Keltner J L, Johnson C A, Quigg J M, Cello K E, Kass M A, Gordon M O
Department of Ophthalmology, University of California, Davis, Sacramento, CA 95817, USA.
Arch Ophthalmol. 2000 Sep;118(9):1187-94. doi: 10.1001/archopht.118.9.1187.
To determine the frequency with which visual field abnormalities observed on follow-up visual fields for patients in the Ocular Hypertension Treatment Study were confirmed on retest.
Between April 1, 1994, and March 1, 1999, 21,603 visual fields were obtained from 1637 patients in the Ocular Hypertension Treatment Study. When follow-up visual fields are outside the normal limits on the Glaucoma Hemifield Test, the Corrected Pattern Standard Deviation (P<.05), or both, subsequent follow-up visual fields are monitored to confirm the abnormality. Abnormalities are confirmed if they are again abnormal on the Glaucoma Hemifield Test, the Corrected Pattern Standard Deviation, or both; if the defect is not artifactual; and if the same index and location are involved. Reliability criteria used by the study consisted of a limit of 33% for false positives, false negatives, and fixation losses.
Of the 21,603 regular follow-up visual fields, 1006 were follow-up retests performed because of an abnormality (n = 748) or unreliability (n = 258). We found that 703 (94%) of the 748 visual fields were abnormal and reliable, and 45 (6%) were abnormal and unreliable. On retesting, abnormalities were not confirmed for 604 (85.9%) of the 703 originally abnormal and reliable visual fields.
Most visual field abnormalities in patients in the Ocular Hypertension Treatment Study were not verified on retest. Confirmation of visual field abnormalities is essential for distinguishing reproducible visual field loss from long-term variability. Arch Ophthalmol. 2000;118:1187-1194
确定在眼压升高治疗研究中,患者随访视野检查中观察到的视野异常在复测时被证实的频率。
在1994年4月1日至1999年3月1日期间,从眼压升高治疗研究中的1637例患者获得了21603次视野检查结果。当随访视野在青光眼半视野检测、校正模式标准差(P<0.05)或两者中超出正常范围时,对后续随访视野进行监测以确认异常。如果在青光眼半视野检测、校正模式标准差或两者中再次出现异常;如果缺陷不是人为造成的;并且如果涉及相同的指标和位置,则异常被证实。该研究使用的可靠性标准包括假阳性、假阴性和固视丢失的限度为33%。
在21603次常规随访视野中,1006次是由于异常(n = 748)或不可靠(n = 258)而进行的随访复测。我们发现,748次视野中有703次(94%)异常且可靠,45次(6%)异常但不可靠。在复测时,703次最初异常且可靠的视野中有604次(85.9%)异常未被证实。
眼压升高治疗研究中患者的大多数视野异常在复测时未得到证实。视野异常的确认对于区分可重复的视野缺损和长期变异性至关重要。《眼科学文献》。2000年;118:1187 - 1194