Visual Outcomes Following Hyperbaric Oxygen Therapy in Acute Central Retinal Artery Occlusion Patients.

Clinical ophthalmology (Auckland, N.Z.) Pub Date : 2025-09-18 eCollection Date: 2025-01-01 DOI:10.2147/OPTH.S510772
Somanus Thoongsuwan, Thanut Sirichayaporn, Nuttawut Rodanant, Nopasak Phasukkijwatana, Supalert Prakhunhungsit, Nida Wongchaisuwat, Chinnapat Montrisuksirikun, Adisak Trinavarat, Kusuma Chinaroonchai, Supathida Jiamsawad
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引用次数: 0

Abstract

Purpose: To evaluate the efficacy of a novel HBOT protocol, characterized by specific pressure levels and treatment duration in patients with CRAO patients presenting within 24 hours, compared to a non-HBOT cohort.

Patients and methods: This retrospective cohort study included patients diagnosed with CRAO presenting within 24 hours from October 2003 to March 2022. Patients treated with intravenous recombinant tissue plasminogen activator (rt-PA) or experiencing treatment-related visual complications were excluded. Of 49 eligible patients, 17 underwent HBOT following the novel protocol, while 32 received standard care (non-HBOT).

Results: Baseline logMAR VA was 2.3 in both groups. At discharge, 76.5% of the HBOT group exhibited a VA improvement of at least 0.3 logMAR, compared to 40.6% in the non-HBOT group (p = 0.02). Mean logMAR VA at discharge was 1.4 ± 0.8 in the HBOT group and 2.0 ± 0.8 in the non-HBOT group. After one month, the mean logMAR VA remained at 1.4 ± 0.9 in the HBOT group and was 1.9 ± 0.9 in the non-HBOT group.

Conclusion: While constrained by the small sample size and short-term outcome data, these results showed the benefits of this unique HBOT protocol in CRAO presenting within the critical 24-hour window. Nevertheless, further prospective validation is necessary before widespread clinical adoption.

急性视网膜中央动脉闭塞患者高压氧治疗后的视力结果。
目的:与非HBOT队列相比,评估以特定压力水平和治疗时间为特征的新型HBOT方案在24小时内出现的CRAO患者中的疗效。患者和方法:本回顾性队列研究纳入2003年10月至2022年3月24小时内诊断为CRAO的患者。排除静脉注射重组组织型纤溶酶原激活剂(rt-PA)或出现治疗相关视觉并发症的患者。在49名符合条件的患者中,17名患者按照新方案接受了HBOT,而32名患者接受了标准治疗(非HBOT)。结果:两组患者基线logMAR VA均为2.3。出院时,76.5%的HBOT组VA改善至少为0.3 logMAR,而非HBOT组为40.6% (p = 0.02)。HBOT组出院时平均logMAR VA为1.4±0.8,非HBOT组为2.0±0.8。1个月后,HBOT组的平均logMAR VA为1.4±0.9,非HBOT组为1.9±0.9。结论:虽然受小样本量和短期结局数据的限制,这些结果表明,这种独特的HBOT方案在CRAO的关键24小时窗口内呈现益处。然而,在广泛的临床应用之前,进一步的前瞻性验证是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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