TY - JOUR
T1 - Transcatheter Valve Replacement in Severe Tricuspid Regurgitation
AU - Hahn, Rebecca T.
AU - Makkar, Raj
AU - Thourani, Vinod H.
AU - Makar, Moody
AU - Sharma, Rahul P.
AU - Haeffele, Christiane
AU - Davidson, Charles J.
AU - Narang, Akhil
AU - O'neill, Brian
AU - Lee, James
AU - Yadav, Pradeep
AU - Zahr, Firas
AU - Chadderdon, Scott
AU - Eleid, Mackram
AU - Pislaru, Sorin
AU - Smith, Robert
AU - Szerlip, Molly
AU - Whisenant, Brian
AU - Sekaran, Nishant K.
AU - Garcia, Santiago
AU - Stewart-Dehner, Terri
AU - Thiele, Holger
AU - Kipperman, Robert
AU - Koulogiannis, Konstantinos
AU - Lim, D. Scott
AU - Fowler, Dale
AU - Kapadia, Samir
AU - Harb, Serge C.
AU - Grayburn, Paul A.
AU - Sannino, Anna
AU - Mack, Michael J.
AU - Leon, Martin B.
AU - Lurz, Philipp
AU - Kodali, Susheel K.
N1 - Publisher Copyright:
© 2024 Massachusetts Medical Society.
PY - 2025/1/9
Y1 - 2025/1/9
N2 - Background Severe tricuspid regurgitation is associated with disabling symptoms and an increased risk of death. Data regarding outcomes after percutaneous transcatheter tricuspid-valve replacement are needed. Methods In this international, multicenter trial, we randomly assigned 400 patients with severe symptomatic tricuspid regurgitation in a 2:1 ratio to undergo either transcatheter tricuspid-valve replacement and medical therapy (valve-replacement group) or medical therapy alone (control group). The hierarchical composite primary outcome was death from any cause, implantation of a right ventricular assist device or heart transplantation, postindex tricuspid-valve intervention, hospitalization for heart failure, an improvement of at least 10 points in the score on the Kansas City Cardiomyopathy Questionnaire overall summary (KCCQ-OS), an improvement of at least one New York Heart Association (NYHA) functional class, and an improvement of at least 30 m on the 6-minute walk distance. A win ratio was calculated for the primary outcome by comparing all possible patient pairs, starting with the first event in the hierarchy. Results A total of 267 patients were assigned to the valve-replacement group and 133 to the control group. At 1 year, the win ratio favoring valve replacement was 2.02 (95% confidence interval [CI], 1.56 to 2.62; P<0.001). In comparisons of patient pairs, those in the valve-replacement group had more wins than the control group with respect to death from any cause (14.8% vs. 12.5%), postindex tricuspid-valve intervention (3.2% vs. 0.6%), and improvement in the KCCQ-OS score (23.1% vs. 6.0%), NYHA class (10.2% vs. 0.8%), and 6-minute walk distance (1.1% vs. 0.9%). The valve-replacement group had fewer wins than the control group with respect to the annualized rate of hospitalization for heart failure (9.7% vs. 10.0%). Severe bleeding occurred in 15.4% of the valve-replacement group and in 5.3% of the control group (P=0.003); new permanent pacemakers were implanted in 17.4% and 2.3%, respectively (P<0.001). Conclusions For patients with severe tricuspid regurgitation, transcatheter tricuspid-valve replacement was superior to medical therapy alone for the primary composite outcome, driven primarily by improvements in symptoms and quality of life.
AB - Background Severe tricuspid regurgitation is associated with disabling symptoms and an increased risk of death. Data regarding outcomes after percutaneous transcatheter tricuspid-valve replacement are needed. Methods In this international, multicenter trial, we randomly assigned 400 patients with severe symptomatic tricuspid regurgitation in a 2:1 ratio to undergo either transcatheter tricuspid-valve replacement and medical therapy (valve-replacement group) or medical therapy alone (control group). The hierarchical composite primary outcome was death from any cause, implantation of a right ventricular assist device or heart transplantation, postindex tricuspid-valve intervention, hospitalization for heart failure, an improvement of at least 10 points in the score on the Kansas City Cardiomyopathy Questionnaire overall summary (KCCQ-OS), an improvement of at least one New York Heart Association (NYHA) functional class, and an improvement of at least 30 m on the 6-minute walk distance. A win ratio was calculated for the primary outcome by comparing all possible patient pairs, starting with the first event in the hierarchy. Results A total of 267 patients were assigned to the valve-replacement group and 133 to the control group. At 1 year, the win ratio favoring valve replacement was 2.02 (95% confidence interval [CI], 1.56 to 2.62; P<0.001). In comparisons of patient pairs, those in the valve-replacement group had more wins than the control group with respect to death from any cause (14.8% vs. 12.5%), postindex tricuspid-valve intervention (3.2% vs. 0.6%), and improvement in the KCCQ-OS score (23.1% vs. 6.0%), NYHA class (10.2% vs. 0.8%), and 6-minute walk distance (1.1% vs. 0.9%). The valve-replacement group had fewer wins than the control group with respect to the annualized rate of hospitalization for heart failure (9.7% vs. 10.0%). Severe bleeding occurred in 15.4% of the valve-replacement group and in 5.3% of the control group (P=0.003); new permanent pacemakers were implanted in 17.4% and 2.3%, respectively (P<0.001). Conclusions For patients with severe tricuspid regurgitation, transcatheter tricuspid-valve replacement was superior to medical therapy alone for the primary composite outcome, driven primarily by improvements in symptoms and quality of life.
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U2 - 10.1056/NEJMoa2401918
DO - 10.1056/NEJMoa2401918
M3 - Article
C2 - 39475399
AN - SCOPUS:85209759989
SN - 0028-4793
VL - 392
SP - 115
EP - 126
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 2
ER -