Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3026827 | Thrombosis Research | 2016 | 7 Pages |
•Pregnant women with a history of VTE have a high risk of recurrent VTE.•The optimal dose of LMWH for thromboprophylaxis ante- and postpartum is unknown.•The Highlow study randomizes to a fixed low dose or an intermediate dose of LMWH.•The primary efficacy outcome is recurrent symptomatic VTE up to 6 weeks postpartum.•The primary safety outcomes are clinically relevant bleeding and mortality.
SummaryBackgroundWomen with a history of venous thromboembolism (VTE) have a 2% to 10% absolute risk of VTE recurrence during subsequent pregnancies. Therefore, current guidelines recommend that all pregnant women with a history of VTE receive pharmacologic thromboprophylaxis. The optimal dose of low-molecular-weight heparin (LMWH) for thromboprophylaxis is unknown. In the Highlow study (NCT 01828697; www.highlowstudy.org), we compare a fixed low dose of LMWH with an intermediate dose of LMWH for the prevention of pregnancy-associated recurrent VTE. We present the rationale and design features of this study.MethodsThe Highlow study is an investigator-initiated, multicentre, international, open-label, randomised trial. Pregnant women with a history of VTE and an indication for ante- and postpartum pharmacologic thromboprophylaxis are included before 14 weeks of gestation. The primary efficacy outcome is symptomatic recurrent VTE during pregnancy and 6 weeks postpartum. The primary safety outcomes are clinically relevant bleeding, blood transfusions before 6 weeks postpartum and mortality. Patients are closely monitored to detect cutaneous reactions to LMWH and are followed for 3 months after delivery. A central independent adjudication committee adjudicates all suspected outcome events.ConclusionThe Highlow study is the first large randomised controlled trial in pregnancy that will provide high-quality evidence on the optimal dose of LWMH thromboprophylaxis for the prevention of recurrent VTE in pregnant women with a history of VTE.