Fugara Nasser A, Shawareb Zaineh A, Rakkad Nancy K, Barhoum Manar L, Shawareb Bana A, Al-Madani Myrna M, Al-Madani Mousa V
Ophthalmology, King Hussein Medical Center, Royal Medical Services of Jordanian Armed Forces, Amman, JOR.
Cureus. 2022 Oct 11;14(10):e30185. doi: 10.7759/cureus.30185. eCollection 2022 Oct.
To report the incidence of non-arteritic ischemic optic neuropathy in diabetic patients treated with intravitreal bevacizumab injection.
A prospective comparative analytic study was done in the King Hussein Medical Center during the period between June 2020 and June 2021. Inclusion criteria included diabetic patients who attended a retina clinic. Exclusion criteria included patients with pre-existing ischemic optic neuropathy. Patients were divided into two groups. The first group included diabetic patients who did not require bevacizumab injection and were treated either with follow-up visits or pan-retinal photocoagulation, and the second group included patients who were treated with intravitreal bevacizumab. Patients were followed up for a period of one year. Data collected in two groups included the total number of patients and the number of patients with non-arteritic ischemic optic neuropathy. Results were compared in both groups. A P-value was used to study the statistical significance and was considered to be statistically significant if ≤0.05.
The mean age for patients in group 1 was 64.3 years, with a male to female ratio of 1.1 to 1. In group 2, the mean age was 66.2 years, with a male to female ratio of 1.2 to 1. The total number of patients in group 1 was 7375, among whom 68 patients had non-arteritic ischemic optic neuropathy. While in group 2, the total number was 2468 and 49 of them had non-arteritic ischemic optic neuropathy. Most cases of non-arteritic ischemic optic neuropathy were seen in patients who had received three or more injections. Conclusion: Intravitreal bevacizumab in diabetic patients is considered a risk factor for the development of non-arteritic ischemic optic neuropathy, especially in patients receiving more than three injections.
报告玻璃体内注射贝伐单抗治疗的糖尿病患者中非动脉炎性缺血性视神经病变的发生率。
2020年6月至2021年6月期间,在侯赛因国王医疗中心进行了一项前瞻性对比分析研究。纳入标准包括就诊于视网膜诊所的糖尿病患者。排除标准包括既往有缺血性视神经病变的患者。患者分为两组。第一组包括不需要注射贝伐单抗、接受随访或全视网膜光凝治疗的糖尿病患者,第二组包括接受玻璃体内贝伐单抗治疗的患者。对患者进行了为期一年的随访。两组收集的数据包括患者总数和非动脉炎性缺血性视神经病变患者数量。对两组结果进行比较。采用P值研究统计学意义,若P值≤0.05,则认为具有统计学意义。
第一组患者的平均年龄为64.3岁,男女比例为1.1:1。第二组患者的平均年龄为66.2岁,男女比例为1.2:1。第一组患者总数为7375例,其中68例患有非动脉炎性缺血性视神经病变。而第二组患者总数为2468例,其中49例患有非动脉炎性缺血性视神经病变。大多数非动脉炎性缺血性视神经病变病例见于接受三次或更多次注射的患者。结论:糖尿病患者玻璃体内注射贝伐单抗被认为是非动脉炎性缺血性视神经病变发生的一个危险因素,尤其是在接受三次以上注射的患者中。