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      <subfield code="a">González Bermúdez, Inmaculada</subfield>
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      <subfield code="a">Bordes Siscar, Pascual</subfield>
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      <subfield code="a">Franco-Peláez, Juan A</subfield>
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      <subfield code="a">Cruz-González, Ignacio</subfield>
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      <subfield code="a">Ruiz Quevedo, Valeriano</subfield>
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      <subfield code="a">Sánchez-Recalde, Ángel</subfield>
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      <subfield code="a">Jiménez Britez, Gustavo</subfield>
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      <subfield code="a">Sánchez-Rubio Lezcano, Juan</subfield>
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      <subfield code="a">Barreiro-Pardal, Cristina</subfield>
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      <subfield code="a">Núñez-Gil, Iván</subfield>
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      <subfield code="a">Abu-Assi, Emad</subfield>
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      <subfield code="a">Iñiguez-Romo, Andrés</subfield>
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      <subfield code="a">Fuster, Valentín</subfield>
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      <subfield code="a">Ibáñez, Borja</subfield>
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      <subfield code="c">2025-04-10</subfield>
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      <subfield code="a">Sodium-glucose cotransporter 2 (SGLT2) inhibitors reduce the risk of heart-failure admission among high-risk patients. However, most patients with valvular heart disease, including those undergoing transcatheter aortic-valve implantation (TAVI), have been excluded from randomized trials.

We conducted this randomized, controlled trial in Spain to evaluate the efficacy of dapagliflozin (at a dose of 10 mg once daily) as compared with standard care alone in patients with aortic stenosis who were undergoing TAVI. All the patients had a history of heart failure plus at least one of the following: renal insufficiency, diabetes, or left ventricular systolic dysfunction. The primary outcome was a composite of death from any cause or worsening of heart failure, defined as hospitalization or an urgent visit, at 1 year of follow-up.
A total of 620 patients were randomly assigned to receive dapagliflozin and 637 to receive standard care alone after TAVI; after exclusions, a total of 1222 patients were included in the primary analysis. A primary-outcome event occurred in 91 patients (15.0%) in the dapagliflozin group and in 124 patients (20.1%) in the standard-care group (hazard ratio, 0.72; 95% confidence interval [CI], 0.55 to 0.95; P = 0.02). Death from any cause occurred in 47 patients (7.8%) in the dapagliflozin group and in 55 (8.9%) in the standard-care group (hazard ratio, 0.87; 95% CI, 0.59 to 1.28). Worsening of heart failure occurred in 9.4% and 14.4% of the patients, respectively (subhazard ratio, 0.63; 95% CI, 0.45 to 0.88). Genital infection and hypotension were significantly more common in the dapagliflozin group.
Among older adults with aortic stenosis undergoing TAVI who were at high risk for heart-failure events, dapagliflozin resulted in a significantly lower incidence of death from any cause or worsening of heart failure than standard care alone. (Funded by Instituto de Salud Carlos III and others; ClinicalTrials.gov number, NCT04696185.).</subfield>
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      <subfield code="a">N Engl J Med. 2025 Apr 10;392(14):1396-1405.</subfield>
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      <subfield code="a">New England Journal of Medicine</subfield>
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      <subfield code="a">40162639</subfield>
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      <subfield code="a">https://hdl.handle.net/20.500.12105/26639</subfield>
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      <subfield code="a">Dapagliflozin in Patients Undergoing Transcatheter Aortic-Valve Implantation.</subfield>
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