AI Article Synopsis

  • The study aimed to evaluate the safety and effectiveness of various anticoagulants in treating isolated superficial vein thrombosis (iSVT) through a systematic review of randomized controlled trials.
  • Eight trials involving 4,721 patients were analyzed, revealing that all anticoagulants significantly reduced thrombotic complications compared to placebo, with fondaparinux showing the best results for preventing deep vein thrombosis (DVT) and pulmonary embolism (PE).
  • Despite some limitations in the data, the review concluded that fondaparinux and rivaroxaban are effective treatments for iSVT, suggesting a potential trend towards better outcomes with longer treatment durations.

Article Abstract

Objective: Assess the safety and efficacy of anticoagulants in treating isolated superficial vein thrombosis (iSVT).

Materials And Methods: A systematic review was conducted according to PRISMA 2020 guidelines, for randomized controlled trials (RCTs) investigating anticoagulants in the treatment of iSVT. The primary endpoint of thrombotic complications encompassed any incident of iSVT progression/recurrence and the development of new-onset (deep vein thrombosis) DVT or (pulmonary embolism) PE.

Results: Eight RCT's and 4721 patients treated once daily with either fondaparinux 2.5 mg, rivaroxaban 10 mg, therapeutic, intermediate, and prophylactic low molecular weight heparin (LMW) were included. While all anticoagulants displayed a statistically significant risk reduction compared to placebo in terms of thrombotic complications and iSVT progression/recurrence, only fondaparinux reduced the risk for DVT/PE. Additionally, fondaparinux exhibited enhanced efficacy in decreasing DVT/PE events relative to prophylactic and therapeutic LMWH. Furthermore, rivaroxaban and fondaparinux demonstrated superior outcomes in terms of preventing thrombotic complications compared to all three dosing regimens of LMWH without significant differences between the two, risk ratio RR 1.00(95%CI:0.51-1.92). SUCRA identified fondaparinux as the most effective treatment regarding thrombotic complications, (SUCRA,91.6) and DVT/PE, (SUCRA,96) and rivaroxaban in terms of iSVT progression/recurrence (SUCRA,94.68). Ultimately and despite certain model limitations, meta-regression analysis suggested a possible trend towards improved outcomes with longer treatment durations for thrombotic complications β = -0.34(95%CI:-16.39to12.23).

Conclusions: Despite inherent limitations such as variations in treatment durations and follow-up periods, this review displayed the efficacy of fondaparinux, rivaroxaban and LMWH in treating iSVT. The improved efficacy of fondaparinux over therapeutic LMWH in terms of DVT/PE outcomes necessitates cautious interpretation underscoring the need for further investigation through adequately powered RCTs.

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Source
http://dx.doi.org/10.1016/j.thromres.2024.109101DOI Listing

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