Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Observational Study
. 2019 Dec 9;7(1):e000884.
doi: 10.1136/bmjdrc-2019-000884. eCollection 2019.

Clinical and economic outcomes among injection-naïve patients with type 2 diabetes initiating dulaglutide compared with basal insulin in a US real-world setting: the DISPEL Study

Affiliations
Observational Study

Clinical and economic outcomes among injection-naïve patients with type 2 diabetes initiating dulaglutide compared with basal insulin in a US real-world setting: the DISPEL Study

Reema Mody et al. BMJ Open Diabetes Res Care. .

Abstract

Aims: To report 1-year clinical and economic outcomes from the retrospective DISPEL (Dulaglutide vs Basal InSulin in Injection Naïve Patients with Type 2 Diabetes: Effectiveness in ReaL World) Study.

Materials and methods: This observational claims study included patients with type 2 diabetes (T2D) and ≥1 claim for dulaglutide or basal insulin between November 2014 and April 2017 (index date=earliest fill date). Propensity score matching was used to address treatment selection bias. Change from baseline in hemoglobin A1c (HbA1c) was compared between the matched cohorts using analysis of covariance; diabetes-related costs were analyzed using generalized linear models.

Results: Matched cohorts (903 pairs total; 523 pairs with complete cost data) were balanced in baseline characteristics with mean HbA1c 8.6%, mean age 54 years. At 1 year postindex, dulaglutide patients had significantly greater reduction in HbA1c than basal insulin (-1.12% vs -0.51%, p<0.01), lower medical costs ($3753 vs $7604, p<0.01), higher pharmacy costs ($9809 vs $6175, p<0.01), and similar total costs ($13 562 vs $13 779, p=0.76). Medical and total costs per 1% HbA1c reduction were lower for dulaglutide than basal insulin (medical: $3128 vs $12 673, p<0.01; total: $11 302 vs $22 965, p<0.01), while pharmacy costs per 1% HbA1c reduction were lower without reaching statistical significance ($8174 vs $10 292, p=0.15).

Conclusions: In this real-world study, patients with T2D initiating dulaglutide demonstrated greater HbA1c reduction compared with those initiating basal insulin. Although total diabetes-related costs were similar, the total diabetes-related costs per HbA1c reduction were lower for dulaglutide, highlighting the importance of evaluating effectiveness along with the economic impact of medications.

Keywords: HbA1c; adherence to medications; claims database analysis; insulin delivery.

PubMed Disclaimer

Conflict of interest statement

Competing interests: RM, MY and HP are employees and stockholders of Eli Lilly and Company. MG is an employee of HealthCore, an independent research organization that received funding from Eli Lilly and Company for the conduct of this study. QH, XZ and LW were employees of HealthCore at the time the study was conducted.

Figures

Figure 1
Figure 1
Glycemic outcomes at 1 year postindex among patients initiating dulaglutide versus basal insulin.*Significant difference between dulaglutide versus basal insulin with p value <0.05. Estimates obtained using ANCOVA with baseline HbA1c level (continuous variable) as covariate.
Figure 2
Figure 2
Longitudinal changes in HbA1c among matched dulaglutide initiators versus basal insulin initiators (MMRM).*Significant difference between dulaglutide versus basal insulin with p value <0.05. Results are from a mixed-effects model with repeated measurements (MMRM). Data represent least square mean ± 95% confidence limit. Baseline reflects HbA1c results obtained between (index date - 183 days) and (index date + 14 days); the value closest to index date was chosen if there were multiple values. 3/6/9/12 months reflects HbA1c results obtained between windows of ±45 days around index date +92/183/274/365 days, with the value closest to and prior to the anchor date chosen if there were multiple values. Point estimates are available in online supplementary appendix table 6.
Figure 3
Figure 3
Healthcare costs in USD per 1% HbA1c reduction at 1 year Post-Index*Significant difference between dulaglutide versus basal insulin with p value <0.05. Costs per 1% HbA1c reduction were calculated from the mean cost across all patients, divided by mean HbA1c reduction. Error bars represent 95% CIs obtained by bootstrapping with 5000 replications.

References

    1. American Diabetes Association 9. Pharmacologic Approaches to Glycemic Treatment: Standards of Medical Care in Diabetes-2019. Diabetes Care 2019;42:S90–102. 10.2337/dc19-S009 - DOI - PubMed
    1. Garber AJ, Abrahamson MJ, Barzilay JI, et al. . Consensus statement by the american association of clinical endocrinologists and american college of endocrinology on the comprehensive type 2 diabetes management algorithm - 2019 EXECUTIVE SUMMARY. Endocr Pract 2019;25:69–100. 10.4158/CS-2018-0535 - DOI - PubMed
    1. Abd El Aziz MS, Kahle M, Meier JJ, et al. . A meta-analysis comparing clinical effects of short- or long-acting GLP-1 receptor agonists versus insulin treatment from head-to-head studies in type 2 diabetic patients. Diabetes Obes Metab 2017;19:216–27. 10.1111/dom.12804 - DOI - PubMed
    1. Brod M, Kongsø JH, Lessard S, et al. . Psychological insulin resistance: patient beliefs and implications for diabetes management. Qual Life Res 2009;18:23–32. 10.1007/s11136-008-9419-1 - DOI - PubMed
    1. Trujillo JM, Nuffer W, Ellis SL. Glp-1 receptor agonists: a review of head-to-head clinical studies. Ther Adv Endocrinol Metab 2015;6:19–28. 10.1177/2042018814559725 - DOI - PMC - PubMed

Publication types

MeSH terms