# The clinical effective of sodium/glucose co-transporter-2 inhibitors on admission frequency, duration and use of acute non-invasive ventilation in patients with chronic obstructive pulmonary disease: A single-centre 24-month retrospective observational study in a UK tertiary care centre

**Authors:** Alan Kan, Joshua De Soyza, Opeyemi Kafi, Ranganatha Rao, Narasimha Murthy, Jayanth Bhat

PMC · DOI: 10.1016/j.clinme.2025.100541 · Clinical Medicine · 2025-12-03

## TL;DR

This study found that SGLT2 inhibitors may reduce hospital stays for COPD patients but do not affect admission frequency or ventilation use.

## Contribution

The study is the first to investigate SGLT2 inhibitors' impact on COPD inpatient outcomes in a UK tertiary care setting.

## Key findings

- SGLT2 inhibitors were associated with a 26% reduction in hospital length of stay for COPD patients.
- No significant effect was observed on admission frequency or acute non-invasive ventilation use.
- The benefit of SGLT2 inhibitors was independent of patients' diabetes or heart failure status.

## Abstract

•Sodium glucose co-transporters-2 (SGLT2) inhibitors are associated with a reduction in length of inpatient admission.•Increasing age and increased severity of FEV1 is associated with increased length of inpatient admission.•SGLT2 inhibitors use did not correlate with a reduction in acute NIV or frequency of admissions.

Sodium glucose co-transporters-2 (SGLT2) inhibitors are associated with a reduction in length of inpatient admission.

Increasing age and increased severity of FEV1 is associated with increased length of inpatient admission.

SGLT2 inhibitors use did not correlate with a reduction in acute NIV or frequency of admissions.

Chronic obstructive pulmonary disease (COPD) contributes significantly to global morbidity and mortality and high economic burdens to healthcare systems. Emerging evidence suggests that sodium/glucose co-transporter-2 inhibitors (SGLT2i), beyond their use in type 2 diabetes mellitus (T2DM) and heart failure (HF), offer multifaceted immunomodulatory and anti-inflammatory effects which may offer positive outcomes in patients with COPD.

Investigate the impact of SGLT2i on inpatient outcomes – specifically, hospital length of stay (LOS), admission frequency, and use of acute non-invasive ventilation (NIV).

We conducted a 24-month retrospective observational study of adults with spirometry-confirmed COPD admitted to University Hospitals Coventry and Warwickshire between April 2022 and April 2024. Patients receiving SGLT2i for ≥30 days prior to study start formed the treatment group. Multivariable Poisson logistic regression was used to analyse the association between SGLT2i use and key outcomes, adjusting for demographics, disease severity, comorbidities and concurrent therapies.

About 1,197 admissions of 627 patients met the inclusion criteria, with 32 patients (5%) prescribed SGLT2i. SGLT2i use was associated with a statistically significant 26% reduction in hospital LOS (95% CI 0.62–0.87; p ≤ 0.001), independent of co-existing HF or T2DM. However, there was no significant reduction in admission frequency (IRR 0.84, 95% CI: 0.62–1.09, p = 0.212) or acute NIV use (OR 2.62, 95% CI: 0.35–13.26, p = 0.277) among SGLT2i users.

SGLT2i therapy in COPD patients was associated with a significantly reduced hospital length of stay during exacerbations, regardless of underlying heart failure or diabetes status. However, no differences were observed in admission frequency or acute NIV utilisation. These findings support the hypothesis of a beneficial anti-inflammatory or cardiopulmonary effect of SGLT2i in COPD and warrant further investigation through prospective trials to explore their therapeutic role in this population.

Image, graphical abstract

## Linked entities

- **Diseases:** chronic obstructive pulmonary disease (MONDO:0005002), type 2 diabetes mellitus (MONDO:0005148), heart failure (MONDO:0005252)

## Full-text entities

- **Diseases:** diabetes (MESH:D003920), inflammatory (MESH:D007249), COPD (MESH:D029424), T2DM (MESH:D003924), HF (MESH:D006333)
- **Chemicals:** SGLT2i (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12800692/full.md

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Source: https://tomesphere.com/paper/PMC12800692