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Brief Summary

GUIDELINE TITLE

Urinary tract infection.

BIBLIOGRAPHIC SOURCE(S)

  • University of Michigan Health System. Urinary tract infection. Ann Arbor (MI): University of Michigan Health System; 2005 May. 9 p. [10 references]

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: University of Michigan Health System. UMHS urinary tract infection guideline. Ann Arbor (MI): University of Michigan Health System; 1999 Jun. 7 p.

** REGULATORY ALERT **

FDA WARNING/REGULATORY ALERT

Note from the National Guideline Clearinghouse (NGC): 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

Note from 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 diagnosis, treatment regimens and costs.

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

Diagnosis

  • History. Diagnosis is made primarily by history. In women with dysuria and frequency, in the absence of vaginitis, the diagnosis is urinary tract infection (UTI) 80% of the time [C].
  • Phone triage. In women with prior history of uncomplicated urinary tract infections (UTIs), consider phone triage [C].
  • Urinalysis. Urinalysis for detection of pyuria by dipstick or microscope has a sensitivity of 80-90% and a specificity of 50% for predicting UTI [B].
  • No urine culture. Urine culture is NOT indicated in the vast majority of UTIs. Urine culture (UC) has a sensitivity of 50% (if threshold for positive is >105 organisms); sensitivity can be increased to >90% if threshold is >102 organisms [C]. Consider urine culture only in recurrent UTI or in the presence of complicating factors.

Treatment

  • First line: three days of trimethoprim/sulfa [A].
  • Second line:
    • three days of quinolone (contraindicated in pregnancy) [A].
    • seven days of nitrofurantoin, amoxicillin, first-generation cephalosporin [A].

Follow-up

  • No tests if asymptomatic. No laboratory follow-up is necessary if asymptomatic [B].
  • For recurrent UTIs. In patients with recurrent UTIs (>3/year):
    • consider prophylaxis/self-initiated therapy [A]
    • urologic structural evaluation rarely indicated [D]

Definitions:

Levels of evidence:

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

CLINICAL ALGORITHM(S)

An algorithm is provided in the original guideline document for the diagnosis and management of urinary tract infection (UTI).

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").

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

  • University of Michigan Health System. Urinary tract infection. Ann Arbor (MI): University of Michigan Health System; 2005 May. 9 p. [10 references]

ADAPTATION

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

DATE RELEASED

1999 Jun (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

Urinary Tract Infection Guideline Team

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Team Leader: Steven E. Gradwohl, MD, General Medicine

Team Members: Carol E. Chenoweth, MD, Infectious Diseases; Karen R. Fonde, MD, Family Practice; R. Van Harrison, PhD, Medical Education; Lauren B. Zoschnick, MD, Obstetrics & Gynecology

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

Carol E. Chenoweth, MD (None)

Karen R. Fonde, MD (None)

Steven E. Gradwohl, MD (None)

R. Van Harrison, PhD (None)

Lauren B. Zoschnick, MD (None)

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: University of Michigan Health System. UMHS urinary tract infection guideline. Ann Arbor (MI): University of Michigan Health System; 1999 Jun. 7 p.

GUIDELINE AVAILABILITY

AVAILABILITY OF COMPANION DOCUMENTS

None available

PATIENT RESOURCES

The following is available:

  • Urinary tract infection in women (UTI). 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. This summary was updated by ECRI Institute on July 28, 2008 following the U.S. Food and Drug Administration advisory on fluoroquinolone antimicrobial drugs.

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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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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