Hashimoto E, Hagiwara T, Hashimoto T, Namba K, Utsumi T, Azuma I
Department of Ophthalmology, Osaka Medical College, Takatsuki, Japan.
Nippon Ganka Gakkai Zasshi. 1991 Mar;95(3):265-72.
The authors previously reported light reflex abnormalities and adrenergic supersensitivity to topical epinephrine (DPE; dipivalyl epinephrine) of the pupils in patients with ocular hypertension (OH) and those with primary open angle glaucoma (POAG). In this investigation, we attempted to reconfirm pupillary light reflex abnormalities we reported previously, and to investigate the relationship between the normotensive effect of 0.1% DPE and the pupillary light reflex abnormalities in OHs and POAGs. A total of 11 OHs and 11 POAGs under good oculotensive control with neither mydriatics nor miotics were examined. They were measured by an open-loop photically stimulated infrared videopupilogram, and were neurologically diagnosed by comparing the simulated patterns of the light reflex made by topical autonomic agents. When we considered the progress of the stage of POAG, both OHs and POAGs showed satisfactory reproducibility of pupillary light reflex abnormalities. Other cases in which light reflexes altered, showed worsening of the visual field deficit, which was prominent when OHs developed into POAG. OHs with significant reduction of intraocular pressure (IOP) after topical administration of 0.1% DPE showed various kinds of abnormal pupillary light reflexes. On the contrary, cases with little reduction of IOP after 0.1% DPE instillation showed normal pupillary light reflexes in OHs and afferent pupillary defect on POAGs.
作者之前报道过高眼压症(OH)患者和原发性开角型青光眼(POAG)患者存在光反射异常以及瞳孔对局部肾上腺素(DPE;二特戊酰肾上腺素)的肾上腺素能超敏反应。在本研究中,我们试图再次确认我们之前报道的瞳孔光反射异常,并研究0.1% DPE的降眼压作用与OH和POAG患者瞳孔光反射异常之间的关系。共检查了11例眼压控制良好、未使用散瞳剂或缩瞳剂的OH患者和11例POAG患者。通过开环光刺激红外视频瞳孔图对他们进行测量,并通过比较局部自主神经药物产生的模拟光反射模式进行神经学诊断。当我们考虑POAG分期的进展时,OH患者和POAG患者的瞳孔光反射异常均显示出令人满意的可重复性。光反射改变的其他病例显示视野缺损恶化,当OH发展为POAG时这种情况尤为明显。局部应用0.1% DPE后眼压显著降低的OH患者表现出各种异常的瞳孔光反射。相反,0.1% DPE滴注后眼压降低很少的病例在OH患者中表现出正常的瞳孔光反射,而在POAG患者中表现出传入性瞳孔缺陷。