Department of Ophthalmology, Casey Eye Institute, Oregon Health & Science University, Portland.
Department of Ophthalmology and Visual Sciences, Illinois Eye and Ear Infirmary, University of Illinois at Chicago.
JAMA Ophthalmol. 2018 May 1;136(5):498-504. doi: 10.1001/jamaophthalmol.2018.0649.
Examinations for retinopathy of prematurity (ROP) are typically performed using binocular indirect ophthalmoscopy. Telemedicine studies have traditionally assessed the accuracy of telemedicine compared with ophthalmoscopy as a criterion standard. However, it is not known whether ophthalmoscopy is truly more accurate than telemedicine.
To directly compare the accuracy and sensitivity of ophthalmoscopy vs telemedicine in diagnosing ROP using a consensus reference standard.
DESIGN, SETTING, AND PARTICIPANTS: This multicenter prospective study conducted between July 1, 2011, and November 30, 2014, at 7 neonatal intensive care units and academic ophthalmology departments in the United States and Mexico included 281 premature infants who met the screening criteria for ROP.
Each examination consisted of 1 eye undergoing binocular indirect ophthalmoscopy by an experienced clinician followed by remote image review of wide-angle fundus photographs by 3 independent telemedicine graders.
Results of both examination methods were combined into a consensus reference standard diagnosis. The agreement of both ophthalmoscopy and telemedicine was compared with this standard, using percentage agreement and weighted κ statistics.
Among the 281 infants in the study (127 girls and 154 boys; mean [SD] gestational age, 27.1 [2.4] weeks), a total of 1553 eye examinations were classified using both ophthalmoscopy and telemedicine. Ophthalmoscopy and telemedicine each had similar sensitivity for zone I disease (78% [95% CI, 71%-84%] vs 78% [95% CI, 73%-83%]; P > .99 [n = 165]), plus disease (74% [95% CI, 61%-87%] vs 79% [95% CI, 72%-86%]; P = .41 [n = 50]), and type 2 ROP (stage 3, zone I, or plus disease: 86% [95% CI, 80%-92%] vs 79% [95% CI, 75%-83%]; P = .10 [n = 251]), but ophthalmoscopy was slightly more sensitive in identifying stage 3 disease (85% [95% CI, 79%-91%] vs 73% [95% CI, 67%-78%]; P = .004 [n = 136]).
No difference was found in overall accuracy between ophthalmoscopy and telemedicine for the detection of clinically significant ROP, although, on average, ophthalmoscopy had slightly higher accuracy for the diagnosis of zone III and stage 3 ROP. With the caveat that there was variable accuracy between examiners using both modalities, these results support the use of telemedicine for the diagnosis of clinically significant ROP.
早产儿视网膜病变(ROP)的检查通常使用双目间接检眼镜进行。远程医疗研究传统上评估了远程医疗与检眼镜作为金标准相比的准确性。然而,尚不清楚检眼镜是否真的比远程医疗更准确。
使用共识参考标准直接比较检眼镜与远程医疗诊断 ROP 的准确性和灵敏度。
设计、地点和参与者:这项多中心前瞻性研究于 2011 年 7 月 1 日至 2014 年 11 月 30 日在美国和墨西哥的 7 个新生儿重症监护病房和学术眼科部门进行,共纳入 281 名符合 ROP 筛查标准的早产儿。
每只眼睛均接受有经验的临床医生进行的双目间接检眼镜检查,然后由 3 名独立的远程医疗分级员远程查看广角眼底照片。
将两种检查方法的结果合并为共识参考标准诊断。使用百分比一致性和加权κ统计量比较这两种方法与该标准的一致性。
在这项研究的 281 名婴儿(127 名女孩和 154 名男孩;平均[SD]胎龄,27.1[2.4]周)中,共有 1553 只眼睛使用检眼镜和远程医疗进行了分类。对于 I 区疾病,检眼镜和远程医疗的敏感性相似(78%[95%CI,71%-84%]与 78%[95%CI,73%-83%];P > .99[n = 165])、外加疾病(74%[95%CI,61%-87%]与 79%[95%CI,72%-86%];P = .41[n = 50])和 2 型 ROP(3 期,I 区或外加疾病:86%[95%CI,80%-92%]与 79%[95%CI,75%-83%];P = .10[n = 251]),但检眼镜在识别 3 期疾病方面略为敏感(85%[95%CI,79%-91%]与 73%[95%CI,67%-78%];P = .004[n = 136])。
在检测临床上有意义的 ROP 方面,检眼镜和远程医疗的整体准确性没有差异,尽管平均而言,检眼镜对诊断 III 区和 3 期 ROP 的准确性略高。需要注意的是,两种方式的检查者之间的准确性存在差异,这些结果支持远程医疗用于诊断临床上有意义的 ROP。