简介:目的:比较白内障超声乳化吸除人工晶状体植入术后和小切口囊外门内障摘除人工品状体植入术后患者生存质量的变化。方法:分别于术前和术后1/4,1,3mo,观察I组108例单眼行白内障超声乳化吸除人工晶状体植入术后患者和II组94例单眼行小切口白内障囊外摘除人工晶状体植入的眼部情况,使用生存质量调杏量表记录分数。结果:术前生存质量总分数和各指标分数,术后1mo和3mo的生存质量总分数,I组和Ⅱ组比较差异均无显著意义(P〉0.05)。术后1/4mo生存质量总分数和各指标分数,I组高于Ⅱ组,两组比较差异有显著意义(P〈0.05)。结论:白内障超声乳化吸除人工品状体植入术患者的生存质量在短期内就得到明显提高。手术效果优于小切口囊外白内障摘除术。中期效果I组和Ⅱ组无明显差异,远期结果尚待进步深入探讨。
简介:AIM:Todescribethecharacteristicsofmodulationtransferfunction(MTF)ofanteriorcornealsurface,andobtainthethenormalreferencerangeofMTFatdifferentspatialfrequenciesandopticalzonesoftheanteriorcornealsurfaceinmyopes.·METHODS:Fourhundredeyesfrom200patientswereexaminedunderSIRIUScornealtopographysystem.PhoenisanalysissoftwarewasappliedtosimulatetheMTFcurvesofanteriorcornealsurfaceatverticalandhorizontalmeridiansatthe3,4,5,6,7mmopticalzonesofcornea.TheMTFvaluesatspatialfrequenciesof5,10,15,20,25,30,35,40,45,50,55and60cycles/degree(c/d)wereselected.·RESULTS:TheMTFcurveofanteriorcornealsurfacedecreasedrapidlyfromlowtointermediatefrequency(0-15cpd)atvariousopticalzonesofcornea,thevaluedecreasedto0slowlyathigherfrequency(>15cpd).Withtheincreaseoftheopticalzonesofcornea,MTFcurvedecreasedgradually.3)Intherangeof3mm-6mmopticalzonesofthecornea,theMTFvaluesmeasuredathorizontalmeridianweregreaterthanthecorrespondingvaluesathorizontalmeridianofeachspatialfrequency,thedifferencewasstatisticallysignificant(P<0.05).At7mmopticalzonesofcornea,theMTFvaluesmeasuredathorizontalmeridianwerelessthanthecorrespondingvaluesatverticalmeridianat10-60spatialfrequencies(cpd),andthedifferencewasstatisticallysignificantin25,30,35,40,45,50cpd(P<0.05).·CONCLUSION:MTFcanbeusedtodescribetheimagingqualityofopticalsystemsatanteriorcornealsurfaceobjectivelyindetail.
简介:目的比较双眼行超声乳化白内障吸除联合植入AcrySofReSTOR与ATLISAtri839MP多焦点人工晶状体(M10L)术后的视觉质量。方法前瞻性非随机对照研究。收集双眼年龄相关性白内障24例(48跟),行超声乳化术,12例(24眼)植入AcrysofReSTOR为对照组,12例(24眼)植入ATLISAtri839MP为实验组,术后3月测量其裸眼远、中及近视力,最佳矫正远、中及近视力,离焦曲线,并通过问卷调查的方式评价患者术后脱镜情况及患者对全程视力的满意度。结果植入ATLISAtri839MP患者的中距离视力高于植入AcrySofReSTOR(P〈0.05),而远、近视力差异无统计学意义(P〉0.05)。离焦曲线显示两组第一峰位均在附加OD处;第二峰位对照组位于附加-3.0D,实验组位于-1.5D至-3.0D之间,此段呈现平台期。两组患者在各空间频率的对比敏感度比较差异均无统计学意义(P〉0.05)。在调查问卷中,实验组的脱镜率及中距离视力满意度高于对照组(P〈0.05)。结论两种人工晶状体植入术后均可获得良好的远近视力,ATLISAtri839MP人工晶状体能够获得更好的中距离视力及较高的患者满意度,具有更为理想的全程视力。
简介:目的:探讨规模化白内障手术中高龄及其伴全身疾病患者安全性。方法:回顾性分析"爱心光明行"活动中高龄及其伴全身疾病患者的临床资料。结果:本组高龄伴全身疾病患者213例(90.6%),其中循环系统疾病、代谢性疾病、呼吸系统疾病分别占65.1%,13.6%和11.1%。术前因首次全身疾病评估暂缓手术25例(10.6%),经有效治疗后手术。手术脱残率95.4%,脱盲率84.2%,12例视力〈0.1患者眼底检查均有不同程度的眼底病变。结论:加强术前综合因素评估,充分治疗全身疾病,严格掌握手术适应证,术中监护,操作轻巧,手术时间10~15min,是保证规模化白内障手术中高龄或伴全身疾病患者安全性的有效措施。
简介:目的对临床可疑青光眼患者进行长期的偏振激光扫描仪联合个体化角膜补偿技术(scanninglaserpolarimetrywithvariablecornealcompensation,GDxVCC)随访,分析GDxVCC对该类患者的诊断价值。方法选取门诊可疑青光眼的眼底检查视乳头杯/盘比(C/D)≥0.4,或双眼不对称且C/D差值〉10.2,静态视野检查结果正常患者68例,随访前后均用GDxVCC检查(采用相同的角膜补偿值)。如双跟C/D值相同,随机选取1眼,如C/D值不同,则选取C/D值大的1眼,对结果进行t检验统计学分析。结果随访时间6~30个月,平均(12.5±7.0)个月,眼底C/D值为0.57±0.17。随访前后GDxVCC检查:椭圆平均值分别为50.33±7.72和49.66±8.12,上方平均值为58.72±13.56和58.18±12.01,下方平均值为60.71±11.31和59.13±11.95,神经纤维指数为30.85±19.62和33.03±21.22,差异无统计学意义,但从绝对数值上,椭圆平均值、上方平均值和下方平均值变小,神经纤维指数变大。其中7例(10.3%)诊断为青光眼,21例(30.9%)排除青光眼,40例(58.8%)仍需进一步随访。结论对临床怀疑青光眼的患者应长期进行随访,GDxVCC随访对青光眼的诊断有一定的价值。(中国眼耳鼻喉科杂志,2009,9:92—94)
简介:目的:探讨激光周边虹膜成形术(laserperipheraliridoplasty,LPIP)治疗急性闭角型青光眼(acuteangle-closureglaucoma,AACG)急性发作期药物不能控制的高眼压持续状态中的疗效。方法:原发性急性闭角型青光眼67例69眼发作期药物治疗3~6h后眼压仍〉30mmHg时,行LPIP治疗。监测术前和术后30,60min和2h眼压、视力变化。应用UBM测量术前、术后2h房角宽度和虹膜厚度,并应用房角镜观察前房角粘连情况。结果:LPIP后2h,房角开放距离(AOD)较术前明显增大(P〈0.01),小梁虹膜夹角(TIA)增宽、部分患者周边虹膜前粘连(PAS)减少、周边虹膜变薄。所有患者眼压在激光虹膜成形术后不同时间均有不同程度下降。术前平均眼压53.81±10.22mmHg,术后30min平均眼压33.81±9.22mmHg,术后60min为21.93±7.19mmHg,2h后眼压下降至15.16±3.07mmHg,治疗前后差异有显著统计学意义(F=151.79,P〈0.01)。同时所有患者视力都有所提高。结论:LPIP可以明显加深患者的周边前房,增宽房角入口,降低患者眼压,是治疗AACG急性发作期药物不能控制高眼压持续状态的重要辅助措施,为青光眼的进一步治疗创造了条件,并且能够改善预后。
简介:AIM:Toadaptthelowvision-relatedqualityoflife(LVQOL)instrumentintoTurkishlanguageandtoassessitsvalidityandreliability.METHODS:Thestudywasconductedin387patientsattendingtheCentreofLowVisionRehabilitation,FacultyofMedicine,AnkaraUniversity.Forstatisticalanalyses,theSpearman’scorrelationcoefficient,Cronbach’salphacoefficientandConfirmatoryFactorAnalysis(CFA)wereused.RESULTS:AccordingtoresultsofCFA,theiteminthe'Adjustment'subscalebecauseofhavingthefactorloadingbelow0.40,wasexcludedfromthequestionnaire.ThereliabilityofthequestionnairewasassessedaccordingtoCronbach’salphacoefficients.Thereliabilityofthe'DistanceVision,Mobility,andLighting'subscalewas?琢=0.863;ofthe'Adjustment'subscalewas?琢=0.694;'ReadingandFineWork'was?琢=0.791,and'ActivitiesofDailyLiving'was?琢=0.770.Sotheseresultsindicatethatthequestionnaireisreliabletomeasurethevisionrelatedqualityoflifeoflow-visionpatients.Thecorrelationsbetweenthesubscaleswerealsoanalyzed,andthecorrelationbetween'Adjustment'and'ReadingandFineWork'wasfoundtobethelowest(rs=0.336,P<0.001),whereasthestrongestcorrelationwasfoundbetweenthe'ReadingandFineWork',and'ActivitiesofDailyLiving'.Additionally,the'Adjustment'dimensionshowedthestrongestcorrelationwithonly'DistanceVision,Mobility,andLighting'dimension.CONCLUSION:Afterremovingthelastitemintheseconddimension,theTurkishadaptationofalldimensionsoftheLVQOLhasbeenshowntobereliable,validandsuitableforuseinpatientswithlowvisioninTurkey.
简介:AIM:Tocomparetheregularityandaccuracyoflaserinsitukeratomileusis(LASIK)flapscreatedbytheZiemerFEMTOLDV'Classic'(Ziemer'Classic')andZiemerFEMTOLDVCrystalLinefemtosecondlaser(ZiemerCrystalLine).METHODS:Fourier-domainopticalcoherencetomography(RTVueOCT)wasusedtomeasurethemorphologyof200LASIKflapsof100consecutivepatientscreatedwiththeZiemerClassic(100flaps)ortheZiemerCrystalLine(100flaps)atoneweekpostoperatively.Flapthicknesswasevaluatedat36specifiedmeasurementpointsoneachflap.Forallprocedureswithbothlasers,thenominalflapthicknesswas110μm.RESULTS:ThemeanflapthicknessoftheZiemerCrystalLinegroup(102.49±2.68μm)wasthinnerthanthatoftheZiemerClassicgroup(107.65±5.09μm)(P<0.01).Averagethicknessofallflapswasuniformwithin4μmatallmeasurementpoints.TheflapsintheZiemerCrystalLinegroupweremoreregularthanthoseintheZiemerClassicgroupwhenmeasuredfromthecentertotheperiphery.Themaximumdeviationfromthenominal110μmof36measurementswas8μmintheZiemerClassicgroup,whileintheZiemerCrystalLinegroupitwas9μm.Withinthe3600measurementsonthe100eyes,differencesgreaterthan20μmwereobserved0.14%intheZiemerClassicgroup,and0.04%intheZiemerCrystalLinegroup.CONCLUSION:TheflapscreatedwiththeZiemerFEMTOLDVCrystalLinefemtosecondlaseraremoreuniformandthinnerthanthosecreatedbytheZiemerFEMTOLDVClassicfemtosecondlaser.
简介:AIM:Toassesstheeffectivenessofimmunosuppressantsintheprophylaxisofcornealallograftrejectionafterhigh-riskkeratoplastyandnormal-riskkeratoplasty.METHODS:WesearchedtheCochraneCentralRegisterofControlledTrials(CENTRAL),MEDLINE,EMBASE,CNKI,VIPandreferencelistsofarticles.Dateofmostrecentsearch:18June,2011.Allrandomisedcontrolledtrials(RCTs)assessingtheuseofimmunosupressantsinthepreventionofgraftrejection,irrespectiveofpublicationlanguage.Twoauthorsassessedtrialqualityandextracteddataindependently.Onlydichotomousoutcomes(cleargraftsurvival,ratioofimmunereactionsandsideeffects)wereavailableandwereexpressedasrelativerisk(RR)and95%confidenceintervals(CI).RESULTS:Sevenstudieswereincludedinthisreview.Inthecomparingofmycophenolatemofetil(MMF)withplacebo,theresultsshowedMMFcouldsignificantlyreduceimmunereactionscomparedwithplacebo(RR1.0895%Cl0.95to1.21),butnoeffectoncleargraftsurvival(RR1.1195%Cl0.90to1.35).Incleargraftsurvivalandimmunereactions,MMFandcyclosporineA(CsA)showedsimilareffect(RR1.1195%Cl0.90to1.35,andRR1.48,95%Cl0.56to3.93,respectively).Tacrolimus(FK506)andsteroidshowedsimilareffectsoncleargraftsurvivalandimmunereactions(RR0.32,95%CI0.02to6.21,andRR1.00,95%CI0.88to1.14,respectively).Nodrugrelativesideeffecthasbeenfound.CONCLUSION:MMFmayreduceimmunereactionsinbothnormal-riskandhigh-riskrejectionofpenetratingkeratoplasty.CsAandFK506showedsimilareffectsasMMF.However,duetothelackoflargeclinicaltrials,theevidenceremainweak,thequalityofevidenceswereratedasverylowtomoderate.Large,properlyrandomised,placebo-controlled,doublemaskedtrialsareneededtoevaluatetheeffectofimmunosuppressants.
简介:AIM:ToIntroduceanewspecializedvisualacuitychartforamblyopicchildrenaged3-5yearsoldanditsclinicalapplications.METHODS:ThenewvisualacuitychartandnotationsweredesignedbasedonWeber-Fechnerlaw.Theoptotypeswereredagainstawhitebackgroundandwerespeciallyshapedfourbasicgeometricsymbols:circle,square,triangle,andcross.Aregulargeometricprogressionoftheoptotypesizesanddistributionwasemployedtoarrangein14lines.Theprogressionrateoftheoptotypesizebetweentwolineswas1.2589andthetestingdistancewas3m.VisualacuityscorecouldberecordedaslogMARnotationordecimalnotation.Agestratifieddiagnosticcriteriaforamblyopiaestablishedbyconsensusstatementondiagnosisofamblyopia(2011)amongmembersoftheStrabismusandPediatricOphthalmologyGroup,OphthalmologySociety,ChineseMedicalAssociation(SPOGOSCMA)wereillustratedinthenewvisualacuitychart.RESULTS:Whenassessingvisualacuityinchildrenaged3-5yearsold,thisnewvisualacuitychartthatconsistsoffoursymmetricalshapes(triangle,square,cross,andcircle)overcameaninabilitytorecognizethelettersofthealphabetanddifficultiesindesignatingthedirectionofblackabstractsymbolssuchasthetumbling’E’orLandolt’C’,whichthesubjectswerepronetoloseinterestin.Thevisualacuityscoremayberecordedindifferentnotations:decimalacuityandlogMAR.Thesetwonotationscanbeeasilyconvertedeachotherintheneweyechart.Themeasurementsofthisnewchartnotonlyshowedasignificantcorrelationandagoodconsistencywiththeinternationalstandardlogarithmicvisualacuitychart(r=0.932,P<0.01),butalsoindicatedahightest-retestreliability(89%ofretestscoreswerewithin0.1logMARunitsoftheinitialtestscore).CONCLUSION:Theresultsofthisstudysupportthevalidityandreliabilityofdistancevisualacuitymeasurementsusingtheneweyechartinchildrenaged3to5yearsoverawiderangeofvisualacuities,andtheneweyechartisgreatforearl