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青光眼患者超声乳化白内障吸除术与超声乳化白内障吸除联合小梁切除术的回顾性比较

A Retrospective Comparison of Phaco-tube vs. Phaco-trabeculectomy in Glaucoma Patients.

机构信息

Department of Ophthalmology, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida.

Division of Ophthalmology, Scripps Clinic, La Jolla, California.

出版信息

Ophthalmol Glaucoma. 2024 Sep-Oct;7(5):466-475. doi: 10.1016/j.ogla.2024.04.008. Epub 2024 Apr 30.

Abstract

PURPOSE

To compare surgical outcomes of phacoemulsification combined with Baerveldt implantation (phaco-tube) or trabeculectomy with mitomycin-C (MMC) (phaco-trab) in patients without prior incisional ocular surgery.

DESIGN

Single-center, retrospective, comparative case series.

PARTICIPANTS

A total of 90 patients underwent surgical treatment, including 45 patients in the phaco-tube group and 45 patients in the phaco-trab group.

METHODS

Eligible patients were identified using current procedural terminology (CPT) codes, and their medical records were retrospectively reviewed.

MAIN OUTCOME MEASURES

The primary outcome measure was the rate of surgical failure (IOP ≤5 mmHg or >21 mmHg or reduced <20% from baseline on 2 consecutive study visits after 3 months, reoperations for glaucoma, or experienced loss of light perception vision). Patients who had successful surgical outcomes without use of glaucoma medications were classified as complete successes, while those who used glaucoma medications were classified as qualified successes. Secondary outcome measures were visual acuity (VA), visual field mean deviation (VFMD), intraocular pressure (IOP), glaucoma medication use, and complications.

RESULTS

The cumulative probability of failure was 6.7% in the phaco-tube group and 32.8% in the phaco-trab group after 3 years (P = 0.005; Restricted Mean Survival Time = 5.9 months, 95% CI = 1.4-10.4 months). The IOP was 13.1 ± 3.4 mmHg in the phaco-tube group and 13.3 ± 6.2 mmHg in the phaco-trab group at 3 years (P = 0.90), and the number of glaucoma medications was 2.6 ± 1.5 in the phaco-tube group and 1.7 ± 1.3 in the phaco-trab group (P = 0.015). The logarithm of the minimum angle of resolution VA was 0.39 ± 0.58 in the phaco-tube group and 0.43 ± 0.73 in the phaco-trab group at 3 years (P = 0.82), and VFMD was -18.3 ± 9.0 dB in the phaco-tube group and -14.1 ± 7.0 dB in the phaco-trab group (P = 0.16). Postoperative complications developed in 21 patients (47%) in the phaco-tube group and 15 patients (33%) in the phaco-trab group (P = 0.28).

CONCLUSIONS

Phaco-tubes had a significantly lower rate of surgical failure compared to phaco-trabs after 3 years of follow-up. However, phaco-trabs used significantly fewer glaucoma medications at multiple postoperative timepoints and had a higher proportion of complete success.

FINANCIAL DISCLOSURE(S): The author(s) have no proprietary or commercial interest in any materials discussed in this article.

摘要

目的

比较超声乳化白内障吸除联合 Baerveldt 植入(超声乳化管)或小梁切除术联合丝裂霉素 C(MMC)(超声乳化小梁切除术)治疗无既往切口眼手术史患者的手术效果。

设计

单中心、回顾性、对照病例系列。

参与者

共有 90 例患者接受了手术治疗,其中 45 例患者在超声乳化管组,45 例患者在超声乳化小梁切除术组。

方法

使用当前程序术语(CPT)代码确定符合条件的患者,并回顾性审查他们的病历。

主要观察指标

主要结局指标是手术失败率(眼压≤5mmHg 或>21mmHg,或在 3 个月后连续 2 次研究访视时基线降低<20%,青光眼再次手术,或出现光感丧失视力)。无青光眼药物治疗且手术成功的患者被归类为完全成功,而使用青光眼药物治疗的患者被归类为合格成功。次要结局指标包括视力(VA)、视野平均偏差(VFMD)、眼压(IOP)、青光眼药物使用情况和并发症。

结果

在 3 年时,超声乳化管组的累积失败概率为 6.7%,超声乳化小梁切除术组为 32.8%(P=0.005;受限平均生存时间为 5.9 个月,95%CI=1.4-10.4 个月)。超声乳化管组和超声乳化小梁切除术组在 3 年时的眼压分别为 13.1±3.4mmHg 和 13.3±6.2mmHg(P=0.90),青光眼药物使用数量分别为 2.6±1.5 和 1.7±1.3(P=0.015)。超声乳化管组和超声乳化小梁切除术组在 3 年时的最小分辨角视力的对数分别为 0.39±0.58 和 0.43±0.73(P=0.82),视野平均偏差分别为-18.3±9.0dB 和-14.1±7.0dB(P=0.16)。超声乳化管组有 21 例(47%)患者和超声乳化小梁切除术组有 15 例(33%)患者发生术后并发症(P=0.28)。

结论

在 3 年的随访后,超声乳化管的手术失败率明显低于超声乳化小梁切除术。然而,在多个术后时间点,超声乳化小梁切除术使用的青光眼药物明显更少,且完全成功率更高。

金融披露

作者在本文讨论的任何材料中均没有任何专有或商业利益。

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