Acute prognostic factors for post-thrombotic syndrome in children with limb DVT: a bi-institutional cohort study

Courtney A Lyle1, Elizabeth Gibson, Amy E Lovejoy

  • 1Department of Pediatrics, Division of Hematology/Oncology, University of California San Diego and Rady Children's Hospital, San Diego, CA, USA. clyle@billingsclinic.org

Thrombosis Research
|December 1, 2012
PubMed

Insights

Early identification of pediatric deep venous thrombosis (DVT) risk factors is crucial. A positive lupus anticoagulant test (dRVVT) within two weeks of DVT diagnosis significantly increases the risk of post-thrombotic syndrome (PTS) in children.

Area of Science:

  • Pediatric Thrombosis and Hemostasis
  • Vascular Medicine
  • Clinical Outcomes Research

Background:

  • Early identification of children at high risk for post-thrombotic syndrome (PTS) after deep venous thrombosis (DVT) is critical for evaluating interventions.
  • Understanding acute prognostic factors for PTS in pediatric limb DVT is essential.

Purpose of the Study:

  • To evaluate acute prognostic factors for the development of PTS in children diagnosed with limb DVT.

Main Methods:

  • A bi-institutional mixed cohort study with prospective PTS ascertainment using a validated pediatric instrument.
  • Data collected included patient/thrombus characteristics, thrombophilia testing, and outcomes in children (<21 years) with acute limb DVT.

Main Results:

  • The cumulative incidence of PTS was 23% at a median follow-up of 33 months.
  • A positive lupus anticoagulant (by dilute Russell Viper venom time - dRVVT) within two weeks of DVT diagnosis was associated with significantly increased odds of clinically significant PTS (OR: 16.8, P=0.02).
  • Infectious or inflammatory conditions at presentation were not associated with PTS risk or dRVVT positivity.

Conclusions:

  • An acutely positive dRVVT test after limb DVT diagnosis is a significant prognostic factor for clinically significant PTS in children.
  • Larger studies are needed to confirm these findings and explore persistent dRVVT positivity or beta-2-glycoprotein-I dependence.
Abstract

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