Persistence of oral antidiabetic treatment for type 2 diabetes characterized by drug class, patient characteristics and severity of renal impairment: A Japanese database analysis

被引:19
作者
Kadowaki, Takashi [1 ]
Sarai, Nobuaki [2 ]
Hirakawa, Takeshi [2 ]
Taki, Kentaro [3 ]
Iwasaki, Kosuke [4 ]
Urushihara, Hisashi [5 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo, Japan
[2] Nippon Boehringer Ingelheim Co Ltd, Clin Dev & Med Affairs, Tokyo, Japan
[3] Eli Lilly Japan KK, Med Dev Unit Japan, Kobe, Hyogo, Japan
[4] Milliman Inc, Tokyo, Japan
[5] Keio Univ, Fac Pharm, Div Drug Dev & Regulatory Sci, Tokyo, Japan
关键词
antidiabetic drug; database research; DPP-4; inhibitor; observational study; pharmacoepidemiology; type; 2; diabetes; HYPOGLYCEMIC AGENTS; KIDNEY-DISEASE; INHIBITOR; RISK; PRESCRIPTION; ADHERENCE; MELLITUS; HEALTH; COHORT;
D O I
10.1111/dom.13463
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim Materials and Methods To evaluate the persistence with oral antidiabetic drug (OAD) treatment characterized by drug class, patient characteristics and severity of renal impairment (RI) in patients with type 2 diabetes (T2DM) in Japan. This retrospective, observational study extracted data from a large-scale hospital database (April 2008 to September 2016). Patients with T2DM aged >= 40 years on the day of their first prescription (index date) of any OAD (biguanides [BGs], thiazolidinediones [TZDs], sulphonylureas [SUs], glinides, dipeptidyl peptidase-4 [DPP-4] inhibitors, or alpha-glucosidase inhibitors [alpha-GIs]) available between January 1, 2014 and September 30, 2016 were identified. Sodium-glucose co-transporter-2 inhibitors were not available at study initiation. Treatment persistence was assessed by Kaplan-Meier survival curves. Patients were also categorized by RI status using estimated glomerular filtration rate: >= 90 mL/min/1.73 m(2) (G1); 60 to <90 mL/min/1.73 m(2) (G2); 30 to <60 mL/min/1.73 m(2) (G3); and <30 mL/min/1.73 m(2) (G4+). Results Conclusions We identified 206 406 index dates from 162 116 eligible patients. The largest number of index dates (91634) was observed for DPP-4 inhibitors, followed by BGs, SUs, alpha-GIs, glinides and TZDs. Treatment persistence was longest for DPP-4 inhibitors (median 17.0 months, 95% confidence interval [CI] 16.4-17.5) and BGs (median 17.3 months, 95% CI 16.6-18.2), and shortest for alpha-GIs (median 5.6 months, 95% CI 5.4-5.9) and SUs (median 4.3 months, 95% CI 4.2-4.6). Persistence was longest with DPP-4 inhibitors at all RI stages (G1-G4+), followed by BGs at stages G1/G2. The longest OAD persistence was observed for BGs and DPP-4 inhibitors at RI stages G1/G2, and for DPP-4 inhibitors at RI stages G3/G4+.
引用
收藏
页码:2830 / 2839
页数:10
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