fmERGs were recorded from 14 eyes of 14 patients with CNV associated with AMD and one patient with idiopathic CNV. fmERGs were recorded before and 3 months after vitrectomy for the removal of CNV between March 1999 and December 2000. The final follow up of these patients ranged from 5 to 27 months (14.2 ± 1.7 months, mean ± SE).
The standard Japanese visual acuity chart was used for acuity measurements, and the results were converted to Snellen visual acuity. The preoperative best corrected visual acuity ranged from counting fingers to 20/25. The size of the CNV lesion was measured on indocyanine green angiograms recorded by confocal scanning laser ophthalmoscopy (HRA; Heidelberg Engineering, Carlsbad, CA). The average size of the lesion was 0.94 ± 0.16 disc diameters (DD, range, 0.25–2.1 DD). The lesions were located subfoveally (beneath the fovea) or juxtafoveally (beneath the foveal avascular area but not beneath the center of the fovea), and the main part of the lesion was located on the RPE, in all cases.
OCT (Humphrey Instruments, San Leandro, CA) was performed before and 3 months after surgery, after the fmERG recordings. The images were cross-sectional scans passing through the fovea horizontally and vertically. The foveal thickness was calculated as the mean of the vertical and horizontal thicknesses at the fovea. The parafoveal thickness was calculated as the mean thickness at four points, 1 mm nasally, temporally, superiorly, and inferiorly from the fovea, according to the OCT images that passed through the fovea.
The surgical technique consisted of a standard three-port pars plana vitrectomy. The posterior hyaloid was separated from the retina after the cortical vitreous was removed. A retinotomy was made, and balanced saline solution was injected into the subretinal space with a 36-gauge subretinal cannula. The CNV membrane was removed through the retinotomy site by subretinal forceps. The irrigation pressure was increased to 60 to 80 mm Hg for 2 minutes, and fluid–air exchange was performed. Six eyes underwent intraocular lens surgery simultaneously, and four eyes underwent intraocular lens surgery 2 to 6 months after the first vitrectomy.
The system and the techniques for recording fmERGs under direct fundus observation have been described in detail.
9 10 Briefly, an infrared fundus camera, equipped with a stimulus light, background illumination, and fixation target, was used. The image from the camera was fed to a cathode-ray tube (CRT) monitor, and the examiner used the monitor to maintain the stimulus on the macula. The size of the stimulus spot was adjustable, and we selected a 15° spot stimulus centered on the fovea. The background light was delivered to the eye from the fundus camera at a visual angle of 45°. Additional background illumination outside the central 45° produced a homogeneous background illumination for nearly the entire visual field.
A Burian-Allen bipolar contact lens electrode was used for the electroretinographic recordings and allowed not only an extremely low noise level but also a clear view of the fundus displayed on the CRT monitor. The intensity of the white stimulus light and background light was 29.46 cd/m2 and 2.89 cd/m2, respectively.
After the patients’ pupils were fully dilated with 0.5% tropicamide and 0.5% phenylephrine hydrochloride, fmERGs were elicited by 5-Hz rectangular stimuli (100-ms light on and 100-ms light off). A total of 512 responses were averaged by a signal processor. A time constant of 0.03 seconds with a 100-Hz high-cut filter on the amplifier was used to record the a- and b-waves, and the time constant was reduced to 0.003 seconds for recording the oscillatory potentials (OPs).
The amplitude of the a-wave was measured from the baseline to the peak of the a-wave. The amplitude of b-wave was measured from the trough of the a-wave to the peak of the b-wave. The amplitude of each OP wavelet was measured from a baseline drawn, as a first order approximation, between the troughs of successive wavelets to its peak.
The research was conducted in accordance with institutional guidelines and conformed to the tenets of the World Medical Association’s Declaration of Helsinki. After providing sufficient information on other treatment options, including observation only, and information that macular electroretinography would bring little immediate benefit but would bring about the recovery of retinal function after surgery, an informed consent was obtained for the surgical removal of the CNV lesion and performance of fmERGs.