Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11498
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dc.contributor.authorKearney, Leighton Gen
dc.contributor.authorOrd, Michelleen
dc.contributor.authorBuxton, Brian Fen
dc.contributor.authorMatalanis, Georgeen
dc.contributor.authorPatel, Sheila Ken
dc.contributor.authorBurrell, Louiseen
dc.contributor.authorSrivastava, Piyush Men
dc.date.accessioned2015-05-16T01:06:41Z
dc.date.available2015-05-16T01:06:41Z
dc.date.issued2012-05-25en
dc.identifier.citationThe American Journal of Cardiology 2012; 110(5): 695-701en
dc.identifier.govdoc22632826en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/11498en
dc.description.abstractThe present study assessed the effect of age and co-morbidity on the outcomes of mild, moderate, and severe aortic stenosis (AS) in patients aged >60 years during 18 years of follow-up. The outcomes evaluated were hemodynamic progression, a composite cardiac mortality or aortic valve replacement (AVR) end point, and all-cause mortality. Consecutive Department of Veterans Affairs patients (aged >60 years) with AS were prospectively enrolled from 1988 to 1994 and followed until 2008 (n = 239). The baseline demographic, co-morbidity, and echocardiographic parameters were recorded. At enrollment, the mean age was 74 ± 6 years, and 78% were men. The annualized mean aortic valve gradient progression was 4 ± 4, 6 ± 5, and 10 ± 8 mm Hg for mild, moderate, and severe AS, respectively (p <0.001). During a mean follow-up of 8 ± 5 years, 206 deaths (52% cardiac) and 91 AVRs were recorded. The AVR/cardiac mortality event rate at 1, 5, and 10 years was 2%, 26%, and 50% for mild AS, 13%, 63%, and 69% for moderate AS, and 66%, 95%, and 95% for severe AS (p <0.001). During the study period, 132 patients developed severe AS. The survival rate at 1, 5, and 10 years was 60 ± 7%, 14 ± 5%, and 5 ± 3% with conservative management and 98 ± 2%, 82 ± 4%, and 50 ± 5% after AVR, respectively (p <0.001). The independent predictors of all-cause mortality were the age-adjusted Charlson co-morbidity index (hazard ratio 1.24, p <0.001), AVR (hazard ratio 0.40, p <0.001), and grade of left ventricular dysfunction (hazard ratio 1.36, p = 0.01). In conclusion, the prognostic significance of AS is determined by the hemodynamic severity, left ventricular function, and the presence of symptoms, in the context of age and co-morbidities. The age-adjusted Charlson co-morbidity index provides crucial prognostic information to guide the surgical risk/benefit discussions for patients with severe AS.en
dc.language.isoenen
dc.subject.otherAge Distributionen
dc.subject.otherAgeden
dc.subject.otherAged, 80 and overen
dc.subject.otherAnalysis of Varianceen
dc.subject.otherAortic Valve Stenosis.diagnosis.epidemiology.surgeryen
dc.subject.otherCohort Studiesen
dc.subject.otherComorbidityen
dc.subject.otherDisease-Free Survivalen
dc.subject.otherFemaleen
dc.subject.otherFollow-Up Studiesen
dc.subject.otherHeart Valve Prosthesisen
dc.subject.otherHeart Valve Prosthesis Implantation.methods.mortalityen
dc.subject.otherHumansen
dc.subject.otherIncidenceen
dc.subject.otherKaplan-Meier Estimateen
dc.subject.otherMaleen
dc.subject.otherMultivariate Analysisen
dc.subject.otherOutcome Assessment (Health Care).methodsen
dc.subject.otherPostoperative Complications.epidemiology.physiopathologyen
dc.subject.otherPredictive Value of Testsen
dc.subject.otherProportional Hazards Modelsen
dc.subject.otherProspective Studiesen
dc.subject.otherSeverity of Illness Indexen
dc.subject.otherSex Distributionen
dc.subject.otherSurvival Analysisen
dc.subject.otherTreatment Outcomeen
dc.subject.otherUltrasonography, Doppler.methodsen
dc.subject.otherVictoriaen
dc.titleUsefulness of the Charlson co-morbidity index to predict outcomes in patients >60 years old with aortic stenosis during 18 years of follow-up.en
dc.typeJournal Articleen
dc.identifier.journaltitleThe American journal of cardiologyen
dc.identifier.affiliationDepartment of Cardiology, Austin Health, Victoria, Australiaen
dc.identifier.doi10.1016/j.amjcard.2012.04.054en
dc.description.pages695-701en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/22632826en
dc.type.austinJournal Articleen
local.name.researcherBuxton, Brian F
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptCardiology-
crisitem.author.deptCardiac Surgery-
crisitem.author.deptCardiac Surgery-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptMedicine (University of Melbourne)-
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