Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/130309
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dc.contributor.authorTrullàs, Joan Carlesen_US
dc.contributor.authorMorales-Rull, José Luísen_US
dc.contributor.authorCasado, Jesúsen_US
dc.contributor.authorCarrera-Izquierdo, Margaritaen_US
dc.contributor.authorSánchez-Marteles, Martaen_US
dc.contributor.authorConde Martel, Aliciaen_US
dc.contributor.authorDávila-Ramos, Melitón Franciscoen_US
dc.contributor.authorLlácer, Pauen_US
dc.contributor.authorSalamanca-Bautista, Pradoen_US
dc.contributor.authorChivite, Daviden_US
dc.contributor.authorJordana-Comajuncosa, Rosaen_US
dc.contributor.authorVillalonga, Mariaen_US
dc.contributor.authorPáez-Rubio, María Inmaculadaen_US
dc.contributor.authorManzano, Luísen_US
dc.contributor.authorFormiga, Francescen_US
dc.date.accessioned2024-05-13T09:31:52Z-
dc.date.available2024-05-13T09:31:52Z-
dc.date.issued2023en_US
dc.identifier.issn1388-9842en_US
dc.identifier.urihttp://hdl.handle.net/10553/130309-
dc.description.abstractAims: In patients with acute heart failure (AHF), the addition of hydrochlorothiazide (HCTZ) to furosemide improved diuretic response in the CLOROTIC trial. This work aimed to evaluate if these effects differ across the estimated glomerular filtration rate (eGFR) spectrum. Methods and results: This post-hoc analysis of the CLOROTIC trial analysed 230 patients with AHF and explored the influence of eGFR on primary and secondary endpoints. The median eGFR was 43 ml/min/1.73 m2 (range 14–109) and 23% had eGFR ≥60 ml/min/1.73 m2 (group 1), 24% from 45 to 59 ml/min/1.73 m2 (group 2), and 53% <45 ml/min/1.73 m2 (group 3). Patients treated with HCTZ had greatest weight loss at 72 h in all three groups, but patients in group 1 had a significantly greater response (−2.1 kg [−3.0 to 0.5]), compared to patients in groups 2 (−1.3 kg [−2.3 to 0.2]) and 3 (−0.1 kg [−1.3 to 0.4]) (p-value for interaction = 0.246). At 96 h, the differences in weight were −1.8 kg (−3.0 to −0.3), −1.4 kg (−2.6 to 0.3), and −0.5 kg (−1.3 to −0.1) in groups 1, 2, and 3, respectively (p-value for interaction = 0.256). There were no significant differences observed with the addition of HCTZ in terms of diuretic response, mortality or rehospitalizations, or safety endpoints (impaired renal function, hyponatraemia, and hypokalaemia) among the three eGFR groups (all p-values for interaction were no significant). Conclusion: The addition of eGFR-adjusted doses of oral HCTZ to loop diuretics in patients with AHF improved diuretic response across the eGFR spectrum. Clinical Trial Registration: ClinicalTrials.gov: NCT01647932; EudraCT number: 2013–001852-36.en_US
dc.languageengen_US
dc.relation.ispartofEuropean Journal of Heart Failureen_US
dc.sourceEuropean Journal of Heart Failure [1388-9842], v. 25, p. 1784–1793 (2023)en_US
dc.subject320501 Cardiologíaen_US
dc.subject.otherDiureticsen_US
dc.subject.otherFurosemideen_US
dc.subject.otherGlomerular filtration rateen_US
dc.subject.otherHeart failureen_US
dc.subject.otherThiazidesen_US
dc.titleCombining loop and thiazide diuretics for acute heart failure across the estimated glomerular filtration rate spectrum: A post-hoc analysis of the CLOROTIC trialen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/ejhf.2988en_US
dc.identifier.pmid37540036-
dc.identifier.scopus2-s2.0-85168145419-
dc.contributor.orcid0000-0002-7380-3475-
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dc.description.lastpage1793en_US
dc.identifier.issue10-
dc.description.firstpage1784en_US
dc.relation.volume25en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.description.numberofpages10en_US
dc.utils.revisionen_US
dc.date.coverdateAgosto 2016en_US
dc.identifier.ulpgcNoen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr5,919
dc.description.jcr18,2
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
dc.description.miaricds10,8
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Patología y Tecnología médica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.orcid0000-0002-2540-3880-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameConde Martel, Alicia-
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