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早期经结膜巩膜穿刺联合 5-氟尿嘧啶与药物治疗在囊泡性滤过泡中的应用:一项 12 个月前瞻性研究。

Early transconjunctival needling revision with 5-fluorouracil versus medical treatment in encapsulated blebs: a 12-month prospective study.

出版信息

Clinics (Sao Paulo). 2013 Oct;68(10):1376-9. doi: 10.6061/clinics/2013(10)14.

Abstract

OBJECTIVE

To compare the efficacy of transconjunctival needling revision with 5-fluorouracil versus medical treatment in glaucomatous eyes with uncontrolled intraocular pressure due to encapsulated bleb after trabeculectomy.

METHODS

Prospective, randomized, interventional study. A total of 40 eyes in 39 patients with elevated intraocular pressure and encapsulated blebs diagnosed at a maximum five months after primary trabeculectomy with mitomycin C were included. The eyes were randomized to either transconjunctival needling revision with 5- fluorouracil or medical treatment (hypotensive eyedrops). A maximum of two transconjunctival needling revisions per patient was allowed in the needling arm. All patients underwent follow-up for 12 months. Successful treatment was defined as an intraocular pressure ≤ 18 mmHg and a 20% reduction from baseline at the final follow-up. Clinicaltrial.gov: NCT01887223.

RESULTS

Mean intraocular pressure at the final 12-month follow-up was lower in the transconjunctival needling revision group compared to the medical treatment group. Similar numbers of eyes reached the criteria for treatment success in both the transconjunctival needling revision group and the medical treatment group.

CONCLUSIONS

Despite similar success rates in eyes randomized to transconjunctival needling revision with 5-fluorouracil compared to eyes receiving medical treatment, there was a significantly lower mean intraocular pressure at 12 months after transconjunctival needling revision.

摘要

目的

比较经结膜穿刺针划切联合丝裂霉素与单纯药物治疗对青光眼术后滤过泡包裹性失败导致眼压控制不良的疗效。

方法

前瞻性、随机、对照研究。共纳入 39 例(40 只眼)患者,这些患者在初次行丝裂霉素 C 联合小梁切除术术后 5 个月内发生眼压升高和包裹性滤过泡,所有患者均于术后 5 个月内行超声生物显微镜检查诊断为包裹性滤过泡失败。将患者随机分为经结膜穿刺针划切联合丝裂霉素组和药物治疗组(降眼压眼药)。如果患者需要再次治疗,经结膜穿刺针划切治疗最多允许进行 2 次。所有患者均随访 12 个月。成功治疗定义为眼压≤18mmHg,且与基线相比,最终随访时眼压下降≥20%。clinicaltrials.gov:NCT01887223。

结果

在最终 12 个月的随访中,经结膜穿刺针划切联合丝裂霉素组的平均眼压明显低于药物治疗组。在经结膜穿刺针划切联合丝裂霉素组和药物治疗组中,达到治疗成功标准的眼数量相似。

结论

尽管经结膜穿刺针划切联合丝裂霉素组和药物治疗组的治疗成功率相似,但经结膜穿刺针划切联合丝裂霉素治疗后 12 个月的平均眼压明显更低。

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