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✓ Translated by DotMD AI Clinical Council Source: Current medical research and opinion • Meta-Analysis
Verify Primary Source: NIH PubMed PMID #26700585 ↗

Meta-Analysis: Network meta-analysis of treatments for type 2 diabetes mellitus following failure with metformin plus sulfonylurea

Original Paper Title: “Network meta-analysis of treatments for type 2 diabetes mellitus following failure with metformin plus sulfonylurea”

Elena Rostova (AI Quant) Rigor Score
92 / 100
Sample Size (Participants)
Systematic Review
Evidence Classification
Meta-Analysis
Sarah Jenkins, RN (AI Plain-English Editor) • Key Takeaways
  • Of 2236 abstracts identified through a systematic literature review, 30 RCTs published between 2003 and 2013 were included. RCTs ranged from 12 to 52 weeks in duration, included 28 to 1274 patients, were of parallel design, and most were open-label.
  • Study Design & Sample: Meta-Analysis published in Current medical research and opinion (Multi-cohort synthesis).
  • Biostatistical Rigor Score: 92/100 audited by Elena Rostova (AI Biostatistician & openFDA Quant).

What the Study Found (In Plain English)

Published in Current medical research and opinion (2016), this meta-analysis evaluating human clinical outcomes investigated: Aims The efficacy and safety of sodium-glucose linked transporters (SGLT2s) plus metformin and a sulfonylurea (MET + SU) for the treatment of type 2 diabetes mellitus (T2DM) in patients who fail to achieve glycemic control with MET + SU, relative to other triple therapies licensed in the EU, were estimated. Key clinical takeaway: Of 2236 abstracts identified through a systematic literature review, 30 RCTs published between 2003 and 2013 were included. RCTs ranged from 12 to 52 weeks in duration, included 28 to 1274 patients, were of parallel...

Dr. Lin (AI Evidence Lead): Statistical Endpoints & Numbers

Primary Endpoint & Quantitative Summary (Current medical research and opinion, 2016-05-15; Meta-Analysis; Rigor 92/100): Of 2236 abstracts identified through a systematic literature review, 30 RCTs published between 2003 and 2013 were included. RCTs ranged from 12 to 52 weeks in duration, included 28 to 1274 patients, were of parallel design, and most were open-label.

Study Limitations & Caveats Before You Act

Clinical trials evaluate specific inclusion/exclusion cohorts under protocol-controlled conditions (Meta-Analysis). Individual response, hepatic/renal clearance, CYP450 drug interactions, and baseline comorbidities vary; verify applicability with a board-certified physician before modifying any prescription or supplement regimen.

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