Literature DB >> 16895283

Safe pharmacologic treatment strategies for osteoarthritis pain in African Americans with hypertension, and renal and cardiac disease.

Jerry Johnson1, Joan Weinryb.   

Abstract

Arthritis is the leading cause of disability in the United States. Osteoarthritis, the most common form of arthritis, is a degenerative joint disease affecting both whites and African Americans similarly. African Americans have a high incidence rate of comorbidities, including hypertension, cardiovascular disease (CVD) risk factors and diabetes. Treatment of osteoarthritic pain in patients with comorbidities is often complicated by potential safety concerns. Traditional nonsteroidal antiinflammatory drugs (NSAIDs) and cyclooxygenase 2 (COX-2) specific NSAIDs have been shown to increase blood pressure in hypertensive patients taking antihypertensive medications. Patients with CVD risk factors taking low-dose aspirin for secondary prevention may be at increased risk for gastrointestinal bleeding with NSAIDs. Diabetics face an increased risk of renal complications. Because NSAIDs are associated with adverse renal effects, they should be used cautiously in patients with advanced renal disease. Acetaminophen is the most appropriate initial analgesic for African Americans with chronic osteoarthritic pain and concurrent hypertension, CVD risk factors or diabetes, and is recommended by the American College of Rheumatology as first-line treatment. Many of the adverse effects commonly associated with NSAIDs are not associated with acetaminophen. Safety concerns surrounding pharmacologic treatment of osteoarthritis in African Americans are reviewed.

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Year:  2006        PMID: 16895283      PMCID: PMC2569481     

Source DB:  PubMed          Journal:  J Natl Med Assoc        ISSN: 0027-9684            Impact factor:   1.798


  54 in total

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Journal:  Am J Gastroenterol       Date:  2000-09       Impact factor: 10.864

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Authors:  R C Dart
Journal:  Am J Manag Care       Date:  2001-12       Impact factor: 2.229

Review 7.  Efficacy, tolerability, and upper gastrointestinal safety of celecoxib for treatment of osteoarthritis and rheumatoid arthritis: systematic review of randomised controlled trials.

Authors:  Jonathan J Deeks; Lesley A Smith; Matthew D Bradley
Journal:  BMJ       Date:  2002-09-21

8.  Abnormal serum transaminases following therapeutic doses of acetaminophen in the absence of known risk factors.

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Journal:  Dig Dis Sci       Date:  1995-09       Impact factor: 3.199

9.  Glucosamine sulfate reduces osteoarthritis progression in postmenopausal women with knee osteoarthritis: evidence from two 3-year studies.

Authors:  Olivier Bruyere; Karel Pavelka; Lucio C Rovati; Rita Deroisy; Marta Olejarova; Jindriska Gatterova; Giampaolo Giacovelli; Jean-Yves Reginster
Journal:  Menopause       Date:  2004 Mar-Apr       Impact factor: 2.953

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Journal:  Lancet       Date:  1978-05-13       Impact factor: 79.321

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  1 in total

1.  Patterns and Perceptions of Self-Management for Osteoarthritis Pain in African American Older Adults.

Authors:  Staja Booker; Keela Herr; Toni Tripp-Reimer
Journal:  Pain Med       Date:  2019-08-01       Impact factor: 3.750

  1 in total

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