The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology
; Santoro, Cristina ; Cid, Ana Rosa ; Orsini, Sara ; Fontana, Pierre ; De Candia, Erica ; Podda, Gianmarco ; Kannan, Meganathan ; Jurk, Kerstin ; Castaman, Giancarlo ; Falaise, Céline ; Guglielmini, Giuseppe ; Noris, Patrizia ; Zaninetti, Carlo ; Fiore, Mathieu ; Tosseto, Alberto ; Zuñiga, Pamela ; Miyazaki, K. ; Dupuis, Arnaud ; Hayward, Catherine ; Casonatto, Alessandra ; Grandone, Elvira ; Mazzuconi Maria Gabriella ; James, Paula ; Fabris, Fabrizio ; Henskens, Yvonne ; Napolitano, Mariasanta ; Curnow, Jennifer ; Gkalea, Vasiliki ; Fedor, Marian ; Lambert, Michele P. ; Zieger, Barbara ; Barcella, Luca ; Cosmi, Benilde ; Giordano, Paola ; Porri, Claudia ; Melazzini, Federica ; Abid, Madiha ; Glembotsky, Ana Claudia
; Ferrara, Gracia ; Russo, Alessandra ; Deckmyn, Hans ; Frelinger, Andrew L. ; Harrison, Paul ; Mezzano, Diego ; Mumford, Andrew D. ; Lordkipanidzé, Marie Otros responsables
Fecha
05/2021
Editorial
Wiley Blackwell Publishing, Inc
Revista
Journal of Thrombosis and Haemostasis
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1538-7933
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Resumen
Background: The ISTH Bleeding Assessment Tool (ISTH-BAT) has been validated for clinical screening of suspected von Willebrand disease (VWD) and for bleeding prediction. Recently it has been validated for subjects with inherited platelet disorders (IPD) (BAT-VAL study). Objectives: To determine whether the ISTH-BAT bleeding score (BS) predicts subsequent bleeding events requiring treatment in IPD patients. Methods: Patients with IPD, type 1 VWD (VWD-1) and age- and sex-matched healthy controls enrolled in the BAT-VAL study were prospectively followed-up for 2 years and bleeding episodes requiring treatment were recorded. Results: Of the 1098 subjects initially enrolled, 955 were followed-up and 124 suffered hemorrhages during follow-up, 60% of whom had inherited platelet function disorders (IPFD). Total number of events was significantly higher in IPFD (n = 235) than VWD-1 (n = 52) or inherited thrombocytopenia (IT; n = 20). Events requiring transfusions were 66% in IPFD, 5.7% in VWD-1, and 3% in IT. Baseline BS was significantly higher in IPFD patients with a bleeding event at follow-up than in those without (p <.01) and the percentage of subjects suffering a bleeding event increased proportionally to baseline BS quartile. A significant association between the BS and the chance of suffering severe bleeding was found in the overall, IPFD, and VWD-1 populations. Similar results were obtained for the pediatric population. Conclusions: Inherited platelet function disorder patients with high BS at enrollment are more likely to suffer from bleeding events requiring treatment at follow-up. Moreover, the higher the baseline BS quartile the greater the incidence of subsequent events, suggesting that independently from diagnosis a high BS is associated with a greater risk of subsequent hemorrhage.
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