Immediate Higher-Dose Prothrombin Complex Concentrate Without Fresh Frozen Plasma or Fibrinogen Concentrate for Significant Coagulopathic Cardiac Surgical Field Bleeding.

Chest tube drainage Coagulopathic cardiac surgical field bleeding Prothrombin complex concentrate Thrombo-embolic complications

Journal

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

Informations de publication

Date de publication:
Sep 2022
Historique:
received: 21 12 2021
revised: 23 05 2022
accepted: 26 05 2022
pubmed: 18 7 2022
medline: 31 8 2022
entrez: 17 7 2022
Statut: ppublish

Résumé

Treatment of significant coagulopathic cardiac surgical field bleeding with immediate higher-dose prothrombin complex concentrate (PCC) without fresh frozen plasma (FFP) or fibrinogen concentrate is unexplored. To study characteristics, chest drainage, and clinical outcomes of patients with significant coagulopathic surgical field bleeding treated with immediate higher-dose (defined at >15 IU/kg based on factor IX) PCC without FFP or fibrinogen concentrate. We screened sequential cardiac surgery patients. We reviewed electronic blood bank data, Australian Society of Cardiothoracic Surgery database information and anaesthetic, intensive care unit (ICU), ward and radiological charts and electronic data. We identified patients deemed by the operating surgeon to require treatment for significant coagulopathic surgical field bleeding who underwent immediate higher-dose PCC without FFP or fibrinogen concentrate. Among 168 patients, we identified 30 who underwent immediate higher-dose PCC without FFP or fibrinogen concentrate. Median age was 68 years, 23 were male, 17 underwent coronary artery bypass surgery and three underwent complex surgery (David procedure, redo mitral valve surgery, and redo thoraco-abdominal aneurysm repair). Median dose of PCC was 2,500 IU. In addition, 27% underwent platelets and one underwent cryoprecipitate. Chest drainage at 24 hours was 505 ml. Survival to hospital discharge was 100%. There were no cases of pulmonary embolism, stroke, or other thrombotic events. Stage 1 AKI occurred in one patient. In a pilot cohort of patients with significant coagulopathic surgical field bleeding, immediate higher-dose PCC without FFP or fibrinogen concentrate was feasible and had an acceptable efficacy and safety profile, which justifies future controlled studies.

Sections du résumé

BACKGROUND BACKGROUND
Treatment of significant coagulopathic cardiac surgical field bleeding with immediate higher-dose prothrombin complex concentrate (PCC) without fresh frozen plasma (FFP) or fibrinogen concentrate is unexplored.
AIMS OBJECTIVE
To study characteristics, chest drainage, and clinical outcomes of patients with significant coagulopathic surgical field bleeding treated with immediate higher-dose (defined at >15 IU/kg based on factor IX) PCC without FFP or fibrinogen concentrate.
METHODS METHODS
We screened sequential cardiac surgery patients. We reviewed electronic blood bank data, Australian Society of Cardiothoracic Surgery database information and anaesthetic, intensive care unit (ICU), ward and radiological charts and electronic data. We identified patients deemed by the operating surgeon to require treatment for significant coagulopathic surgical field bleeding who underwent immediate higher-dose PCC without FFP or fibrinogen concentrate.
RESULTS RESULTS
Among 168 patients, we identified 30 who underwent immediate higher-dose PCC without FFP or fibrinogen concentrate. Median age was 68 years, 23 were male, 17 underwent coronary artery bypass surgery and three underwent complex surgery (David procedure, redo mitral valve surgery, and redo thoraco-abdominal aneurysm repair). Median dose of PCC was 2,500 IU. In addition, 27% underwent platelets and one underwent cryoprecipitate. Chest drainage at 24 hours was 505 ml. Survival to hospital discharge was 100%. There were no cases of pulmonary embolism, stroke, or other thrombotic events. Stage 1 AKI occurred in one patient.
CONCLUSION CONCLUSIONS
In a pilot cohort of patients with significant coagulopathic surgical field bleeding, immediate higher-dose PCC without FFP or fibrinogen concentrate was feasible and had an acceptable efficacy and safety profile, which justifies future controlled studies.

Identifiants

pubmed: 35843859
pii: S1443-9506(22)00969-6
doi: 10.1016/j.hlc.2022.05.048
pii:
doi:

Substances chimiques

Blood Coagulation Factors 0
prothrombin complex concentrates 37224-63-8
Factor IX 9001-28-9
Fibrinogen 9001-32-5

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1300-1306

Informations de copyright

Copyright © 2022 Australian and New Zealand Society of Cardiac and Thoracic Surgeons (ANZSCTS) and the Cardiac Society of Australia and New Zealand (CSANZ). All rights reserved.

Auteurs

Prashant Pruthi (P)

Intensive Care Unit, Warringal Private Hospital, Melbourne, Vic, Australia.

Christine Culliver (C)

Dorevitch Blood Bank at Warringal Private Hospital, Melbourne, Vic, Australia.

Hasan Emel (H)

Dorevitch Blood Bank at Warringal Private Hospital, Melbourne, Vic, Australia.

Sophie Georghie (S)

Department of Anaesthesia, Warringal Private Hospital, Melbourne, Vic, Australia.

Matthew J Benson (MJ)

Department of Anaesthesia, Warringal Private Hospital, Melbourne, Vic, Australia.

George Matalanis (G)

Department of Cardiac Surgery, Warringal Private Hospital, Melbourne, Vic, Australia.

Fumitaka Yanase (F)

Department of Intensive Care, Austin Hospital, Melbourne, Vic, Australia.

Rinaldo Bellomo (R)

Intensive Care Unit, Warringal Private Hospital, Melbourne, Vic, Australia; Department of Intensive Care, Austin Hospital, Melbourne, Vic, Australia; Department of Critical Care, University of Melbourne, Melbourne, Vic, Australia; Australian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, Vic, Australia; Data Analytics Research and Evaluation Centre, Austin Hospital, Melbourne, Vic, Australia. Electronic address: Rinaldo.bellomo@austin.org.au.

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Classifications MeSH