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Dual Therapy Appears Superior to Monotherapy for Low-Income Individuals With Newly Diagnosed Type 2 Diabetes. | LitMetric

AI Article Synopsis

  • Variable recommendations exist for treating newly diagnosed type 2 diabetes (T2D), especially in low-income settings where access to care is limited.
  • A study analyzed data from 309 low-income patients receiving oral hypoglycemic agents, focusing on the effects of monotherapy versus dual therapy on hemoglobin A1c levels over 12 months.
  • Results showed that dual therapy led to a more significant decrease in A1c levels compared to metformin monotherapy, suggesting dual therapy might be the preferred approach for these patients.

Article Abstract

Background: There are variable recommendations regarding initiating monotherapy or dual therapy in patients with newly diagnosed type 2 diabetes (T2D). Clear initial strategies are of particular importance in underserved settings where access to care and financial burdens are significant barriers.

Objectives: To provide descriptive data of metabolic outcomes to therapy regimens for low-income individuals with newly diagnosed T2D placed on oral hypoglycemic agents (OAs).

Methods: We conducted a retrospective chart review of low-income individuals with newly diagnosed T2D initiated on OAs. We provided descriptive data and then evaluated the effects of OA regimens (ie, mono-, dual-, transition [from mono to dual or vice versa] therapy) on hemoglobin A1c (A1c) (baseline to 12 months).

Results: A total of 309 patients were included in the study. At 12 months, the mean decrease in A1c for the entire sample was -2.36% (9.37% to 7.01%). Patients prescribed dual therapy had a greater change of A1c compared to those taking monotherapy with metformin (-1.11%, P < .01). Patients who transitioned therapies did not differ in change of A1c compared to monotherapy.

Conclusion: Initiation of dual therapy was superior to metformin monotherapy or transitioning therapies and may be preferred for low-income individuals with newly diagnosed T2D.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748290PMC
http://dx.doi.org/10.1177/2150131917745760DOI Listing

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