Keck School of Medicine at the University of Southern California, Los Angeles, California.
Roski Eye Institute, Department of Ophthalmology, Keck School of Medicine at the University of Southern California, Los Angeles, California.
Ophthalmol Glaucoma. 2023 Mar-Apr;6(2):169-176. doi: 10.1016/j.ogla.2022.08.016. Epub 2022 Sep 2.
To assess rates of diagnostic conversion from anatomical narrow angle (ANA) to primary angle-closure glaucoma (PACG) in the United States and identify factors associated with diagnostic conversion.
Retrospective case-control study.
Patients diagnosed with ANA between the years 2007 and 2019 were identified based on International Classification of Diseases (ICD) codes in the Optum Clinformatics Data Mart Database. Inclusion was limited to newly diagnosed ANA, defined as the following: (1) continuous enrollment during a 2-year look back period and 6-year study period from index (first) date of ANA diagnosis; (2) diagnosis by an ophthalmologist or optometrist and record of gonioscopy; and (3) no history of intraocular pressure (IOP)-lowering drops, laser peripheral iridotomy (LPI), or intraocular surgery.
Cox proportional hazards models were developed to assess factors associated with diagnostic conversion, defined as a change in ICD code from ANA to PACG.
New diagnosis of PACG within the 6-year study period recorded after an index diagnosis of ANA.
Among 3985 patients meeting inclusion criteria, 459 (11.52%) had detected diagnostic conversion to PACG within the study period. The conversion rate was stable at 3.54% per year after the first 6 months of ANA diagnosis. In the Cox proportional hazards model, age > 70 years and early (within 6 months of ANA diagnosis) need for LPI or IOP-lowering drops were positively associated with diagnostic conversion (hazard ratio [HR] > 1.59; P < 0.02). Cataract surgery at any time and late (after 6 months of ANA diagnosis) need for IOP-lowering drops appeared protective against diagnostic conversion (HR < 0.46; P < 0.004).
Annual risk of diagnostic conversion from ANA to PACG is relatively low overall; elderly patients are at higher risk whereas patients receiving cataract surgery are at lower risk. The utility of long-term monitoring seems low for most patients with ANA, highlighting the need for improved clinical methods to identify patients at higher risk for PACG.
FINANCIAL DISCLOSURE(S): Proprietary or commercial disclosure may be found after the references.
评估美国解剖性窄房角(ANA)至原发性闭角型青光眼(PACG)的诊断转化率,并确定与诊断转化相关的因素。
回顾性病例对照研究。
根据 Optum Clinformatics Data Mart 数据库中的国际疾病分类(ICD)代码,确定 2007 年至 2019 年间诊断为 ANA 的患者。纳入标准仅限于新诊断的 ANA,定义如下:(1)在 ANA 诊断的前 2 年回顾期和 6 年研究期内持续入组;(2)由眼科医生或验光师诊断,并记录房角镜检查结果;(3)无眼压(IOP)降低滴注、激光周边虹膜切开术(LPI)或眼内手术史。
采用 Cox 比例风险模型评估与诊断转化相关的因素,诊断转化定义为 ICD 代码从 ANA 变为 PACG。
ANA 诊断后 6 年内新诊断为 PACG。
在符合纳入标准的 3985 名患者中,459 名(11.52%)在研究期间发现诊断为 PACG。ANA 诊断后前 6 个月的转化率为每年 3.54%,此后转化率稳定。在 Cox 比例风险模型中,年龄>70 岁和早期(ANA 诊断后 6 个月内)需要行 LPI 或 IOP 降低滴注与诊断转化呈正相关(风险比[HR]>1.59;P<0.02)。任何时候行白内障手术和晚期(ANA 诊断后 6 个月后)需要 IOP 降低滴注似乎可预防诊断转化(HR<0.46;P<0.004)。
ANA 至 PACG 的诊断转化率总体上相对较低;老年患者风险较高,而接受白内障手术的患者风险较低。对于大多数 ANA 患者,长期监测的效用似乎较低,这凸显了需要改进临床方法来识别 PACG 风险较高的患者。
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