Hospital de día en la unidad de insuficiencia cardíaca como una estrategia de abordaje integral: análisis de un único centro en América Latina / Heart Failure Day Hospital as a Comprehensive Approach Strategy in the Heart Failure Unit: Analysis of a Single Center in Latin America

RESUMEN Objetivos: Describir las características clínicas, el impacto en la calidad de vida, la clase funcional (CF), el número de internaciones y la supervivencia de los pacientes que ingresaron a un hospital de día (HD) de insuficiencia cardíaca (IC). Material y métodos: Se analizaron en forma retrospectiva aquellos pacientes que ingresaron a un HD para la infusión de hierro, furosemida, levosimendán o la combinación de estos dos últimos fármacos, durante un período de 3 años. Las variables analizadas, al inicio y a los 6 meses, fueron la CF (NYHA), la prueba de marcha de 6 minutos (PM6M) y calidad de vida mediante el cuestionario de Minnesota (MLHFQ). El número de internaciones por IC fue comparado con el del año previo al ingreso al HD y la supervivencia fue evaluada al año de seguimiento. Resultados: Se observó una mejoría significativa de la CF en los 4 grupos, y del número de internaciones por IC en los primeros 3. Conclusiones: El desarrollo del HD puede modificar el presente y futuro de esta población.

ABSTRACT Objectives: To describe the clinical characteristics, impact on quality of life, functional class (FC), number of hospitalizations, and survival rate of patients with heart failure (HF) enrolled in an outpatient heart failure clinic (HFC). Methods: Patients enrolled in a HFC for infusion of iron, furosemide, levosimendan -or the combination of these two drugsover a 3-year period were retrospectively analyzed. Baseline and 6-month variables were FC (NYHA), 6-minute walk test (6MWT) and quality of life using the Minnesota questionnaire (MLHFQ). The number of HF hospitalizations was compared with that of the year prior to HFC enrollment, and survival was assessed at 1-year follow-up. Results: A significant improvement in FC was observed in all four groups, and a decrease of HF hospitalizations in the first three. Conclusions: Outpatient HFC development can change the present and future of this population.

Heart Failure and Diabetes: Perspective of a Dangerous Association.

The relationship between diabetes and risk of heart failure has been described in previous trials, releasing the importance of the hyperglycemic state that, added to other risk factors, favors the development of coronary heart disease. The mechanism by which, in the absence of hypertension, obesity and/or dyslipidemia, diabetic patients develop cardiomyopathy has been less studied. Recently, the Sodium Glucose Co-transporter type 2 inhibitors (SGLT2 inhibitors) used for the treatment of heart failure patients with or without diabetes has been a breakthrough in the field of medicine. This review describes the established pathophysiology of diabetic cardiomyopathy and SGLT2 inhibitors, their mechanisms of action, and benefits in this group of patients.

Short-term mechanical circulatory support devices as bridge to heart transplantation: A prospective single-center experience in Argentina.

BACKGROUND: Patients with cardiogenic shock may require hemodynamic stabilization with short-term mechanical circulatory support devices (ST-MCS) such as extracorporeal membrane oxygenation (ECMO) and centrifugal pump (CP) as bridge to transplantion (BTT). This study aimed to describe ECMO and CP during BTT and after heart transplant. METHODS: A cohort of patients on ECMO or CP as BTT between April 2006 and April 2018 in a single hospital. RESULTS: Thirty-seven consecutive patients with ECMO (n = 14) or CP (n = 23) were included. Acute kidney injury was more prevalent during CP (28.6% vs 69.6%, P = .02). There were no differences in stroke, thrombosis, sepsis, or vasoplegia. Bleeding (0% vs 56.5%, P = .0003) and reoperation (0% vs 47.8%, P = .002) were more frequent in CP group as well as mortality (0 vs 7 [30.4%], P = .03). The remaining 30 patients (81.1%) underwent heart transplantation, without differences in primary graft dysfunction, vasoplegia, reoperation for bleeding, or hospital stay. Mortality was 23.3% at 30 days, similar in both groups, with no further deaths at median follow-up of 44.2 months. CONCLUSIONS: In patients with cardiogenic shock, ST-MCS with ECMO or CP as BTT are a lifesaving approach allowing successful transplantation in the majority of cases, with good short- and long-term survival.

High-dose plasmid-mediated VEGF gene transfer is safe in patients with severe ischemic heart disease (Genesis-I). A phase I, open-label, two-year follow-up trial.

OBJECTIVES: We aimed to assess safety and, secondarily, the efficacy of intramyocardial high-dose plasmid-vascular endothelial growth factor (VEGF) 165 (pVEGF165) gene transfer in no-option patients with coronary artery disease (CAD). BACKGROUND: Controlled trials of pVEGF165 in CAD have shown little benefit. One possible reason is shortness of dosage. We have shown in large mammalian models of chronic myocardial ischemia and acute myocardial infarction that intramyocardial pVEGF165 at doses significantly higher than those used in recent phase II trials is safe and efficacious on myocardial perfusion, left ventricular function, and infarct size limitation. METHODS: Using an injection catheter, 10 patients with severe CAD not amenable for revascularization received 10 intramyocardial injections of 0.38 mg (total dose, 3.8 mg) pVEGF165 in zones exhibiting myocardial ischemia, as assessed by combined stress 99mTc-sestamibi single-photon emission computed tomography and stress echocardiography. RESULTS: No serious adverse events related to either VEGF or the injection procedure occurred over the 2-year follow-up. One patient suffered femoral artery thrombosis after a follow-up coronary angiography, successfully resolved with medical treatment. Six patients suffered uncomplicated coronary ischemic events during the second year follow-up. Angina functional class decreased from 2.6 ± 0.2 to 1.2 ± 0.3 (mean ± SEM, P < 0.05), quality of life increased from 56.9 ± 3.2 to 82.6 ± 2.4 (P < 0.05), the summed difference score of myocardial perfusion decreased from 13.4 ± 2 to 7.7 ± 1.8 (P < 0.04), and stress ejection fraction did not change (44.2 ± 3.6% to 47.8 ± 3.1%, P = NS). CONCLUSIONS: High-dose intramyocardial pVEGF165 is safe at 2 years follow-up in patients with severe CAD. The efficacy results observed must be taken cautiously given the uncontrolled, open-label study design.