Activated Prothrombin Complex Concentrate in Pediatric Cardiac Patients, Our Early Experience

Author:

Ashikhmina Swan Elena1ORCID,Brinkman Nathan J.2,Lahr Brian D.3,Nemergut Michael E.4,Dearani Joseph A.5ORCID,Stephens Elizabeth H.5

Affiliation:

1. Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, MN, USA

2. Department of Pharmacy, Mayo Clinic, Rochester, MN, USA

3. Department of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, USA

4. Divison of Pediatric Critical Care, Mayo Clinic, Rochester, MN, USA

5. Department of Cardiovascular Surgery, Mayo Clinic, Rochester, MN, USA

Abstract

Background Pediatric cardiac surgery is associated with abnormal coagulation, bleeding, and nearly ubiquitous transfusions. With the popularization of patient blood management, attempts are being made to decrease liberal transfusions by administering prothrombin complex concentrates (PCCs). The safety and efficacy of PCCs in adult cardiac surgery has been studied extensively, but only few reports address this in children. We performed an observational study focused on transfusion requirements after off-label use of activated PCC Factor Eight Inhibitor Bypassing Activity (FEIBA) as an adjunct to post-cardiopulmonary bypass (CPB) hemostatic protocol. Methods We reviewed the medical records of children ≤15 kg undergoing cardiac operations with CPB between May 2018 and March 2022. A propensity score (PS) analysis was performed to identify matched pairs of patients who did and did not receive FEIBA. Results Out of 210 patients who met the inclusion criteria, 44 patients received FEIBA. Propensity score-based analysis identified 40 matched pairs of patients with similar baseline characteristics. There was no statistically significant difference in the primary outcome—the volume of transfusion after CPB, which included all allogeneic blood products and salvaged washed red cells administered after protamine. Specifically, FEIBA patients were transfused 28 (22-34) mL/kg and controls were transfused 22 (11-49) mL/kg, P = .989. Upon arrival to ICU, the FEIBA group averaged an 8% lower international normalized ratio, compared with the controls ( P = .009) and a 1.08 g/dL higher hemoglobin ( P = .050). Neither difference remained significant on POD 1. Conclusions In this exploratory study, we found no change in transfusion requirements after CPB despite FEIBA administration.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,General Medicine,Pediatrics, Perinatology and Child Health,Surgery

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