Trivedi Rupal H, Lambert Scott R, Lynn Michael J, Wilson M Edward
Department of Ophthalmology, Storm Eye Institute, Medical University of South Carolina, Charleston, South Carolina.
Department of Ophthalmology, Emory University School of Medicine, Atlanta, Georgia.
J AAPOS. 2014 Jun;18(3):251-4. doi: 10.1016/j.jaapos.2014.01.012.
To investigate the role of preoperative biometry for selecting initial contact lens power.
Patients randomized to receive contact lenses in the Infant Aphakia Treatment Study (IATS) were retrospectively analyzed. Inclusion criteria were availability of both a preoperative immersion axial length measurement and a 1-month postoperative refractive value. The target contact lens power for distance was determined using 1-month postoperative spherical equivalent refraction (after adjusting for a vertex distance) over the known contact lens power. We compared targeted contact lens power for distance with three other treatment techniques: (1) 30 D contact lens (32 D minus 2 D overcorrection for near vision based on IATS protocol); (2) regression-estimated contact lens power of 84.4 - 3.2 × axial length; and (3) IOL power calculated using the Sanders-Retzlaff-Kraff (SRK/T) regression formula with a modified A-constant (112.176). Prediction error (targeted minus estimated contact lens power) and its absolute values were calculated.
A total of 34 eyes of 34 patients met inclusion criteria. Age at the time of cataract surgery was 2.4 ± 1.7 months. Follow-up refraction was performed at 31 ± 3 days after surgery. Target contact lens power for distance was 26.0 ± 4.5 D for the IATS cohort (which excluded infants with corneal diameter <9 mm). The mean prediction error was -4.0, -1.0, and -2.0 D and mean absolute prediction error was 4.4, 2.2, and 2.9 D, respectively, for 30 D contact lens, regression, and SRK/T-estimated power.
Preoperative biometry can be used to estimate contact lens power for distance if an accurate refraction cannot be obtained initially.
探讨术前生物测量在选择初始隐形眼镜屈光度中的作用。
对婴儿无晶状体治疗研究(IATS)中随机接受隐形眼镜的患者进行回顾性分析。纳入标准为术前有浸入式眼轴长度测量值以及术后1个月的屈光值。根据已知的隐形眼镜屈光度,使用术后1个月的等效球镜度(调整顶点距离后)确定远距离目标隐形眼镜屈光度。我们将远距离目标隐形眼镜屈光度与其他三种治疗技术进行比较:(1)30D隐形眼镜(根据IATS方案,为近视力进行32D减2D的过矫正);(2)通过回归估计的隐形眼镜屈光度为84.4 - 3.2×眼轴长度;(3)使用修正A常数(112.176)的Sanders-Retzlaff-Kraff(SRK/T)回归公式计算的人工晶状体屈光度。计算预测误差(目标屈光度减去估计的隐形眼镜屈光度)及其绝对值。
共有34例患者的34只眼符合纳入标准。白内障手术时的年龄为2.4±1.7个月。术后31±3天进行随访验光。IATS队列(排除角膜直径<9mm的婴儿)的远距离目标隐形眼镜屈光度为26.0±4.5D。对于30D隐形眼镜、回归法和SRK/T估计的屈光度,平均预测误差分别为-4.0、-1.0和-2.0D,平均绝对预测误差分别为4.4、2.2和2.9D。
如果最初无法获得准确的验光结果,术前生物测量可用于估计远距离隐形眼镜屈光度。