The Food and Drug Administration requires certified providers to dispense mifepristone, one of the drugs used in medication abortion, directly to the patient in a clinic, medical office, or hospital. This study’s findings indicate that removing that requirement could lead to more providers of medication abortion, including in regions with limited abortion access.
Key Findings
Study Design
Researchers conducted a survey survey between August 2016 and March 2017 of a national sample of practicing OB-GYNs. They limited their sample to the 868 respondents who had reported having any abortion-seeking patients in the last year.
Implications
Currently, clinicians who want to provide medication abortions must stock the drug in their practice, adding up-front costs and administrative burdens. Removing this requirement could increase the number of medication abortion providers across the country, including in settings with limited access.
“The in-person dispensing requirement for mifepristone codified in the drug’s REMS is a barrier to clinician provision of the method. Removing this requirement could increase the number of medication abortion providers across the country, including in settings with limited access.”
The article, Obstetrician-gynecologist willingness to provide medication abortion with removal of the in-person dispensing requirement for mifepristone, is available in Contraception.