Title: New Guidelines streamline Diabetes Diagnosis
1New GuidelinesstreamlineDiabetes Diagnosis
- Clev Clin J Med 19986510-12
2Guideline Development
- 1979 National Diabetes Data Group
- 1997 American Diabetes Association
Diabetes 1979281039-1057Diabetes Care
1997201183-1197
3National Diabetes Data Group
- Issued in 1979
- fasting plasma glucose gt 140 mg/dl
- 2 hr glucose tolerance test gt 200 mg/dl
- tests not equivalent only 1/4 of patients with
abnormal GTT have abnormal FBS - GTT is expensive, time-consuming, inconvenient
- FBS is more reliable and consistent
Diabetes 1979281039-1057
4American Diabetes Association
- Report of the Expert Committee on the
Diagnosis and Classification of Diabetes
Mellitus - Diabetes Care 1997201183-1197
5American Diabetes Association
- Issued in 1997
- fasting plasma glucose gt126 mg/dl
- glucose tolerance test not used
- simplify the diagnostic process
- identify more patients with previously
unidentified diabetes
Diabetes Care 1997201183-1197
6ADA criteria for the diagnosis of diabetes
mellitus
- Symptoms of diabetes (polyuria, polydipsia,
unexplained weight loss) plus a casual plasma
glucose concentration ? 200 mg/dl - A fasting plasma glucose concentration ? 126
mg/dl (measured after at least 8 hours of no
caloric intake) - An abnormal oral glucose tolerance test result (a
plasma glucose concentration ? 200 mg/dl two
hours after a glucose load of 75 grams of
anhydrous glucose dissolved in water)
Diabetes Care 1997201183-1197
7Usefulness of Hemoglobin A1cfor follow-up but
not for screening
- HbA1c level reflect long-term glucose level
useful in the follow-up of diabetics - Problems
- methods not standardized for all labs
- abnormal low values in patients with abnormal
hemoglobins or those with reduced red blood cell
life span
8Who should be screened?
- Prevalence of diabetes (ages 40-74)
- 12.27 using the 1979 criteria
- 14.26 using the 1997 criteria
- Currently, only 50 of diabetics are identified
- Earlier identification and treatment may lead to
fewer complications
The 3rd National Health and Nutrition Survey
9Who should be screened?
- Consider testing all persons age 45 and older (if
normal, repeat every 3 years) - Consider testing at a younger age, or more
frequently, for higher risk individuals
Diabetes Care 1997201183-1197
10Who should be screened?high risk patients
- Obese persons (? 120 desired body wt or body
mass index ? 27 kg/m2) - first-degree relatives with diabetes
- high-risk ethnic groups (African Americans,
Hispanic, American Indians) - mothers of babies weighing ? 9 lb at birth
- women with a history of gestational diabetes
Diabetes Care 1997201183-1197
11Who should be screened?high risk patients
- hypertensive patients (? 140/90)
- dyslipidemic patients (HDL ? 35 mg/dl or
triglyceride ? 250 mg/dl or both) - patients with previous finding of impaired
glucose tolerance (140-199 mg/dl on 2-hr test) or
impaired fasting glucose (110-125 mg/dl)
Diabetes Care 1997201183-1197
12Old Nomenclatureclassification by disease
treatment
- Discard the use of IDDM (insulin-dependent
DM)NIDDM (non-insulin-dependent DM) - classification based on treatment
- not all patients fit into either category
Diabetes Care 1997201183-1197
13New Nomenclatureclassification by disease process
- Type 1 diabetes
- due to beta cell destruction, usually leading to
absolute insulin deficiency - Type 2 diabetes
- range from predominantly insulin resistance with
relative insulin deficiency to predominantly
secretory defect with insulin resistance
Diabetes Care 1997201183-1197
14New Nomenclatureclassification by disease process
- Other types of diabetes
- specific genetic defects, diseases of the
exocrine pancreas, endocrinopathies, drugs or
chemicals, infections, immune-mediated diseases - Gestational diabetes
- screen women at high risk (age gt25, obesity,
family history, ethnic groups)
Diabetes Care 1997201183-1197
15Oral Hypoglycemic Agents
- Sulfonylreas
- increase insulin secretion by the pancreas
- Acarbose
- delay carbohydrate absorption by inhibiting
enzymes that break down starches in the small
intestine
16Oral Hypoglycemic Agents
- Metformin
- decrease hepatic glucose production
- increase insulin sensitivity in muscle cells
- Troglitazone
- increase insulin sensitivity
- isolated reports of severe hepatotoxicity
17Toward rational use of Oral Hypoglycemic Agents
- One approach is to choose the drug appropriate
for the stage of the disease based on the natural
history of type 2 diabetes
18Natural history of Type 2 diabetes
- Early phase
- ? insulin sensitivity
- gradual rise in blood glucose
- ? insulin secretion to compensate
- Late phase
- ? insulin levels as beta cell wears out
- sharp rise in blood sugar level
19Natural history of Type 2 diabetes Clue to
disease progression
- Weight gain
- Is the patient is still gaining weight at the
time of diagnosis ? - weight gain, in the absence of therapy, indicates
that the patient still has adequate insulin
secretion
20Toward rational use of Oral Hypoglycemic Agents
- General guidelines
- monitor FBS and HbA1c at regular intervals (2 - 4
times / yr) and adjust treatment as needed - Treatment guided by disease stage
- early phase acarbose, metformin, troglitazone
- late phase sulfonylureas and insulin
21Toward rational use of Oral Hypoglycemic Agents
- A M T S
- Postprandial ? sugar
- Liver disease -- --
- Obese patients
- Kidney disease --
- Elderly patients
- FBS gt 200 mg/dl
A acarbose, M metformin, T troglitazone, S
sulfonylureas favored or indicated,
low-dose, -- avoid
22References
- Expert Committee on the Diagnosis and
Classification of Diabetes Mellitus. Diabetes
Care 1997201183-1197. - National Diabetes Data Group. Classification and
diagnosis of diabetes and other categories of
glucose intolerance.Diabetes 1979281039-1057. - Comparison of fasting and 2-hour glucose and
HBA1c levels for diagnosing diabetes diagnostic
criteria and performance revisited.Engelgau MM,
Thompson TJ, et al. Diabetes Care
199720785-791. - New guidelines streamline diabetes diagnosis.
Reddy S.Clev Clinic j Med 199865(1)10-12.