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Bleeding Severity and Phenotype in 22q11.2 Deletion Syndrome—A Cross-Sectional Investigation - 22/07/21

Doi : 10.1016/j.jpeds.2021.03.071 
Priyal O. Patel, DO 1, 2, Adriane L. Baylis, PhD 2, 3, Scott E. Hickey, MD 2, 4, Joseph Stanek, MS 1, Richard E. Kirschner, MD 2, 3, Margaret L. Rand, PhD 5, 6, Riten Kumar, MD 7, 8,
1 Division of Hematology-Oncology-Blood and Marrow Transplantation, Nationwide Children's Hospital, Columbus, OH 
2 Department of Pediatrics, The Ohio State University, Columbus, OH 
3 Department of Plastic and Reconstructive Surgery, Nationwide Children's Hospital, Columbus, OH 
4 Division of Genetic and Genomic Medicine, Nationwide Children's Hospital, Columbus, OH 
5 Departments of Laboratory Medicine & Pathobiology, Biochemistry, and Pediatrics, University of Toronto, Toronto, Ontario, Canada 
6 Translational Medicine, Research Institute, Division of Hematology/Oncology, The Hospital for Sick Children, Toronto, Ontario, Canada 
7 Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA 
8 Department of Pediatrics, Harvard Medical School, Boston, MA 

Reprint requests: Riten Kumar, MD, MSc, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, 300 Longwood Ave, Boston, MA 02115Dana-Farber/Boston Children's Cancer and Blood Disorders Center300 Longwood AveBostonMA02115

Abstract

Objectives

To prospectively quantify bleeding severity and elaborate hemorrhagic symptoms in children with 22q11.2 deletion syndrome (22q11DS) using 2 validated bleeding assessment tools (BATs), namely the Pediatric Bleeding Questionnaire and the International Society on Thrombosis and Hemostasis BAT (ISTH-BAT). We also sought to compare subjects’ bleeding scores to unaffected first-degree family members.

Study design

Children with 22q11DS and unaffected first-degree family members were recruited for the study. Two validated BATs were administered by a pediatric hematologist. Additional clinical and laboratory data were abstracted from patient medical records. Standard descriptive and nonparametric statistical methods were used.

Results

In total, 29 eligible subjects and controls were assessed. Median age (range) of subjects and controls was 8 (5-17) years and 38 (9-56) years, respectively. In total, 17 of 29 subjects had a positive bleeding score on ISTH-BAT compared with 1 of 29 control patients (P < .0001). Median ISTH-BAT score in subjects was 3 (0-12), compared with 2 (0-6) in control patients (P = .022). Median Pediatric Bleeding Questionnaire score in subjects was 2 (−1 to 12). The most frequent bleeding symptoms reported in subjects with 22q11DS were epistaxis (69%) and bruising (52%). Eighteen subjects had been surgically challenged, and 6 were noted to have increased perioperative hemorrhage.

Conclusions

Children with 22q11DS have increased bleeding scores compared with their first-degree unaffected relatives. The majority of the bleeding symptoms described were mucocutaneous.

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Abbreviations : 22q11DS, AVWS, BAT, BSS, CD, CNS, ISTH-BAT, MPV, PBQ, PFA-100, VWD, VWF


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 The authors declare no conflicts of interest.


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Vol 235

P. 220-225 - agosto 2021 Ritorno al numero
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