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SALIM-TAMUZ ABBOUD<br />

Reproducibility <strong>of</strong> Serial Optical Coherence Tomography<br />

Without Pharmacologic Pupillary Dilatation<br />

Background:<br />

Salim Abboud<br />

Department <strong>of</strong> Neurology, The Cleveland Clinic, Mellen Center<br />

Optical Coherence Tomography (OCT) is a technique proposed for longitudinal monitoring <strong>of</strong> multiple sclerosis,<br />

and as an outcome measure in clinical trials. However, little is known about the precision <strong>of</strong> serial<br />

measurements when implemented without the use <strong>of</strong> pharmacologic pupillary dilatation (PPD). Quantification <strong>of</strong><br />

the variability <strong>of</strong> serial measurements is necessary for sample size calculations in planning clinical trials.<br />

Methods:<br />

Peripapillary retinal nerve fiber layer thickness (RNFLT) and macular volume (MV) were serially measured in ten<br />

consecutive healthy volunteers (20 eyes) using the Zeiss Stratus OCT system by ―Fast RNFL‖ and ―Fast macular<br />

thickness‖ scan protocols without PPD. In each subject, two serial measurements were obtained at least one<br />

week apart by a single operator. A third set <strong>of</strong> measurements was acquired using the ―repeat‖ scan registration<br />

function to evaluate its reproducibility compared to serial independent measurements. Only signal strengths <strong>of</strong><br />

6 and above were accepted for each scan. The relationship between signal strength and reproducibility was<br />

evaluated.<br />

Results:<br />

Mean RNFLT in the group was 96.65uM. Mean macular volume was 6.81mm3. Coefficients <strong>of</strong> variation (COV) for<br />

independent serial measures was 2.86% for RNFLT and 1.90% for MV. COV for RNFLT and MV using the repeat<br />

function were 3.14% and 1.16%, respectively. Median signal strength for RNFLT was 8 (range 6.5-10), and for<br />

MV was 9 (range 6.5-10). The correlation between OCT signal strength and individual COV for serial<br />

independent measure <strong>of</strong> RNFL approached significance (r=-.41, p=0.07).<br />

Conclusions:<br />

Serial measurements <strong>of</strong> RNFL and MV are sufficiently precise to employ as outcome measures in clinical trials<br />

when implemented without PPD. Despite a trend for higher signal strengths to provide more precise data, signal<br />

strengths greater than 6 are easily achievable and highly precise. Reproducibility may be lower in patients with<br />

MS who potentially have impairment <strong>of</strong> visual acuity and ocular motility.<br />

Supported by the Crile Fellowship<br />

4

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