Comparative Analysis of Prothrombin Complex Concentrate and Fresh Frozen Plasma in Coronary Surgery.


Journal

Heart, lung & circulation
ISSN: 1444-2892
Titre abrégé: Heart Lung Circ
Pays: Australia
ID NLM: 100963739

Informations de publication

Date de publication:
Dec 2019
Historique:
received: 09 10 2018
accepted: 30 10 2018
pubmed: 3 2 2019
medline: 16 4 2020
entrez: 3 2 2019
Statut: ppublish

Résumé

Recent studies suggested that prothrombin complex concentrate (PCC) might be more effective than fresh frozen plasma (FFP) to reduce red blood cell (RBC) transfusion requirement after cardiac surgery. This is a comparative analysis of 416 patients who received FFP postoperatively and 119 patients who received PCC with or without FFP after isolated coronary artery bypass grafting (CABG). Mixed-effects regression analyses adjusted for multiple covariates and participating centres showed that PCC significantly decreased RBC transfusion (67.2% vs. 87.5%, adjusted OR 0.319, 95%CI 0.136-0.752) and platelet transfusion requirements (11.8% vs. 45.2%, adjusted OR 0.238, 95%CI 0.097-0.566) compared with FFP. The PCC cohort received a mean of 2.7±3.7 (median, 2.0, IQR 4) units of RBC and the FFP cohort received a mean of 4.9±6.3 (median, 3.0, IQR 4) units of RBC (adjusted coefficient, -1.926, 95%CI -3.357-0.494). The use of PCC increased the risk of KDIGO (Kidney Disease: Improving Global Outcomes) acute kidney injury (41.4% vs. 28.2%, adjusted OR 2.300, 1.203-4.400), but not of KDIGO acute kidney injury stage 3 (6.0% vs. 8.0%, OR 0.850, 95%CI 0.258-2.796) when compared with the FFP cohort. These results suggest that the use of PCC compared with FFP may reduce the need of blood transfusion after CABG.

Sections du résumé

BACKGROUND BACKGROUND
Recent studies suggested that prothrombin complex concentrate (PCC) might be more effective than fresh frozen plasma (FFP) to reduce red blood cell (RBC) transfusion requirement after cardiac surgery.
METHODS METHODS
This is a comparative analysis of 416 patients who received FFP postoperatively and 119 patients who received PCC with or without FFP after isolated coronary artery bypass grafting (CABG).
RESULTS RESULTS
Mixed-effects regression analyses adjusted for multiple covariates and participating centres showed that PCC significantly decreased RBC transfusion (67.2% vs. 87.5%, adjusted OR 0.319, 95%CI 0.136-0.752) and platelet transfusion requirements (11.8% vs. 45.2%, adjusted OR 0.238, 95%CI 0.097-0.566) compared with FFP. The PCC cohort received a mean of 2.7±3.7 (median, 2.0, IQR 4) units of RBC and the FFP cohort received a mean of 4.9±6.3 (median, 3.0, IQR 4) units of RBC (adjusted coefficient, -1.926, 95%CI -3.357-0.494). The use of PCC increased the risk of KDIGO (Kidney Disease: Improving Global Outcomes) acute kidney injury (41.4% vs. 28.2%, adjusted OR 2.300, 1.203-4.400), but not of KDIGO acute kidney injury stage 3 (6.0% vs. 8.0%, OR 0.850, 95%CI 0.258-2.796) when compared with the FFP cohort.
CONCLUSIONS CONCLUSIONS
These results suggest that the use of PCC compared with FFP may reduce the need of blood transfusion after CABG.

Identifiants

pubmed: 30709591
pii: S1443-9506(18)32004-3
doi: 10.1016/j.hlc.2018.10.025
pii:
doi:

Substances chimiques

Blood Coagulation Factors 0
prothrombin complex concentrates 37224-63-8

Types de publication

Clinical Trial Comparative Study Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1881-1887

Informations de copyright

Copyright © 2018 Australian and New Zealand Society of Cardiac and Thoracic Surgeons (ANZSCTS) and the Cardiac Society of Australia and New Zealand (CSANZ). Published by Elsevier B.V. All rights reserved.

Auteurs

Fausto Biancari (F)

Heart Center, Turku University Hospital and Department of Surgery, University of Turku, Turku, Finland; Department of Surgery, Oulu University Hospital and University of Oulu, Oulu, Finland. Electronic address: faustobiancari@yahoo.it.

Vito G Ruggieri (VG)

Division of Cardiothoracic and Vascular Surgery, Robert Debré University Hospital, Reims, France.

Andrea Perrotti (A)

Department of Thoracic and Cardio-Vascular Surgery, University Hospital Jean Minjoz, Besançon, France.

Riccardo Gherli (R)

Department of Cardiovascular Sciences, Cardiac Surgery Unit, S. Camillo-Forlanini Hospital, Rome, Italy.

Till Demal (T)

Hamburg University Heart Center, Hamburg, Germany.

Ilaria Franzese (I)

Division of Cardiovascular Surgery, Verona University Hospital, Verona, Italy.

Magnus Dalén (M)

Department of Molecular Medicine and Surgery, Department of Cardiac Surgery, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.

Giuseppe Santarpino (G)

Cardiovascular Center, Paracelsus Medical University, Nuremberg, Germany.

Antonino S Rubino (AS)

Centro Clinico-Diagnostico "G.B. Morgagni", Centro Cuore, Pedara, Italy.

Daniele Maselli (D)

Department of Cardiac Surgery, St. Anna Hospital, Catanzaro, Italy.

Antonio Salsano (A)

Division of Cardiac Surgery, University of Genoa, Genoa, Italy.

Francesco Nicolini (F)

Division of Cardiac Surgery, University of Parma, Parma, Italy.

Matteo Saccocci (M)

Department of Cardiac Surgery, Centro Cardiologico - Fondazione Monzino IRCCS, Milan, Italy.

Giuseppe Gatti (G)

Division of Cardiac Surgery, Ospedali Riuniti, Trieste, Italy.

Stefano Rosato (S)

National Center of Global Health, Istituto Superiore di Sanità, Rome, Italy.

Paola D'Errigo (P)

National Center of Global Health, Istituto Superiore di Sanità, Rome, Italy.

Eeva-Maija Kinnunen (EM)

Department of Surgery, Oulu University Hospital and University of Oulu, Oulu, Finland.

Marisa De Feo (M)

Department of Cardiothoracic Sciences, University of Campania "Luigi Vanvitelli", Naples, Italy.

Tuomas Tauriainen (T)

Department of Surgery, Oulu University Hospital and University of Oulu, Oulu, Finland.

Francesco Onorati (F)

Division of Cardiovascular Surgery, Verona University Hospital, Verona, Italy.

Giovanni Mariscalco (G)

Department of Cardiovascular Sciences, Clinical Sciences Wing, University of Leicester, Glenfield Hospital, Leicester, UK.

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Classifications MeSH