HapticV1, PascalFrancis, Corpus, bibRecord, 000B18

Long-term effect of 1-piece and 3-piece hydrophobic acrylic intraocular lens on posterior capsule opacification : A Randomized Trial

Identifieur interne : 000B18 ( PascalFrancis/Corpus ); précédent : 000B17; suivant : 000B19

Long-term effect of 1-piece and 3-piece hydrophobic acrylic intraocular lens on posterior capsule opacification : A Randomized Trial

Auteurs : Christina Leydolt ; Sofija Davidovic ; Stefan Sacu ; Rupert Menapace ; Thomas Neumayer ; Ana Prinz ; Wolf Buehl ; Oliver Findl

Source :

Ophthalmology : (Rochester, MN) [ 0161-6420 ] ; 2007.

RBID : Pascal:07-0410735

Descripteurs français

Pascal (Inist)
- Long terme, Acrylique dérivé polymère, Postérieur, Capsule, Opacification, Randomisation, Ophtalmologie.

English descriptors

KwdEn :
- Acrylic polymer, Capsule, Long term, Opacification, Ophthalmology, Posterior, Randomization.

Abstract

Purpose: To compare the intensity of posterior capsule opacification (PCO) between the 1-piece and 3-piece haptic designs of the foldable hydrophobic acrylic AcrySof intraocular lens (IOL) over a 5-year period. Design: Randomized, prospective, patient- and examiner-masked clinical trial with intraindividual comparison. Participants: Fifty-two patients with bilateral age-related cataract (104 eyes). Methods: Each study patient had cataract surgery in both eyes and received a 1 -piece AcrySof IOL in 1 eye and a 3-piece AcrySof IOL in the other eye. Follow-up examinations were performed at 1 week, 1 month, 6 months, and 1, 2, and 5 years. Digital retroillumination images were obtained of each eye. The amount of posterior capsule opacification (score range, 0-10) was assessed subjectively at the slit lamp and objectively using automated image analysis software 1, 2, and 5 years after surgery. Main Outcome Measure: Posterior capsule opacification score (scale, 0-10). Results: There was no significant difference between the 1 -piece and 3-piece AcrySof IOL in best-corrected visual acuity, overlap of rhexis and IOL, capsular folds, anterior capsule opacification, and posterior capsule opacification (1-piece AcrySof PCO score, 1.7±1.7; 3-piece AcrySof PCO score, 1.3±1.4; P = 0.30). Conclusions: Modification of the IOL haptic design of the sharp optic edged AcrySof IOL from a 3-piece to a 1-piece haptic design caused no significant change in PCO intensity and neodymium:yttrium-aluminium-garnet laser treatment rate 5 years after surgery.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

A01	`01`	`1`		`@0 0161-6420`
A02	`01`			`@0 OPHTDG`
A03		`1`		`@0 Ophthalmology : (Rochester MN)`
A05				`@2 114`
A06				`@2 9`
A08	`01`	`1`	`ENG`	`@1 Long-term effect of 1-piece and 3-piece hydrophobic acrylic intraocular lens on posterior capsule opacification : A Randomized Trial`
A11	`01`	`1`		`@1 LEYDOLT (Christina)`
A11	`02`	`1`		`@1 DAVIDOVIC (Sofija)`
A11	`03`	`1`		`@1 SACU (Stefan)`
A11	`04`	`1`		`@1 MENAPACE (Rupert)`
A11	`05`	`1`		`@1 NEUMAYER (Thomas)`
A11	`06`	`1`		`@1 PRINZ (Ana)`
A11	`07`	`1`		`@1 BUEHL (Wolf)`
A11	`08`	`1`		`@1 FINDL (Oliver)`
A14	`01`			`@1 Department of Ophthalmology, Medical University of Vienna @2 Vienna @3 AUT @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut. @Z 5 aut. @Z 6 aut. @Z 7 aut. @Z 8 aut.`
A14	`02`			`@1 Novi Sad Clinical Centre Eye Clinic @2 Novi Sad @3 SCG @Z 2 aut.`
A20				`@1 1663-1669`
A21				`@1 2007`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 18914 @5 354000161579690100`
A44				`@0 0000 @1 © 2007 INIST-CNRS. All rights reserved.`
A45				`@0 31 ref.`
A47	`01`	`1`		`@0 07-0410735`
A60				`@1 P`
A61				`@0 A`
A64	`01`	`1`		`@0 Ophthalmology : (Rochester, MN)`
A66	`01`			`@0 USA`
C01	`01`		`ENG`	@0 Purpose: To compare the intensity of posterior capsule opacification (PCO) between the 1-piece and 3-piece haptic designs of the foldable hydrophobic acrylic AcrySof intraocular lens (IOL) over a 5-year period. Design: Randomized, prospective, patient- and examiner-masked clinical trial with intraindividual comparison. Participants: Fifty-two patients with bilateral age-related cataract (104 eyes). Methods: Each study patient had cataract surgery in both eyes and received a 1 -piece AcrySof IOL in 1 eye and a 3-piece AcrySof IOL in the other eye. Follow-up examinations were performed at 1 week, 1 month, 6 months, and 1, 2, and 5 years. Digital retroillumination images were obtained of each eye. The amount of posterior capsule opacification (score range, 0-10) was assessed subjectively at the slit lamp and objectively using automated image analysis software 1, 2, and 5 years after surgery. Main Outcome Measure: Posterior capsule opacification score (scale, 0-10). Results: There was no significant difference between the 1 -piece and 3-piece AcrySof IOL in best-corrected visual acuity, overlap of rhexis and IOL, capsular folds, anterior capsule opacification, and posterior capsule opacification (1-piece AcrySof PCO score, 1.7±1.7; 3-piece AcrySof PCO score, 1.3±1.4; P = 0.30). Conclusions: Modification of the IOL haptic design of the sharp optic edged AcrySof IOL from a 3-piece to a 1-piece haptic design caused no significant change in PCO intensity and neodymium:yttrium-aluminium-garnet laser treatment rate 5 years after surgery.
C02	`01`	`X`		`@0 002B09N`
C03	`01`	`X`	`FRE`	`@0 Long terme @5 02`
C03	`01`	`X`	`ENG`	`@0 Long term @5 02`
C03	`01`	`X`	`SPA`	`@0 Largo plazo @5 02`
C03	`02`	`X`	`FRE`	`@0 Acrylique dérivé polymère @2 NK @5 03`
C03	`02`	`X`	`ENG`	`@0 Acrylic polymer @2 NK @5 03`
C03	`02`	`X`	`SPA`	`@0 Acrilico derivado polímero @2 NK @5 03`
C03	`03`	`X`	`FRE`	`@0 Postérieur @5 05`
C03	`03`	`X`	`ENG`	`@0 Posterior @5 05`
C03	`03`	`X`	`SPA`	`@0 Posterior @5 05`
C03	`04`	`X`	`FRE`	`@0 Capsule @5 06`
C03	`04`	`X`	`ENG`	`@0 Capsule @5 06`
C03	`04`	`X`	`SPA`	`@0 Cápsula @5 06`
C03	`05`	`X`	`FRE`	`@0 Opacification @5 08`
C03	`05`	`X`	`ENG`	`@0 Opacification @5 08`
C03	`05`	`X`	`SPA`	`@0 Opacificación @5 08`
C03	`06`	`X`	`FRE`	`@0 Randomisation @5 09`
C03	`06`	`X`	`ENG`	`@0 Randomization @5 09`
C03	`06`	`X`	`SPA`	`@0 Aleatorización @5 09`
C03	`07`	`X`	`FRE`	`@0 Ophtalmologie @5 11`
C03	`07`	`X`	`ENG`	`@0 Ophthalmology @5 11`
C03	`07`	`X`	`SPA`	`@0 Oftalmología @5 11`
N21				`@1 267`
N44	`01`			`@1 OTO`
N82				`@1 OTO`

Format Inist (serveur)

NO :	PASCAL 07-0410735 INIST
ET :	Long-term effect of 1-piece and 3-piece hydrophobic acrylic intraocular lens on posterior capsule opacification : A Randomized Trial
AU :	LEYDOLT (Christina); DAVIDOVIC (Sofija); SACU (Stefan); MENAPACE (Rupert); NEUMAYER (Thomas); PRINZ (Ana); BUEHL (Wolf); FINDL (Oliver)
AF :	Department of Ophthalmology, Medical University of Vienna/Vienna/Autriche (1 aut., 2 aut., 3 aut., 4 aut., 5 aut., 6 aut., 7 aut., 8 aut.); Novi Sad Clinical Centre Eye Clinic/Novi Sad/Serbie-et-Monténégro (2 aut.)
DT :	Publication en série; Niveau analytique
SO :	Ophthalmology : (Rochester, MN); ISSN 0161-6420; Coden OPHTDG; Etats-Unis; Da. 2007; Vol. 114; No. 9; Pp. 1663-1669; Bibl. 31 ref.
LA :	Anglais
EA :	Purpose: To compare the intensity of posterior capsule opacification (PCO) between the 1-piece and 3-piece haptic designs of the foldable hydrophobic acrylic AcrySof intraocular lens (IOL) over a 5-year period. Design: Randomized, prospective, patient- and examiner-masked clinical trial with intraindividual comparison. Participants: Fifty-two patients with bilateral age-related cataract (104 eyes). Methods: Each study patient had cataract surgery in both eyes and received a 1 -piece AcrySof IOL in 1 eye and a 3-piece AcrySof IOL in the other eye. Follow-up examinations were performed at 1 week, 1 month, 6 months, and 1, 2, and 5 years. Digital retroillumination images were obtained of each eye. The amount of posterior capsule opacification (score range, 0-10) was assessed subjectively at the slit lamp and objectively using automated image analysis software 1, 2, and 5 years after surgery. Main Outcome Measure: Posterior capsule opacification score (scale, 0-10). Results: There was no significant difference between the 1 -piece and 3-piece AcrySof IOL in best-corrected visual acuity, overlap of rhexis and IOL, capsular folds, anterior capsule opacification, and posterior capsule opacification (1-piece AcrySof PCO score, 1.7±1.7; 3-piece AcrySof PCO score, 1.3±1.4; P = 0.30). Conclusions: Modification of the IOL haptic design of the sharp optic edged AcrySof IOL from a 3-piece to a 1-piece haptic design caused no significant change in PCO intensity and neodymium:yttrium-aluminium-garnet laser treatment rate 5 years after surgery.
CC :	002B09N
FD :	Long terme; Acrylique dérivé polymère; Postérieur; Capsule; Opacification; Randomisation; Ophtalmologie
ED :	Long term; Acrylic polymer; Posterior; Capsule; Opacification; Randomization; Ophthalmology
SD :	Largo plazo; Acrilico derivado polímero; Posterior; Cápsula; Opacificación; Aleatorización; Oftalmología
LO :	INIST-18914.354000161579690100
ID :	07-0410735

Links to Exploration step

Pascal:07-0410735

Le document en format XML

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<series><title level="j" type="main">Ophthalmology : (Rochester, MN)</title>
<title level="j" type="abbreviated">Ophthalmology : (Rochester MN)</title>
<idno type="ISSN">0161-6420</idno>
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<seriesStmt><title level="j" type="main">Ophthalmology : (Rochester, MN)</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Acrylic polymer</term>
<term>Capsule</term>
<term>Long term</term>
<term>Opacification</term>
<term>Ophthalmology</term>
<term>Posterior</term>
<term>Randomization</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Long terme</term>
<term>Acrylique dérivé polymère</term>
<term>Postérieur</term>
<term>Capsule</term>
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<term>Ophtalmologie</term>
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<front><div type="abstract" xml:lang="en">Purpose: To compare the intensity of posterior capsule opacification (PCO) between the 1-piece and 3-piece haptic designs of the foldable hydrophobic acrylic AcrySof intraocular lens (IOL) over a 5-year period. Design: Randomized, prospective, patient- and examiner-masked clinical trial with intraindividual comparison. Participants: Fifty-two patients with bilateral age-related cataract (104 eyes). Methods: Each study patient had cataract surgery in both eyes and received a 1 -piece AcrySof IOL in 1 eye and a 3-piece AcrySof IOL in the other eye. Follow-up examinations were performed at 1 week, 1 month, 6 months, and 1, 2, and 5 years. Digital retroillumination images were obtained of each eye. The amount of posterior capsule opacification (score range, 0-10) was assessed subjectively at the slit lamp and objectively using automated image analysis software 1, 2, and 5 years after surgery. Main Outcome Measure: Posterior capsule opacification score (scale, 0-10). Results: There was no significant difference between the 1 -piece and 3-piece AcrySof IOL in best-corrected visual acuity, overlap of rhexis and IOL, capsular folds, anterior capsule opacification, and posterior capsule opacification (1-piece AcrySof PCO score, 1.7±1.7; 3-piece AcrySof PCO score, 1.3±1.4; P = 0.30). Conclusions: Modification of the IOL haptic design of the sharp optic edged AcrySof IOL from a 3-piece to a 1-piece haptic design caused no significant change in PCO intensity and neodymium:yttrium-aluminium-garnet laser treatment rate 5 years after surgery.</div>
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<inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0161-6420</s0>
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<fA02 i1="01"><s0>OPHTDG</s0>
</fA02>
<fA03 i2="1"><s0>Ophthalmology : (Rochester MN)</s0>
</fA03>
<fA05><s2>114</s2>
</fA05>
<fA06><s2>9</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG"><s1>Long-term effect of 1-piece and 3-piece hydrophobic acrylic intraocular lens on posterior capsule opacification : A Randomized Trial</s1>
</fA08>
<fA11 i1="01" i2="1"><s1>LEYDOLT (Christina)</s1>
</fA11>
<fA11 i1="02" i2="1"><s1>DAVIDOVIC (Sofija)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>SACU (Stefan)</s1>
</fA11>
<fA11 i1="04" i2="1"><s1>MENAPACE (Rupert)</s1>
</fA11>
<fA11 i1="05" i2="1"><s1>NEUMAYER (Thomas)</s1>
</fA11>
<fA11 i1="06" i2="1"><s1>PRINZ (Ana)</s1>
</fA11>
<fA11 i1="07" i2="1"><s1>BUEHL (Wolf)</s1>
</fA11>
<fA11 i1="08" i2="1"><s1>FINDL (Oliver)</s1>
</fA11>
<fA14 i1="01"><s1>Department of Ophthalmology, Medical University of Vienna</s1>
<s2>Vienna</s2>
<s3>AUT</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
</fA14>
<fA14 i1="02"><s1>Novi Sad Clinical Centre Eye Clinic</s1>
<s2>Novi Sad</s2>
<s3>SCG</s3>
<sZ>2 aut.</sZ>
</fA14>
<fA20><s1>1663-1669</s1>
</fA20>
<fA21><s1>2007</s1>
</fA21>
<fA23 i1="01"><s0>ENG</s0>
</fA23>
<fA43 i1="01"><s1>INIST</s1>
<s2>18914</s2>
<s5>354000161579690100</s5>
</fA43>
<fA44><s0>0000</s0>
<s1>© 2007 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45><s0>31 ref.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>07-0410735</s0>
</fA47>
<fA60><s1>P</s1>
</fA60>
<fA61><s0>A</s0>
</fA61>
<fA64 i1="01" i2="1"><s0>Ophthalmology : (Rochester, MN)</s0>
</fA64>
<fA66 i1="01"><s0>USA</s0>
</fA66>
<fC01 i1="01" l="ENG"><s0>Purpose: To compare the intensity of posterior capsule opacification (PCO) between the 1-piece and 3-piece haptic designs of the foldable hydrophobic acrylic AcrySof intraocular lens (IOL) over a 5-year period. Design: Randomized, prospective, patient- and examiner-masked clinical trial with intraindividual comparison. Participants: Fifty-two patients with bilateral age-related cataract (104 eyes). Methods: Each study patient had cataract surgery in both eyes and received a 1 -piece AcrySof IOL in 1 eye and a 3-piece AcrySof IOL in the other eye. Follow-up examinations were performed at 1 week, 1 month, 6 months, and 1, 2, and 5 years. Digital retroillumination images were obtained of each eye. The amount of posterior capsule opacification (score range, 0-10) was assessed subjectively at the slit lamp and objectively using automated image analysis software 1, 2, and 5 years after surgery. Main Outcome Measure: Posterior capsule opacification score (scale, 0-10). Results: There was no significant difference between the 1 -piece and 3-piece AcrySof IOL in best-corrected visual acuity, overlap of rhexis and IOL, capsular folds, anterior capsule opacification, and posterior capsule opacification (1-piece AcrySof PCO score, 1.7±1.7; 3-piece AcrySof PCO score, 1.3±1.4; P = 0.30). Conclusions: Modification of the IOL haptic design of the sharp optic edged AcrySof IOL from a 3-piece to a 1-piece haptic design caused no significant change in PCO intensity and neodymium:yttrium-aluminium-garnet laser treatment rate 5 years after surgery.</s0>
</fC01>
<fC02 i1="01" i2="X"><s0>002B09N</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE"><s0>Long terme</s0>
<s5>02</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG"><s0>Long term</s0>
<s5>02</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA"><s0>Largo plazo</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE"><s0>Acrylique dérivé polymère</s0>
<s2>NK</s2>
<s5>03</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG"><s0>Acrylic polymer</s0>
<s2>NK</s2>
<s5>03</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Acrilico derivado polímero</s0>
<s2>NK</s2>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Postérieur</s0>
<s5>05</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Posterior</s0>
<s5>05</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Posterior</s0>
<s5>05</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Capsule</s0>
<s5>06</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Capsule</s0>
<s5>06</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Cápsula</s0>
<s5>06</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE"><s0>Opacification</s0>
<s5>08</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Opacification</s0>
<s5>08</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Opacificación</s0>
<s5>08</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Randomisation</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Randomization</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Aleatorización</s0>
<s5>09</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Ophtalmologie</s0>
<s5>11</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Ophthalmology</s0>
<s5>11</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Oftalmología</s0>
<s5>11</s5>
</fC03>
<fN21><s1>267</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
</fN82>
</pA>
</standard>
<server><NO>PASCAL 07-0410735 INIST</NO>
<ET>Long-term effect of 1-piece and 3-piece hydrophobic acrylic intraocular lens on posterior capsule opacification : A Randomized Trial</ET>
<AU>LEYDOLT (Christina); DAVIDOVIC (Sofija); SACU (Stefan); MENAPACE (Rupert); NEUMAYER (Thomas); PRINZ (Ana); BUEHL (Wolf); FINDL (Oliver)</AU>
<AF>Department of Ophthalmology, Medical University of Vienna/Vienna/Autriche (1 aut., 2 aut., 3 aut., 4 aut., 5 aut., 6 aut., 7 aut., 8 aut.); Novi Sad Clinical Centre Eye Clinic/Novi Sad/Serbie-et-Monténégro (2 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Ophthalmology : (Rochester, MN); ISSN 0161-6420; Coden OPHTDG; Etats-Unis; Da. 2007; Vol. 114; No. 9; Pp. 1663-1669; Bibl. 31 ref.</SO>
<LA>Anglais</LA>
<EA>Purpose: To compare the intensity of posterior capsule opacification (PCO) between the 1-piece and 3-piece haptic designs of the foldable hydrophobic acrylic AcrySof intraocular lens (IOL) over a 5-year period. Design: Randomized, prospective, patient- and examiner-masked clinical trial with intraindividual comparison. Participants: Fifty-two patients with bilateral age-related cataract (104 eyes). Methods: Each study patient had cataract surgery in both eyes and received a 1 -piece AcrySof IOL in 1 eye and a 3-piece AcrySof IOL in the other eye. Follow-up examinations were performed at 1 week, 1 month, 6 months, and 1, 2, and 5 years. Digital retroillumination images were obtained of each eye. The amount of posterior capsule opacification (score range, 0-10) was assessed subjectively at the slit lamp and objectively using automated image analysis software 1, 2, and 5 years after surgery. Main Outcome Measure: Posterior capsule opacification score (scale, 0-10). Results: There was no significant difference between the 1 -piece and 3-piece AcrySof IOL in best-corrected visual acuity, overlap of rhexis and IOL, capsular folds, anterior capsule opacification, and posterior capsule opacification (1-piece AcrySof PCO score, 1.7±1.7; 3-piece AcrySof PCO score, 1.3±1.4; P = 0.30). Conclusions: Modification of the IOL haptic design of the sharp optic edged AcrySof IOL from a 3-piece to a 1-piece haptic design caused no significant change in PCO intensity and neodymium:yttrium-aluminium-garnet laser treatment rate 5 years after surgery.</EA>
<CC>002B09N</CC>
<FD>Long terme; Acrylique dérivé polymère; Postérieur; Capsule; Opacification; Randomisation; Ophtalmologie</FD>
<ED>Long term; Acrylic polymer; Posterior; Capsule; Opacification; Randomization; Ophthalmology</ED>
<SD>Largo plazo; Acrilico derivado polímero; Posterior; Cápsula; Opacificación; Aleatorización; Oftalmología</SD>
<LO>INIST-18914.354000161579690100</LO>
<ID>07-0410735</ID>
</server>
</inist>
</record>

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Long-term effect of 1-piece and 3-piece hydrophobic acrylic intraocular lens on posterior capsule opacification : A Randomized Trial

Long-term effect of 1-piece and 3-piece hydrophobic acrylic intraocular lens on posterior capsule opacification : A Randomized Trial

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