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柔红霉素辅助治疗增生性玻璃体视网膜病变:一项多中心临床试验的结果。柔红霉素研究组

Adjunctive daunorubicin in the treatment of proliferative vitreoretinopathy: results of a multicenter clinical trial. Daunomycin Study Group.

作者信息

Wiedemann P, Hilgers R D, Bauer P, Heimann K

机构信息

University Eye Hospital Leipzig, Germany.

出版信息

Am J Ophthalmol. 1998 Oct;126(4):550-9. doi: 10.1016/s0002-9394(98)00115-9.

Abstract

PURPOSE

To assess the efficacy and safety of adjunctive daunorubicin during vitrectomy surgery in eyes with idiopathic proliferative vitreoretinopathy (PVR).

METHODS

Two hundred eighty-six eyes (286 patients) with stage C2 (Retina Society Classification, 1983) or more advanced preoperative PVR in which surgery with silicone oil was planned were enrolled in a multicenter, prospective, randomized, controlled clinical trial. Standardized surgery plus adjunctive daunorubicin perfusion was compared with surgery alone. Outcomes assessed were retinal attachment without additional vitreoretinal surgery 6 months after standardized surgery, number of and time until vitreoretinal reoperations within 1 year of standardized surgery, and change in visual acuity 1 year after standardized surgery, evaluated by photodocumentation, number of reoperations, and measurement of best-corrected visual function. Outcomes were determined 6 months after operation and reevaluated after 1 year of follow-up.

RESULTS

Six months after standardized surgery, complete retinal reattachment without additional vitreoretinal surgery was achieved in 62.7% (89/142) of eyes in the daunorubicin group vs 54.1% (73/135) in the control group (P = .07, one-sided). However, in the daunorubicin group, significantly fewer vitreoretinal reoperations were performed within 1 year postoperatively (P = .005, one-sided) to achieve the same overall 1-year retinal reattachment rate (80.2% [105/131] vs 81.8% [103/126]). The rate of patients with no vitreoretinal reoperations was 65.5% (95/145) in the daunorubicin group vs 53.9% (76/141) in the control group. There was no difference in the best-corrected visual acuity. No severe adverse effect related to daunorubicin was identified.

CONCLUSIONS

Although the rate of anatomic success after 6 months failed to show significance, some benefit of the adjunctive treatment exists, especially a tendency toward increased rate of reattachment and a significant reduction in the number of reoperations. This shows that human PVR is amenable to pharmacologic treatment.

摘要

目的

评估柔红霉素辅助治疗特发性增生性玻璃体视网膜病变(PVR)患者玻璃体切除术的疗效和安全性。

方法

286只眼(286例患者)术前PVR为C2期(视网膜协会分类,1983年)或更晚期且计划行硅油手术,纳入一项多中心、前瞻性、随机、对照临床试验。将标准化手术联合柔红霉素辅助灌注与单纯手术进行比较。评估的结局包括标准化手术后6个月无需额外玻璃体视网膜手术的视网膜复位情况、标准化手术后1年内玻璃体视网膜再次手术的次数和时间,以及标准化手术后1年的视力变化,通过照片记录、再次手术次数和最佳矫正视力功能测量进行评估。术后6个月确定结局,并在随访1年后重新评估。

结果

标准化手术后6个月,柔红霉素组62.7%(89/142)的眼在无需额外玻璃体视网膜手术的情况下实现了完全视网膜复位,而对照组为54.1%(73/135)(P = 0.07,单侧)。然而,在柔红霉素组,术后1年内进行的玻璃体视网膜再次手术显著减少(P = 0.005,单侧),以达到相同的总体1年视网膜复位率(80.2% [105/131] 对81.8% [103/126])。柔红霉素组无玻璃体视网膜再次手术的患者比例为65.5%(95/145),而对照组为53.9%(76/141)。最佳矫正视力无差异。未发现与柔红霉素相关 的严重不良反应。

结论

尽管6个月后的解剖学成功率未显示出显著性差异,但辅助治疗存在一些益处,尤其是视网膜复位率有增加的趋势,且再次手术次数显著减少。这表明人类PVR适合药物治疗。

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