Evaluation of medication withdrawal in patients with non-systemic juvenile idiopathic arthritis in Japan using a web-based survey

Author:

Ebato Takasuke1,Kishi Takayuki2,Akamine Keiji3,Nozawa Tomo4,Imagawa Tomoyuki5,Bando Yuki6,Miyamae Takako78

Affiliation:

1. Department of Pediatrics, Kitasato University , Kanagawa, Japan

2. Department of Pediatrics, Tokyo Women’s Medical University , Tokyo, Japan

3. Department of Nephrology and Rheumatology, Tokyo Metropolitan Children’s Medical Center , Tokyo, Japan

4. Department of Pediatrics, Graduate School of Medicine, Yokohama City University , Kanagawa, Japan

5. Department of Infection and Immunology, Kanagawa Children’s Medical Center , Kanagawa, Japan

6. Department of Pediatrics, Kitasato University Medical Center , Saitama, Japan

7. Department of Pediatric Rheumatology, Institute of Rheumatology, Tokyo Women’s Medical University Hospital , Tokyo, Japan

8. Division of Rheumatology, Department of Internal Medicine, Tokyo Women’s Medical University School of Medicine , Tokyo, Japan

Abstract

ABSTRACT Objectives Although treatments for juvenile idiopathic arthritis (JIA) have seen considerable advancements, there remains a lack of clear guidelines on withdrawing medications. This study aimed to investigate the current strategies for discontinuing non-systemic JIA treatment. Methods A web-based questionnaire was distributed to members of the Pediatric Rheumatology Association of Japan. Results According to 126 responses, the most significant factors influencing JIA treatment tapering were the duration of clinically inactive disease, medication toxicity, and a history of arthritis flares. Respondents were often cautious about discontinuing medication if symptoms, e.g. ‘morning stiffness’ or ‘intermittent joint pain’, persisted. Among subtypes, oligoarticular JIA was more amenable to treatment tapering, whereas rheumatoid factor–positive polyarticular JIA proved less amenable. Most respondents started medication tapering after a continuous clinical inactive duration exceeding 12 months, and >50% of them required >6 months to achieve treatment discontinuation. Additionally, 40% of the respondents consistently underwent imaging before treatment tapering. Conclusions The relative risks of treatment continuation and withdrawal should be considered, and decisions should be made accordingly. To obtain improved understanding of and more robust evidence for the optimal strategies for safely discontinuing JIA treatment, it is crucial to continue investigations including long-term outcomes.

Publisher

Oxford University Press (OUP)

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