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dc.contributor.authorYan, Raymond T.
dc.contributor.authorYan, Andrew T.
dc.contributor.authorGranger, Christopher B.
dc.contributor.authorLopez-Sendon, Jose
dc.contributor.authorBrieger, David
dc.contributor.authorKennelly, Brian M.
dc.contributor.authorBudaj, Andrzej
dc.contributor.authorSteg, Phillippe Gabriel
dc.contributor.authorGeorgescue, Alina A.
dc.contributor.authorHassan, Quamrul
dc.contributor.authorGoodman, Shaun G.
dc.contributor.authorGRACE Electrocardiogram Substudy Group
dc.date2022-08-11T08:08:08.000
dc.date.accessioned2022-08-23T15:44:00Z
dc.date.available2022-08-23T15:44:00Z
dc.date.issued2008-03-25
dc.date.submitted2011-09-23
dc.identifier.citationAm J Cardiol. 2008 Apr 1;101(7):919-24. Epub 2008 Feb 15. <a href="http://dx.doi.org/10.1016/j.amjcard.2007.11.041">Link to article on publisher's site</a>
dc.identifier.issn0002-9149 (Linking)
dc.identifier.doi10.1016/j.amjcard.2007.11.041
dc.identifier.pmid18359308
dc.identifier.urihttp://hdl.handle.net/20.500.14038/27220
dc.description.abstractThis aim of this study was to assess the clinical utility of quantitative ST-segment depression (STD) for refining the risk stratification of non-ST elevation acute coronary syndromes in the prospective, multinational Global Registry of Acute Coronary Events (GRACE). Quantitative measurements of STD on admission electrocardiograms were evaluated independently by a core laboratory, and their predictive value for in-hospital and cumulative 6-month mortality was examined. Although more severe STD is a marker of increased short- and long-term mortality, it is also associated with higher risk clinical features and biomarkers. Thus, after adjustment for these clinically important predictors, quantitative STD does not provide incremental prognostic value beyond simple dichotomous evaluation for the presence of STD. Furthermore, adopting quantitative instead of the prognostically proven qualitative evaluation of STD does not improve risk discrimination afforded by the validated GRACE risk models. In conclusion, the findings do not support the quantification of STD in routine clinical practice beyond simple evaluation for the presence of STD as an integral part of comprehensive risk stratification using the GRACE risk score.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=18359308&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.amjcard.2007.11.041
dc.subjectAcute Coronary Syndrome
dc.subjectAged
dc.subject*Electrocardiography
dc.subjectFemale
dc.subjectHumans
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectPredictive Value of Tests
dc.subjectRegistries
dc.subjectRisk Assessment
dc.subjectHealth Services Research
dc.titleUsefulness of quantitative versus qualitative ST-segment depression for risk stratification of non-ST elevation acute coronary syndromes in contemporary clinical practice
dc.typeJournal Article
dc.source.journaltitleThe American journal of cardiology
dc.source.volume101
dc.source.issue7
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/cor_grace/38
dc.identifier.contextkey2254957
html.description.abstract<p>This aim of this study was to assess the clinical utility of quantitative ST-segment depression (STD) for refining the risk stratification of non-ST elevation acute coronary syndromes in the prospective, multinational Global Registry of Acute Coronary Events (GRACE). Quantitative measurements of STD on admission electrocardiograms were evaluated independently by a core laboratory, and their predictive value for in-hospital and cumulative 6-month mortality was examined. Although more severe STD is a marker of increased short- and long-term mortality, it is also associated with higher risk clinical features and biomarkers. Thus, after adjustment for these clinically important predictors, quantitative STD does not provide incremental prognostic value beyond simple dichotomous evaluation for the presence of STD. Furthermore, adopting quantitative instead of the prognostically proven qualitative evaluation of STD does not improve risk discrimination afforded by the validated GRACE risk models. In conclusion, the findings do not support the quantification of STD in routine clinical practice beyond simple evaluation for the presence of STD as an integral part of comprehensive risk stratification using the GRACE risk score.</p>
dc.identifier.submissionpathcor_grace/38
dc.contributor.departmentCenter for Outcomes Research
dc.source.pages919-24


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