Evaluating the Use of Unfractionated Heparin with Intra-Aortic Balloon Counterpulsation.

Anti-Xa Anticoagulation Heparin IABP Intra-aortic balloon pump Mechanical circulatory support aPTT

Journal

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

Informations de publication

Date de publication:
03 Apr 2024
Historique:
received: 12 06 2023
revised: 07 12 2023
accepted: 28 01 2024
medline: 5 4 2024
pubmed: 5 4 2024
entrez: 4 4 2024
Statut: aheadofprint

Résumé

Evidence supporting anticoagulation with unfractionated heparin (UFH) in patients with an intra-aortic balloon pump (IABP) to prevent limb ischaemia remains limited, while bleeding risks remain high. Monitoring heparin in this setting with anti-factor Xa (anti-Xa) is not previously described. The study objective is to describe the incidence of thromboembolic and bleeding events with the use of UFH in patients with an IABP utilising monitoring with both anti-Xa and activated partial thromboplastin time (aPTT). This is a retrospective study of adults who received an IABP and UFH for ≥24 hours. Electronic medical records were reviewed for pertinent data. The primary outcome was the incidence of limb ischaemia during IABP. Secondary outcomes included myocardial infarction, thrombus on IABP, or stroke. Exploratory outcomes included any venous thromboembolism and bleeding events. Of 159 patients, 88% received an IABP for cardiogenic shock and median duration of IABP support was 118 hours (interquartile range, 67-196). Limb ischaemia occurred in four of 159 patients (2.5%). Strokes occurred in 3.8% of the cohort, and bleeding events occurred in 33%. Despite anticoagulation use in all patients, 11% experienced a venous thromboembolism, with most identified upon asymptomatic screening with concern for heparin-induced thrombocytopenia. We found no differences in outcomes that occurred with a hybrid anti-Xa and aPTT versus aPTT monitoring alone. We observed a high rate of thrombotic and bleeding complications with the use of UFH in patients with an IABP. Use of anti-Xa versus aPTT for monitoring was not associated with complications. These data suggest safer anticoagulation strategies are needed in this setting.

Sections du résumé

BACKGROUND BACKGROUND
Evidence supporting anticoagulation with unfractionated heparin (UFH) in patients with an intra-aortic balloon pump (IABP) to prevent limb ischaemia remains limited, while bleeding risks remain high. Monitoring heparin in this setting with anti-factor Xa (anti-Xa) is not previously described.
OBJECTIVES OBJECTIVE
The study objective is to describe the incidence of thromboembolic and bleeding events with the use of UFH in patients with an IABP utilising monitoring with both anti-Xa and activated partial thromboplastin time (aPTT).
METHODS METHODS
This is a retrospective study of adults who received an IABP and UFH for ≥24 hours. Electronic medical records were reviewed for pertinent data. The primary outcome was the incidence of limb ischaemia during IABP. Secondary outcomes included myocardial infarction, thrombus on IABP, or stroke. Exploratory outcomes included any venous thromboembolism and bleeding events.
RESULTS RESULTS
Of 159 patients, 88% received an IABP for cardiogenic shock and median duration of IABP support was 118 hours (interquartile range, 67-196). Limb ischaemia occurred in four of 159 patients (2.5%). Strokes occurred in 3.8% of the cohort, and bleeding events occurred in 33%. Despite anticoagulation use in all patients, 11% experienced a venous thromboembolism, with most identified upon asymptomatic screening with concern for heparin-induced thrombocytopenia. We found no differences in outcomes that occurred with a hybrid anti-Xa and aPTT versus aPTT monitoring alone.
CONCLUSIONS CONCLUSIONS
We observed a high rate of thrombotic and bleeding complications with the use of UFH in patients with an IABP. Use of anti-Xa versus aPTT for monitoring was not associated with complications. These data suggest safer anticoagulation strategies are needed in this setting.

Identifiants

pubmed: 38575436
pii: S1443-9506(24)00067-2
doi: 10.1016/j.hlc.2024.01.032
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 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.

Déclaration de conflit d'intérêts

Disclosures JH reports a relationship with Inari Medical Inc. that includes: consulting or advisory; and with Penumbra Inc. that includes: consulting or advisory. ON, CM, JP, SVR and TA have no conflicts of interest to disclose.

Auteurs

Olivia Nuti (O)

Department of Pharmacy, NYU Langone Hospital, Brooklyn, NY, USA. Electronic address: https://www.twitter.com/olivia_nuti.

Cristian Merchan (C)

Department of Pharmacy, NYU Langone Health, New York, NY, USA. Electronic address: https://www.twitter.com/ColombianpharmD.

John Papadopoulos (J)

Department of Pharmacy, NYU Langone Health, New York, NY, USA. Electronic address: https://www.twitter.com/JPCritCarePharm.

James Horowitz (J)

Department of Medicine - Cardiology at NYU Grossman School of Medicine, New York, NY, USA. Electronic address: https://www.twitter.com/jameshorowitmd.

Sunil V Rao (SV)

Department of Medicine - Interventional Cardiology, NYU Grossman School of Medicine, New York, NY, USA. Electronic address: https://www.twitter.com/SVRaoMD.

Tania Ahuja (T)

Department of Pharmacy, NYU Langone Health, New York, NY, USA; Department of Medicine - Cardiology at NYU Grossman School of Medicine, New York, NY, USA. Electronic address: tania.ahuja@nyulangone.org.

Classifications MeSH