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Brief Summary

GUIDELINE TITLE

Management of type 2 diabetes mellitus.

BIBLIOGRAPHIC SOURCE(S)

  • University of Michigan Health System. Management of type 2 diabetes mellitus. Ann Arbor (MI): University of Michigan Health System; 2008 Jan. 21 p. [15 references]

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: University of Michigan Health System. Management of type 2 diabetes mellitus. Ann Arbor (MI): University of Michigan Health System; 2007 Jul. 20 p. [15 references]

The University of Michigan Health System updated this guideline to include information on exenatide (Byetta), dipeptidyl peptidase-4, and Exubera that was released after the publication of the July 2007 version of the guideline.

** REGULATORY ALERT **

FDA WARNING/REGULATORY ALERT

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

  • February 26, 2008, Avandia (rosiglitazone): A new Medication Guide for Avandia must be provided with each prescription that is dispensed due to the U.S. Food and Drug Administration's (FDA's) determination that this medication could pose a serious and significant public health concern.
  • December 12, 2007, Carbamazepine: The U.S. Food and Drug Administration (FDA) has provided recommendations for screening that should be performed on specific patient populations before starting treatment with carbamazepine.
  • November 14, 2007, Avandia (rosiglitazone): New information has been added to the existing boxed warning in Avandia's prescribing information about potential increased risk for heart attacks.
  • October 16, 2007, Byetta (exenatide): Amylin Pharmaceuticals, Inc. has agreed to include information about acute pancreatitis in the PRECAUTIONS section of the product label.
  • August 14, 2007, Thiazolidinedione class of antidiabetic drugs: Addition of a boxed warning to the updated label of the entire thiazolidinedione class of antidiabetic drugs to warn of the risks of heart failure.
  • May 2, 2007, Antidepressant drugs: Update to the existing black box warning on the prescribing information on all antidepressant medications to include warnings about the increased risks of suicidal thinking and behavior in young adults ages 18 to 24 years old during the first one to two months of treatment.

BRIEF SUMMARY CONTENT

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

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Note from the National Guideline Clearinghouse (NGC): The following key points summarize the content of the guideline. Refer to the full text for additional information, including dosing and cost considerations for oral agents for the management of type 2 diabetes and self-management topics. The levels of evidence [A–D] are defined at the end of the "Major Recommendations" field.

Screening

Although little evidence is available on screening for diabetes, one may consider beginning screening at age 45 at 3–year intervals, earlier particularly if body mass index (BMI) >25 kg/m2 [D].

Prevention

In individuals at risk for diabetes (see Table 1 in original guideline document), diet, exercise, and pharmacologic interventions can delay or prevent type 2 diabetes [A].

Diagnosis

Either two separate fasting glucoses >126 mg/dL, or if symptoms, a glucose >200 mg/dL confirmed on a separate day by a fasting glucose >126 mg/dL, or 2-hour postload glucose > 200 mg/dL during an oral glucose tolerance test [B]. (See Table 1 in the original guideline document.) Glycated hemoglobin (HbA1c) has low sensitivity, but high specificity, for the diagnosis of diabetes, and most experts feel that it should not be used as a primary diagnostic test.

Treatment

Diet, exercise, and pharmacologic interventions should be initiated for:

  • Hypertension control [A]
  • Glycemic control [A]
  • Lipid control [A]
  • Cardiovascular risk reduction [A]

Ongoing Screening and Management

Routine screening and prevention efforts for cardiovascular risk factors (hypertension, hyperlipidemia, tobacco use) and for microvascular disease (retinopathy, nephropathy, neuropathy) are recommended to be performed in the following time frames. (See the original guideline document for management of risk factors, complications, and glycemia.)

Each Regular Diabetes Visit Every 3 to 6 Months Annually (see Table 2 in the original guideline document)
  • Diabetes visit every 3 months for patients on insulin; every 6 months for patients on oral agents or diet only [D]
  • Blood pressure measured and controlled [A] (see Table 2 in the original guideline document)
  • Weight checked [D]
  • Inspect feet each visit if presence of neuropathy; otherwise annually [A] (see Tables 2 and 8 in the original guideline document)
  • Smoking cessation counseling provided for patients with tobacco dependence [B] (see Table 2 in the original guideline document)
  • Very important self-management goals reviewed and reinforced [A] (see Table 8 in the original guideline document)
  • Check HbA1c and optimize glycemic control [A] (see Table 4 in the original guideline document)
  • Dilated retinal examination by an eye care specialist [B] and treatment of retinopathy [A] (Biannually if previous eye exam was normal, see Table 2 in the original guideline document)
  • Screen for microalbuminuria if not on an angiotensin-converting enzyme (ACE) inhibitor or angiotensin II receptor antagonist (ARB) [B]. Prescribe an ACE-1 or ARB for microalbuminuria or proteinuria [A]
  • Serum creatinine and estimated glomerular filtration rate (eGRF) [D].
  • Monofilament testing of feet [A] (see Table 9 in the original guideline document)
  • Lipids measured [B] and treated [A] (see Table 2 in the original guideline document)
  • Smoking status assessed
  • Other important self-management goals reviewed and reinforced (see Table 8 in the original guideline document)

Special considerations: Pregnancy. Preconception counseling and glycemic control in women with diabetes mellitus results in optimal maternal and fetal outcomes [B].

Definitions:

Levels of Evidence

  1. Randomized controlled trials
  2. Controlled trials, no randomization
  3. Observational trials
  4. Opinion of expert panel

CLINICAL ALGORITHM(S)

None provided

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of evidence is identified and graded for the most significant recommendations (see "Major Recommendations").

Conclusions were based on prospective randomized clinical trials if available, to the exclusion of other data. If randomized controlled trials were not available, observational studies were admitted to consideration. If no such data were available for a given link in the problem formulation, expert opinion was used to estimate effect size.

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

  • University of Michigan Health System. Management of type 2 diabetes mellitus. Ann Arbor (MI): University of Michigan Health System; 2008 Jan. 21 p. [15 references]

ADAPTATION

This guideline was partially adapted as follows:

  • Screening and glycemic goal recommendations were based on "American Diabetes Association. Clinical practice recommendations 2004. Diabetes Care. 2004;27(Suppl 1):S1-S140."
  • Screening and treatment of hypertension and lipid levels in type 2 diabetes recommendations are based on "Lipid control in the management of type 2 diabetes mellitus: A Clinical Practice Guideline from the American College of Physicians, Clinical Efficacy Assessment Subcommittee (2004)."

DATE RELEASED

1996 May (revised 2008 Jan)

GUIDELINE DEVELOPER(S)

University of Michigan Health System - Academic Institution

SOURCE(S) OF FUNDING

University of Michigan Health System

GUIDELINE COMMITTEE

Diabetes Mellitus Guideline Team

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Team Leaders: Sandeep Vijan, MD, General Internal Medicine

Team Members: Hae Mi Choe, PharmD, College of Pharmacy; Martha M. Funnell, MS, RN, CDE, Diabetes Research and Training Center; Steven J. Bernstein, MD, General Internal Medicine; R. Van Harrison, PhD, Medical Education; William H. Herman, MD, Endocrinology and Metabolism; Denise Campbell-Scherer, MD, PhD, Family Medicine; Robert W. Lash, MD, Endocrinology and Metabolism

Guidelines Oversight Team: William E. Chavey, MD; Connie J. Standiford, MD; R. Van Harrison, PhD

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

The University of Michigan Health System endorses the Guidelines of the Association of American Medical Colleges and the Standards of the Accreditation Council for Continuing Medical Education that the individuals who present educational activities disclose significant relationships with commercial companies whose products or services are discussed. Disclosure of a relationship is not intended to suggest bias in the information presented, but is made to provide readers with information that might be of potential importance to their evaluation of the information.

Team Member/Relationship/Company

Steven Bernstein, MD (None)

Denise Campbell-Scherer, MD, PhD (None)

Hae Mi Choe, PharmD (None)

Martha Funnell, MS, RN, Consultant: Eli Lilly, Home Diagnostics Inc, Novo Nordisk

Van Harrison, PhD (None)

William Herman, MD, Consultant: Aventis, Eli Lilly, GlaxoSmithKline, Merck, Sanofi-Aventis, Takeda

Robert Lash, MD (None)

Sandeep Vijan, MD (None)

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: University of Michigan Health System. Management of type 2 diabetes mellitus. Ann Arbor (MI): University of Michigan Health System; 2007 Jul. 20 p. [15 references]

The University of Michigan Health System updated this guideline to include information on exenatide (Byetta), dipeptidyl peptidase-4, and Exubera that was released after the publication of the July 2007 version of the guideline.

GUIDELINE AVAILABILITY

AVAILABILITY OF COMPANION DOCUMENTS

PATIENT RESOURCES

Several patient education resources about diabetes are available from the University of Michigan Health System Web site.

Please note: This patient information is intended to provide health professionals with information to share with their patients to help them better understand their health and their diagnosed disorders. By providing access to this patient information, it is not the intention of NGC to provide specific medical advice for particular patients. Rather we urge patients and their representatives to review this material and then to consult with a licensed health professional for evaluation of treatment options suitable for them as well as for diagnosis and answers to their personal medical questions. This patient information has been derived and prepared from a guideline for health care professionals included on NGC by the authors or publishers of that original guideline. The patient information is not reviewed by NGC to establish whether or not it accurately reflects the original guideline's content.

NGC STATUS

This summary was completed by ECRI on May 20, 1999. The information was verified by the guideline developer on June 17, 1999. This NGC summary was updated by ECRI on October 12, 2004. The updated information was verified by the guideline developer on October 22, 2004. This summary was updated on May 3, 2005 following the withdrawal of Bextra (valdecoxib) from the market and the release of heightened warnings for Celebrex (celecoxib) and other nonselective nonsteroidal anti-inflammatory drugs (NSAIDs). This summary was updated by ECRI on June 16, 2005, following the U.S. Food and Drug Administration advisory on COX-2 selective and non-selective non-steroidal anti-inflammatory drugs (NSAIDs). 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 6, 2007, following the U.S. Food and Drug Administration advisory on Antidepressant drugs. This NGC summary was updated by ECRI Institute on January 23, 2008. The information was verified by the guideline developer on February 11, 2008. 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 copyrighted by the University of Michigan Health System (UMHS).

DISCLAIMER

NGC DISCLAIMER

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


 

 

   
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