Quality of life after transcatheter or surgical aortic valve replacement using the Toronto Aortic Stenosis Quality of Life Questionnaire
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články, multicentrická studie, pozorovací studie, práce podpořená grantem
PubMed
34810276
PubMed Central
PMC8609945
DOI
10.1136/openhrt-2021-001821
PII: openhrt-2021-001821
Knihovny.cz E-zdroje
- Klíčová slova
- aortic diseases, aortic valve stenosis, healthcare, heart valve prosthesis implantation, outcome assessment, quality of healthcare,
- MeSH
- aortální chlopeň chirurgie MeSH
- aortální stenóza epidemiologie psychologie chirurgie MeSH
- kvalita života * MeSH
- lidé MeSH
- morbidita trendy MeSH
- následné studie MeSH
- pooperační období MeSH
- prospektivní studie MeSH
- průzkumy a dotazníky * MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- transkatetrální implantace aortální chlopně psychologie MeSH
- zdravotní stav * MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- pozorovací studie MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Evropa epidemiologie MeSH
- Kanada epidemiologie MeSH
BACKGROUND: The Toronto Aortic Stenosis Quality of Life Questionnaire (TASQ) is a validated instrument for assessing quality of life (QoL) in patients with severe aortic stenosis (AS). In this study, we evaluated health status outcomes, based on the TASQ, in patients with severe AS undergoing transcatheter aortic valve replacement (TAVR) or surgical aortic valve replacement (SAVR). METHODS: The TASQ registry was a prospective observational registry. Patients with severe AS from nine centres in Europe and one in Canada underwent either SAVR or transfemoral TAVR. Patients completed the TASQ, Kansas City Cardiomyopathy Questionnaire and Short Form-12 V.2 prior to the intervention, predischarge, and at 30-day and 3-month follow-ups. Primary end point was the TASQ score. RESULTS: In both the TAVR (n=137) and SAVR (n=137) cohorts, significant increases were observed in all three scores. The overall TASQ score improved as did all but one of the individual domains at 3 months after the intervention (p<0.001). TASQ health expectations were the only domain which worsened (p<0.001). Across TASQ subscores, significant changes were evident from the time of discharge in the TAVR and 30-day follow-up in the SAVR cohort. In a categorical analysis of the TASQ, 39.7% of the TAVR group and 35.0% of the SAVR group had a substantially improved health status at 3 months compared with baseline. CONCLUSIONS: The TASQ captured changes in QoL among patients with severe AS who were treated with TAVR or SAVR. QoL improved substantially after either intervention, as indicated by changes in the TASQ overall score at 3 months. TRIAL REGISTRATION NUMBER: NCT03186339.
Department of Cardiac Surgery Innsbruck Medical University Innsbruck Austria
Department of Cardiology Barts Heart Centre St Bartholomew's Hospital London UK
Department of Cardiology Bichat Claude Bernard Hospital Paris France
Department of Cardiology Department of Cardiovascular Surgery Hospital Juan Canalejo Coruna Spain
Department of Cardiology Hospital Vall d'Hebron CIBER CV Barcelona Spain
Department of Internal Medicine 3 Kiel Germany
Department of Psychiatry University Health Network Toronto Ontario Canada
Department of Thoracic and Cardiovascular Surgery Hopital Prive Jacques Cartier Massy France
Division of Cardiology Department of Medicine University of Verona Verona Italy
Institut Jacques Cartier Massy France
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ClinicalTrials.gov
NCT03186339