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Central and peripheral vision loss associated with nefazodone usage

机译:与奈法唑酮使用相关的中枢和周围视力丧失

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A 35-year-old woman who reported persistent significant vision loss for 3 years after taking the antidepressant nefazodone was referred for electrophysiological assessment of vision. The vision changes included reduced acuities, reduced colour vision and visual field constriction in both eyes and were thought to be associated with the use of nefazodone for 6 – 8 weeks, 3 years earlier. Multifocal electroretinograms and visual evoked potentials were recorded using the Visual Evoked Response Imaging System (VERIS) to investigate the nature and site of the neural deficit. The summed retinal response showed a normal a- and b-wave latency and amplitude, however, the retinal topographic mfERGs showed a severe depression of the macular response in both eyes. The cortical topographic multifocal VEP mapping also showed a central depression in the right eye compared with the left. Two-frame motion and pattern custom mfVEP were also measured to assess different forms of cortical processing and especially of motion as nefazodone has previously been associated with image persistence with moving stimuli. The responses to two frame-motion showed signs of abnormality. Thus these results suggest that the primary locus of neural damage is retinal and is likely to have resulted from neurotoxicity. Other competing hypotheses such as hysterical blindness must be ruled out.
机译:一名35岁的妇女在服用抗抑郁药奈法唑酮后连续3年出现持续严重的视力丧失,因此被转介进行视力的电生理评估。视力变化包括敏锐度降低,双眼色觉减弱和视野狭窄,被认为与3年前使用奈法唑酮有关6-8周。使用视觉诱发反应成像系统(VERIS)记录多焦视网膜电图和视觉诱发电位,以研究神经缺陷的性质和部位。总计的视网膜反应显示出正常的a和b波潜伏期和振幅,但是,视网膜地形图mfERGs显示两只眼睛的黄斑反应均严重降低。与左眼相比,皮层地形多焦点VEP映射在右眼也显示出中央凹陷。还测量了两帧运动和模式自定义mfVEP,以评估不同形式的皮层处理,尤其是运动,因为奈法唑酮以前曾与运动刺激的图像持久性相关。对两次框架运动的反应均显示异常迹象。因此,这些结果表明神经损伤的主要部位是视网膜,并且很可能是由神经毒性引起的。必须排除其他竞争假设,例如歇斯底里的盲目性。

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