William D Toff1,2, David Hildick-Smith3, Jan Kovac1,2, Michael J Mullen4, Olaf Wendler5, Anita Mansouri6, Ines Rombach6, Keith R Abrams7,8,9, Simon P Conroy9, Marcus D Flather10, Alastair M Gray11, Philip MacCarthy12, Mark J Monaghan12, Bernard Prendergast13, Simon Ray14, Christopher P Young15, David C Crossman16, John G F Cleland17, Mark A de Belder18, Peter F Ludman19, Stephen Jones20, Cameron G Densem21, Steven Tsui22, Manoj Kuduvalli23, Joseph D Mills24, Adrian P Banning25, Rana Sayeed26, Ragheb Hasan27, Douglas G W Fraser28, Uday Trivedi3, Simon W Davies29, Alison Duncan29, Nick Curzen30, Sunil K Ohri30, Christopher J Malkin31, Pankaj Kaul32, Douglas F Muir33, W Andrew Owens34, Neal G Uren35, Renzo Pessotto35, Simon Kennon36, Wael I Awad36, Saib S Khogali37, Maciej Matuszewski37, Richard J Edwards38, Bandigowdanapalya C Ramesh38, Miles Dalby39, Shahzad G Raja40, Giovanni Mariscalco1,2, Clinton Lloyd41, Ian D Cox42, Simon R Redwood43, Mark G Gunning44, Paul D Ridley45. 1. Department of Cardiovascular Sciences, University of Leicester, Leicester, England. 2. National Institute for Health Research Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, England. 3. Sussex Cardiac Centre, Brighton and Sussex University Hospitals NHS Trust, Brighton, England. 4. Institute of Cardiovascular Science, University College London, London, England. 5. Department of Cardiothoracic Surgery, King's College Hospital NHS Foundation Trust, London, England. 6. Oxford Clinical Trials Research Unit, Nuffield Department of Orthopedics, Rheumatology, and Musculoskeletal Sciences, University of Oxford, Oxford, England. 7. Centre for Health Economics, University of York, York, England. 8. Department of Statistics, University of Warwick, Coventry, England. 9. Department of Health Sciences, University of Leicester, Leicester, England. 10. Norwich Medical School, University of East Anglia, Norwich, England. 11. Health Economics Research Centre, Nuffield Department of Population Health, University of Oxford, Oxford, England. 12. Department of Cardiology, King's College Hospital NHS Foundation Trust, London, England. 13. Department of Cardiology, St Thomas' Hospital, London, England. 14. Department of Cardiology, Manchester University NHS Foundation Trust, Manchester, England. 15. Department of Cardiothoracic Surgery, St Thomas' Hospital, London, England. 16. School of Medicine, University of St Andrews, Fife, Scotland. 17. Robertson Centre for Biostatistics and Glasgow Clinical Trials Unit, Institute of Health and Wellbeing, University of Glasgow, Glasgow, Scotland. 18. National Institute for Cardiovascular Outcomes Research, Barts Health NHS Trust, London, England. 19. Institute of Cardiovascular Sciences, Birmingham University, Birmingham, England. 20. Surgical Intervention Trials Unit, Nuffield Department of Surgical Sciences, University of Oxford, Oxford, England. 21. Department of Cardiology, Royal Papworth Hospital, Cambridge, England. 22. Department of Cardiothoracic Surgery, Royal Papworth Hospital, Cambridge, England. 23. Department of Cardiothoracic Surgery, Liverpool Heart and Chest Hospital NHS Foundation Trust, Liverpool, England. 24. Department of Cardiology, Liverpool Heart and Chest Hospital NHS Foundation Trust, Liverpool, England. 25. Department of Cardiology, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, England. 26. Department of Cardiothoracic Surgery, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, England. 27. Department of Cardiothoracic Surgery, Manchester University NHS Foundation Trust, Manchester, England. 28. Department of Cardiovascular Medicine, University of Manchester, Manchester, England. 29. Cardiac Department, Royal Brompton Hospital, Royal Brompton and Harefield NHS Foundation Trust, London, England. 30. Wessex Cardiothoracic Centre, University Hospital Southampton, Southampton, England. 31. Department of Cardiology, Leeds Teaching Hospitals NHS Trust, Leeds, England. 32. Department of Cardiac Surgery, Leeds Teaching Hospitals NHS Trust, Leeds, England. 33. Department of Cardiology, James Cook University Hospital, South Tees Hospitals NHS Foundation Trust, Middlesbrough, England. 34. Department of Cardiothoracic Surgery, James Cook University Hospital, South Tees Hospitals NHS Foundation Trust, Middlesbrough, England. 35. Edinburgh Heart Centre, Royal Infirmary of Edinburgh, Edinburgh, Scotland. 36. Barts Heart Centre, Barts Health NHS Trust, London, England. 37. Heart and Lung Centre, New Cross Hospital, Wolverhampton, England. 38. Cardiothoracic Department, Newcastle upon Tyne Hospitals, Newcastle upon Tyne, England. 39. Department of Cardiology, Harefield Hospital, Royal Brompton and Harefield NHS Foundation Trust, London, England. 40. Department of Cardiac Surgery, Harefield Hospital, Royal Brompton and Harefield NHS Foundation Trust, London, England. 41. Department of Cardiothoracic Surgery, Derriford Hospital, Plymouth, England. 42. Department of Cardiology, Derriford Hospital, Plymouth, England. 43. Cardiovascular Division, King's College London, British Heart Foundation Centre of Research Excellence, Rayne Institute, St Thomas' Hospital, London, England. 44. Cardiology Department, Royal Stoke University Hospital, Stoke-on-Trent, England. 45. Department of Cardiothoracic Surgery, Royal Stoke University Hospital, Stoke-on-Trent, England.
Abstract
Importance: Transcatheter aortic valve implantation (TAVI) is a less invasive alternative to surgical aortic valve replacement and is the treatment of choice for patients at high operative risk. The role of TAVI in patients at lower risk is unclear. Objective: To determine whether TAVI is noninferior to surgery in patients at moderately increased operative risk. Design, Setting, and Participants: In this randomized clinical trial conducted at 34 UK centers, 913 patients aged 70 years or older with severe, symptomatic aortic stenosis and moderately increased operative risk due to age or comorbidity were enrolled between April 2014 and April 2018 and followed up through April 2019. Interventions: TAVI using any valve with a CE mark (indicating conformity of the valve with all legal and safety requirements for sale throughout the European Economic Area) and any access route (n = 458) or surgical aortic valve replacement (surgery; n = 455). Main Outcomes and Measures: The primary outcome was all-cause mortality at 1 year. The primary hypothesis was that TAVI was noninferior to surgery, with a noninferiority margin of 5% for the upper limit of the 1-sided 97.5% CI for the absolute between-group difference in mortality. There were 36 secondary outcomes (30 reported herein), including duration of hospital stay, major bleeding events, vascular complications, conduction disturbance requiring pacemaker implantation, and aortic regurgitation. Results: Among 913 patients randomized (median age, 81 years [IQR, 78 to 84 years]; 424 [46%] were female; median Society of Thoracic Surgeons mortality risk score, 2.6% [IQR, 2.0% to 3.4%]), 912 (99.9%) completed follow-up and were included in the noninferiority analysis. At 1 year, there were 21 deaths (4.6%) in the TAVI group and 30 deaths (6.6%) in the surgery group, with an adjusted absolute risk difference of -2.0% (1-sided 97.5% CI, -∞ to 1.2%; P < .001 for noninferiority). Of 30 prespecified secondary outcomes reported herein, 24 showed no significant difference at 1 year. TAVI was associated with significantly shorter postprocedural hospitalization (median of 3 days [IQR, 2 to 5 days] vs 8 days [IQR, 6 to 13 days] in the surgery group). At 1 year, there were significantly fewer major bleeding events after TAVI compared with surgery (7.2% vs 20.2%, respectively; adjusted hazard ratio [HR], 0.33 [95% CI, 0.24 to 0.45]) but significantly more vascular complications (10.3% vs 2.4%; adjusted HR, 4.42 [95% CI, 2.54 to 7.71]), conduction disturbances requiring pacemaker implantation (14.2% vs 7.3%; adjusted HR, 2.05 [95% CI, 1.43 to 2.94]), and mild (38.3% vs 11.7%) or moderate (2.3% vs 0.6%) aortic regurgitation (adjusted odds ratio for mild, moderate, or severe [no instance of severe reported] aortic regurgitation combined vs none, 4.89 [95% CI, 3.08 to 7.75]). Conclusions and Relevance: Among patients aged 70 years or older with severe, symptomatic aortic stenosis and moderately increased operative risk, TAVI was noninferior to surgery with respect to all-cause mortality at 1 year. Trial Registration: isrctn.com Identifier: ISRCTN57819173.
Importance: Transcatheter aortic valve implantation (TAVI) is a less invasive alternative to surgical aortic valve replacement and is the treatment of choice for patients at high operative risk. The role of TAVI in patients at lower risk is unclear. Objective: To determine whether TAVI is noninferior to surgery in patients at moderately increased operative risk. Design, Setting, and Participants: In this randomized clinical trial conducted at 34 UK centers, 913 patients aged 70 years or older with severe, symptomatic aortic stenosis and moderately increased operative risk due to age or comorbidity were enrolled between April 2014 and April 2018 and followed up through April 2019. Interventions: TAVI using any valve with a CE mark (indicating conformity of the valve with all legal and safety requirements for sale throughout the European Economic Area) and any access route (n = 458) or surgical aortic valve replacement (surgery; n = 455). Main Outcomes and Measures: The primary outcome was all-cause mortality at 1 year. The primary hypothesis was that TAVI was noninferior to surgery, with a noninferiority margin of 5% for the upper limit of the 1-sided 97.5% CI for the absolute between-group difference in mortality. There were 36 secondary outcomes (30 reported herein), including duration of hospital stay, major bleeding events, vascular complications, conduction disturbance requiring pacemaker implantation, and aortic regurgitation. Results: Among 913 patients randomized (median age, 81 years [IQR, 78 to 84 years]; 424 [46%] were female; median Society of Thoracic Surgeons mortality risk score, 2.6% [IQR, 2.0% to 3.4%]), 912 (99.9%) completed follow-up and were included in the noninferiority analysis. At 1 year, there were 21 deaths (4.6%) in the TAVI group and 30 deaths (6.6%) in the surgery group, with an adjusted absolute risk difference of -2.0% (1-sided 97.5% CI, -∞ to 1.2%; P < .001 for noninferiority). Of 30 prespecified secondary outcomes reported herein, 24 showed no significant difference at 1 year. TAVI was associated with significantly shorter postprocedural hospitalization (median of 3 days [IQR, 2 to 5 days] vs 8 days [IQR, 6 to 13 days] in the surgery group). At 1 year, there were significantly fewer major bleeding events after TAVI compared with surgery (7.2% vs 20.2%, respectively; adjusted hazard ratio [HR], 0.33 [95% CI, 0.24 to 0.45]) but significantly more vascular complications (10.3% vs 2.4%; adjusted HR, 4.42 [95% CI, 2.54 to 7.71]), conduction disturbances requiring pacemaker implantation (14.2% vs 7.3%; adjusted HR, 2.05 [95% CI, 1.43 to 2.94]), and mild (38.3% vs 11.7%) or moderate (2.3% vs 0.6%) aortic regurgitation (adjusted odds ratio for mild, moderate, or severe [no instance of severe reported] aortic regurgitation combined vs none, 4.89 [95% CI, 3.08 to 7.75]). Conclusions and Relevance: Among patients aged 70 years or older with severe, symptomatic aortic stenosis and moderately increased operative risk, TAVI was noninferior to surgery with respect to all-cause mortality at 1 year. Trial Registration: isrctn.com Identifier: ISRCTN57819173.
Authors: Jeffrey J Popma; G Michael Deeb; Steven J Yakubov; Mubashir Mumtaz; Hemal Gada; Daniel O'Hair; Tanvir Bajwa; John C Heiser; William Merhi; Neal S Kleiman; Judah Askew; Paul Sorajja; Joshua Rovin; Stanley J Chetcuti; David H Adams; Paul S Teirstein; George L Zorn; John K Forrest; Didier Tchétché; Jon Resar; Antony Walton; Nicolo Piazza; Basel Ramlawi; Newell Robinson; George Petrossian; Thomas G Gleason; Jae K Oh; Michael J Boulware; Hongyan Qiao; Andrew S Mugglin; Michael J Reardon Journal: N Engl J Med Date: 2019-03-16 Impact factor: 91.245
Authors: Raj R Makkar; Gregory Fontana; Hasan Jilaihawi; Tarun Chakravarty; Klaus F Kofoed; Ole De Backer; Federico M Asch; Carlos E Ruiz; Niels T Olsen; Alfredo Trento; John Friedman; Daniel Berman; Wen Cheng; Mohammad Kashif; Vladimir Jelnin; Chad A Kliger; Hongfei Guo; Augusto D Pichard; Neil J Weissman; Samir Kapadia; Eric Manasse; Deepak L Bhatt; Martin B Leon; Lars Søndergaard Journal: N Engl J Med Date: 2015-10-05 Impact factor: 91.245
Authors: A Pieter Kappetein; Stuart J Head; Philippe Généreux; Nicolo Piazza; Nicolas M van Mieghem; Eugene H Blackstone; Thomas G Brott; David J Cohen; Donald E Cutlip; Gerrit-Anne van Es; Rebecca T Hahn; Ajay J Kirtane; Mitchell W Krucoff; Susheel Kodali; Michael J Mack; Roxana Mehran; Josep Rodés-Cabau; Pascal Vranckx; John G Webb; Stephan Windecker; Patrick W Serruys; Martin B Leon Journal: J Am Coll Cardiol Date: 2012-10-09 Impact factor: 24.094
Authors: John V Conte; James Hermiller; Jon R Resar; G Michael Deeb; Thomas G Gleason; David H Adams; Jeffrey J Popma; Steven J Yakubov; Daniel Watson; Jia Guo; George L Zorn; Michael J Reardon Journal: Semin Thorac Cardiovasc Surg Date: 2017-06-19
Authors: Thomas G Gleason; Michael J Reardon; Jeffrey J Popma; G Michael Deeb; Steven J Yakubov; Joon S Lee; Neal S Kleiman; Stan Chetcuti; James B Hermiller; John Heiser; William Merhi; George L Zorn; Peter Tadros; Newell Robinson; George Petrossian; G Chad Hughes; J Kevin Harrison; John V Conte; Mubashir Mumtaz; Jae K Oh; Jian Huang; David H Adams Journal: J Am Coll Cardiol Date: 2018-09-21 Impact factor: 24.094
Authors: Ahmed A Kolkailah; Rami Doukky; Marc P Pelletier; Annabelle S Volgman; Tsuyoshi Kaneko; Ashraf F Nabhan Journal: Cochrane Database Syst Rev Date: 2019-12-20