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Expansion of a direct-to-patient telemedicine abortion service in the United States and experience during the COVID-19 pandemic
OBJECTIVE: To present updated evidence on the safety, efficacy and acceptability of a direct-to-patient telemedicine abortion service and describe how the service functioned during the COVID-19 pandemic. STUDY DESIGN: We offered the study at 10 sites that provided the service in 13 states and Washin...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9748604/ https://www.ncbi.nlm.nih.gov/pubmed/33781762 http://dx.doi.org/10.1016/j.contraception.2021.03.019 |
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author | Chong, Erica Shochet, Tara Raymond, Elizabeth Platais, Ingrida Anger, Holly A. Raidoo, Shandhini Soon, Reni Grant, Melissa S. Haskell, Susan Tocce, Kristina Baldwin, Maureen K. Boraas, Christy M. Bednarek, Paula H. Banks, Joey Coplon, Leah Thompson, Francine Priegue, Esther Winikoff, Beverly |
author_facet | Chong, Erica Shochet, Tara Raymond, Elizabeth Platais, Ingrida Anger, Holly A. Raidoo, Shandhini Soon, Reni Grant, Melissa S. Haskell, Susan Tocce, Kristina Baldwin, Maureen K. Boraas, Christy M. Bednarek, Paula H. Banks, Joey Coplon, Leah Thompson, Francine Priegue, Esther Winikoff, Beverly |
author_sort | Chong, Erica |
collection | PubMed |
description | OBJECTIVE: To present updated evidence on the safety, efficacy and acceptability of a direct-to-patient telemedicine abortion service and describe how the service functioned during the COVID-19 pandemic. STUDY DESIGN: We offered the study at 10 sites that provided the service in 13 states and Washington DC. Interested individuals obtained any needed preabortion tests locally and had a videoconference with a study clinician. Sites sent study packages containing mifepristone and misoprostol by mail and had remote follow-up consultations within one month by telephone (or by online survey, if the participant could not be reached) to evaluate abortion completeness. The analysis was descriptive. RESULTS: We mailed 1390 packages between May 2016 and September 2020. Of the 83% (1157/1390) of abortions for which we obtained outcome information, 95% (1103/1157) were completed without a procedure. Participants made 70 unplanned visits to emergency rooms or urgent care centers for reasons related to the abortion (6%), and 10 serious adverse events occurred, including 5 transfusions (0.4%). Enrollment increased substantially with the onset of COVID-19. Although a screening ultrasound was required, sites determined in 52% (346/669) of abortions that occurred during COVID that those participants should not get the test to protect their health. Use of urine pregnancy test to confirm abortion completion increased from 67% (144/214) in the 6 months prior to COVID to 90% (602/669) in the 6 months during COVID. Nearly all satisfaction questionnaires (99%, 1013/1022) recorded that participants were satisfied with the service. CONCLUSIONS: This direct-to-patient telemedicine service was safe, effective, and acceptable, and supports the claim that there is no medical reason for mifepristone to be dispensed in clinics as required by the Food and Drug Administration. In some cases, participants did not need to visit any facilities to obtain the service, which was critical to protecting patient safety during the COVID-19 pandemic. IMPLICATIONS: Medical abortion using telemedicine and mail is effective and can be safely provided without a pretreatment ultrasound. This method of service delivery has the potential to greatly improve access to abortion care in the United States. |
format | Online Article Text |
id | pubmed-9748604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97486042022-12-14 Expansion of a direct-to-patient telemedicine abortion service in the United States and experience during the COVID-19 pandemic Chong, Erica Shochet, Tara Raymond, Elizabeth Platais, Ingrida Anger, Holly A. Raidoo, Shandhini Soon, Reni Grant, Melissa S. Haskell, Susan Tocce, Kristina Baldwin, Maureen K. Boraas, Christy M. Bednarek, Paula H. Banks, Joey Coplon, Leah Thompson, Francine Priegue, Esther Winikoff, Beverly Contraception Original Research Article OBJECTIVE: To present updated evidence on the safety, efficacy and acceptability of a direct-to-patient telemedicine abortion service and describe how the service functioned during the COVID-19 pandemic. STUDY DESIGN: We offered the study at 10 sites that provided the service in 13 states and Washington DC. Interested individuals obtained any needed preabortion tests locally and had a videoconference with a study clinician. Sites sent study packages containing mifepristone and misoprostol by mail and had remote follow-up consultations within one month by telephone (or by online survey, if the participant could not be reached) to evaluate abortion completeness. The analysis was descriptive. RESULTS: We mailed 1390 packages between May 2016 and September 2020. Of the 83% (1157/1390) of abortions for which we obtained outcome information, 95% (1103/1157) were completed without a procedure. Participants made 70 unplanned visits to emergency rooms or urgent care centers for reasons related to the abortion (6%), and 10 serious adverse events occurred, including 5 transfusions (0.4%). Enrollment increased substantially with the onset of COVID-19. Although a screening ultrasound was required, sites determined in 52% (346/669) of abortions that occurred during COVID that those participants should not get the test to protect their health. Use of urine pregnancy test to confirm abortion completion increased from 67% (144/214) in the 6 months prior to COVID to 90% (602/669) in the 6 months during COVID. Nearly all satisfaction questionnaires (99%, 1013/1022) recorded that participants were satisfied with the service. CONCLUSIONS: This direct-to-patient telemedicine service was safe, effective, and acceptable, and supports the claim that there is no medical reason for mifepristone to be dispensed in clinics as required by the Food and Drug Administration. In some cases, participants did not need to visit any facilities to obtain the service, which was critical to protecting patient safety during the COVID-19 pandemic. IMPLICATIONS: Medical abortion using telemedicine and mail is effective and can be safely provided without a pretreatment ultrasound. This method of service delivery has the potential to greatly improve access to abortion care in the United States. Elsevier Inc. 2021-07 2021-03-27 /pmc/articles/PMC9748604/ /pubmed/33781762 http://dx.doi.org/10.1016/j.contraception.2021.03.019 Text en © 2021 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Original Research Article Chong, Erica Shochet, Tara Raymond, Elizabeth Platais, Ingrida Anger, Holly A. Raidoo, Shandhini Soon, Reni Grant, Melissa S. Haskell, Susan Tocce, Kristina Baldwin, Maureen K. Boraas, Christy M. Bednarek, Paula H. Banks, Joey Coplon, Leah Thompson, Francine Priegue, Esther Winikoff, Beverly Expansion of a direct-to-patient telemedicine abortion service in the United States and experience during the COVID-19 pandemic |
title | Expansion of a direct-to-patient telemedicine abortion service in the United States and experience during the COVID-19 pandemic |
title_full | Expansion of a direct-to-patient telemedicine abortion service in the United States and experience during the COVID-19 pandemic |
title_fullStr | Expansion of a direct-to-patient telemedicine abortion service in the United States and experience during the COVID-19 pandemic |
title_full_unstemmed | Expansion of a direct-to-patient telemedicine abortion service in the United States and experience during the COVID-19 pandemic |
title_short | Expansion of a direct-to-patient telemedicine abortion service in the United States and experience during the COVID-19 pandemic |
title_sort | expansion of a direct-to-patient telemedicine abortion service in the united states and experience during the covid-19 pandemic |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9748604/ https://www.ncbi.nlm.nih.gov/pubmed/33781762 http://dx.doi.org/10.1016/j.contraception.2021.03.019 |
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