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Brief Summary

GUIDELINE TITLE

Type 2 diabetes practice guidelines.

BIBLIOGRAPHIC SOURCE(S)

  • International Diabetes Center. Type 2 diabetes practice guidelines. Minneapolis (MN): International Diabetes Center; 2003. 1 p.

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: Staged diabetes management: a systematic approach. Minneapolis (MN): Matrex, International Diabetes Center; 2000. Type 2 diabetes practice guidelines. p. 63-131.

** REGULATORY ALERT **

FDA WARNING/REGULATORY ALERT

Note from the National Guideline Clearinghouse: This guideline references a drug(s) for which important revised regulatory and/or warning information has been released.

BRIEF SUMMARY CONTENT

 ** REGULATORY ALERT **
 RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

The following is an outline of practice guidelines for management of type 2 diabetes mellitus. A detailed management plan and accompanying DecisionPaths can be found in the original guidelines:

Screening

Screen all patients every 3 years starting at age 45; if risk factors present, start earlier and screen annually.

Risk Factors

  • Family history of type 2 diabetes (especially first-degree relatives)
  • Body mass index >25 kg/m2 (especially waist-to-hip ratio >1)
  • Age (risk increases with age)
  • Hypertension (>140/90 mm Hg)
  • Dyslipidemia (high-density lipoprotein <35 mg/dL and/or triglyceride >250 mg/dL)
  • Previous impaired fasting glucose with fasting plasma glucose 110 to 125 mg/dL
  • Previous impaired glucose tolerance with oral glucose tolerance test 2 hour glucose value 140 to 199 mg/dL
  • Previous gestational diabetes: macrosomic or large-for-gestational age infant (>9lbs.)
  • Acanthosis nigricans/polycystic ovary syndrome (PCOS)
  • History of vascular disease
  • American Indian or Alaska Native, African American, Hispanic, Asian, Pacific Islander

Diagnosis

Plasma Glucose

Casual >200 mg/dL plus symptoms, fasting >126 mg/dL, or 75 g Oral Glucose Tolerance Test 2 hour glucose value >200 mg/dL; if positive, confirm diagnosis with casual or fasting plasma glucose on subsequent day within one week.

Symptoms

Often none

Common: Blurred vision, urinary tract infection, yeast infection, dry/itchy skin, numbness or tingling in extremities, fatigue

Occasional: Increased urination, thirst, and appetite; nocturia; weight loss

Urine Ketones

Usually negative

Treatment Options

Medical nutrition therapy and activity, oral agent monotherapy, combination therapy (oral agents or oral agent-insulin), insulin stages 2, 3, 4 (see Type 2 Master DecisionPath in the original guideline document)

Targets

Self-Monitored Blood Glucose

  • More than 50% of self-monitored blood glucose values within target range
  • Pre-meal: 70 to140 mg/dL
  • Post-meal (2 hr after start of meal): <160 mg/dL
  • Bedtime: 100 to 160 mg/dL
  • No severe (assisted) or nocturnal hypoglycemia

Adjust pre-meal target upwards (e.g. 100 to 160 mg/dL) if frail elderly, cognitive disorders, or other medical concerns (cardiac disease, stroke, hypoglycemia unawareness, end-stage renal disease)

Hemoglobin A1c

  • Within 1.0% point of upper limit of normal (e.g. normal 6.0%; target <7.0%)
  • Frequency: every 3 to 4 months
  • Use hemoglobin A1c to verify self-monitored blood glucose data

Blood Pressure

<130/80 mm Hg

Lipids

Low-density lipoprotein <100 mg/dL; high-density lipoprotein >40 mg/dL; triglyceride <150 mg/dL

Monitoring

Self-Monitored Blood Glucose

2 to 4 times/day (e.g., before breakfast, before main meal, 2 hrs after main meal); if on insulin, check 3 a.m. self-monitored blood glucose as needed; self-monitored blood glucose may be modified due to cost, technical ability, or availability of meters.

Method

Meter with memory that is downloadable and log book

Follow Up

Monthly

Office visit during Adjust Phase (weekly phone contact may be necessary)

Every 3 Months

Hypoglycemia, medications, weight or body mass index, blood pressure, self-monitored blood glucose data (download and check meter), hemoglobin A1c, eye and foot screen, medical nutrition therapy, preconception planning for women of childbearing age, smoking cessation counseling, aspirin therapy

Yearly

In addition to the 3 month follow-up, complete the following: history and physical, fasting lipid profile, albuminuria screen, dilated eye examination, dental examination, neurologic assessment, complete foot examination (pulses, sensation, and inspection), referral for diabetes and nutrition education, adult immunizations

Complications Surveillance

Cardiovascular, renal, retinal, neurological, foot, oral, and dermatological

CLINICAL ALGORITHM(S)

Algorithms are provided for management of type 2 diabetes mellitus in the form of a Master DecisionPath and separate, detailed DecisionPaths for:

  • Screening and Diagnosis
  • Master DecisionPath for Individuals Under Age 18
  • Screening and Diagnosis for Individuals Under Age 18
  • Impaired Glucose Homeostasis/Start
  • Medical Nutrition Therapy (Start)
  • Medical Nutrition Therapy (Adjust)
  • Exercise Assessment
  • Oral Agent Selection for Individuals 18 Years and Older
  • Insulin Stage 2/Start
  • Insulin Stage 2/ Adjust
  • Insulin Stage 3A/Start
  • Treating Hypoglycemia
  • Medical Nutrition Adherence Assessment
  • Psychological and Social Assessment
  • Pregestational and Gestational Diabetes

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of supporting evidence is not specifically stated for each recommendation. However, throughout the guideline document, the evidence used as the basis for the recommendations is discussed.

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

  • International Diabetes Center. Type 2 diabetes practice guidelines. Minneapolis (MN): International Diabetes Center; 2003. 1 p.

ADAPTATION

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

DATE RELEASED

2000 (revised 2003)

GUIDELINE DEVELOPER(S)

International Diabetes Center - Private Nonprofit Organization

GUIDELINE DEVELOPER COMMENT

The International Diabetes Center is part of the Institute for Research and Education HealthSystem Minnesota. HealthSystem Minnesota, an integrated care system, also includes Methodist Hospital, Park Nicollet Clinic, and The Foundation.

The International Diabetes Center is a World Health Organization (WHO) Collaborating Center for Diabetes Education, Translation and Computer Technology.

SOURCE(S) OF FUNDING

This publication is supported by an unrestricted educational grant from Becton Dickinson and Company.

GUIDELINE COMMITTEE

Not stated

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Authors: Roger S. Mazze, PhD, Ellie S. Strock, RN, ANP, CDE; Gregg D. Simonson, PhD, Richard M. Bergenstal, MD, Donnell D. Etzwiler, MD

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

Not stated

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: Staged diabetes management: a systematic approach. Minneapolis (MN): Matrex, International Diabetes Center; 2000. Type 2 diabetes practice guidelines. p. 63-131.

GUIDELINE AVAILABILITY

AVAILABILITY OF COMPANION DOCUMENTS

None available

PATIENT RESOURCES

None available

NGC STATUS

This summary was completed by ECRI on May 21, 2001. This summary was updated by ECRI on February 18, 2004. The information was verified by the guideline developer on March 11, 2004. This summary was updated by ECRI on January 11, 2006 following the U.S. Food and Drug Administration advisory on rosiglitazone. This summary was updated by ECRI Institute on September 5, 2007 following the U.S. Food and Drug Administration advisory on the Thiazolidinedione class of antidiabetic drugs. This summary was updated by ECRI Institute on November 28, 2007 following the U.S. Food and Drug Administration advisory on the Avandia (rosiglitazone maleate) Tablets. This summary was updated by ECRI Institute on March 10, 2008 following the U.S. Food and Drug Administration advisory on Avandia (rosiglitazone maleate).

COPYRIGHT STATEMENT

This NGC summary is based on the original guideline, which is subject to the guideline developer's copyright restrictions.

Copyright 2000. International Diabetes Center, Institute for Research and Education. All rights reserved. No part of these Guidelines may be reproduced, stored in a retrieval system or transmitted, in any form or by any means, electronic, photocopying, recording or otherwise, without prior written permissions of the International Diabetes Center. These Guidelines should not be interpreted as including all available and proper methods of diabetes care. The decision regarding any specific treatment modality must be made by the health care professional with consideration of the particular circumstances presented by the patient and the needs and resources particular to the community or institution.

DISCLAIMER

NGC DISCLAIMER

The National Guideline Clearinghouse™ (NGC) does not develop, produce, approve, or endorse the guidelines represented on this site.

All guidelines summarized by NGC and hosted on our site are produced under the auspices of medical specialty societies, relevant professional associations, public or private organizations, other government agencies, health care organizations or plans, and similar entities.

Guidelines represented on the NGC Web site are submitted by guideline developers, and are screened solely to determine that they meet the NGC Inclusion Criteria which may be found at http://www.guideline.gov/about/inclusion.aspx .

NGC, AHRQ, and its contractor ECRI Institute make no warranties concerning the content or clinical efficacy or effectiveness of the clinical practice guidelines and related materials represented on this site. Moreover, the views and opinions of developers or authors of guidelines represented on this site do not necessarily state or reflect those of NGC, AHRQ, or its contractor ECRI Institute, and inclusion or hosting of guidelines in NGC may not be used for advertising or commercial endorsement purposes.

Readers with questions regarding guideline content are directed to contact the guideline developer.


 

 

   
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