TY - JOUR
T1 - Dynamic prediction of bleeding risk in thrombocytopenic preterm neonates
AU - Fustolo-Gunnink, Susanna F
AU - Fijnvandraat, Karin
AU - Putter, Hein
AU - Ree, Isabelle M
AU - Caram-Deelder, Camila
AU - Andriessen, Peter
AU - d'Haens, Esther J
AU - Hulzebos, Christian V
AU - Onland, Wes
AU - Kroon, André A
AU - Vijlbrief, Daniël C
AU - Lopriore, Enrico
AU - van der Bom, Johanna G
N1 - Funding Information:
1Sanquin/LUMC, Center for Clinical Transfusion Research, Leiden; 2Amsterdam University Medical Center, Emma Children’s Hospital, Department ofPediatric Hematology, Amsterdam-Zuidoost; 3Sanquin Blood Supply Foundation, Department ofPlasma Proteins, Sanquin Research, Amsterdam; 4Leiden University Medical Center, Department ofMedical Statistics, Leiden; 5Leiden University Medical Center, Willem Alexander Children’s Hospital, Department ofNeonatology, Leiden; 6Máxima Medical Center, Department of Neonatology, Veldhoven; 7Isala Zwolle, Amalia Children’s Center, Department of Neonatology, Zwolle; 8University Medical Center Groningen, Beatrix Children’s Hospital, Department ofNeonatology, Groningen; 9Amsterdam University Medical Center, Emma Children’s Hospital, Department ofNeonatology, Amsterdam-Zuidoost; 10Erasmus Medical Center, Sophia Children’s Hospital, Department ofNeonatology, Rotterdam; 11University Medical Center Utrecht, Utrecht University, Wilhelmina Children’s Hospital, Department of Neonatology, Utrecht and 12Leiden University Medical Center, Department ofClinical Epidemiology, Leiden, the Netherlands.
Publisher Copyright:
© 2019 Ferrata Storti Foundation.
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2019/10/30
Y1 - 2019/10/30
N2 - Over 75% of severely thrombocytopenic neonates receive platelet transfusions, though little evidence supports this practice, and only 10% develop major bleeding. In a recent randomized trial, giving platelet transfusions at a threshold platelet count of 50x109/L compared to a threshold of 25x109/L was associated with an increased risk of major bleeding or mortality. This finding highlights the need for improved and individualized guidelines on neonatal platelet transfusion, which require accurate prediction of bleeding risk. Therefore, the objective of this study was to develop a dynamic prediction model for major bleeding in thrombocytopenic preterm neonates. This model allows for calculation of bleeding risk at any time-point during the first week after the onset of severe thrombocytopenia. In this multicenter cohort study, we included neonates with a gestational age <34 weeks, admitted to a neonatal intensive care unit, who developed severe thrombocytopenia (platelet count <50×10
9/L). The study endpoint was major bleeding. We obtained predictions of bleeding risk using a proportional baselines landmark supermodel. Of 640 included neonates, 71 (11%) had a major bleed. We included the variables gestational age, postnatal age, intrauterine growth retardation, necrotizing enterocolitis, sepsis, platelet count and mechanical ventilation in the model. The median cross-validated c-index was 0.74 (interquartile range, 0.69-0.82). This is a promising dynamic prediction model for bleeding in this population that should be explored further in clinical studies as a potential instrument for supporting clinical decisions.
AB - Over 75% of severely thrombocytopenic neonates receive platelet transfusions, though little evidence supports this practice, and only 10% develop major bleeding. In a recent randomized trial, giving platelet transfusions at a threshold platelet count of 50x109/L compared to a threshold of 25x109/L was associated with an increased risk of major bleeding or mortality. This finding highlights the need for improved and individualized guidelines on neonatal platelet transfusion, which require accurate prediction of bleeding risk. Therefore, the objective of this study was to develop a dynamic prediction model for major bleeding in thrombocytopenic preterm neonates. This model allows for calculation of bleeding risk at any time-point during the first week after the onset of severe thrombocytopenia. In this multicenter cohort study, we included neonates with a gestational age <34 weeks, admitted to a neonatal intensive care unit, who developed severe thrombocytopenia (platelet count <50×10
9/L). The study endpoint was major bleeding. We obtained predictions of bleeding risk using a proportional baselines landmark supermodel. Of 640 included neonates, 71 (11%) had a major bleed. We included the variables gestational age, postnatal age, intrauterine growth retardation, necrotizing enterocolitis, sepsis, platelet count and mechanical ventilation in the model. The median cross-validated c-index was 0.74 (interquartile range, 0.69-0.82). This is a promising dynamic prediction model for bleeding in this population that should be explored further in clinical studies as a potential instrument for supporting clinical decisions.
UR - http://www.scopus.com/inward/record.url?scp=85071356195&partnerID=8YFLogxK
U2 - 10.3324/haematol.2018.208595
DO - 10.3324/haematol.2018.208595
M3 - Article
C2 - 30819913
SN - 0390-6078
VL - 104
SP - 2300
EP - 2306
JO - Haematologica
JF - Haematologica
IS - 11
ER -