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. (Funded by Edwards Lifesciences; TRISCEND II ClinicalTrials.gov number, NCT04482062.).

Transcatheter Valve Replacement in Severe Tricuspid Regurgitation / Hahn, Rebecca T; Makkar, Raj; Thourani, Vinod H; Makar, Moody; Sharma, Rahul P; Haeffele, Christiane; Davidson, Charles J; Narang, Akhil; O'Neill, Brian; Lee, James; Yadav, Pradeep; Zahr, Firas; Chadderdon, Scott; Eleid, Mackram; Pislaru, Sorin; Smith, Robert; Szerlip, Molly; Whisenant, Brian; Sekaran, Nishant K; Garcia, Santiago; Stewart-Dehner, Terri; Thiele, Holger; Kipperman, Robert; Koulogiannis, Konstantinos; Lim, D Scott; Fowler, Dale; Kapadia, Samir; Harb, Serge C; Grayburn, Paul A; Sannino, Anna; Mack, Michael J; Leon, Martin B; Lurz, Philipp; Kodali, Susheel K. - In: THE NEW ENGLAND JOURNAL OF MEDICINE. - ISSN 0028-4793. - 392:2(2025). [10.1056/NEJMoa2401918]

Transcatheter Valve Replacement in Severe Tricuspid Regurgitation

Sannino, Anna
Data Curation
;
2025

Abstract

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. (Funded by Edwards Lifesciences; TRISCEND II ClinicalTrials.gov number, NCT04482062.).
2025
Transcatheter Valve Replacement in Severe Tricuspid Regurgitation / Hahn, Rebecca T; Makkar, Raj; Thourani, Vinod H; Makar, Moody; Sharma, Rahul P; Haeffele, Christiane; Davidson, Charles J; Narang, Akhil; O'Neill, Brian; Lee, James; Yadav, Pradeep; Zahr, Firas; Chadderdon, Scott; Eleid, Mackram; Pislaru, Sorin; Smith, Robert; Szerlip, Molly; Whisenant, Brian; Sekaran, Nishant K; Garcia, Santiago; Stewart-Dehner, Terri; Thiele, Holger; Kipperman, Robert; Koulogiannis, Konstantinos; Lim, D Scott; Fowler, Dale; Kapadia, Samir; Harb, Serge C; Grayburn, Paul A; Sannino, Anna; Mack, Michael J; Leon, Martin B; Lurz, Philipp; Kodali, Susheel K. - In: THE NEW ENGLAND JOURNAL OF MEDICINE. - ISSN 0028-4793. - 392:2(2025). [10.1056/NEJMoa2401918]
File in questo prodotto:
File Dimensione Formato  
NEJMoa2401918.pdf

accesso aperto

Tipologia: Versione Editoriale (PDF)
Licenza: Dominio pubblico
Dimensione 591.87 kB
Formato Adobe PDF
591.87 kB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/993562
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact