# Acetazolamide Use in the Management of Refractory Acute Decompensated Heart Failure in the ICU

**Authors:** Meher Ayyazuddin, Adelyn Mendoza, Vismay Patel, Rubba Shoukat Khan, Rehan Shah

PMC · DOI: 10.15190/d.2026.2 · Discoveries · 2026-03-03

## TL;DR

This paper presents a case where acetazolamide helped manage severe heart failure when traditional treatments failed.

## Contribution

The paper introduces acetazolamide as a potential solution for diuretic resistance in acute heart failure.

## Key findings

- Acetazolamide led to significant diuresis and resolution of pulmonary edema in 72 hours.
- The patient showed clinical improvement after acetazolamide treatment.

## Abstract

Diuretic resistance is a major therapeutic challenge in acute decompensated heart failure (ADHF). Acetazolamide, a carbonic anhydrase inhibitor, has emerged as a potential adjunct to conventional loop diuretics, as demonstrated in the ADVOR trial. We present a 74-year-old woman with acute coronary syndrome complicated by cardiogenic shock and refractory pulmonary edema despite inotropic support and guideline-directed therapy. The patient received intravenous acetazolamide 500 mg daily for three days, resulting in marked diuresis and radiographic resolution of pulmonary edema within 72 hours. The patient improved clinically. This case supports the potential utility of acetazolamide as an adjunctive strategy for overcoming diuretic resistance in ADHF.

## Linked entities

- **Chemicals:** Acetazolamide (PubChem CID 1986)
- **Diseases:** acute coronary syndrome (MONDO:0005542), cardiogenic shock (MONDO:0800175), pulmonary edema (MONDO:0006932)

## Full-text entities

- **Genes:** AP2B1 (adaptor related protein complex 2 subunit beta 1) [NCBI Gene 163] {aka ADTB2, AP105B, AP2-BETA, CLAPB1}, ACE (angiotensin I converting enzyme) [NCBI Gene 1636] {aka ACE1, CD143, DCP, DCP1}
- **Diseases:** ADHF (MESH:D006333), impaired renal function (MESH:D007674), depression (MESH:D003866), cardiomegaly (MESH:D006332), somnolence (MESH:D006970), pulmonary congestion (MESH:D001261), stent thrombosis (MESH:D013927), hypertension (MESH:D006973), impaired cardiac output (MESH:D002303), alveolar opacities (MESH:D003318), pleural effusions (MESH:D010996), alveolar infiltrates (MESH:D017254), chest pain (MESH:D002637), COPD (MESH:D029424), fatigue (MESH:D005221), renal function (MESH:D058186), hypotension (MESH:D007022), WRF (MESH:D000067251), mitral regurgitation (MESH:D008944), hypoxemia (MESH:D000860), volume overload (MESH:D019190), acute coronary syndrome (MESH:D054058), nephron (MESH:D007683), dyspnea (MESH:D004417), cardiogenic shock (MESH:D012770), -motion abnormalities (MESH:D009041), weakness (MESH:D018908), diuretic resistance (MESH:D060467), PRESENTATION (MESH:D001946), pulmonary edema (MESH:D011654)
- **Chemicals:** Spironolactone (MESH:D013148), milrinone (MESH:D020105), creatinine (MESH:D003404), clopidogrel (MESH:D000077144), Diuretic resistance (-), ticagrelor (MESH:D000077486), sodium (MESH:D012964), aspirin (MESH:D001241), thiazide (MESH:D049971), oxygen (MESH:D010100), Acetazolamide (MESH:D000086)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12962849/full.md

## References

14 references — full list in the complete paper: https://tomesphere.com/paper/PMC12962849/full.md

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Source: https://tomesphere.com/paper/PMC12962849