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首页> 外文期刊>American Journal of Ophthalmology: The International Journal of Ophthalmology >Anti-inflammatory effect of low-molecular-weight heparin in pediatric cataract surgery: A randomized clinical trial
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Anti-inflammatory effect of low-molecular-weight heparin in pediatric cataract surgery: A randomized clinical trial

机译:低分子量肝素在小儿白内障手术中的抗炎作用:一项随机临床试验

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? PURPOSE: To determine if intraocular infusion of low-molecular-weight heparin (enoxaparin) reduces postoperative inflammation in pediatric eyes undergoing cataract surgery with IOL implantation. ? DESIGN: Prospective masked randomized controlled trial. ? METHODS: SETTING: Private, institutional practice. STUDY POPULATION: Twenty children (40 eyes) undergoing bilateral cataract surgery with IOL implantation were randomized to receive enoxaparin in the intraocular infusion fluid (BSS) (Group I) or not to receive enoxaparin (Group II). The first eye was randomly assigned to 1 of the 2 groups and the second eye received alternate treatment. OBSERVATION PROCEDURE: Patients were followed up in the first week and 1 and 3 months after surgery. MAIN OUTCOME MEASURES: Anterior chamber flare and cells (Hogan's criteria), cell deposits on IOL, posterior synechiae. ? RESULTS: One week postoperatively, no eyes had >grade 2 flare/cells. Proportion of eyes with grade 2 cells was higher in eyes that did not receive enoxaparin (Group II: 80% vs Group I: 40%, P = .009). In the first week >10 small cell deposits were noted in the eyes that received enoxaparin (Group I: 20%, Group II: none, P = .005). Large cell deposits first appeared at 1 month in 40% of eyes in Group I and 55% of eyes in Group II (P = .34) and increased at 3 months (60% in both groups, P > .999). Posterior synechiae were seen in 10% of eyes in Group I at 1 month, which persisted at 3 months; no eyes in Group II showed posterior synechiae (P = .14). ? CONCLUSION: The results of our study suggest that there does not seem to be a benefit of using enoxaparin in the infusion fluid with respect to early postoperative inflammation.
机译:?目的:确定眼内输注低分子量肝素(依诺肝素)是否可降低接受白内障人工晶状体植入术的小儿眼睛的术后炎症。 ?设计:前瞻性隐蔽随机对照试验。 ?方法:环境:私人机构实践。研究人群:接受双眼白内障人工晶状体植入术的二十名儿童(40眼)被随机分配接受眼内输注液(BSS)中的依诺肝素(I组)或不接受依诺肝素(II组)。将第一只眼随机分配到两组中的一组中,第二只眼接受替代治疗。观察程序:在手术后的第一周和第一,第三个月对患者进行随访。主要观察指标:前房耀斑和细胞(霍根标准),IOL上的细胞沉积,后粘连。 ?结果:术后一周,没有眼睛有> 2级眩光/细胞。未接受依诺肝素的眼中具有2级细胞的眼比例更高(第二组:80%,第一组:40%,P = .009)。在第一周中,接受依诺肝素的眼中发现有10多个小细胞沉积物(I组:20%,II组:无,P = .005)。大细胞沉积首先出现在第一组的40%的眼睛和第二组的55%的眼睛的1个月(P = .34),并在3个月时增加(两组的60%,P> .999)。 I组在第1个月时有10%的眼睛出现后粘连,并持续3个月。第二组中没有眼睛显示后粘连(P = .14)。 ?结论:我们的研究结果表明,就术后早期炎症而言,在输液中使用依诺肝素似乎没有益处。

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