TY - JOUR
T1 - Early versus delayed follow-up after misoprostol treatment for early pregnancy loss
AU - Mizrachi, Yossi
AU - Tamayev, Liliya
AU - Shemer, Ofer
AU - Kleiner, Ilia
AU - Bar, Jacob
AU - Sagiv, Ron
N1 - Publisher Copyright:
© 2019 Reproductive Healthcare Ltd.
PY - 2019/7
Y1 - 2019/7
N2 - Research question: Does extending the follow-up after misoprostol treatment for early pregnancy loss increase the success rate? Design: Patients who had experienced early pregnancy loss (<12 weeks) and were treated with misoprostol in a single university-affiliated medical centre were prospectively followed before and after the implementation of a new treatment protocol extending the follow-up from 1 to 2 weeks. All patients received misoprostol 800 μg vaginally on day 1 and a second dose, when needed, on day 4 or 8. Patients underwent surgical aspiration after 1 week in the early follow-up group (n = 84) or 2 weeks in the delayed follow-up group (n = 85) if complete expulsion was not achieved (defined as endometrial thickness ≤15 mm and absence of gestational sac on transvaginal sonography). The primary outcome was treatment success, defined as no need for surgical aspiration. Results: Women in the delayed follow-up group had a higher rate of successful treatment compared with women in the early follow-up group (88.2% versus 76.2%, respectively; P = 0.040), and a lower rate of second dose administration (32.9% versus 51.2%, respectively; P = 0.016). The incidence of non-expulsion of the gestational sac was also lower in the delayed follow-up group (1.2% versus 10.7%; P = 0.009). Treatment acceptability did not differ between the study groups. Conclusion: In women with early pregnancy loss treated with misoprostol, extending the follow-up protocol from 1 to 2 weeks resulted in an increase in treatment success.
AB - Research question: Does extending the follow-up after misoprostol treatment for early pregnancy loss increase the success rate? Design: Patients who had experienced early pregnancy loss (<12 weeks) and were treated with misoprostol in a single university-affiliated medical centre were prospectively followed before and after the implementation of a new treatment protocol extending the follow-up from 1 to 2 weeks. All patients received misoprostol 800 μg vaginally on day 1 and a second dose, when needed, on day 4 or 8. Patients underwent surgical aspiration after 1 week in the early follow-up group (n = 84) or 2 weeks in the delayed follow-up group (n = 85) if complete expulsion was not achieved (defined as endometrial thickness ≤15 mm and absence of gestational sac on transvaginal sonography). The primary outcome was treatment success, defined as no need for surgical aspiration. Results: Women in the delayed follow-up group had a higher rate of successful treatment compared with women in the early follow-up group (88.2% versus 76.2%, respectively; P = 0.040), and a lower rate of second dose administration (32.9% versus 51.2%, respectively; P = 0.016). The incidence of non-expulsion of the gestational sac was also lower in the delayed follow-up group (1.2% versus 10.7%; P = 0.009). Treatment acceptability did not differ between the study groups. Conclusion: In women with early pregnancy loss treated with misoprostol, extending the follow-up protocol from 1 to 2 weeks resulted in an increase in treatment success.
KW - Misoprostol
KW - Pregnancy loss
KW - Spontaneous abortion
UR - http://www.scopus.com/inward/record.url?scp=85064462002&partnerID=8YFLogxK
U2 - 10.1016/j.rbmo.2019.02.011
DO - 10.1016/j.rbmo.2019.02.011
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C2 - 31023610
AN - SCOPUS:85064462002
SN - 1472-6483
VL - 39
SP - 155
EP - 160
JO - Reproductive BioMedicine Online
JF - Reproductive BioMedicine Online
IS - 1
ER -