HapticV1, PascalFrancis, Corpus, bibRecord, 000599

Three-haptic intraocular lens for myopia: Early results

Identifieur interne : 000599 ( PascalFrancis/Corpus ); précédent : 000598; suivant : 000600

Three-haptic intraocular lens for myopia: Early results

Auteurs : Imran J. Khan ; Joseph Abbott ; Ajay J. Bhatnager ; Nicholas J. Price

Source :

Journal of cataract and refractive surgery [ 0886-3350 ] ; 2010.

RBID : Pascal:10-0366539

Descripteurs français

Pascal (Inist)
- Myopie, Lentille intraoculaire, Précoce, Ophtalmologie, Chirurgie, Traitement.

English descriptors

KwdEn :
- Early, Intraocular lens, Myopia, Ophthalmology, Surgery, Treatment.

Abstract

PURPOSE: To report the intraoperative experience and early postoperative results of implantation of an intraocular lens (IOL) developed specifically for myopic eyes. SETTING: Wolverhampton Eye Infirmary, Wolverhampton, United Kingdom. METHODS: This retrospective study evaluated consecutive highly myopic eyes having implantation of a Bigbag IOL from November 2003 to December 2007. Before IOL placement, a 2.8 mm clear corneal incision was created and phacoemulsification performed. The IOL was implanted using the dedicated folder and injector supplied by the manufacturer. RESULTS: The study evaluated 67 eyes (48 patients) with a mean follow-up of 8.5 months (range 0.75 to 31 months). Intraoperative complications were IOL haptic damage from the injector system (3 eyes; 4.5%) and posterior capsule tear (1 eye; 1.5%). Postoperative complications were posterior capsule opacification (29 eyes; 43%), retinal detachment (1 eye; 1.5%), and iritis (1 eye; 1.5%). The postoperative corrected distance visual acuity was 0.10 logMAR or better in 24 eyes (35.8%) and 0.18 to 0.48 logMAR in 32 eyes (47.8%). Forty-three eyes (64.2%) were within ±1.00 diopter of the intended refractive outcome. CONCLUSION: Preliminary results indicate that this 3-haptic IOL is safe and appropriate for use in highly myopic patients having cataract surgery. Financial Disclosure: No author has a financial or proprietary interest in any material or method mentioned.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A08	`01`	`1`	`ENG`	`@1 Three-haptic intraocular lens for myopia: Early results`
A11	`01`	`1`		`@1 KHAN (Imran J.)`
A11	`02`	`1`		`@1 ABBOTT (Joseph)`
A11	`03`	`1`		`@1 BHATNAGER (Ajay J.)`
A11	`04`	`1`		`@1 PRICE (Nicholas J.)`
A14	`01`			`@1 Wolverhampton Eye Infirmary, New Cross Hospital @2 Wolverhampton @3 GBR @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut.`
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A44				`@0 0000 @1 © 2010 INIST-CNRS. All rights reserved.`
A45				`@0 27 ref.`
A47	`01`	`1`		`@0 10-0366539`
A60				`@1 P`
A61				`@0 A`
A64	`01`	`1`		`@0 Journal of cataract and refractive surgery`
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C01	`01`		`ENG`	@0 PURPOSE: To report the intraoperative experience and early postoperative results of implantation of an intraocular lens (IOL) developed specifically for myopic eyes. SETTING: Wolverhampton Eye Infirmary, Wolverhampton, United Kingdom. METHODS: This retrospective study evaluated consecutive highly myopic eyes having implantation of a Bigbag IOL from November 2003 to December 2007. Before IOL placement, a 2.8 mm clear corneal incision was created and phacoemulsification performed. The IOL was implanted using the dedicated folder and injector supplied by the manufacturer. RESULTS: The study evaluated 67 eyes (48 patients) with a mean follow-up of 8.5 months (range 0.75 to 31 months). Intraoperative complications were IOL haptic damage from the injector system (3 eyes; 4.5%) and posterior capsule tear (1 eye; 1.5%). Postoperative complications were posterior capsule opacification (29 eyes; 43%), retinal detachment (1 eye; 1.5%), and iritis (1 eye; 1.5%). The postoperative corrected distance visual acuity was 0.10 logMAR or better in 24 eyes (35.8%) and 0.18 to 0.48 logMAR in 32 eyes (47.8%). Forty-three eyes (64.2%) were within ±1.00 diopter of the intended refractive outcome. CONCLUSION: Preliminary results indicate that this 3-haptic IOL is safe and appropriate for use in highly myopic patients having cataract surgery. Financial Disclosure: No author has a financial or proprietary interest in any material or method mentioned.
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C07	`02`	`X`	`SPA`	`@0 Trastorno refracción ocular @5 38`
C07	`03`	`X`	`FRE`	`@0 Trouble de la vision @5 39`
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C07	`03`	`X`	`SPA`	`@0 Trastorno visión @5 39`
N21				`@1 235`
N44	`01`			`@1 OTO`
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Format Inist (serveur)

NO :	PASCAL 10-0366539 INIST
ET :	Three-haptic intraocular lens for myopia: Early results
AU :	KHAN (Imran J.); ABBOTT (Joseph); BHATNAGER (Ajay J.); PRICE (Nicholas J.)
AF :	Wolverhampton Eye Infirmary, New Cross Hospital/Wolverhampton/Royaume-Uni (1 aut., 2 aut., 3 aut., 4 aut.)
DT :	Publication en série; Niveau analytique
SO :	Journal of cataract and refractive surgery; ISSN 0886-3350; Coden JCSUEV; Etats-Unis; Da. 2010; Vol. 36; No. 7; Pp. 1161-1166; Bibl. 27 ref.
LA :	Anglais
EA :	PURPOSE: To report the intraoperative experience and early postoperative results of implantation of an intraocular lens (IOL) developed specifically for myopic eyes. SETTING: Wolverhampton Eye Infirmary, Wolverhampton, United Kingdom. METHODS: This retrospective study evaluated consecutive highly myopic eyes having implantation of a Bigbag IOL from November 2003 to December 2007. Before IOL placement, a 2.8 mm clear corneal incision was created and phacoemulsification performed. The IOL was implanted using the dedicated folder and injector supplied by the manufacturer. RESULTS: The study evaluated 67 eyes (48 patients) with a mean follow-up of 8.5 months (range 0.75 to 31 months). Intraoperative complications were IOL haptic damage from the injector system (3 eyes; 4.5%) and posterior capsule tear (1 eye; 1.5%). Postoperative complications were posterior capsule opacification (29 eyes; 43%), retinal detachment (1 eye; 1.5%), and iritis (1 eye; 1.5%). The postoperative corrected distance visual acuity was 0.10 logMAR or better in 24 eyes (35.8%) and 0.18 to 0.48 logMAR in 32 eyes (47.8%). Forty-three eyes (64.2%) were within ±1.00 diopter of the intended refractive outcome. CONCLUSION: Preliminary results indicate that this 3-haptic IOL is safe and appropriate for use in highly myopic patients having cataract surgery. Financial Disclosure: No author has a financial or proprietary interest in any material or method mentioned.
CC :	002B09K; 002B25B
FD :	Myopie; Lentille intraoculaire; Précoce; Ophtalmologie; Chirurgie; Traitement
FG :	Pathologie de l'oeil; Trouble de la réfraction oculaire; Trouble de la vision
ED :	Myopia; Intraocular lens; Early; Ophthalmology; Surgery; Treatment
EG :	Eye disease; Refractive error; Vision disorder
SD :	Miopía; Lente intraocular; Precoz; Oftalmología; Cirugía; Tratamiento
LO :	INIST-20937.354000193818970160
ID :	10-0366539

Links to Exploration step

Pascal:10-0366539

Le document en format XML

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<front><div type="abstract" xml:lang="en">PURPOSE: To report the intraoperative experience and early postoperative results of implantation of an intraocular lens (IOL) developed specifically for myopic eyes. SETTING: Wolverhampton Eye Infirmary, Wolverhampton, United Kingdom. METHODS: This retrospective study evaluated consecutive highly myopic eyes having implantation of a Bigbag IOL from November 2003 to December 2007. Before IOL placement, a 2.8 mm clear corneal incision was created and phacoemulsification performed. The IOL was implanted using the dedicated folder and injector supplied by the manufacturer. RESULTS: The study evaluated 67 eyes (48 patients) with a mean follow-up of 8.5 months (range 0.75 to 31 months). Intraoperative complications were IOL haptic damage from the injector system (3 eyes; 4.5%) and posterior capsule tear (1 eye; 1.5%). Postoperative complications were posterior capsule opacification (29 eyes; 43%), retinal detachment (1 eye; 1.5%), and iritis (1 eye; 1.5%). The postoperative corrected distance visual acuity was 0.10 logMAR or better in 24 eyes (35.8%) and 0.18 to 0.48 logMAR in 32 eyes (47.8%). Forty-three eyes (64.2%) were within ±1.00 diopter of the intended refractive outcome. CONCLUSION: Preliminary results indicate that this 3-haptic IOL is safe and appropriate for use in highly myopic patients having cataract surgery. Financial Disclosure: No author has a financial or proprietary interest in any material or method mentioned.</div>
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<AU>KHAN (Imran J.); ABBOTT (Joseph); BHATNAGER (Ajay J.); PRICE (Nicholas J.)</AU>
<AF>Wolverhampton Eye Infirmary, New Cross Hospital/Wolverhampton/Royaume-Uni (1 aut., 2 aut., 3 aut., 4 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Journal of cataract and refractive surgery; ISSN 0886-3350; Coden JCSUEV; Etats-Unis; Da. 2010; Vol. 36; No. 7; Pp. 1161-1166; Bibl. 27 ref.</SO>
<LA>Anglais</LA>
<EA>PURPOSE: To report the intraoperative experience and early postoperative results of implantation of an intraocular lens (IOL) developed specifically for myopic eyes. SETTING: Wolverhampton Eye Infirmary, Wolverhampton, United Kingdom. METHODS: This retrospective study evaluated consecutive highly myopic eyes having implantation of a Bigbag IOL from November 2003 to December 2007. Before IOL placement, a 2.8 mm clear corneal incision was created and phacoemulsification performed. The IOL was implanted using the dedicated folder and injector supplied by the manufacturer. RESULTS: The study evaluated 67 eyes (48 patients) with a mean follow-up of 8.5 months (range 0.75 to 31 months). Intraoperative complications were IOL haptic damage from the injector system (3 eyes; 4.5%) and posterior capsule tear (1 eye; 1.5%). Postoperative complications were posterior capsule opacification (29 eyes; 43%), retinal detachment (1 eye; 1.5%), and iritis (1 eye; 1.5%). The postoperative corrected distance visual acuity was 0.10 logMAR or better in 24 eyes (35.8%) and 0.18 to 0.48 logMAR in 32 eyes (47.8%). Forty-three eyes (64.2%) were within ±1.00 diopter of the intended refractive outcome. CONCLUSION: Preliminary results indicate that this 3-haptic IOL is safe and appropriate for use in highly myopic patients having cataract surgery. Financial Disclosure: No author has a financial or proprietary interest in any material or method mentioned.</EA>
<CC>002B09K; 002B25B</CC>
<FD>Myopie; Lentille intraoculaire; Précoce; Ophtalmologie; Chirurgie; Traitement</FD>
<FG>Pathologie de l'oeil; Trouble de la réfraction oculaire; Trouble de la vision</FG>
<ED>Myopia; Intraocular lens; Early; Ophthalmology; Surgery; Treatment</ED>
<EG>Eye disease; Refractive error; Vision disorder</EG>
<SD>Miopía; Lente intraocular; Precoz; Oftalmología; Cirugía; Tratamiento</SD>
<LO>INIST-20937.354000193818970160</LO>
<ID>10-0366539</ID>
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Three-haptic intraocular lens for myopia: Early results

Three-haptic intraocular lens for myopia: Early results

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