TY - JOUR
T1 - Disease Recapture Rates After Medication Discontinuation and Flare in Juvenile Idiopathic Arthritis
T2 - An Observational Study Within the Childhood Arthritis and Rheumatology Research Alliance Registry
AU - the Childhood Arthritis and Rheumatology Research Alliance Registry Investigators
AU - Ringold, Sarah
AU - Dennos, Anne C.
AU - Kimura, Yukiko
AU - Beukelman, Timothy
AU - Shrader, Peter
AU - Phillips, Thomas A.
AU - Kohlheim, Melanie
AU - Schanberg, Laura E.
AU - Yeung, Rae S.M.
AU - Horton, Daniel B.
AU - Abel, N.
AU - Abulaban, K.
AU - Adams, A.
AU - Adams, M.
AU - Agbayani, R.
AU - Aiello, J.
AU - Akoghlanian, S.
AU - Alejandro, C.
AU - Allenspach, E.
AU - Alperin, R.
AU - Alpizar, M.
AU - Amarilyo, G.
AU - Ambler, W.
AU - Anderson, E.
AU - Ardoin, S.
AU - Armendariz, S.
AU - Baker, E.
AU - Balboni, I.
AU - Balevic, S.
AU - Ballenger, L.
AU - Ballinger, S.
AU - Balmuri, N.
AU - Barbar-Smiley, F.
AU - Barillas-Arias, L.
AU - Basiaga, M.
AU - Baszis, K.
AU - Becker, M.
AU - Bell-Brunson, H.
AU - Beltz, E.
AU - Benham, H.
AU - Benseler, S.
AU - Bernal, W.
AU - Beukelman, T.
AU - Bigley, T.
AU - Binstadt, B.
AU - Black, C.
AU - Blakley, M.
AU - Bohnsack, J.
AU - Boland, J.
AU - Boneparth, A.
AU - Bowman, S.
AU - Bracaglia, C.
AU - Brooks, E.
AU - Brothers, M.
AU - Brown, A.
AU - Brunner, H.
AU - Buckley, M.
AU - Buckley, M.
AU - Bukulmez, H.
AU - Bullock, D.
AU - Cameron, B.
AU - Canna, S.
AU - Cannon, L.
AU - Carper, P.
AU - Cartwright, V.
AU - Cassidy, E.
AU - Cerracchio, L.
AU - Chalom, E.
AU - Chang, J.
AU - Chang-Hoftman, A.
AU - Chauhan, V.
AU - Chira, P.
AU - Chinn, T.
AU - Chundru, K.
AU - Clairman, H.
AU - Co, D.
AU - Confair, A.
AU - Conlon, H.
AU - Connor, R.
AU - Cooper, A.
AU - Cooper, J.
AU - Cooper, S.
AU - Correll, C.
AU - Corvalan, R.
AU - Costanzo, D.
AU - Cron, R.
AU - Curiel-Duran, L.
AU - Curington, T.
AU - Curry, M.
AU - Dalrymple, A.
AU - Davis, A.
AU - Davis, C.
AU - Davis, C.
AU - Davis, T.
AU - De Benedetti, F.
AU - De Ranieri, D.
AU - Dean, J.
AU - Dedeoglu, F.
AU - DeGuzman, M.
AU - Delnay, N.
AU - Dempsey, V.
AU - DeSantis, E.
AU - Dickson, T.
AU - Dingle, J.
AU - Donaldson, B.
AU - Dorsey, E.
AU - Dover, S.
AU - Dowling, J.
AU - Drew, J.
AU - Driest, K.
AU - Du, Q.
AU - Duarte, K.
AU - Durkee, D.
AU - Duverger, E.
AU - Dvergsten, J.
AU - Eberhard, A.
AU - Eckert, M.
AU - Ede, K.
AU - Edelheit, B.
AU - Edens, C.
AU - Edens, C.
AU - Edgerly, Y.
AU - Elder, M.
AU - Ervin, B.
AU - Fadrhonc, S.
AU - Failing, C.
AU - Fair, D.
AU - Falcon, M.
AU - Favier, L.
AU - Federici, S.
AU - Feldman, B.
AU - Fennell, J.
AU - Ferguson, I.
AU - Ferguson, P.
AU - Ferreira, B.
AU - Ferrucho, R.
AU - Fields, K.
AU - Finkel, T.
AU - Fitzgerald, M.
AU - Fleming, C.
AU - Flynn, O.
AU - Fogel, L.
AU - Fox, E.
AU - Fox, M.
AU - Franco, L.
AU - Freeman, M.
AU - Fritz, K.
AU - Froese, S.
AU - Fuhlbrigge, R.
AU - Fuller, J.
AU - George, N.
AU - Gerhold, K.
AU - Gerstbacher, D.
AU - Gilbert, M.
AU - Gillispie-Taylor, M.
AU - Giverc, E.
AU - Godiwala, C.
AU - Goh, I.
AU - Goheer, H.
AU - Goldsmith, D.
AU - Gotschlich, E.
AU - Gotte, A.
AU - Gottlieb, B.
AU - Gracia, C.
AU - Graham, T.
AU - Grevich, S.
AU - Griffin, T.
AU - Griswold, J.
AU - Grom, A.
AU - Guevara, M.
AU - Guittar, P.
AU - Guzman, M.
AU - Hager, M.
AU - Hahn, T.
AU - Halyabar, O.
AU - Hammelev, E.
AU - Hance, M.
AU - Hanson, A.
AU - Harel, L.
AU - Haro, S.
AU - Harris, J.
AU - Harry, O.
AU - Hartigan, E.
AU - Hausmann, J.
AU - Hay, A.
AU - Hayward, K.
AU - Heiart, J.
AU - Hekl, K.
AU - Henderson, L.
AU - Henrickson, M.
AU - Hersh, A.
AU - Hickey, K.
AU - Hill, P.
AU - Hillyer, S.
AU - Hiraki, L.
AU - Kitcharoensakkul, M.
AU - Schmitt, E.
AU - Syed, R.
AU - White, A.
AU - Yomogida, K.
N1 - Funding Information:
Supported by the Rheumatology Research Foundation Innovative Research Award.
Publisher Copyright:
© 2022 American College of Rheumatology.
PY - 2023/4
Y1 - 2023/4
N2 - Objective: Children with well-controlled juvenile idiopathic arthritis (JIA) frequently experience flares after medication discontinuation, but the outcomes of these flares have not been well described. The objective of this study was to characterize the rates and predictors of disease recapture among children with JIA who restarted medication to treat disease flare. Methods: Children with JIA who discontinued conventional synthetic or biologic disease-modifying antirheumatic drugs for well-controlled disease but subsequently experienced a flare and restarted medication were identified from the Childhood Arthritis and Rheumatology Research Alliance (CARRA) registry. The primary outcome was inactive disease (ID) (physician global assessment <1 and active joint count = 0) 6 months after flare. Results: A total of 333 patients had complete data for ID at 6 months after flare. The recapture rate for the cohort was 55%, ranging from 47% (persistent oligoarthritis) to 69% (systemic arthritis) (P = 0.4). Approximately 67% of children achieved ID by 12 months. In the multivariable model, history and reinitiation of biologic drugs were associated with increased odds of successful recapture (odds ratio [OR] 4.79 [95% confidence interval (95% CI) 1.22–18.78] and OR 2.74 [95% CI 1.62–4.63], respectively). Number of joints with limited range of motion was associated with decreased odds (OR 0.83 per 1 joint increase [95% CI 0.72–0.95]). Conclusion: Approximately half of JIA flares post-discontinuation were recaptured within 6 months, but rates of recapture varied across JIA categories. These findings inform shared decision-making for patients, families, and clinicians regarding the risks and benefits of medication discontinuation. Better understanding of biologic predictors of successful recapture in JIA are needed.
AB - Objective: Children with well-controlled juvenile idiopathic arthritis (JIA) frequently experience flares after medication discontinuation, but the outcomes of these flares have not been well described. The objective of this study was to characterize the rates and predictors of disease recapture among children with JIA who restarted medication to treat disease flare. Methods: Children with JIA who discontinued conventional synthetic or biologic disease-modifying antirheumatic drugs for well-controlled disease but subsequently experienced a flare and restarted medication were identified from the Childhood Arthritis and Rheumatology Research Alliance (CARRA) registry. The primary outcome was inactive disease (ID) (physician global assessment <1 and active joint count = 0) 6 months after flare. Results: A total of 333 patients had complete data for ID at 6 months after flare. The recapture rate for the cohort was 55%, ranging from 47% (persistent oligoarthritis) to 69% (systemic arthritis) (P = 0.4). Approximately 67% of children achieved ID by 12 months. In the multivariable model, history and reinitiation of biologic drugs were associated with increased odds of successful recapture (odds ratio [OR] 4.79 [95% confidence interval (95% CI) 1.22–18.78] and OR 2.74 [95% CI 1.62–4.63], respectively). Number of joints with limited range of motion was associated with decreased odds (OR 0.83 per 1 joint increase [95% CI 0.72–0.95]). Conclusion: Approximately half of JIA flares post-discontinuation were recaptured within 6 months, but rates of recapture varied across JIA categories. These findings inform shared decision-making for patients, families, and clinicians regarding the risks and benefits of medication discontinuation. Better understanding of biologic predictors of successful recapture in JIA are needed.
UR - http://www.scopus.com/inward/record.url?scp=85141945959&partnerID=8YFLogxK
U2 - 10.1002/acr.24994
DO - 10.1002/acr.24994
M3 - Article
C2 - 35921198
AN - SCOPUS:85141945959
SN - 2151-464X
VL - 75
SP - 715
EP - 723
JO - Arthritis Care and Research
JF - Arthritis Care and Research
IS - 4
ER -