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Brief Summary

GUIDELINE TITLE

Standards of medical care in diabetes. II. Testing for prediabetes and diabetes in asymptomatic patients.

BIBLIOGRAPHIC SOURCE(S)

  • American Diabetes Association (ADA). Standards of medical care in diabetes. II. Testing for pre-diabetes and diabetes in asymptomatic patients. Diabetes Care 2008 Jan;31(Suppl 1):S13-4.

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: American Diabetes Association (ADA). Standards of medical care in diabetes. II. Screening for diabetes. Diabetes Care 2007 Jan;30(Suppl 1):S5-7.

BRIEF SUMMARY CONTENT

 
RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

The evidence grading system (A through C, E) is defined at the end of the "Major Recommendations" field.

Testing for Pre-diabetes and Diabetes in Asymptomatic Patients

  • Testing to detect pre-diabetes and type 2 diabetes in asymptomatic people should be considered in adults who are overweight or obese (body mass index [BMI] >25 kg/m2) and who have one or more additional risk factors for diabetes. In those without these risk factors, testing should begin at age 45. (B)
  • If tests are normal, repeat testing should be carried out at least at 3-year intervals. (E)
  • To test for pre-diabetes or diabetes, either a fasting plasma glucose (FPG) test or a 2-h oral glucose tolerance test (OGTT) (75-g glucose load) or both are appropriate. (B)
  • An oral glucose tolerance test may be considered in patients with impaired fasting glucose (IFG) to better define the risk of diabetes. (E)
  • In those identified with pre-diabetes, identify and, if appropriate, treat other cardiovascular disease (CVD) risk factors. (B)

Criteria for Testing for Pre-Diabetes and Diabetes in Asymptomatic Adult Individuals

1. Testing should be considered in all adults who are overweight (BMI >25 kg/m2*) and have additional risk factors:
  • Physical inactivity
  • First-degree relative with diabetes
  • Members of a high-risk ethnic population (e.g., African American, Latino, Native American, Asian American, and Pacific Islander)
  • Women who delivered a baby weighing >9 lb or have been diagnosed with gestational diabetes mellitus (GDM)
  • Hypertension (>140/90 mmHg or on therapy for hypertension)
  • High-density lipoprotein (HDL) cholesterol level <35 mg/dL (0.90 mmol/L) and/or a triglyceride level >250 mg/dL (2.82 mmol/L)
  • Women with polycystic ovarian syndrome (PCOS)
  • Impaired glucose tolerance (IGT) or IFG on previous testing
  • Other clinical conditions associated with insulin resistance (e.g., severe obesity and acanthosis nigricans)
  • History of CVD
2. In the absence of the above criteria, testing for pre-diabetes and diabetes should begin at age 45 years
3. If results are normal, testing should be repeated at least at 3-year intervals, with consideration of more frequent testing depending on initial results and risk status.

*At-risk BMI may be lower in some ethnic groups.

Testing for Type 2 Diabetes in Asymptomatic Children

Criteria
  • Overweight (BMI >85th percentile for age and sex, weight for height >85th percentile, or weight >120% of ideal for height)

    Plus any two of the following risk factors:

    • Family history of type 2 diabetes in first or second-degree relative
    • Race/ethnicity (Native American, African American, Latino, Asian American, and Pacific Islander)
    • Signs of insulin resistance or conditions associated with insulin resistance (e.g., acanthosis nigricans, hypertension, dyslipidemia, or PCOS)
    • Maternal history of diabetes or gestational diabetes mellitus
Age of initiation Age 10 years or at onset of puberty, if puberty occurs at a younger age
Frequency Every 2 years
Test FPG preferred

Definitions:

American Diabetes Association's Evidence Grading System for Clinical Practice Recommendations

A

Clear evidence from well-conducted, generalizable, randomized controlled trials that are adequately powered, including:

  • Evidence from a well-conducted multicenter trial
  • Evidence from a meta-analysis that incorporated quality ratings in the analysis
  • Compelling non-experimental evidence (i.e., "all or none" rule developed by the Center for Evidence Based Medicine at Oxford*)

Supportive evidence from well-conducted randomized, controlled trials that are adequately powered, including:

  • Evidence from a well-conducted trial at one or more institutions
  • Evidence from a meta-analysis that incorporated quality ratings in the analysis

*Either all patients died before therapy and at least some survived with therapy, or some patients died without therapy and none died with therapy. Example: use of insulin in the treatment of diabetic ketoacidosis.

B

Supportive evidence from well-conducted cohort studies, including:

  • Evidence from a well-conducted prospective cohort study or registry
  • Evidence from a well-conducted meta-analysis of cohort studies

Supportive evidence from a well-conducted case-control study

C

Supportive evidence from poorly controlled or uncontrolled studies, including:

  • Evidence from randomized clinical trials with one or more major or three or more minor methodological flaws that could invalidate the results
  • Evidence from observational studies with high potential for bias (such as case series with comparison with historical controls)
  • Evidence from case series or case reports

Conflicting evidence with the weight of evidence supporting the recommendation

E

Expert consensus or clinical experience

CLINICAL ALGORITHM(S)

None provided

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of supporting evidence is identified and graded for each recommendation (see the "Major Recommendations" field).

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

  • American Diabetes Association (ADA). Standards of medical care in diabetes. II. Testing for pre-diabetes and diabetes in asymptomatic patients. Diabetes Care 2008 Jan;31(Suppl 1):S13-4.

ADAPTATION

Not applicable: The guideline was not adapted from another source.

DATE RELEASED

1998 (revised 2008 Jan)

GUIDELINE DEVELOPER(S)

American Diabetes Association - Professional Association

SOURCE(S) OF FUNDING

The American Diabetes Association (ADA) received an unrestricted educational grant from LifeScan, Inc., a Johnson and Johnson Company, to support publication of the 2008 Diabetes Care Supplement.

GUIDELINE COMMITTEE

Professional Practice Committee

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Committee Members: Irl Hirsch, MD, Chair; Martin Abrahamson, MD; Andrew Ahmann, MD; Lawrence Blonde, MD; Silvio Inzucchi, MD; Mary T. Korytkowski, MN, MD, MSN; Melinda Maryniuk, MEd, RD, CDE; Elizabeth Mayer-Davis, MS, PhD, RD; Janet H. Silverstein, MD; Robert Toto, MD

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

Not stated

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: American Diabetes Association (ADA). Standards of medical care in diabetes. II. Screening for diabetes. Diabetes Care 2007 Jan;30(Suppl 1):S5-7.

GUIDELINE AVAILABILITY

AVAILABILITY OF COMPANION DOCUMENTS

PATIENT RESOURCES

None available

NGC STATUS

This summary was completed by ECRI on April 2, 2001. The information was verified by the guideline developer on August 24, 2001. This summary was updated by ECRI on March 14, 2002, July 29, 2003, March 23, 2004, July 1, 2005, and March 16, 2006, and April 24, 2007. This summary was updated most recently by ECRI Institute on March 31, 2008. The updated information was verified by the guideline developer on May 15, 2008.

COPYRIGHT STATEMENT

DISCLAIMER

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