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Bleeding risk of surgery and its prevention in patients with inherited platelet disorders.
Orsini, Sara; Noris, Patrizia; Bury, Loredana; Heller, Paula G; Santoro, Cristina; Kadir, Rezan A; Butta, Nora C; Falcinelli, Emanuela; Cid, Ana Rosa; Fabris, Fabrizio; Fouassier, Marc; Miyazaki, Koji; Lozano, Maria Luisa; Zúñiga, Pamela; Flaujac, Claire; Podda, Gian Marco; Bermejo, Nuria; Favier, Remi; Henskens, Yvonne; De Maistre, Emmanuel; De Candia, Erica; Mumford, Andrew D; Ozdemir, Gul Nihal; Eker, Ibrahim; Nurden, Paquita; Bayart, Sophie; Lambert, Michele P; Bussel, James; Zieger, Barbara; Tosetto, Alberto; Melazzini, Federica; Glembotsky, Ana C; Pecci, Alessandro; Cattaneo, Marco; Schlegel, Nicole; Gresele, Paolo.
Afiliación
  • Orsini S; Department of Medicine, Section of Internal and Cardiovascular Medicine, University of Perugia, Italy.
  • Noris P; Department of Internal Medicine, IRCCS Policlinico S. Matteo Foundation, University of Pavia, Italy.
  • Bury L; Department of Medicine, Section of Internal and Cardiovascular Medicine, University of Perugia, Italy.
  • Heller PG; Hematología Investigación, Instituto de Investigaciones Médicas Alfredo Lanari, Universidad de Buenos Aires, CONICET, Argentina.
  • Santoro C; La Sapienza University of Rome, Italy.
  • Kadir RA; Haemophilia Centre and Haemostasis Unit, Royal Free Hospital, London, UK.
  • Butta NC; Unidad de Hematología, Hospital Universitario La Paz-IDIPaz, Madrid, Spain.
  • Falcinelli E; Department of Medicine, Section of Internal and Cardiovascular Medicine, University of Perugia, Italy.
  • Cid AR; Department of Medicine, Section of Internal and Cardiovascular Medicine, University of Perugia, Italy.
  • Fabris F; Clinica Medica 1 - Medicina Interna CLOPD, Dipartimento Assistenziale Integrato di Medicina, Azienda-Ospedale Università di Padova and Dipartimento di Medicina, Università di Padova, Italy.
  • Fouassier M; Consultations d'Hémostase - CRTH, CHU de Nantes, France.
  • Miyazaki K; Department of Hematology, Kitasato University School of Medicine, Sagamihara, Japan.
  • Lozano ML; 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 Sa
  • Zúñiga P; Department of Hematology-Oncology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Flaujac C; Service d'Hématologie Biologique Cochin Hospital, Paris, France.
  • Podda GM; Medicina III, ASST Santi Paolo e Carlo, Dipartimento di Scienze della Salute, Università degli Studi di Milano, Italy.
  • Bermejo N; Department of Hematology, Hospital San Pedro de Alcántara, Cáceres, Spain.
  • Favier R; Assistance Publique-Hôpitaux de Paris, Armand Trousseau Children's Hospital, French Reference Centre for Inherited Platelet Disorders, Paris, France.
  • Henskens Y; Hematological Laboratory, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • De Maistre E; Department of Biology and Haematology, Centre Hospitalier Universitaire Dijon, France.
  • De Candia E; Hemostasis and Thrombosis Unit, Institute of Internal Medicine, Policlinico Agostino Gemelli-Università Cattolica Sacro Cuore, Rome, Italy.
  • Mumford AD; School of Clinical Sciences, University of Bristol, UK.
  • Ozdemir GN; Cerrahpasa Medical Faculty, Pediatric Hematology Department, Istanbul, Turkey.
  • Eker I; Gülhane Military Medical Faculty, Pediatric Hematology Department, Ankara, Turkey.
  • Nurden P; Reference Centre for Platelet Disorders, Bordeaux University Hospital Centre, Rythmology and Cardiac Modeling Institute (LIRYC), Xavier Arnozan Hospital, Pessac, France.
  • Bayart S; Centre Régional de Traitement des Hémophiles, Centre Hospitalier Universitaire de Rennes, France.
  • Lambert MP; 1 Division of Hematology, Department of Pediatrics, Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PN, USA.
  • Bussel J; Department of Pediatrics, Division of Hematology, Weill Cornell Medicine, New York, NY, USA.
  • Zieger B; Department of Pediatrics and Adolescent Medicine, University Medical Center Freiburg, Germany.
  • Tosetto A; Hematology Department, S. Bortolo Hospital, Vicenza, Italy.
  • Melazzini F; Department of Internal Medicine, IRCCS Policlinico S. Matteo Foundation, University of Pavia, Italy.
  • Glembotsky AC; Hematología Investigación, Instituto de Investigaciones Médicas Alfredo Lanari, Universidad de Buenos Aires, CONICET, Argentina.
  • Pecci A; Department of Internal Medicine, IRCCS Policlinico S. Matteo Foundation, University of Pavia, Italy.
  • Cattaneo M; Medicina III, ASST Santi Paolo e Carlo, Dipartimento di Scienze della Salute, Università degli Studi di Milano, Italy.
  • Schlegel N; Centre de Référence des Pathologies Plaquettaires (CRPP), Service d'Hématologie Biologique, CHU Robert Debré, AP-HP, Paris, France.
  • Gresele P; Department of Medicine, Section of Internal and Cardiovascular Medicine, University of Perugia, Italy paolo.gresele@unipg.it.
Haematologica ; 102(7): 1192-1203, 2017 07.
Article en En | MEDLINE | ID: mdl-28385783
ABSTRACT
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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Procedimientos Quirúrgicos Operativos / Trastornos de las Plaquetas Sanguíneas / Hemorragia Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Haematologica Año: 2017 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Procedimientos Quirúrgicos Operativos / Trastornos de las Plaquetas Sanguíneas / Hemorragia Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Haematologica Año: 2017 Tipo del documento: Article País de afiliación: Italia