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Diabetes

Comparative persistence and adherence with newer anti-hyperglycemic agents to treat patients with type 2 diabetes in the United States

, , , &
Pages 1175-1186 | Received 24 Mar 2016, Accepted 27 Jun 2016, Published online: 12 Jul 2016

Figures & data

Figure 1. Sample selection.

Figure 1. Sample selection.

Table 1. Key baseline characteristics, index costs, and days of supply by index anti-hyperglycemic agent.

Figure 2. Kaplan-Meier analysis of persistence, using the time to treatment discontinuation. Cana, canagliflozin; Dapa, dapagliflozin; Exen, exenatide; Exen LA, long-acting exenatide; Lina, linagliptin; Lira, liraglutide; Saxa, saxagliptin; Sita, sitagliptin.

Figure 2. Kaplan-Meier analysis of persistence, using the time to treatment discontinuation. Cana, canagliflozin; Dapa, dapagliflozin; Exen, exenatide; Exen LA, long-acting exenatide; Lina, linagliptin; Lira, liraglutide; Saxa, saxagliptin; Sita, sitagliptin.

Figure 3. Cox proportional hazards model ratios for treatment non-persistence. * p < 0.05 vs reference. Included combinations with the previous items in the list and excluded combinations with the subsequent items. For example, “DPP-4 inhibitors” included DPP-4 inhibitors either alone or in combination with metformin, sulfonylureas, meglitinides, α-glucosidase inhibitors, and/or thiazolidinediones; and excluded combinations of DPP-4 inhibitors with GLP-1 agonists, SGLT2 inhibitors, or insulin. Co-payment/co-insurance for each pharmacy claim was adjusted to 30 days. CDHP, consumer-directed health plan; CI, confidence interval; DCSI, Diabetes Complications Severity Index; DPP-4 inhibitors, dipeptidyl peptidase-4 inhibitors (e.g. sitagliptin, saxagliptin, linagliptin); EPO, exclusive provider organization; GLP-1 agonists, glucagon-like peptide-1 receptor agonist (e.g. exenatide, liraglutide); HDHP, high-deductible health plan; HMO, health maintenance organization; POS, point of service; PPO, preferred provider organization; SGLT2 inhibitors, sodium/glucose cotransporter 2 inhibitors (e.g. canagliflozin, dapagliflozin).

Figure 3. Cox proportional hazards model ratios for treatment non-persistence. * p < 0.05 vs reference. † Included combinations with the previous items in the list and excluded combinations with the subsequent items. For example, “DPP-4 inhibitors” included DPP-4 inhibitors either alone or in combination with metformin, sulfonylureas, meglitinides, α-glucosidase inhibitors, and/or thiazolidinediones; and excluded combinations of DPP-4 inhibitors with GLP-1 agonists, SGLT2 inhibitors, or insulin. Co-payment/co-insurance for each pharmacy claim was adjusted to 30 days. CDHP, consumer-directed health plan; CI, confidence interval; DCSI, Diabetes Complications Severity Index; DPP-4 inhibitors, dipeptidyl peptidase-4 inhibitors (e.g. sitagliptin, saxagliptin, linagliptin); EPO, exclusive provider organization; GLP-1 agonists, glucagon-like peptide-1 receptor agonist (e.g. exenatide, liraglutide); HDHP, high-deductible health plan; HMO, health maintenance organization; POS, point of service; PPO, preferred provider organization; SGLT2 inhibitors, sodium/glucose cotransporter 2 inhibitors (e.g. canagliflozin, dapagliflozin).

Figure 4. Median (mean) adherence rate for the index anti-hyperglycemic agent.

Figure 4. Median (mean) adherence rate for the index anti-hyperglycemic agent.

Figure 5. Proportion of patients with good adherence to the index anti-hyperglycemic agent.

Figure 5. Proportion of patients with good adherence to the index anti-hyperglycemic agent.

Table 2. Odds ratios for treatment adherence, defined as either proportion of days covered ≥80% or medication possession ratio ≥80%, using multivariable logistic regression analyses.

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