学科分类
/ 1
7 个结果
  • 简介:目的总结老年性白内障复明手术护理配合经验。方法对489例老年性白内障摘除+人工晶体植入术的护理配合过程进行回顾。重点是确保器械灭菌效果以及手术问空气质量,各种手术用品的充分准备。结果489例手术医护配合顺利。结论充分的术前准备,熟练的术中配合,正确及时的术后处理是保证手术顺利进行的关键。

  • 标签: 复明手术 护理配合 老年患者 临床护理
  • 简介:目的:研究当归芍药散配合小梁切除术联合bevacizumab治疗新生血管性青光眼的疗效。方法:将2011-01/2014-02期间我院收治的新生血管性青光眼患者纳入研究,根据治疗方法不同分为接受中西医药物配合小梁切除术治疗的观察组和接受西医药物配合小梁切除术治疗的对照组,比较两组患者的视力水平、眼压、视网膜神经纤维层厚度。结果:视力水平:治疗后1wk;6,12mo,观察组的患眼视力水平均明显高于对照组(0.41±0.07vs0.27±0.04,0.52±0.08vs0.38±0.06,0.72±0.14vs0.54±0.08);眼压:治疗后1wk;6,12mo,观察组眼压明显低于对照组(15.11±3.22vs22.32±5.34,18.64±5.08vs26.67±6.22,17.18±3.76vs22.42±4.32)mmHg;视网膜神经纤维层厚度:治疗后12mo,观察组上方视野、下方视野、颞侧视野、鼻侧视野等神经纤维层厚度等神经纤维层厚度均明显高于对照组(90.41±10.52vs78.64±8.24,88.38±12.12vs72.37±8.82,73.21±8.46vs60.25±7.23,75.35±8.13vs62.63±7.29)μm。结论:当归芍药散配合小梁切除术联合bevacizumab治疗新生血管性青光眼有助于促进视力水平的恢复、控制眼压、改善视网膜神经纤维层厚度。

  • 标签: 新生血管性青光眼 BEVACIZUMAB 玻璃体腔注射 小梁切除术 当归芍药散
  • 简介:目的总结有晶体眼后房型人工晶体植人术手术护理配合经验。方法对我院26例52只眼后房型人工晶体植入术矫正高度近视的手术配合进行回顾。结果26例52只眼后房型人工晶体矫正高度近视的手术配合顺利,效果满意。结论充分的术前准备,熟练有效的手术配合是保证手术成功的关键。

  • 标签: 后房型 有晶体眼 植入术 高度近视 手术配合
  • 简介:目的:评价图形视觉诱发电位(patternvisualevokedpotentials,P-VEP)、眼底照相、视野和光学相干断层扫描(opticalcoherencetomography,OCT)对青光眼患者检查的可靠性。方法:对83例95眼青光眼患者应用眼科电生理仪、眼底照相、视野和OCT,根据P-VEP、眼底照相、OCT、视野检查结果的阳性率进行相关性分析。结果:患者83例95眼中,视野检查成功获取阳性病例图像73眼(76.8%),无法获取图像22眼(23.2%);眼底照像成功获取阳性病例图像75眼(78.9%),无法获取图像20眼(21.1%);获得P-VEP阳性病例47眼(49.5%),未见明显异常26眼(27.3%),无法采集图像22眼(23.2%);成功获取OCT阳性病例图像81眼(85.3%),无法获取OCT图像14眼(14.7%)。结论:视觉诱发电位、眼底照相、视野和光学相干断层图像结果对青光眼患者的视功能状况进行综合评估。

  • 标签: 青光眼 视觉诱发电位 视野 眼底照相 光学相干断层扫描
  • 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.

  • 标签: LOW vision-related quality of life TURKISH
  • 简介:目的:系统评价拉坦前列素(Latanoprost)滴眼液与噻吗心安(Timolol)滴眼液降眼压的有效性和安全性。方法:计算机检索PubMed,Medline,CNKI及中国生物医学文献数据库收录的,并辅以手工检索、因特网搜索的有关拉坦前列素与噻吗心安治疗原发性开角型青光眼和高眼压症的随机对照试验(RCT)。按照纳入和排除标准限定研究对象,通过Jadad评分量表进行文献质量评估后,针对眼压下降比例、药物不良反应2项内容,使用Cochrane协作网提供的RevMan5.0软件进行Meta分析。结果:共纳入9项RCT,合计555例患者。Meta分析结果显示:(1)拉坦前列素滴眼液与噻吗心安滴眼液降眼压效果,在2,6,12wk时差异均有统计学意义(P<0.01),加权平均差(WMD)分别为:在2wk[WMD=-0.76,95%CI(-1.32,-0.20)],在6wk[WMD=-1.15,95%CI(-1.68,0.63)]和12wk[WMD=-1.01,95%CI(-1.42,-0.61)]。(2)随访结束时,结膜充血、异物感为拉坦前列素的两种较为常见的不良反应,但其发生率拉坦前列素组与噻吗心安组比较,结膜充血的发生率[OR=2.25,95%CI(0.99,5.08)],异物感的发生率[OR=2.48,95%CI(1.02,6.03)],显示二者差异均无统计学意义。结论:治疗原发性开角型青光眼和高眼压症,拉坦前列素降眼压效果在用药12wk内较噻吗心安好;两者在12wk内引起结膜充血、异物感、虹膜色素加深、视野损害等的不良反应方面,差异不明显。由于纳入研究的样本量偏小,且方法学质量中等,致使本系统评价结果论证强度不高,因此还需要开展更多的高质量的临床随机对照研究,以便更客观、准确、全面地评价其疗效和安全性。

  • 标签: 拉坦前列素 噻吗心安 原发性开角型青光眼 高眼压症 有效性 安全性
  • 简介:AIM:Tofindouttheoutcomeoflaserphotocoagulationinclinicallysignificantmacularedema(CSME)byopticalcoherencetomography(OCT).·METHODS:Itwasaprospective,non-controlled,caseseriesstudyenrolling81eyesof64patientswithCSMEbetweenAugust2008andJanuary2010.AllpatientsreceivedmodifiedgridphotocoagulationwithfrequencydoubledNd:YAGlaser.Eachpatientwasevaluatedintermsofbest-correctedvisualacuity(BCVA)andregressionorprogressionofmaculopathyafterlasertherapyat1,3and6months.Spearman’scorrelationtestwasusedtoshowthecorrelationbetweenBCVAandtotalmacularvolume(TMV).Analysisofvariance(ANOVA)wasusedtocompareamonggroupsandindependentt-testwasusedtocompareineachgroup.·RESULTS:ThereishighcorrelationbetweenBCVAandTMV(P≤0.001).BCVAimprovedin50.6%,remainedstaticin39.5%anddeterioratedin9.9%patientsafter6monthoftreatment.TheBaselineTMV(meanandSD)were9.26±1.83,10.4±2.38,11.5±3.05,8.89±0.75and9.47±1.98mm3fordifferentOCTpatterns,ST(spongelikethickening),CMO(cystoidmacularedema),SFD(subfovealdetachment),VMIA(Vitreomacularinterfaceabnormality)andaverageTMVrespectively(P=0.04).After6monthsoflasertreatment,themeanTMVdecreasedfrom9.47±1.98mm3to8.77±1.31mm3(P=0.01).InSTtherewassignificantdecreaseinTMV,P=0.01,Furtherwithinthesegroupsat6months,theyweresignificantlydifferent,P=0.01.·CONCLUSION:OCTshowedthedifferentmorphologicalvariantofCSMEwhiletheresponseoftreatmentisdifferent.TMVdecreasedthemostandhenceshowedtheimprovementinvisionafter6monthsoflasertreatment.IntheeraofAntivascularendothelialgrowthfactors(VEGFs),efficacyoflaserseemstobeinshadowbutitisstillfirstlineoftreatmentindevelopingnationlikeNepalwhereantiVEGFsmaynotbeeasilyavailableandaffordable.

  • 标签: Clinically SIGNIFICANT MACULAR EDEMA Grid laser