Literature DB >> 14756580

Benefit-risk assessment of rofecoxib in the treatment of osteoarthritis.

Helmut Schmidt1, Barry G Woodcock, Gerd Geisslinger.   

Abstract

NSAIDs are widely used to treat pain and inflammation in osteoarthritis. Their use in this indication is generally intermittent and fluctuates with the intensity of the disease. Nonetheless, success of the therapy is frequently limited by injury to the gastrointestinal mucosa and complications such as bleeding, ulceration and perforation. A careful and detailed evaluation of these aspects in regard to the newly introduced NSAIDs is of considerable clinical importance. This review focuses on the NSAID rofecoxib, one of the selective cyclo-oxygenase (COX)-2 inhibitors, which are claimed to be as effective as nonselective NSAIDs with better gastrointestinal tolerability. Indeed, phase II, phase III and epidemiological studies have revealed that the efficacy of rofecoxib is comparable to that of conventional NSAIDs but with lower gastrointestinal toxicity, although this advantage may not be demonstrable in every patient. In patients treated with low-dose aspirin (acetylsalicylic acid) for cardiovascular prophylaxis, celecoxib (another selective COX-2 inhibitor) seems to have no obvious advantages over conventional NSAIDs, and similar conclusions may be applied to rofecoxib. A comparison of NSAID therapy +/- concomitant low-dose aspirin was not a primary outcome in this trial with celecoxib and there is thus a need for further studies which compare the gastrointestinal risk of a selective COX-2 inhibitor plus aspirin versus a conventional NSAID. Recent debate has emerged regarding the cardiovascular safety of rofecoxib. Although there is evidence both for and against higher cardiovascular risk with rofecoxib, a retrospective cohort study recently published suggested that there is no increased risk of acute myocardial infarction in the short-term when compared with non-selective NSAIDs. The renal toxicity of rofecoxib has been thoroughly investigated. Clinical studies revealed renal effects of rofecoxib similar to those of conventional NSAIDs. Since adverse effects increase with the degree of renal impairment, monitoring of renal function should be carried out in patients at risk. Although there are still insufficient data concerning certain important adverse effects of rofecoxib, this drug is becoming an important alternative in the therapy of osteoarthritis, especially in high-risk patients. Clinicians need to weigh up the benefits and risks of rofecoxib on a case-by-base basis.

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Year:  2004        PMID: 14756580     DOI: 10.2165/00002018-200427030-00003

Source DB:  PubMed          Journal:  Drug Saf        ISSN: 0114-5916            Impact factor:   5.606


  70 in total

1.  No reduction in cardiovascular risk with NSAIDs-including aspirin?

Authors:  John G F Cleland
Journal:  Lancet       Date:  2002-01-12       Impact factor: 79.321

2.  Celecoxib loses its anti-inflammatory efficacy at high doses through activation of NF-kappaB.

Authors:  E Niederberger; I Tegeder; G Vetter; A Schmidtko; H Schmidt; C Euchenhofer; L Bräutigam; S Grösch; G Geisslinger
Journal:  FASEB J       Date:  2001-07       Impact factor: 5.191

3.  Hemostatic factors and cardiovascular disease in active rheumatoid arthritis: an 8 year followup study.

Authors:  S Wållberg-Jonsson; M Cederfelt; S Rantapää Dahlqvist
Journal:  J Rheumatol       Date:  2000-01       Impact factor: 4.666

Review 4.  The clinical significance of inhibition of renal prostaglandin synthesis.

Authors:  C Patrono; M J Dunn
Journal:  Kidney Int       Date:  1987-07       Impact factor: 10.612

5.  Chronic cyclooxygenase-2 inhibition blunts low sodium-stimulated renin without changing renal haemodynamics.

Authors:  P Harding; O A Carretero; W H Beierwaltes
Journal:  J Hypertens       Date:  2000-08       Impact factor: 4.844

6.  Gastrointestinal toxicity with celecoxib vs nonsteroidal anti-inflammatory drugs for osteoarthritis and rheumatoid arthritis: the CLASS study: A randomized controlled trial. Celecoxib Long-term Arthritis Safety Study.

Authors:  F E Silverstein; G Faich; J L Goldstein; L S Simon; T Pincus; A Whelton; R Makuch; G Eisen; N M Agrawal; W F Stenson; A M Burr; W W Zhao; J D Kent; J B Lefkowith; K M Verburg; G S Geis
Journal:  JAMA       Date:  2000-09-13       Impact factor: 56.272

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.  Results from a patient survey to assess gastrointestinal burden of non-steroidal anti-inflammatory drug therapy contrasted with a review of data from EVA to determine satisfaction with rofecoxib.

Authors:  S Steinfeld; P A Bjørke
Journal:  Rheumatology (Oxford)       Date:  2002-04       Impact factor: 7.580

9.  Prostaglandin synthase 1 gene disruption in mice reduces arachidonic acid-induced inflammation and indomethacin-induced gastric ulceration.

Authors:  R Langenbach; S G Morham; H F Tiano; C D Loftin; B I Ghanayem; P C Chulada; J F Mahler; C A Lee; E H Goulding; K D Kluckman; H S Kim; O Smithies
Journal:  Cell       Date:  1995-11-03       Impact factor: 41.582

Review 10.  Review article: NSAIDs, gastroprotection and cyclo-oxygenase-II-selective inhibitors.

Authors:  R Micklewright; S Lane; W Linley; C McQuade; F Thompson; N Maskrey
Journal:  Aliment Pharmacol Ther       Date:  2003-02       Impact factor: 8.171

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  1 in total

1.  Development and evaluation of a common data model enabling active drug safety surveillance using disparate healthcare databases.

Authors:  Stephanie J Reisinger; Patrick B Ryan; Donald J O'Hara; Gregory E Powell; Jeffery L Painter; Edward N Pattishall; Jonathan A Morris
Journal:  J Am Med Inform Assoc       Date:  2010 Nov-Dec       Impact factor: 4.497

  1 in total

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