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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,...
Language English Country Great Britain
Document type Comparative Study, Journal Article, Multicenter Study, Observational Study, Research Support, Non-U.S. Gov't
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- MeSH
- Aortic Valve Stenosis diagnostic imaging nursing therapy MeSH
- Balloon Valvuloplasty * adverse effects MeSH
- Time-to-Treatment * MeSH
- Time Factors MeSH
- Heart Valve Prosthesis Implantation * adverse effects MeSH
- Echocardiography MeSH
- Clinical Decision-Making MeSH
- Referral and Consultation * MeSH
- Humans MeSH
- Watchful Waiting * MeSH
- Prospective Studies MeSH
- Cross-Sectional Studies MeSH
- Registries MeSH
- Nurse's Role * MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Severity of Illness Index MeSH
- Transcatheter Aortic Valve Replacement * adverse effects MeSH
- Eligibility Determination MeSH
- Patient Selection MeSH
- Treatment Outcome MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Observational Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Geographicals
- Europe 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
References provided by 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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