Screening for Type 2 Diabetes Author: Lorraine Lipscombe, MD, FRCPC; Denice S. Feig, MD, MSc, FRCPC
Editorial changes - 2012-02-07
Author information and module status
Key Points
Population at Risk
Effectiveness/Harms of Screening Tests
Effectiveness/Harms of Early Treatment
Direct Evidence that Screening Reduces Adverse Outcomes
Timeline
Cost-Effectiveness
Patient Education
Referral/Consultation
Guidelines

Tables
References
Glossary
What's New
Patient Information
Additional Resources
Tools
Effectiveness/Harms of Screening Tests
  • Know that a 2-hour PG value of 200 mg/dL (11.1 mmol/L) after a 75-g OGTT is considered the gold standard for diagnosing diabetes mellitus.B
  • Recognize that the ADA criterion for diabetes of an FBG of 126 mg/dL (7.0 mmol/L) is more reproducible than the 2-hour PG and has excellent specificity for diagnosing diabetes, but its sensitivity is only approximately 50%.B
  • Know that lowering the threshold FBG value increases the sensitivity but decreases the specificity for a diagnosis of diabetes; therefore, although the optimal threshold FBG value to exclude diabetes may be <100 mg/dL (5.6 mmol/L), a 2-hour PG would be required to confirm diabetes in patients with an FBG 100 mg/dL (5.6 mmol/L).B
  • Recognize that the HbA1ctest has good specificity but only moderate sensitivity for detecting undiagnosed diabetes, and its performance varies depending on the population and cutpoint used.B
  • Recognize that consideration of age, BMI, and race/ethnicity in screening to detect diabetes and pre-diabetes may be less important than evaluation of random plasma glucose.B
  • Know that risk assessment questionnaires developed to screen for diabetes have inadequate sensitivity and specificity in identifying persons with undiagnosed diabetes.B
  • Know that there is limited evidence regarding the harms of screening for diabetes; however, screening tests appear to be safe and have minimal effect on quality of life.B
FAQs
Denice S. Feig, MD, MSc, FRCPC has no financial relationships with pharmaceutical companies, biomedical device manufacturers, or health-care related organizations. Lorraine Lipscombe, MD, FRCPC has no financial relationships with pharmaceutical companies, biomedical device manufacturers, or health-care related organizations. Sonal Singh, MD, editorial consultant, has no financial relationships with pharmaceutical companies, biomedical device manufacturers, or health-care related organizations.
Deborah Korenstein, MD, FACP, Co-Editor, PIER, has no financial relationships with pharmaceutical companies, biomedical device manufacturers, or health-care related organizations. Richard B. Lynn, MD, FACP, Co-Editor, PIER, has no financial relationships with pharmaceutical companies, biomedical device manufacturers, or health-care related organizations.


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