NIH. The institution of Dr. Ontaneda has received research support from PCORI. The institution of Dr. Ontaneda has received research support from NMSS. The institution of Dr. Ontaneda has received research support from Genetech.
Blake Buchalter, PhD Dr. Buchalter has nothing to disclose.