Consensus neuropathological diagnosis of common dementia syndromes: testing and standardising the use of multiple diagnostic criteria

被引:47
作者
Halliday, G
Ng, T
Rodriguez, M
Harding, A
Blumbergs, P
Evans, W
Fabian, V
Fryer, J
Gonzales, M
Harper, C
Kalnins, R
Masters, CL
McLean, C
Milder, DG
Pamphlett, R
Scott, G
Tannenberg, A
Kril, J
机构
[1] Prince Wales Med Res Inst, Randwick, NSW 2031, Australia
[2] Westmead Hosp, Inst Clin Pathol & Med Res, Westmead, NSW 2145, Australia
[3] Cent Sydney Area Hlth Serv, Dept Forens Med, Glebe, NSW 2037, Australia
[4] Inst Med & Vet Sci, Neuropathol Lab, Adelaide, SA 5000, Australia
[5] Royal Perth Hosp, Dept Neuropathol, Perth, WA 6001, Australia
[6] Royal N Shore Hosp, St Leonards, NSW 2065, Australia
[7] Royal Melbourne Hosp, Melbourne, Vic 3050, Australia
[8] Univ Sydney, Dept Pathol, Sydney, NSW 2006, Australia
[9] Austin Hosp, Melbourne, Vic 3084, Australia
[10] Univ Melbourne, Dept Pathol, Melbourne, Vic 3010, Australia
[11] Mater Misericordiae Publ Hosp, Dept Pathol, Brisbane, Qld 4101, Australia
[12] Concord Hosp, Ctr Educ & Res Ageing, Concord, NSW 2139, Australia
[13] Univ Sydney, Concord, NSW 2139, Australia
基金
英国医学研究理事会;
关键词
Alzheimer's disease; dementia; diagnosis; Lewy body; neuropathology;
D O I
10.1007/s00401-002-0529-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The aim of this study was to assess the variation between neuropathologists in the diagnosis of common dementia syndromes when multiple published protocols are applied. Fourteen out of 18 Australian neuropathologists participated in diagnosing 20 cases (16 cases of dementia, 4 age-matched controls) using consensus diagnostic methods. Diagnostic criteria, clinical synopses and slides from multiple brain regions were sent to participants who were asked for case diagnoses. Diagnostic sensitivity, specificity, predictive value, accuracy and variability were determined using percentage agreement and kappa statistics. Using CERAD criteria, there was a high inter-rater agreement for cases with probable and definite Alzheimer's disease but low agreement for cases with possible Alzheimer's disease. Braak staging and the application of criteria for dementia with Lewy bodies also resulted in high inter-rater agreement. There was poor agreement for the diagnosis of frontotemporal dementia and for identifying small vessel disease. Participants rarely diagnosed more than one disease in any case. To improve efficiency when applying multiple diagnostic criteria, several simplifications were proposed and tested on 5 of the original 210 cases. Inter-rater reliability for the diagnosis of Alzheimer's disease and dementia with Lewy bodies significantly improved. Further development of simple and accurate methods to identify small vessel lesions and diagnose frontotemporal dementia is warranted.
引用
收藏
页码:72 / 78
页数:7
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