# Peritoneal Dialysis Versus Extracorporeal Ultrafiltration Modalities in the Management of Acute Cardiorenal Syndrome with Diuretic Resistance

**Authors:** Laura Elena Zamora-Cervantes, Enzo Vásquez-Jiménez, José Manuel Rodríguez-Chagolla, Mayra Eugenia Avilés-Ramírez, Viridiana Galicia Galicia, Roberto Galindo-López, Alberto Ramírez-Gil, Diego Sánchez-Hernández, Octavio René García-Flores, Hiram José Serrano-García

PMC · DOI: 10.3390/life16020249 · 2026-02-02

## TL;DR

The paper compares peritoneal dialysis and extracorporeal ultrafiltration for managing acute cardiorenal syndrome with diuretic resistance.

## Contribution

It highlights the lack of comparative evidence and calls for trials focusing on fluid removal and broader patient outcomes.

## Key findings

- Non-pharmacological ultrafiltration therapies improve fluid removal and reduce rehospitalizations in refractory cases.
- Peritoneal dialysis offers hemodynamic benefits without anticoagulation, but is not first-line.
- Few studies compare renal replacement therapies in acute cardiorenal syndrome with diuretic resistance.

## Abstract

In cardiorenal Syndrome (CRS), diuretic resistance is frequent and congestion predominates in acute forms. In refractory cases, non-pharmacological ultrafiltration therapies have shown effectiveness on fluid removal, improved diuresis, and reduced rehospitalizations. However, the choice of modality remains individualized and resource-dependent. Both continuous renal replacement therapy (CRRT) and peritoneal dialysis (PD) offer hemodynamic advantages, but CRRT carries risks such as infection, bleeding, and high cost. PD has also demonstrated benefits in acute settings, providing effective sodium removal, and no need for anticoagulation, though it is not considered first-line therapy. There are few studies comparing different renal replacement therapies (RRT) in patients with acute CRS and there is no evidence on diuretic resistance. So, the question arises: could there be an advantage of a modality beyond fluid removal? The scarcity of comparative studies underscores the need for randomized trials that move beyond the cardiocentric perspective and include patients at risk of diuretic resistance.

## Linked entities

- **Diseases:** cardiorenal Syndrome (MONDO:0044079)

## Full-text entities

- **Genes:** AVP (arginine vasopressin) [NCBI Gene 551] {aka ADH, ARVP, AVP-NPII, AVRP, VP}, MUC16 (mucin 16, cell surface associated) [NCBI Gene 94025] {aka CA125}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, NPPB (natriuretic peptide B) [NCBI Gene 4879] {aka BNP, Iso-ANP}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}
- **Diseases:** infection (MESH:D007239), Congestion (MESH:D002311), effusion (MESH:D000080324), PD (MESH:D010538), hypertrophy (MESH:D006984), weight loss (MESH:D015431), vascular damage (MESH:D057772), acidosis (MESH:D000138), Pulmonary congestion (MESH:D001261), 2 CRS (MESH:D059347), death (MESH:D003643), left ventricular hypertrophy (MESH:D017379), kidney disease (MESH:D007674), HF (MESH:D006333), cardiac disease (MESH:D006331), cardiogenic shock (MESH:D012770), Diuretic Resistance (MESH:D060467), myocardial stunning (MESH:D017682), pulmonary edema (MESH:D011654), hyponatremia (MESH:D007010), CKD (MESH:D051436), edema (MESH:D004487), uremia (MESH:D014511), inflammation (MESH:D007249), shock (MESH:D012769), injury to (MESH:D014947), fluid loss (MESH:D002559), hyperkalemia (MESH:D006947), acute coronary syndromes (MESH:D054058), renal hypoperfusion (MESH:D006030), hypotension (MESH:D007022), bleeding (MESH:D006470), arrhythmias (MESH:D001145), venous congestion (MESH:D006940), AKI (MESH:D058186)
- **Chemicals:** furosemide (MESH:D005665), ATHENA (-), potassium (MESH:D011188), sodium (MESH:D012964), creatinine (MESH:D003404), icodextrin (MESH:D000077607), glucose (MESH:D005947), spironolactone (MESH:D013148), acetazolamide (MESH:D000086), aldosterone (MESH:D000450), phosphorus (MESH:D010758), tolvaptan (MESH:D000077602), Thiazides (MESH:D049971), water (MESH:D014867), empagliflozin (MESH:C570240)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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Source: https://tomesphere.com/paper/PMC12941509