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Brief Summary

GUIDELINE TITLE

Osteoporosis: prevention and treatment.

BIBLIOGRAPHIC SOURCE(S)

  • University of Michigan Health System. Osteoporosis: prevention and treatment. Ann Arbor (MI): University of Michigan Health System; 2005 Jul. 13 p.

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: University of Michigan Health System. Osteoporosis: prevention and treatment. Ann Arbor (MI): University of Michigan Health System; 2002 Mar. 12 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 on drug dosing, Dexa-T scoring, and patient screening criteria.

The levels of evidence (A, B, C, D) are repeated at the end of the "Major Recommendations" field.

Definitions

  • Bone mineral density (BMD) correlates with skeletal strength and fracture risk.
  • Dual emission X-ray absorptiometry (DEXA) measures BMD.
  • A DEXA T-score is the number of standard deviations from mean BMD in young adult women.
  • Osteoporosis is defined as a DEXA T-score <-2.5, osteopenia as >-2.5 but <-1.0 (refer to Table 1 in the original guideline document for details).

General Clinical Relevance

Fractures related to osteoporosis are common and have high morbidity [C].

Glucocorticoids can cause significant bone loss, particularly during the first 6 to 12 months of use [C].

Prevention

Recommend weight bearing exercise and adequate calcium (1200-1500 mg/day) and vitamin D (400-800 IU/day) across the life span (refer to Table 6 in the original guideline document for details) [D]. Most older persons need vitamin D 700-800 IU/day [A].

Risk Assessment and Diagnosis

  • Assess all adults for clinical risk factors for osteoporotic fracture (refer to Table 2 in the original guideline document for details) [C]
    • Postmenopausal woman with one or more of the following:
      • Age >65 years
      • Current smoking
      • Low body weight
      • Frailty
      • Personal history of fracture without substantial trauma age >40
      • Hip, wrist, or spine fracture without substantial trauma in 1st degree relative >50
    • Chronic glucocorticoid use (prednisone >7.5 mg daily, or equivalent, for >6 months)
    • Organ transplant or pending transplant
    • Other associated medical conditions and medications
  • Order DEXA based on clinical risk factors and potential impact of results on management (refer to Table 3 in the original guideline document for details).
  • Evaluate appropriately and refer, when indicated, for secondary causes of osteoporosis (refer to Table 4 in the original guideline document for details) [D].

Treatment

  • Treat based on DEXA T-score and clinical risk factors for fracture (refer to Table 2 and Table 6 in the original guideline document for details)
    • Prior osteoporosis-related fracture [A].
    • T-score <-1 and (a) glucocorticoid use or (b) pending or post-transplant, especially if on steroids or (c) postmenopausal woman at high risk (i.e., with other risk factors for fracture but not already receiving hormone replacement therapy [HRT] [A]).
    • T-score <-2 and (a) postmenopausal woman [A] or (b) man [A] or (c) person with other risk factors [D].
  • When starting glucocorticoids consider therapy for prevention or treatment of osteoporosis [A].
  • Base management strategies on benefits and risks (refer to Table 6, Table 7, and Table 8 in the original guideline document for details)
    • In post-menopausal women with osteoporosis:
      • Alendronate and risedronate reduce hip and vertebral fracture risk [A].
      • Raloxifene and calcitonin reduce vertebral fracture risk [A].
      • HRT reduces vertebral [A] and hip [A] fracture risk, but overall poses health risks >placebo [A]. Consider use of HRT for osteoporosis only if there are other indications to use HRT.
    • In men with osteoporosis, alendronate reduces vertebral fracture risk [A].
    • In glucocorticoid use, risedronate (and perhaps alendronate) reduces vertebral fracture risk [A].

Follow-up

  • Follow-up osteoporosis or osteopenia with a repeat DEXA based on a patient's situation (refer to Table 3 and Table 5 in the original guideline document for details).
  • For most persons an interval of >2 years between DEXAs provides the most meaningful information.
  • Early in glucocorticoid use and/or after transplantation consider repeating DEXA in 6 to 12 months.

Definitions:

Levels of Evidence

Levels of evidence reflect the best available literature in support of an intervention or test.

  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 supporting evidence is identified and graded for each recommendation (see Major Recommendations).

Conclusions were based on prospective randomized clinical trials, if available, to the exclusion of other data. If randomized controlled trials (RCTs) 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. Osteoporosis: prevention and treatment. Ann Arbor (MI): University of Michigan Health System; 2005 Jul. 13 p.

ADAPTATION

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

DATE RELEASED

2002 Mar (revised 2005 Jul)

GUIDELINE DEVELOPER(S)

University of Michigan Health System - Academic Institution

SOURCE(S) OF FUNDING

University of Michigan Health System

GUIDELINE COMMITTEE

Osteoporosis Guideline Team

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Team Leader: Jane McCort, MD, General Medicine

Team Members: Van Harrison, PhD, Medical Education; Robert Lash, MD, Endocrinology; Yolanda Smith, MD, Obstetrics/Gynecology; Lourdes Velez, MD, Family Medicine

Guidelines Oversight Team: Connie Standiford, MD; Lee Green, MD, MPH; 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
Van Harrison, PhD (None)  
Robert Lash, MD (None)  
Jane McCort, MD (None)  
Yolanda Smith, MD Lilly, Forest, Abbott, Wyeth, Glaxo-Smith-Kline
Pfizer
Speaker's Bureau

Consultant
Lourdes Velez, MD (None)  

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: University of Michigan Health System. Osteoporosis: prevention and treatment. Ann Arbor (MI): University of Michigan Health System; 2002 Mar. 12 p.

GUIDELINE AVAILABILITY

AVAILABILITY OF COMPANION DOCUMENTS

PATIENT RESOURCES

The following are available:

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 NGC summary was completed by ECRI on March 19, 2003. The information was verified by the guideline developer on April 23, 2003. This NGC summary was updated by ECRI on September 22, 2005. The updated information was verified by the guideline developer on November 1, 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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Readers with questions regarding guideline content are directed to contact the guideline developer.


 

 

   
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