Screening for juvenile idiopathic arthritis associated uveitis with laser flare photometry in the pediatric rheumatology office: a prospective observational study.

IF 2.8 3区 医学 Q1 PEDIATRICS Pediatric Rheumatology Pub Date : 2024-01-26 DOI:10.1186/s12969-024-00961-9
Kaleo Ede, Michael Shishov, Elisa Wershba, Nikita Goswami, Sabrina Gorry, Malin Joseph, Lucia Mirea, James O'Neil
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Abstract

Background: Juvenile Idiopathic Arthritis (JIA) Associated Uveitis (JIA-U) remains one of the most serious complications of JIA in children. Historically, pediatric JIA is diagnosed by an Optometrist or Ophthalmologist; however, barriers to scheduling increase wait times that may delay diagnosis and treatment. The purpose of this study was to evaluate laser flare photometry (LFP) use to diagnose JIA-U in the Pediatric Rheumatology clinic for patients with JIA.

Methods: This prospective, observational study assessed pediatric patients diagnosed with JIA without a previous history of uveitis between January 2020 and September 2022. All patients underwent at least one evaluation of both eyes using a Kowa FM-600 laser flare photometer during a routine Rheumatology appointment, as well as a standard slit lamp examination (SLE) by optometry or ophthalmology during routine clinical care. Data collected at patient visits included demographics, JIA characteristics, treatment, LFP readings, and anterior chamber (AC) cell grade score utilizing the SUN grading system. Data were summarized using descriptive analyses and the uveitis false positive rate was calculated.

Results: The study cohort included 58 pediatric patients diagnosed with JIA. The mean age was 8.4 years (1.2-16.3 years) at diagnosis and 11.9 (4.8-16.5 years) at enrollment. The mean duration of disease at time of enrollment was 42 months (range; 0-157 months). Participants were predominantly female (n = 43, 74.1%) and white/Caucasian race (n = 37, 63.8%). The most common JIA subtypes included persistent oligoarticular JIA (n = 19, 32.8%), and RF negative polyarticular JIA (n = 12, 20.7%). There were 12 ANA positive patients (20.7%). At enrollment, 16 patients (27.6%) were not on medications, with 20 (34.5%) on methotrexate, 20 (34.5%) on adalimumab, 6 (10.3%) on tocilizumab, and 5 (8.6%) on etanercept. During the study period, no eye exams detected active uveitis based on SLE with a SUN grade over 0. However, of the 135 LFP readings, 131 (97.0%) were normal, yielding a false positive rate of 3% (95% CI: 0.8%, 7.4%).

Conclusions: LFP is a non-invasive tool that can be utilized in the pediatric rheumatology clinic to evaluate for JIA-U. There is a low false positive rate of LFP when compared with standard slit lamp exam.

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在儿科风湿病诊室用激光耀斑光度法筛查幼年特发性关节炎相关葡萄膜炎:一项前瞻性观察研究。
背景:青少年特发性关节炎(JIA)相关性葡萄膜炎(JIA-U)仍然是儿童 JIA 最严重的并发症之一。一直以来,小儿 JIA 都是由验光师或眼科医生诊断的;然而,排期方面的障碍增加了等待时间,可能会延误诊断和治疗。本研究的目的是评估激光耀斑光度计(LFP)在儿科风湿病诊所诊断 JIA-U 的使用情况:这项前瞻性观察研究评估了2020年1月至2022年9月期间诊断为JIA且既往无葡萄膜炎病史的儿科患者。所有患者均在风湿科常规就诊期间使用科瓦 FM-600 激光耀斑光度计对双眼进行了至少一次评估,并在常规临床护理期间接受了验光或眼科的标准裂隙灯检查(SLE)。在患者就诊时收集的数据包括人口统计学特征、JIA 特征、治疗、LFP 读数以及使用 SUN 分级系统的前房(AC)细胞等级评分。通过描述性分析对数据进行总结,并计算葡萄膜炎假阳性率:研究队列包括58名确诊为JIA的儿童患者。确诊时的平均年龄为8.4岁(1.2-16.3岁),注册时的平均年龄为11.9岁(4.8-16.5岁)。入组时的平均病程为 42 个月(0-157 个月)。参与者主要为女性(43 人,占 74.1%)和白人/白种人(37 人,占 63.8%)。最常见的 JIA 亚型包括持续性少关节型 JIA(19 人,32.8%)和 RF 阴性多关节型 JIA(12 人,20.7%)。ANA阳性患者有12人(20.7%)。入组时,16 名患者(27.6%)未服用药物,其中 20 人(34.5%)服用甲氨蝶呤,20 人(34.5%)服用阿达木单抗,6 人(10.3%)服用妥昔单抗,5 人(8.6%)服用依那西普。然而,在135个LFP读数中,131个(97.0%)正常,假阳性率为3%(95% CI:0.8%, 7.4%):LFP是一种无创工具,可用于儿科风湿病诊所评估JIA-U。与标准裂隙灯检查相比,LFP的假阳性率较低。
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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.
期刊最新文献
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