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Quantifying the Costs of Transcatheter Aortic Valve Replacement Hesitancy
Author(s) -
Garcia Santiago,
Gössl Mario,
Sorajja Paul
Publication year - 2018
Publication title -
journal of the american heart association
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.494
H-Index - 85
ISSN - 2047-9980
DOI - 10.1161/jaha.118.010610
Subject(s) - medicine , aortic valve replacement , stenosis , valvular heart disease , valve replacement , population , aortic valve stenosis , cardiology , surgery , environmental health
A ortic stenosis (AS) is one the most common valvular heart diseases. It affects 5% of the adult population ≥65 years of age. Current guidelines recommend surgical or transcatheter aortic valve replacement (AVR) for patients with severe and symptomatic AS. Because there is no medical therapy that can halt disease progression or effectively treat symptoms, prognosis is dismal without AVR, with 1-year mortality of 25% to 50% in symptomatic patients with severe AS. The goal of informed consent is to provide patients and families with estimates of the risks and benefits of the procedure and to discuss alternative treatments, whether medical or procedural based, whenever available. In general, when the perceived benefits of the procedure exceed the potential risks, most patients decide to consent to the performance of the procedure. Given the safety of modern surgery and dismal prognosis of medical therapy, pursuit of transcatheter AVR (TAVR) is usually a straightforward proposition. Confronted with a 25% to 50% risk of dying without TAVR, most patients with symptomatic severe AS prefer to take the <5% risk of mortality associated with the procedure. Understanding the pros and cons of valve replacement is a hallmark of an effective shared decision-making process. Variables associated with and outcome of initial TAVR refusal have not been previously studied in a systematicmanner using a large national database, in part because most registries were designed to capture procedural outcomes, not refusals. The study by Yamamoto et al in this issue of the Journal of the American Heart Association (JAHA) sheds light into this subject by evaluating factors associated with and prognosis of initial refusal to a TAVR procedure in patients with symptomatic AS. How often do patients refuse TAVR? What are the reasons for TAVR refusal and why do patients change their mind? Finally, what are the outcomes of those patients who, having refused TAVR, change their mind and undergo the procedure at a later time? Using a large (n=1542) Japanese TAVR registry (Optimized Catheter Valvular Intervention Transcatheter Aortic Valve Implantation), the authors make several interesting observations. First, TAVR refusal is uncommon (1.8%). Second, most patients who refuse a TAVR procedure do so out of fear (47%) or perception of clinical stability, despite a majority reporting class II or III New York Heart Association functional class symptoms. Third, 75% of patients who initially refused TAVR changed their mind after a heart failure exacerbation. Fourth, the median time from refusal to acceptance was 5 months. Finally, the shortand long-term outcomes of patients who initially refused TAVR were significantly worse than those of patients who initially accepted the procedure (30-day mortality, 7% versus 1.3%; 1-year mortality, 28% versus 10%). The study has important limitations inherent to observational registries. First, the sample size of the refusal group is small (n=28), which tends to generate imprecise estimates of harm. Second, patients who initially refused TAVR were sicker than patients who accepted the procedure, because they were older (87 versus 84 years of age), were more likely to have a high-risk Society of Thoracic Surgeons score (67% versus 32%), and presented with comorbid conditions, such as clinical frailty, mitral regurgitation, and peripheral arterial disease at a much higher rate. The refusal group was also more likely to undergo nontransfemoral TAVR (32% versus 20%), which carries a higher risk of complications and prolonged length of stay. Are the poor outcomes of the refusal group attributable to treatment delay, comorbid conditions, or a combination of both? The authors attempted to adjust with statistical analysis, and TAVR refusal was independently associated with increased long-term mortality, with a hazard ratio of 3.37 (95% confidence interval, 1.52– 7.48; P=0.003). It is well accepted that such adjustments are helpful but can never fully account for selection bias in retrospective analyses. The opinions expressed in this article are not necessarily those of the editors or of the American Heart Association. From the University of Minnesota and Minneapolis VA Healthcare System, Minneapolis, MN (S.G.); and Minneapolis Heart Institute, Minneapolis, MN (M.G., P.S.). Correspondence to: Santiago Garcia, MD, Structural Heart Program, University of Minnesota, Minneapolis VAHCS, Minneapolis, MN. E-mail: santiagogarcia@me.com J Am Heart Assoc. 2018;7:e010610. DOI: 10.1161/JAHA.118.010610. a 2018 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

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