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Abstract Details

Preference for Inebilizumab Home Infusion Among People with Neuromyelitis Optica Spectrum Disorder
Autoimmune Neurology
P12 - Poster Session 12 (11:45 AM-12:45 PM)
8-003

To determine whether people with neuromyelitis optica spectrum disorder (NMOSD) prefer to receive inebilizumab (Uplizna) infusions at home versus in an infusion center or hospital, and to assess how that choice affects their quality of life.

 Recently, inebilizumab was approved for treating NMOSD and was deemed safe for at-home use. However, there is no data on preferences for home infusion and its impact on patient quality of life.

This was an observational study on AQP4 + NMOSD patients. Participants completed a preference survey and the short-form quality of life (SF-36) questionnaire at baseline, and at one week after the first and second home infusions. Descriptive statistics for the baseline characteristics were calculated and linear regression analyses were conducted to identify whether the first or second home infusion was associated with significant improvements or declines in the SF-36 subdomains.

Nine patients met the inclusion criteria, with an average age of 60 ± 12 years (8 females, 1 male). Post home-infusion data showed that 8 out of 9 patients preferred home, felt "very safe"  and that it was "much more convenient". Lastly, all 9 participants strongly preferred future infusions to be at home. Although no significant difference was noted, two SF-36 subdomains are highlighted. Physical functioning demonstrated a slight improvement, with a change of 7.7 (95% CI: -21.9 to 37.5, p = 0.59) following the first home infusion and 3.3 (95% CI: -26.4 to 33.0, p = 0.82) after the second. Also, social functioning showed slight improvement, reflecting a change of 4.2 (95% CI: -26.5 to 34.9, p = 0.78) after the first home infusion and 0 (95% CI: -30.7 to 30.6, p = 1.00) after the second.

Results suggest that inebilizumab home infusion may be a feasible and preferred option among NMOSD patients, potentially improving their quality of life.

Authors/Disclosures
Gerome B. Vallejos, MD
PRESENTER
Mr. Vallejos has nothing to disclose.
Gabriela Romanow (Massachusetts General Hospital) Gabriela Romanow has nothing to disclose.
Michael Levy, MD, PhD, FAAN (Massachusetts General Hospital/Harvard Medical School) Dr. Levy has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Mitsubishi Pharma. Dr. Levy has received personal compensation in the range of $500-$4,999 for serving as a Consultant for UCB Pharma. Dr. Levy has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Sanofi. Dr. Levy has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Alexion. Dr. Levy has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Horizon. Dr. Levy 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. Levy has received personal compensation in the range of $500-$4,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for Elsevier. Dr. Levy has received personal compensation in the range of $10,000-$49,999 for serving as an Expert Witness for Various law firms. The institution of Dr. Levy has received research support from National Institutes Health.