Comparison of Two Tube-Modification Techniques in Baerveldt Glaucoma Implantation in Refractory Glaucoma

难治性青光眼Baerveldt青光眼植入术中两种导管改良技术的比较

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Abstract

IMPORTANCE: To compare treatment outcomes among a stent group, ligature group and combined group in eyes with refractory glaucoma. BACKGROUND: Various techniques have been used intra-operatively to restrict the aqueous flow in Baerveldt glaucoma implantation. DESIGN: Retrospective chart review. PARTICIPANTS: All glaucoma patients aged over 18-years old who had Baerveldt implantation in Ramathibodi Hospital, Bangkok, Thailand, between October 2011 and February 2018 were included for analysis. METHODS: Retrospective interventional research was conducted. All glaucoma patients who underwent drainage device implantations were retrospectively reviewed from medical records and divided into three groups: stent group, ligature group, and combined group. The primary outcome was post-operative intraocular pressure (IOP) changes and BCVA (logMAR) change. The secondary outcome is treatment failure. Repeated measurements with mixed models and multi-level parametric survival model stratified by propensity score and eye side were used to compare the primary and secondary outcomes between stent group and ligature group. MAIN OUTCOME MEASURES: Treatment failure between two groups. RESULTS: A total of 163 patients with a mean age of 57.11 ± 19.04 years, implanted with Baerveldt tube, were eligible. There were no significant differences between stent and ligature groups in terms of post-operative IOP changes [mean difference with 95% confidence interval = 0.53 (-0.49, +1.55) vs -0.02 (-0.84, +0.81); P = 0.411] and post-operative BCVA (logMAR) change (0.02 (-0.13, +0.18) vs -0.05 (-0.18, +0.07); P = 0.465). The hazard ratio and 95% confidence interval of treatment failure in ligature group were 2.57 (0.72-9.19) compared with the stent group. CONCLUSION: This study suggests a trend toward a better result in the stent group compared with the ligature group. Further research with a larger sample size and randomized control trial is warranted.

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