Validation of a symptom-based questionnaire for pediatric CNS demyelinating diseases

被引:3
|
作者
Waldman, Amy T. [1 ,3 ,4 ,5 ]
Yeshokumar, Anusha K. [6 ]
Lavery, Amy [1 ]
Liu, Geraldine [1 ]
Pineles, Stacy L. [7 ]
Repka, Michael X. [8 ]
Adang, Laura [1 ,3 ,4 ,5 ]
Narula, Sona [1 ,3 ,4 ,5 ]
Liu, Grant T. [2 ,3 ,5 ]
机构
[1] Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USA
[2] Childrens Hosp Philadelphia, Div Ophthalmol, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Neurol, Perelman Sch Med, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USA
[5] Univ Penn, Dept Ophthalmol, Perelman Sch Med, Philadelphia, PA 19104 USA
[6] Icahn Sch Med Mt Sinai, New York, NY 10029 USA
[7] Univ Calif Los Angeles, Jules Stein Eye Inst, Los Angeles, CA 90024 USA
[8] Johns Hopkins Univ, Sch Med, Wilmer Eye Inst, Baltimore, MD 21205 USA
来源
JOURNAL OF AAPOS | 2019年 / 23卷 / 03期
关键词
MULTIPLE-SCLEROSIS; DISABILITY; CRITERIA;
D O I
10.1016/j.jaapos.2019.01.016
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE Optic neuritis is a manifestation of numerous neuroinflammatory disorders. Recognition of current and prior symptoms may facilitate identification of an underlying multifocal neurologic disease. The purpose of this study was to determine whether a symptom-based questionnaire could inform clinical decision making by identifying children with visual complaints who may have a systemic demyelinating disorder. METHODS Children with visual changes from non-demyelinating disease were compared with patients with confirmed pediatric-onset multiple sclerosis (MS) or neuromyelitis optica spectrum disorder (NMOSD). Participants completed a 21-item questionnaire to capture their recent (<30 days) and remote (>30 days) symptoms of neurologic dysfunction. The questionnaire scores were compared using t tests, and the 95% confidence interval for each group was used to determine a threshold score suggesting demyelinating disease. RESULTS We enrolled 51 participants (30 females [59%]) with a mean age of 14.6 years (range, 4-21): 25 in the non-demyelinating disease group and 26 with MS/NMOSD. The mean questionnaire score for the non-demyelinating group was 5.0 points (95%CI, 3.3-6.9); for the MS/NMOSD group, 9.4 points (95% CI, 7.4-11.4) for the MS/NMOSD group (P < 0.002). Questionnaire results were dichotomized using a score of >= 7 as indicative of demyelinating disease, with 69% sensitivity and 72% specificity. An abbreviated questionnaire, using 8 questions that differed between groups, had a sensitivity of 65% and specificity (92%). CONCLUSIONS A symptom-based questionnaire is sensitive and specific for identifying children with CNS demyelinating disease and may be useful as a screening tool for children with vision complaints and possible demyelination.
引用
收藏
页码:157 / 158
页数:2
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