Ang Robert Edward T
Cataract and Refractive Surgery Department, Asian Eye Institute, Makati City, Philippines.
Clin Ophthalmol. 2023 Feb 21;17:623-632. doi: 10.2147/OPTH.S403351. eCollection 2023.
To show the visual and refractive outcomes in Asian eyes with cataract when bilaterally implanted with either a hydrophobic FineVision POD F GF or a hydrophilic FineVision POD F intraocular lens (IOL).
Forty-six patients were randomized to receive POD F GF or POD F IOLs. Visual and refractive outcomes were assessed up to 24 months post-surgery. Measurements included uncorrected-distance visual acuity, corrected-distance visual acuity (CDVA), distance-corrected intermediate visual acuity (DCIVA), distance-corrected near visual acuity (DCNVA), refraction, defocus curve, photopic and mesopic contrast sensitivity, and patient-reported outcomes.
Mean spherical equivalent was close to emmetropia for both groups and stable across postoperative visits. Overall, 97.73% and 100% of eyes in the POD F GF IOL group and 95.65% and 100%, of eyes in the POD F IOL group were within ±1.00D of the target refraction at 12 and 24 months, respectively. All patients showed a CDVA of ≥20/25 at 12- and 24-months post-surgery. In both groups, 24 months post-surgery 91% of patients presented a DCIVA of ≥20/25 and 83.3% of patients had a DCNVA of ≥20/25. Defocus curve showed continuous visual acuity, being 20/32 or better in both groups over a 4.00D range between 1.00D and -3.00/-3.50D. Both groups showed good contrast sensitivity values for photopic and mesopic conditions. Overall, 86.4%, 86.4%, and 72.7% of patients implanted with the POD F GF IOL reported not wearing glasses at all for distance, intermediate, and near vision, respectively. These values were 81.8%, 86.4%, and 90.9% for patients implanted with the POD F IOL. Both groups of patients reported similar satisfaction percentages (100% very satisfied/satisfied) and would recommend the procedure (100% definitively yes/probably yes).
This study demonstrates good visual and refractive outcomes for both the FineVision POD F GF and the FineVision POD F IOLs when implanted in Asian eyes.
展示亚洲白内障患者双眼植入疏水性FineVision POD F GF或亲水性FineVision POD F人工晶状体(IOL)后的视觉和屈光效果。
46例患者被随机分配接受POD F GF或POD F IOL。术后24个月内评估视觉和屈光效果。测量指标包括未矫正远视力、矫正远视力(CDVA)、距离矫正中间视力(DCIVA)、距离矫正近视力(DCNVA)、验光、散焦曲线、明视觉和 mesopic 对比敏感度以及患者报告的结果。
两组的平均球镜等效度均接近正视且术后随访期间稳定。总体而言,POD F GF IOL组分别有97.73%和100%的眼睛在12个月和24个月时目标屈光在±1.00D范围内,POD F IOL组分别为95.65%和100%。所有患者术后12个月和24个月时的CDVA均≥20/25。两组在术后24个月时,91%的患者DCIVA≥2 /25,83.3%的患者DCNVA≥20/25。散焦曲线显示视力持续良好,两组在1.00D至 -3.00/-3.50D的4.00D范围内视力均为20/32或更好。两组在明视觉和mesopic条件下均显示出良好的对比敏感度值。总体而言,植入POD F GF IOL的患者分别有86.4%、86.4%和72.7%报告在远、中、近视力时完全不戴眼镜。植入POD F IOL的患者这些值分别为81.8%、86.4%和90.9%。两组患者报告的满意度百分比相似(100%非常满意/满意),并会推荐该手术(100%肯定会/可能会)。
本研究表明,FineVision POD F GF和FineVision POD F IOL植入亚洲人眼中均具有良好的视觉和屈光效果。