Evidence map›Paper›PMID 41485833›Full record

ReviewAmerican journal of obstetrics and gynecology2026

Postoperative venous thromboembolism following cesarean delivery: prevalence, pathophysiology, diagnosis, treatment, and prevention.

Jerome J Federspiel, Marc A Rodger, Maureane R Hoffman, Leslie Skeith, Thomas L Ortel, Ann M Bruno, Andra H James

Abstract readReview
In one paragraph

Review in American journal of obstetrics and gynecology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Jerome J FederspielDivision of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, Duke University School of Medicine, Durham, NC; Division of Hematology, Department of Medicine, Duke University School of Medicine, Durham, NC; Department of Population Health Sciences, Duke University School of Medicine, Durham, NC. Electronic address: jerome.federspiel@duke.edu.
Marc A RodgerDepartment of Medicine, Faculty of Medicine and Health Sciences, McGill University, Montreal, Quebec, Canada.
Maureane R HoffmanDepartment of Pathology, Duke University School of Medicine, Durham, NC.
Leslie SkeithDivision of Hematology and Hematological Malignancies, Department of Medicine, University of Calgary, Calgary, Alberta, Canada.
Thomas L OrtelDivision of Hematology, Department of Medicine, Duke University School of Medicine, Durham, NC.
Ann M BrunoDivision of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, University of Utah School of Medicine, Salt Lake City, UT.
Andra H JamesDivision of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, Duke University School of Medicine, Durham, NC; Division of Hematology, Department of Medicine, Duke University School of Medicine, Durham, NC.

Funding

Utah Women's Reproductive Health Research Career Development ProgramK12HD085816 · NICHD · UNIVERSITY OF UTAH · PI SILVER, ROBERT M. · 2015 to 2024
$3.2M
Duke Women's Reproductive Health Research ScholarsK12HD103083 · NICHD · DUKE UNIVERSITY · PI Cindy Amundsen · 2020 to 2026
$2.2M
NICHD NIH HHS K12 HD085816NICHD NIH HHS K12 HD103083
6 · The paper itself

Abstract

Venous thromboembolism contributes to approximately 10% of pregnancy-associated deaths in the United States, with the highest incidence rate in the immediate postpartum period. Cesarean deliveries are associated with 4-fold relative risk of venous thromboembolism vs vaginal delivery. While most patients have some evidence of thrombosis in the pelvic veins after cesarean delivery, only a small proportion of patients (2.6-4.3 per 1000 deliveries) develop a clinically relevant venous thromboembolism. We outline the normal physiologic process of postcesarean hemostasis and the pathways by which aberrant balance in hemostasis may result in venous thromboembolism. With respect to diagnosis, vascular ultrasound remains the cornerstone of deep vein thrombosis diagnosis, while ventilation/perfusion studies and computed tomographic angiography are bedrocks of pulmonary embolism diagnosis. Venous thromboembolism prediction rules have not been validated in the postcesarean population and high rates of elevated D-dimer concentrations in the weeks after cesarean delivery limit their use. For the treatment of postpartum venous thromboembolism, low-molecular-weight heparin is the mainstay of acute management, but a wide range of alternative agents are now available, including warfarin and direct oral anticoagulants. In contemporary practice, there is large variation in the use of postpartum pharmacologic prophylaxis within the United States and internationally. Whether broader use of postpartum pharmacologic prophylaxis reduces the incidence of postcesarean venous thromboembolism with acceptable rates of adverse events (eg, bleeding complications) is unclear; observational evidence has come to conflicting conclusions. There is an urgent need for further study of the effectiveness of postpartum prophylaxis, and its optimal agent, dose, and duration, in randomized trials. Contemporary guidelines regarding which patients should receive postpartum pharmacologic prophylaxis are based largely on expert opinion; well-validated postpartum venous thromboembolism prediction models and patient preference data are needed to inform risk stratification and counseling.

Indexed as

Cesarean SectionPostoperative ComplicationsVenous ThromboembolismAnticoagulantsFemaleHeparin, Low-Molecular-WeightHumansPregnancyPrevalencePulmonary EmbolismAnticoagulantsHeparin, Low-Molecular-Weightanticoagulantscesarean sectioncomputed tomography angiographyepidemiologyfibrin fragment Dheparinlow-molecular-weightmagnetic resonance angiographypatient preferencepregnancypulmonary embolismultrasonography/Doppler/duplexvenous thromboembolismventilation-perfusion scan

Identifiers

PMID41485833
PMCPMC12774447

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.