Synthetic hydroxyapatite-based integrated orbital implants: A human pilot trial

<b>Purpose: </b> Orbital implants are used as fillers following enucleation or evisceration surgeries to replace the lost volume for better cosmesis and motility of the artificial eye. Over the last decade porous hydroxyapatite (HAp) implants derived from the naturally occurring corals,...

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Main Authors: Kundu Biswanath, Sinha Mithlesh, Mitra Santanu, Basu Debabrata
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2005-01-01
Series:Indian Journal of Ophthalmology
Subjects:
Online Access:http://www.ijo.in/article.asp?issn=0301-4738;year=2005;volume=53;issue=4;spage=235;epage=241;aulast=Kundu
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spelling doaj-76e5394d22a84bafa1e38e1487adbb372020-11-24T21:03:10ZengWolters Kluwer Medknow PublicationsIndian Journal of Ophthalmology0301-47382005-01-01534235241Synthetic hydroxyapatite-based integrated orbital implants: A human pilot trialKundu BiswanathSinha MithleshMitra SantanuBasu Debabrata<b>Purpose: </b> Orbital implants are used as fillers following enucleation or evisceration surgeries to replace the lost volume for better cosmesis and motility of the artificial eye. Over the last decade porous hydroxyapatite (HAp) implants derived from the naturally occurring corals, are increasingly used. Recently synthetic HAp-based implants have been introduced. After fibrovasculrisation they have the added advantage of being directly integrated with the artificial shell, thereby increasing the motility to a great extent. The current study, evaluated the efficacy of two different models of synthetic HAp with 75&#x0025; porosity and pore sizes ranging from 100 to 300 mm.<b> Methods: </b> Synthetic HAp powders were prepared with a novel wet chemical route. Two models of porous orbital implants with the characteristic designs for both evisceration and enucleation surgery were developed, characterised and implanted to consecutive 25 human subjects, 17 following evisceration, and 8 following enucleation. The postoperative performances of these implants were evaluated in respect to the degree of volume replacement (implant &#x002B; prosthesis), presence/absence of lagophthalmos and lower eye-lid laxity, status of socket and fornices. Magnetic resonance imaging assessed the stability of the implants within the socket and progressive fibro-vascularisation within the porous scaffold as a function of time. Finally, motility of the implants as well as the prostheses (horizontal movements by Lister Perimeter) and subjective cosmetic results (qualitative) were also evaluated.<b> Results: </b>During the 2.5 years of follow-up study, no significant postoperative complications were noticed. One case, showed an anterior implant exposure of 3-4 mm, and was managed with donor scleral patch graft and one case of conjunctival thinning was corrected by re-suturing the conjunctival dehiscence. Fourteen of the 25 patients had a very good movement of the prostheses (> 20&#x00B0; horizontal movement) and the other 11 patients had a fair motility (10 - 20&#x00B0;). The degree of volume replacement (with prosthesis) was found to be very good in 21 patients and fair in other 4 patients. All patients reported cosmetic satisfaction.<b> Conclusion: </b> Synthetic HAp-based integrated orbital implants with this modified design were found clinically safe and cosmetically acceptable.http://www.ijo.in/article.asp?issn=0301-4738;year=2005;volume=53;issue=4;spage=235;epage=241;aulast=KunduCosmesisenucleationeviscerationsynthetic hydroxyapatite orbital implants
collection DOAJ
language English
format Article
sources DOAJ
author Kundu Biswanath
Sinha Mithlesh
Mitra Santanu
Basu Debabrata
spellingShingle Kundu Biswanath
Sinha Mithlesh
Mitra Santanu
Basu Debabrata
Synthetic hydroxyapatite-based integrated orbital implants: A human pilot trial
Indian Journal of Ophthalmology
Cosmesis
enucleation
evisceration
synthetic hydroxyapatite orbital implants
author_facet Kundu Biswanath
Sinha Mithlesh
Mitra Santanu
Basu Debabrata
author_sort Kundu Biswanath
title Synthetic hydroxyapatite-based integrated orbital implants: A human pilot trial
title_short Synthetic hydroxyapatite-based integrated orbital implants: A human pilot trial
title_full Synthetic hydroxyapatite-based integrated orbital implants: A human pilot trial
title_fullStr Synthetic hydroxyapatite-based integrated orbital implants: A human pilot trial
title_full_unstemmed Synthetic hydroxyapatite-based integrated orbital implants: A human pilot trial
title_sort synthetic hydroxyapatite-based integrated orbital implants: a human pilot trial
publisher Wolters Kluwer Medknow Publications
series Indian Journal of Ophthalmology
issn 0301-4738
publishDate 2005-01-01
description <b>Purpose: </b> Orbital implants are used as fillers following enucleation or evisceration surgeries to replace the lost volume for better cosmesis and motility of the artificial eye. Over the last decade porous hydroxyapatite (HAp) implants derived from the naturally occurring corals, are increasingly used. Recently synthetic HAp-based implants have been introduced. After fibrovasculrisation they have the added advantage of being directly integrated with the artificial shell, thereby increasing the motility to a great extent. The current study, evaluated the efficacy of two different models of synthetic HAp with 75&#x0025; porosity and pore sizes ranging from 100 to 300 mm.<b> Methods: </b> Synthetic HAp powders were prepared with a novel wet chemical route. Two models of porous orbital implants with the characteristic designs for both evisceration and enucleation surgery were developed, characterised and implanted to consecutive 25 human subjects, 17 following evisceration, and 8 following enucleation. The postoperative performances of these implants were evaluated in respect to the degree of volume replacement (implant &#x002B; prosthesis), presence/absence of lagophthalmos and lower eye-lid laxity, status of socket and fornices. Magnetic resonance imaging assessed the stability of the implants within the socket and progressive fibro-vascularisation within the porous scaffold as a function of time. Finally, motility of the implants as well as the prostheses (horizontal movements by Lister Perimeter) and subjective cosmetic results (qualitative) were also evaluated.<b> Results: </b>During the 2.5 years of follow-up study, no significant postoperative complications were noticed. One case, showed an anterior implant exposure of 3-4 mm, and was managed with donor scleral patch graft and one case of conjunctival thinning was corrected by re-suturing the conjunctival dehiscence. Fourteen of the 25 patients had a very good movement of the prostheses (> 20&#x00B0; horizontal movement) and the other 11 patients had a fair motility (10 - 20&#x00B0;). The degree of volume replacement (with prosthesis) was found to be very good in 21 patients and fair in other 4 patients. All patients reported cosmetic satisfaction.<b> Conclusion: </b> Synthetic HAp-based integrated orbital implants with this modified design were found clinically safe and cosmetically acceptable.
topic Cosmesis
enucleation
evisceration
synthetic hydroxyapatite orbital implants
url http://www.ijo.in/article.asp?issn=0301-4738;year=2005;volume=53;issue=4;spage=235;epage=241;aulast=Kundu
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AT sinhamithlesh synthetichydroxyapatitebasedintegratedorbitalimplantsahumanpilottrial
AT mitrasantanu synthetichydroxyapatitebasedintegratedorbitalimplantsahumanpilottrial
AT basudebabrata synthetichydroxyapatitebasedintegratedorbitalimplantsahumanpilottrial
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