Jaeb Center for Health Research, Tampa, FL 33647, USA
Ophthalmology. 2010 May;117(5):998-1004.e6. doi: 10.1016/j.ophtha.2009.10.014. Epub 2010 Feb 16.
To determine whether visual acuity improvement with Bangerter filters is similar to improvement with patching as initial therapy for children with moderate amblyopia.
Randomized, clinical trial.
We enrolled 186 children, 3 to <10 years old, with moderate amblyopia (20/40-20/80).
Children were randomly assigned to receive either daily patching or to use a Bangerter filter on the spectacle lens in front of the fellow eye. Study visits were scheduled at 6, 12, 18, and 24 weeks.
Visual acuity in amblyopic eyes at 24 weeks.
At 24 weeks, amblyopic eye improvement averaged 1.9 lines in the Bangerter group and 2.3 lines in the patching group (difference in mean visual acuities between groups adjusted for baseline acuity = 0.38 line). The upper limit of a 1-sided 95% confidence interval was 0.76 line, which slightly exceeded a prespecified noninferiority limit of <0.75 line. Similar percentages of subjects in each group improved > or =3 lines (Bangerter group 38% vs patching group 35%; P = 0.61) or had > or =20/25 amblyopic eye acuity (36% vs 31%, respectively; P = 0.86). There was a lower treatment burden in the Bangerter group as measured with the Amblyopia Treatment Index. With Bangerter filters, neither a fixation switch to the amblyopic eye nor induced blurring in the fellow eye to worse than that of the amblyopic eye was required for visual acuity improvement.
Because the average difference in visual acuity improvement between Bangerter filters and patching was less than half a line, and there was lower burden of treatment on the child and family, Bangerter filter treatment is a reasonable option to consider for initial treatment of moderate amblyopia.
确定邦加特滤光镜治疗中度弱视儿童的视力提高是否与遮盖治疗相似。
随机临床试验。
我们招募了 186 名 3 至<10 岁的中度弱视(20/40-20/80)儿童。
儿童随机分为接受每日遮盖或在对侧眼镜片上使用邦加特滤光镜治疗。研究访问计划在 6、12、18 和 24 周进行。
24 周时弱视眼的视力。
在 24 周时,邦加特组弱视眼的平均改善为 1.9 行,遮盖组为 2.3 行(调整基线视力后两组平均视力差异=0.38 行)。单侧 95%置信区间上限为 0.76 行,略超过预定的<0.75 行非劣效性限值。每组中视力提高>或=3 行的患者比例相似(邦加特组 38%对遮盖组 35%;P=0.61)或弱视眼视力>或=20/25 的比例相似(分别为 36%和 31%,P=0.86)。邦加特组的治疗负担用弱视治疗指数衡量时较低。使用邦加特滤光镜,无需将注视点转移到弱视眼,也无需使对侧眼的模糊度降低到比弱视眼更差的程度,即可提高视力。
由于邦加特滤光镜和遮盖治疗的视力提高平均差异小于半行,而且对儿童和家庭的治疗负担较低,因此邦加特滤光镜治疗是中度弱视初始治疗的合理选择。