THE FORGOTTEN POPULATIONS: REAL-WORLD PATIENTS WITH T2DM NOT MEETING ELIGIBILITY CRITERIA OF THE GLARGINE 300 U/ML EDITION AND BRIGHT RCTS

Session Name
NEW INSULIN ANALOGUES
Session Type
E-POSTER VIEWING (EXHIBITION HOURS)
Date
20.02.2020, Thursday
Session Time
09:30 - 15:30
Channel
E-Poster Area
Lecture Time
09:34 - 09:35
Presenter
  • Jukka Westerbacka, France
Authors
  • Didac Mauricio, Spain
  • Jukka Westerbacka, France
  • Charlie Nicholls, United Kingdom
  • Jasmanda Wu, United States of America
  • Rishab Gupta, United States of America
  • Arjun A. Menon, United States of America
  • Björn Eliasson, Sweden

Abstract

Background and Aims

Randomised controlled trials (RCTs) are the gold standard for comparing therapies’ efficacy and safety but can have strict eligibility criteria and may not reflect real-life clinical practice. Electronic medical records such as those from the Predictive Health Intelligence Environment (PHIE) database may be used to assess clinical effectiveness in real-world populations missed by clinical trials. We describe here the proportion and characteristics of patients with type 2 diabetes mellitus (T2DM) who would have been excluded from RCTs using eligibility criteria adapted from the EDITION 1–3 and BRIGHT trials.

Methods

Records from people with T2DM, with a basal insulin prescription on the index date (01 March 2015) and ≥1 HbA1c value in the previous 12 months, were evaluated. Exclusion criteria included HbA1c <7.0 % / >10.0 %, systolic blood pressure >180 mmHg and/or diastolic blood pressure >95 mmHg, or key comorbidities (e.g. heart failure or stroke) in the previous 12 months.

Results

Of 191,218 evaluated records, 157,873 (83%) met ≥1 exclusion criterion; only 33,345 (17%) could have been included in RCTs (Table). Excluded patients were older, with more previous hypoglycaemia vs included patients, and were less likely to have HbA1c between 7 and 9 %.

table.png

Conclusions

This divergence in clinical characteristics and patient numbers highlights the need for real-world studies assessing clinical effectiveness in populations of interest typically excluded from RCTs.

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