简介:对有晶状体眼植入后房型人工晶状体是矫正屈光不正的有效方法,植入的后房型人工晶状体目前主要有可植入式接触镜(implantablecontactlens,ICL)和有晶状体眼屈光性晶状体(phakicrefractivelens,PRL)。对术后患者主观视觉质量(视力、对比敏感度)、客观视觉质量(波前像差、点扩散函数、斯特尔比率及光学传递函数)的研究显示,主观视力的提高也伴随着客观视觉质量的改善,但部分患者术后出现光晕及眩光症状。本文主要对ICL和PRL植入术后主观及客观视觉质量的临床研究做一综述,对可影响视觉质量的术后并发症如晶状体前囊膜下混浊、青光眼及角膜内皮功能异常等需进一步远期随访。
简介:目的:探讨舌状截囊方法在过熟期白内障囊外摘除联合人工晶状体植入术的临床效果。方法:对380眼过熟期白内障囊外摘除联合人工晶状体植入术中采用舌状截囊方法,术后观察及随访其疗效。结果:所有患眼术后视力均有不同程度提高,视力恢复情况:术后1d,0.1以下85眼(22.4%),0.1-0.3者162眼(42.6%),0.4-0.6者87眼(22.9%),0.6以上者46眼(12.1%)。术后1mo0.1以下33眼(8.7%),0.1-0.3者152眼(40.0%),0.4-0.6者117眼(30.8%),0.6以上者78眼(20.5%)。术中术后并发症:术中悬韧带断离16眼(4.2%),后囊膜破裂25眼(6.6%),角膜水肿53眼(13.9%),人工晶状体偏位12眼(3.2%)。结论:舌状截囊方法容易掌握,手术的安全性更好,更适合在援非过熟期白内障囊外摘除联合人工晶状体植入术中的应用。
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:目的了解531例患者(含家属)对我院民生工程白内障手术疗效的评价。方法我院固定1名眼科主治医师在不同时间段进行电话回访(含手机),如固定电话打不通再换手机打,打1-2次通话者为1次打通,3次(含3次者)以上为多次打通,打4-7次不通者放弃。结果531例共打电话1327次,平均每名患者2.49次,回访率为100%,最终获得有效通话者427例,回访成功率为80.41%。手术满意380例,占88.99%;基本满意33例,占7.73%;满意率为96.72%。不满意14例,占3.28%。术后复查1-3次者314例,占73.53%;未复查93例,占21.77%;不知道是否复查20例,占4.68%;复查率最高者琅琊区100%,最低者定远县63.44%。无1例在住院手术期间花钱。未发现严重并发症和医疗事故及医疗纠纷。结论电话回访能有效获得民生工程白内障手术患者的疗效评价,且经济方便,应纳入常规内容。
简介:目的评价甲基纤维素联合透明质酸钠制作软壳技术在白内障小切口非超声乳化手术中的效果.方法白内障“复明工程”患者261例295眼.随机分为A、B两组,其中A组术中单用透明质酸钠,B组术中联合使用甲基纤维素和透明质酸钠.手术方法为小切口非超声乳化加人工晶体植入.结果术后第ld裸眼视力大于0.3者,A组78.79%(104/132),B组87.1%(142/163),两组之间差异显著(P<0.05);术后第7d视力在0.3以上者,A组93.9%(124/132),B组94.5%(154/163).两组间差异无统计学意义(P>0.05).术后角膜水肿情况:术后第1天,A组17.42%(23/132),B组9.8%(16/163),两组间比较差异有统计学意义(P<0.05).术后第7天,A组2.27%(3/132),B组2.45%(4/163),两组间比较差异无统计学意义(P>0.05).结论甲基纤维素联合透明质酸钠制作软壳技术比单用透明质酸钠更安全.
简介:目的以接受免费白内障手术的患者电话随访结果为依据,对我省防盲项目完成效果进行评价、分析,探讨提出加强和完善基层医院眼科参与大规模防盲项目患者的可持续随访体系。方法通过以电话随访的方式,对2012年云南省'光明工程'6万例免费白内障手术患者中随机抽取2000例患者就手术视力提高程度及满意度进行电话随访。随访统一使用云南省卫生厅《2012年云南省'光明工程'患者电话随访表》,由专人于4周内完成电话随访。结果患者术后视力明显提高者占90.20%;患者对术后满意度达93.27%;从生活不能自理到能自理占86.41%;术后生活质量明显提高占85.79%;术后患眼有不适者占17.76%;知道如出现不适如何处理的患者占70%;新农合占93.81%,居民医保5.56%,职工医保1.64%,其他医保占0.88%;所有患者均为免费手术,无自付比例。结论在基层开展大规模集中白内障防盲项目的过程中,在严格监控患者术后质量、手术费用、住院天数、降低患者的医疗费用的同时,更应该加强对手术患者的长效管理机制,建立合理的患者随访体系,总结经验,不断完善工作流程,真正改善患者的生活质量,提高患者满意度,体现防盲工作的真正含义。