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Brief Summary

GUIDELINE TITLE

Peptic ulcer disease.

BIBLIOGRAPHIC SOURCE(S)

  • University of Michigan Health System. Peptic ulcer disease. Ann Arbor (MI): University of Michigan Health System; 2005 May. 9 p. [7 references]

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: University of Michigan Health System. UMHS peptic ulcer guideline. Ann Arbor (MI): University of Michigan Health System; 1999 May. 6 p.

BRIEF SUMMARY CONTENT

 
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 detailed information on dosing and cost considerations for therapy for Helicobacter pylori (H. pylori [HP]) associated peptic ulcer disease (PUD).

The levels of evidence [A-D] are defined at the end of the "Major Recommendations" field.

  • Clinical approach.

    Ulcers are caused by an infection of a bacterium known as Helicobacter pylori (HP) or H. pylori. Eradication of HP infection alters the natural history of peptic ulcer disease. Successful eradication reduces PUD recurrence rate from 90% to <5% per year [A]. PUD generally does not recur in the successfully treated patient unless nonsteroidal anti-inflammatory drug (NSAID) use is present.

  • Diagnosis.

    Economic analyses demonstrate a cost effectiveness advantage of non-invasive testing and antibiotic therapy for HP in patients with symptoms suggestive of PUD when compared to immediate endoscopy. [C] Testing for active HP infection (stool antigen or urea breath testing) is more appropriate than serology testing in areas with low prevalence of active HP infection to reduce unnecessary treatment of individuals without active HP infection.

  • Treatment.

    HP eradication therapy consists of antibiotics and anti-secretory drugs. [A] Long-term acid inhibition is inappropriate in the management of HP-related PUD in most instances. [B]

  • Follow-up.

    Referral to the gastroenterologist should occur for all patients with signs and symptoms of complicated ulcer disease and for patients who fail initial therapy based on a non-invasive HP test. Persistent symptoms after 2 weeks of therapy suggest an alternative diagnosis.

Definitions:

Levels of evidence for the most significant recommendations:

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

CLINICAL ALGORITHM(S)

An algorithm is provided in the original guideline document for the management of peptic ulcer disease.

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" field).

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

  • University of Michigan Health System. Peptic ulcer disease. Ann Arbor (MI): University of Michigan Health System; 2005 May. 9 p. [7 references]

ADAPTATION

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

DATE RELEASED

1996 Oct (revised 2005 May)

GUIDELINE DEVELOPER(S)

University of Michigan Health System - Academic Institution

SOURCE(S) OF FUNDING

The University of Michigan Health System (UMHS) provides funding for guideline development. No external funds are used.

GUIDELINE COMMITTEE

Peptic Ulcer Guideline Team

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Team Members: A. Mark Fendrick, M.D., General Internal Medicine; Randall T. Forsch, M.D., Family Medicine; R. Van Harrison, Ph.D., Medical Education; James M. Scheiman, M.D., Gastroenterology

Guidelines Oversight Team: Connie J. Standiford, MD; Lee A. Green, 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

Mark Fendrick, MD, Speaker's bureau, Astra Zeneca, Tap

Consultant, Astra Zeneca, Tap, Meridian Diagnostics

Randall Forsch, MD (None)

Van Harrison, PhD (None)

James Scheiman, MD, Grant/research support, AstraZeneca, Pfizer, Merck Consultant, AstraZeneca, Merck, Nitromed, McNeil, Novartis, TAP, Pfizer, Pozen, The GI Company

Speaker's bureau, AstraZeneca, TAP, Wyeth, Boheringer Ingelheim

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: University of Michigan Health System. UMHS peptic ulcer guideline. Ann Arbor (MI): University of Michigan Health System; 1999 May. 6 p.

GUIDELINE AVAILABILITY

AVAILABILITY OF COMPANION DOCUMENTS

None available

PATIENT RESOURCES

The following is available:

  • Peptic ulcer disease (PUD). University of Michigan Health System; 2005 Apr. Various p.

Electronic copies: 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 August 21, 2000. The information was verified by the guideline developer on November 22, 2000. This summary was updated by ECRI on August 4, 2005. The updated information was verified by the guideline developer on August 10, 2005.

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

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

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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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