Comparative Efficacy of Insulin Delivery Modalities on Glycaemic Control in Adults With Type 2 Diabetes: A Systematic Review and Network Meta-Analysis.

Diabetes Obes MetabJul 13, 2026 (epub)
Clinical ResearchEndocrinology

Ruining Yang, Xiyi Lu, Yixian Liang et al.

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In 30 seconds

This systematic review and network meta-analysis compared insulin delivery modalities in adults with insulin-treated type 2 diabetes, using parallel-group randomised trials identified through searches of eight databases and two trial registries. Thirty-seven reports covering 36 trials and 4157 participants were included; median follow-up was 12 weeks. In the primary analysis, hybrid closed-loop delivery versus multiple daily injections reduced HbA1c by MD -0.79% (95% CI -1.33 to -0.25) and increased time in range by MD +16.00 percentage points (95% CI +8.77 to +23.22), while also increasing body weight.

Key findings

  • Hybrid closed-loop versus multiple daily injections reduced HbA1c (MD -0.79%, 95% CI -1.33 to -0.25).
  • Hybrid closed-loop increased time in range by MD +16.00 percentage points (95% CI +8.77 to +23.22) and reduced time above range by MD -13.48 percentage points (95% CI -23.05 to -3.91).
  • Hybrid closed-loop increased body weight (MD +1.58 kg, 95% CI +0.75 to +2.40) and reduced insulin dose (MD -15.69 U/day, 95% CI -31.33 to -0.06).
  • Continuous subcutaneous insulin infusion reduced HbA1c (MD -0.47%, 95% CI -0.74 to -0.20) and insulin dose.

Why it matters

The findings suggest that insulin delivery modality may influence glycaemic control as well as insulin requirements in adults with insulin-treated type 2 diabetes. The observed weight increase with hybrid closed-loop delivery and limited safety evidence are relevant when weighing potential benefits. Results for fully closed-loop delivery remain uncertain, as they derive from one short trial.

What to keep in mind

Median follow-up was 12 weeks; most trials had risk-of-bias concerns, and a low-risk sensitivity analysis was infeasible. Fully closed-loop estimates came from one short trial.

Source

Published in Diabetes Obes Metab. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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