Table 1

Characteristics of selected studies for the prognostic value of mitral regurgitation in patients undergoing TAVI

Author, country, year, refDesignProspectiveUniversalConsecutive recruitmentNo. centresValve typeInclusion periodnFollow-up% patients lost to follow-upIndependent adjudication event committee
Rodes-Cabau, Canada, 201016National RegistryYesYes*Yes6BEVJanuary 2005 to June 2009339240 days0No
Leon, USA, 20105RCTYesYesNo25BEVMay 2007 to March 20091711.6 years0Yes
Smith, USA, 20116RCTYesYesNo25BEVMay 2007 to August 20093341.4 years0.6Yes
Gilard, France, 201217National RegistryYesYesYes34BEV/SEVJanuary 2010 to October 20113195114 days0.2Yes
Zahn, Germany, 201318National RegistryYesNoYes22BEV/SEVJanuary 2009 to June 2010139112.9 months5.2No
D'Onofrio, Italy, 201319National RegistryYesNoYes21BEVApril 2008 to June 201277412 months0No
Bedogni, Italy, 20139National RegistryYesYes†Yes14SEVJune 2007 to April 20111007>1 year (97.3%)0Yes
Sabaté, Spain, 201320National RegistryNoNoNo37BEV/SEVJanuary 2010 to December 2011883244 days3.7No
  • *For Edwards valve.

  • †For initial Corevalve System experience.

  • BEV, balloon-expandable valve; RCT, randomised clinical trial; SEV, self-expandable valve.