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European retrospective study of real-life haemophilia treatment.
Berntorp, E; Dolan, G; Hay, C; Linari, S; Santagostino, E; Tosetto, A; Castaman, G; Álvarez-Román, M T; Parra Lopez, R; Oldenburg, J; Albert, T; Scholz, U; Holmström, M; Schved, J-F; Trossaërt, M; Hermans, C; Boban, A; Ludlam, C; Lethagen, S.
Afiliación
  • Berntorp E; Clinical Coagulation Research Unit, Lund University, Malmö, Sweden.
  • Dolan G; St Thomas' Hospital Haemophilia Centre, St Thomas' Hospital, London, UK.
  • Hay C; Department of Haematology, Manchester Royal Infirmary, Manchester, UK.
  • Linari S; Center for Bleeding Disorders, Careggi University Hospital, Florence, Italy.
  • Santagostino E; Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, IRCCS Ca' Granda Foundation, Maggiore Hospital Policlinico, Milan, Italy.
  • Tosetto A; Department of Cell Therapy and Hematology, Hemophilia and Thrombosis Center, San Bortolo Hospital, Vicenza, Italy.
  • Castaman G; Center for Bleeding Disorders, Careggi University Hospital, Florence, Italy.
  • Álvarez-Román MT; Department of Cell Therapy and Hematology, Hemophilia and Thrombosis Center, San Bortolo Hospital, Vicenza, Italy.
  • Parra Lopez R; Hospital Universitario La Paz, Thrombosis and Haemostasis Unit, Madrid, Spain.
  • Oldenburg J; Unidad de Hemofilia, Hospital Vall d'Hebrón, Barcelona, Spain.
  • Albert T; Institut für Experimentelle Hämatologie und Transfusionsmedizin, Universitätsklinik Bonn, Bonn, Germany.
  • Scholz U; Institut für Experimentelle Hämatologie und Transfusionsmedizin, Universitätsklinik Bonn, Bonn, Germany.
  • Holmström M; Center of Haemostasis, Leipzig, Germany.
  • Schved JF; Coagulation Unit, Hematology Centre Karolinska, Karolinska University Hospital, Stockholm, Sweden.
  • Trossaërt M; Department of Medicine, Karolinska Institutet, Solna, Sweden.
  • Hermans C; Hôpital Saint Eloi, Laboratoire d'hématologie, Montpellier, France.
  • Boban A; Centre Régional de Traitement de l'Hémophilie CHU, Nantes, France.
  • Ludlam C; Haemostasis and Thrombosis Unit, Haemophilia Clinic St-Luc University Hospital, Brussels, Belgium.
  • Lethagen S; Haemostasis and Thrombosis Unit, Haemophilia Clinic St-Luc University Hospital, Brussels, Belgium.
Haemophilia ; 23(1): 105-114, 2017 Jan.
Article en En | MEDLINE | ID: mdl-27761962
ABSTRACT

INTRODUCTION:

Haemophilia treatment varies significantly between individuals, countries and regions and details of bleed rates, factor consumption and injection frequency are often not available.

AIM:

To provide an overview of the FVIII/FIX treatment practice and outcome for patients with haemophilia A (HA) or haemophilia B (HB) across Europe.

METHODS:

Non-interventional, 12-month retrospective study where anonymized data were retrieved from haemophilia centres/registers in Belgium, France, Germany, Italy, Spain, Sweden and the United Kingdom. Male patients (all ages) receiving coagulation factor treatment 24 months prior to the study, with basal FVIII/FIX levels ≤5 IU dL-1 , without inhibitors, were included. Data were summarized descriptively.

RESULTS:

In total, 1346 patients with HA and 312 with HB were included in the analysis; 75% and 57% had severe disease (FVIII/FIX < 1 IU dL-1 ) respectively. Prophylaxis was most common for severe haemophilia, especially for children, whereas on-demand treatment was more common for moderate haemophilia in most countries. The mean (SD) prescribed prophylactic treatment ranged from 67.9 (30.4) to 108.4 (78.1) (HA) and 32.3 (10.2) to 97.7 (32.1) (HB) IU kg-1 per week, across countries. Most patients on prophylaxis were treated ≥3 times/week (HA) or two times/week (HB). The median annual bleeding rate (ABR) for patients on prophylaxis ranged from 1.0 to 4.0 for severe HA, and from 1.0 to 6.0 for severe HB, while those with moderate haemophilia generally had slightly higher ABRs. Median ABRs for on-demand-treated severe HA ranged from 4.5 to 18.0, and for HB, 1.5 to 14.0.

CONCLUSION:

Treatment practice varied greatly between centres and countries and patients treated on-demand and prophylactically both experienced bleeds, emphasizing the need for further optimization of care.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Hemofilia A Tipo de estudio: Observational_studies Límite: Adult / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Haemophilia Asunto de la revista: HEMATOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Hemofilia A Tipo de estudio: Observational_studies Límite: Adult / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Haemophilia Asunto de la revista: HEMATOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Suecia