Author
Listed:
- Kah Suan Chong
(National Cheng Kung University)
- Chun-Ting Yang
(National Cheng Kung University
Brigham and Women’s Hospital, Harvard Medical School)
- Chi-Chuan Wang
(National Taiwan University
National Taiwan University
National Taiwan University Hospital)
- Huang-Tz Ou
(National Cheng Kung University
National Cheng Kung University)
- Shihchen Kuo
(National Cheng Kung University
University of Michigan Medical School)
Abstract
Background and Objective Although heterogeneous treatment effects of sodium-glucose cotransporter 2 inhibitors (SGLT2is) have been revealed, the heterogeneous economic value of SGLT2is in real-world type 2 diabetes (T2D) populations with diverse clinical characteristics remains unclear. We conducted subgroup cost-effectiveness analyses of SGLT2is versus dipeptidyl peptidase 4 inhibitors (DPP4is) among patients with T2D. Methods A multi-state transition model was used to estimate the incremental cost-effectiveness ratios (ICERs, in US$ per quality-adjusted life-years [QALYs] gained) and value-based pricing (VBP) among patients with T2D stratified by age, estimated glomerular filtration rate (eGFR), glycated hemoglobin (HbA1c), and body mass index (BMI) over 5 years and a Lifetime horizon from a healthcare sector perspective, with both costs and quality-adjusted Life years discounted at 3% annually. Model inputs included treatment effects derived from analysis of individual-level data in Taiwan, and health utilities and costs sourced from published Literature of Taiwanese populations. Deterministic and probabilistic sensitivity analyses across subgroups were performed. All costs were standardized to 2022. Results Over 5 years, the ICERs of SGLT2is versus DPP4is were as follows: age subgroups (
Suggested Citation
Kah Suan Chong & Chun-Ting Yang & Chi-Chuan Wang & Huang-Tz Ou & Shihchen Kuo, 2025.
"Heterogeneity in Economic Value of SGLT2is for Type 2 Diabetes: Subgroup Modeling Cost-Effectiveness Analyses,"
PharmacoEconomics, Springer, vol. 43(12), pages 1451-1461, December.
Handle:
RePEc:spr:pharme:v:43:y:2025:i:12:d:10.1007_s40273-025-01536-6
DOI: 10.1007/s40273-025-01536-6
Download full text from publisher
As the access to this document is restricted, you may want to
for a different version of it.
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:spr:pharme:v:43:y:2025:i:12:d:10.1007_s40273-025-01536-6. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.springer.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.