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
相关论文
共 50 条
  • [21] Non-infectious meningitis and CNS demyelinating diseases: A conceptual review
    Etemadifar, M.
    Fereidan-Esfahani, M.
    Sedaghat, N.
    Kargaran, P. K.
    Mansouri, A. R.
    Abhari, A. P.
    Aghababaei, A.
    Jannesari, A.
    Salari, M.
    Ganjalikhani-Hakemi, M.
    Nouri, H.
    REVUE NEUROLOGIQUE, 2023, 179 (06) : 533 - 547
  • [22] Phosphorylated neurofilament heavy subunits as a marker of neurodegeneration in demyelinating diseases of the CNS
    Vorobyeva, A. A.
    Fominykh, V. V.
    Onufriev, M. V.
    Zakharova, M. N.
    Gulyaeva, N. V.
    NEUROCHEMICAL JOURNAL, 2014, 8 (03) : 221 - 225
  • [23] Phosphorylated neurofilament heavy subunits as a marker of neurodegeneration in demyelinating diseases of the CNS
    A. A. Vorobyeva
    V. V. Fominykh
    M. V. Onufriev
    M. N. Zakharova
    N. V. Gulyaeva
    Neurochemical Journal, 2014, 8 : 221 - 225
  • [24] Pediatric acquired CNS demyelinating syndromes Features associated with multiple sclerosis
    Hintzen, Rogier Q.
    Dale, Russell C.
    Neuteboom, Rinze F.
    Mar, Soe
    Banwell, Brenda
    NEUROLOGY, 2016, 87 (09) : S67 - S73
  • [25] Atypical Pediatric Demyelinating Diseases of the Central Nervous System
    Troxell, Regina M.
    Christy, Alison
    CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS, 2019, 19 (12)
  • [26] Atypical Pediatric Demyelinating Diseases of the Central Nervous System
    Regina M. Troxell
    Alison Christy
    Current Neurology and Neuroscience Reports, 2019, 19
  • [27] Clinical and immunological follow-up of B-cell depleting therapy in CNS demyelinating diseases
    Gredler, Viktoria
    Mader, Simone
    Schanda, Kathrin
    Hegen, Harald
    Di Pauli, Franziska
    Kuenz, Bettina
    Deisenhammer, Florian
    Berger, Thomas
    Reindl, Markus
    Lutterotti, Andreas
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2013, 328 (1-2) : 77 - 82
  • [28] Digital symbol-digit modalities test with modified flexible protocols in patients with CNS demyelinating diseases
    Seo, Dayoung
    So, Jeong Min
    Kim, Jiyon
    Jung, Heejae
    Jang, Inhye
    Kim, Hyunjin
    Kang, Dong-Wha
    Lim, Young-Min
    Choi, Jaesoon
    Lee, Eun-Jae
    SCIENTIFIC REPORTS, 2024, 14 (01):
  • [29] New clinical implications of anti-myelin oligodendrocyte glycoprotein antibodies in children with CNS demyelinating diseases
    Di Pauli, Franziska
    Reindl, Markus
    Berger, Thomas
    MULTIPLE SCLEROSIS AND RELATED DISORDERS, 2018, 22 : 35 - 37
  • [30] CSF oligoclonal bands in neurological diseases besides CNS inflammatory demyelinating disorders
    Ren, Jingru
    Wang, Jianchun
    Liu, Ran
    Guo, Jing
    Yao, Yan
    Hao, Hongjun
    Gao, Feng
    BMJ NEUROLOGY OPEN, 2025, 7 (01)