Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/21872
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dc.contributor.authorAnderson, James J-
dc.contributor.authorLau, Edmund M-
dc.contributor.authorLavender, Melanie-
dc.contributor.authorBenza, Raymond-
dc.contributor.authorCelermajer, David S-
dc.contributor.authorCollins, Nicholas-
dc.contributor.authorCorrigan, Carolyn-
dc.contributor.authorDwyer, Nathan-
dc.contributor.authorFeenstra, John-
dc.contributor.authorHorrigan, Mark-
dc.contributor.authorKeating, Dominic-
dc.contributor.authorKermeen, Fiona-
dc.contributor.authorKotlyar, Eugene-
dc.contributor.authorMcWilliams, Tanya-
dc.contributor.authorRhodes, Bronwen-
dc.contributor.authorSteele, Peter-
dc.contributor.authorThakkar, Vivek-
dc.contributor.authorWilliams, Trevor-
dc.contributor.authorWhitford, Helen-
dc.contributor.authorWhyte, Kenneth-
dc.contributor.authorWeintraub, Robert-
dc.contributor.authorWrobel, Jeremy P-
dc.contributor.authorKeogh, Anne-
dc.contributor.authorStrange, Geoff-
dc.date2020-01-
dc.date.accessioned2019-10-07T21:40:27Z-
dc.date.available2019-10-07T21:40:27Z-
dc.date.issued2019-09-26-
dc.identifier.citationChest 2020; 157(1): 162-172en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/21872-
dc.description.abstractPulmonary arterial hypertension (PAH) prognosis has improved with targeted therapies although the long-term outlook remains poor. Objective multi-parametric risk assessment is recommended to identify patients at risk of early morbidity and mortality, and for optimization of treatment. The REVEAL 2.0 Risk Score is a new model proposed for the follow-up of PAH patients but has not been externally validated. The REVEAL 2.0 Risk Score was applied to a mixed prevalent and incident cohort of PAH patients (n=1,011) from the Pulmonary Hypertension Society of Australia and New Zealand (PHSANZ) Registry. Kaplan-Meier (KM) survival was estimated for each REVEAL 2.0 Risk Score strata and for a broader three-category (low, intermediate, high-risk) model. Sensitivity analysis was performed on an incident-only cohort. The REVEAL 2.0 model effectively discriminated risk in the large external PHSANZ registry cohort, with c-statistic 0.74 (both for full 8-tier and three-category models). When applied to incident cases only, c-statistic was 0.73. The three-category REVEAL 2.0 model demonstrated robust separation of 12 and 60-months survival estimates (all risk categories comparisons p<0.001). Although the full 8-tier REVEAL 2.0 model separated low, intermediate and high-risk patients, survival estimates overlapped within some of the intermediate and high-risk strata. The REVEAL 2.0 risk score was validated in a large external cohort from the PHSANZ Registry. The REVEAL 2.0 model can be applied for risk assessment of PAH patients at follow-up. The simplified 3-category model may be preferred for clinical use and for future comparison with other prognostic models.en_US
dc.language.isoeng-
dc.titleRetrospective validation of the REVEAL 2.0 Risk Score with the Australian and New Zealand Pulmonary Hypertension Registry Cohort.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleChesten_US
dc.identifier.affiliationRespiratory Department, Sunshine Coast University Hospital, Birtinya, Australiaen_US
dc.identifier.affiliationSydney Medical School, University of Sydney, Camperdown, Australiaen_US
dc.identifier.affiliationAllegheny General Hospital, Pittsburgh, USAen_US
dc.identifier.affiliationDepartment of Cardiology, Royal Prince Alfred Hospital, Sydney, Australiaen_US
dc.identifier.affiliationDepartment of Respiratory Medicine, Royal Prince Alfred Hospital, Sydney, Australiaen_US
dc.identifier.affiliationSchool of Medicine, University of Notre Dame, Fremantle, Australiaen_US
dc.identifier.affiliationDepartment of Cardiovascular Services, Royal Adelaide Hospital, Adelaide, Australiaen_US
dc.identifier.affiliationThoracic Medicine, The Prince Charles Hospital, Brisbane, Australiaen_US
dc.identifier.affiliationAustin Healthen_US
dc.identifier.affiliationCardiology Department, Royal Hobart Hospital, Hobart, Australiaen_US
dc.identifier.affiliationHeart and Lung Transplant Unit, St Vincent's Hospital, Sydney, Australiaen_US
dc.identifier.affiliationJohn Hunter Hospital, Newcastle, Australiaen_US
dc.identifier.affiliationAdvanced Lung Disease Unit, Fiona Stanley Hospital, Perth, Australiaen_US
dc.identifier.affiliationGreenlane Respiratory Services, Auckland City Hospital, Auckland, New Zealand; NZ Respiratory and Sleep Institute, Auckland, New Zealanden_US
dc.identifier.affiliationDepartment of Respiratory Medicine, Christchurch Hospital, Christchurch, New Zealanden_US
dc.identifier.affiliationGreenlane Respiratory Services, Auckland City Hospital, Auckland, New Zealanden_US
dc.identifier.affiliationUniversity of New South Wales, Sydney, Australiaen_US
dc.identifier.affiliationRoyal Children's Hospital, Melbourne, Australiaen_US
dc.identifier.affiliationMurdoch Children's Research Institute, Melbourne, Australiaen_US
dc.identifier.affiliationUniversity of Melbourne, Melbourne, Australiaen_US
dc.identifier.affiliationRespiratory Medicine, Alfred Hospital, Melbourne, Australiaen_US
dc.identifier.affiliationMonash University, Melbourne, Australiaen_US
dc.identifier.affiliationMacquarie University, Department of Clinical Medicine, Macquarie Park, Australiaen_US
dc.identifier.affiliationLiverpool Hospital, Department of Rheumatology, Liverpool, Australiaen_US
dc.identifier.doi10.1016/j.chest.2019.08.2203en_US
dc.type.contentTexten_US
dc.identifier.pubmedid31563497-
dc.type.austinJournal Article-
local.name.researcherHorrigan, Mark
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptCardiology-
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