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Treatment patterns, persistence and adherence rates in patients with type 2 diabetes mellitus in Japan: a claims-based cohort study.
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- Author(s): Nishimura R;Nishimura R; Kato H; Kato H; Kisanuki K; Kisanuki K; Oh A; Oh A; Hiroi S; Hiroi S; Onishi Y; Onishi Y; Guelfucci F; Guelfucci F; Shimasaki Y; Shimasaki Y
- Source:
BMJ open [BMJ Open] 2019 Mar 01; Vol. 9 (3), pp. e025806. Date of Electronic Publication: 2019 Mar 01.- Publication Type:
Journal Article; Research Support, Non-U.S. Gov't- Language:
English - Source:
- Additional Information
- Source: Publisher: BMJ Publishing Group Ltd Country of Publication: England NLM ID: 101552874 Publication Model: Electronic Cited Medium: Internet ISSN: 2044-6055 (Electronic) Linking ISSN: 20446055 NLM ISO Abbreviation: BMJ Open Subsets: MEDLINE
- Publication Information: Original Publication: [London] : BMJ Publishing Group Ltd, 2011-
- Subject Terms:
- Abstract: Objective: To determine real-world trends in antidiabetic drug use, and persistence and adherence, in Japanese patients with type 2 diabetes mellitus (T2DM).
Design: Retrospective evaluation of administrative claims data (2011-2015) using the Japan Medical Data Center (JMDC) and Medical Data Vision (MDV) databases.
Setting: Analysis of two administrative claims databases for Japanese patients with T2DM.
Participants: Adults (aged ≥18 years) with an International Classification of Diseases, 10th Revision code of T2DM and at least one antidiabetic drug prescription.
Main Outcome Measures: Treatment patterns in untreated (UT) or previously treated (PT) patients receiving antidiabetic therapy; persistence with treatment at 12 months; adherence to treatment at 12 months.
Results: 40 908 and 90 421 patients were included from the JMDC and MDV databases, respectively. The most frequently prescribed therapy at the index (first prescription) date was dipeptidyl peptidase-4 inhibitor (DPP-4i) in UT patients (JMDC: 44.0%, MDV: 54.8%) and combination therapy in PT patients (74.6%, 81.1%). Most common combinations were DPP-4i plus: biguanide (BG; 11.4%, 10.9%), sulfonylurea (SU; 8.4%, 11.0%) or BG+SU (7.8%, 9.1%). In UT or PT patients from either database whose index prescription was for any antidiabetic drug class(es) other than DPP-4i, the most frequent add-on or switch was to DPP-4i. 12-month persistence with index monotherapy was highest with DPP-4i and BG. Adherence was high (≥80%) for all monotherapy schedules, except insulin and glucagon-like peptide-1 agonist, and for the five most frequent two-drug and three-drug combinations. Persistence was greater in elderly UT patients and in those receiving ≤5 medications, but comparatively worse in UT patients with ≥3 index antidiabetic drug classes.
Conclusions: The findings indicate that DPP-4i is the most commonly used antidiabetic drug class in Japanese patients with T2DM, and persistence and adherence to this antidiabetic drug class are high.
Competing Interests: Competing interests: RN has received speaker honoraria from Astellas Pharma, Nippon Boehringer Ingelheim, Eli Lilly Japan K.K., Kissei Pharmaceutical, Medtronic Japan, MSD, Novartis Pharma KK, Novo Nordisk Pharma, Sanofi KK and Takeda Pharmaceutical and contract research fees for collaborative research with the Japan Diabetes Foundation. HK, KK, AO and YS are employees of Takeda Pharmaceutical. SH was an employee of Takeda Pharmaceutical at the time the study was conducted. FG and YO are employees of Creativ-Ceutical K.K.
(© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.) - References: J Diabetes Investig. 2012 Dec 20;3(6):498-502. (PMID: 24843614)
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J Diabetes Investig. 2017 Jan;8(1):123-125. (PMID: 27935263) - Contributed Indexing: Keywords: adherence; administrative claims-based study; antidiabetic drug therapy; dipeptidyl peptidase-4 inhibitors; persistence; type 2 diabetes
- Accession Number: 0 (Drug Combinations)
0 (Hypoglycemic Agents) - Publication Date: Date Created: 20190304 Date Completed: 20200330 Latest Revision: 20220409
- Publication Date: 20221213
- Accession Number: PMC6429930
- Accession Number: 10.1136/bmjopen-2018-025806
- Accession Number: 30826768
- Source:
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