Standardization of bleeding assessment in immune thrombocytopenia: report from the International Working Group

Author:

Rodeghiero Francesco1,Michel Marc2,Gernsheimer Terry3,Ruggeri Marco1,Blanchette Victor4,Bussel James B.5,Cines Douglas B.6,Cooper Nichola7,Godeau Bertrand2,Greinacher Andreas8,Imbach Paul9,Khellaf Mehdi2,Klaassen Robert J.10,Kühne Thomas9,Liebman Howard11,Mazzucconi Maria Gabriella12,Newland Adrian13,Pabinger Ingrid14,Tosetto Alberto1,Stasi Roberto15

Affiliation:

1. Department of Cell Therapy and Hematology, San Bortolo Hospital, Vicenza, Italy;

2. Universitè Paris-Est Crétéil, Assistance Publique Hôpitaux de Paris, Hopital Henri Mondor, Department of Internal Medicine, Creteil, France;

3. Puget Sound Blood Center, University of Washington School of Medicine, Spokane, WA;

4. Division of Hematology/Oncology, The Hospital for Sick Children, Department of Pediatrics, University of Toronto, Toronto, ON, Canada;

5. Division of Pediatric Hematology/Oncology, Weill Medical College of Cornell University, New York, NY;

6. Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA;

7. Department of Hematology, Imperial College NHS Trust, Hammersmith Hospital, London, United Kingdom;

8. Department of Immunology and Transfusion Medicine, Ernst-Moritz-Arndt-University, Greifswald, Germany;

9. University Children’s Hospital Basel, Pediatric Oncology/Hematology, Basel, Switzerland;

10. Children’s Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canada;

11. Jane Anne Nohl Division of Hematology and Center for the Study of Blood Diseases, Los Angeles, CA;

12. Department of Cellular Biotechnology and Hematology, La Sapienza University, Rome, Italy;

13. Pathology Clinical Academic Unit-Barts and the London NHS Trust, London, United Kingdom;

14. Division of Haematology and Haemostaseology, Department of Medicine I, Medical University, Vienna, Austria; and

15. Department of Haematology, St. George’s Hospital NHS Trust, London, United Kingdom

Abstract

Abstract In a previous publication on new terminology, definitions, and outcome criteria for immune thrombocytopenia (ITP), the International Working Group (IWG) on ITP acknowledged that response to treatment should consist of clinically meaningful end points such as bleeding manifestations and that platelet count may not be the ideal parameter for capturing the benefits of therapy. The IWG now proposes a consensus-based ITP-specific bleeding assessment tool (ITP-BAT) with definitions and terminology consistent with those adopted for other bleeding disorders. Bleeding manifestations were grouped into three major domains: skin (S), visible mucosae (M), and organs (O), with gradation of severity (SMOG). Each bleeding manifestation is assessed at the time of examination. Severity is graded from 0 to 3 or 4, with grade 5 for any fatal bleeding. Bleeding reported by the patient without medical documentation is graded 1. Within each domain, the same grade is assigned to bleeding manifestations of similar clinical impact. The “worst bleeding manifestation since the last visit” (observation period) is graded (a suitable database collection form is provided), and the highest grade within each domain is recorded. The SMOG system provides a consistent description of the bleeding phenotype in ITP, and the IWG unanimously supports its adoption and validation in future clinical studies.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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