Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/38774
Title: Acetazolamide in Acute Decompensated Heart Failure with Volume Overload
Authors: MULLENS, Wilfried 
DAUW, Jeroen 
MARTENS, Pieter 
VERBRUGGE, Frederik 
NIJST, Petra 
MEEKERS, Evelyne 
Tartaglia, Katrien
Chenot, Fabien
Moubayed, Samer
Dierckx, Riet
Blouard, Philippe
Troisfontaines, Pierre
Derthoo, David
Smolders, Walter
BRUCKERS, Liesbeth 
Droogne, Walter
Ter Maaten, Jozine M.
Damman, Kevin
Lassus, Johan
Mebazaa, Alexandre
Filippatos, Gerasimos
Ruschitzka, Frank
DUPONT, Matthias 
ADVOR Study Grp
Issue Date: 2022
Publisher: MASSACHUSETTS MEDICAL SOC
Source: NEW ENGLAND JOURNAL OF MEDICINE, 387 (13), p. 1185-1195
Abstract: BACKGROUND Whether acetazolamide, a carbonic anhydrase inhibitor that reduces proximal tubular sodium reabsorption, can improve the efficiency of loop diuretics, potentially leading to more and faster decongestion in patients with acute decompensated heart failure with volume overload, is unclear. METHODS In this multicenter, parallel-group, double-blind, randomized, placebo-controlled trial, we assigned patients with acute decompensated heart failure, clinical signs of volume overload (i.e., edema, pleural effusion, or ascites), and an N-terminal pro-B-type natriuretic peptide level of more than 1000 pg per milliliter or a B-type natriuretic peptide level of more than 250 pg per milliliter to receive either intravenous acetazolamide (500 mg once daily) or placebo added to standardized intravenous loop diuretics (at a dose equivalent to twice the oral maintenance dose). Randomization was stratified according to the left ventricular ejection fraction (& LE;40% or > 40%). The primary end point was successful decongestion, defined as the absence of signs of volume overload, within 3 days after randomization and without an indication for escalation of decongestive therapy. Secondary end points included a composite of death from any cause or rehospitalization for heart failure during 3 months of follow-up. Safety was also assessed. REUSLTS A total of 519 patients underwent randomization. Successful decongestion occurred in 108 of 256 patients (42.2%) in the acetazolamide group and in 79 of 259 (30.5%) in the placebo group (risk ratio, 1.46; 95% confidence interval [CI], 1.17 to 1.82; P < 0.001). Death from any cause or rehospitalization for heart failure occurred in 76 of 256 patients (29.7%) in the acetazolamide group and in 72 of 259 patients (27.8%) in the placebo group (hazard ratio, 1.07; 95% CI, 0.78 to 1.48). Acetazolamide treatment was associated with higher cumulative urine output and natriuresis, findings consistent with better diuretic efficiency. The incidence of worsening kidney function, hypokalemia, hypotension, and adverse events was similar in the two groups. CONCLUSIONS The addition of acetazolamide to loop diuretic therapy in patients with acute decompensated heart failure resulted in a greater incidence of successful decongestion. (Funded by the Belgian Health Care Knowledge Center; ADVOR ClinicalTrials.gov number, .)
Notes: Mullens, W (corresponding author), Ziekenhuis Oost Limburg, Schiepse Bos 6, B-3600 Genk, Belgium.
Document URI: http://hdl.handle.net/1942/38774
ISSN: 0028-4793
e-ISSN: 1533-4406
DOI: 10.1056/NEJMoa2203094
ISI #: 000861026900001
Rights: 2022 Massachusetts Medical Society.
Category: A1
Type: Journal Contribution
Validations: ecoom 2023
Appears in Collections:Research publications

Files in This Item:
File Description SizeFormat 
plSTO.pdfPublished version413.39 kBAdobe PDFView/Open
Show full item record

WEB OF SCIENCETM
Citations

167
checked on Apr 24, 2024

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.