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Brief Summary

GUIDELINE TITLE

American Gastroenterological Association medical position statement: guidelines on osteoporosis in gastrointestinal diseases.

BIBLIOGRAPHIC SOURCE(S)

GUIDELINE STATUS

This is the current release of the guideline.

According to the guideline developer, the Clinical Practice Committee meets three times a year to review all American Gastroenterological Association Institute (AGAI) guidelines. This review includes new literature searches of electronic databases followed by expert committee review of new evidence that has emerged since the original publication date.

BRIEF SUMMARY CONTENT

 
RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Definitions for the strength of evidence (Grade A-D) are repeated at the end of the Major Recommendations.

The following steps outline a possible approach to managing osteoporosis in gastrointestinal (GI) disease:

  1. All patients should receive education on the importance of lifestyle changes (e.g., engaging in regular weight-bearing exercise, quitting smoking, avoiding excessive alcohol intake), as well as vitamin D and calcium supplementation (level D evidence).
  2. Dual energy x-ray absorptiometry (DXA) scans should be selectively ordered in inflammatory bowel disease (IBD) patients based on a thorough risk factor assessment (level D evidence).
  3. DXA scans are likely unnecessary in patients with newly diagnosed uncomplicated pediatric celiac disease, but should be considered for adults with newly diagnosed celiac disease 1 year after initiation of a gluten-free diet, to allow for stabilization of bone density (level D evidence).
  4. Patients who are at least 10 years postgastrectomy, especially postmenopausal females, males over age 50, and patients with low-trauma fractures should undergo DXA testing (level D evidence).
  5. In patients with IBD and celiac disease, serum calcium level, corrected for albumin, should be measured at diagnosis. In IBD, celiac disease, and postgastrectomy states in which the patient is found to be osteoporotic or has a low-trauma fracture, screening for other causes of low bone density should be performed through a complete blood count, total SAP level, calcium level, creatinine level, 25-(OH) vitamin D level, protein electrophoresis, and testosterone level (in males) (level D evidence).
  6. Serum measurements of parathyroid hormone (PTH) are unnecessary unless a patient is found to have an abnormal serum or urinary calcium level (level D evidence).
  7. Implementation of a gluten-free diet in celiac disease and correction of nutritional deficiencies is necessary in all GI diseases (level A evidence).
  8. Corticosteroid dosing in IBD should be kept to a minimum, and other immunomodulatory agents should be considered to help withdraw patients from corticosteroids once corticosteroid dependence becomes evident (level D evidence in IBD; level A evidence regarding fracture risk reduction by minimizing the corticosteroid dosage for other non-GI diseases).
  9. Vitamin D and calcium supplementation should be given to those deemed to be at high risk for osteoporosis or with proven osteoporosis. Younger men and premenopausal women require 1000 mg/day of elemental calcium, whereas men and women over age 50 require up to 1500 mg/day. Vitamin D 400 to 800 IU/day is usually an adequate replacement dose in healthy individuals; it can be obtained from many multivitamin preparations (level D evidence in GI disease, level B evidence regarding nonvertebral and vertebral fracture risk reduction by optimizing calcium and vitamin D intake in older men and women).
  10. Estrogen therapy has received U.S. Food and Drug Administration (FDA) approval for the prevention of osteoporosis in postmenopausal or hypogonadal premenopausal women, but must be balanced against the significant risks (level D evidence in GI disease, level A evidence for vertebral and nonvertebral fracture risk reduction in generally healthy postmenopausal women).
  11. A selective estrogen receptor modulator (SERM) has been approved by the FDA for the prevention and treatment of osteoporosis in menopausal women (level D evidence in GI disease, level A evidence for vertebral fracture risk reduction in osteoporotic postmenopausal women). A bone disease specialist should participate in the decision to choose a SERM in patients with GI diseases.
  12. Testosterone should be used to treat hypogonadism in males (level D evidence).
  13. Bisphosphonates are FDA-approved for the prevention and treatment of osteoporosis in patients with known osteoporosis, patients with atraumatic fractures, and patients who cannot withdraw from corticosteroids after 3 months of use (level D evidence in GI disease, level A evidence regarding vertebral and nonvertebral fracture risk reduction in postmenopausal women).
  14. Nasal or subcutaneous calcitonin can be considered as an alternative treatment approach when the preceding antiresorptive agents are contraindicated or poorly tolerated (level D evidence in GI disease, level A evidence regarding vertebral fracture risk reduction in postmenopausal women).
  15. Fluoride is not recommended as treatment for osteoporosis associated with GI disease (level D evidence in GI disease, no consistent evidence for fracture risk reduction in postmenopausal women).

Definitions:

Quality of Evidence on Which a Recommendation is Based

Grade A: Homogeneous evidence from multiple well-designed randomized (therapeutic) or cohort (descriptive) controlled trials, each involving a number of participants to be of sufficient statistical power

Grade B: Evidence from at least 1 large well-designed clinical trial with or without randomization, from cohort or case-control analytic studies, or well-designed meta-analysis

Grade C: Evidence based on clinical experience, descriptive studies, or reports of expert committees

Grade D: Not rated

CLINICAL ALGORITHM(S)

An algorithm is provided in the technical review (see "Companion Documents" field) for management approach for osteoporosis in gastrointestinal disease

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").

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

ADAPTATION

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

DATE RELEASED

2003 Mar

GUIDELINE DEVELOPER(S)

American Gastroenterological Association Institute - Medical Specialty Society

SOURCE(S) OF FUNDING

American Gastroenterological Association Institute

GUIDELINE COMMITTEE

American Gastroenterological Association Patient Care Committee

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Not stated

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

Dr. Charles Bernstein is supported in part by a Research Scientist Award from the Crohn’s and Colitis Foundation of Canada and an Investigator Award from the Canadian Institutes of Health Research.

GUIDELINE STATUS

This is the current release of the guideline.

According to the guideline developer, the Clinical Practice Committee meets three times a year to review all American Gastroenterological Association Institute (AGAI) guidelines. This review includes new literature searches of electronic databases followed by expert committee review of new evidence that has emerged since the original publication date.

GUIDELINE AVAILABILITY

Electronic copies: Available from the American Gastroenterological Association Institute (AGAI) Gastroenterology journal Web site.

Print copies: Available from the American Gastroenterological Association Institute, 4930 Del Ray Avenue, Bethesda, MD 20814.

AVAILABILITY OF COMPANION DOCUMENTS

PATIENT RESOURCES

None available

NGC STATUS

This summary was completed by ECRI on August 20, 2003.

COPYRIGHT STATEMENT

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

DISCLAIMER

NGC DISCLAIMER

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