A survey of factor prophylaxis in the Canadian haemophilia A population

P Blanchette1, G Rivard, S Israels

  • 1Institute of Medical Sciences, University of Toronto, Toronto, Canada.

Insights

High-dose factor (F) VIII prophylaxis in severe haemophilia A prevents joint damage but is costly. Canadian data show prophylaxis use increased FVIII consumption significantly between 1999-2003.

Area of Science:

  • Hematology
  • Pediatric Medicine
  • Pharmacoeconomics

Background:

  • High-dose factor (F) VIII prophylaxis (25-40 IU/kg ≥3 times/week) initiated early prevents arthropathy in severe haemophilia A.
  • Prophylaxis programs are expensive and pose venous access challenges.
  • A global shortage of recombinant FVIII concentrate prompted a survey of prophylaxis patterns in Canada.

Purpose of the Study:

  • To ascertain patterns of FVIII prophylaxis in Canada during a period of FVIII concentrate shortage.
  • To analyze FVIII consumption trends related to prophylaxis.

Main Methods:

  • A survey was conducted in 2001 across 14 Canadian haemophilia treatment centers.
  • Data were collected on 247 inhibitor-negative, severe haemophilia A patients receiving regular FVIII prophylaxis (≥1 infusion/week).
  • Analysis included patient demographics, FVIII infusion doses, frequency, and overall FVIII consumption.

Main Results:

  • The median age of patients on prophylaxis was 13 years (range: 1-65), with 95% having severe haemophilia A.
  • Median FVIII dose was 26 IU/kg (range: 16-33), with 67% receiving ≥3 infusions/week.
  • High-dose prophylaxis was most common in boys <5 years (82%) and significantly contributed to a 10% increase in Canadian FVIII consumption (19.3 million IU) from 1999-2003.

Conclusions:

  • Prophylaxis, particularly high-dose regimens, is a substantial driver of FVIII consumption in Canada.
  • The economic implications of widespread prophylaxis necessitate further research into optimal regimens.
  • Prospective studies are warranted to define cost-effective and efficient prophylaxis strategies for severe haemophilia A.

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