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Joint health and treatment modalities in Nordic patients with moderate haemophilia A and B - The MoHem study.
Måseide, Ragnhild J; Berntorp, Erik; Astermark, Jan; Olsson, Anna; Bruzelius, Maria; Frisk, Tony; Nummi, Vuokko; Lassila, Riitta; Tjønnfjord, Geir E; Holme, Pål A.
  • Måseide RJ; Department of Haematology, Oslo University Hospital, Oslo, Norway.
  • Berntorp E; Research Institute of Internal Medicine, Oslo University Hospital, Oslo, Norway.
  • Astermark J; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
  • Olsson A; Department of Translational Medicine, Lund University, Malmö, Sweden.
  • Bruzelius M; Department of Translational Medicine, Lund University, Malmö, Sweden.
  • Frisk T; Department of Haematology, Skåne University Hospital, Malmö, Sweden.
  • Nummi V; Department of Medicine, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Lassila R; Molecular Medicine and Surgery, Karolinska Institute, Stockholm, Sweden.
  • Tjønnfjord GE; Department of Haematology, Karolinska University Hospital, Stockholm, Sweden.
  • Holme PA; Pediatric Coagulation, Karolinska University Hospital, Stockholm, Sweden.
Haemophilia ; 26(5): 891-897, 2020 Sep.
Article en En | MEDLINE | ID: mdl-33021747
ABSTRACT

INTRODUCTION:

The prevalence of arthropathy in moderate haemophilia A (MHA) and B (MHB) is not well known.

AIM:

We evaluated joint health in Nordic patients in relation to their treatment modality.

METHODS:

A cross-sectional, multicentre study covering MHA and MHB in Sweden, Finland and Norway. Arthropathy was evaluated by ultrasound (HEAD-US) and Haemophilia Joint Health Score (HJHS).

RESULTS:

We report on 145 patients median age 28 years (IQR 13-52) and 61% MHA. Baseline factor VIII/factor IX activity (FVIII/FIXC) was 2 IU/dL (median) (IQR 2-4) lower for MHB (2 IU/dL, IQR 1-2) than MHA (3 IU/dL, IQR 2-4) (P < .01). Eighty-five per cent of MHA and 73% MHB had a history of haemarthrosis (P = .07). Age at first joint bleed was lower for MHA (5 years [median], IQR 3-7) than MHB (7 years, IQR 5-12) (P = .01). Thirty-eight per cent received prophylaxis, started at median 10 years of age (IQR 4-24). Median joint bleeds and serious other bleeds during the last 12 months were both zero (IQR 0-1). Total HEAD-US captured 0/48 points (median) (IQR 0-2) and HJHS 4/120 points (IQR 1-10) with strong correlation between them (r = .72). FVIII/FIX C ≤ 3 IU/dL was associated with higher HJHS (P = .04). Fifteen per cent had undergone orthopaedic surgery.

CONCLUSION:

The current joint health in Nordic moderate haemophilia patients was rather good, but a subgroup had severe arthropathy. FVIII/FIX C ≤ 3 IU/dL and MHA were associated with a more severe bleeding phenotype. We suggest primary prophylaxis to all patients with FVIII/FIXC ≤ 3 IU/dL.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hemofilia B / Hemofilia A Tipo de estudio: Clinical_trials / Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Adolescent / Adult / Female / Humans / Male / Middle aged País como asunto: Europa Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hemofilia B / Hemofilia A Tipo de estudio: Clinical_trials / Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Adolescent / Adult / Female / Humans / Male / Middle aged País como asunto: Europa Idioma: En Año: 2020 Tipo del documento: Article