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Facilitated Data Relay and Effects on Treatment of Severe Aortic Stenosis in Europe
RP. Steeds, M. Lutz, J. Thambyrajah, A. Serra, E. Schulz, J. Maly, M. Aiello, TK. Rudolph, G. Lloyd, AS. Bortone, KE. Hauptmann, A. Clerici, G. Delle-Karth, J. Rieber, C. Indolfi, M. Mancone, L. Belle, A. Lauten, M. Arnold, BJ. Bouma, C. Deutsch,...
Jazyk angličtina Země Velká Británie
Typ dokumentu srovnávací studie, časopisecké články, multicentrická studie, pozorovací studie, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2012
Free Medical Journals
od 2012
PubMed Central
od 2012
Europe PubMed Central
od 2012
Open Access Digital Library
od 2012-01-01
Open Access Digital Library
od 2012-01-01
Open Access Digital Library
od 2015-01-01
Wiley-Blackwell Open Access Titles
od 2012
ROAD: Directory of Open Access Scholarly Resources
od 2012
PubMed
31549578
DOI
10.1161/jaha.119.013160
Knihovny.cz E-zdroje
- MeSH
- aortální stenóza diagnostické zobrazování ošetřování terapie MeSH
- balónková valvuloplastika * škodlivé účinky MeSH
- čas zasáhnout při rozvinutí nemoci * MeSH
- časové faktory MeSH
- chirurgická náhrada chlopně * škodlivé účinky MeSH
- echokardiografie MeSH
- klinické rozhodování MeSH
- konziliární vyšetření a konzultace * MeSH
- lidé MeSH
- pozorné vyčkávání * MeSH
- prospektivní studie MeSH
- průřezové studie MeSH
- registrace MeSH
- role ošetřovatelky * MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- stupeň závažnosti nemoci MeSH
- transkatetrální implantace aortální chlopně * škodlivé účinky MeSH
- určení vhodnosti pacienta MeSH
- výběr pacientů MeSH
- výsledek terapie 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
- srovnávací studie MeSH
- Geografické názvy
- Evropa MeSH
Background Many patients with severe aortic stenosis are referred late with advanced symptoms or inappropriately denied intervention. The objective was to investigate whether a structured communication to referring physicians (facilitated data relay) might improve the rate and timeliness of intervention. Methods and Results A prospective registry of consecutive patients with severe aortic stenosis at 23 centers in 9 European countries with transcatheter as well as surgical aortic valve replacement being available was performed. The study included a 3-month documentation of the status quo (phase A), a 6-month intervention phase (implementing facilitated data relay), and a 3-month documentation of a legacy effect (phase-B). Two thousand one hundred seventy-one patients with severe aortic stenoses were enrolled (phase A: 759; intervention: 905; phase-B: 507). Mean age was 77.9±10.0 years, and 80% were symptomatic, including 52% with severe symptoms. During phase A, intervention was planned in 464/696 (67%), 138 (20%) were assigned to watchful waiting, 8 (1%) to balloon aortic valvuloplasty, 60 (9%) were listed as not for active treatment, and in 26 (4%), no decision was made. Three hundred sixty-three of 464 (78%) patients received the planned intervention within 3 months. Timeliness of the intervention improved as shown by the higher number of aortic valve replacements performed within 3 months (59% versus 51%, P=0.002) and a significant decrease in the time to intervention (36±38 versus 30±33 days, P=0.002). Conclusions A simple, low-cost, facilitated data relay improves timeliness of treatment for patients diagnosed with severe aortic stenosis, resulting in a shorter time to transcatheter aortic valve replacement. This effect was mainly driven by a significant improvement in timeliness of intervention in transcatheter aortic valve replacement but not surgical aortic valve replacement. Clinical Trial Registration URL: https://www.clinicaltrials.gov/. Unique identifier: NCT02241447.
4th Medical Department Hietzing Hospital Vienna Austria
Cardiology Department 1 University Clinic Mainz Germany
Centre Hospital d'Annecy France
Department of Cardiology and Angiology University of Kiel Germany
Department of Cardiology University Hospital Erlangen Germany
Department of Cardiology University of Cologne Heart Center Cologne Germany
Department of Cardiothoracic Surgery Foundation IRCCS Policlinico S Matteo Pavia Italy
Division of Cardiology and URT CNR of IFC University Magna Graecia Catanzaro Italy
Edwards Lifesciences Nyon Switzerland
German Centre for Cardiovascular Research University Heart Center and Charité Berlin Germany
Herzkatheterlabor Nymphenburg and Department of Cardiology University of Munich Germany
Institute for Pharmacology and Preventive Medicine Cloppenburg Germany
Interventional Cardiology Unit Hospital de la Santa Creu i Sant Pau Barcelona Spain
James Cook Hospital Middlesbrough UK
Krankenhaus der Barmherzigen Brüder Trier Germany
Queen Elizabeth Hospital and Institute of Cardiovascular Sciences University of Birmingham UK
Sapienza University of Rome Italy
St Bartholomew's Hospital London UK
University of Amsterdam Netherlands
Citace poskytuje Crossref.org
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- $a Background Many patients with severe aortic stenosis are referred late with advanced symptoms or inappropriately denied intervention. The objective was to investigate whether a structured communication to referring physicians (facilitated data relay) might improve the rate and timeliness of intervention. Methods and Results A prospective registry of consecutive patients with severe aortic stenosis at 23 centers in 9 European countries with transcatheter as well as surgical aortic valve replacement being available was performed. The study included a 3-month documentation of the status quo (phase A), a 6-month intervention phase (implementing facilitated data relay), and a 3-month documentation of a legacy effect (phase-B). Two thousand one hundred seventy-one patients with severe aortic stenoses were enrolled (phase A: 759; intervention: 905; phase-B: 507). Mean age was 77.9±10.0 years, and 80% were symptomatic, including 52% with severe symptoms. During phase A, intervention was planned in 464/696 (67%), 138 (20%) were assigned to watchful waiting, 8 (1%) to balloon aortic valvuloplasty, 60 (9%) were listed as not for active treatment, and in 26 (4%), no decision was made. Three hundred sixty-three of 464 (78%) patients received the planned intervention within 3 months. Timeliness of the intervention improved as shown by the higher number of aortic valve replacements performed within 3 months (59% versus 51%, P=0.002) and a significant decrease in the time to intervention (36±38 versus 30±33 days, P=0.002). Conclusions A simple, low-cost, facilitated data relay improves timeliness of treatment for patients diagnosed with severe aortic stenosis, resulting in a shorter time to transcatheter aortic valve replacement. This effect was mainly driven by a significant improvement in timeliness of intervention in transcatheter aortic valve replacement but not surgical aortic valve replacement. Clinical Trial Registration URL: https://www.clinicaltrials.gov/. Unique identifier: NCT02241447.
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