De Gregorio F, Pecori Giraldi J, Pannarale L, Saccucci S, Virno M
Department of Ocular Physio-Pharmacology, Eye Clinic, University La Sapienza, Rome, Italy.
Int Ophthalmol. 1996;20(1-3):151-5. doi: 10.1007/BF00212962.
Ibopamine is used when performing provocative tests, thanks to its pharmacological property of increasing ocular pressure in eyes with outflow system impairment. This study summarizes the latest results that we have achieved with reference to its clinical-diagnostic use.
175 (250 eyes) POAG patients, 101 (190 eyes) glaucoma suspects with mild ocular hypertension, 39 (64 eyes) NTG patients and 163 (326 eyes) healthy volunteers underwent an ibopamine provocative test. Among the POAG and the glaucoma suspects, 49 (92 eyes) and 20 (38 eyes) patients were selected who, starting from the performing of ibopamine test, had at least one year of perimetric follow-up. These patients have been assessed for the perimetric defect progression in relation to the (negative or positive) response to ibopamine.
the ibopamine test was positive for 92% of the glaucomatous patients, 61% of the glaucoma suspects, 52% of the NTG patients and 0% of the healthy volunteers. It was observed that 28% of the ibopamine-positive glaucoma suspects showed a perimetric deterioration during an average 2.5-year follow-up. No perimetric deterioration was found on ibopamine-negative glaucoma suspects (Fisher's exact test: p = 0.038). Among glaucomatous patients, 46% of the test-positive individuals showed a progressive trend of the perimetric defect, as against about 8% of glaucomatous test-negative patients (Fisher's exact test: p = 0.003).
We believe that the ibopamine provocative test can be usefully applied especially to epidemiological screening studies to identify patients who might develop ocular hypertension or glaucoma and in the follow-up of glaucoma suspects, to identify individuals who have a greater risk of developing perimetric defects.
由于异波帕明具有使房水流出系统受损的眼睛眼压升高的药理特性,因此在进行激发试验时会使用该药物。本研究总结了我们在其临床诊断应用方面取得的最新成果。
175例(250只眼)原发性开角型青光眼(POAG)患者、101例(190只眼)轻度高眼压青光眼疑似患者、39例(64只眼)正常眼压性青光眼(NTG)患者和163例(326只眼)健康志愿者接受了异波帕明激发试验。在POAG患者和青光眼疑似患者中,分别选取了49例(92只眼)和20例(38只眼)从进行异波帕明试验开始至少有一年视野随访的患者。对这些患者根据异波帕明试验(阴性或阳性)反应评估视野缺损进展情况。
异波帕明试验在92%的青光眼患者、61%的青光眼疑似患者、52%的NTG患者中呈阳性,在健康志愿者中呈阳性的比例为0%。观察到,在平均2.5年的随访期间,28%异波帕明试验阳性的青光眼疑似患者出现了视野恶化。异波帕明试验阴性的青光眼疑似患者未发现视野恶化(Fisher精确检验:p = 0.038)。在青光眼患者中,46%试验阳性个体的视野缺损呈进行性趋势,而异波帕明试验阴性的青光眼患者这一比例约为8%(Fisher精确检验:p = 0.003)。
我们认为,异波帕明激发试验尤其可有效地应用于流行病学筛查研究,以识别可能发生高眼压或青光眼的患者,以及在青光眼疑似患者的随访中,识别发生视野缺损风险更高的个体。