Improving Multiple Sclerosis Plaque Detection Using a Semiautomated Assistive Approach

被引:18
作者
van Heerden, J. [1 ,2 ]
Rawlinson, D. [3 ]
Zhang, A. M. [3 ]
Chakravorty, R. [4 ]
Tacey, M. A. [5 ,6 ]
Desmond, P. M. [1 ,2 ]
Gaillard, F. [1 ,2 ]
机构
[1] Royal Melbourne Hosp, Dept Radiol, Parkville, Vic 3050, Australia
[2] Univ Melbourne, Parkville, Vic 3052, Australia
[3] Univ Melbourne, Sch Engn, Dept Elect & Elect Engn, Parkville, Vic 3052, Australia
[4] IBM Res, Melbourne, Vic, Australia
[5] Univ Melbourne, Royal Melbourne Hosp, Melbourne EpiCtr, Parkville, Vic 3052, Australia
[6] Univ Melbourne, Dept Med, Parkville, Vic 3052, Australia
基金
澳大利亚研究理事会;
关键词
WHITE-MATTER LESIONS; AUTOMATIC SEGMENTATION; LOAD; IMAGES; FLAIR; DISABILITY;
D O I
10.3174/ajnr.A4375
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: Treating MS with disease-modifying drugs relies on accurate MR imaging follow-up to determine the treatment effect. We aimed to develop and validate a semiautomated software platform to facilitate detection of new lesions and improved lesions. MATERIALS AND METHODS: We developed VisTarsier to assist manual comparison of volumetric FLAIR sequences by using interstudy registration, resectioning, and color-map overlays that highlight new lesions and improved lesions. Using the software, 2 neuroradiologists retrospectively assessed MR imaging MS comparison study pairs acquired between 2009 and 2011 (161 comparison study pairs met the study inclusion criteria). Lesion detection and reading times were recorded. We tested inter-and intraobserver agreement and comparison with original clinical reports. Feedback was obtained from referring neurologists to assess the potential clinical impact. RESULTS: More comparison study pairs with new lesions (reader 1, n = 60; reader 2, n = 62) and improved lesions (reader 1, n = 28; reader 2, n = 39) were recorded by using the software compared with original radiology reports (new lesions, n = 20; improved lesions, n = 5); the difference reached statistical significance (P < .001). Interobserver lesion number agreement was substantial (>= 1 new lesion: kappa = 0.87; 95% CI, 0.79-0.95; >= 1 improved lesion: kappa = 0.72; 95% CI, 0.59-0.85), and overall interobserver lesion number correlation was good (Spearman rho : new lesion = 0.910, improved lesion = 0.774). Intraobserver agreement was very good (new lesion: kappa = 1.0, improved lesion: kappa = 0.94; 95% CI, 0.82-1.00). Mean reporting times were <3 minutes. Neurologists indicated retrospective management alterations in 79% of comparative study pairs with newly detected lesion changes. CONCLUSIONS: Using software that highlights changes between study pairs can improve lesion detection. Neurologist feedback indicated a likely impact on management.
引用
收藏
页码:1465 / 1471
页数:7
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