Back to Search Start Over

Diuretic Strategies in Acute Heart Failure and Renal Dysfunction: Conventional vs Carbohydrate Antigen 125-guided Strategy. Clinical Trial Design

Authors :
García-Blas S
Bonanad C
Llàcer P
Ventura S
Núñez JM
Sánchez R
Chamorro C
Fácila L
de la Espriella R
Vaquer JM
Cordero A
Roqué M
Ortiz V
Racugno P
Bodí V
Valero E
Santas E
Moreno MDC
Miñana G
Carratalá A
Bondanza L
Paya A
Cardells I
Heredia R
Pellicer M
Valls G
Palau P
Bosch MJ
Raso R
Sánchez A
Bertomeu-González V
Bertomeu-Martínez V
Montagud-Balaguer V
Albiach-Montañana C
Pendás-Meneau J
Marcaida G
Cervantes-García S
San Antonio R
de Mingo E
Chorro FJ
Sanchis J
Núñez J
IMPROVE-HF Investigators
Source :
REVISTA ESPANOLA DE CARDIOLOGIA, r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA, instname, r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante, r-FISABIO. Repositorio Institucional de Producción Científica, Revista espanola de cardiologia (English ed.), r-FISABIO: Repositorio Institucional de Producción Científica, Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
Publication Year :
2017
Publisher :
EDICIONES DOYMA S A, 2017.

Abstract

Introduction and objectives: The optimal treatment of patients with acute heart failure (AHF) and cardiorenal syndrome type 1 (CRS-1) is far from being well-defined. Arterial hypoperfusion in concert with venous congestion plays a crucial role in the pathophysiology of CRS-I. Plasma carbohydrate antigen 125 (CA125) has emerged as a surrogate of fluid overload in AHF. The aim of this study was to evaluate the clinical usefulness of CA125 for tailoring the intensity of diuretic therapy in patients with CRS-1. Methods: Multicenter, open-label, parallel clinical trial, in which patients with AHF and serum creatinine >= 1.4 mg/dL on admission will be randomized to: a) standard diuretic strategy: titration-based on conventional clinical and biochemical evaluation, or b) diuretic strategy based on CA125: high dose if CA125 > 35 U/mL, and low doses otherwise. The main endpoint will be renal function changes at 24 and 72 hours after therapy initiation. Secondary endpoints will include: a) clinical and biochemical changes at 24 and 72 hours, and b) renal function changes and major clinical events at 30 days. Results: The results of this study will add important knowledge on the usefulness of CA125 for guiding diuretic treatment in CRS-1. In addition, it will pave the way toward a better knowledge of the pathophysiology of this challenging situation. Conclusions: We hypothesize that higher levels of CA125 will identify a patient population with CRS-1 who could benefit from the use of a more intense diuretic strategy. Conversely, low levels of this glycoprotein could select those patients who would be harmed by high diuretic doses. (C) 2017 Sociedad Espanola de Cardiologia. Published by Elsevier Espana, S.L.U. All rights reserved.

Details

ISSN :
03008932 and 18855857
Database :
OpenAIRE
Journal :
REVISTA ESPANOLA DE CARDIOLOGIA, r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA, instname, r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante, r-FISABIO. Repositorio Institucional de Producción Científica, Revista espanola de cardiologia (English ed.), r-FISABIO: Repositorio Institucional de Producción Científica, Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
Accession number :
edsair.dedup.wf.001..21ea35406840c53200094de0efeb13b4