Zhongshan Ophthalmic Center, State Key Laboratory of Ophthalmology, Sun Yat-sen University, Guangzhou, 510060, China.
Department of Ophthalmology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
BMC Ophthalmol. 2020 Jun 17;20(1):236. doi: 10.1186/s12886-020-01509-7.
To explore the effects of enhanced external counterpulsation (EECP) and its underlying influencing factors in nonarteritic anterior ischemic optic neuropathy (NAION) patients.
Patients at Zhongshan Ophthalmic Center with recent-onset (< 8 weeks) NAION were retrospectively recruited. The patients had decided whether or not they would undergo EECP treatment, and the patients who declined were included in the control group. The effectiveness of EECP was evaluated by comparing the visual function and fellow eye involvement in patients with and without EECP treatment.
In total, 61 patients (76 eyes) were included. Twenty-nine patients (37 eyes) underwent EECP treatment, while 32 patients (39 eyes) were included in the control group. Mean time from NAION onset to EECP initiation was 27.59 ± 16.70 days. In the EECP group, the mean EECP duration was 31.57 ± 18.45 days. EECP was well tolerated by all patients. However, there was no significant difference in visual function between the EECP and control groups. Furthermore, there was no evidence of the effectiveness of EECP in the subgroup analysis of patients with different systemic health conditions. Among the 42 patients with monocular NAION, the sequential attack rate was comparable between the EECP (27.78%) and control (25.00%) groups.
This study is the first nonrandomized controlled study to evaluate the effectiveness of EECP in NAION patients. Unfortunately, we failed to demonstrate the effectiveness of EECP in NAION at the 6-month follow-up. Any further application of EECP in NAION patients should be cautious.
探讨增强型体外反搏(EECP)对非动脉炎性前部缺血性视神经病变(NAION)患者的影响及其潜在影响因素。
回顾性招募中山大学中山眼科中心近期(<8 周)发生的 NAION 患者。患者决定是否接受 EECP 治疗,拒绝接受 EECP 治疗的患者被纳入对照组。通过比较接受和未接受 EECP 治疗的患者的视力功能和对侧眼受累情况来评估 EECP 的疗效。
共纳入 61 例(76 只眼)患者。29 例(37 只眼)患者接受 EECP 治疗,32 例(39 只眼)患者纳入对照组。NAION 发病至开始 EECP 的平均时间为 27.59±16.70 天。EECP 组 EECP 持续时间的平均时间为 31.57±18.45 天。所有患者均能耐受 EECP。然而,EECP 组和对照组之间的视力功能无显著差异。此外,在不同全身健康状况患者的亚组分析中,也没有证据表明 EECP 的有效性。在 42 例单眼 NAION 患者中,EECP 组(27.78%)和对照组(25.00%)的序贯攻击率相当。
本研究是首个评估 EECP 对 NAION 患者有效性的非随机对照研究。遗憾的是,我们未能在 6 个月随访时证明 EECP 在 NAION 中的有效性。EECP 在 NAION 患者中的进一步应用应谨慎。