Latest News

Warfarin best for thrombotic antiphospholipid syndrome?


 

FROM THE JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

‘Important implications’

In an accompanying editorial,Mark A. Crowther, MD, McMaster University, Hamilton, Ont., and Aubrey E. Jones, PharmD, and Daniel M. Witt, PharmD, both of the University of Utah College of Pharmacy, Salt Lake City, say that: “As the quality of the evidence was rated ‘high’ for the arterial thrombosis outcome and ‘moderate’ for the venous thrombosis and bleeding outcomes, these results should lead to a revision of evidence-based guidelines to recommend against using DOACs as an option for most patients with thrombotic antiphospholipid syndrome.”

They add that this recommendation for vitamin K antagonists also applies to patients previously thought to be at lower risk from antiphospholipid syndrome – including those with only one or two positive serological tests and those with only prior venous thrombosis.

The editorialists point out that this will have important implications, particularly for the accurate diagnosis of antiphospholipid syndrome, including confirmation and documentation of positive laboratory tests at least 12 weeks after the initial positive test.

They recommend that while awaiting confirmatory testing, patients with suspected antiphospholipid syndrome should avoid DOACs, and that “strong consideration” should be given to switching essentially all antiphospholipid syndrome patients currently receiving DOACs to vitamin K antagonists.

Dr. Bikdeli is a consulting expert, on behalf of the plaintiff, for litigation related to two specific brand models of IVC filters and is supported by the Scott Schoen and Nancy Adams IGNITE Award from the Mary Horrigan Connors Center for Women’s Health and Gender Biology at Brigham and Women’s Hospital and a Career Development Award from the American Heart Association and VIVA Physicians. Dr. Crowther has received personal funding from AstraZeneca, Precision Biologics, Hemostasis Reference Laboratories, Syneos Health, Bayer, Pfizer, and CSL Behring; and holds the Leo Pharma Chair in Thromboembolism Research, which is endowed at McMaster University. Dr. Jones is supported by a career development award from the National Heart, Lung, and Blood Institute; and Dr. Witt is supported by grant funding from the Agency for Healthcare Research and Quality.

A version of this article first appeared on Medscape.com.

Pages

Recommended Reading

AXIOMATIC-SSP: Cautious optimism on factor XI inhibitor in stroke
MDedge Emergency Medicine
Rivaroxaban outmatched by VKAs for AFib in rheumatic heart disease
MDedge Emergency Medicine
Blood type linked to higher risk for early onset stroke
MDedge Emergency Medicine
New deep dive into Paxlovid interactions with CVD meds
MDedge Emergency Medicine
Collateral flow flags stroke patients for late thrombectomy
MDedge Emergency Medicine
Best anticoagulant for minimizing bleeding risk identified
MDedge Emergency Medicine
Combo thrombolytic approach fails to reduce ICH in stroke
MDedge Emergency Medicine
EHR-based thromboembolism risk tool boosted prophylaxis
MDedge Emergency Medicine
No benefit of rivaroxaban in COVID outpatients: PREVENT-HD
MDedge Emergency Medicine
Statins tied to lower ICH risk regardless of bleed location
MDedge Emergency Medicine