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https://accedacris.ulpgc.es/handle/10553/143144
Título: | Hypokalemia during Decongestion with Loop Diuretics and Hydrochlorothiazide, a Post Hoc Analysis of the CLOROTIC Trial | Autores/as: | Conde Martel, Alicia Hernández-Meneses, Marta Morales-Rull, José Luís Casado, Jesús Carrera-Izquierdo, Margarita León, Marta Sánchez-Marteles, Marta Dávila-Ramos, Melitón Francisco Hernández-Carballo, Carolina Llàcer Iborra, Pau Moreno-García, Mari Carmen Salamanca-Bautista, María del Prado Formiga, Francesc Manzano, Luís Trullàs, Joan Carles Solé, Cristina Garcés Horna, Vanesa Zabaleta, Juan Pedro Bisbe, Josep Aramburu Bodas, Óscar Ruiz, Raúl Pérez Silvestre, José Plasín, Miguel Ángel Cerqueiro González, José Manuel Chivite, David Gil, Paloma Jordana, Rosa Villalonga, María Paéz Rubio, M. Inmaculada Cepeda Rodrigo, José M. Pérez-Barquero, Manuel Montero Muela, Alberto Mateos, Lourdes Grau, Jordi Armengou, Arola Herrero, Almudena Quirós López, Raúl |
Clasificación UNESCO: | 32 Ciencias médicas 3205 Medicina interna 320501 Cardiología 3209 Farmacología |
Palabras clave: | Diuretics Heart Failure Hypokalemia Potassium Risk Factors |
Fecha de publicación: | 2025 | Publicación seriada: | Circulation. Heart failure | Resumen: | BACKGROUND: In patients with acute heart failure, the addition of hydrochlorothiazide (HCTZ) to furosemide increased the diuretic response in the CLOROTIC trial (Combining Loop with Thiazide Diuretics for Decompensated Heart Failure). The aim of this subanalysis was to evaluate the incidence and risk factors for hypokalemia, and its impact on mortality and readmissions. METHODS: This is a post hoc analysis of the CLOROTIC trial that randomized 230 patients with acute heart failure and volume overload to receive HCTZ or placebo in addition to intravenous furosemide. The incidence and risk factors for the development of hypokalemia (K+ <3.5 mmol/L) and its association with 30- and 90-day mortality and readmissions were analyzed. The Monte Carlo simulation method was applied to predict the development of hypokalemia. RESULTS: The incidence of hypokalemia was significantly higher in the HCTZ group (compared with the placebo group) at 48 and 96 hours after randomization, and at discharge (P<0.001). In a multivariate analysis, the following variables were independently associated with the development of hypokalemia: baseline K+ values (OR per 0.1 units, 0.82 [95% CI, 0.76-0.87]; P<0.001), treatment with HCTZ (OR, 4.90 [95% CI, 2.50-9.90]; P<0.001), and treatment with a mineralocorticoid receptor antagonist at baseline (OR, 0.42 [95% CI, 0.20-0.84]; P=0.017). There was no association between the development of hypokalemia and 30- and 90-day mortality and readmissions. The Monte Carlo simulation method predicted in patients treated with furosemide alone a higher risk of hypokalemia when baseline K+ values are ≤3.7 mmol/L. When HCTZ is added to furosemide, the risk of hypokalemia is present with higher baseline K+ values (≤4.3 mmol/L). CONCLUSIONS: Adding HCTZ to intravenous furosemide increases the risk of hypokalemia a especially when baseline K+ is ≤4.3 mmol/L and when patients are not treated with a mineralocorticoid receptor antagonist. In patients treated with furosemide and HCTZ, it is advisable to add potassium supplements and a mineralocorticoid receptor antagonist. | URI: | https://accedacris.ulpgc.es/handle/10553/143144 | ISSN: | 1941-3289 | DOI: | 10.1161/CIRCHEARTFAILURE.125.012914 | Fuente: | Circulation: Heart Failure [ISSN 1941-3289], (Enero 2025) |
Colección: | Artículos |
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