Fundamentals for a Systematic Approach to Mild and Moderate Inherited Bleeding Disorders: An EHA Consensus Report.


Journal

HemaSphere
ISSN: 2572-9241
Titre abrégé: Hemasphere
Pays: United States
ID NLM: 101740619

Informations de publication

Date de publication:
10 2019
Historique:
received: 26 03 2019
revised: 08 07 2019
accepted: 15 07 2019
entrez: 17 1 2020
pubmed: 17 1 2020
medline: 17 1 2020
Statut: epublish

Résumé

Healthy subjects frequently report minor bleedings that are frequently 'background noise' of normality rather than a true disorder. Nevertheless, unexpected or unusual bleeding may be alarming. Thus, the distinction between normal and pathologic bleeding is critical. Understanding the underlying pathologic mechanism in patients with an excessive bleeding is essential for their counseling and treatment. Most of these patients with significant bleeding will result affected by non-severe inherited bleeding disorders (BD), collectively denominated mild or moderate BD for their relatively benign course. Unfortunately, practical recommendations for the management of these disorders are still lacking due to the current state of fragmented knowledge of pathophysiology and lack of a systematic diagnostic approach. To address this gap, an International Working Group (IWG) was established by the European Hematology Association (EHA) to develop consensus-based guidelines on these disorders. The IWG agreed that grouping these disorders by their clinical phenotype under the single category of mild-to-moderate bleeding disorders (MBD) reflects current clinical practice and will facilitate a systematic diagnostic approach. Based on standardized and harmonized definitions a conceptual unified framework is proposed to distinguish normal subjects from affected patients. The IWG proposes a provisional comprehensive patient-centered initial diagnostic approach that will result in classification of MBD into distinct clinical-pathological entities under the overarching principle of clinical utility for the individual patient. While we will present here a general overview of the global management of patients with MBD, this conceptual framework will be adopted and validated in the evidence-based, disease-specific guidelines under development by the IWG.

Identifiants

pubmed: 31942541
doi: 10.1097/HS9.0000000000000286
pii: HemaSphere-2019-0075
pmc: PMC6919472
doi:

Types de publication

Review

Langues

eng

Pagination

e286

Subventions

Organisme : NHLBI NIH HHS
ID : P01 HL144457
Pays : United States

Informations de copyright

Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the European Hematology Association.

Déclaration de conflit d'intérêts

The authors have indicated they have no potential conflicts of interest to disclose.

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Auteurs

Francesco Rodeghiero (F)

Hematology Project Foundation, Vicenza, Italy, affiliated to the Hematology Department, San Bortolo Hospital, Vicenza, Italy.

Ingrid Pabinger (I)

Clinical Division of Hematology and Hemostaseology, Department of Medicine I, Medical University of Vienna, Austria.

Margaret Ragni (M)

Department of Medicine - Division Hematology/Oncology, University of Pittsburgh Medical Center Hemophilia Center of Western PA, Pittsburgh, USA.

Rezan Abdul-Kadir (R)

Department of Obstetrics and Gynecology and Katharine Dormandy Hemophilia and Thrombophilia Centre, The Royal Free Foundation Hospital and University College London, London, UK.

Erik Berntorp (E)

Department of Translational Medicine & Centre for Thrombosis and Hemostasis, Lund University, Malmö, Sweden.

Victor Blanchette (V)

Department of Pediatrics, University of Toronto and Division of Hematology/Oncology, Hospital for Sick Children, Toronto, Canada.

Imre Bodó (I)

3rd Dept of Internal Medicine, Semmelweis University, Budapest, Hungary.

Alessandro Casini (A)

Division of Angiology and Hemostasis, Faculty of Medicine, University Hospitals of Geneva, Switzerland.

Paolo Gresele (P)

Department of Medicine - Section of Internal and Cardiovascular Medicine jUniversity of Perugia, Perugia, Italy.

Riitta Lassila (R)

Coagulation Disorders Unit, Department of Haematology, Research Program in Oncology, Helsinki University Hospital;, Helsinki, Finland.

Frank Leebeek (F)

Department of Haematology, Erasmus University Medical Center, Rotterdam, the Netherlands.

David Lillicrap (D)

Department of Pathology and Molecular Medicine, Queen's University, Kingston, Canada.

Diego Mezzano (D)

Department of Hematology-Oncology, School of Medicine, Pontificia Universidad Católica de Chile.

Patrizia Noris (P)

Department of Internal Medicine and Medical Therapy, University of Pavia and Department of Medical Sciences and Infectious Diseases, IRCCS Policlinico San Matteo Foundation, Pavia, Italy.

Alok Srivastava (A)

Department of Haematology, Christian Medical College, Vellore, India.

Alberto Tosetto (A)

Hemophilia and Thrombosis Center, Hematology Department, S. Bortolo Hospital, Vicenza, Italy.

Jerzy Windyga (J)

Department of Hemostasis Disorders and Internal Medicine, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.

Barbara Zieger (B)

Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Center - University of Freiburg, Faculty of Medicine, Germany.

Mike Makris (M)

Sheffield Hemophilia and Thrombosis Centre, Royal Hallamshire Hospital, Sheffield, UK.

Nigel Key (N)

Department of Medicine, Division of Heamtology-Oncology, University of North Carolina at Chapel Hill, NC, USA.

Classifications MeSH