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Primary prophylaxis implementation and long-term joint outcomes in Swedish haemophilia A patients

Arvanitakis, Alexandros LU ; Jepsen, Caroline ; Andersson, Nadine G. LU ; Baghaei, Fariba and Astermark, Jan LU (2024) In Haemophilia 30(3). p.671-677
Abstract

Introduction: Primary prophylaxis is the gold standard in severe haemophilia A (SHA) but time to escalate the prophylaxis regimen varies. Aim: Assess prophylaxis implementation and long-term joint health outcomes in SHA with primary prophylaxis. Methods: Adult male patients born after 1980, with SHA on primary prophylaxis, started before the age of 3 years and second joint bleed, and no history of FVIII inhibitors, were enrolled. Repeated joint-health examinations were performed with HJHS or HEAD-US; VERITAS-PRO assessed adherence. Results: Thirty patients were enrolled with, at inclusion, median age 33.5 years, annualized bleed rate and joint bleed rate 0, and FVIII consumption 4232 IU/kg/year, respectively. The median age was 1.2... (More)

Introduction: Primary prophylaxis is the gold standard in severe haemophilia A (SHA) but time to escalate the prophylaxis regimen varies. Aim: Assess prophylaxis implementation and long-term joint health outcomes in SHA with primary prophylaxis. Methods: Adult male patients born after 1980, with SHA on primary prophylaxis, started before the age of 3 years and second joint bleed, and no history of FVIII inhibitors, were enrolled. Repeated joint-health examinations were performed with HJHS or HEAD-US; VERITAS-PRO assessed adherence. Results: Thirty patients were enrolled with, at inclusion, median age 33.5 years, annualized bleed rate and joint bleed rate 0, and FVIII consumption 4232 IU/kg/year, respectively. The median age was 1.2 years, at prophylaxis start once weekly with a median FVIII dose of 47.7 IU/kg, and 1.7 years, by the time escalation to a final regimen had occurred, with a median infusion frequency of thrice weekly and FVIII dose 41.7 IU/kg, respectively. Older age correlated with later transition to escalated prophylaxis (p <.001). Longer time to escalated prophylaxis correlated to more bleeds (p <.001). Median HJHS increased slowly, reaching 4 at 35–40 years. HJHS at 15–20 years correlated with higher HJHS afterwards. Median total HEAD-US score was 1 and correlated with HJHS (p <.001). Median VERITAS-PRO score was 36, indicating good treatment adherence. Conclusion: Primary prophylaxis is effective but does not completely prevent the gradual development of arthropathy in SHA. Joint assessments with HJHS should start at an early age, as they correlate with arthropathy in later life. Prophylaxis escalation should proceed expeditiously to prevent bleeds.

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author
; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
adherence, arthropathy, early bleeding phenotype, haemophilia, HEAD-US, primary prophylaxis
in
Haemophilia
volume
30
issue
3
pages
671 - 677
publisher
John Wiley & Sons Inc.
external identifiers
  • pmid:38575549
  • scopus:85189454006
ISSN
1351-8216
DOI
10.1111/hae.15013
language
English
LU publication?
yes
id
b3f67776-f36f-45bf-8f86-f7c2b73b970d
date added to LUP
2024-04-22 12:58:06
date last changed
2025-03-11 19:33:02
@article{b3f67776-f36f-45bf-8f86-f7c2b73b970d,
  abstract     = {{<p>Introduction: Primary prophylaxis is the gold standard in severe haemophilia A (SHA) but time to escalate the prophylaxis regimen varies. Aim: Assess prophylaxis implementation and long-term joint health outcomes in SHA with primary prophylaxis. Methods: Adult male patients born after 1980, with SHA on primary prophylaxis, started before the age of 3 years and second joint bleed, and no history of FVIII inhibitors, were enrolled. Repeated joint-health examinations were performed with HJHS or HEAD-US; VERITAS-PRO assessed adherence. Results: Thirty patients were enrolled with, at inclusion, median age 33.5 years, annualized bleed rate and joint bleed rate 0, and FVIII consumption 4232 IU/kg/year, respectively. The median age was 1.2 years, at prophylaxis start once weekly with a median FVIII dose of 47.7 IU/kg, and 1.7 years, by the time escalation to a final regimen had occurred, with a median infusion frequency of thrice weekly and FVIII dose 41.7 IU/kg, respectively. Older age correlated with later transition to escalated prophylaxis (p &lt;.001). Longer time to escalated prophylaxis correlated to more bleeds (p &lt;.001). Median HJHS increased slowly, reaching 4 at 35–40 years. HJHS at 15–20 years correlated with higher HJHS afterwards. Median total HEAD-US score was 1 and correlated with HJHS (p &lt;.001). Median VERITAS-PRO score was 36, indicating good treatment adherence. Conclusion: Primary prophylaxis is effective but does not completely prevent the gradual development of arthropathy in SHA. Joint assessments with HJHS should start at an early age, as they correlate with arthropathy in later life. Prophylaxis escalation should proceed expeditiously to prevent bleeds.</p>}},
  author       = {{Arvanitakis, Alexandros and Jepsen, Caroline and Andersson, Nadine G. and Baghaei, Fariba and Astermark, Jan}},
  issn         = {{1351-8216}},
  keywords     = {{adherence; arthropathy; early bleeding phenotype; haemophilia; HEAD-US; primary prophylaxis}},
  language     = {{eng}},
  number       = {{3}},
  pages        = {{671--677}},
  publisher    = {{John Wiley & Sons Inc.}},
  series       = {{Haemophilia}},
  title        = {{Primary prophylaxis implementation and long-term joint outcomes in Swedish haemophilia A patients}},
  url          = {{http://dx.doi.org/10.1111/hae.15013}},
  doi          = {{10.1111/hae.15013}},
  volume       = {{30}},
  year         = {{2024}},
}