Description:
<jats:title>Abstract</jats:title><jats:sec><jats:title>Background</jats:title><jats:p>The purpose of the study was to evaluate the safety and selectivity of the retinal pigment epithelium lesions by using automatic energy ramping and dosimetry technique for selective retina therapy and to investigate the healing response.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Ten eyes of <jats:styled-content style="fixed-case">C</jats:styled-content>hinchilla <jats:styled-content style="fixed-case">B</jats:styled-content>astard rabbits were treated with an automatic dosage controlled selective retina therapy laser (frequency doubled <jats:styled-content style="fixed-case">Q</jats:styled-content>‐switched <jats:styled-content style="fixed-case">N</jats:styled-content>d:<jats:styled-content style="fixed-case">YLF</jats:styled-content>, wavelength: 527 nm, pulse duration: 1.7 μs, repetition rate: 100 <jats:styled-content style="fixed-case">H</jats:styled-content>z, pulse energy: linear increasing from pulse to pulse up to shut down – maximal 110 μ<jats:styled-content style="fixed-case">J</jats:styled-content>, max. number of pulses in a burst: 30, retinal spot diameter: 133 μm). After treatment, fundus photography, optical coherence tomography and fluorescein angiography were performed at three time points from 1 h to 3 weeks. Histological analysis was performed.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>A total of 381 selective retina therapy laser spots were tested (range 13–104 μ<jats:styled-content style="fixed-case">J</jats:styled-content>).Typical fundus photographs obtained at 1 h after irradiation showed that 379 out of 381 lesions produced by selective retina therapy were not visible ophthalmoscopically and the lesions could be detected by angiography only. Optical coherence tomography images revealed that the structure of photoreceptors was preserved, but a disrupted retinal pigment epithelium layer was observed as was expected. By 3 weeks, histology showed selective retinal pigment epithelium damage without any effect on the inner retina and focal proliferation of the retinal pigment epithelium layer.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>Automatically controlled selective retina therapy is a significant improvement in this innovative treatment. It could be demonstrated that the non‐contact, reflectometric technique with a controlled pulse energy ramp is safe and selective.</jats:p></jats:sec>