Department of Ophthalmology, Başkent University School of Medicine, Fevzi Çakmak Blv. Bahçelievler, 06490, Ankara, Turkey.
Int Ophthalmol. 2024 Aug 25;44(1):354. doi: 10.1007/s10792-024-03281-9.
We aimed to evaluate distance stereoacuity (DS) in patients with successfully treated accommodative esotropia (AET) and its association with other clinical factors.
The medical records of 176 children with refractive AET with a follow-up period ≥ 1 year were reviewed to identify a cohort of patients who achieved a stable alignment within 4 prism diopters (PD) of orthotropia at both distance and near fixation. Age of onset, duration of misalignment, uncorrected near and distance deviation, accommodative convergence/accommodation ratio, refractive error, presence of anisometropia and amblyopia, near stereopsis were evaluated as predictors of outcome. DS was measured using the Distance Randot Stereo test and near stereoacuity by Randot Stereotest. The patient group was compared with 50 age-matched normal controls for DS.
Fifty-six patients were included, and 38 patients had DS at the final visit. All patients with DS attained uncontoured near stereopsis (UCNS). UCNS was present only in 11 patients without DS (p = 0.001). Anisometropia (p = 0.997), uncorrected near deviation (p = 0.224), distance deviation with correction (p = 0.255), and high hypermetropia (p = 0.998) were not associated with DS. The multivariable regression model showed a significant positive correlation between UCNS and DS (OR = 31.14 (95% CI 2.25-430.48); p = 0.01). Contoured near stereopsis outcome was significantly different between the patients with and without DS (p = 0.001 for animals and p = 0.003 for circles). Compared with the control group, the patient group yielded lower DS scores (p = 0.001).
Distance Randot Stereotest can be useful in measuring binocular vision recovery after successful realignment in refractive AET patients. Patients attaining normal scores for near stereopsis tests after optical correction revealed subnormal thresholds for DS.
评估成功治疗的调节性内斜视(AET)患者的远距立体视锐度(DS)及其与其他临床因素的关系。
回顾了 176 例屈光性 AET 儿童的病历,这些儿童的随访时间≥1 年,以确定一组在远距和近距注视时,在 4 棱镜屈光度(PD)内达到正位的稳定斜视患者。评估发病年龄、斜视持续时间、未矫正的近距和远距偏斜、调节性集合/调节比值、屈光不正、是否存在屈光参差和弱视、近立体视等作为预测结果的因素。使用距离 Randot 立体视检查(Distance Randot Stereo test)测量 DS,使用 Randot 立体试验(Randot Stereotest)测量近立体视锐度。将患者组与 50 名年龄匹配的正常对照组进行 DS 比较。
纳入 56 例患者,其中 38 例在最后一次就诊时具有 DS。所有具有 DS 的患者均获得未校正的近立体视锐度(UCNS)。而在没有 DS 的 11 例患者中仅存在 UCNS(p=0.001)。屈光参差(p=0.997)、未矫正的近距偏斜(p=0.224)、矫正后的远距偏斜(p=0.255)和高度远视(p=0.998)与 DS 无相关性。多变量回归模型显示,UCNS 与 DS 之间存在显著正相关(OR=31.14(95%CI 2.25-430.48);p=0.01)。具有和不具有 DS 的患者的近立体视锐度结果有显著差异(动物图的 p=0.001,圆形图的 p=0.003)。与对照组相比,患者组的 DS 评分较低(p=0.001)。
在屈光性 AET 患者成功矫正后,距离 Randot Stereotest 可用于测量双眼视觉恢复情况。经光学矫正后近立体视测试获得正常分数的患者,其 DS 阈值较低。