Renal Function and Decongestion With Acetazolamide in Acute Decompensated Heart Failure: The ADVOR Trial

Link to article at PubMed

Eur Heart J. 2023 Aug 25:ehad557. doi: 10.1093/eurheartj/ehad557. Online ahead of print.


BACKGROUND AND AIMS: In the ADVOR trial, acetazolamide improved decongestion in acute decompensated heart failure (ADHF). Whether the beneficial effects of acetazolamide are consistent across the entire range of renal function remains unclear.

METHODS: This is a prespecified analysis of the ADVOR trial that randomized 519 patients with ADHF to intravenous acetazolamide or matching placebo on top of intravenous loop diuretics. The main endpoints of decongestion, diuresis, natriuresis and clinical outcomes are assessed according to baseline renal function. Changes in renal function are evaluated between treatment arms.

RESULTS: On admission, median estimated glomerular filtration rate (eGFR) was 40 (30-52) mL/min/1.73 m². Acetazolamide consistently increased the likelihood of decongestion across the entire spectrum of eGFR (p-interaction=0.977). Overall, natriuresis and diuresis were higher with acetazolamide, with a higher treatment effect for patients with low eGFR (both p-interaction <0.007). Acetazolamide was associated with a higher incidence of worsening renal function (WRF) (rise in creatinine ≥0.3 mg/dL) during the treatment period (40.5% vs. 18.9%; p<0.001), but there was no difference in creatinine after 3 months (p=0.565). This was not associated with a higher incidence of heart failure hospitalizations and mortality (p-interaction=0.467). However, decongestion at discharge was associated with a lower incidence of adverse clinical outcomes irrespective of the onset of WRF (p-interaction=0.805).

CONCLUSIONS: Acetazolamide is associated with a higher rate of successful decongestion across the entire range of renal function with more pronounced effects regarding natriuresis and diuresis in patients with a lower eGFR. While WRF occurred more frequently with acetazolamide, this was not associated with adverse clinical outcomes.


PMID:37623428 | DOI:10.1093/eurheartj/ehad557

Leave a Reply

Your email address will not be published. Required fields are marked *