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Evaluation of cone function by a handheld non-mydriatic flicker electroretinogram device

机译:通过手持式非散瞳闪烁视网膜电图仪评估锥体功能

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Purpose: Full-field electroretinograms (ERGs) are used to evaluate retinal function in patients with various types of hereditary and acquired retinal diseases. However, ERG recordings require relatively invasive procedures, including pupillary dilation and the use of contact lens electrodes. Thus, it would be helpful to have a simpler and noninvasive screening method. The purpose of this study was to determine whether a new, handheld, portable ERG device, RETeval?, can be used to screen patients for cone dysfunction. Patients and methods: Thirty-five eyes of 35 patients who had reduced cone responses ascertained by a conventional ERG system using contact lens electrodes were studied. The causative diseases included achromatopsia, cone dystrophy, cone-rod dystrophy, retinitis pigmentosa, choroidal dystrophy, autoimmune retinopathy, and Stargardt disease. The flicker ERGs were recorded with the RETeval? under undilated conditions with skin electrodes (stimulus strength, 3.0 cd·s/m2; frequency, 28.3 Hz), and the responses were compared to that of 50 healthy eyes. The amplitudes and implicit times of the fundamental component of the flicker ERGs were analyzed in three age groups: Group A, ≤20 years; Group B, 21–40 years; and Group C, ≥41 years. Results: In all of the age groups, the amplitudes of the ERGs were significantly smaller and the implicit times significantly longer in patients with cone dysfunction than in the control eyes. All but one of the patients had flicker amplitudes lower than the mean ?2.0 standard deviation of control eyes. Conclusion: The RETeval? has a potential of being used to screen for cone dysfunction. The entire examination takes <5 minutes and does not require pupil dilatation or a contact lens electrode. Although the flicker responses do not provide information on the scotopic functions, the RETeval? device can be used to determine which patients require additional full-field ERG testing with dilated pupils under both scotopic and photopic conditions.
机译:目的:全场视网膜电图(ERG)用于评估患有各种遗传性和后天性视网膜疾病的患者的视网膜功能。然而,ERG记录需要相对侵入性的程序,包括瞳孔扩张和使用隐形眼镜电极。因此,拥有一种更简单,无创的筛查方法将很有帮助。这项研究的目的是确定是否可以使用新的手持式便携式ERG设备RETeval?筛查视锥功能障碍的患者。患者和方法:研究了35例通过使用隐形眼镜电极的常规ERG系统确定的视锥反应降低的35眼患者。致病性疾病包括无色症,视锥细胞营养不良,视锥杆营养不良,色素性视网膜炎,脉络膜营养不良,自身免疫性视网膜病和Stargardt病。用RETeval记录闪烁的ERG。在未扩张的条件下使用皮肤电极(刺激强度为3.0 cd·s / m 2 ;频率为28.3 Hz),并将其响应与50只健康的眼睛进行比较。在三个年龄组中分析了闪烁ERGs基本成分的振幅和隐含时间:A组,≤20岁; A组,≤20岁; A组,≤20岁。 B组,21–40岁; C组,≥41岁。结果:在所有年龄组中,视锥细胞功能障碍患者的ERGs幅度均明显小于对照组,而隐性时间明显更长。除一名患者外,所有患者的闪烁幅度均低于对照眼的平均±2.0标准差。结论:RETeval?有可能被用于筛查锥体功能障碍。整个检查过程少于5分钟,不需要瞳孔散大或隐形眼镜电极。尽管闪烁响应未提供有关暗视功能的信息,但RETeval?该设备可用于确定哪些患者需要在暗视和明视条件下对散瞳进行额外的全视野ERG测试。

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