Ruiz-Mesa Ramón, Abengózar-Vela Antonio, Aramburu Ana, Ruiz-Santos María
Oftalvist CIO Jerez, Puerta del Sur, Hospital Jerez de la Frontera, Cádiz - Spain.
Eur J Ophthalmol. 2017 Jun 26;27(4):460-465. doi: 10.5301/ejo.5000935. Epub 2017 Jan 28.
To compare visual outcomes after cataract surgery with bilateral implantation of 2 intraocular lenses (IOLs): extended range of vision and trifocal.
Each group of this prospective study comprised 40 eyes (20 patients). Phacoemulsification followed by bilateral implantation of a FineVision IOL (group 1) or a Symfony IOL (group 2) was performed. The following outcomes were assessed up to 1 year postoperatively: binocular uncorrected distance visual acuity (UDVA), binocular uncorrected intermediate visual acuity (UIVA) at 60 cm, binocular uncorrected near visual acuity (UNVA) at 40 cm, spherical equivalent (SE) refraction, defocus curves, mesopic and photopic contrast sensitivity, halometry, posterior capsule opacification (PCO), and responses to a patient questionnaire.
The mean binocular values in group 1 and group 2, respectively, were SE -0.15 ± 0.25 D and -0.19 ± 0.18 D; UDVA 0.01 ± 0.03 logMAR and 0.01 ± 0.02 logMAR; UIVA 0.11 ± 0.08 logMAR and 0.09 ± 0.08 logMAR; UNVA 0.06 ± 0.07 logMAR and 0.17 ± 0.06 logMAR. Difference in UNVA between IOLs (p<0.05) was statistically significant. There were no significant differences in contrast sensitivity, halometry, or PCO between groups. Defocus curves were similar between groups from 0 D to -2 D, but showed significant differences from -2.50 D to -4.00 D (p<0.05).
Both IOLs provided excellent distance and intermediate visual outcomes. The FineVision IOL showed better near visual acuity. Predictability of the refractive results and optical performance were excellent; all patients achieved spectacle independence. The 2 IOLs gave similar and good contrast sensitivity in photopic and mesopic conditions and low perception of halos by patients.
比较白内障手术后双眼植入两种人工晶状体(IOL)后的视觉效果:扩展视力范围型和三焦点型。
这项前瞻性研究的每组包括40只眼(20例患者)。进行超声乳化白内障吸除术,随后双眼植入FineVision IOL(第1组)或Symfony IOL(第2组)。在术后长达1年的时间里评估以下结果:双眼未矫正远视力(UDVA)、60cm处的双眼未矫正中间视力(UIVA)、40cm处的双眼未矫正近视力(UNVA)、等效球镜度(SE)屈光度、散焦曲线、中间视觉和明视觉对比敏感度、眩光测量、后囊膜混浊(PCO)以及患者问卷的回答。
第1组和第2组的平均双眼值分别为:SE -0.15±0.25D和-0.19±0.18D;UDVA 0.01±0.03 logMAR和0.01±0.02 logMAR;UIVA 0.11±0.08 logMAR和0.09±0.08 logMAR;UNVA 0.06±0.07 logMAR和0.17±0.06 logMAR。两种IOL之间的UNVA差异(p<0.05)具有统计学意义。两组之间在对比敏感度、眩光测量或PCO方面没有显著差异。两组从0D到-2D的散焦曲线相似,但在-2.50D到-4.00D之间存在显著差异(p<0.05)。
两种IOL均提供了出色的远视力和中间视力效果。FineVision IOL显示出更好的近视力。屈光结果的可预测性和光学性能都非常出色;所有患者都无需佩戴眼镜。这两种IOL在明视觉和中间视觉条件下具有相似且良好的对比敏感度,患者对眩光的感知较低。