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The American Journal of Medicine
Volume 119, Issue 3
, Pages 255-266
, March 2006
Celecoxib Versus Naproxen and Diclofenac in Osteoarthritis Patients: SUCCESS-I Study
References
- . Gastrointestinal toxicity of nonsteroidal antiinflammatory drugs . N Engl J Med . 1999;340:1888–1899
-
.
Epidemiology of NSAID-induced GI complications
.
J Rheumatol
. 1999;26(suppl):18–24
- . Efficacy, tolerability, and upper gastrointestinal safety of celecoxib for treatment of osteoarthritis and rheumatoid arthritis (systematic review of randomised controlled trials) . BMJ . 2002;325:619–626
-
.
Efficacy of celecoxib versus ibuprofen in the treatment of acute pain
(a multicenter, double-blind, randomized controlled trial in acute ankle sprain)
.
Am J Orthop
. 2002;31:445–451
- Rofecoxib, a new cyclooxygenase 2 inhibitor, shows sustained efficacy, comparable with other nonsteroidal anti-inflammatory drugs (a 6-week and a 1-year trial in patients with osteoarthritis) . Arch Fam Med . 2000;9:1124–1134
- A placebo and active comparator-controlled trial of rofecoxib for the treatment of rheumatoid arthritis . Scand J Rheumatol . 2002;31:230–238
- Analgesic efficacy of the cyclooxygenase-2-specific inhibitor rofecoxib in post-dental surgery pain (a randomized, controlled trial) . Clin Ther . 1999;21:943–953
- Reduced risk of upper gastrointestinal ulcer complications with celecoxib, a novel COX-2 inhibitor . Am J Gastroenterol . 2000;95:1681–1690
- Adverse upper gastrointestinal effects of rofecoxib compared with NSAIDs . JAMA . 1999;282:1929–1933
- 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 . JAMA . 2000;284:1247–1255
- Comparison of upper gastrointestinal toxicity of rofecoxib and naproxen in patients with rheumatoid arthritis . N Engl J Med . 2000;343:1520–1528
- Comparison of lumiracoxib with naproxen and ibuprofen in the Therapeutic Arthritis Research and Gastrointestinal Event Trial (TARGET), reduction in ulcer complications (randomised controlled trial) . Lancet . 2004;364:665–674
- . The American College of Rheumatology 1991 revised criteria for the classification of global functional status in rheumatoid arthritis . Arthritis Rheum . 1992;35:498–502
- . Osteoarthritis clinical trials (candidate variables and clinimetric properties) . J Rheumatol . 1997;24:768–778
- Validation study of WOMAC (a health status instrument for measuring clinically important patient relevant outcomes to antirheumatic drug therapy in patients with osteoarthritis of the hip or knee) . J Rheumatol . 1988;15:1833–1840
-
Merck Research Laboratories. Vioxx Gastrointestinal Outcomes Research Study. Available at: www.fda.gov/ohrms/dockets/ac/01/briefing/3677b2_01_merck.pdf. Accessed July 22, 2004.
- . A general parametric approach to meta-analysis of randomized clinical trials . Stat Med . 1991;10:1665–1677
- Observational study of upper gastrointestinal haemorrhage in elderly patients given selective cyclo-oxygenase-2 inhibitors or conventional non-steroidal anti-inflammatory drugs . BMJ . 2002;325:624
- Prophylactic aspirin and risk of peptic ulcer bleeding . BMJ . 1995;310:827–830
-
Systemic biosynthesis of prostacyclin by cyclooxygenase (COX)-2
(the human pharmacology of a selective inhibitor of COX-2)
.
Proc Natl Acad Sci USA
. 1999;96:272–277
[published erratum appears in Proc Natl Acad Sci USA. 1999;96:5890]
- . The coxibs, selective inhibitors of cyclooxygenase-2 . N Engl J Med . 2001;345:433–442
- Cardiovascular events associated with rofecoxib in a colorectal adenoma chemoprevention trial . N Engl J Med . 2005;352:1092–1102
- Efficacy and safety of the cyclooxygenase 2 inhibitors parecoxib and valdecoxib in patients undergoing coronary artery bypass surgery . J Thorac Cardiovasc Surg . 2003;125:1481–1492
- Complications of the COX-2 inhibitors parecoxib and valdecoxib after cardiac surgery . N Engl J Med . 2005;352:1081–1091
-
Baraf HSB, Fuentealba C, Greenwald M, et al. Gastrointestinal tolerability and effectiveness of etoricoxib compared to diclofenac sodium in patients with osteoarthritis: a randomized, blinded clinical study (EDGE Trial). Poster presented at the American College of Rheumatology annual meeting, October 19, 2004.
- Comparison of thromboembolic events in patients treated with celecoxib, a cyclooxygenase-2 specific inhibitor, versus ibuprofen or diclofenac . Am J Cardiol . 2002;89:425–430
- . Cardiovascular thrombotic events in arthritis trials of the cyclooxygenase-2 inhibitor celecoxib . Am J Cardiol . 2003;92:411–418
- Effect of selective cyclooxygenase 2 inhibitors and naproxen on short-term risk of acute myocardial infarction in the elderly . Arch Intern Med . 2003;163:481–486
-
Risk of acute cardiac events among patients treated with cyclooxygenase-2 selective and non-selective-nonsteroidal anti-inflammatory drugs
.
[abstract 1756]
Arthritis Rheum
. 2004;50(suppl 9):S657
-
Patients exposed to rofecoxib and celecoxib have different odds of nonfatal myocardial infarction
.
Ann Intern Med
. 2005;142:157–164
- COX-2 selective non-steroidal anti-inflammatory drugs and risk of serious coronary heart disease . Lancet . 2002;360:1071–1073
- Relationship between selective cyclooxygenase-2 inhibitors and acute myocardial infarction in older adults . Circulation . 2004;109:2068–2073
- Cardiovascular risk associated with celecoxib in a clinical trial for colorectal adenoma prevention . N Engl J Med . 2005;352:1071–1080
-
http://www.fda.gov/cder/drug/infopage/celebrex/celebrex-hcp.pdf. Accessed January 12, 2005.
-
http://www.fda.gov/cder/drug/InfoSheets/HCP/Naproxen-hcp.pdf. Accessed January 12, 2005.
-
Selective COX-2 inhibition improves endothelial function in coronary artery disease
.
Circulation
. 2003;28:107;
405-409
- Sulfone COX-2 inhibitors increase susceptibility of human LDL and plasma to oxidative modification (comparison to sulfonamide COX-2 inhibitors and NSAIDs) . Atherosclerosis . 2004;177:235–243
- Misoprostol reduces serious gastrointestinal complications in patients with rheumatoid arthritis receiving nonsteroidal anti-inflammatory drugs (A randomized, double-blind, placebo-controlled trial) . Ann Intern Med . 1995;123:241–249
- Association of upper gastrointestinal toxicity of nonsteroidal anti-inflammatory drugs with continued exposure (cohort study) . BMJ . 1997;315:1333–1337
-
The effect of exposure duration on NSAID-related serious gastrointestinal adverse event rates
.
J Gastroentrol Hepatol
. 2003;18(Suppl):B15
This study was supported by a grant from Pharmacia Corporation and Pfizer, Inc. The study design as well as data analysis and interpretation were performed by the study design committee, of which the sponsor was a member. The study sponsors were responsible for data collection and management, in collaboration with the authors. Two independent Gastrointestinal Events adjudication committees performed the data analysis and interpretation of gastrointestinal events. The authors had full access to all the data and had final responsibility for data analysis, interpretation, manuscript preparation and the decision to submit for publication.Conflict of Interest Statement: Gurkirpal Singh received research support from Searle, Pharmacia, Pfizer, Merck, Boehringer Ingelheim, TAP Pharmaceuticals, Wyeth, Altana, Glaxo Smith Kline, Novartis, and Centocor; consultancies, travel grants, speakers bureau from Searle, Pharmacia, Pfizer, Merck and Boehringer Ingelheim. John G. Fort and Carl Wallmark were employees of Pharmacia/Pfizer and own stock in Pfizer, Inc. Jay L. Goldstein: consultancies, honoraria, travel grants, travel expenses, speakers bureau, and research grants from Searle, Pharmacia, Pfizer, TAP Pharmaceuticals, and Astra-Zeneca. Roger A. Levy: Investigator and Speakers bureau (Pfizer, Aventis, Wyeth and Schering-Plough); Advisory board (Pfizer and Novartis). Patrick S. Hanrahan: travel grants from Pfizer. Alfonso E. Bello: former employee of Pharmacia/Pfizer. Lilia Andrade-Ortega: Advisory board (Pfizer); travel grants (Schering Plough). Naurang M. Agrawal: honoraria (Pharmacia and Pfizer); advisory board (Pfizer). Glenn M. Eisen: consultancies and honoraria (Pfizer). William F. Stenson: consultancies (Pharmacia and Pfizer). George Triadafilopoulos: research support from Pfizer, Astra-Zeneca and TAP Pharmaceuticals; consultant to Pfizer, Merck, Boerhinger-Ingelheim, Astra-Zeneca, TAP Pharmaceuticals, Janssen and Wyeth; honoraria and travel support for lectures and meetings from Pfizer, Merck, Boerhinger-Ingelheim, Astra-Zeneca, TAP Pharmaceuticals, Janssen and Wyeth.
PII: S0002-9343(05)00913-7
doi: 10.1016/j.amjmed.2005.09.054
© 2006 Elsevier Inc. All rights reserved.
« Previous
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The American Journal of Medicine
Volume 119, Issue 3
, Pages 255-266
, March 2006

