2016
DOI: 10.1111/trf.13332
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Efficacy and safety of pathogen‐reduced platelet concentrates in children with cancer: a retrospective cohort study

Abstract: In spite of lower numerical increase in PLT count, the hemostatic efficacy and safety of PR PLT transfusions was comparable with the control group. Adverse event rates did not differ between groups, but the sample size was relatively small.

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Cited by 18 publications
(13 citation statements)
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“…Our comparative study shows that neonates transfused with PLTs diluted in PAS and treated with riboflavin and UV light‐PRT require the transfusion of more PLTs than neonates receiving standard PLTs. Additionally, the adverse transfusion reaction rate in children transfused with PAS‐PLTs treated with riboflavin and UV light was found to be in accordance with data in the literature for children and adults receiving PLTs treated with the same PRT. PRT‐treated PLTs seem to be safe for children, since in 5 years (2013‐2017) not a single severe PLT transfusion reaction was reported in children transfused with riboflavin and UV light‐treated PLTs.…”
Section: Discussionsupporting
confidence: 87%
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“…Our comparative study shows that neonates transfused with PLTs diluted in PAS and treated with riboflavin and UV light‐PRT require the transfusion of more PLTs than neonates receiving standard PLTs. Additionally, the adverse transfusion reaction rate in children transfused with PAS‐PLTs treated with riboflavin and UV light was found to be in accordance with data in the literature for children and adults receiving PLTs treated with the same PRT. PRT‐treated PLTs seem to be safe for children, since in 5 years (2013‐2017) not a single severe PLT transfusion reaction was reported in children transfused with riboflavin and UV light‐treated PLTs.…”
Section: Discussionsupporting
confidence: 87%
“…The only previous report describing the use of such PRT‐treated‐PLTs in children included only 51 pediatric patients (age range: 0.4‐18 years; mean: 11 years) transfused with 141 riboflavin and UV light treated‐PLTs and 86 controls (age range: 0.4‐18 years; mean 11 years) transfused with 291 standard PLTs. These authors found that the CCI at 1 to 4 hours and at 18 to 24 hours were significantly higher in the control group, although both groups reached clinically effective CCI …”
Section: Discussionmentioning
confidence: 93%
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“…Limited data suggest that Mirasol ® ‐treated platelets have comparable hemostatic efficacy to untreated (i.e. standard) platelets . A single‐blind, randomized, clinical trial ( n = 24 healthy, adult volunteers) comparing red‐blood‐cell (RBC) components prepared from Mirasol ® ‐treated versus untreated whole blood showed that the Mirasol ® ‐treated whole blood‐derived RBCs met FDA acceptability criteria for red cell recovery (82·5 ± 3·9% [of the pre‐PR count] vs. 91·7 ± 6·8% in treated and control groups, respectively).…”
Section: Resultsmentioning
confidence: 99%