Randomized Trial of Very Early Medication Abortion

随机对照试验 流产 医学 产科 怀孕 内科学 生物 遗传学
作者
Karin Brandell,Tagrid Jar‐Allah,John Joseph Reynolds-Wright,Helena Kopp Kallner,Helena Hognert,Frida Gyllenberg,Janina Kaislasuo,Anand Tamang,Heera Tuladhar,Clare Boerma,Karen Schimanski,Gillian Gibson,Mette Løkeland,Pia Teleman,Marie Bixo,Michael Kjær,Ervin Kallfa,Johan Bring,Oskari Heikinheimo,Sharon Cameron,Kristina Gemzell‐Danielsson
出处
期刊:The New England Journal of Medicine [Massachusetts Medical Society]
卷期号:391 (18): 1685-1695
标识
DOI:10.1056/nejmoa2401646
摘要

BackgroundMedication abortion, with a combination of mifepristone and misoprostol, is highly effective and safe. However, there is insufficient evidence on efficacy and safety at very early gestations before a pregnancy can be visualized with ultrasonography.MethodsWe conducted a multicenter, noninferiority, randomized, controlled trial involving women requesting medication abortion at up to 42 days of gestation with an unconfirmed intrauterine pregnancy on ultrasound examination (visualized as an empty cavity or a sac-like structure without a yolk sac or embryonic pole). Participants were randomly assigned to either immediate start of abortion (early-start group) or standard-care treatment delayed until intrauterine pregnancy was confirmed (standard group). The primary outcome was complete abortion. The noninferiority margin was set at 3.0 percentage points for the absolute between-group difference.Download a PDF of the Plain Language Summary.ResultsIn total, 1504 women were included at 26 sites in nine countries and were randomly assigned to the early-start group (754 participants) or the standard group (750 participants). In an intention-to-treat analysis, a complete abortion occurred in 676 of 710 participants (95.2%) in the early-start group and in 656 of 688 (95.3%) in the standard group; the absolute between-group difference was −0.1 percentage points (95% confidence interval, −2.4 to 2.1). Ectopic pregnancies occurred in 10 of 741 participants (1.3%) in the early-start group and in 6 of 724 (0.8%) in the standard group, with one rupture before diagnosis (early-start group). Serious adverse events occurred in 12 of 737 participants (1.6%) in the early-start group and in 5 of 718 (0.7%) in the standard group (P=0.10); the majority were uncomplicated hospitalizations for treatment of ectopic pregnancy or incomplete abortion.ConclusionsMedication abortion before confirmed intrauterine pregnancy was noninferior to standard, delayed treatment with respect to complete abortion. (Funded by the Swedish Research Council and others; VEMA EudraCT number, 2018-003675-35; ClinicalTrials.gov number, NCT03989869.) Quick Take A Trial of Very Early Medication Abortion 1m 48s
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