Maturi Raj K, Bleau Laura A, Wilson Donald L
Vitreo-retinal Service, Midwest Eye Institute, Indianapolis, Indiana 46280, USA.
Retina. 2006 Mar;26(3):270-4. doi: 10.1097/00006982-200603000-00003.
To evaluate the short-term electrophysiologic effects of intravitreal bevacizumab in the treatment of exudative age-related macular degeneration (AMD).
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).
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 15 degrees 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.
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.
评估玻璃体内注射贝伐单抗治疗渗出性年龄相关性黄斑变性(AMD)的短期电生理效应。
9例接受玻璃体内注射贝伐单抗治疗渗出性AMD的患者,在治疗前接受了多焦视网膜电图(mf-ERG)或全视野视网膜电图(G-ERG)检查。所有5例接受G-ERG检查的患者在玻璃体内注射贝伐单抗后1周进行了重复检查。所有4例接受mf-ERG检查的患者以及5例接受G-ERG检查患者中的4例,在治疗后1个月按照相同的治疗前方案进行了重复检查。1例接受G-ERG检查的患者在初始治疗后6周还接受了第二次玻璃体内注射贝伐单抗,并在第二次注射后1个月(初始治疗后3个月)进行了重复检查。
所有4例接受mf-ERG检查的患者在治疗后1个月黄斑反应均有改善。黄斑反应中心15度区域反应密度的平均改善率为35%(范围为11%-65%)。接受G-ERG检查的患者电生理反应无显著变化,尽管在不同检查时间点观察到波幅和潜伏时存在一些差异。光学相干断层扫描中心子野厚度从基线时的298微米降至治疗后1个月的274微米。大多数患者的视力有所改善。
在本研究中,玻璃体内注射贝伐单抗可改善mf-ERG黄斑功能反应,并使G-ERG反应相对稳定。黄斑电生理反应表明黄斑功能随治疗而改善。G-ERG提示短期内玻璃体内注射贝伐单抗不存在可测量的显著光感受器毒性。