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6 - The Promise of Telehealth for Abortion

from Part II - Digital Home Diagnostics for Specific Conditions

Published online by Cambridge University Press:  25 April 2024

I. Glenn Cohen
Affiliation:
Harvard Law School, Massachusetts
Daniel B. Kramer
Affiliation:
Harvard Medical School, Massachusetts
Julia Adler-Milstein
Affiliation:
University of California, San Francisco
Carmel Shachar
Affiliation:
Harvard Law School, Massachusetts

Summary

The COVID-19 pandemic revolutionized abortion care. What seemed impossible a few years ago – entirely virtual abortion – is now a reality. The Food and Drug Administration (FDA) has historically required patients to collect abortion medication, a two-drug regimen that terminates a pregnancy in the first ten weeks, in-person at a health care facility. In July 2020, a federal district court suspended that requirement during the pandemic, allowing providers to mail abortion medication directly to patients. In December 2021, President Biden removed the in-person requirement permanently. Over the last two years, virtual clinics have begun offering “no-touch” abortions, eliminating many of the costs associated with travel to an abortion clinic. The FDA’s most recent decision has cleared the way for the supervised mail delivery and pharmacy dispensation of abortion medication. The expansion of virtual clinics, however, faces significant obstacles and limitations – most acutely, the fact that nineteen states prohibit telabortion explicitly or indirectly. This chapter maps the emergence of virtual abortion care and analyzes its significance for early abortion access, particularly in the post-Roe world. It then considers the limits of telabortion, concluding that, over the long term, the portability of abortion medication will test how closely state officials (or anyone else) can police access to early abortion care, even if abortion is banned in a particular state.

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