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Abstract Details

Use of Anti-Parkinsonian Medications among Incident Parkinson Disease Patients
General Neurology
S24 - Hot Topics in Global Health and Neuroepidemiology (1:36 PM-1:48 PM)
004

Anti-parkinsonian medications, especially levodopa, are critical for managing motor symptoms in PD. Understanding demographic and geographic differences in medication initiation is essential to ensure equitable care.

To compare demographic and geographic characteristics of U.S. Medicare beneficiaries newly diagnosed with Parkinson disease (PD) who did or did not fill a prescription for an anti-parkinsonian medication within 12 months of diagnosis.

We used comprehensive 2014-2018 Medicare data to identify incident PD cases aged 67-105 with Part D (prescription medication) coverage at diagnosis in 2017 and the following 12 months (N=54,755). We used multivariable logistic regression to estimate odds ratios (ORs) and 95% confidence intervals (CIs) for age, sex, and race/ethnicity in relation to use of anti-parkinsonian medications within 12 months of diagnosis. We included levodopa, COMT inhibitors, MAO-B inhibitors, dopamine agonists, and anticholinergics. We also mapped medication use nationwide.

Among incident PD patients followed for 12 months, 62.2% filled a prescription for levodopa or other anti-parkinsonian medication. Older patients were less likely than younger patients to receive anti-parkinsonian medications (OR=0.966, 95% CI: 0.963-0.968 per additional year). Women had lower odds of receiving anti-parkinsonian medications than men (OR=0.92, 95% CI: 0.89-0.96). Black patients were less likely to receive anti-parkinsonian medications compared to non-Hispanic White patients (OR=0.66, 95% CI: 0.61-0.71), while Hispanic beneficiaries demonstrated intermediate levels of anti-parkinsonian medication use (OR=0.77, 95% CI: 0.72-0.83). Even when accounting for demographics, we observed the greatest use of anti-parkinsonian medications in the Central U.S., while the lowest use was seen in the Northeast and Southwest. All results remained similar with further adjustment for urban-rural status and Area Deprivation Index.

Demographic and geographic differences in the use of anti-parkinsonian medications among newly diagnosed PD patients in the Medicare population suggest potential gaps in the treatment of older and minoritized beneficiaries.

Authors/Disclosures
Sai Anmisha Doddamreddy, MS
PRESENTER
Miss Doddamreddy has nothing to disclose.
Brad A. Racette, MD, FAAN (Barrow Neurological Institute) Dr. Racette has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for American Regent. Dr. Racette has received personal compensation in the range of $500-$4,999 for serving as a advisory council with NIEHS.
Jordan A. Killion, PhD (Barrow Neurological Institute) Dr. Killion has received personal compensation for serving as an employee of CommonSpirit Health. Dr. Killion has received personal compensation for serving as an employee of Seneca Solutions. Dr. Killion has received personal compensation for serving as an employee of Univeristy of California, San Diego. The institution of Dr. Killion has received research support from NIAID/NIDA R01AI147490 through University of California, San Diego. The institution of Dr. Killion has received research support from California HIV/AIDS Research Program (H21PC3601) through University of California, San Diego. The institution of Dr. Killion has received research support from NIDA R01DA049644 through University of California, San Diego. The institution of Dr. Killion has received research support from The Michael J. Fox Foundation for Parkinson's Research (MJFF-000939). The institution of Dr. Killion has received research support from Department of Defense Grant (PD190057).
Brittany Krzyzanowski, PhD (Barrow Neurological Institute) Dr. Krzyzanowski has nothing to disclose.
ALEJANDRA CAMACHOSOTO, MD The institution of Dr. CAMACHOSOTO has received research support from Michael J Fox Foundation . The institution of Dr. CAMACHOSOTO has received research support from NIH NCATS KL2 Career Development.
Susan Nielsen (Washington University in St. Louis) The institution of Susan Nielsen has received research support from National Institutes of Health. The institution of Susan Nielsen has received research support from Department of Defense. The institution of Susan Nielsen has received research support from The Michael J. Fox Foundation for Parkinson's Research. The institution of Susan Nielsen has received research support from Cure Alzheimer's. Susan Nielsen has received personal compensation in the range of $0-$499 for serving as a Panel/committee member with The Michael J. Fox Foundation for Parkinson's Research. Susan Nielsen has received personal compensation in the range of $0-$499 for serving as a Reviewer with Parkinson's Disease Foundation.