Rotationally Asymmetric Refractive Low Addition Multifocal IOL Implantation in Patients With Previous Hyperopic Corneal Laser Refractive Surgery
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00179906%3A_____%2F25%3A10507210" target="_blank" >RIV/00179906:_____/25:10507210 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216208:11150/25:10507210
Výsledek na webu
<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=_GujoCznRv" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=_GujoCznRv</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3928/1081597X-20251024-02" target="_blank" >10.3928/1081597X-20251024-02</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Rotationally Asymmetric Refractive Low Addition Multifocal IOL Implantation in Patients With Previous Hyperopic Corneal Laser Refractive Surgery
Popis výsledku v původním jazyce
Purpose: To evaluate visual, refractive, and quality-of-vision outcomes after cataract surgery with a low-addition rotationally asymmetric refractive multifocal intraocular lens (Lentis Comfort Mplus LS-313 MF15; Teleon) in eyes with prior hyperopic corneal laser refractive surgery. Methods: This was a retrospective observational study of 26 eyes (26 patients) implanted with the LENTIS Comfort Mplus LS-313 MF15 after uneventful surgery. Distance, intermediate, and near visual acuity, manifest refraction, ocular/corneal wavefront aberrations, contrast sensitivity, and defocus curves were assessed preoperatively and at 1, 3, and 6 months and at the final visit. Subjective quality was measured with the Quality of Vision (QoV) questionnaire. Results: At 6 months and the final visit, uncorrected (UDVA), corrected (CDVA), uncorrected near (UNVA), and corrected near (CNVA) visual acuity improved to 0.10 +/- 0.14, 0.05 +/- 0.06, 0.27 +/- 0.22, and 0.08 +/- 0.10 logarithm of the minimum angle of resolution (logMAR), respectively (all P < .05). UIVA and CDIVA were 0.12 +/- 0.07 and 0.10 +/- 0.09 logMAR, respectively. Refractive cylinder decreased to -0.40 +/- 0.38 diopters (D) (P < .05); mean spherical equivalent at 6 months was 0.00 +/- 0.70 D. Ocular root mean square for total, astigmatism, coma, asymmetry, HOAs, spherical-like, and coma-like aberrations were 0.59 +/- 0.36, 0.42 +/- 0.28, 0.20 +/- 0.12, 0.05 +/- 0.03, 0.39 +/- 0.28, 0.16 +/- 0.12, and 0.30 +/- 0.20 mu m, respectively. Defocus showed 0.05 +/- 0.01 logMAR at 0.00 D, 0.13 +/- 0.01 at -1.50 D, and 0.27 +/- 0.20 at -2.50 D; contrast sensitivity remained within normal limits. QoV scores were 32.97 +/- 24.31 (frequency), 30.47 +/- 22.19 (severity), and 28.59 +/- 21.32 (bothersomeness). Corneal higher order aberrations (HOAs) and angle kappa correlated with postoperative uncorrected acuity, especially at intermediate and near. Conclusions: The aberration-neutral, rotationally asymmetric LENTIS Comfort Mplus LS-313 MF15 provided safe, predictable rehabilitation in eyes after hyperopic corneal surgery, with high-quality distance/intermediate vision and low photic phenomena. Preoperative HOAs and angle kappa significantly influenced postoperative uncorrected vision.
Název v anglickém jazyce
Rotationally Asymmetric Refractive Low Addition Multifocal IOL Implantation in Patients With Previous Hyperopic Corneal Laser Refractive Surgery
Popis výsledku anglicky
Purpose: To evaluate visual, refractive, and quality-of-vision outcomes after cataract surgery with a low-addition rotationally asymmetric refractive multifocal intraocular lens (Lentis Comfort Mplus LS-313 MF15; Teleon) in eyes with prior hyperopic corneal laser refractive surgery. Methods: This was a retrospective observational study of 26 eyes (26 patients) implanted with the LENTIS Comfort Mplus LS-313 MF15 after uneventful surgery. Distance, intermediate, and near visual acuity, manifest refraction, ocular/corneal wavefront aberrations, contrast sensitivity, and defocus curves were assessed preoperatively and at 1, 3, and 6 months and at the final visit. Subjective quality was measured with the Quality of Vision (QoV) questionnaire. Results: At 6 months and the final visit, uncorrected (UDVA), corrected (CDVA), uncorrected near (UNVA), and corrected near (CNVA) visual acuity improved to 0.10 +/- 0.14, 0.05 +/- 0.06, 0.27 +/- 0.22, and 0.08 +/- 0.10 logarithm of the minimum angle of resolution (logMAR), respectively (all P < .05). UIVA and CDIVA were 0.12 +/- 0.07 and 0.10 +/- 0.09 logMAR, respectively. Refractive cylinder decreased to -0.40 +/- 0.38 diopters (D) (P < .05); mean spherical equivalent at 6 months was 0.00 +/- 0.70 D. Ocular root mean square for total, astigmatism, coma, asymmetry, HOAs, spherical-like, and coma-like aberrations were 0.59 +/- 0.36, 0.42 +/- 0.28, 0.20 +/- 0.12, 0.05 +/- 0.03, 0.39 +/- 0.28, 0.16 +/- 0.12, and 0.30 +/- 0.20 mu m, respectively. Defocus showed 0.05 +/- 0.01 logMAR at 0.00 D, 0.13 +/- 0.01 at -1.50 D, and 0.27 +/- 0.20 at -2.50 D; contrast sensitivity remained within normal limits. QoV scores were 32.97 +/- 24.31 (frequency), 30.47 +/- 22.19 (severity), and 28.59 +/- 21.32 (bothersomeness). Corneal higher order aberrations (HOAs) and angle kappa correlated with postoperative uncorrected acuity, especially at intermediate and near. Conclusions: The aberration-neutral, rotationally asymmetric LENTIS Comfort Mplus LS-313 MF15 provided safe, predictable rehabilitation in eyes after hyperopic corneal surgery, with high-quality distance/intermediate vision and low photic phenomena. Preoperative HOAs and angle kappa significantly influenced postoperative uncorrected vision.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30207 - Ophthalmology
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2025
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Refractive Surgery
ISSN
1081-597X
e-ISSN
1938-2391
Svazek periodika
41
Číslo periodika v rámci svazku
12
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
9
Strana od-do
"e1296"-"e1304"
Kód UT WoS článku
001638760700005
EID výsledku v databázi Scopus
2-s2.0-105024385667