Switching From Liraglutide to Semaglutide Improved Blood Sugar, Weight, and Saved Over $400,000 at a VA Hospital

Converting 304 veterans from daily liraglutide to weekly semaglutide significantly reduced HbA1c from 8.1% to 7.6%, decreased body weight, and saved over $400,000 in pharmacy costs.

RPEP-069412023RETHINKTHC RESEARCH DATABASErethinkthc.com/research

Quick Facts

Study Type
Not classified
Evidence
Not graded
Sample
Not reported

What This Study Found

Among 304 veterans converted from liraglutide (0.6 or 1.2 mg daily) to semaglutide (0.25 mg weekly, titrated to 0.5 mg weekly):

- Mean HbA1c decreased significantly from 8.1% (SD 1.5) to 7.6% (SD 1.4) at 3–12 months (P significant)

- Mean baseline blood glucose: 187.4 mg/dL (SD 44.2)

- Mean baseline body weight: 112.9 kg (SD 23.0); significant weight loss observed (P < 0.001)

- Minimal changes to antihyperglycemic regimens were needed

- Cost savings exceeded $400,000 from the conversion

- Common adverse effects: hypoglycemia and gastrointestinal intolerance

Key Numbers

How They Did This

Retrospective chart review of veterans without retinopathy treated at the Michael E. DeBakey VA Medical Center between March and November 2021. Patients on liraglutide 0.6 or 1.2 mg daily were converted to semaglutide 0.25 mg weekly (titrated to 0.5 mg after 4 weeks). HbA1c values were compared at baseline and 3–12 months post-conversion. Cost savings were calculated using outpatient pharmacy data.

Why This Research Matters

With GLP-1 drugs being expensive, finding ways to optimize both clinical outcomes and costs is important for healthcare systems. This study shows that switching from an older daily GLP-1 peptide to a newer weekly one can improve blood sugar control, promote weight loss, and generate significant cost savings — a win across the board.

The Bigger Picture

As healthcare systems manage the growing costs of GLP-1 medications, studies like this provide evidence-based guidance for formulary decisions and drug switching protocols. The VA system, which serves millions of veterans, demonstrated that therapeutic conversions between GLP-1 peptides can be done safely while improving outcomes and reducing costs.

What This Study Doesn't Tell Us

This was a retrospective study without a control group, making it impossible to determine whether improvements were due to the drug switch or other factors. The conversion used relatively low semaglutide doses (0.5 mg), not the maximum approved dose (2.0 mg for diabetes, 2.4 mg for weight loss). The VA patient population (predominantly male veterans) may not be representative of the general population. A full cost-effectiveness analysis was not conducted.

Questions This Raises

  • ?Would higher doses of semaglutide (1.0 or 2.0 mg) have produced even greater improvements after conversion from liraglutide?
  • ?How do long-term outcomes beyond 12 months compare after liraglutide-to-semaglutide conversion?
  • ?Could similar cost savings be achieved in other healthcare systems by standardizing GLP-1 formulary decisions?

Trust & Context

Key Stat:
$400,000+ saved Switching 304 veterans from daily liraglutide to weekly semaglutide, while also improving HbA1c from 8.1% to 7.6% and reducing body weight
Evidence Grade:
This is a retrospective chart review without a control group — a real-world observational study. While it demonstrates meaningful clinical and cost improvements, the lack of randomization and blinding limits causal conclusions.
Study Age:
Published in 2023 with data from 2021, this reflects early experience with GLP-1 drug conversions during a period of rapidly evolving prescribing patterns.
Original Title:
Impact of Liraglutide to Semaglutide Conversion on Glycemic Control and Cost Savings at a Veterans Affairs Medical Center.
Published In:
Federal practitioner : for the health care professionals of the VA, DoD, and PHS, 40(Suppl 6), S24-S30 (2023)
Database ID:
RPEP-06941

Evidence Hierarchy

Meta-Analysis / Systematic Review
Randomized Controlled Trial
Cohort / Case-Control
Cross-Sectional / ObservationalSnapshot without intervening
This study
Case Report / Animal Study
What do these levels mean? →

Frequently Asked Questions

Is it safe to switch from liraglutide to semaglutide?

This study found that switching was safe for most patients. Blood sugar control improved and weight decreased. Some patients experienced hypoglycemia or GI symptoms, which are common with all GLP-1 drugs. Minimal changes to other diabetes medications were needed.

Why would a hospital switch patients between GLP-1 drugs?

Semaglutide is given weekly instead of daily (more convenient), showed better blood sugar and weight outcomes, and cost less for the VA system — saving over $400,000. These combined benefits made the conversion worthwhile for both patients and the institution.

Read More on RethinkPeptides

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Cite This Study

RPEP-06941·https://rethinkpeptides.com/research/RPEP-06941

APA

Hardin, Maiah; Adanse, Fiona; Schexnayder, Chandler; Malveaux, Janeca; Agbahiwe, Sylvester. (2023). Impact of Liraglutide to Semaglutide Conversion on Glycemic Control and Cost Savings at a Veterans Affairs Medical Center.. Federal practitioner : for the health care professionals of the VA, DoD, and PHS, 40(Suppl 6), S24-S30. https://doi.org/10.12788/fp.0413

MLA

Hardin, Maiah, et al. "Impact of Liraglutide to Semaglutide Conversion on Glycemic Control and Cost Savings at a Veterans Affairs Medical Center.." Federal practitioner : for the health care professionals of the VA, 2023. https://doi.org/10.12788/fp.0413

RethinkPeptides

RethinkPeptides Research Database. "Impact of Liraglutide to Semaglutide Conversion on Glycemic ..." RPEP-06941. Retrieved from https://rethinkpeptides.com/research/hardin-2023-impact-of-liraglutide-to

Access the Original Study

Study data sourced from PubMed, a service of the U.S. National Library of Medicine, National Institutes of Health.

This study breakdown was produced by the RethinkPeptides research team. We analyze and report published research findings without making health recommendations. All interpretations are based solely on the published abstract and study data.