4.7 Article

Bleeding risks are higher in children versus adults given prophylactic platelet transfusions for treatment-induced hypoproliferative thrombocytopenia

Journal

BLOOD
Volume 120, Issue 4, Pages 748-760

Publisher

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2011-11-389569

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Funding

  1. National Heart, Lung, and Blood Institute of the National Institutes of Health to the Data Coordinating Center at New England Research Institutes [HL072268]
  2. Case Western Reserve University [HL072033]
  3. Children's Hospital Boston [HL072291]
  4. Cornell University [HL072196]
  5. Duke University [HL072291]
  6. Emory University [HL072248]
  7. Johns Hopkins University [HL072191]
  8. Massachusetts General Hospital [HL072299]
  9. Puget Sound Blood Center [HL072305]
  10. Tulane [HL072274]
  11. University of Iowa [HL072028]
  12. University of Maryland [HL072359]
  13. University of Minnesota [HL072027]
  14. University of North Carolina [HL072355]
  15. University of Oklahoma [HL072283]
  16. University of Pennsylvania [HL072346]
  17. University of Pittsburgh [HL072331]
  18. Blood Center of Wisconsin [HL072290]

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Age-group analyses were conducted of patients in the prophylactic platelet dose trial (PLADO), which evaluated the relation between platelet dose per transfusion and bleeding. Hospitalized patients with treatment-induced hypoproliferative thrombocytopenia were randomly assigned to 1 of 3 platelet doses: 1.1 x 10(11), 2.2 x 10(11), or 4.4 x 10(11) platelets/m(2) per transfusion, given for morning counts of <= 10 000 platelets/mu L. Daily hemostatic assessments were performed. The primary end point (percentage of patients who developed grade 2 or higher World Health Organization bleeding) was evaluated in 198 children (0-18 years) and 1044 adults. Although platelet dose did not predict bleeding for any age group, children overall had a significantly higher risk of grade 2 or higher bleeding than adults (86%, 88%, 77% vs 67% of patients aged 0-5 years, 6-12 years, 13-18 years, vs adults, respectively) and more days with grade 2 or higher bleeding (median, 3 days in each pediatric group vs 1 day in adults; P < .001). The effect of age on bleeding differed by disease treatment category and was most pronounced among autologous transplant recipients. Pediatric subjects were at higher risk of bleeding over a wide range of platelet counts, indicating that their excess bleeding risk may be because of factors other than platelet counts. This trial was registered at www.clinicaltrials.gov as #NCT00128713. (Blood. 2012; 120(4):748-760)

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