| Return |
Compared to those who took placebo, about 9 fewer people out of 100 taking apixaban had another blood clot.
Major bleeding was rare and did not differ between groups. Mild bleeding, such as nosebleeds or bruising, happened in a few more people taking apixaban, but the difference was small.
People who develop a blood clot (deep vein thrombosis or pulmonary embolism) after a temporary cause, such as surgery, trauma, or being bedridden for at least 3 days (called provoked blood clots), usually take a blood thinner for about three months. After that, treatment is often stopped because the risk of another blood clot is low. However, some people have ongoing health conditions, such as obesity, chronic inflammation, or lung disease, which may increase their risk of another blood clot.
Researchers wanted to know if patients with provoked blood clots and an ongoing health condition should continue a low-dose blood thinner to prevent another blood clot or stop treatment to avoid bleeding.
This randomized, double-blind, placebo-controlled trial (HI-PRO) included 600 adults (average age 59 years, 57% women) who had a blood clot after a temporary trigger but with at least one lasting risk factor such as obesity, chronic lung disease, inflammation, or heart disease.
Patients were randomly assigned to receive either apixaban 2.5 mg twice daily for 12 months or placebo after at least three months of full dose anticoagulation.
Apixaban vs placebo for prevention of recurrent VTE after a provoked VTE
Outcome (12 months) | Apixaban 2.5 mg twice daily | Placebo | Result |
Symptomatic recurrent DVT or PE | 1 in 100 people | 10 in 100 people | About 9 fewer per 100 people who continued apixaban had another blood clot compared to those taking placebo |
Major bleeding | 1 in 100 people | 0 people | No difference* |
Non-major bleeding | 5 in 100 people | 2 in 100 people | No difference* |
*Although the rates for the 2 groups look different, the differences were not statistically significant - this means that the difference could be simply due to chance rather than due to the different treatments
This Evidence Summary is based on the following article:
Piazza G, Bikdeli B, Pandey AK, et al. Apixaban for Extended Treatment of Provoked Venous Thromboembolism. N Engl J Med. 2025 Sep 25;393(12):1166-1176. doi: 10.1056/NEJMoa2509426. Epub 2025 Aug 30. PubMed
Talal Alghamdi, MD
Dr Talal Alghamdi is an Internal Medicine resident and an incoming General Internal Medicine resident at McMaster University. He has a strong interest in thrombosis, evidence-based medicine, and clinical education. Dr Alghamdi is actively involved in research and teaching initiatives focused on venous thromboembolism management and patient-centered communication.
Anthony Sandre, MD
Dr. Sandre is an Assistant Professor in the Division of General Internal Medicine at McMaster University with additional training in Vascular Medicine. Within the Division of Hematology and Thromboembolism, Dr. Sandre provides care to patients with arterial and venous thrombosis, arteriopathies, and high-risk primary or secondary prevention of cardiovascular disease.
Published: Monday, November 10, 2025
Please note that the information contained herein is not to be interpreted as an alternative to medical advice from a professional healthcare provider. If you have any questions about any medical matter, you should consult your professional healthcare providers, and should never delay seeking medical advice, disregard medical advice or discontinue medication based on information provided here.
|
This Evidence Summary was printed from the CLOT+ website on 2025/12/14. To view other Evidence Summaries or to register to receive email notifications about new Evidence Summaries, please visit us at https://plus.mcmaster.ca/ClotPlus/Articles/EvidenceSummaries |
|