Evaluation of a "smart" screening tool for asynchronous assessment of medication abortion eligibility: A pilot study.

Asynchronous Feasibility Medication abortion Safety Telemedicine

Journal

Contraception
ISSN: 1879-0518
Titre abrégé: Contraception
Pays: United States
ID NLM: 0234361

Informations de publication

Date de publication:
20 Nov 2023
Historique:
received: 23 08 2023
revised: 06 11 2023
accepted: 16 11 2023
pubmed: 23 11 2023
medline: 23 11 2023
entrez: 22 11 2023
Statut: aheadofprint

Résumé

This study aimed to assess the feasibility, safety, and acceptability of asynchronous screening for medication abortion eligibility using a programmed questionnaire. For this study, we developed an informational website about medication abortion with a linked questionnaire programmed to produce a conclusion regarding eligibility according to standard criteria. We enrolled people in Colorado and Minnesota who submitted questionnaires indicating eligibility. A study physician reviewed each questionnaire and medical records if available and determined whether the responses warranted treatment without a synchronous clinical consultation or ultrasound. If so, the physician prescribed a standard regimen of mifepristone and misoprostol. We collected posttreatment data on abortion outcome, adverse events, and satisfaction. We received questionnaires from 197 individuals, of whom 160 remained in the study until the physician made a final treatment decision. Physicians prescribed medication abortion to 156 (97.5%) individuals based on the questionnaire responses, whereas four needed further assessment to confirm eligibility. Of the 156 individuals, 130 had sufficient follow-up to assess abortion outcome, and 123 (95%) had complete medication abortions without additional treatment. One participant was hospitalized for bleeding, and one expelled a 15-week fetus; however, it is not clear that conventional synchronous history-based screening would have averted these events. Of the 197 questionnaires, 42% were submitted outside business hours. On satisfaction questionnaires, 134 (96%) of 144 participants said they would recommend the study to a friend who needed an abortion. Data from this pilot project suggest that providing medication abortion based only on a self-administered, programmed questionnaire is likely to be effective, safe, efficient, and acceptable. A programmed self-administered patient questionnaire to assess eligibility for medication abortion could reduce the cost of the service, augment clinic efficiency, improve quality of care, and enhance access to abortion.

Identifiants

pubmed: 37992850
pii: S0010-7824(23)00460-2
doi: 10.1016/j.contraception.2023.110340
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

110340

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Auteurs

Elizabeth G Raymond (EG)

Gynuity Health Projects, New York, NY, United States. Electronic address: eraymond@gynuity.org.

Laura J Frye (LJ)

Gynuity Health Projects, New York, NY, United States.

Kristina Tocce (K)

Planned Parenthood of the Rocky Mountains, Denver, CO, United States.

Shay Gingras (S)

Planned Parenthood North Central States, Saint Paul, MN, United States.

Amy Almquist (A)

Planned Parenthood North Central States, Saint Paul, MN, United States.

Ann Firstenberg (A)

Planned Parenthood of the Rocky Mountains, Denver, CO, United States.

Cynthia Ortega (C)

Planned Parenthood of the Rocky Mountains, Denver, CO, United States.

Paul D Blumenthal (PD)

Department of Obstetrics and Gynecology, Stanford University, Palo Alto, CA, United States.

Beverly Winikoff (B)

Gynuity Health Projects, New York, NY, United States.

Christy Boraas (C)

Planned Parenthood North Central States, Saint Paul, MN, United States.

Classifications MeSH