VTE Prophylaxis

Published on Nov 18, 2015

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PRESENTATION OUTLINE

VTE prophylaxis for Haematology Patients:

not to treat (Fionnuala Fagan)

Current guidelines

  • Based on RCT that exclude subjects with a potentially high bleeding risk (including platelet count
  • No recommendations/ algorithms for prophylaxis in pateints with thrombocytopaenia
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Not even in allogeneic transplant

  • Current BCSH/BSBMT do not recommend heparin (unfractionated or low molecular weight) for prophylaxis of veno-occlusive disease (sinusoidal obstruction syndrome) in allogeneic bone marrow transplants
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How common a problem is it?

  • In acute leukaemia rate is 3.7 per 100 person years
  • In acute lymphoblastic leukaemia 4.2 per 100 person years
  • In acute myeloid leukaemia 3.4 per 100 person years
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Where to go from here...

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Bleeding is a major concern

1.7% of all patients of prophylactic enxoparin have major bleeding.
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Is thrombocytopenia protective?

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Platelet count at the time of VTE diagnosis ALL

Platelet count at the time of VTE diagnosis: AML

Does increased risk of VTE matter?

Does increased risk of VTE matter?

  • Hazard ratio for death in the presence of VTE
  • AML: 1.0 (95%CI 0.8-1.2; p value 0.99)
  • ALL: 1.4 (95% CI 1.0-2.0; p value 0.3)

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Better risk stratification?

Instead of a blanket approach?
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Risk Factors for VTE

  • Previous VTE
  • Chemotherapy (especially aspariginase)
  • Central venous catheter
  • Comorbid conditions
  • Body mass index >30
  • Immobolity
  • Use of eythopoiesis--stimulating agent

In ALL patients Risk Factors

  • Baseline platelet count 50-99x10^9/L (aOR 3.7)
  • Philadelphia chromasome positivity (aOR 2.8)
  • Age >40yo (aOR 2.7)
  • presence of additional haematologic malignancy (myeloma, lymphoma; aOR 8.3)
  • In women, hormonal therapy (aOR 2.4)
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Risk Factors in AML

  • Male (aOR 1.9)
  • Liver disease (aOR 3.7)
  • Use of Erythroid Stimulating Agent (aOR 2.4)
  • Women, hormonal therapy (aOR 2.6)
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How to implement risk stratification?

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Conclusion

  • While there is an increased risk of VTE the routine use of chemical prophylaxis confers an increased risk of bleeding
  • No conclusive evidence about what to use and when to withold
  • VTE is not associated with increased mortality in AML (and probably not ALL either)
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Reference

  • Vu, K. et al. A retrospective study of venothromboembolism in acute leukaemia patients treated at the University of Texas MD Anderson Cancer Center. Cancer Medicine. 2015; 4(1)27-35
  • Tufano, A. et al. Prevention of Venous thromboembolism in Medical patients with Thrombocytopaenia or Platelet dysfunction: A review of literatures. Seminars in thrombosis and Haemostasis. 2011. 37(3):267-273
  • Grace, H K. Venous thromboembolism in patient with with acute leukaemia: incidence, risk factors and effect on survival. Blood. 2009. 113(17):3911-3917
  • Crowther, M. Bleeding risk and the management of bleeding complications in patients undergoing anticoagulant therapy: focus on new anticoagulant agents. Blood. 2008. 111(10): 4871 - 4879
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Fionnuala Fagan

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