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Quality of life in a large multinational haemophilia B cohort (The B-Natural study) - Unmet needs remain.
Berntorp, Erik; LeBeau, Petra; Ragni, Margaret V; Borhany, Munira; Abajas, Yasmina L; Tarantino, Michael D; Holstein, Katharina; Croteau, Stacy E; Liesner, Raina; Tarango, Cristina; Carvalho, Manuela; McGuinn, Catherine; Funding, Eva; Kempton, Christine L; Bidlingmaier, Christoph; Cohen, Alice; Oldenburg, Johannes; Kearney, Susan; Knoll, Christine; Kuriakose, Philip; Acharya, Suchitra; Reiss, Ulrike M; Kulkarni, Roshni; Witkop, Michelle; Lethagen, Stefan; Krouse, Rebecca; Shapiro, Amy D; Astermark, Jan.
Afiliación
  • Berntorp E; Clinical Coagulation Research, Department of Translational Medicine, Lund University, Malmö, Sweden.
  • LeBeau P; Rho, Inc., Durham, North Carolina, USA.
  • Ragni MV; University of Pittsburgh and Hemophilia Center of Western Pennsylvania, Pittsburgh, Pennsylvania, USA.
  • Borhany M; National Institute of Blood Disease and Bone Marrow Transplantation, Karachi, Pakistan.
  • Abajas YL; Hemophilia and Thrombosis Center, University of North Carolina, Chapel Hill, North Carolina, USA.
  • Tarantino MD; Bleeding and Clotting Disorders Institute, Peoria, Illinois, USA.
  • Holstein K; University Medical Center Hamburg-Eppendorf, Medical Department, Haemophilia Center, Hamburg, Germany.
  • Croteau SE; Boston Children's Hospital, Boston Hemophilia Center, Boston, Massachusetts, USA.
  • Liesner R; Great Ormond Street Hospital for Children, NHS Trust supported by NIHR, GOSH, BRC, London, UK.
  • Tarango C; Cancer and Blood Diseases Institute, Cincinnati Children's Hospital Medical Center, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
  • Carvalho M; Congenital Coagulopathies Reference Centre, Centro Hospitalar Universitário São João, Porto, Portugal.
  • McGuinn C; Weill Cornell Medical College, New York, New York, USA.
  • Funding E; Department of Hematology, University Hospital Rigshospitalet, Institute of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Kempton CL; Emory University School of Medicine, Emory University, Atlanta, Georgia, USA.
  • Bidlingmaier C; Dr. v. Hauner's Childrens University Hospital, Hemophilia Center, LMU Hospital, Munich, Germany.
  • Cohen A; Newark Beth Israel Medical Center, Newark, New Jersey, USA.
  • Oldenburg J; University Clinic Bonn, Bonn, Germany.
  • Kearney S; Children's Minnesota Center for Bleeding and Clotting Disorders, Minneapolis, Minnesota, USA.
  • Knoll C; Phoenix Children's Hospital, Phoenix, Arizona, USA.
  • Kuriakose P; Henry Ford Hospital, Detroit, Michigan, USA.
  • Acharya S; Northwell Hemostasis and Thrombosis Center, New Hyde Park, New York, New York, USA.
  • Reiss UM; St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Kulkarni R; Michigan State University, East Lansing, Michigan, USA.
  • Witkop M; Munson Medical Center, Northern Regional Bleeding Disorders Center, Traverse City, Michigan, USA.
  • Lethagen S; Sobi, Stockholm, Sweden.
  • Krouse R; Rho, Inc., Durham, North Carolina, USA.
  • Shapiro AD; Indiana Hemophilia and Thrombosis Center, Indianapolis, Indiana, USA.
  • Astermark J; Department of Translational Medicine, Lund University and Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Malmö, Sweden.
Haemophilia ; 28(3): 453-461, 2022 May.
Article en En | MEDLINE | ID: mdl-35263495
INTRODUCTION: The B-Natural study is a multicentre, multinational, observational study of haemophilia B (HB) designed to increase understanding of clinical manifestations, treatment and quality of life (QoL). AIM: To characterise and compare QoL in HB across disease severity groups and individuals with inhibitors to identify gaps in treatment. METHODS: A total of 224 individuals from 107 families were enrolled from a total of 24 centres in North America (n = 16), Europe (n = 7) and Asia (n = 1). Of these, 68 (30.4%) subjects had severe (<1 IU/dL), median age 15.6 years, 114 (50.9%) moderate (1-5 IU/dL), age 13.3 years, and 42 (18.8%) mild (>5-< 40 IU/dL), age 12.1 years, disease. Twenty-nine participants had inhibitors or a history of inhibitors. Three versions of the EQ-5D instrument were used as a measure of QoL: proxy (ages 4-7), youth (ages 8-15) and self (age 16+). Each instrument included a visual analogue scale ranging from 100 (best health) to 0 (worst health) to assess current day's health (EQ VAS). Range-of-motion (ROM) for elbows, knees and ankles was assessed using a four-point scale, from which a composite score was calculated. RESULTS: In all severity groups, a proportion of subjects showed less than optimal QoL. The majority of the mild and moderate severe participants reported a normal EQ-5D health profile (79% and 72%, respectively), whereas about half (47%) of the severe participants and only 13% of the inhibitor participants reported this profile. CONCLUSION: The B-Natural study reveals impacted QoL in all disease severities of HB including those with inhibitors. Unmet needs remain and include nonsevere HB.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Hemofilia B Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Humans Idioma: En Revista: Haemophilia Asunto de la revista: HEMATOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Hemofilia B Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Humans Idioma: En Revista: Haemophilia Asunto de la revista: HEMATOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Suecia