The long-term effects of non-steroidal antiinflammatory drugs in osteoarthritis of the knee: a randomized placebo-controlled trial

被引:59
|
作者
Scott, DL
Berry, H
Capell, H
Coppock, J
Daymond, T
Doyle, DV
Fernandes, L
Hazleman, B
Hunter, J
Huskisson, EC
Jawad, A
Jubb, R
Kennedy, T
McGill, P
Nichol, F
Palit, J
Webley, M
Woolf, A
Wotjulewski, J
机构
[1] Kings Coll London Hosp Dulwich, Dept Rheumatol, London SE22 8PT, England
[2] Coventry & Warwickshire Hosp, Dept Rheumatol, Coventry CV1 4FH, W Midlands, England
[3] Whipps Cross Hosp & Chest Clin, London E11 1NR, England
[4] Glasgow Royal Infirm, Ctr Rheumat Dis, Glasgow G4 0SF, Lanark, Scotland
[5] Dist Hosp, Dept Rheumatol, Sunderland SR4 7TP, England
[6] Royal Sussex Cty Hosp, Dept Rheumatol, Brighton BN2 5BE, E Sussex, England
[7] Addenbrookes Hosp, Dept Rheumatol, Cambridge CB2 2QQ, England
[8] Gartnavel Royal Hosp, Glasgow G12 0YN, Lanark, Scotland
[9] Royal London Hosp Mile End, Musculoskeletal Directorate, London E1 4DG, England
[10] Selly Oak Hosp, Dept Rheumatol, Birmingham B29 6JD, W Midlands, England
[11] Wirral Hosp NHS Trust, Wirral L49 5PE, Merseyside, England
[12] Stobhill Gen Hosp, Glasgow G21 3UW, Lanark, Scotland
[13] Leicester Royal Infirm, Dept Rheumatol, Leicester, Leics, England
[14] Basildon Hosp, Dept Rheumatol, Basildon SS16 5NL, Essex, England
[15] Stoke Mandeville Hosp, Aylesbury HP21 8AL, Bucks, England
[16] Royal Cornwall Hosp, Dept Rheumatol, Truro TR1 2HZ, Cornwall, England
[17] Dist Gen Hosp, Eastbourne BN21 2UD, E Sussex, England
关键词
NSAIDs; osteoarthritis; knee; randomized controlled trial;
D O I
10.1093/rheumatology/39.10.1095
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Non-steroidal anti-inflammatory drugs (NSAIDs) are widely used to treat osteoarthritis (OA), though their long-term efficacy is uncertain. We report a comparison of the symptomatic responses to therapy with tiaprofenic acid, indomethacin and placebo over 5 yr. Methods. A parallel-group, randomized, single-blind trial of patients with knee OA recruited 812 patients from 20 centres; 307 patients received tiaprofenic acid (300 mg b.d.), 202 indomethacin (25 mg t.d.s.) and 303 matching placebo for up to 5 yr. At the end of the parallel-group study, patients receiving tiaprofenic acid or placebo entered a 4-week blinded cross-over study of tiaprofenic acid or placebo, both given for 2 weeks. Assessments were at baseline, 4 weeks, then at 6-month intervals for up to 5 yr in the parallel group study and at 2-week intervals in the cross-over study. They comprised pain scores, duration of morning stiffness, patients' global assessments, paracetamol consumption, adverse reactions, withdrawals and functional outcomes. Results. There were significant falls in overall pain scores in patients receiving NSAIDs compared with placebo at 4 weeks in the parallel-group phase. Thereafter there were no advantages favouring active therapy. In the cross-over phase, pain scores were significantly lower in patients receiving tiaprofenic acid than placebo. Patients who had been receiving long-term tiaprofenic acid showed significant rises in their pain scores when receiving placebo therapy and vice versa. Adverse events were reported by 61% of patients receiving tiaprofenic acid, 63% on indomethacin and 51% on placebo. Potentially severe side-effects were rare: for example, there were only three cases of gastrointestinal bleeding on NSAIDs. The pattern of withdrawal was similar in patients taking NSAIDs and placebo in the parallel-group study; at 48 weeks 53% of the patients remained on tiaprofenic acid, 50% on indomethacin and 54% on placebo. Conclusions. NSAIDs significantly reduce overall pain over 4 weeks. This short-term responsiveness is retained, and even after several years of therapy with tiaprofenic acid pain scores increased over 2 weeks when it was changed to placebo. Our results do not show long-term benefits from the use of NSAIDs in OA and the majority of patients had persisting pain and disability despite therapy.
引用
收藏
页码:1095 / 1101
页数:7
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