Induced Abortion, Instrumental Induced Abortion Between 14 and 16 Weeks of Amenorrhea
Conditions
Keywords
interruption of pregnancy, Induced abortion, instrumental technique, women complications
Brief summary
In France, induced abortions can be carried out by two different methods: the medicinal one, which involves taking medications to expel the pregnancy (MIFEPRISTONE and then MISOPROSTOL), and the instrumental one, which involves aspiration in the operating room. According to the high authority of health, before 9 weeks of amenorrhea, both methods are possible if there is no contraindication to one of them. After 9 weeks of amenorrhea, only the instrumental method is authorized. Until March 2022, the maximal deadline to abort was 14 weeks of amenorrhea. On March 2nd 2022, a change in the law extended this time limit from 14 to 16 weeks of amenorrhea. Only one study was carried out following this change in France to assess the complication rate of late abortions (between 14 and 16 weeks of amenorrhea (AW)). This study was carried out at Trousseau Hospital in Paris, with a total of 46 patients. The results of this study were reassuring, with bleeding \> 500 mL for only one patient (2.2%, 95% CI \[0.0-6.4\]) and no complications such as perforation, postoperative infection or revision surgery, or need for transfusion. However, this paper is the only French study which evaluated the operative risks of late abortion since the change in the law, and its power is small. There is a need to assess the operative risks of late abortion on a larger cohort. That's why the investigators had the idea to conduct a study looking at all instrumental abortions performed in Croix Rousse Hospital in Lyon between March 2022 and March 2023, representing around 700 procedures. The aim of the study is to compare the complication rates of instrumental abortions between 14 and 16 weeks of amenorrhea versus those carried out before 14 weeks.
Interventions
OTHERRetrospective
Retrospective Operative risk in patients undergoing instrumental abortion
Sponsors
Hospices Civils de Lyon
Study design
Observational model
COHORT
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No
Inclusion criteria
Eligibility Criteria \* * Inclusion Criteria \* : * Surgical induced abortion * At Croix Rousse hospital, Lyon * Between March 2022 and March 2023 *
Exclusion criteria
\* : * Minor patients
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Proportion of patients with intraoperative bleeding > 500 mL | Primary endpoint is measured during the intervention by collecting the total blood quantity collected into a reservoir connected to the aspiration probe. | Evaluated by collecting blood loss during the procedure (in 50 mL increments) |
Countries
France
Outcome results
None listed