The cost-effectiveness of cyclooxygenase-2 selective inhibitors in the management of chronic arthritis

被引:87
作者
Spiegel, BMR [1 ]
Targownik, L [1 ]
Dulai, GS [1 ]
Gralnek, IM [1 ]
机构
[1] Univ Calif Los Angeles, CURE Digest Dis Res Ctr,David Geffen Sch Med, Ctr Study Digest Healthcare Qual & Outcomes, Vet Adm Greater Los Angeles Healthcare Syst, Los Angeles, CA 90073 USA
关键词
D O I
10.7326/0003-4819-138-10-200305200-00007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Rofecoxib and celecoxib (coxibs) effectively treat chronic arthritis pain and reduce ulcer complications by 50% compared with nonselective nonsteroidal anti-inflammatory drugs (NSAIDs). However, their absolute risk reduction is small and the cost-effectiveness of treatment is uncertain. Objective: To determine whether the degree of risk reduction in gastrointestinal complications by coxibs offsets their increased cost compared with a generic nonselective NSAID. Design: Cost-utility analysis. Data Sources: Systematic review of MEDLINE and published abstracts. Target Population: Patients with osteoarthritis or rheumatoid arthritis who are not taking aspirin and who require long-term NSAID therapy for moderate to severe arthritis pain. Perspective: Third-party payer. Interventions: Naproxen, 500 mg twice daily, and coxib, once daily. Patients intolerant of naproxen were switched to a coxib. Outcome Measures: Incremental cost per quality-adjusted life-year (QALY) gained. Results of Base-Case Analysis: Using a coxib instead of a nonselective NSAID in average-risk patients cost an incremental $275 809 per year to gain 1 additional QALY. Results of Sensitivity Analysis: The incremental cost per QALY gained decreased to $55 803 when the analysis was limited to the subset of patients with a history of bleeding ulcers. The coxib strategy became dominant when the cost of coxibs was reduced by 90% of the current average wholesale price. In probabilistic sensitivity analysis, if a third-party payer was willing to pay $150 000 per QALY gained, then 4.3% of average-risk patients would fall within the budget. Conclusions: The risk reduction seen with coxibs does not offset their increased costs compared with nonselective NSAIDs in the management of average-risk patients with chronic arthritis. However, coxibs may provide an acceptable incremental cost-effectiveness ratio in the subgroup of patients with a history of bleeding ulcers.
引用
收藏
页码:795 / 806
页数:12
相关论文
共 92 条
[71]   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 [J].
Saag, K ;
van der Heijde, D ;
Fisher, C ;
Samara, A ;
DeTora, L ;
Bolognese, J ;
Sperling, R ;
Daniels, B .
ARCHIVES OF FAMILY MEDICINE, 2000, 9 (10) :1124-1134
[72]   Potential cost-effectiveness of prophylactic use of the implantable cardioverter defibrillator or amiodarone after myocardial infarction [J].
Sanders, GD ;
Hlatky, MA ;
Every, NR ;
McDonald, KM ;
Heidenreich, PA ;
Parsons, LS ;
Owens, DK .
ANNALS OF INTERNAL MEDICINE, 2001, 135 (10) :870-883
[73]  
SCHNITZER T, 2002, ARTHRITIS RHEUM, V46, pA326
[74]   MISOPROSTOL REDUCES SERIOUS GASTROINTESTINAL COMPLICATIONS IN PATIENTS WITH RHEUMATOID-ARTHRITIS RECEIVING NONSTEROIDAL ANTIINFLAMMATORY DRUGS - A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL [J].
SILVERSTEIN, FE ;
GRAHAM, DY ;
SENIOR, JR ;
DAVIES, HW ;
STRUTHERS, BJ ;
BITTMAN, RM ;
GEIS, GS .
ANNALS OF INTERNAL MEDICINE, 1995, 123 (04) :241-249
[75]   Gastrointestinal toxicity with celecoxib vs nonsteroidal anti-inflammatory drugs for osteoarthritis and rheumatoid arthritis - The CLASS study: A randomized controlled trial [J].
Silverstein, FE ;
Faich, G ;
Goldstein, JL ;
Simon, LS ;
Pincus, T ;
Whelton, A ;
Makuch, R ;
Eisen, G ;
Agarwal, NM ;
Stenson, WF ;
Burr, AM ;
Zhao, WW ;
Kent, JD ;
Lefkowith, JB ;
Verburg, KM ;
Geis, GS .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 284 (10) :1247-1255
[76]   Anti-inflammatory and upper gastrointestinal effects of celecoxib in rheumatoid arthritis - A randomized controlled trial [J].
Simon, LS ;
Weaver, AL ;
Graham, DY ;
Kivitz, AJ ;
Lipsky, PE ;
Hubbard, RC ;
Isakson, PC ;
Verburg, KM ;
Yu, SS ;
Zhao, WW ;
Geis, GS .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 282 (20) :1921-1928
[77]  
Soll AH, 1996, JAMA-J AM MED ASSOC, V275, P622
[78]  
Sonnenberg A, 1997, AM J GASTROENTEROL, V92, P614
[79]   LANSOPRAZOLE - A REAPPRAISAL OF ITS PHARMACODYNAMIC AND PHARMACOKINETIC PROPERTIES, AND ITS THERAPEUTIC EFFICACY IN ACID-RELATED DISORDERS [J].
SPENCER, CM ;
FAULDS, D .
DRUGS, 1994, 48 (03) :404-430
[80]   Dyspepsia management in primary care: A decision analysis of competing strategies [J].
Spigel, BMR ;
Vakil, NB ;
Ofman, JJ .
GASTROENTEROLOGY, 2002, 122 (05) :1270-1285