Long-term follow-up of posterior capsule opacification after AquaLase and NeoSoniX phacoemulsification
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00179906%3A_____%2F16%3A10316843" target="_blank" >RIV/00179906:_____/16:10316843 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216208:11150/16:10316843
Výsledek na webu
<a href="http://dx.doi.org/10.5507/bp.2015.039" target="_blank" >http://dx.doi.org/10.5507/bp.2015.039</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.5507/bp.2015.039" target="_blank" >10.5507/bp.2015.039</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Long-term follow-up of posterior capsule opacification after AquaLase and NeoSoniX phacoemulsification
Popis výsledku v původním jazyce
Aim. To compare the degree of posterior capsule opacification (PCO) after AquaLase and NeoSoniX phacoemulsification methods during an 8-year follow-up period using two types of software. Design. Prospective, randomized clinical trial. Methods. AquaLase was used in the right eye and NeoSoniX in the left eye of each patient with bilateral cataract. Results. Fifty patients were analyzed 1 year, 46 patients 3 years, and 37 patients 8 years after cataract surgery. Mean EPCO 2000 values were for the AquaLase group 0.324 +- 0.305 and for the NeoSoniX group 0.298 +- 0.341 (P = 0.53) 1 year after surgery, for the AquaLase group 0.582 +- 0.506 and for the NeoSoniX group 0.594 +- 0.515 (P = 0.87) 3 years after surgery, and for the AquaLase group 0.648 +- 0.567 and for the NeoSoniX group 0.673 +- 0.542 (P = 0.30) 8 years after surgery. The OSCA results were for the AquaLase group 0.7097 +- 0.3778 and for the NeoSoniX group 0.8584 +- 0.4323 (P = 0.046) 1 year after surgery, for the AquaLase group 0.9667 +- 0.736 and for the NeoSoniX group 0.9540 +- 0.5250 (P = 0.91) 3 years after surgery, and for the AquaLase group 1,035 +- 0,952 and for the NeoSoniX group 1,103 +- 0,741 (P = 0.44) 8 years after surgery. Conclusion. There was minimal PCO difference between these 2 approaches, AquaLase and NeoSoniX. Neither AquaLase nor NeoSoniX technique was able to prevent a natural progression of PCO.
Název v anglickém jazyce
Long-term follow-up of posterior capsule opacification after AquaLase and NeoSoniX phacoemulsification
Popis výsledku anglicky
Aim. To compare the degree of posterior capsule opacification (PCO) after AquaLase and NeoSoniX phacoemulsification methods during an 8-year follow-up period using two types of software. Design. Prospective, randomized clinical trial. Methods. AquaLase was used in the right eye and NeoSoniX in the left eye of each patient with bilateral cataract. Results. Fifty patients were analyzed 1 year, 46 patients 3 years, and 37 patients 8 years after cataract surgery. Mean EPCO 2000 values were for the AquaLase group 0.324 +- 0.305 and for the NeoSoniX group 0.298 +- 0.341 (P = 0.53) 1 year after surgery, for the AquaLase group 0.582 +- 0.506 and for the NeoSoniX group 0.594 +- 0.515 (P = 0.87) 3 years after surgery, and for the AquaLase group 0.648 +- 0.567 and for the NeoSoniX group 0.673 +- 0.542 (P = 0.30) 8 years after surgery. The OSCA results were for the AquaLase group 0.7097 +- 0.3778 and for the NeoSoniX group 0.8584 +- 0.4323 (P = 0.046) 1 year after surgery, for the AquaLase group 0.9667 +- 0.736 and for the NeoSoniX group 0.9540 +- 0.5250 (P = 0.91) 3 years after surgery, and for the AquaLase group 1,035 +- 0,952 and for the NeoSoniX group 1,103 +- 0,741 (P = 0.44) 8 years after surgery. Conclusion. There was minimal PCO difference between these 2 approaches, AquaLase and NeoSoniX. Neither AquaLase nor NeoSoniX technique was able to prevent a natural progression of PCO.
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
FF - ORL, oftalmologie, stomatologie
OECD FORD obor
—
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2016
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Biomedical Papers
ISSN
1213-8118
e-ISSN
—
Svazek periodika
160
Číslo periodika v rámci svazku
1
Stát vydavatele periodika
CZ - Česká republika
Počet stran výsledku
6
Strana od-do
143-148
Kód UT WoS článku
000373390800020
EID výsledku v databázi Scopus
2-s2.0-84962339948