In-hospital gastrointestinal bleeding following percutaneous coronary intervention.


Journal

Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions
ISSN: 1522-726X
Titre abrégé: Catheter Cardiovasc Interv
Pays: United States
ID NLM: 100884139

Informations de publication

Date de publication:
01 2020
Historique:
received: 28 11 2018
revised: 26 02 2019
accepted: 23 03 2019
pubmed: 10 4 2019
medline: 15 9 2020
entrez: 10 4 2019
Statut: ppublish

Résumé

This study aims to examine in-hospital gastrointestinal (GI) bleeding, its predictors and clinical outcomes, including long-term outcomes, in a national cohort of patients undergoing percutaneous coronary intervention (PCI) in England and Wales. GI bleeding remains associated with significant morbidity, mortality, and socioeconomic burden. We examined the temporal changes in in-hospital GI bleeding in a national cohort of patients undergoing PCI between 2007 and 2014 in England and Wales, its predictors and prognostic consequences. Multivariate analysis was performed to identify independent risk factors between GI bleeding and 30-day mortality. Survival analysis was performed comparing patients with, and without, GI bleeding. There were 480 in-hospital GI bleeds in 549,298 patients (0.09%). Overall, rates of GI bleeding remained stable over time but a significant decline was observed for patients with ST segment elevation myocardial infarction (STEMI). The strongest predictors of bleeding events were STEMI-odds ratio (OR) 7.28 (95% confidence interval [95% CI] 4.82-11.00), glycoprotein IIb/IIIa inhibitor use OR 3.42 (95% CI 2.76-4.24) and use of circulatory support OR 2.65 (95% CI 1.90-3.71). Antiplatelets/coagulants (clopidogrel, prasugrel, and warfarin) were not independently associated with GI bleeding. GI bleeding was independently associated with a significant increase in all-cause 30-day mortality (OR 2.08 [1.52-2.83]). Patients with in-hospital GI bleed who survived to 30-days had increased all-cause mortality risk at 1 year compared to non-bleeders (HR 1.49 [1.07-2.09]). In-hospital GI bleeding following PCI is rare but is a clinically important event associated with increased 30-day and long-term mortality.

Sections du résumé

OBJECTIVES
This study aims to examine in-hospital gastrointestinal (GI) bleeding, its predictors and clinical outcomes, including long-term outcomes, in a national cohort of patients undergoing percutaneous coronary intervention (PCI) in England and Wales.
BACKGROUND
GI bleeding remains associated with significant morbidity, mortality, and socioeconomic burden.
METHODS
We examined the temporal changes in in-hospital GI bleeding in a national cohort of patients undergoing PCI between 2007 and 2014 in England and Wales, its predictors and prognostic consequences. Multivariate analysis was performed to identify independent risk factors between GI bleeding and 30-day mortality. Survival analysis was performed comparing patients with, and without, GI bleeding.
RESULTS
There were 480 in-hospital GI bleeds in 549,298 patients (0.09%). Overall, rates of GI bleeding remained stable over time but a significant decline was observed for patients with ST segment elevation myocardial infarction (STEMI). The strongest predictors of bleeding events were STEMI-odds ratio (OR) 7.28 (95% confidence interval [95% CI] 4.82-11.00), glycoprotein IIb/IIIa inhibitor use OR 3.42 (95% CI 2.76-4.24) and use of circulatory support OR 2.65 (95% CI 1.90-3.71). Antiplatelets/coagulants (clopidogrel, prasugrel, and warfarin) were not independently associated with GI bleeding. GI bleeding was independently associated with a significant increase in all-cause 30-day mortality (OR 2.08 [1.52-2.83]). Patients with in-hospital GI bleed who survived to 30-days had increased all-cause mortality risk at 1 year compared to non-bleeders (HR 1.49 [1.07-2.09]).
CONCLUSIONS
In-hospital GI bleeding following PCI is rare but is a clinically important event associated with increased 30-day and long-term mortality.

Identifiants

pubmed: 30963681
doi: 10.1002/ccd.28222
doi:

Substances chimiques

Platelet Aggregation Inhibitors 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

109-117

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Références

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Auteurs

Chun Shing Kwok (CS)

Keele Cardiovascular Research Group, Keele University, Stoke-on-Trent, UK.
Department of Cardiology, Royal Stoke University Hospital, Stoke-on-Trent, UK.

Alex Sirker (A)

Department of Cardiology, University College London Hospitals and St. Bartholomew's Hospital, London, UK.

Adam D Farmer (AD)

Department of Gastroenterology and Institute of Applied Clinical Sciences, Royal Stoke University Hospital, Stoke-on-Trent, UK.

Evangelos Kontopantelis (E)

Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.

Jessica Potts (J)

Department of Cardiology, Queen Elizabeth Hospital, Birmingham, UK.

Muhammad Ayyaz Ul Haq (M)

Keele Cardiovascular Research Group, Keele University, Stoke-on-Trent, UK.
Department of Cardiology, Royal Stoke University Hospital, Stoke-on-Trent, UK.

Peter Ludman (P)

Department of Cardiology, The James Cook University Hospital, Middlesbrough, UK.

Mark de Belder (M)

Department of Cardiology, Freeman Hospital and Institute of Cellular Medicine, Newcastle University, Newcastle Upon Tyne, UK.

John Townend (J)

Department of Cardiology, The James Cook University Hospital, Middlesbrough, UK.

Azfar Zaman (A)

Department of Cardiology, Freeman Hospital and Institute of Cellular Medicine, Newcastle University, Newcastle Upon Tyne, UK.

Adrian Large (A)

Department of Cardiology, Royal Stoke University Hospital, Stoke-on-Trent, UK.

Tim Kinnaird (T)

Department of Cardiology, University Hospital of Wales, Cardiff, UK.

Mamas A Mamas (MA)

Keele Cardiovascular Research Group, Keele University, Stoke-on-Trent, UK.
Department of Cardiology, Royal Stoke University Hospital, Stoke-on-Trent, UK.

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