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Analysis of gout remission definitions in a randomised controlled trial of colchicine prophylaxis for people with gout initiating allopurinol.
Tabi-Amponsah, Adwoa Dansoa; Stamp, Lisa K; Horne, Anne; Drake, Jill; Stewart, Sarah; Gamble, Greg; Petrie, Keith J; Dalbeth, Nicola.
Afiliación
  • Tabi-Amponsah AD; A.D. Tabi-Amponsah, BBiomedSc(Hons). Department of Medicine, The Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
  • Stamp LK; L.K. Stamp, PhD, FRACP. Department of Medicine, University of Otago, Christchurch, Christchurch, New Zealand.
  • Horne A; A. Horne, MBChB, Department of Medicine, The Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
  • Drake J; J. Drake, RN. Department of Rheumatology, Immunology and Allergy, Te Whatu Ora Health New Zealand Waitaha Canterbury, Christchurch, New Zealand.
  • Stewart S; S. Stewart, PhD. Department of Medicine, The Faculty of Medical and Health Sciences, University of Auckland; School of Clinical Sciences, Faculty of Health and Environmental Sciences, Auckland University of Technology, Auckland, New Zealand.
  • Gamble G; G. Gamble, MSc, Department of Medicine, The Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
  • Petrie KJ; K.J. Petrie, PhD. Department of Psychological Medicine, Faculty of Medical and Health Sciences, University of Auckland.
  • Dalbeth N; N. Dalbeth, MD, FRACP, Department of Medicine, The Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
J Rheumatol ; 2024 Aug 01.
Article en En | MEDLINE | ID: mdl-39089837
ABSTRACT

OBJECTIVE:

To investigate the effect of colchicine prophylaxis on gout remission when commencing urate lowering therapy (ULT), and illness perceptions of people in remission, using two definitions of gout remission.

METHODS:

Data from a 12-month double-blind placebo-controlled trial of 200 people with gout commencing allopurinol were analyzed. Participants were randomly assigned to prophylaxis with 0.5mg daily colchicine or placebo for six months, followed by six months of additional follow-up. Gout remission was assessed using the 2016 preliminary definition or simplified definition without patient reported outcomes. Illness perceptions were assessed using a gout-specific brief illness perception questionnaire (BIPQ).

RESULTS:

In the first six months, few participants were in remission according to either the 2016 preliminary definition (3% for colchicine and 4% for placebo) or the simplified definition (7% for colchicine and 12% for placebo). In the second six months, after study drug (colchicine or placebo) discontinuation, fewer participants in the colchicine group than in the placebo group were in remission according to the 2016 preliminary definition (4% vs. 14%, p=0.03), and the simplified definition (14% vs 28%, p=0.02). Participants fulfilling remission using either definition had more favorable perceptions about their gout symptoms and illness concerns, as well as consequences, when using the simplified definition.

CONCLUSION:

Using either definition, six months of colchicine prophylaxis when initiating ULT does not provide an advantage in the fulfilment of gout remission. People fulfilling either definition report fewer symptoms, lower concern about their gout, and when using the simplified definition, are less affected by gout.

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Rheumatol Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Rheumatol Año: 2024 Tipo del documento: Article