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Pathogen-reduced platelets in pediatric and neonatal patients: Demographics, transfusion rates, and transfusion
Baia Lasky1, Joseph Nolasco2, Jazmin Graff3
1Division of Biomedical Services, American Red Cross, Biomedical Services, Washington, District of Columbia, USA.
Insights
Pathogen-reduced platelets (PR PLT) are safe for pediatric transfusions. This study found no increased risk of transfusion reactions in children receiving PR PLT compared to conventional platelets.
Area of Science:
- Hematology
- Transfusion Medicine
- Pediatric Medicine
Background:
- Pathogen-reduced platelets (PR PLT) are increasingly used to prevent transfusion-transmitted infections (TTIs).
- Hesitancy exists regarding PR PLT use in pediatric populations due to limited data.
- This study addresses the safety and efficacy of PR PLT in children.
Purpose of the Study:
- To evaluate the safety and transfusion reaction rates of PR PLT in pediatric and neonatal patients.
- To compare transfusion outcomes between PR PLT and conventional (CONV) platelets in young patients.
Main Methods:
- Retrospective review of patients under 18 years old receiving platelet transfusions.
- Comparison of PR PLT and CONV PLT use and associated transfusion reactions over a 300-day period.
- Statistical analysis using Fisher Exact Test to determine significance.
Main Results:
- 191 patients received 1010 platelet units; 68 received PR PLT only, 56 received CONV PLT only.
- Patients with hematologic malignancies received the most transfusions, often of both types.
- No significant difference in transfusion reactions between PR PLT (5/506 units) and CONV PLT (2/386 units); p=0.7052. No TTIs identified.
Conclusions:
- PR PLT can be safely transfused to pediatric and neonatal patients.
- There is no increased risk of acute adverse events with PR PLT compared to CONV PLT in this population.
- This study supports the expanded use of PR PLT in pediatric transfusion medicine.
Background:
Pathogen-reduced platelets (PR PLT) are the emerging standard for proactive transfusion-transmitted infection (TTI) mitigation. There is, however, continued hesitation to transfuse PR PLT in children due to limited published data. We report demographics, rates of transfusion, and transfusion reactions (TR) associated with FDA-approved PR PLT in pediatric and neonatal patients at an academic medical center.
Methods:
Retrospective review was performed for patients <18 years receiving at least one platelet over a 300-day period at a large, tertiary care hospital. Patients were transfused PR or conventional (CONV) PLT, based on inventory availability. Statistical analysis was performed using Fisher Exact Test.
Results:
During the study period, 191 patients received 1010 platelet transfusions (892 units). Sixty-eight patients received PR PLT only (1.3 units/patient, 95% confidence interval [CI] 1.1-1.5; 1.8 transfusions/patient, 95% CI 1.4-2.2), and 56 patients received CONV PLT only (1.4 units/patient, 95% CI 1.1-1.7; 1.6 transfusions/patient, 95% CI 1.3-1.9). Patients with hematologic malignancies undergoing chemotherapy/radiation and allogeneic hematopoietic stem cell transplant received the most platelet transfusions and more commonly received both platelet types. Of 506 PR PLT units, 5 TRs occurred; 386 CONV PLT resulted in two TRs (p = .7052). Of 51 neonates, 37 received PR PLT without adverse events, including 13 receiving phototherapy. No TTIs were identified in any group.
Conclusion:
There was no significant difference in rates of transfusion or TRs between PR and CONV PLT. Our study provides additional evidence that PR PLT can be transfused to pediatric and neonatal patients without increasing the risk of acute adverse events.
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