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Cold platelet transfusion: The effects of a fluid warmer on platelet function.
Valencia Morales, Diana J; Klompas, Allan M; Torbenson, Jenna M; Finney, Robyn E; Chen, Dong; Stubbs, James R; Nuttall, Gregory A.
Afiliação
  • Valencia Morales DJ; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.
  • Klompas AM; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.
  • Torbenson JM; Division of Transfusion Medicine, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.
  • Finney RE; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.
  • Chen D; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.
  • Stubbs JR; Division of Hematopathology, Department of Laboratory Medicine and Pathology, Clinical Core Laboratory, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.
  • Nuttall GA; Division of Transfusion Medicine, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.
Transfusion ; 64(1): 47-52, 2024 01.
Article em En | MEDLINE | ID: mdl-38115202
ABSTRACT

BACKGROUND:

Recently the US Food and Drug Administration has granted variances to select blood centers to supply cold-stored platelet components (CSP). In hemorrhage resuscitation warming of blood components with approved fluid warming devices is common. STUDY DESIGN AND

METHODS:

Pathogen-reduced apheresis platelet units were collected and stored in one of two ways (1) CSP-I, (2) CSP-D. CSP-I were collected and immediately stored at 1-6°C until used. CSP-D were collected and stored at 20-24°C for 5 days and transferred to storage at 1-6°C until use. Aggregometry using arachidonic acid (AA), adenosine diphosphate (ADP) and collagen as agonists was performed on the unit samples before and after the units were infused through a Ranger blood-warming device.

RESULTS:

CSP-I, 23 units, had very high aggregation responses to all agonists (all ≥47.6 ± 20.7). There was a statistically significant reduction in ADP-induced aggregometry results from 55.1 ± 23.2 before compared to 33.5 ± 14.6 following infusion of the PLT through the blood warmer (p < .001). There were no differences in AA and collagen aggregometry results before and after the infusion of the platelets through the blood warmer. CSP-D had 5 of the 15 units with visible clotting in the bag. The 10 CSP-Ds studied had lower aggregation than all agonists before and after infusion through the blood-warming device (all ≤49.9 ± 35.9).

CONCLUSION:

We detected a statistically significant reduction in ADP-induced aggregometry in CSP-I run through a Ranger blood-warming device with no change with AA or collagen agonist aggregometry.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Agregação Plaquetária / Transfusão de Plaquetas Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Agregação Plaquetária / Transfusão de Plaquetas Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article