Table 3.

How we manage thrombosis in myeloproliferative disease (MPD).

Abbreviations: ET, essential thrombocythemia; PV, polycythemia vera 
  1. Risk stratification

    At least one of the following defines high-risk patients:

    • - age above 60 years

    • - previous major thrombotic complication

    • - platelet count > 1500 × 109/L in ET

  2. Therapy

    • Primary prevention

      Low-risk patients

      • - PV: Target hematocrit below 45% plus aspirin 100 mg/day

      • - ET: aspirin 100 mg/day if cardiovascular risk factors

      High-risk patients

      As above, plus

      • - Myelosuppressive therapy (see text)

    • Acute events

      • - Manage ongoing thrombosis according to current guidelines30 

      • - Aspirin 500 mg/day for acute microvascular symptoms in ET

    • Secondary thromboprophylaxis

      • - Aspirin 100 mg/day long-life after arterial or microvascular thrombosis

      • - Warfarin, PT INR 2.0–3.0 (long-life ?) after venous thromboembolism

      • - Myelosuppressive therapy (see text)

 
Abbreviations: ET, essential thrombocythemia; PV, polycythemia vera 
  1. Risk stratification

    At least one of the following defines high-risk patients:

    • - age above 60 years

    • - previous major thrombotic complication

    • - platelet count > 1500 × 109/L in ET

  2. Therapy

    • Primary prevention

      Low-risk patients

      • - PV: Target hematocrit below 45% plus aspirin 100 mg/day

      • - ET: aspirin 100 mg/day if cardiovascular risk factors

      High-risk patients

      As above, plus

      • - Myelosuppressive therapy (see text)

    • Acute events

      • - Manage ongoing thrombosis according to current guidelines30 

      • - Aspirin 500 mg/day for acute microvascular symptoms in ET

    • Secondary thromboprophylaxis

      • - Aspirin 100 mg/day long-life after arterial or microvascular thrombosis

      • - Warfarin, PT INR 2.0–3.0 (long-life ?) after venous thromboembolism

      • - Myelosuppressive therapy (see text)

 
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