Prematurity
Poster Session 4
Louise Ghesquiere, MD, PhD (she/her/hers)
Centre de recherche du CHU de Québec-Université Laval
Quebec, QC, Canada
Paul Guerby, MD, PhD (he/him/his)
Head of Obstetrics Department
Hopital Paule de Viguier, CHU Toulouse, Toulouse III University
Toulouse, Midi-Pyrenees, France
Jean-Claude Forest, MD, PhD
CHU de Québec
Quebec City, QC, Canada
Yves Giguère, MD, PhD
Research Center of the CHU de Québec-Université Laval, QC, Canada
Chantale Vachon-Marceau, MD
CHU de Québec
Quebec City, QC, Canada
Caroline Carpentier, MD
CHU de Québec
Quebec City, QC, Canada
Emmanuel Bujold, MD, MSc
Professor
Centre de recherche du CHU de Québec-Université Laval
Quebec, QC, Canada
Vaginal progesterone in women with a short cervix reduces spontaneous preterm births (sPTB) and particularly the early forms of sPTB. Aspirin initiated in the first-trimester can reduces preeclampsia (PE), particularly early PE, but also other outcomes related to deep placentation disorders (Great Obstetrical Syndromes). We wanted to study the impact of combined 1st trimester (early PE) and 2nd trimester (sPTB) screening on pregnancy outcomes.
Study Design:
We carried out an historical comparative study. From 2014 to 2017, we recruited nulliparous pregnant women with a singleton pregnancy in the 1st trimester of pregnancy. The 1st trimester FMF screening was performed, but the result remained secret and no intervention was proposed. From 2020 to 2022, we recruited nulliparous pregnant women with the same criteria in the same center to whom we gave the result of the FMF screening (giving aspirin in high-risk women) and to whom we performed a mid-trimester assessment of cervical length (giving vaginal progesterone in cases of short cervix). We compared the pregnancy outcomes, including PTB, sPTB before 37 weeks, 34 weeks, and before 32 weeks along with PE, PE < 37 weeks, and PE≤ 34 weeks, and intra-uterine fetal death (IUFD).
Results:
We compared the pregnancy outcomes of 5593 participants who did not receive screening results (2014-2017) with 1703 participants who received screening results (2021-2022). We observed no significant change in terms of PTB and PE overall, but a significant reduction of sPTB< 32 weeks – RR: 0.32; 95%CI 0.13 – 0.83 (p=0.01), and a favorable trend for the other outcomes: all sPTB – RR : 0.83; 95%CI 0.63 – 1.09; sPTB < 34 weeks – RR: 0.60; 95%CI 0.36 – 1.03, p=0.06; early PE – RR: 0.86; 95%CI 0.32 – 2.31; IUFD – RR: 0.75 95%CI : 0.22 – 2.65.
Conclusion:
The introduction of 1st trimester PE screening combined to a 2nd trimester sPTB screening does not reduce the overall rates of PTB and PE, but can have a significant impact on the most severe forms of those diseases, particularly sPTB < 32 weeks. A randomized trial with larger number of participants is warranted.