Lynn M Malec1, Charity G Moore, Carolyn M Bennett, Donald L Yee, Bryce A Kerlin, Char M Witmer, Roshni Kulkarni, Sweta Gupta, Sriya Gunawardena, Peter A Kouides, Deborah Brown, Margaret V Ragni. 1. *Children's Hospital of Pittsburgh, Hemophilia Center of Western PA ††Children's Hospital of Pittsburgh, University of Pittsburgh †Center for Healthcare Research Data Center, University of Pittsburgh School of Medicine ∥∥University of Pittsburgh, Hemophilia Center of Western PA, Pittsburgh ¶The Children's Hospital of Philadelphia, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA ‡Children's Healthcare of Atlanta at Scottish Rite, Emory University School of Medicine, Atlanta, GA §Texas Children's Hospital, Baylor College of Medicine §§University of Texas, Houston, TX ∥Nationwide Children's Hospital, The Ohio State University, Columbus, OH #Pediatrics & Human Development, Michigan State University, East Lansing, MI **Indiana Hemophilia & Thrombosis Center, Indianapolis, IN ‡‡Rochester General Hospital, Rochester, NY.
Abstract
BACKGROUND: The diagnosis of type 1 von Willebrand disease (VWD) presents a diagnostic challenge in children. In fact, 25% or more of children with VWD may be diagnosed only after they experience postoperative bleeding. We previously described a 4-variable composite score that has 92.5% sensitivity and 95% specificity for diagnosing VWD in children with known VWD when 2 of 4 criteria are positive: (1) Tosetto bleeding score ≥ 1; (2) family history of VWD; (3) personal history of iron deficiency anemia; and/or (4) positive James early bleeding score. The purpose of this study was to prospectively validate a composite score of ≥ 2 for identifying children with VWD. PROCEDURE: Children without a previously diagnosed bleeding disorder presenting for hematology evaluation were enrolled. Sensitivity, specificity, positive, and negative predictive value of the composite score was determined. RESULTS: A total of 193 subjects were enrolled from 12 participating centers were included in the analysis. Forty-seven children had type 1 VWD, including 11 with von Willebrand Ristocetin Cofactor (VWF):RCo < 30 IU/dL, 14 subjects with a VWF:RCo 30 to 39 IU/dL, and 22 with a VWF:RCo 40 to 49 IU/dL. Including all 4 variables, a composite score of ≥ 2 had a sensitivity of 63.6% to 76.0%, specificity of 33.5% to 35.1%, negative predictive value of 76.9% to 93.8%, and positive predictive value of 5.5% to 25%. CONCLUSIONS: The negative predictive value of the composite score was robust, especially at lower VWF:RCo suggesting that VWD testing could be eliminated in nearly a third of children referred for VWD testing.
BACKGROUND: The diagnosis of type 1 von Willebrand disease (VWD) presents a diagnostic challenge in children. In fact, 25% or more of children with VWD may be diagnosed only after they experience postoperative bleeding. We previously described a 4-variable composite score that has 92.5% sensitivity and 95% specificity for diagnosing VWD in children with known VWD when 2 of 4 criteria are positive: (1) Tosetto bleeding score ≥ 1; (2) family history of VWD; (3) personal history of iron deficiency anemia; and/or (4) positive James early bleeding score. The purpose of this study was to prospectively validate a composite score of ≥ 2 for identifying children with VWD. PROCEDURE: Children without a previously diagnosed bleeding disorder presenting for hematology evaluation were enrolled. Sensitivity, specificity, positive, and negative predictive value of the composite score was determined. RESULTS: A total of 193 subjects were enrolled from 12 participating centers were included in the analysis. Forty-seven children had type 1 VWD, including 11 with von Willebrand Ristocetin Cofactor (VWF):RCo < 30 IU/dL, 14 subjects with a VWF:RCo 30 to 39 IU/dL, and 22 with a VWF:RCo 40 to 49 IU/dL. Including all 4 variables, a composite score of ≥ 2 had a sensitivity of 63.6% to 76.0%, specificity of 33.5% to 35.1%, negative predictive value of 76.9% to 93.8%, and positive predictive value of 5.5% to 25%. CONCLUSIONS: The negative predictive value of the composite score was robust, especially at lower VWF:RCo suggesting that VWD testing could be eliminated in nearly a third of children referred for VWD testing.
Authors: Paula D James; Nathan T Connell; Barbara Ameer; Jorge Di Paola; Jeroen Eikenboom; Nicolas Giraud; Sandra Haberichter; Vicki Jacobs-Pratt; Barbara Konkle; Claire McLintock; Simon McRae; Robert R Montgomery; James S O'Donnell; Nikole Scappe; Robert Sidonio; Veronica H Flood; Nedaa Husainat; Mohamad A Kalot; Reem A Mustafa Journal: Blood Adv Date: 2021-01-12
Authors: Mohamad A Kalot; Nedaa Husainat; Sammy Tayiem; Abdallah El Alayli; Ahmad B Dimassi; Osama Diab; Omar Abughanimeh; Bader Madoukh; Aref Qureini; Barbara Ameer; Jorge Di Paola; Jeroen C J Eikenboom; Vicky Jacobs-Pratt; Claire McLintock; Robert Montgomery; James S O'Donnell; Robert Sidonio; Romina Brignardello-Petersen; Veronica Flood; Nathan T Connell; Paula D James; Reem A Mustafa Journal: Blood Adv Date: 2021-12-14
Authors: Erik Berntorp; Sonata S Trakymienė; Augusto B Federici; Katharina Holstein; Fernando F Corrales-Medina; Glenn F Pierce; Alok Srivastava; Mario von Depka Prondzinski; Jill M Johnsen; Irena P Zupan; Susan Halimeh; Vuokko Nummi; Jonathan C Roberts Journal: Haemophilia Date: 2022-07 Impact factor: 4.263