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Assessing the Efficacy of Prothrombin Complex Concentrate in Multiply Injured Patients With High-Energy Pelvic and Extremity Fractures

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Published:1st Dec 2016
Author: Joseph B, Khalil M, Harrison C, Swartz T, Kulvatunyou N, Haider AA et al.
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Ref.:J Orthop Trauma. 2016 Dec;30(12):653-658.
DOI:10.1097/BOT.0000000000000665
Assessing the Efficacy of Prothrombin Complex Concentrate in Multiply Injured Patients With High-Energy Pelvic and Extremity Fractures


Objectives:
Prothrombin complex concentrate (PCC) is being increasingly used for reversing induced coagulopathy of trauma. However, the use of PCC for reversing coagulopathy in multiply injured patients with pelvic and/or lower extremity fractures remains unclear. The aim of our study was to assess the efficacy of PCC for reversing coagulopathy in this group of patients.

Design: Two-year retrospective analysis.

Setting: Our level I trauma center.

Patients/Participants: All coagulopathic [International normalized ratio (INR) ≥1.5] trauma patients. Patients with femur, tibia, or pelvic fracture were included. Patients were divided into 2 groups: PCC (single dose) and fresh frozen plasma (FFP). Patients in the 2 groups were matched using propensity score matching.

Main Outcome Measurements: Time to correction of INR, time to intervention, development of thromboembolic complications, mortality, and cost of therapy.

Results: A total of 81 patients (PCC: 27, FFP: 54) were included. Patients who received PCC had faster correction of INR and shorter time to surgical intervention in comparison to patients who received FFP. PCC therapy was also associated with lower overall blood product requirement (P = 0.02) and lower transfusion costs (P = 0.0001).

Conclusions: In a matched cohort of multiply injured patients with pelvic and/or lower extremity fractures, administration of a single dose of PCC significantly reduced the time to correction of INR and time to intervention compared with patients who received FFP therapy. This may allow orthopaedic surgeons to more safely proceed with early, definitive fixation strategies.

Level of Evidence: Therapeutic level III. See Instructions for Authors for a complete description of levels of evidence.


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