- Blondom M. Anticoagulation during pregnancy - who, when and for how long. EHA 2025, Milan, Italy, June 12-15
Pregnancy induces a well-recognized prothrombotic state due to profound physiological changes in the coagulation system. The management of anticoagulation during pregnancy remains a complex clinical challenge, requiring careful balancing of maternal and fetal risks. In his presentation at EHA 2025, “Anticoagulation during pregnancy: who, when and for how long,” Dr. Marc Blondom (Division of Angiology and Haemostasis, Geneva University Hospitals) provided an evidence-based overview of current strategies and practical recommendations for clinicians.
Dr. Blondom opened his presentation by emphasizing the importance of risk stratification. Not all pregnant women require anticoagulation. Appropriate selection hinges on a careful assessment of thrombotic risk factors.
Key groups to consider for prophylactic or therapeutic anticoagulation include:
It is important to note that pregnancy-related risk factors, such as immobilisation, caesarean section, obesity or multiple pregnancy, can alter the overall risk and should influence treatment decisions.
Dr. Blondom stressed that individual risk assessment remains paramount: blanket anticoagulation for all thrombophilic women is not warranted, and overtreatment can introduce unnecessary bleeding risk.
Optimal timing for initiating anticoagulation depends on baseline risk and prior clinical history. For high-risk patients (e.g., with a history of VTE), anticoagulant therapy is usually started before conception or as soon as pregnancy is confirmed. For patients identified during pregnancy (e.g., with a diagnosis of a new episode of VTE), treatment should be started immediately after diagnosis.
In women with intermediate risk (e.g., heterozygous thrombophilia without prior thrombosis), prophylactic anticoagulation may be considered starting from the second trimester, when the hypercoagulable state intensifies.
Dr. Blondom also discussed perioperative and peripartum management, highlighting the importance of close coordination between obstetricians and hematologists. Ideally, delivery should be planned to allow for temporary cessation of anticoagulation, thereby minimizing bleeding risk during labor. In emergency situations, the use of reversal agents or the administration of regional anesthesia requires careful timing in relation to the patient’s anticoagulation status.
Duration of anticoagulation must encompass both pregnancy and the high-risk postpartum period, when thrombotic risk peaks. Dr. Blondom highlighted that:
He also underlined that many VTE events occur postpartum (thus, adequate postpartum coverage is critical). Early mobilization, compression therapy, and thromboprophylaxis are key components of comprehensive care.
Although not the primary focus of this session, Dr. Blondom briefly reviewed drug selection.
In his concluding remarks, Dr. Blondom reinforced key principles for clinical practice:
As research continues to evolve, clinicians must remain attentive to updated guidelines and emerging data on the safety of newer agents. For now, LMWH-based regimens, tailored to patient risk profiles, remain the standard of care for managing anticoagulation during pregnancy.