Predictors of persisting pain in children with Juvenile Idiopathic Arthritis: a case control study nested in the ReACCh-Out cohort

Author:

McGrath TaraORCID,Guzman Jaime,Tucker Lori,Shiff Natalie J.,Yaskina Maryna,Tupper Susan,Rumsey Dax G.,Benseler Susanne,Berard Roberta,Boire Gilles,Bolaria Roxana,Cabral David,Cameron Bonnie,Campillo Sarah,Chan Mercedes,Chédeville Gaëlle,Chetaille Anne-Laure,Dancey Paul,Dorval Jean,Duffy Ciarán,Ellsworth Janet,Feldman Brian,Feldman Debbie,Gross Katherine,Haddad Ellie,Houghton Kristin,Huber Adam,Johnson Nicole,Jurencak Roman,Lang Bianca,Larché Maggie,Laxer Ronald,LeBlanc Claire,Levy Deborah,Luca Nadia,Miettunen Paivi,Morishita Kimberly,Oen Kiem,Petty Ross,Ramsey Suzanne,Rosenberg Alan,Roth Johannes,Saint-Cyr Claire,Schmeling Heinrike,Schneider Rayfel,Silverman Earl,Spiegel Lynn,Stringer Elizabeth,Scuccimarri Rosie,Tse Shirley,Turvey Stuart,Duffy Karen Watanabe,Yeung Rae,

Abstract

Abstract Background To identify baseline predictors of persisting pain in children with Juvenile Idiopathic Arthritis (JIA), relative to patients with JIA who had similar baseline levels of pain but in whom the pain did not persist. Methods We used data from the Research in Arthritis in Canadian Children emphasizing Outcomes (ReACCh-Out) inception cohort to compare cases of ‘moderate persisting pain’ with controls of ‘moderate decreasing pain’. Moderate pain was defined as a Visual Analogue Scale (VAS) for pain measurement score of > 3.5 cm. Follow-up was minimum 3 years. Univariate and Multivariate logistic regression models ascertained baseline predictors of persisting pain. Results A total of 31 cases and 118 controls were included. Mean pain scores at baseline were 6.4 (SD 1.6) for cases and 5.9 (1.5) for controls. A greater proportion of cases than controls were females (77.4% vs 65.0%) with rheumatoid factor positive polyarthritis (12.9% vs 4.2%) or undifferentiated JIA (22.6% vs 8.5%). Oligoarthritis was less frequent in cases than controls (9.7% vs 33%). At baseline, cases had more active joints (mean of 11.4 vs 7.7) and more sites of enthesitis (4.6 vs 0.7) than controls. In the final multivariate regression model, enthesitis count at baseline (OR 1.40, CI 95% 1.19–1.76), female sex (4.14, 1.33–16.83), and the overall Quality of My Life (QoML) baseline score (0.82, 0.69–0.98) predicted development of persisting pain. Conclusions Among newly diagnosed children with JIA with moderate pain, female sex, lower overall quality of life, and higher enthesitis counts at baseline predicted development of persisting pain. If our findings are confirmed, patients with these characteristics may be candidates for interventions to prevent development of chronic pain.

Funder

Women and Children's Research Institute

Publisher

Springer Science and Business Media LLC

Subject

Immunology and Allergy,Rheumatology,Pediatrics, Perinatology and Child Health

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