Bleeding risk of surgery and its prevention in patients with inherited platelet disorders
Sara Orsini,
Patrizia Noris,
Loredana Bury,
Paula G. Heller,
Cristina Santoro,
Rezan A. Kadir,
Nora C. Butta,
Emanuela Falcinelli,
Ana Rosa Cid,
Fabrizio Fabris,
Marc Fouassier,
Koji Miyazaki,
Maria Luisa Lozano,
Pamela Zúñiga,
Claire Flaujac,
Gian Marco Podda,
Nuria Bermejo,
Remi Favier,
Yvonne Henskens,
Emmanuel De Maistre,
Erica De Candia,
Andrew D. Mumford,
Gul Nihal Ozdemir,
Ibrahim Eker,
Paquita Nurden,
Sophie Bayart,
Michele P. Lambert,
James Bussel,
Barbara Zieger,
Alberto Tosetto,
Federica Melazzini,
Ana C. Glembotsky,
Alessandro Pecci,
Marco Cattaneo,
Nicole Schlegel,
Paolo Gresele
Affiliations
Sara Orsini
Department of Medicine, Section of Internal and Cardiovascular Medicine, University of Perugia, Italy
Patrizia Noris
Department of Internal Medicine, IRCCS Policlinico S. Matteo Foundation, University of Pavia, Italy
Loredana Bury
Department of Medicine, Section of Internal and Cardiovascular Medicine, University of Perugia, Italy
Paula G. Heller
Hematología Investigación, Instituto de Investigaciones Médicas Alfredo Lanari, Universidad de Buenos Aires, CONICET, Argentina
Cristina Santoro
La Sapienza University of Rome, Italy
Rezan A. Kadir
Haemophilia Centre and Haemostasis Unit, Royal Free Hospital, London, UK
Nora C. Butta
Unidad de Hematología, Hospital Universitario La Paz-IDIPaz, Madrid, Spain
Emanuela Falcinelli
Department of Medicine, Section of Internal and Cardiovascular Medicine, University of Perugia, Italy
Ana Rosa Cid
Department of Medicine, Section of Internal and Cardiovascular Medicine, University of Perugia, Italy
Fabrizio Fabris
Clinica Medica 1 - Medicina Interna CLOPD, Dipartimento Assistenziale Integrato di Medicina, Azienda-Ospedale Università di Padova and Dipartimento di Medicina, Università di Padova, Italy
Marc Fouassier
Consultations d’Hémostase – CRTH, CHU de Nantes, France
Koji Miyazaki
Department of Hematology, Kitasato University School of Medicine, Sagamihara, Japan
Maria Luisa Lozano
Servicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguery Centro Regional de Hemodonación, IMIB-Arrixaca, Universidad de Murcia, Murcia 30003 and Grupo de Investigación CB15/00055 del Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain
Pamela Zúñiga
Department of Hematology-Oncology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile
Claire Flaujac
Service d’Hématologie Biologique Cochin Hospital, Paris, France
Gian Marco Podda
Medicina III, ASST Santi Paolo e Carlo, Dipartimento di Scienze della Salute, Università degli Studi di Milano, Italy
Nuria Bermejo
Department of Hematology, Hospital San Pedro de Alcántara, Cáceres, Spain
Remi Favier
Assistance Publique-Hôpitaux de Paris, Armand Trousseau Children’s Hospital, French Reference Centre for Inherited Platelet Disorders, Paris, France
Yvonne Henskens
Hematological Laboratory, Maastricht University Medical Centre, Maastricht, The Netherlands
Emmanuel De Maistre
Department of Biology and Haematology, Centre Hospitalier Universitaire Dijon, France
Erica De Candia
Hemostasis and Thrombosis Unit, Institute of Internal Medicine, Policlinico Agostino Gemelli-Università Cattolica Sacro Cuore, Rome, Italy
Andrew D. Mumford
School of Clinical Sciences, University of Bristol, UK
Gul Nihal Ozdemir
Cerrahpasa Medical Faculty, Pediatric Hematology Department, Istanbul, Turkey
Ibrahim Eker
Gülhane Military Medical Faculty, Pediatric Hematology Department, Ankara, Turkey
Paquita Nurden
Reference Centre for Platelet Disorders, Bordeaux University Hospital Centre, Rythmology and Cardiac Modeling Institute (LIRYC), Xavier Arnozan Hospital, Pessac, France
Sophie Bayart
Centre Régional de Traitement des Hémophiles, Centre Hospitalier Universitaire de Rennes, France
Michele P. Lambert
1st Division of Hematology, Department of Pediatrics, Children’s Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PN, USA
James Bussel
Department of Pediatrics, Division of Hematology, Weill Cornell Medicine, New York, NY, USA
Barbara Zieger
Department of Pediatrics and Adolescent Medicine, University Medical Center Freiburg, Germany
Alberto Tosetto
Hematology Department, S. Bortolo Hospital, Vicenza, Italy
Federica Melazzini
Department of Internal Medicine, IRCCS Policlinico S. Matteo Foundation, University of Pavia, Italy
Ana C. Glembotsky
Hematología Investigación, Instituto de Investigaciones Médicas Alfredo Lanari, Universidad de Buenos Aires, CONICET, Argentina
Alessandro Pecci
Department of Internal Medicine, IRCCS Policlinico S. Matteo Foundation, University of Pavia, Italy
Marco Cattaneo
Medicina III, ASST Santi Paolo e Carlo, Dipartimento di Scienze della Salute, Università degli Studi di Milano, Italy
Nicole Schlegel
Centre de Référence des Pathologies Plaquettaires (CRPP), Service d’Hématologie Biologique, CHU Robert Debré, AP-HP, Paris, France
Paolo Gresele
Department of Medicine, Section of Internal and Cardiovascular Medicine, University of Perugia, Italy
Excessive bleeding at surgery is a feared complication in patients with inherited platelet disorders. However, very few studies have evaluated the frequency of surgical bleeding in these hemorrhagic disorders. We performed a worldwide, multicentric, retrospective study to assess the bleeding complications of surgery, the preventive and therapeutic approaches adopted, and their efficacy in patients with inherited platelet disorders: the Surgery in Platelet disorders And Therapeutic Approach (SPATA) study. We rated the outcome of 829 surgical procedures carried out in 423 patients with well-defined forms of inherited platelet disorders: 238 inherited platelet function disorders and 185 inherited platelet number disorders. Frequency of surgical bleeding was high in patients with inherited platelet disorders (19.7%), with a significantly higher bleeding incidence in inherited platelet function disorders (24.8%) than in inherited platelet number disorders (13.4%). The frequency of bleeding varied according to the type of inherited platelet disorder, with biallelic Bernard Soulier syndrome having the highest occurrence (44.4%). Frequency of bleeding was predicted by a pre-operative World Health Organization bleeding score of 2 or higher. Some types of surgery were associated with a higher bleeding incidence, like cardiovascular and urological surgery. The use of pre-operative pro-hemostatic treatments was associated with a lower bleeding frequency in patients with inherited platelet function disorders but not in inherited platelet number disorders. Desmopressin, alone or with antifibrinolytic agents, was the preventive treatment associated with the lowest bleedings. Platelet transfusions were used more frequently in patients at higher bleeding risk. Surgical bleeding risk in inherited platelet disorders is substantial, especially in inherited platelet function disorders, and bleeding history, type of disorder, type of surgery and female sex are associated with higher bleeding frequency. Prophylactic pre-operative pro-hemostatic treatments appear to be required and are associated with a lower bleeding incidence.