Identificador persistente para citar o vincular este elemento: 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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