Long-term outcomes of inoperable patients with aortic stenosis randomly assigned to transcatheter aortic valve replacement or standard therapy
- PMID: 25205802
- DOI: 10.1161/CIRCULATIONAHA.114.009834
Long-term outcomes of inoperable patients with aortic stenosis randomly assigned to transcatheter aortic valve replacement or standard therapy
Abstract
Background: The long-term outcomes of transcatheter aortic valve replacement (TAVR) in inoperable patients with severe aortic stenosis remain unknown.
Methods and results: In the Placement of Aortic Transcatheter Valves (PARTNER) study, 358 patients were randomly assigned to TAVR or standard therapy. We report the 3-year outcomes on these patients, and the pooled outcomes for all randomly assigned inoperable patients (n=449) in PARTNER, as well, including the randomized portion of the continued access study (n=91). The 3-year mortality rate in the TAVR and standard therapy groups was 54.1% and 80.9%, respectively (P<0.001; hazard ratio, 0.53; 95% confidence interval, 0.41-0.68; P<0.001). In survivors, there was significant improvement in New York Heart Association functional class sustained at 3 years. The cumulative incidence of strokes at 3-year follow-up was 15.7% in TAVR patients versus 5.5% in patients undergoing standard therapy (hazard ratio, 2.81; 95% confidence interval, 1.26-6.26; P=0.012); however, the composite of death or strokes was significantly lower after TAVR versus standard therapy (57.4% versus 80.9%, P<0.001; hazard ratio, 0.60; 95% confidence interval, 0.46-0.77; P<0.001). Echocardiography showed a sustained increase in aortic valve area and decrease in transvalvular gradient after TAVR. Analysis of the 449 pooled randomly assigned patients (TAVR, n=220; standard therapy, n=229) demonstrated significant improvement in all-cause mortality and functional status during early and 3-year follow-up. The results of the pooled cohort were similar to the results obtained from the pivotal PARTNER trial.
Conclusions: TAVR resulted in better survival and functional status in inoperable patients with severe aortic stenosis with durable hemodynamic benefit on long-term follow-up. However, high residual mortality, even in successfully treated TAVR patients, highlights the need for more strategic patient selection.
Clinical trial registration url: http://www.clinicaltrials.gov. Unique identifier: NCT00530894.
Keywords: aortic valve; aortic valve stenosis; outcome assessment (health care).
© 2014 American Heart Association, Inc.
Comment in
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Death and interventional cardiology: a tale of 2 trials.Circulation. 2014 Oct 21;130(17):1442-4. doi: 10.1161/CIRCULATIONAHA.114.012740. Epub 2014 Sep 9. Circulation. 2014. PMID: 25205803 No abstract available.
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Letter by Frigerio et al Regarding Article, "Long-Term Outcomes of Inoperable Patients With Aortic Stenosis Randomly Assigned to Transcatheter Aortic Valve Replacement or Standard Therapy".Circulation. 2015 Aug 11;132(6):e117. doi: 10.1161/CIRCULATIONAHA.114.014377. Circulation. 2015. PMID: 26260503 No abstract available.
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Response to Letter Regarding Article, "Long-Term Outcomes of Inoperable Patients With Aortic Stenosis Randomly Assigned to Transcatheter Aortic Valve Replacement or Standard Therapy".Circulation. 2015 Aug 11;132(6):e118-9. doi: 10.1161/CIRCULATIONAHA.115.015363. Circulation. 2015. PMID: 26260504 No abstract available.
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