Duration of effect in treatment of methotrexate intolerance in juvenile idiopathic arthritis using Eye Movement Desensitization and Reprocessing (EMDR) can be improved by Bi-lateral Alternating Stimulation Tactile (BLAST) wristbands.

IF 2.8 3区 医学 Q1 PEDIATRICS
Lea Höfel, Bruno Eppler, Johannes-Peter Haas, Boris Hügle
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引用次数: 0

Abstract

Background: Methotrexate (MTX) intolerance in juvenile idiopathic arthritis (JIA) frequently leads to discontinuation due to anticipatory and associative gastrointestinal symptoms. Eye Movement Desensitization and Reprocessing (EMDR) has successfully been used in MTX intolerance, with lasting effects but frequently diminishing efficacy over time. BLAST (bi-lateral alternating stimulation tactile) wristbands utilize a similar process to EMDR. The aim of this study was to determine if utilization of BLAST wristbands could improve and prolong the effect of EMDR on patients with MTX intolerance.

Methods: Consecutive patients admitted to the German Center for Pediatric and Adolescent Rheumatology with JIA and signs of MTX intolerance from October 2016 until March 2024 were included in this study. Treatment was performed using an adapted 8 phase EMDR protocol implementing BAST wristbands. Initial patients were treated with EMDR, subsequent patients additionally with BLAST wristbands. Health-related quality of live was determined using the PedsQL. Measurements of MISS (Methotrexate Intolerance Severity Score) and PedsQL were taken at 4 time points: directly before and after (MISS only) treatment, as well as 4 and 12 months after treatment. Changes in MISS and PedsQL were compared using descriptive statistics and repeated measures ANOVA.

Results: 87 patients with MTX intolerance were included, 53 in group 1 without BLAST wristbands and 34 in group 2 which were concurrently treated with BLAST wristbands. All patients reported marked improvement of MTX intolerance symptoms (mean MISS score group 1: 15.0 ± 5.5 before treatment, 1.3 ± 1.5 after treatment, group 2: 16.8 ± 5.6 and 2.5 ± 2.5, respectively). After 4 and 12 months, MISS in group 1 was 8.1 ± 7.1 and 8.7 ± 8.4, and in group 2: 7.1 ± 6.3 and 6.5 ± 5.7. A repeated measures ANOVA showed a significant difference between the MISS results over time (F(3,114) = 64.6, p < 0.001), and also demonstrated a significant difference of the PedsQL results between the two groups over time (F(2,64) = 8.9, p < 0.001).

Conclusion: Treatment with Eye Movement Desensitization and Reprocessing (EMDR) could present an effective treatment of MTX intolerance, and using BLAST wristbands, further potential improvement is possible.

使用眼动脱敏和再处理疗法(EMDR)治疗幼年特发性关节炎患者甲氨蝶呤不耐受的疗效持续时间可通过双侧交替刺激触觉(BLAST)腕带得到改善。
背景:幼年特发性关节炎(JIA)患者对甲氨蝶呤(MTX)的不耐受常常会因为预期和联想性胃肠道症状而导致停药。眼动脱敏和再处理疗法(EMDR)已成功用于治疗MTX不耐受症,效果持久,但随着时间的推移,疗效往往会减弱。BLAST(双侧交替刺激触觉)腕带采用了与 EMDR 相似的过程。本研究旨在确定使用 BLAST 腕带能否改善和延长 EMDR 对 MTX 不耐受患者的疗效:从2016年10月至2024年3月,德国儿童和青少年风湿病学中心连续收治了患有JIA并有MTX不耐受症状的患者。治疗采用经调整的8阶段EMDR方案,使用BAST腕带。最初的患者接受了 EMDR 治疗,随后的患者则接受了 BLAST 腕带治疗。使用 PedsQL 测定与健康相关的生活质量。在四个时间点测量 MISS(甲氨蝶呤不耐受严重程度评分)和 PedsQL:治疗前后(仅测量 MISS)、治疗后 4 个月和 12 个月。采用描述性统计和重复测量方差分析比较了 MISS 和 PedsQL 的变化:共纳入了 87 名 MTX 不耐受患者,其中 53 人属于不使用 BLAST 腕带的第一组,34 人属于同时使用 BLAST 腕带治疗的第二组。所有患者的 MTX 不耐受症状均有明显改善(第 1 组平均 MISS 评分:治疗前为 15.0 ± 5.5,治疗后为 1.3 ± 1.5;第 2 组分别为 16.8 ± 5.6 和 2.5 ± 2.5)。4 个月和 12 个月后,第 1 组的 MISS 分别为 8.1 ± 7.1 和 8.7 ± 8.4,第 2 组分别为 7.1 ± 6.3 和 6.5 ± 5.7。重复测量方差分析显示,随着时间的推移,MISS 结果之间存在显著差异(F(3,114) = 64.6,P 结论:眼动脱敏和再处理疗法(EMDR)是治疗 MTX 不耐受的有效方法,使用 BLAST 腕带还可能进一步改善症状。
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来源期刊
Pediatric Rheumatology
Pediatric Rheumatology PEDIATRICS-RHEUMATOLOGY
CiteScore
4.10
自引率
8.00%
发文量
95
审稿时长
>12 weeks
期刊介绍: Pediatric Rheumatology is an open access, peer-reviewed, online journal encompassing all aspects of clinical and basic research related to pediatric rheumatology and allied subjects. The journal’s scope of diseases and syndromes include musculoskeletal pain syndromes, rheumatic fever and post-streptococcal syndromes, juvenile idiopathic arthritis, systemic lupus erythematosus, juvenile dermatomyositis, local and systemic scleroderma, Kawasaki disease, Henoch-Schonlein purpura and other vasculitides, sarcoidosis, inherited musculoskeletal syndromes, autoinflammatory syndromes, and others.
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