Impact of Heparin- or Nonheparin-Coated Circuits on Platelet Function in Pediatric Cardiac Surgery.


Journal

The Annals of thoracic surgery
ISSN: 1552-6259
Titre abrégé: Ann Thorac Surg
Pays: Netherlands
ID NLM: 15030100R

Informations de publication

Date de publication:
04 2019
Historique:
received: 12 06 2018
revised: 14 09 2018
accepted: 14 09 2018
pubmed: 6 11 2018
medline: 18 12 2019
entrez: 6 11 2018
Statut: ppublish

Résumé

Extracorporeal circuit coating has been shown to improve coagulation derangements during pediatric cardiopulmonary bypass (CPB). This study compared platelet function and hemostasis activation in pediatric cardiac surgery conducted with nonheparin coating (Balance; Medtronic, Minneapolis, MN) versus heparin-based coating (Carmeda; Medtronic) circuits. A prospective, randomized, double-center trial was conducted in children older than 1 month undergoing congenital heart disease treatment. Blood samples were collected at baseline (T0), 15 minutes after the start of CPB (T1), and 15 minutes (T2) and 1 hour after the conclusion of CPB (T3). The primary end point of the study was to detect potential differences in β-thromboglobulin levels between the two groups at T2. Other coagulation and platelet function indicators were analyzed as secondary end points. The concentration of β-thromboglobulin increased significantly at T2 in both groups. However, there was no significant difference between the groups across all time points. There was no difference in the secondary end points between the groups. The two circuits showed similar biological effects on platelet function and coagulation. This observation may be useful in optimizing the conduct of CPB and in rationalizing its cost for the treatment of congenital heart disease.

Sections du résumé

BACKGROUND
Extracorporeal circuit coating has been shown to improve coagulation derangements during pediatric cardiopulmonary bypass (CPB). This study compared platelet function and hemostasis activation in pediatric cardiac surgery conducted with nonheparin coating (Balance; Medtronic, Minneapolis, MN) versus heparin-based coating (Carmeda; Medtronic) circuits.
METHODS
A prospective, randomized, double-center trial was conducted in children older than 1 month undergoing congenital heart disease treatment. Blood samples were collected at baseline (T0), 15 minutes after the start of CPB (T1), and 15 minutes (T2) and 1 hour after the conclusion of CPB (T3). The primary end point of the study was to detect potential differences in β-thromboglobulin levels between the two groups at T2. Other coagulation and platelet function indicators were analyzed as secondary end points.
RESULTS
The concentration of β-thromboglobulin increased significantly at T2 in both groups. However, there was no significant difference between the groups across all time points. There was no difference in the secondary end points between the groups.
CONCLUSIONS
The two circuits showed similar biological effects on platelet function and coagulation. This observation may be useful in optimizing the conduct of CPB and in rationalizing its cost for the treatment of congenital heart disease.

Identifiants

pubmed: 30395857
pii: S0003-4975(18)31550-9
doi: 10.1016/j.athoracsur.2018.09.032
pii:
doi:

Substances chimiques

Heparin 9005-49-6

Types de publication

Clinical Trial, Phase IV Comparative Study Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1241-1247

Informations de copyright

Copyright © 2019 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.

Auteurs

Chiara Giorni (C)

Pediatric Intensive Care, Cardiac Surgery and Perfusion Unit, Bambino Gesù Children's Hospital, Rome, Italy. Electronic address: c_giorni@yahoo.it.

Chiara Pezzella (C)

Pediatric Intensive Care, Cardiac Surgery and Perfusion Unit, Bambino Gesù Children's Hospital, Rome, Italy.

Mirela Bojan (M)

Department of Anesthesiology and Critical Care, Assistance Publique-Hôpitaux de Paris, Hôpital Necker-Enfants Malades, Paris, France.

Zaccaria Ricci (Z)

Pediatric Intensive Care, Cardiac Surgery and Perfusion Unit, Bambino Gesù Children's Hospital, Rome, Italy.

Philippe Pouard (P)

Department of Anesthesiology and Critical Care, Assistance Publique-Hôpitaux de Paris, Hôpital Necker-Enfants Malades, Paris, France.

Olivier Raisky (O)

Department of Pediatric Cardiac Surgery, Assistance Publique-Hôpitaux de Paris, Hôpital Necker-Enfants Malades, Paris, France.

Laurent Tourneur (L)

Department of Pediatric Cardiac Surgery, Assistance Publique-Hôpitaux de Paris, Hôpital Necker-Enfants Malades, Paris, France.

Ondina La Salvia (O)

Pediatric Intensive Care, Cardiac Surgery and Perfusion Unit, Bambino Gesù Children's Hospital, Rome, Italy.

Isabella Favia (I)

Pediatric Intensive Care, Cardiac Surgery and Perfusion Unit, Bambino Gesù Children's Hospital, Rome, Italy.

Delphine Borgel (D)

Hematology Laboratory, Assistance Publique-Hôpitaux de Paris, Hôpital Necker-Enfants Malades, Paris, France; Hémostase Inflammation Thrombose, Unité Mixte de Recherche -S1176, Institut National de la Santé et de la Recherche Médicale, University Paris-Sud, Université Paris-Saclay, Le Kremlin-Bicêtre, France.

Paola Cogo (P)

Pediatric Intensive Care, Cardiac Surgery and Perfusion Unit, Bambino Gesù Children's Hospital, Rome, Italy.

Adriano Carotti (A)

Pediatric Intensive Care, Cardiac Surgery and Perfusion Unit, Bambino Gesù Children's Hospital, Rome, Italy.

Dominique Lasne (D)

Hematology Laboratory, Assistance Publique-Hôpitaux de Paris, Hôpital Necker-Enfants Malades, Paris, France; Hémostase Inflammation Thrombose, Unité Mixte de Recherche -S1176, Institut National de la Santé et de la Recherche Médicale, University Paris-Sud, Université Paris-Saclay, Le Kremlin-Bicêtre, France.

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