Publication:
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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cris.virtualsource.author-orcid101f1394-72d5-4dda-b28f-666a3dee6c70
datacite.rightsopen.access
dc.contributor.authorPilgrim, Thomas
dc.contributor.authorVranckx, Pascal
dc.contributor.authorValgimigli, Marco
dc.contributor.authorStefanini, Giulio
dc.contributor.authorPiccolo, Raffaele
dc.contributor.authorRat, Julie
dc.contributor.authorRothenbühler, Martina
dc.contributor.authorStortecky, Stefan
dc.contributor.authorRäber, Lorenz
dc.contributor.authorBlöchlinger, Stefan
dc.contributor.authorHunziker Munsch, Lukas Christoph
dc.contributor.authorSilber, Sigmund
dc.contributor.authorJüni, Peter
dc.contributor.authorSerruys, Patrick W
dc.contributor.authorWindecker, Stephan
dc.date.accessioned2024-10-24T18:24:29Z
dc.date.available2024-10-24T18:24:29Z
dc.date.issued2016-05
dc.description.abstractBACKGROUND 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.
dc.description.numberOfPages10
dc.description.sponsorshipUniversitätsklinik für Kardiologie
dc.description.sponsorshipDepartement Klinische Forschung, Core Facility, Clinical Trials Unit (CTU) Bern
dc.identifier.doi10.7892/boris.89742
dc.identifier.pmid27179724
dc.identifier.publisherDOI10.1016/j.ahj.2016.01.021
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/146016
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofAmerican Heart Journal
dc.relation.issn0002-8703
dc.relation.organizationInstitute of Social and Preventive Medicine
dc.relation.organizationDepartment of Clinical Research (DCR)
dc.relation.organizationClinic of Cardiology
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.subject.ddc300 - Social sciences, sociology & anthropology::360 - Social problems & social services
dc.titleRisk 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.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
dspace.file.typetext
oaire.citation.endPage65
oaire.citation.startPage56
oaire.citation.volume175
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationDepartement Klinische Forschung, Core Facility, Clinical Trials Unit (CTU) Bern
oairecerif.author.affiliationDepartement Klinische Forschung, Core Facility, Clinical Trials Unit (CTU) Bern
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliation2Institut für Sozial- und Präventivmedizin (ISPM)
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unibe.date.licenseChanged2019-10-24 04:33:37
unibe.description.ispublishedpub
unibe.eprints.legacyId89742
unibe.journal.abbrevTitleAM HEART J
unibe.refereedtrue
unibe.subtype.articlejournal

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