Sarac, Ozge MD; Tasci, Yelda Y. MD; Gurdal, Canan MD; Can, Izzet MD
Optic disc edema (ODE) is usually due to increased intracranial pressure or an optic neuropathy that may necessitate neurologic or systemic evaluation and medical or surgical treatment. Optic nerve head drusen (ONHD) are laminated calcified hyaline bodies that form anterior to the lamina cribrosa of the optic nerve and are not associated with neurologic disease, yet may simulate ODE (1–4).
During patient evaluation, differentiation of ODE from ONHD is crucial. Examination techniques commonly performed in the diagnosis of ONHD are B-scan ultrasonography, fluorescein angiography, and CT (1,5). Application of optical coherence tomography (OCT), a noninvasive imaging technique that creates images closely resembling histologic sections, recently has achieved increasing popularity in differentiating ODE vs ONHD. OCT parameters studied included peripapillary retinal nerve fiber layer (RNFL) thickness (6,7) and direct visualization of the optic nerve head (8).
We assessed the efficacy of spectral-domain optical coherence tomography (SD-OCT) in differentiating ODE and ONHD by visualizing the optic nerve head and the peripapillary RNFL. In addition, we sought to identify SD-OCT features that would differentiate ODE from ONHD.
This prospective study was conducted in compliance with the institutional and government review board regulations, informed consent regulations, and the Declaration of Helsinki. Written informed consent was obtained from all patients and control subjects.
Twenty-five eyes of 25 ODE patients (11 with papilledema, 8 with nonarteritic anterior ischemic optic neuropathy, and 6 with optic neuritis), 25 eyes of 25 ONHD patients, and 25 eyes of 25 normal subjects were recruited from the Department of Neuro-Ophthalmology of Yildirim Beyazit University, Ataturk Hospital, from December 2009 to April 2011. Patients with ODE formed group 1, and patients with ONHD formed group 2. The degree of ODE was variable from subtle to severe. In bilateral asymmetric cases, only the more edematous optic disc was evaluated, and in bilateral symmetric cases, only the right eye was included for study. Those excluded were patients younger than 7 years or older than 70 years and individuals with high hyperopia (greater than +7.00 diopters [D]) or high myopia (greater than −6.00 D).
All patients underwent complete ophthalmologic examination, including visual acuity testing, slit-lamp examination, dilated funduscopy, color fundus photography, autofluorescence imaging, and ocular echography. Supplemental testing included visual fields and fluorescein angiography. Patients suspected of having a neurologic disorder underwent neurologic examination, brain CT imaging, and cerebrospinal fluid analysis. If the diagnosis of ONHD could not be made with funduscopy, it was established by fulfilling at least 2 of the following 4 criteria: autofluorescence on fundus photography, calcification on B-scan ultrasonography or CT, and normal opening pressure on lumbar puncture. Patients with ODE who were included in the study had documented resolution of ODE during the follow-up period.
Patients were evaluated with SD-OCT (RTVue, software version 2.7; Optovue, Inc, Fremont, CA) imaging the optic disc and the peripapillary RNFL. This instrument takes 26,000 A-scans per second, with a frame rate of 256 to 4,096 A-scans per frame. It has a depth resolution of 5 μm and a transverse resolution of 15 μm. The scan range is 2–2.3 mm in depth and 2–12 mm in the transverse plane. The scan beam wavelength is 840 ± 10 nm (9).
All OCT measurements were performed by a single examiner (Y.Y.T.). Each participant was instructed to fixate on an external target positioned in the primary position. Multiple horizontal and vertical scans centered 3.45 mm diameter (radius, 1.73 mm) on the optic disc were performed. The configurations of the optic nerve head and retinal layers around the optic nerve head and the average peripapillary RNFL thickness of the superior, inferior, nasal, and temporal quadrants in group 1, group 2, and the control groups were evaluated. The hyporeflective space located between the sensory retina and the retinal pigment epithelium and choriocapillaris complex, designated as the subretinal hyporeflective space (SHYPS), was determined in groups 1 and 2 (10). With the caliper tool provided by the SD-OCT, the thickness (Fig. 1A) and area (Fig. 1B) of the SHYPS were measured. The thickness of the SHYPS was measured from the highest point in each patient. The angle between the retinal pigment epithelium and the outer nuclear layer at the optic nerve head margin, termed the α-angle (Fig. 1C), was measured manually with a caliper tool from the computer screen in the section where the optic nerve head had the highest configuration. Finally, the horizontal length of the optic nerve was determined (Fig. 1D).
Statistical analysis was performed using the Statistical Package for Social Sciences software (version 16.0; SPSS, Inc, Chicago, IL). The significance of the difference in the RNLF thickness and optic nerve head parameters were assessed by the analysis of variance test between the study groups and the control group. Differences were considered statistically significant at P ≤ 0.05.
Group 1 was composed of 17 women (68%) and 8 men (32%), and group 2 included 15 women (60%) and 10 men (40%). The average age in group 1 was 38.13 ± 18.84 years (range, 19–61 years) and that in group 2 was 29.29 ± 15.58 years (range, 7–55 years). The control group consisted of 15 women (60%) and 10 men (40%), with an average age of 32.53 ± 15.05 years (range, 18–52 years).
The mean RNFL thickness was significantly greater in group 1 when compared with group 2 and the control group (P < 0.001; Table 1). No statistically significant difference between group 2 and the control group was seen (P = 0.320; Table 1). While differentiating groups 1 and 2, the receiver operating characteristic (ROC) curve areas were calculated in each quadrant for the RNFL thickness. The ROC curve area for temporal RNFL thickness was 0.819. When the cutoff point for temporal RNFL thickness was set at 101.5 μm, 92% sensitivity and 65% specificity were obtained. The area under the ROC curve for nasal RNFL thickness was 0.851 (for RNFL thickness >74.5 μm: sensitivity 92%, specificity 47%).
The mean thickness of the highest point of the SHYPS was 582.27 ± 208.16 μm in group 1 and 456.77 ± 112.07 μm in group 2 (P = 0.04). When the cutoff point for the thickness of the highest point of the SHYPS was set at 464 μm, 85% sensitivity and 60% specificity were obtained. The mean area of the SHYPS was 1,110 ± 210 μm2 in group 1 and it was decreased to 620 ± 120 μm2 in group 2 (P = 0.008). The area under the ROC curve for this parameter was 0.851 (for area >811 μm2: sensitivity 85%, specificity 89%).
The mean degree of the α-angle was 145.77 ± 6.34° in group 1 compared with 131.18 ± 11.89° in group 2 (P < 0.001). The area under the ROC curve for this parameter was 0.896 (for angle >141°: sensitivity 77%, specificity 95%).
The mean horizontal length of the optic nerve head was 2,530 ± 830 μm in group 1. The value was 1,920 ± 241 μm in group 2 and 1,530 ± 200 μm in the control subjects. The differences between groups 1 and 2 (P = 0.007) and group 1 and the control group (P < 0.01) were statistically significant. The mean horizontal length of the optic nerve head was positively correlated with the mean RNFL thickness (r = 0.557, P < 0.001), the mean SHYPS thickness (r = 0.757, P < 0.001), and the mean area of the SHYPS (r = 0.927, P < 0.001).
ONHD are a common, benign, congenital anomaly of the optic nerve, which rarely lead to decreased visual acuity (1,11). It is thought that the formation of ONHD is caused by axoplasmic transport alteration and axonal degeneration in the presence of a small scleral canal (12). In affected patients, the configuration of the optic nerve head is variable, and the drusen may be visible on the disc surface or buried within the disc.
It is buried ONHD that may simulate ODE and lead to diagnostic uncertainty. Techniques to differentiate these 2 conditions include funduscopy, optic disc autofluorescence, fluorescein angiography, B-scan ultrasonography, and CT scanning. B-scan ultrasonography has been shown to be superior to autofluorescence and CT (13). In recent years, there have been a number of reports evaluating OCT to distinguish between ODE and ONHD, focused primarily on measurements of the peripapillary RNFL thickness (6,8,10,14). RNFL thickness, especially in the nasal quadrant, has been shown to be decreased in ONHD when compared with ODE (8). In some patients with ONHD, photoreceptor changes also have been documented (15).
Using OCT, Savini et al (10) identified the SHYPS, a hyporeflective space located between the sensory retina and the retinal pigment epithelium and choriocapillaris in ODE patients. Johnson et al (7) found a decrease in the mean SHYPS thickness in ONHD patients compared with those with ODE. They considered the extravasated fluid from the optic nerve head, percolating into and elevating the subretinal space, as the most plausible cause for the increased SHYPS thickness. These investigators characterized the OCT appearance of ODE as an elevated optic nerve head with a smooth internal contour and a SHYPS thickness under the optic nerve head with a gradient taper away from the disc. A “lumpy bumpy” internal optic nerve contour and a more abrupt taper of the SHYPS (Fig. 2) were suggestive of ONHD (7). We differentiated ODE from ONHD using quantitative measures obtained with SD-OCT: peripapillary RNFL thickness, SHYPS thickness, area of the SHYPS, and degree of the α-angle.
Measuring RNFL thickness with SD-OCT, differentiation of ODE from ONHD ranged in sensitivity from 77% to 92% (temporal and nasal RNFL thicknesses greater than 101.5 and 74.5 μm, respectively) and specificity from 47% to 95% (α-angle greater than 141°). The mean RNFL thickness was higher in ODE patients in all quadrants when compared with that of ONHD patients. When we evaluated the respective peripapillary RNFL thicknesses, the ROC curve showed that the temporal and nasal RNFL thicknesses were the most important parameters for differentiating these 2 disorders. The temporal RNFL thickness greater than 101.5 μm had 92% sensitivity and 65% specificity. The nasal RNFL thickness greater than 74.5 μm had 92% sensitivity and 47% specificity. Johnson et al (7) reported 80% specificity and 70% sensitivity for the temporal RNFL thickness greater than 97 μm and nasal RNFL thickness greater than 86 μm for the differentiation of ONHD from ODE. Lee et al (8) investigated the differentiation of ONHD from ODE with SD-OCT and demonstrated the nasal RNFL thickness as the most important factor. They detected 80.0% sensitivity and 88.9% specificity for nasal RNFL thickness greater than 78.0 μm.
Measuring the thickness of the SHYPS also helped distinguish between ODE and ONHD, being greater in ODE patients. SHYPS thickness greater than 464 μm had 85% sensitivity and 60% specificity. Johnson et al (7) measured the SHYPS thickness at radii of 0.75, 1.5, and 2 mm in ONHD and ODE patients and reported the sensitivity and specificity for the 2-mm radius for SHYPS thickness as 70% and 90%, respectively (for SHYPS thickness >169 μm). Their cutoff point for this parameter was thinner than that of 464 μm in our study.
The area of the SHYPS and the α-angle were significantly higher in ODE patients than in patients with ONHD. These 2 parameters had the highest specificity values. The area of the SHYPS greater than 811 μm2 had 89% specificity and proved to be a better method of distinguishing ODE from ONHD than the thickness of the SHYPS, both in our study and previous reports (7,8). Measurement of the α-angle was also a highly predictive parameter as a measurement greater than 141° had a 95% specificity.
While the horizontal length of the optic nerve head in ODE patients was significantly greater than that in patients with ONHD and control subjects, it did not distinguish between patients with ONHD and control subjects. Our findings are in agreement with those of Floyd et al (16) and do not support the hypothesis that ONHD patients have a small scleral canal that causes a crowding effect on axonal transport or neural development.
We recognize the limitations of our study. First, the sample sizes were small with wide age range in all groups. Second, measurement of the α-angle was performed manually. Third, we did not evaluate the qualitative parameters of the optic nerve head and the peripapillary RNFL. Despite these limitations, we believe that our study presents promising findings in support of the use of SD-OCT in differentiating ODE from ONHD. Further studies with large patient groups are needed to validate the proposed cutoff values that we obtained.
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