Global optical coherence tomography measures for detecting the progression of glaucoma have fundamental flaws.
Global optical coherence tomography measures for detecting the progression of glaucoma have fundamental flaws.
复制标题
用于检测青光眼进展的全球光学相干断层扫描措施具有基本缺陷。
DOI:
10.1038/s41433-020-01296-x
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发表时间:
2021-11
期刊:
影响因子:
--
通讯作者:
Hood DC
中科院分区:
文献类型:
--
作者:
Sun A;Tsamis E;Eguia MD;Liebmann JM;Blumberg DM;Al-Aswad LA;Cioffi GA;Gustavo De Moraes C;Hood DC
To understand the problems involved in using global OCT measures for detecting progression in early glaucoma. Eyes from 76 patients and 28 healthy controls (HC) had a least two OCT scans at least 1 year apart. To determine the 95% confidence intervals (CI), 151 eyes (49 HC and 102 patients) had at least two scans within 6 months. All eyes had 24-2 mean deviation ≥-6dB. The average (global) thicknesses of the circumpapillary retinal nerve fibre layer (cRNFL), GONH, and of the retinal ganglion cell layer plus inner plexiform layer (RGCLP), Gmac, were calculated. Using quantile regression, the 95% CI intervals were determined. Eyes outside the CIs were classified as “progressors.” For a reference standard (RS), four experts evaluated OCT and VF information. Compared to the RS, 31 of the 76 (40.8%) patient eyes were identified as progressors (RS-P), and 45 patient, and all 28 HC, eyes as nonprogressors (RS-NP). The metrics missed (false negative, FN) 15 (48%) (GONH) and 9 (29%) (Gmac) of the 31 RS-P. Further, GONH and/or Gmac falsely identified (false positive, FP) 10 (22.2%) of 45 patient RS-NP eyes and 7 (25%) of the 28 HC eyes as progressing. Post-hoc analysis identified three reasons (segmentation, centring, and local damage) for these errors. Global metrics lead to FPs and FNs because of problems inherent in OCT scanning (segmentation and centring), and to FNs because they can miss local damage. These problems are difficult, if not impossible, to correct, and raise concerns about the advisability of using GONH and Gmac for detecting progression.
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影响因子:
4.4
作者:
Medeiros FA;Zangwill LM;Alencar LM;Bowd C;Sample PA;Susanna R Jr;Weinreb RN
通讯作者:
Weinreb RN
影响因子:
2
作者:
Muhammad H;Fuchs TJ;De Cuir N;De Moraes CG;Blumberg DM;Liebmann JM;Ritch R;Hood DC
通讯作者:
Hood DC
影响因子:
3.4
作者:
Kim, Mi Jeung;Park, Ki Ho;Kim, Dong Myung
通讯作者:
Kim, Dong Myung
影响因子:
4.4
作者:
Hood, Donald C.;Tsamis, Emmanouil;De Moraes, Carlos G.
通讯作者:
De Moraes, Carlos G.
影响因子:
3
作者:
Tsamis, Emmanouil;Bommakanti, Nikhil K.;Hood, Donald C.
通讯作者:
Hood, Donald C.