TY - JOUR
T1 - Changes in multifocal electroretinograms induced by transpupillary thermotherapy
AU - Shimada, Yoshiaki
AU - Horiguchi, Masayuki
PY - 2005/8
Y1 - 2005/8
N2 - Objective: To determine retinal function after transpupillary thermotherapy (TTT) for subfoveal choroidal neovascularization using multifocal electroretinograms (mfERGs). Methods: Multifocal electroretinograms were recorded before and after TTT (wavelength, 810 nm; diameter, 3 mm; duration, 60 seconds; power, 350 mW) in 9 eyes in 9 patients with subfoveal choroidal neovascularizations. The stimulus consisted of 7 hexagons; the central hexagon covered the laser-irradiated area and the surrounding 6 hexagons covered the nonirradiated area. Each recording was completed within 1 minute, and mfERGs were recorded periodically during the first 60 minutes after TTT and also at 24 hours and 1 week after TTT. Results: The amplitude of mfERGs from irradiated areas was significantly reduced at 1 minute after TTT (P<.01) and then recovered soon. The peak time was prolonged at 15 minutes after TTT (P<.01), recovered to pre-TTT levels at 60 minutes, and then was prolonged again at 24 hours (P<.05) and 1 week (P<.05) after TTT. The mfERGs in nonirradiated areas were unchanged during the observational period. Conclusions: We found amplitude reduction in central focal ERGs at 1 minute after TTT, transient peak-time delay at 15 minutes, and a delay at 24 hours. Early reduction is probably directly caused by an increase in temperature during TTT as previously reported in focal flicker ERGs. Peak-time delays at 15 minutes and 24 hours may be caused by other factors, such as increased intracellular calcium (Ca 2+), the release of nitric oxide or heat shock proteins, vasodilation, or change in choroidal neovascularization. Our findings indicate that recording mfERGs may be a useful tool for evaluating TTT procedures.
AB - Objective: To determine retinal function after transpupillary thermotherapy (TTT) for subfoveal choroidal neovascularization using multifocal electroretinograms (mfERGs). Methods: Multifocal electroretinograms were recorded before and after TTT (wavelength, 810 nm; diameter, 3 mm; duration, 60 seconds; power, 350 mW) in 9 eyes in 9 patients with subfoveal choroidal neovascularizations. The stimulus consisted of 7 hexagons; the central hexagon covered the laser-irradiated area and the surrounding 6 hexagons covered the nonirradiated area. Each recording was completed within 1 minute, and mfERGs were recorded periodically during the first 60 minutes after TTT and also at 24 hours and 1 week after TTT. Results: The amplitude of mfERGs from irradiated areas was significantly reduced at 1 minute after TTT (P<.01) and then recovered soon. The peak time was prolonged at 15 minutes after TTT (P<.01), recovered to pre-TTT levels at 60 minutes, and then was prolonged again at 24 hours (P<.05) and 1 week (P<.05) after TTT. The mfERGs in nonirradiated areas were unchanged during the observational period. Conclusions: We found amplitude reduction in central focal ERGs at 1 minute after TTT, transient peak-time delay at 15 minutes, and a delay at 24 hours. Early reduction is probably directly caused by an increase in temperature during TTT as previously reported in focal flicker ERGs. Peak-time delays at 15 minutes and 24 hours may be caused by other factors, such as increased intracellular calcium (Ca 2+), the release of nitric oxide or heat shock proteins, vasodilation, or change in choroidal neovascularization. Our findings indicate that recording mfERGs may be a useful tool for evaluating TTT procedures.
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U2 - 10.1001/archopht.123.8.1066
DO - 10.1001/archopht.123.8.1066
M3 - Article
C2 - 16087839
AN - SCOPUS:23844504740
SN - 0003-9950
VL - 123
SP - 1066
EP - 1072
JO - Archives of Ophthalmology
JF - Archives of Ophthalmology
IS - 8
ER -