首页期刊导航|眼视光学杂志(英文版)
期刊信息/Journal information
眼视光学杂志(英文版)
眼视光学杂志(英文版)

双月刊

眼视光学杂志(英文版)/Journal Eye and VisionCSCDSCI
正式出版
收录年代

    Prospective 12-month outcomes of combined iStent inject implantation and phacoemulsification in Asian eyes with normal tension glaucoma

    Bryan Chin Hou AngWenqi ChiewVivien Cherng Hui YipChun Hau Chua...
    1-11页
    查看更多>>摘要:Background:Glaucoma is the leading cause of irreversible blindness.Normal tension glaucoma(NTG)is a subset of open-angle glaucoma,demonstrating glaucomatous optic nerve damage in the absence of raised intraocular pres-sure(IOP).NTG is more prevalent in Asian populations.While generally slow-progressing,NTG may be associated with significant central visual field loss.In recent years,minimally invasive glaucoma surgery has been added to the arma-mentarium of glaucoma surgery.This prospective study aims to evaluate 12-month surgical outcomes of combined iStent inject(Glaukos Corporation,Laguna Hills,CA)implantation and phacoemulsification in Asian eyes with NTG.Methods:This is a prospective,single-center case series of 30 eyes followed up until 12 months after surgery.Out-come measures included IOP,number of glaucoma medications,best-corrected visual acuity(BCVA)and intra-and postoperative complications.Results:Mean age of subjects was 73.1±6.3 years.Majority were ethnic Chinese(n=27,90%).Baseline medicated mean IOP was 13.8±2.4 mmHg and mean number of glaucoma medications was 1.3±0.7.Mean Humphrey visual field mean deviation was-13.7±7.6 dB.The mean IOP reduction at all timepoints from postoperative month(POM)3 onwards was statistically significant(all P<0.05),with mean reduction of 1.2 mmHg(95%CI:0.1-2.2,P=0.037)by POM12.There was statistically significant reduction in mean number of medications from postoperative day(POD)1 onwards(all P<0.05),with mean decrease of 1.0 medication(95%CI:0.9-1.1,P<0.001)by POM12.By POM12,25(83.3%)eyes were medication-free.Three(10%)eyes had stent occlusion by iris requiring laser iridoplasty.One eye had gross hyphema which resolved on conservative management before POM1.Mean BCVA improved from the baseline 0.3±0.3 logMAR to 0.1±0.1 logMAR postoperatively(P<0.001).There were no major adverse or sight-threat-ening events.No eyes required further glaucoma surgery during the 12-month follow-up period.Conclusion:Asian eyes with NTG which underwent combined iStent inject implantation and phacoemulsifica-tion demonstrated a significant and sustained reduction in IOP and glaucoma medications,up to 12 months postoperatively.

    Visual acuity,near phoria and accommodation in myopic children using spectacle lenses with aspherical lenslets:results from a randomized clinical trial

    Yingying HuangXue LiChu WangFengchao Zhou...
    12-19页
    查看更多>>摘要:Objectives:To investigate the short-and long-term effects of myopia control spectacle lenses with highly aspherical lenslets(HAL)and slightly aspherical lenslets(SAL)on visual function and visual quality using data obtained from a randomized controlled clinical trial.Methods:This was a prospective,randomized,controlled,and double-blinded study;170 myopic children aged 8-13 years were randomly assigned to the HAL,SAL,or single-vision spectacle lenses(SVL)groups.Distance and near visual acuity(VA)at high(100%)and low(10%)contrast in photopic and scotopic conditions,near phoria,stereoacu-ity,and accommodative lag,microfluctuations(AMFs),amplitude(AA)were measured after wearing lenses for 10 min,6 months,and 12 months.Results:In total,161 subjects completed all follow-ups in 12 months and were included in the analysis.After 10 min of wearing,the HAL and SAL groups had lower scotopic and low-contrast VA than the SVL group(decreased 0.03-0.08 logMAR and 0.01-0.04 logMAR in different VAs in the HAL and SAL groups,respectively,all P<0.05).The reduction in VA was recovered at 12 months as the HAL and SAL groups exhibited significant VA improvements,and the VA was not different among the three groups(all P>0.05).The HAL and SAL groups had significantly larger AMFs than the SVL group(HAL vs.SAL vs.SVL:0.21±0.08 D vs.0.16±0.05 D vs.0.15±0.06 D at baseline,0.19±0.07 D vs.0.17±0.05 D vs.0.13±0.07 D at 12 months,all P<0.05).There were no significant differences in accommodative lag,AA,or phoria between the groups(all P>0.05).The HAL and SAL groups had reduced stereoacuity compared to the SVL group at baseline(70"vs.60"vs.50",P=0.005),but no difference was observed at 12 months(70"vs.70"vs.70",P=0.11).Conclusions:HAL and SAL have no significant influence on accommodation and phoria except having larger AMF than SVL.Scotopic VA and low-contrast VA are reduced with short-term HAL and SAL use but recovered to be at same level with the SVL after 1 year of use.

    Q-value customized versus wavefront-optimized ablation in femtosecond laser-assisted LASIK for myopia and myopic astigmatism:a prospective contralateral comparative study

    Magdi Mohammad MostafaHazem AbdelmotaalKhaled AbdelazeemIslam Goda...
    20-32页
    查看更多>>摘要:Background:Corneal refractive surgery for myopia results in an oblate shift with increased postoperative aberrations inversely affecting the quality of vision.Aspheric ablation profiles have been introduced to minimize such a prob-lem.The aim of this study was to compare changes in corneal asphericity,central and mid-peripheral pachymetry between the Q-value customized and the wavefront-optimized(WFO)ablation profiles.Methods:A prospective,comparative non-randomized fellow eye study was conducted.Eighty eyes of 40 eligible patients underwent femtosecond laser-assisted laser in situ keratomileusis for myopia and myopic astigmatism.In each patient,the more myopic eye was included in the custom-Q ablation experimental group and the other less myopic eye was included in the WFO control group.For the custom-Q group,the target asphericity was set to the preoperative Q-value.Corneal asphericity,central and mid-peripheral pachymetric changes and the root mean square of corneal higher-order aberrations(RMSh)were assessed 6 months following surgery.Visual and refractive outcomes were also evaluated in both platforms 6 months postoperatively.Results:The mean preoperative refractive spherical equivalent was significantly more myopic in the custom-Q group than in the WFO group(P=0.001).The mean Q-value changed from-0.2±0.1 to 0.6±0.7 and from-0.2±0.1 to 0.4±0.5 in the custom-Q and WFO groups,respectively.The oblate shift in corneal asphericity was not significantly different between both treatment groups(P=0.094).The mean ablation depth at the pupillary center was signifi-cantly greater in the custom-Q group(P=0.011),while there was no significant difference at the mid-peripheral pachymetry(P=0.256).The RMSh significantly increased in both treatment profiles(P<0.001)with no significant dif-ference between the two groups(P=0.06).The uncorrected distance visual acuity(UDVA)and the manifest refraction spherical equivalents(MRSE)significantly improved in both treatment groups(P<0.001).Conclusions:The custom-Q treatment profile with target asphericity set at the preoperative Q-value achieved com-parable outcomes vs.the WFO profile in terms of postoperative corneal asphericity and mid-peripheral pachymetry despite the greater amount of ablation,the smaller optical zone,and the resulting increase in postoperative corneal flattening in the custom-Q group.

    Comparison of efficacy and safety of intravitreal ranibizumab and conbercept before vitrectomy in Chinese proliferative diabetic retinopathy patients:a prospective randomized controlled trial

    Siying LiLili GuoPingping ZhouJiyang Tang...
    33-40页
    查看更多>>摘要:Background:To compare the efficacy and safety of preoperative intravitreal injections of ranibizumab and conber-cept in Chinese proliferative diabetic retinopathy(PDR)patients.Methods:This prospective randomized controlled trial enrolled 90 eyes of 80 patients with PDR.Forty-four eyes of 40 patients that received intravitreal ranibizumab(IVR)injections(0.5 mg/0.05 mL)before vitreous surgeries were assigned to the IVR group.Forty-six eyes of 40 patients that received intravitreal conbercept(IVC)injections(0.5 mg/0.05 mL)before vitreous surgeries were assigned to the IVC group.Intraoperative and postoperative indices were assessed for further comparison between the two groups.Results:There were no statistically significant differences in all surgery indices,including intraoperative indices(sur-gery time,P=0.225;intraoperative bleeding,P=0.808;endodiathermy use,P=0.693;incidence of iatrogenic retinal breaks,P=0.740;relaxing retinotomy,P=0.682;retinal reattachment,P=0.682 and silicone oil tamponade,P=0.814)and postoperative indices[postoperative vitreous hemorrhage(VH),P=0.808;neovascular glaucoma(NVG),P=0.964;recurrent retinal detachment,P=0.531;postoperative fibrovascular proliferation progression,P=0.682 and reoperation,P=0.955]between the two groups.There were no statistically significant differences in best-corrected visual acuity(BCVA)at each follow-up visit(P=0.939,0.669,0.741 and 0.717,respectively)or in central retinal thick-ness(CRT)(P=0.976,0.699,0.551 and 0.686,respectively).As for safety profile,both groups had no ocular or system adverse events during the observation period.Conclusions:IVR and IVC as a pretreatment of vitrectomy had similar efficacy and safety profile for Chinese PDR patients.

    INSTRUCTIONS FOR AUTHORS

    封3页