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Topical autologous platelet-rich plasma eyedrops for acute corneal chemical injury

机译:局部自体富血小板血浆滴眼液用于急性角膜化学损伤

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Purpose: Evaluation of efficacy of autologous platelet-rich plasma eyedrops as an adjunct to standard medical treatment as compared with standard medical treatment with artificial tears in acute ocular chemical injury. Methods: Twenty eyes with grade III to grade V chemical injury were randomly assigned to 2 groups. Group I (10 eyes) received autologous platelet-rich plasma eyedrops along with standard medical treatment, and group II (10 eyes) received standard medical treatment alone. Follow-up was on days 3, 7, 14, 21, 30, 60, and 90. Chi-square test for categorical variables and Mann-Whitney test for quantitative variables were applied for statistical analysis. Results: The mean time between exposure and presentation was 2.15 ± 0.93 days (group I, 2.2 ± 0.73 days; group II, 2.1 ± 0.98 days; P = 0.81). Complete epithelialization was achieved in all the eyes. The mean ± SD and median (range) time to complete epithelialization were 40 ± 31.57 days and 25.5 (7-90) days in group I and 47 ± 26.15 days and 30.0 (21-90) days in group II (P = 0.29). For grade III injuries, mean ± SD and median (range) time to complete epithelialization were 14 ± 7 days and 14 (7-21) days in group I and 28.5 ± 3.67 days and 28.5 (21-30) days in group II (P = 0.006) [Wilcoxon rank sum (Mann-Whitney) test]. At 3 months, corneal clarity showed significant improvement in grade I compared with grade II (P = 0.048). Similarly, the percentage improvement in best-corrected visual acuity was 63.64 ± 55.75 and 37.74 ± 9.66 for grades I and II, respectively (P = 0.082). Conclusions: Topical autologous platelet-rich plasma therapy is safe and effective, and it promotes rapid reepithelialization of ocular surface and can be administered along with standard medical therapy.
机译:目的:与使用人工泪液的标准药物治疗急性眼部化学损伤的标准药物治疗相比,评估自体富含血小板的血浆滴眼剂作为标准药物治疗的疗效。方法:将20只III级至V级化学损伤的眼睛随机分为2组。第一组(10眼)接受自体富血小板血浆滴眼液以及标准药物治疗,第二组(10眼)仅接受标准药物治疗。在第3、7、14、21、30、60和90天进行随访。分类变量采用卡方检验,定量变量采用Mann-Whitney检验进行统计分析。结果:暴露和表现之间的平均时间为2.15±0.93天(I组为2.2±0.73天; II组为2.1±0.98天; P = 0.81)。所有人的眼睛都完全上皮化。 I组的平均±SD和完成上皮形成的中位(范围)时间分别为40±31.57天和25.5(7-90)天,I组为47±26.15天,II组为30.0(21-90)天(P = 0.29) 。对于III级损伤,第一组的平均±SD和完成上皮形成的中位(范围)时间分别为I组的14±7天和14(7-21)天,II组的28.5±3.67天和28.5(21-30)天( P = 0.006)[Wilcoxon秩和(Mann-Whitney)检验]。在3个月时,与II级相比,I级角膜清晰度显着改善(P = 0.048)。同样,I级和II级的最佳矫正视力的改善百分比分别为63.64±55.75和37.74±9.66(P = 0.082)。结论:局部自体富血小板血浆疗法安全有效,可促进眼表快速上皮再形成,可与标准药物疗法同时使用。

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