Alberto Tozzi · A simulation model estimates lifetime health and economic outcomes of screening prediabetes using the 1-h plasma glucose
Article1 min read·Published Sep 2023Older

A simulation model estimates lifetime health and economic outcomes of screening prediabetes using the 1-h plasma glucose

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Article · Sep 2023 · 1 min read

In brief

In brief

This health economic analysis uses Markov simulation to compare 1-hour versus 2-hour plasma glucose screening for prediabetes over 35 years. The 1-hour test demonstrated superior cost-effectiveness, delaying type 2 diabetes onset by one year per patient and gaining 0.58 QALYs while reducing complication incidence.

Written by the GCMD Library team from the article.

Alberto Tozzi

Aims: The current method to diagnose impaired glucose tolerance (IGT) is based on the 2-h plasma glucose (2-hPG) value during a 75-g oral glucose tolerance test (OGTT). Robust evidence demonstrates that the 1-h post-load plasma glucose (1-hPG) ≥ 8.6 mmol/L in those with normal glucose tolerance is highly predictive of type 2 diabetes (T2D), micro and macrovascular complications and mortality. The aim of this study was to conduct a health economic analysis to estimate long-term cost-effectiveness of using the 1-hPG compared to the 2-hPG for screening and assessing the risk of diabetes over 35 years. The main outcome was cost per quality-adjusted life year (QALY) gained. Methods: A Monte Carlo-based Markov simulation model was developed to forecast long-term effects of two screening strategies with regards to clinical and cost-effectiveness outcomes. The base case model included 20,000 simulated patients over 35-years follow-up. Transition probabilities on disease progression, mortality, effects on preventive treatments and complications were retrieved from landmark diabetes studies. Direct medical costs were sourced from published literature and inflated to 2019 Euros. Results: In the lifetime analysis, the 1-hPG was projected to increase the number of years free from disease (2 years per patient); to delay the onset of T2D (1 year per patient); to reduce the incidence of T2D complications (0·6 RR-Relative Risk per patient) and to increase the QALY gained (0·58 per patient). E

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