Geospatial distribution of the adoption of dipeptidyl-peptidase-4 inhibitors for type 2 diabetes among Medicare beneficiaries

被引:0
作者
Cordes, Jack [1 ,2 ]
Glynn, Robert J. [1 ,3 ]
Walker, Alexander M. [1 ,2 ]
Schneeweiss, Sebastian S. [1 ,2 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Dept Med, Div Pharmacoepidemiol & Pharmacoecon, Boston, MA 02115 USA
[2] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[3] Harvard TH Chan Sch Publ Hlth, Dept Biostat, Boston, MA USA
关键词
Diabetes; Clustering; DPP-4i; Sulfonylureas; ASSOCIATION;
D O I
10.1016/j.sste.2025.100711
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Objective: To characterize the geospatial distribution of the adoption of dipeptidyl-peptidase-4 inhibitor (DPP-4i) antidiabetics versus second generation sulfonylureas (SU). Methods: Using Medicare claims data 2012-2017, two cohorts were built with new-users of either sitagliptin or saxagliptin each versus active comparator SU. For each ZIP Code tabulation area (ZCTA), the proportion DPP-4i prescribing was used in a local indicator of spatial association hotspot analysis. Multilevel logistic models were used to quantify the variation in medication use at the individual, ZCTA, state, and region levels. Results: DPP-4i utilization proportion was low (sitagliptin median = 0.22; interquartile range 0.15 to 0.33; saxagliptin median = 0.025; 0.00 to 0.069). Clustering was observed for sitagliptin (Moran's I = 0.32) and saxagliptin (Moran's I = 0.20). States and ZCTAs accounted for 8.1 % and 13.3 % of variation in sitagliptin and saxagliptin prescribing, respectively. Conclusions: Variation across ZCTAs suggests neighborhood factors may be important determinants of prescribing.
引用
收藏
页数:7
相关论文
共 50 条
[31]   Dipeptidyl peptidase-4 inhibitors and the risk of community-acquired pneumonia in patients with type 2 diabetes [J].
Faillie, J. -L. ;
Filion, K. B. ;
Patenaude, V. ;
Ernst, P. ;
Azoulay, L. .
DIABETES OBESITY & METABOLISM, 2015, 17 (04) :379-385
[32]   PROTECTIVE EFFECTS OF DIPEPTIDYL PEPTIDASE-4 INHIBITORS ON PROGRESSION OF DIABETIC RETINOPATHY IN PATIENTS WITH TYPE 2 DIABETES [J].
Chung, Yoo-Ri ;
Park, Sung Wook ;
Kim, Jong Wan ;
Kim, Jeong Hun ;
Lee, Kihwang .
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 2016, 36 (12) :2357-2363
[33]   Bullous Pemphigoid Associated with Dipeptidyl Peptidase 4 Inhibitors for the Treatment of Type 2 Diabetes: A Multicenter Study in Istanbul [J].
Ugurer, Ece ;
Ozkur, Ezgi ;
Altunay, Ilknur Kivanc ;
Sen, Esra Cil ;
Aksu, Ayse Esra Koku ;
Ozcan, Ilknur ;
Altuntas, Yuksel ;
Gurel, Mehmet Salih .
MEDICAL BULLETIN OF SISLI ETFAL HOSPITAL, 2022, 56 (03) :375-380
[34]   Vildagliptin, a dipeptidyl peptidase-4 inhibitor, for the treatment of type 2 diabetes [J].
Stein, Stephanie A. ;
Lamos, Elizabeth M. ;
Davis, Stephen N. .
EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, 2014, 10 (04) :599-608
[35]   Saxagliptin A New Dipeptidyl Peptidase-4 Inhibitor for Type 2 Diabetes [J].
Lam, Sum ;
Saad, Maha .
CARDIOLOGY IN REVIEW, 2010, 18 (04) :213-217
[36]   Food insecurity and glycemic goals among Medicare beneficiaries with type 2 diabetes [J].
Massey, Mckayla ;
Stewart, Morgan P. ;
Lamanna, Jacqueline B. ;
Park, Chanhyun ;
Ng, Boon Peng .
CHRONIC ILLNESS, 2024, 20 (03) :527-534
[37]   Dipeptidyl peptidase 4 inhibition with sitagliptin: a new therapy for Type 2 diabetes [J].
Deacon, Carolyn F. .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2007, 16 (04) :533-545
[38]   Nationwide Trends in Pancreatitis and Pancreatic Cancer Risk Among Patients With Newly Diagnosed Type 2 Diabetes Receiving Dipeptidyl Peptidase 4 Inhibitors [J].
Lee, Minyoung ;
Sun, Jiyu ;
Han, Minkyung ;
Cho, Yongin ;
Lee, Ji-Yeon ;
Nam, Chung Mo ;
Kang, Eun Seok .
DIABETES CARE, 2019, 42 (11) :2057-2064
[39]   Addition of dipeptidyl peptidase-4 inhibitors to insulin treatment in type 2 diabetes patients: A meta-analysis [J].
Yang, Wenjia ;
Cai, Xiaoling ;
Gao, Xueying ;
Chen, Yifei ;
Chen, Ling ;
Ji, Linong .
JOURNAL OF DIABETES INVESTIGATION, 2018, 9 (04) :813-821
[40]   Dipeptidyl peptidase IV inhibitors: A promising new therapeutic approach for the management of type 2 diabetes [J].
Deacon, CF ;
Holst, JJ .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2006, 38 (5-6) :831-844