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                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Pérez-Belmonte, Luis M.</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Ricci, Michele</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Sanz-Cánovas, Jaime</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Cobos-Palacios, Lidia</mods:namePart>
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               <mods:name>
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                  <mods:namePart>López-Carmona, María D.</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Ruiz-Moreno, M. Isabel</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Millán-Gómez, Mercedes</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Bernal-López, M. Rosa</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Jansen-Chaparro, Sergio</mods:namePart>
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               <mods:name>
                  <mods:role>
                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Gómez-Huelgas, Ricardo</mods:namePart>
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                  <mods:namePart>[Pérez-Belmonte,LM; Ricci,M; Sanz-Cánovas,J; Cobos-Palacios,L; López-Carmona,MD; Ruiz-Moreno,MI; Bernal-López,MR; Jansen-Chaparro,S; Gómez-Huelgas,R] Servicio de Medicina Interna, Hospital Regional Universitario de Málaga, Instituto de Investigación Biomédica de Málaga (IBIMA), Universidad de Málaga (UMA), Málaga, Spain. [Pérez-Belmonte,LM] Servicio de Medicina Interna, Hospital Helicópteros Sanitarios, Marbella, Spain. [Pérez-Belmonte,LM; Millán-Gómez,M] Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares (CIBERCV), Instituto de Salud Carlos III, Madrid, Spain. [Bernal-López,MR; Gómez-Huelgas,R] Centro de Investigación Biomédica en Red Fisiopatología de la Obesidad y Nutrición (CIBERobn), Instituto de Salud Carlos III, Madrid, Spain.</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-02-19T15:28:10Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2021-05-08</mods:dateIssued>
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               <mods:identifier type="doi">10.3390/jcm10092013</mods:identifier>
               <mods:identifier type="e-issn">2077-0383</mods:identifier>
               <mods:identifier type="journal">Journal of Clinical Medicine</mods:identifier>
               <mods:identifier type="other">http://hdl.handle.net/10668/4533</mods:identifier>
               <mods:identifier type="pubmedID">34066707</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/18335</mods:identifier>
               <mods:abstract>Canagliflozin is a sodium-glucose co-transporter 2 inhibitor that reduces glycemia as well as the risk of cardiovascular events. Our main objective was to analyze antidiabetic treatment de-intensification and the glycemic efficacy of replacing antidiabetic agents (excluding metformin) with canagliflozin in patients with heart failure and type 2 diabetes with poor glycemic control. In this observational, retrospective, real-world study, we selected patients treated with metformin in combination with ≥2 non-insulin antidiabetic agents or metformin in combination with basal insulin plus ≥1 non-insulin antidiabetic agent. Non-insulin antidiabetic agents were replaced with canagliflozin. Patients were followed-up on at three, six, and 12 months after the switch and a wide range of clinical variables were recorded. A total of 121 patients were included. From baseline to 12 months, the number of antidiabetic agents (3.1 ± 1.0 vs. 2.1 ± 0.8, p &lt; 0.05), basal insulin dose (20.1 ± 9.8 vs. 10.1 ± 6.5 units, p &lt; 0.01), and percentage of patients who used basal insulin (47.9% vs. 31.3%, p &lt; 0.01) decreased. The proportion of patients who used diuretics also declined significantly. In addition, we observed improvement in glycemic control, with an increase in the proportion of patients with glycated hemoglobin &lt;7% from 16.8% at three months to 63.5% at 12 (p &lt; 0.001). Canagliflozin use was also beneficial in terms of body weight, blood pressure, heart failure status, functional class, and cardiovascular-renal risk. There were also reductions in the number of emergency department visits and hospitalizations for heart failure. Moreover, canagliflozin was well-tolerated, with a low rate of drug-related discontinuation. Mounting evidence from randomized controlled trials and real-world studies point to the beneficial profile of sodium-glucose co-transporter type 2 inhibitors such as canagliflozin in patients with heart failure.</mods:abstract>
               <mods:language>
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               <mods:subject>
                  <mods:topic>De-intensification</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Efficacy</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Canagliflozin</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Heart failure</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Type 2 diabetes</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Capacidad de respuesta</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Eficacia</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Canagliflozina</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Insuficiencia cardíaca</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Diabetes mellitus tipo 2</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Hipoglucemiantes</mods:topic>
               </mods:subject>
               <mods:titleInfo>
                  <mods:title>De-Intensification of Antidiabetic Treatment Using Canagliflozin in Patients with Heart Failure and Type 2 Diabetes: Cana-Switch-HF Study</mods:title>
               </mods:titleInfo>
               <mods:genre>research article</mods:genre>
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