Newman Nancy J, Scherer Roberta, Langenberg Patricia, Kelman Shalom, Feldon Steven, Kaufman David, Dickersin Kay
Department of Ophthalmology, Neurology, and Neurological Surgery, Emory University School of Medicine, Atlanta, Georgia, USA.
Am J Ophthalmol. 2002 Sep;134(3):317-28. doi: 10.1016/s0002-9394(02)01639-2.
To examine the prevalence and incidence of second eye nonarteritic anterior ischemic optic neuropathy (NAION) and associated patient characteristics in patients enrolled in the Ischemic Optic Neuropathy Decompression Trial (IONDT) Follow-up Study.
Randomized clinical trial with observational cohort.
Patients randomized to optic nerve sheath decompression surgery or careful follow-up had a diagnosis of acute unilateral NAION, visual acuity between 20/64 and light perception, and were aged 50 years or older. Eligible patients who declined randomization or whose visual acuity was better than 20/64 were not randomized but followed as part of an observational cohort. Follow-up examinations took place at 3, 6, 12, 18, and 24 months and annually thereafter.
Four hundred eighteen patients were enrolled; 258 randomized and 160 observed. Previous NAION or other optic neuropathy was present in the fellow eye of 21.1% (88/418) of patients at baseline. Four patients developed optic neuropathy in the fellow eye at follow up that could not be conclusively diagnosed as NAION. New NAION in the fellow eye occurred in 14.7% (48/326) of patients at risk during a median follow up of 5.1 years. Randomized patients experienced a higher incidence (35/201; 17.4%) than nonrandomized patients (13/125; 10.4%). A history of diabetes and baseline visual acuity of 20/200 or worse in the study eye, but not age, sex, aspirin use, or smoking were significantly associated with new NAION in the fellow eye. Final fellow eye visual acuity was significantly worse in those patients with new fellow eye NAION whose baseline study eye visual acuity was 20/200 or worse.
Follow-up data from the IONDT cohort provide evidence that the incidence of fellow eye NAION is lower than expected: new NAION was diagnosed in 14.7% of IONDT patients over approximately 5 years. Increased incidence is associated with poor baseline visual acuity in the study eye and diabetes, but not age, sex, smoking history, or aspirin use.
在缺血性视神经病变减压试验(IONDT)随访研究的患者中,研究对侧眼非动脉炎性前部缺血性视神经病变(NAION)的患病率、发病率及相关患者特征。
随机临床试验及观察性队列研究。
随机分为视神经鞘减压手术组或密切随访组的患者,均诊断为急性单侧NAION,视力在20/64至光感之间,年龄50岁及以上。拒绝随机分组或视力优于20/64的符合条件患者未进行随机分组,而是作为观察性队列的一部分进行随访。随访检查在3、6、12、18和24个月时进行,此后每年进行一次。
共纳入418例患者;258例随机分组,160例观察。基线时,21.1%(88/418)的患者对侧眼存在既往NAION或其他视神经病变。4例患者在随访期间对侧眼发生视神经病变,但无法明确诊断为NAION。在中位随访5.1年期间,有发生对侧眼新NAION风险的患者中,14.7%(48/326)出现了对侧眼新NAION。随机分组患者的发病率(35/201;17.4%)高于非随机分组患者(13/125;10.4%)。糖尿病病史以及研究眼基线视力为20/200或更差,而非年龄、性别、阿司匹林使用情况或吸烟,与对侧眼新NAION显著相关。基线研究眼视力为20/200或更差的对侧眼发生新NAION的患者,其对侧眼最终视力明显更差。
IONDT队列的随访数据表明,对侧眼NAION的发病率低于预期:在大约5年的时间里,14.7%的IONDT患者被诊断为对侧眼新NAION。发病率增加与研究眼基线视力差和糖尿病有关,但与年龄、性别、吸烟史或阿司匹林使用无关。