Fondaparinux During Intra-Aortic Balloon Pump Counterpulsation in Acute Myocardial Infarction Patients Undergoing Percutaneous Coronary Intervention.


Journal

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

Informations de publication

Date de publication:
Oct 2021
Historique:
received: 25 11 2020
revised: 28 03 2021
accepted: 12 04 2021
pubmed: 18 5 2021
medline: 30 9 2021
entrez: 17 5 2021
Statut: ppublish

Résumé

Although anticoagulation with unfractionated heparin (UFH) is commonly used during intra-aortic balloon pump (IABP) counterpulsation to prevent thromboembolic events, no data or guidelines exist to support this strategy, especially in the setting of acute myocardial infarction (AMI). This study sought to compare the short-term outcome of UFH vs fondaparinux in AMI patients who underwent successful percutaneous coronary intervention (PCI) and IABP insertion. The anticoagulation therapy of revascularised AMI patients who received IABP counterpulsation and admitted to a tertiary hospital in the last decade was retrospectively evaluated. The primary outcome was the occurrence of all-cause mortality, stroke or transient ischaemic attack, reinfarction, unplanned revascularisation, major or minor limb ischaemia, and any bleeding at 1 month. Propensity score matching was performed to compare the primary outcome between UFH and fondaparinux. Of 1,355 AMI survivors at 2 days after hospital admission and who underwent successful PCI, an IABP was inserted in 197 (14.5%): 72 (36.5%) were treated with UFH and 125 (63.5%) with fondaparinux (2.5 mg o.d.). At clinical follow-up, completed in 98.5% of cases, the incidence of the primary outcome was 22.5% in UFH and 5.7% in fondaparinux groups (p=0.0009). More than two-thirds of the events included in the primary outcome were related to early bleeding complications. In the matched cohort of 62 patients, the primary outcome occurred in 14 (45.2%) patients in the UFH and two (6.5%) in the fondaparinux group (p=0.01). This study suggested that fondaparinux is safer, by reducing early bleeding complications at one month, than UFH in the management of IABP.

Sections du résumé

BACKGROUND BACKGROUND
Although anticoagulation with unfractionated heparin (UFH) is commonly used during intra-aortic balloon pump (IABP) counterpulsation to prevent thromboembolic events, no data or guidelines exist to support this strategy, especially in the setting of acute myocardial infarction (AMI). This study sought to compare the short-term outcome of UFH vs fondaparinux in AMI patients who underwent successful percutaneous coronary intervention (PCI) and IABP insertion.
METHODS METHODS
The anticoagulation therapy of revascularised AMI patients who received IABP counterpulsation and admitted to a tertiary hospital in the last decade was retrospectively evaluated. The primary outcome was the occurrence of all-cause mortality, stroke or transient ischaemic attack, reinfarction, unplanned revascularisation, major or minor limb ischaemia, and any bleeding at 1 month. Propensity score matching was performed to compare the primary outcome between UFH and fondaparinux.
RESULTS RESULTS
Of 1,355 AMI survivors at 2 days after hospital admission and who underwent successful PCI, an IABP was inserted in 197 (14.5%): 72 (36.5%) were treated with UFH and 125 (63.5%) with fondaparinux (2.5 mg o.d.). At clinical follow-up, completed in 98.5% of cases, the incidence of the primary outcome was 22.5% in UFH and 5.7% in fondaparinux groups (p=0.0009). More than two-thirds of the events included in the primary outcome were related to early bleeding complications. In the matched cohort of 62 patients, the primary outcome occurred in 14 (45.2%) patients in the UFH and two (6.5%) in the fondaparinux group (p=0.01).
CONCLUSIONS CONCLUSIONS
This study suggested that fondaparinux is safer, by reducing early bleeding complications at one month, than UFH in the management of IABP.

Identifiants

pubmed: 33994282
pii: S1443-9506(21)00421-2
doi: 10.1016/j.hlc.2021.04.012
pii:
doi:

Substances chimiques

Heparin 9005-49-6
Fondaparinux J177FOW5JL

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1545-1551

Informations de copyright

Copyright © 2021 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

Leonardo De Luca (L)

Department of Cardiosciences, A. O. San Camillo-Forlanini, Roma, Italy. Electronic address: leo.deluca@libero.it.

Massimo Uguccioni (M)

Department of Cardiosciences, A. O. San Camillo-Forlanini, Roma, Italy.

Rita Lucia Putini (RL)

Department of Cardiosciences, A. O. San Camillo-Forlanini, Roma, Italy.

Enrico Natale (E)

Department of Cardiosciences, A. O. San Camillo-Forlanini, Roma, Italy.

Antonio Terranova (A)

Department of Cardiosciences, A. O. San Camillo-Forlanini, Roma, Italy.

Marco Pugliese (M)

Department of Cardiosciences, A. O. San Camillo-Forlanini, Roma, Italy.

Elisabetta Biffani (E)

Department of Cardiosciences, A. O. San Camillo-Forlanini, Roma, Italy.

Lucia De Lio (L)

Department of Cardiosciences, A. O. San Camillo-Forlanini, Roma, Italy.

Vito Piazza (V)

Department of Cardiosciences, A. O. San Camillo-Forlanini, Roma, Italy.

Francesco Musumeci (F)

Department of Cardiosciences, A. O. San Camillo-Forlanini, Roma, Italy.

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