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首页> 外文期刊>Ophthalmology >Safety and efficacy of phacoemulsification compared with manual small-incision cataract surgery by a randomized controlled clinical trial: six-week results.
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Safety and efficacy of phacoemulsification compared with manual small-incision cataract surgery by a randomized controlled clinical trial: six-week results.

机译:随机对照临床试验与人工小切口白内障手术相比,超声乳化的安全性和有效性:六周结果。

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OBJECTIVE: To compare the efficacy, safety, and refractive errors of astigmatism after cataract surgery by phacoemulsification and manual small-incision cataract surgery techniques. DESIGN: Masked randomized control clinical trial. PARTICIPANTS: Four hundred eyes of 400 patients, 1:1 randomization with half in each arm of the trial. METHODS: A total of 400 eyes was assigned randomly to either phacoemulsification or small-incision groups after informed consent and were operated on by 4 surgeons. They were masked to the technique of surgery before, during, and after cataract surgery and followed up to 1 year after surgery. The intraoperative and postoperative complications, uncorrected and best-corrected visual acuity, and astigmatism were recorded at 1 and 6 weeks postoperatively. MAIN OUTCOME MEASURES: The proportion of patients achieving visual acuity better than or equal to 6/18 with and without spectacles after cataract surgery in the operated eye up to 6 weeks, postoperative astigmatism, and complications during and after surgery. RESULTS: This article reports clinical outcomes up to 6 weeks. Three hundred eighty-three of 400 (95.75%) patients completed the 1-week follow-up, and 372 of 400 (93%) patients completed the 6-week follow-up. One hundred thirty-one of 192 (68.2%) patients in the phacoemulsification group and 117 of 191 (61.25%) patients in the small-incision group had uncorrected visual acuity better than or equal to 6/18 at 1 week (P = 0.153). One hundred fifty of 185 (81.08%) patients of the phacoemulsification group and 133 of 187 (71.1%) patients of the small-incision group (P = 0.038) were better than or equal to 6/18 at the 6-week follow-up for presenting visual activity. Visual acuity improved to > or = 6/18 with best correction in 182 of 185 patients (98.4%) and 184 of 187 (98.4%) patients (P = 0.549), respectively. Poor outcome (postoperative visual acuity < 6/60) was noted in 1 of 185 (0.5%) in the phacoemulsification group and none in the small-incision group. The mode of astigmatism was 0.5 diopters (D) for the phacoemulsification group and 1.5 D for the small-incision group, and the average astigmatism was 1.1 D and 1.2 D, respectively. There was an intra-surgeon variation in astigmatism. The phacoemulsification group had 7 posterior capsular rents compared with 12 in the small-incision group, but the phacoemulsification group had more corneal edema on the first postoperative day. CONCLUSIONS: Both the phacoemulsification and the small-incision techniques are safe and effective for visual rehabilitation of cataract patients, although phacoemulsification gives better uncorrected visual acuity in a larger proportion of patients at 6 weeks.
机译:目的:通过超声乳化和人工小切口白内障手术技术,比较白内障手术后散光的疗效,安全性和屈光不正。设计:蒙面随机对照临床试验。参与者:400位患者的400只眼,按1:1随机分配,试验的每只手臂各占一半。方法:经知情同意后,将400只眼睛随机分配至超声乳化或小切口组,并由4名外科医生进行手术。他们在白内障手术之前,期间和之后对手术技术视而不见,并在手术后长达一年。术后1和6周记录术中和术后并发症,未矫正和最佳矫正视力以及散光。主要观察指标:白内障手术后6周以内,未配戴眼镜,术后散光及术后并发症的视力≥6/ 18的患者比例。结果:本文报告长达6周的临床结果。 400名患者中的383名(95.75%)完成了1周的随访,而400名患者中的372名(93%)完成了6周的随访。超声乳化术组中192例患者中的113例(68.2%)和小切口组中191例中191例患者(61.25%)的未矫正视力在1周时好于或等于6/18(P = 0.153) )。在6周的随访中,超声乳化组的185名患者中有150名(81.08%),小切口组的187名患者中有133名(71.1%)(P = 0.038)优于或等于6/18。用于呈现视觉活动。视力改善至>或= 6/18,分别在185例患者中的182例(98.4%)和187例患者中的184例(98.4%)中进行了最佳矫正(P = 0.549)。超声乳化组185例中有1例(0.5%)的预后较差(术后视力<6/60),小切口组未见。晶状体乳化组的散光模式为0.5屈光度(D),小切口组的散光模式为1.5 D,平均散光分别为1.1 D和1.2D。外科医生在散光方面有差异。超声乳化组的后囊租金为7例,而小切口超声乳化组为12例,但是超声乳化组术后第一天角膜水肿更大。结论:超声乳化术和小切口技术对于白内障患者的视觉康复都是安全有效的,尽管超声乳化在6周时能为更大比例的患者提供更好的未矫正视力。

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