Open-label randomised pragmatic trial (CONTACT) comparing naproxen and low-dose colchicine for the treatment of gout flares in primary care

被引:41
|
作者
Roddy, Edward [1 ,2 ,3 ]
Clarkson, Kris [1 ,2 ,4 ]
Blagojevic-Bucknall, Milica [1 ,2 ,4 ]
Mehta, Rajnikant [5 ]
Oppong, Raymond [6 ]
Avery, Anthony [7 ]
Hay, Elaine M. [1 ,2 ]
Heneghan, Carl [8 ]
Hartshorne, Liz [1 ,2 ,4 ]
Hooper, Julie [9 ]
Hughes, Gemma [1 ,2 ,4 ]
Jowett, Sue [1 ,2 ,6 ]
Lewis, Martyn [1 ,2 ,4 ]
Little, Paul [9 ]
McCartney, Karen [7 ]
Mahtani, Kamal R. [8 ]
Nunan, David [8 ]
Santer, Miriam [9 ]
Williams, Sam [9 ]
Mallen, Christian D. [1 ,2 ]
机构
[1] Keele Univ, Primary Care Ctr Versus Arthrit, Keele ST5 5BG, Staffs, England
[2] Keele Univ, Sch Primary Community & Social Care, Keele ST5 5BG, Staffs, England
[3] Midland Partnership NHS Fdn Trust, Haywood Acad Rheumatol Ctr, Stoke On Trent, Staffs, England
[4] Keele Univ, Keele Clin Trials Unit, Keele, Staffs, England
[5] Univ Birmingham, Inst Appl Hlth Res BCTU, Heart England NHS Fdn Trust, Birmingham Acute Care Res, Birmingham, W Midlands, England
[6] Univ Birmingham, Hlth Econ, Birmingham, W Midlands, England
[7] Univ Nottingham, Div Primary Care, Nottingham, England
[8] Univ Oxford, Nuffield Dept Primary Care Hlth Sci, Oxford, England
[9] Univ Southampton, Primary Care & Populat Sci, Southampton, Hants, England
关键词
AMERICAN-COLLEGE; RECURRENT GOUT; DOUBLE-BLIND; MANAGEMENT; GUIDELINE; ARTHRITIS; DRUGS;
D O I
10.1136/annrheumdis-2019-216154
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives To compare the effectiveness and safety of naproxen and low-dose colchicine for treating gout flares in primary care. Methods This was a multicentre open-label randomised trial. Adults with a gout flare recruited from 100 general practices were randomised equally to naproxen 750 mg immediately then 250 mg every 8 hours for 7 days or low-dose colchicine 500 mcg three times per day for 4 days. The primary outcome was change in worst pain intensity in the last 24 hours (0-10 Numeric Rating Scale) from baseline measured daily over the first 7 days: mean change from baseline was compared between groups over days 1-7 by intention to treat. Results Between 29 January 2014 and 31 December 2015, we recruited 399 participants (naproxen n=200, colchicine n=199), of whom 349 (87.5%) completed primary outcome data at day 7. There was no significant between-group difference in average pain-change scores over days 1-7 (colchicine vs naproxen: mean difference -0.18; 95% CI -0.53 to 0.17; p=0.32). During days 1-7, diarrhoea (45.9% vs 20.0%; OR 3.31; 2.01 to 5.44) and headache (20.5% vs 10.7%; 1.92; 1.03 to 3.55) were more common in the colchicine group than the naproxen group but constipation was less common (4.8% vs 19.3%; 0.24; 0.11 to 0.54). Conclusion We found no difference in pain intensity over 7 days between people with a gout flare randomised to either naproxen or low-dose colchicine. Naproxen caused fewer side effects supporting naproxen as first-line treatment for gout flares in primary care in the absence of contraindications.
引用
收藏
页码:276 / 284
页数:9
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