{"title":"The timing of discontinuation of low-dose aspirin and postpartum hemorrhage risk","authors":"Muhammad Badarna , Neta Hoffman , Shai Stern , Raneen Sawaid Kayal , Ala Aiob , Lior Lowenstein , Inshirah Sgayer","doi":"10.1016/j.preghy.2025.101247","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><div>To evaluate associations of the timing of low-dose aspirin (LDA) discontinuation, with postpartum hemorrhage (PPH) and bleeding-related complications.</div></div><div><h3>Study design</h3><div>A retrospective cohort study was conducted at a tertiary medical center, of pregnant women who received LDA and delivered beyond 23 weeks of gestation. The women were categorized as having discontinued LDA ≤7 days or >7 days before delivery. Exclusion criteria were: severe fetal malformations, intrauterine fetal death, multiple pregnancy, pre-conceptional use of LDA, and missing data on the timing of LDA discontinuation.</div></div><div><h3>Main outcome measures</h3><div>The primary outcome was a composite bleeding outcome that included at least one of the following: PPH, blood loss greater than 1000 ml, the need for blood product transfusions, and a drop in hemoglobin of ≥4 g/dL after delivery.</div></div><div><h3>Results</h3><div>Among 763 women, 192 (25.2 %) discontinued LDA ≤7 days of delivery, while 571 (74.8 %) discontinued >7 days before delivery. Comparing these groups, PPH rates, severe blood loss, and transfusion requirements did not differ significantly, nor did the composite bleeding outcome (9.9 % vs. 8.6 %, p = 0.661). Placental abruption occurred more frequently among women who discontinued LDA ≤7 days compared to >7 days before delivery (5.2 % vs. 1.1 %, p = 0.002). However, in multivariate analysis, the timing of LDA discontinuation was not independently associated with an increased risk of placental abruption.</div></div><div><h3>Conclusion</h3><div>The timing of LDA discontinuation was not associated with increased PPH or major bleeding complications.</div></div>","PeriodicalId":48697,"journal":{"name":"Pregnancy Hypertension-An International Journal of Womens Cardiovascular Health","volume":"41 ","pages":"Article 101247"},"PeriodicalIF":2.9000,"publicationDate":"2025-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pregnancy Hypertension-An International Journal of Womens Cardiovascular Health","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2210778925000637","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives
To evaluate associations of the timing of low-dose aspirin (LDA) discontinuation, with postpartum hemorrhage (PPH) and bleeding-related complications.
Study design
A retrospective cohort study was conducted at a tertiary medical center, of pregnant women who received LDA and delivered beyond 23 weeks of gestation. The women were categorized as having discontinued LDA ≤7 days or >7 days before delivery. Exclusion criteria were: severe fetal malformations, intrauterine fetal death, multiple pregnancy, pre-conceptional use of LDA, and missing data on the timing of LDA discontinuation.
Main outcome measures
The primary outcome was a composite bleeding outcome that included at least one of the following: PPH, blood loss greater than 1000 ml, the need for blood product transfusions, and a drop in hemoglobin of ≥4 g/dL after delivery.
Results
Among 763 women, 192 (25.2 %) discontinued LDA ≤7 days of delivery, while 571 (74.8 %) discontinued >7 days before delivery. Comparing these groups, PPH rates, severe blood loss, and transfusion requirements did not differ significantly, nor did the composite bleeding outcome (9.9 % vs. 8.6 %, p = 0.661). Placental abruption occurred more frequently among women who discontinued LDA ≤7 days compared to >7 days before delivery (5.2 % vs. 1.1 %, p = 0.002). However, in multivariate analysis, the timing of LDA discontinuation was not independently associated with an increased risk of placental abruption.
Conclusion
The timing of LDA discontinuation was not associated with increased PPH or major bleeding complications.
期刊介绍:
Pregnancy Hypertension: An International Journal of Women''s Cardiovascular Health aims to stimulate research in the field of hypertension in pregnancy, disseminate the useful results of such research, and advance education in the field.
We publish articles pertaining to human and animal blood pressure during gestation, hypertension during gestation including physiology of circulatory control, pathophysiology, methodology, therapy or any other material relevant to the relationship between elevated blood pressure and pregnancy. The subtitle reflects the wider aspects of studying hypertension in pregnancy thus we also publish articles on in utero programming, nutrition, long term effects of hypertension in pregnancy on cardiovascular health and other research that helps our understanding of the etiology or consequences of hypertension in pregnancy. Case reports are not published unless of exceptional/outstanding importance to the field.