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Two-year outcomes following a randomised platelet transfusion trial in preterm infants

Abstract:
Objective: Assess mortality and neurodevelopmental outcomes at 2 years of corrected age in children who participated in the PlaNeT-2/MATISSE (Platelets for Neonatal Transfusion - 2/Management of Thrombocytopenia in Special Subgroup) study, which reported that a higher platelet transfusion threshold was associated with significantly increased mortality or major bleeding compared to a lower one. Design: Randomised clinical trial, enrolling from June 2011 to August 2017. Follow-up was complete by January 2020. Caregivers were not blinded; however, outcome assessors were blinded to treatment group. Setting: 43 level II/III/IV neonatal intensive care units (NICUs) across UK, Netherlands and Ireland. Patients: 660 infants born at less than 34 weeks' gestation with platelet counts less than 50×109/L. Interventions: Infants were randomised to undergo a platelet transfusion at platelet count thresholds of 50×109/L (higher threshold group) or 25×109/L (lower threshold group). Main outcomes measures: Our prespecified long-term follow-up outcome was a composite of death or neurodevelopmental impairment (developmental delay, cerebral palsy, seizure disorder, profound hearing or vision loss) at 2 years of corrected age. Results: Follow-up data were available for 601 of 653 (92%) eligible participants. Of the 296 infants assigned to the higher threshold group, 147 (50%) died or survived with neurodevelopmental impairment, as compared with 120 (39%) of 305 infants assigned to the lower threshold group (OR 1.54, 95% CI 1.09 to 2.17, p=0.017). Conclusions: Infants randomised to a higher platelet transfusion threshold of 50×109/L compared with 25×109/L had a higher rate of death or significant neurodevelopmental impairment at a corrected age of 2 years. This further supports evidence of harm caused by high prophylactic platelet transfusion thresholds in preterm infants. Trial registration number: ISRCTN87736839
Publication status:
Published
Peer review status:
Peer reviewed

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Role:
Author
ORCID:
0000-0003-4164-3195
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Role:
Author
ORCID:
0000-0002-5831-5959
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Role:
Author
ORCID:
0009-0009-1437-7953


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Funder identifier:
10.13039/100009033
Grant:
BS06/1
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Funder identifier:
10.13039/100018270
Grant:
Aspire 2020
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Funder identifier:
10.13039/501100012023
Grant:
PPOC-12-012027
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Funder identifier:
10.13039/501100000272


Publisher:
BMJ Publishing Group
Journal:
Archives of Disease in Childhood. Fetal and Neonatal Edition More from this journal
Volume:
108
Issue:
5
Pages:
fetalneonatal-2022
Publication date:
2023-02-21
DOI:
EISSN:
1468-2052
ISSN:
1359-2998


Language:
English
Keywords:
Pubs id:
1331615
Local pid:
pubs:1331615
Source identifiers:
W4321613064
Deposit date:
2026-05-05
ARK identifier:
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