简介:目的:探索通过共焦激光眼底血管造影仪(HRA2)观测正常大鼠视网膜血管的形态和分布以及荧光标记的白细胞在眼底的运动情况的方法。方法:大鼠麻醉后散瞳并将其置于动物台上,荧光素钠血管造影观察大鼠视网膜血管的形态和分布,并照相和进行视频记录。另外,体外分离大鼠的外周血白细胞并用CFDA(6-carboxyfluoresceindiacetate)进行荧光标记,之后通过尾静脉将其回输进入同窝另一只大鼠的体内,观察白细胞在眼底血管的运动情况。结果:通过HRA2能够清楚而有效的观察到大鼠视网膜4级以上血管的形态和分布情况,并能够观察到白细胞在眼底血管中的各种运动状态。结论:建立了一种通过HRA2观测大鼠视网膜血管及白细胞运动的方法。
简介:目的:研究及观察视神经萎缩患者球后动脉血流动力学及球结膜微循环指标的变化情况。方法:选取2013-04/2014-10于本院进行诊治的70例视神经萎缩患者为观察组,同时期的70名健康同龄人员为对照组,然后将两组的球后动脉血流动力学及球结膜微循环指标进行比较,并比较观察组中不同分类及严重程度患者的上述检测指标。结果:观察组的球后动脉血流动力学及球结膜微循环指标均差于对照组,且观察组中重度患者的检测结果差于轻度及中度患者,中度患者的检测结果则差于轻度患者,均有显著性差异(P〈0.05),而不同分类患者之间的检测结果则无显著性差异(P〉0.05)。结论:视神经萎缩患者球后动脉血流动力学及球结膜微循环指标的变化较大,且本病患者的检测结果受疾病严重程度的影响较大。
简介:目的:评价超声乳化白内障吸除联合人工晶状体植入术后人工晶状体眼的波前像差,讨论不同设计的人工晶状体对术后人工晶状体眼波前像差的影响。方法:选择年龄相关性白内障患者62例(69眼),年龄41~84(平均63.4±4.0)岁。其中男24例(28眼),女38例(41眼),右眼38例,左眼31例。随机平均分为3组,使年龄性别相匹配。其中A组植入三片式人工晶状体(ACRYsof^@MA60BM),B组植入一片式人工晶状体(ACRYsof^@SA60AT),C组植入蓝光滤过型一片式人工晶状体(ACRYsof^@SN60AT)。同一术者,同一超声乳化仪(Alcon^@INFINITIVISIONSYSTEM)和手术显微镜(CarlZeissStativS88),术中均采用角膜曲率最高经线上宽3.2mm长1.75mm的角巩膜缘隧道切口。术后1mo使用客观型波前像差仪(NidekOPD-scanARK-10000)进行波前像差检测,得出总体高阶像差的均方根(RMSh)。结果:A组三片式(ACRYsof^@MA60BM)的RMSh平均达到0.702±0.090μm,B组一片式(ACRYsof^@SA60AT)的RMSh平均达到0.529±0.067μm,C组蓝光滤过型一片式(ACRYsof^@SN60AT)的RMSh平均达到0.566±0.066μm。三组比较采用单向方差分析,5.0mm瞳孔大小时A组的总体像差值最高(P〈0.01),其余两组没有显著性差异(P=0.126)。组间差异有统计学意义。结论:人工晶状体襻的设计对超声乳化白内障吸除联合人工晶状体植入术后人工晶状体眼的像差有明显影响,但光学区染色对单色像差的影响无统计学差异。这一结果对进一步完善白内障手术以及人工晶状体材料和设计的改善提供了有意义的信息。
简介:目的探讨一组特殊设计镜片对周边屈光度、周边清晰视力范围和主观感受的影响。方法3例(4眼)被试者,年龄22-31岁,屈光度-2.0D,按随机顺序分别在单眼配戴普通非球面镜片、成长乐镜片、视特保大、中、小光区镜片的情况下进行周边屈光度、周边清晰视力范围测量和主观评分,主观评分包括远距和近距戴镜舒适度、清晰度和接受度。结果配戴5种镜片时,被试眼相对周边屈光度均为远视状态,远视度数随周边角度增加而增加。配戴普通非球面镜片和视特保大光区镜片时周边远视度数最大,视特保中光区镜片其次,成长乐镜片和视特保小光区镜片最小;配戴普通非球面镜片和视特保大光区镜片时的周边清晰视力范围最大,其次是视特保中光区镜片,最小的是成长乐镜片和视特保小光区镜片;远距评分为普通非球面镜片最高,视特保大光区镜片其次,然后为视特保中光区镜片,成长乐镜片及视特保小光区镜片最差;近距评分视特保大光区镜片接近普通非球面镜片,视特保中光区镜片和成长乐镜片其次,视特保小光区镜片最差。结论不同设计的中周部加光镜片对改变周边屈光度的作用存在差异,其配戴后的顺应性与镜片改变周边屈光度的程度呈负相关。
简介:Thekeratoprosthesis(KPro;artificialcornea)isaspecialrefractivedevicetoreplacehumancorneabyusingheterogeneousformingmaterialsfortheimplantationintothedamagedeyesinordertoobtainacertainvision.Themainproblemsofartificialcorneaarethebiocompatibilityandstabilityofthetissueparticularlyinpenetratingkeratoplasty.Thecurrentstudiesoftissue-engineeredscaffoldmaterialsthroughcomprisingcompositesofnaturalandsyntheticbiopolymerstogetherhavedevelopedanewwaytoartificialcornea.Althoughawideagreementthatthelong-termstabilityofthesedeviceswouldbegreatlyimprovedbythepresenceofcorneacells,modificationofkeratoprosthesistosupportcorneacellsremainselusive.Mostofthestudiesoncornealsubstratematerialsandsurfacemodificationofcompositeshavetriedtoimprovethegrowthandbiocompatibilityofcorneacellswhichcannotonlyreducethestimulusofheterogeneousmaterials,butalsomoreimportantlycontinuousandstablecorneacellscanpreventthedestructionofcollagenase.Thenecrosisofstromaandspontaneousextrusionofthedevice,allowformaintenanceofaprecornealtearlayer,andplaytheroleofensuringagoodopticalsurfaceandresistingbacterialinfection.Asaresult,improvementincornealcellshasbeenthemainaimofseveralrecentinvestigations;someefforthasfocusedonbiomaterialforitswellbiologicalpropertiessuchaspromotingthegrowthofcorneacells.Thepurposeofthisreviewistosummarythegrowthstatusofthecornealcellsaftertheimplantationofseveralartificialcorneas.
简介:AIM:Todescribethedesignandpreliminaryresultsofthehospitalbasedepidemiologicalstudyfordiabeticretinopathy(HBESDR),anongoingepidemiologicalstudytoestimatetheprevalenceofdiabeticretinopathy(DR)andtoelucidatetheclinical,anthropometric,biochemicalandanyotherriskfactorsassociatedwithdiabeticretinopathy.METHODS:Totally2000diabeteswillberecruitedfromtheDiabeteseyeclinicintheFirstAffiliatedHospitalofChinaMedicalUniversity.AllsubjectsunderwentbloodsugarestimationandOralGlucoseToleranceTesttodiagnosediabetes.Alldiabeteswouldundergocompletequestionnaire,acomprehensiveeyeexamination.Bloodandurinewouldbecollectedforbiochemicalinvestigations.AllfundusphotographsforanyDRwillbegraded.Participantswhoneedtreatmentwillbesenttotheophthalmicclinicandfollow-upintervalprogramforallsubjectswillbesuggested.Acomputerizeddatabaseiscreatedfortherecords.RESULTS:Todate,1174diabeteshavebeenrecruited,therewere350(29.81%)DRinalldiabetes,mostofthemwerewithmildnon-proliferativediabeticretinopathy(NPDR)(139,39.71%);71(20.29%)moderateNPDR,66(18.86%)severeNPDR,74(21.14%)proliferativediabeticretinopathy(PDR).Females,longerdurationofdiabetes,familyhistoryofdiabetesandhypertensionhadastatisticallysignificantincreaseinriskofanyDR.CONCLUSION:ThestudyisexpectedtoprovideanestimateoftheoverallprevalenceofDRandtheprevalencewithdifferentdurationofdiabetesandalsoabetterunderstandingoftheriskfactorsassociatedwithDR.
简介:AIM:Todemonstratethemorphologyandstructureofinvitroreconstructedtissue-engineeredhumancornealepithelium(TE-HCEP)withseedercellsfromanuntransfectedHCEPcellline.·METHODS:TheTE-HCEPswerereconstructedinvitrowithseedercellsfromanuntransfectedHCEPcellline,andscaffoldcarriersofdenudedamnioticmembrane(dAM)inair-liquidinterfaceculturefor3,5,7and9days,respectively.Thespecimenswereexaminedwithhematoxylin-eosin(HE)stainingofparaffin-section,immunocytochemicalstaining,scanningandtransmissionelectronmicroscopy.·RESULTS:DuringinvitroreconstructionofTE-HCEP,HCEPcellsformeda3-4,6-7and8-10layersofanHCEP-likestructureondAMsinair-liquidinterfaceculturefor3,5and7days,respectively.Butthecellsdeceasedto5-6layersandthestructureofstraifiedepitheliumbecamelooseatday9.Andthecellsmaintainedpositiveexpressionofmarkerproteins(keratin3andkeratin12),cell-junctionproteins(zonulaoccludens-1,E-cadherin,connexin43andintegrinβ1)andmembranetransportproteinofNa+-K+ATPase.TheHCEPcellsinTE-HCEPwererichinmicrovillionapicalsurfaceandestablishednumerouscell-cellandcell-dAMjunctionsatday5.·CONCLUSION:ThemorphologyandstructureofthereconstructedTE-HCEPweresimilartothoseofHCEPinvivo.TheHCEPcellsinthereconstructedTE-HCEPmaintainedthepropertiesofHCEPcells,includingabilitiesofformingintercellularandcell-extracellularmatrixjunctionsandabilitiesofperformingmembranetransportation.TheuntransfectedHCEPcellsanddAMscouldpromisinglybeusedinreconstructionHCEPequivalentforclinicalcornealepitheliumtransplantation.