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  3. Risk and timing of recurrent ischemic events among patients with stable ischemic heart disease, non-ST-segment elevation acute coronary syndrome, and ST-segment elevation myocardial infarction.
 

Risk and timing of recurrent ischemic events among patients with stable ischemic heart disease, non-ST-segment elevation acute coronary syndrome, and ST-segment elevation myocardial infarction.

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BORIS DOI
10.7892/boris.89742
Date of Publication
May 2016
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Departement Klinische...

Contributor
Pilgrim, Thomas
Universitätsklinik für Kardiologie
Vranckx, Pascal
Valgimigli, Marco
Universitätsklinik für Kardiologie
Stefanini, Giulio
Universitätsklinik für Kardiologie
Piccolo, Raffaele
Universitätsklinik für Kardiologie
Rat, Julie
Departement Klinische Forschung, Core Facility, Clinical Trials Unit (CTU) Bern
Rothenbühler, Martinaorcid-logo
Departement Klinische Forschung, Core Facility, Clinical Trials Unit (CTU) Bern
Institut für Sozial- und Präventivmedizin (ISPM)
Stortecky, Stefan
Universitätsklinik für Kardiologie
Räber, Lorenz
Universitätsklinik für Kardiologie
Blöchlinger, Stefan
Universitätsklinik für Kardiologie
Hunziker Munsch, Lukas Christoph
Universitätsklinik für Kardiologie
Silber, Sigmund
Jüni, Peter
Serruys, Patrick W
Windecker, Stephan
Universitätsklinik für Kardiologie
Subject(s)

600 - Technology::610...

300 - Social sciences...

Series
American Heart Journal
ISSN or ISBN (if monograph)
0002-8703
Publisher
Elsevier
Language
English
Publisher DOI
10.1016/j.ahj.2016.01.021
PubMed ID
27179724
Description
BACKGROUND

We aimed to compare differences in risk and timing of recurrent ischemic events among patients with stable ischemic heart disease (SIHD), non-ST-segment elevation acute coronary syndrome (NSTE-ACS), and ST-segment elevation myocardial infarction (STEMI) undergoing percutaneous coronary intervention (PCI).

METHODS

We performed an individual data pooled analysis of 5 randomized controlled all-comer trials including a total of 8,859 patients and investigated the risk and timing of recurrent ischemic events among patients with SIHD (n = 3,543), NSTE-ACS (n = 3,364), and STEMI (n = 1,952) throughout 2 years of follow-up.

RESULTS

At 2 years, all-cause mortality was higher among patients with STEMI (6.4%) and NSTE-ACS (6.1%) compared with those with SIHD (4.2%) (STEMI vs SIHD: hazard ratio [HR] 1.40, 95% CI 1.09-1.78, P = .007; NSTE-ACS vs SIHD: 1.40, 95% CI 1.13-1.73, P = .002). In a landmark analysis, the risk of mortality among patients with STEMI compared with those with SIHD was confined to the first 30 days after PCI (HR 6.19, 95% CI 3.15-12.16, P < .001) but was similar between 30 days and 2 years (HR 1.00, 95% CI 0.76-1.33, P = .974) (Pinteraction < .001). Conversely, patients with NSTE-ACS had a higher risk of mortality compared with those with SIHD both within the first 30 days (HR 2.19, 95% CI 1.08-4.47, P = .031) and beyond (HR 1.34, 95% CI 1.07-1.67, P = .012) (Pinteraction < .001). A similar pattern in the differential timing of events was observed for cardiac death. Beyond 30 days, the risk of myocardial infarction was comparable in patients with STEMI and SIHD, whereas the risk in patients with NSTE-ACS was increased (HR 1.65, 95% CI 1.23-2.21, P = .001).

CONCLUSION

Whereas patients with NSTE-ACS are at increased risk for death at any time after PCI, the mortality of STEMI patients is higher during the first 30 days after PCI but not thereafter compared with patients with SIHD.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/146016
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FileFile TypeFormatSizeLicensePublisher/Copright statementContent
1-s2.0-S0002870316000533-main.pdftextAdobe PDF739.73 KBpublisherpublished restricted
Pilgrim AmHeartJ 2016_postprint.pdftextAdobe PDF1.37 MBAttribution-NonCommercial-NoDerivatives (CC BY-NC-ND 4.0)acceptedOpen
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