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A comparison between leukocyte reduced low titer whole blood vs non-leukocyte reduced low titer whole blood for massive transfusion activation.
Fadeyi, Emmanuel A; Saha, Amit K; Naal, Tawfeq; Martin, Harrison; Fenu, Elena; Simmons, Julie H; Jones, Mary Rose; Pomper, Gregory J.
Affiliation
  • Fadeyi EA; Department of Pathology & Laboratory Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
  • Saha AK; Department of Pathology & Laboratory Medicine, Wake Forest Baptist Health, Winston-Salem, North Carolina, USA.
  • Naal T; Department of Anesthesiology, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
  • Martin H; Department of Pathology & Laboratory Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
  • Fenu E; Department of Pathology & Laboratory Medicine, Wake Forest Baptist Health, Winston-Salem, North Carolina, USA.
  • Simmons JH; Department of Pathology & Laboratory Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
  • Jones MR; Department of Pathology & Laboratory Medicine, Wake Forest Baptist Health, Winston-Salem, North Carolina, USA.
  • Pomper GJ; Department of Pathology & Laboratory Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
Transfusion ; 60(12): 2834-2840, 2020 12.
Article in En | MEDLINE | ID: mdl-32888344
ABSTRACT

BACKGROUND:

Hemorrhagic shock is the leading cause of survivable death in trauma patients and recent literature has focused on resuscitation strategies including transfusing low-titer group O whole blood (LTOWB). Debate remains regarding whether leukocyte reduced (LR) whole blood is of clinical benefit or detriment to patients requiring massive transfusion. This study compares survival outcomes between LR-LTOWB and non-LR LTOWB. STUDY DESIGN AND

METHODS:

The objective of this prospective, observational study was to detect any difference in 24-hour survival between patients receiving LR-LTOWB and non-LR LTOWB during their massive transfusion activation. Secondary objectives were to report any difference in ICU LOS, ventilation days, in-hospital survival, and hospital LOS. Data collected included patient sex, age, mechanism of injury, Injury Severity Score (ISS), Trauma Injury Severity Score (TRISS), cause of death, and number of LTOWB transfused.

RESULTS:

A total of 167 patients received 271 LTOWB transfusions. There were 97 patients that received 168 units of LR-LTOWB while 70 patients received 103 units of non-LR LTOWB. The two study groups were comparable in terms of age, sex, ISS, TRISS, and the number of LTOWB transfused. The use of LR LTOWB during the initial massive transfusion activation in traumatically injured patients was not associated with increased 24-hour survival compared to when using non-LR LTOWB. No transfusion associated adverse events were reported.

CONCLUSIONS:

The administration of either LR or non-LR LTOWB was not associated with >24 hours survival in patients presenting with massive hemorrhage. The high cost and the rapid decline in platelet count of LR whole blood may be a consideration.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Resuscitation / Shock, Hemorrhagic / Blood Transfusion / Transfusion Reaction Type of study: Observational_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Transfusion Year: 2020 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Main subject: Resuscitation / Shock, Hemorrhagic / Blood Transfusion / Transfusion Reaction Type of study: Observational_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Transfusion Year: 2020 Type: Article Affiliation country: United States