Thomas Pilgrim1, Anna Franzone2, Stefan Stortecky2, Fabian Nietlispach2, Alan G Haynes2, David Tueller2, Stefan Toggweiler2, Oliver Muller2, Enrico Ferrari2, Stéphane Noble2, Francesco Maisano2, Raban Jeger2, Marco Roffi2, Jürg Grünenfelder2, Christoph Huber2, Peter Wenaweser2, Stephan Windecker2. 1. From the Department of Cardiology, Swiss Cardiovascular Center Bern (T.P., A.F., S.S., P.W., S.W.) and Clinical Trials Unit (A.G.H.), Bern University Hospital, Switzerland; Department of Cardiology and Cardiovascular Surgery, University Hospital Zurich, Switzerland (F.N., F.M.); Institute of Social and Preventive Medicine, Bern, Switzerland (A.G.H.); Department of Cardiology, Triemlispital, Zurich, Switzerland (D.T.); Department of Cardiology, Kantonsspital, Lucerne, Switzerland (S.T.); Department of Cardiology, Lausanne University Hospital, Switzerland (O.M.); Cardiac Surgery Unit, Cardiocentro Ticino Foundation, Lugano, Switzerland (E.F.); Division of Cardiology (S.N., M.R.) and Department of Cardiovascular Surgery (C.H.), University Hospital Geneva, Switzerland; Department of Cardiology, University Hospital of Basel, Switzerland (R.J.); Department of Cardiovascular Surgery, Hirslanden Klinik, Zurich, Switzerland (J.G.); and Department of Cardiology, Klinik im Park, Zurich, Switzerland (P.W.). thomas.pilgrim@insel.ch. 2. From the Department of Cardiology, Swiss Cardiovascular Center Bern (T.P., A.F., S.S., P.W., S.W.) and Clinical Trials Unit (A.G.H.), Bern University Hospital, Switzerland; Department of Cardiology and Cardiovascular Surgery, University Hospital Zurich, Switzerland (F.N., F.M.); Institute of Social and Preventive Medicine, Bern, Switzerland (A.G.H.); Department of Cardiology, Triemlispital, Zurich, Switzerland (D.T.); Department of Cardiology, Kantonsspital, Lucerne, Switzerland (S.T.); Department of Cardiology, Lausanne University Hospital, Switzerland (O.M.); Cardiac Surgery Unit, Cardiocentro Ticino Foundation, Lugano, Switzerland (E.F.); Division of Cardiology (S.N., M.R.) and Department of Cardiovascular Surgery (C.H.), University Hospital Geneva, Switzerland; Department of Cardiology, University Hospital of Basel, Switzerland (R.J.); Department of Cardiovascular Surgery, Hirslanden Klinik, Zurich, Switzerland (J.G.); and Department of Cardiology, Klinik im Park, Zurich, Switzerland (P.W.).
Abstract
BACKGROUND: The Transcatheter Valve Therapy (TVT) registry model was recently developed to predict the risk of in-hospital mortality in patients undergoing transcatheter aortic valve replacement. We sought to externally validate the model in an independent data set of consecutively enrolled patients in the Swiss Transcatheter Aortic Valve Implantation registry. METHODS AND RESULTS: The original prediction model was retrospectively applied to 3491 consecutive patients undergoing transcatheter aortic valve replacement in Switzerland between February 2011 and February 2016. We examined model performance in terms of discrimination (Harrel C index) and calibration (Hosmer-Lemeshow goodness-of-fit test) for prediction of in-hospital and 30-day mortality and compared its predictive accuracy with the Society of Thoracic Surgeons Predicted Risk of Mortality score. Rates of in-hospital and 30-day mortality in the external validation cohort were 2.9% and 3.8%, respectively. The TVT registry model was found to have moderate discrimination (C index, 0.66; 95% confidence interval, 0.60-0.72 and C index, 0.67; 95% confidence interval, 0.62-0.72 for in-hospital and 30-day mortality, respectively) and good calibration. Compared with the Society of Thoracic Surgeons Predicted Risk of Mortality score, the TVT registry model demonstrated improved calibration for in-hospital (slope, 0.83; P=0.23 versus slope, 0.24; P<0.001, respectively) and 30-day (slope, 1.11; P=0.40 versus slope, 0.41; P<0.001, respectively) mortality. CONCLUSIONS: In a large, multicenter, non-US cohort of patients with transcatheter aortic valve replacement, the validation of the TVT registry model demonstrated moderate discrimination and good calibration for the prediction of in-hospital and 30-day mortality. As a result, the TVT registry model should be considered an alternative to the Society of Thoracic Surgeons Predicted Risk of Mortality score for decision making and assessment of early outcome in patients eligible for transcatheter aortic valve replacement.
BACKGROUND: The Transcatheter Valve Therapy (TVT) registry model was recently developed to predict the risk of in-hospital mortality in patients undergoing transcatheter aortic valve replacement. We sought to externally validate the model in an independent data set of consecutively enrolled patients in the Swiss Transcatheter Aortic Valve Implantation registry. METHODS AND RESULTS: The original prediction model was retrospectively applied to 3491 consecutive patients undergoing transcatheter aortic valve replacement in Switzerland between February 2011 and February 2016. We examined model performance in terms of discrimination (Harrel C index) and calibration (Hosmer-Lemeshow goodness-of-fit test) for prediction of in-hospital and 30-day mortality and compared its predictive accuracy with the Society of Thoracic Surgeons Predicted Risk of Mortality score. Rates of in-hospital and 30-day mortality in the external validation cohort were 2.9% and 3.8%, respectively. The TVT registry model was found to have moderate discrimination (C index, 0.66; 95% confidence interval, 0.60-0.72 and C index, 0.67; 95% confidence interval, 0.62-0.72 for in-hospital and 30-day mortality, respectively) and good calibration. Compared with the Society of Thoracic Surgeons Predicted Risk of Mortality score, the TVT registry model demonstrated improved calibration for in-hospital (slope, 0.83; P=0.23 versus slope, 0.24; P<0.001, respectively) and 30-day (slope, 1.11; P=0.40 versus slope, 0.41; P<0.001, respectively) mortality. CONCLUSIONS: In a large, multicenter, non-US cohort of patients with transcatheter aortic valve replacement, the validation of the TVT registry model demonstrated moderate discrimination and good calibration for the prediction of in-hospital and 30-day mortality. As a result, the TVT registry model should be considered an alternative to the Society of Thoracic Surgeons Predicted Risk of Mortality score for decision making and assessment of early outcome in patients eligible for transcatheter aortic valve replacement.
Authors: Vittal Hejjaji; David J Cohen; John D Carroll; Zhuokai Li; Pratik Manandhar; Sreekanth Vemulapalli; Adam J Nelson; Ali O Malik; Michael J Mack; John A Spertus; Suzanne V Arnold Journal: Circ Cardiovasc Qual Outcomes Date: 2021-02-18