# Efficacy and Safety of Sodium-Glucose Cotransporter-2 Inhibitors in Patients With Refractory Cirrhotic Ascites and Diabetes: Scoping Review Protocol

**Authors:** Tooba Laeeq, Ayesha Mehak Kamal, Arbab Burhan Uddin Kasi, Umm E Salma Shabbar Banatwala, Aniqa Baloch, Roberto Sagaribay, Vidhani Goel, Aditi Singh, Kavita Batra

PMC · DOI: 10.2196/77587 · JMIR Research Protocols · 2026-01-13

## TL;DR

This study aims to explore how well a new type of diabetes drug, called SGLT2 inhibitors, works in treating hard-to-manage fluid buildup in patients with liver disease and diabetes.

## Contribution

The study introduces a scoping review protocol to evaluate the use of SGLT2 inhibitors in refractory cirrhotic ascites among diabetic or insulin-resistant patients.

## Key findings

- The review will summarize evidence on the efficacy of SGLT2 inhibitors in managing refractory cirrhotic ascites.
- It will identify knowledge gaps and research priorities in using SGLT2 inhibitors for this patient population.
- The findings will support the potential for further clinical investigation into this drug class.

## Abstract

Hepatic cirrhosis is a complex condition leading to multiple complications, including ascites, hepatic encephalopathy, bleeding varices, and eventually liver failure. Patients with diabetes mellitus or insulin resistance are more likely to fail treatment, leading to the worsening of hepatic fibrosis. Sodium-glucose cotransporter-2 (SGLT2) inhibitors are a new class of drugs with the potential for use in cirrhotic ascites. This scoping review will focus on the response of the addition of SGLT2 inhibitors (SGLT2i) on refractory ascites.

The objective of this scoping review is to understand the extent and type of evidence in relation to the response of the addition of SGLT2i on refractory ascites in patients with diabetes mellitus or insulin resistance.

A comprehensive literature search will be conducted across five databases using variations of the keywords “Sodium-glucose Cotransporter-2 Inhibitors” and “ascites” to identify original studies published from inception through December 2023. The search will be limited to English-language human studies evaluating the efficacy of SGLT2 inhibitors, excluding studies focused on other drugs or conducted in animal models. This review will include studies involving patients over 21 years of age with cirrhotic ascites and will exclude studies involving noncirrhotic causes. Only studies containing original patient data will be considered, regardless of health care setting, to ensure clinical relevance and consistency in interpretation.

The results of this scoping review will offer a comprehensive overview of the available evidence on the use of SGLT2i in the management of cirrhotic ascites. This review will summarize key study characteristics, patient populations, interventions, and outcomes, and identify existing knowledge gaps and research priorities. Findings will be presented narratively and in tabular format to facilitate interpretation and comparison. The review process began with protocol development and registration in February 2025. A structured literature search and database screening will follow, continuing through June. Title and abstract screening, along with full-text review and eligibility assessment, will be completed by July 2025. Data extraction and charting will take place in July, with synthesis and analysis of findings occurring through August. Manuscript drafting will begin in August, and the final review and submission of the completed scoping review are anticipated by September 2025.

By systematically identifying and summarizing original studies that assess the efficacy of SGLT2i in this unique patient population, the review will provide insight into the therapeutic potential of this drug class beyond glycemic control. It will also highlight the strengths and limitations of the existing literature, identify key knowledge gaps, and suggest directions for future research. Ultimately, this review may support the rationale for further clinical investigation and the development of targeted therapies for a high-risk group of patients with limited treatment options.

## Linked entities

- **Diseases:** diabetes mellitus (MONDO:0005015), liver failure (MONDO:0100192), hepatic encephalopathy (MONDO:0001711)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}
- **Diseases:** Insulin resistance (MESH:D007333), viral hepatitis (MESH:D014777), nonalcoholic fatty liver disease (MESH:D065626), glucose intolerance (MESH:D018149), Diabetes (MESH:D003920), chronic liver disease (MESH:D008107), heart failure (MESH:D006333), dehydration (MESH:D003681), alcohol-related liver disease (MESH:D008108), bleeding varices (MESH:D014648), kidney injury (MESH:D007674), inflammation (MESH:D007249), hepatic encephalopathy (MESH:D006501), acute kidney injury (MESH:D058186), OSF (MESH:D005597), Ascites (MESH:D001201), genital infections (MESH:D007239), liver failure (MESH:D017093), PBC (MESH:D008105), fluid retention (MESH:D016055), T2DM (MESH:D003924), hyponatremia (MESH:D007010), cirrhotic (MESH:D000094724), euglycemic ketoacidosis (MESH:D007662), urinary tract infection (MESH:D014552), cirrhosis (MESH:D005355), Hepatic cirrhosis (MESH:D008103)
- **Chemicals:** aldosterone (MESH:D000450), dapagliflozin (MESH:C529054), ertugliflozin (MESH:C570288), sulfonylureas (MESH:D013453), glucose (MESH:D005947), sodium (MESH:D012964), metformin (MESH:D008687), SGLT2i (-), canagliflozin (MESH:D000068896)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** KB — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_0372)

## Full text

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## Figures

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## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12799079/full.md

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Source: https://tomesphere.com/paper/PMC12799079