Inter- and Intrarater Agreement of CT Brain Calcification Scoring in Primary Familial Brain Calcification

被引:0
|
作者
Snijders, Birgitta M. G. [1 ]
Koek, Huiberdina L. [1 ]
Peters, Mike J. L. [1 ,2 ]
Mali, Willem P. T. M. [3 ]
van Beek, Michelle M. [1 ]
Betman, Merel J. C. [3 ]
Goluke, Nienke M. S. [4 ]
Kruyswijk, Tijl [1 ]
de Lange, Stephanie V. [3 ]
Lith, Bouke D. W. T. [1 ]
Pekelharing, Ruth M. [1 ]
Roos, Marvin J. [1 ]
Rutgers, Dirk R. [3 ]
Venema, Simone M. Uniken [3 ]
Verberne, Wouter R. [1 ,2 ]
Emmelot-Vonk, Marielle H. [1 ]
de Jong, Pim A. [3 ]
机构
[1] Univ Med Ctr Utrecht, Dept Geriatr, Heidelberglaan 100, NL-3584 CX Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Dept Internal Med, Utrecht, Netherlands
[3] Univ Med Ctr Utrecht, Dept Radiol, Utrecht, Netherlands
[4] Ziekenhuis Gelderse Vallei, Dept Geriatr, Ede, Netherlands
关键词
D O I
10.3174/ajnr.A8446
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND AND PURPOSE: The total calcification score (TCS) is a visual rating scale to measure primary familial brain calcification (PFBC)?related calcification severity on CT. We investigated the inter- and intrarater agreement of a modified TCS. MATERIALS AND METHODS: Patients aged ?18?years with PFBC or Fahr syndrome who visited the outpatient clinic of a Dutch academic hospital were included. The TCS was modified, for example, by adding hippocampal calcification, and ranged from 0 to 95 points. Fifteen raters evaluated all CTs, of whom 3 evaluated the CTs twice. Their entrustable professional activity (EPA) level ranged from II (medical student) to V (neuroradiologist). Agreement was assessed by using the intraclass correlation coefficient (ICC) for the total score. Kendall?s W and weighted Cohen ? were used to determine the inter- and intrarater agreement for individual locations, respectively. RESULTS: Forty patients were included (mean age 60?years, 53% women). The median modified TCS was 34 (range 4?76). For all EPA levels, the interrater agreement of the modified TCS was excellent (ICC?= 0.97 [95% CI 0.95?0.98]). The Kendall W values were good to excellent for commonly affected locations, but poor to moderate for less commonly affected locations for raters with lower levels of expertise. The intrarater agreement of the modified TCS was excellent. The Cohen ? of most locations were substantial to almost perfect. CONCLUSIONS: The modified TCS can be used with excellent reproducibility of the overall amount of brain calcifications and with limited training, although for some individual calcification locations more expertise is needed.
引用
收藏
页码:147 / 152
页数:6
相关论文
共 50 条
  • [31] Evaluation of MYORG mutations as a novel cause of primary familial brain calcification
    Chen, You
    Fu, Feng
    Chen, Si
    Cen, Zhidong
    Tang, Haiyan
    Huang, Jinxiu
    Xie, Fei
    Zheng, Xiaosheng
    Yang, Dehao
    Wang, Haotian
    Huang, Xuerong
    Zhang, Yun
    Zhou, Yongji
    Liu, Jing-Yu
    Luo, Wei
    MOVEMENT DISORDERS, 2019, 34 (02) : 291 - 297
  • [32] MICROANGIOPATHY IN PRIMARY FAMILIAL BRAIN CALCIFICATION: EVIDENCE FROM SKIN BIOPSIES
    Nicolas, Gael
    Marguet, Florent
    Laquerriere, Annie
    Mendes de Oliveira, Joao Ricardo
    Hannequin, Didier
    NEUROLOGY-GENETICS, 2017, 3 (02)
  • [33] Biallelic MYORG mutations: Primary familial brain calcification goes recessive
    Alvarez-Fischer, Daniel
    Westenberger, Ana
    MOVEMENT DISORDERS, 2019, 34 (03) : 322 - 322
  • [34] Primary familial brain calcification - The impact of calcifications on the development of motor symptoms
    Alvarez-Fischer, D.
    Schiemenz, C.
    Mahlke, G.
    Keller, A.
    Westenberger, A.
    Erdmann, J.
    Aherrahrou, Z.
    Klein, C.
    MOVEMENT DISORDERS, 2018, 33 : S205 - S205
  • [35] Refractory focal epilepsy in a paediatric patient with primary familial brain calcification
    Knowles, Juliet K.
    Santoro, Jonathan D.
    Porter, Brenda E.
    Baumer, Fiona M.
    SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2018, 56 : 50 - 52
  • [37] Clinical and radiological diversity in genetically confirmed primary familial brain calcification
    Koyama, Shingo
    Sato, Hidenori
    Kobayashi, Ryota
    Kawakatsu, Shinobu
    Kurimura, Masayuki
    Wada, Manabu
    Kawanami, Toru
    Kato, Takeo
    SCIENTIFIC REPORTS, 2017, 7
  • [38] Cognitive profiling in a cohort of Primary Familial Brain Calcification (PFBC) patients
    Garon, M.
    Carecchio, M.
    Weis, L.
    Pistonesi, F.
    Mainardi, M.
    Bonato, G.
    Salviati, L.
    Antonini, A.
    Biundo, R.
    MOVEMENT DISORDERS, 2021, 36 : S93 - S93
  • [39] A New Gene for Primary Familial Brain Calcification: The Importance of Phosphate Homeostasis
    Westenberger, Ana
    Klein, Christine
    MOVEMENT DISORDERS, 2015, 30 (09) : 1213 - 1213
  • [40] Clinical and radiological diversity in genetically confirmed primary familial brain calcification
    Shingo Koyama
    Hidenori Sato
    Ryota Kobayashi
    Shinobu Kawakatsu
    Masayuki Kurimura
    Manabu Wada
    Toru Kawanami
    Takeo Kato
    Scientific Reports, 7