Prognosis of Type 2 Myocardial Infarction Patients Implanted With a Prophylactic Defibrillator (from the Very-High-Rate Registry)

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Deharo, Pierre | Bisson, Arnaud | Herbert, Julien | Lacour, Thibaud | Saint Etienne, Christophe | Grammatico-Guillon, Leslie | Porto, Alizée | Collart, Frederic | Bourguignon, Thierry | Cuisset, Thomas | Fauchier, Laurent | Garcia, Rodrigue | Boveda, Serge | Defaye, Pascal | Sadoul, Nicolas | Narayanan, Kumar | Perier, Marie-Cécile | Klug, Didier | Leclercq, Christophe | Babuty, Dominique | Bordachar, Pierre | Gras, Daniel | Deharo, Jean-Claude | Piot, Olivier | Providencia, Rui | Marijon, Eloi | Algalarrondo, Vincent | Theron, Alexis | David, Charlotte | André, Clémentine | Pierre, Bertrand | Bernard, Anne | Angoulvant, Denis | Clementy, Nicolas

Edité par CCSD ; Elsevier -

International audience. Background: Two competing transcatheter aortic valve replacement (TAVR) technologies are currently available. Head-to-head comparisons of the relative performances of these 2 devices have been published. However, long-term clinical outcome evaluation remains limited by the number of patients analyzed, in particular, for recent-generation devices. Methods: Based on the French administrative hospital-discharge database, the study collected information for all consecutive patients treated with a TAVR device commercialized in France between 2014 and 2018. Propensity score matching was used for the analysis of outcomes during follow-up. The objective of this study was to analyze the outcomes of TAVR according to Sapien 3 balloon-expandable (BE) versus Evolut R self-expanding TAVR technology at a nationwide level in France. Results: A total of 31 113 patients treated with either Sapien 3 BE or Evolut R self-expanding TAVR were found in the database. After matching on baseline characteristics, 20 918 patients were analyzed (10 459 in each group with BE or self-expanding valves). During follow-up (mean [SD], 358 [384]; median [interquartile range], 232 [10–599] days), BE TAVR was associated with a lower yearly incidence of all-cause death (relative risk, 0.88; corrected P =0.005), cardiovascular death (relative risk, 0.82; corrected P =0.002), and rehospitalization for heart failure (relative risk, 0.84; corrected P <0.0001). BE TAVR was also associated with lower rates of pacemaker implantation after the procedure (relative risk, 0.72; corrected P <0.0001). Conclusions: On the basis of the largest cohort available, we observed that Sapien 3 BE valves were associated with lower rates of all-cause death, cardiovascular death, rehospitalization for heart failure, and pacemaker implantation after a TAVR procedure.

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