Long-term results and biocompatibility of heparin-surface-modified intraocular lenses.
Identifieur interne : 002168 ( PubMed/Corpus ); précédent : 002167; suivant : 002169Long-term results and biocompatibility of heparin-surface-modified intraocular lenses.
Auteurs : M. Amon ; R. MenapaceSource :
- Journal of cataract and refractive surgery [ 0886-3350 ] ; 1993.
English descriptors
- KwdEn :
- Adult, Aged, Aged, 80 and over, Biocompatible Materials, Cataract Extraction, Female, Fibroblasts (pathology), Foreign-Body Reaction (pathology), Giant Cells (pathology), Heparin, Humans, Lenses, Intraocular, Longitudinal Studies, Male, Methylmethacrylate, Methylmethacrylates, Middle Aged, Prospective Studies, Prosthesis Design, Treatment Outcome, Visual Acuity.
- MESH :
- chemical : Biocompatible Materials, Heparin, Methylmethacrylate, Methylmethacrylates.
- pathology : Fibroblasts, Foreign-Body Reaction, Giant Cells.
- Adult, Aged, Aged, 80 and over, Cataract Extraction, Female, Humans, Lenses, Intraocular, Longitudinal Studies, Male, Middle Aged, Prospective Studies, Prosthesis Design, Treatment Outcome, Visual Acuity.
Abstract
A prospective in vivo study of 50 intraocular lenses was done to document the long-term results and biocompatibility of heparin-surface-modified poly(methyl methacrylate) posterior chamber lenses. Continuous curvilinear capsulorhexis and phacoemulsification were performed throughout and examinations were by slit-lamp and specular microscopy. Decentrations of more than 1 mm were seen in 4% of eyes. Stress folds from the haptic traction forces were detected in 16%. A posterior capsulotomy was performed in 10% because of fibrosis or Elschnig pearl formation. Fine fibers were found on the lens surface in 76%. During the first postoperative days only a moderate number of fibroblast-like cells was observed. Foreign-body giant cells were seen in 8%. All cases with foreign-body giant cells had posterior synechias. Visual performance and clinical results were comparable to those of other well-approved intraocular lenses. The low percentage of cellular reaction on the lens surface suggests good biocompatibility.
PubMed: 8487171
Links to Exploration step
pubmed:8487171Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Long-term results and biocompatibility of heparin-surface-modified intraocular lenses.</title>
<author><name sortKey="Amon, M" sort="Amon, M" uniqKey="Amon M" first="M" last="Amon">M. Amon</name>
<affiliation><nlm:affiliation>1. Universität Augenklinik Wien, Vienna, Austria.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Menapace, R" sort="Menapace, R" uniqKey="Menapace R" first="R" last="Menapace">R. Menapace</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="1993">1993</date>
<idno type="RBID">pubmed:8487171</idno>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Long-term results and biocompatibility of heparin-surface-modified intraocular lenses.</title>
<author><name sortKey="Amon, M" sort="Amon, M" uniqKey="Amon M" first="M" last="Amon">M. Amon</name>
<affiliation><nlm:affiliation>1. Universität Augenklinik Wien, Vienna, Austria.</nlm:affiliation>
</affiliation>
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<author><name sortKey="Menapace, R" sort="Menapace, R" uniqKey="Menapace R" first="R" last="Menapace">R. Menapace</name>
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<series><title level="j">Journal of cataract and refractive surgery</title>
<idno type="ISSN">0886-3350</idno>
<imprint><date when="1993" type="published">1993</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Biocompatible Materials</term>
<term>Cataract Extraction</term>
<term>Female</term>
<term>Fibroblasts (pathology)</term>
<term>Foreign-Body Reaction (pathology)</term>
<term>Giant Cells (pathology)</term>
<term>Heparin</term>
<term>Humans</term>
<term>Lenses, Intraocular</term>
<term>Longitudinal Studies</term>
<term>Male</term>
<term>Methylmethacrylate</term>
<term>Methylmethacrylates</term>
<term>Middle Aged</term>
<term>Prospective Studies</term>
<term>Prosthesis Design</term>
<term>Treatment Outcome</term>
<term>Visual Acuity</term>
</keywords>
<keywords scheme="MESH" type="chemical" xml:lang="en"><term>Biocompatible Materials</term>
<term>Heparin</term>
<term>Methylmethacrylate</term>
<term>Methylmethacrylates</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Fibroblasts</term>
<term>Foreign-Body Reaction</term>
<term>Giant Cells</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Cataract Extraction</term>
<term>Female</term>
<term>Humans</term>
<term>Lenses, Intraocular</term>
<term>Longitudinal Studies</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Prospective Studies</term>
<term>Prosthesis Design</term>
<term>Treatment Outcome</term>
<term>Visual Acuity</term>
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<front><div type="abstract" xml:lang="en">A prospective in vivo study of 50 intraocular lenses was done to document the long-term results and biocompatibility of heparin-surface-modified poly(methyl methacrylate) posterior chamber lenses. Continuous curvilinear capsulorhexis and phacoemulsification were performed throughout and examinations were by slit-lamp and specular microscopy. Decentrations of more than 1 mm were seen in 4% of eyes. Stress folds from the haptic traction forces were detected in 16%. A posterior capsulotomy was performed in 10% because of fibrosis or Elschnig pearl formation. Fine fibers were found on the lens surface in 76%. During the first postoperative days only a moderate number of fibroblast-like cells was observed. Foreign-body giant cells were seen in 8%. All cases with foreign-body giant cells had posterior synechias. Visual performance and clinical results were comparable to those of other well-approved intraocular lenses. The low percentage of cellular reaction on the lens surface suggests good biocompatibility.</div>
</front>
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<DateCreated><Year>1993</Year>
<Month>06</Month>
<Day>07</Day>
</DateCreated>
<DateCompleted><Year>1993</Year>
<Month>06</Month>
<Day>07</Day>
</DateCompleted>
<DateRevised><Year>2013</Year>
<Month>11</Month>
<Day>21</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0886-3350</ISSN>
<JournalIssue CitedMedium="Print"><Volume>19</Volume>
<Issue>2</Issue>
<PubDate><Year>1993</Year>
<Month>Mar</Month>
</PubDate>
</JournalIssue>
<Title>Journal of cataract and refractive surgery</Title>
<ISOAbbreviation>J Cataract Refract Surg</ISOAbbreviation>
</Journal>
<ArticleTitle>Long-term results and biocompatibility of heparin-surface-modified intraocular lenses.</ArticleTitle>
<Pagination><MedlinePgn>258-62</MedlinePgn>
</Pagination>
<Abstract><AbstractText>A prospective in vivo study of 50 intraocular lenses was done to document the long-term results and biocompatibility of heparin-surface-modified poly(methyl methacrylate) posterior chamber lenses. Continuous curvilinear capsulorhexis and phacoemulsification were performed throughout and examinations were by slit-lamp and specular microscopy. Decentrations of more than 1 mm were seen in 4% of eyes. Stress folds from the haptic traction forces were detected in 16%. A posterior capsulotomy was performed in 10% because of fibrosis or Elschnig pearl formation. Fine fibers were found on the lens surface in 76%. During the first postoperative days only a moderate number of fibroblast-like cells was observed. Foreign-body giant cells were seen in 8%. All cases with foreign-body giant cells had posterior synechias. Visual performance and clinical results were comparable to those of other well-approved intraocular lenses. The low percentage of cellular reaction on the lens surface suggests good biocompatibility.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Amon</LastName>
<ForeName>M</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>1. Universität Augenklinik Wien, Vienna, Austria.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Menapace</LastName>
<ForeName>R</ForeName>
<Initials>R</Initials>
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<Language>eng</Language>
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<MedlineJournalInfo><Country>UNITED STATES</Country>
<MedlineTA>J Cataract Refract Surg</MedlineTA>
<NlmUniqueID>8604171</NlmUniqueID>
<ISSNLinking>0886-3350</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D001672">Biocompatible Materials</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D008768">Methylmethacrylates</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>196OC77688</RegistryNumber>
<NameOfSubstance UI="D020366">Methylmethacrylate</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>9005-49-6</RegistryNumber>
<NameOfSubstance UI="D006493">Heparin</NameOfSubstance>
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</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D000328">Adult</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D000368">Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D000369">Aged, 80 and over</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D001672">Biocompatible Materials</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D002387">Cataract Extraction</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005260">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005347">Fibroblasts</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005549">Foreign-Body Reaction</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D015726">Giant Cells</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="Y" UI="D006493">Heparin</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="Y" UI="D007910">Lenses, Intraocular</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008137">Longitudinal Studies</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008297">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D020366">Methylmethacrylate</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008768">Methylmethacrylates</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008875">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D011446">Prospective Studies</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D011474">Prosthesis Design</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D016896">Treatment Outcome</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D014792">Visual Acuity</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1993</Year>
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