简介：目的：探讨去上皮瓣机械法准分子激光角膜上皮瓣下磨镶术（Epi—LASIK）矫治高度近视的临床疗效。方法：对86例169眼高度近视患者施行去上皮瓣Epi-LASIK，术后随访6mo。观察术后刺激症状、角膜上皮愈合时间、视力、屈光度、角膜上皮下雾状混浊程度（haze）。结果：所有患者术后均未主诉明显疼痛，仅表现有轻中度的异物感、畏光、流泪。角膜上皮愈合时间3～4d。术后6mo，全部86例169眼术后等效球镜均在±1．00D以内，未见最佳矫正视力下降，23眼（13．6％）最佳矫正视力提高1行以上。术后1mo，142眼（84．0％）角膜haze为0级，27眼（16．0％）角膜haze为0．5级；术后3mo，2例4眼不明原因出现3级haze；术后6too，所有患者角膜haze均为0级。结论：去上皮瓣Epi—LASIK治疗高度近视安全、有效，具有良好的可预测性和稳定性。个别患者在术后发生不明原因的迟发性haze有待于进一步研究。

简介：【药品名称】通用名称：小牛血清去蛋白眼用凝胶。英文名称：eproteinisedCalfSerumEyeGel。【成分】本品主要成份：本品含50%的小牛血清去蛋白提取物,小牛血清去蛋白提取物主要含有多种游离氨基酸、低分子肽和寡糖。

简介：目的：观察小牛血去蛋白提取物眼用凝胶对复发性翼状胬肉术后角膜切口修复的应用疗效。方法：将68例68眼行复发性翼状胬肉术后发生角膜切口水肿的患者随机分为2组,每组34例。对照组常规应用双氯芬酸钠滴眼液加抗生素滴眼液同时加用贝复舒滴眼液交替点眼,4次/d。治疗组除每日应用双氯芬酸钠滴眼液加抗生素滴眼液交替点眼外,使用小牛血去蛋白提取物眼用凝胶,4次/d,疗程1mo,于用药前和用药后3,7,14d;1mo分别对患者主觉症状、体征、角膜切口修复情况进行对比分析。结果：复发性翼状胬肉术后3,7,14d,治疗组角膜切口水肿较对照组明显消退,切口修复较快,主觉症状在短时间消退,术后1mo,两组无显著性差异。结论：小牛血去蛋白提取物眼用凝胶对复发性翼状胬肉术后角膜切口的早期修复起效时间短、舒适度好、安全性良好,对减少术后感染性角膜病的发生及术后角膜散光有良好的作用。

简介：AIM:Toestablishanuntransfectedhumancornealstromal(HCS)celllineandcharacterizeitsbiocompatibilitytoacellularporcinecornealstroma(aPCS).·METHODS:PrimaryculturewasinitiatedwithapurepopulationofHCScellsinDMEM/F12media(pH7.2)containing20%fetalbovineserumandvariousnecessarygrowthfactors.Theestablishedcelllinewascharacterizedbygrowthproperty,chromosomeanalysis,tumorigenicityassay,expressionofmarkerproteinsandfunctionalproteins.Furthermore,thebiocompatibilityofHCScellswithaPCSwasexaminedthroughhistologicalandimmunocytochemistryanalysesandwithlight,electronmicroscopies.·RESULTS:HCScellsproliferatedtoconfluence2weekslaterinprimarycultureandhavebeensubculturedtopassage140sofar.AcontinuousuntransfectedHCScelllinewithapopulationdoublingtimeof41.44hoursatpassage80hasbeendetermined.Resultsofchromosomeanalysis,morphology,combinedwiththeresultsofexpressionofmarkerproteinandfunctionalproteinssuggestedthatthecellsretainedHCScellproperties.Furthermore,HCScellshavenotumorigenicity,andwithexcellentbiocompatibilitytoaPCS.·CONCLUSION:Anuntransfectedandnon-tumorigenicHCScelllinehasbeenestablished,andthecellsmaintainedpositiveexpressionofmarkerproteinsandfunctionalproteins.Thecellline,withexcellentbiocompatibilitytoaPCS,mightbeusedforinvitroreconstructionoftissue-engineeredHCS.

简介：AIM:Todeterminewhethersinglenucleotidepolymorphism(SNP)rs641153isassociatedwiththeriskofage-relatedmaculardegeneration(AMD),weperformedasystematicmeta-analysisof15eligiblestudies.SNPinthecomplementfactorB(CFB)geneisconsideredtohavesignificantassociationwithAMDsusceptibility,butthereisgreatdiscrepancyintheseresults.METHODS:TheeligiblestudieswereidentifiedbysearchingthedatabasesofPubMed,EMBASE,andWebofScience.Oddsratios(ORs)with95%confidenceintervals(CIs)wereusedtoassesstheassociation.AlldatawereanalyzedusingStatasoftware.RESULTS:Theassociationbetweenrs641153andAMDriskwasstatisticallysignificantunderthehomozygousmodel(AAvsGG:OR=0.26,95%CI=0.15-0.45,P_h=0.973,/~2=0.0%,fixedeffects),dominantmodel(AA+GAvsGG:OR=0.49,95%CI=0.40-0.59,P_h=0.004,/~2=56.4%,randomeffects)andrecessivemodel(AAvsGA+GG:OR=0.30,95%CI=0.17-0.51,R_n=0.983,I~2=0.0%,fixedeffects).Thesameresultswerealsoobservedinthestratifiedanalysesbyethnicity,sourceofcontrolandsamplesize.CONCLUSION:Ourmeta-analysissuggeststhatrs641153intheCFBgenemayplayaprotectiveroleinAMDsusceptibility,thelateAMDinparticular,bothinCaucasiansandinAsians.