Abstract
High-dose prophylaxis for severe hemophilia A [25–40 factor (F) VIII Units (u) kg−1 on alternate days] reduces arthropathy, but does so at great cost. (
Objectives: To assess the degree of joint damage in the 6 index joints for subjects receiving tailored prophylaxis.
Methods: We studied an inception cohort of boys ages 1–2.5 years with severe hemophilia A (<2% FVIII) and no inhibitors treated with tailored prophylaxis. Patients were followed at 6 monthly intervals and parents have kept detailed diaries. Joint damage was measured using a validated physiotherapy joint score and function was assessed using the Child Health Assessment Questionnaire (CHAQ)
Results: 54 boys were enrolled from 11 Canadian hemophilia treatment centers. The total follow-up is 3423 patient months (mean 62.2 months, median 54 months and range 5–117 months). 16 (29.6%) boys have been escalated to Step 2 and 14 (25.9%) have escalated to Step 3. 11 of the escalations were due to target joint bleeding. Subjects on study had a mean of 1.4 joint bleeds/patient-year. Physiotherapy Scores Maximum Possible Score Median Observed Range Ankles 56 2 0–20 Elbows 48 0 0–13 Knees 56 0 0–15 All Joints Swelling 18 0 0–4 Muscle Atrophy 18 0 0–3 CHAQ 3 0 0–2 89% of participants were compliant with the primary prophylaxis protocol. Non compliant subjects had the poorest outcomes. No treatment related adverse events have occurred.
Conclusion: Tailored primary prophylaxis should be considered as a valid option for long term prophylaxis in young boys with severe hemophilia A.
. | Maximum Possible Score . | Median . | Observed Range . |
---|---|---|---|
Ankles | 56 | 2 | 0–20 |
Elbows | 48 | 0 | 0–13 |
Knees | 56 | 0 | 0–15 |
All Joints | |||
Swelling | 18 | 0 | 0–4 |
Muscle Atrophy | 18 | 0 | 0–3 |
CHAQ | 3 | 0 | 0–2 |
. | Maximum Possible Score . | Median . | Observed Range . |
---|---|---|---|
Ankles | 56 | 2 | 0–20 |
Elbows | 48 | 0 | 0–13 |
Knees | 56 | 0 | 0–15 |
All Joints | |||
Swelling | 18 | 0 | 0–4 |
Muscle Atrophy | 18 | 0 | 0–3 |
CHAQ | 3 | 0 | 0–2 |
Author notes
Disclosure:Research Funding: The study was funded by CIHR and Bayer Canada. Honoraria Information: Honourarium for speaking at symposium. Membership Information: Sits on advisory board for Bayer, Baxer and Amgen.