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Electrophysiologic findings after intravitreal bevacizumab (Avastin) treatment.

机译:玻璃体内贝伐单抗(Avastin)治疗后的电生理结果。

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PURPOSE: To evaluate the short-term electrophysiologic effects of intravitreal bevacizumab in the treatment of exudative age-related macular degeneration (AMD). METHODS: Nine subjects with AMD who received treatment with intravitreal bevacizumab for exudative AMD underwent pretreatment testing with multifocal electroretinography (mf-ERG) or Ganzfeld electroretinography (G-ERG). All five G-ERG subjects underwent repeated testing at 1 week after intravitreal bevacizumab. All four mf-ERG subjects and four of the five G-ERG subjects underwent repeated testing with the same pretreatment protocol at 1 month after treatment. One G-ERG subject also received a second intravitreal injection of bevacizumab at 6 weeks after initial treatment and underwent repeated testing at 1 month after the second dose (3 months after initial treatment). RESULTS: All four subjects undergoing mf-ERG had improvement of the macular response at 1 month of after treatment. The average improvement in response density of the central 15degrees of macular response was 35% (range, 11-65%). Subjects undergoing G-ERG testing had no significant changes in electrophysiologic response, although some variation in amplitude and implicit time was noted at different testing times. Optical coherence tomography central subfield thickness decreased from 298 microm at baseline to 274 microm at 1 month after treatment. Visual acuity improved in a majority of subjects. CONCLUSION: In this study, the intravitreal use of bevacizumab resulted in improvement of mf-ERG macular function responses and relatively stable G-ERG responses. The macular electrophysiologic response suggests that macular function improves with treatment. G-ERG suggests that there is no significant measurable photoreceptor toxicity with the use of intravitreal bevacizumab over the short term.
机译:目的:评估玻璃体内贝伐单抗在治疗渗出性年龄相关性黄斑变性(AMD)中的短期电生理作用。方法:9名接受玻璃体内贝伐单抗治疗渗出性AMD的AMD患者接受了多焦点视网膜电图(mf-ERG)或甘兹菲尔德视网膜电图(G-ERG)的预处理测试。玻璃体内贝伐单抗治疗后1周,所有5名G-ERG受试者均接受了重复测试。在治疗后1个月,所有四名mf-ERG受试者和五名G-ERG受试者中的四名均接受了相同的预处理方案重复测试。一名G-ERG受试者在初次治疗后第6周也接受了贝伐单抗的第二次玻璃体内注射,并在第二次给药后1个月(初次治疗后3个月)进行了重复测试。结果:所有接受mf-ERG治疗的4名受试者在治疗后1个月时黄斑反应均得到改善。黄斑中心点15度中心反应密度的平均改善幅度为35%(范围为11-65%)。进行G-ERG测试的受试者的电生理反应没有明显变化,尽管在不同的测试时间注意到幅度和隐性时间有些变化。治疗后1个月,光学相干断层扫描的中央子场厚度从基线的298微米降低到274微米。大多数受试者的视力得到改善。结论:在这项研究中,贝伐单抗的玻璃体内使用可改善mf-ERG黄斑功能反应和相对稳定的G-ERG反应。黄斑电生理反应表明黄斑功能随着治疗而改善。 G-ERG表明,短期内使用玻璃体内贝伐单抗没有明显的可测量光感受器毒性。

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