The Effect of Biomicroscope Illumination System on Grading Anterior Chamber Inflammation

Purpose To determine how a biomicroscope illumination system affects the grading of anterior chamber (AC) inflammation. Design Laboratory investigation. Methods An artificial AC was designed to replicate optically a human AC and was filled with 5-μm polystyrene beads suspended in ethanol. A high-def...

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Published inAmerican journal of ophthalmology Vol. 148; no. 4; pp. 516 - 520.e2
Main Authors Wong, Ira G, Nugent, Alex K, Vargas-Martín, Fernando
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.10.2009
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Abstract Purpose To determine how a biomicroscope illumination system affects the grading of anterior chamber (AC) inflammation. Design Laboratory investigation. Methods An artificial AC was designed to replicate optically a human AC and was filled with 5-μm polystyrene beads suspended in ethanol. A high-definition video eyepiece camera recorded the moving beads. Using image processing software, the main outcomes measures determined were the average number of beads in a 1 × 1-mm field at varying widths of the slit-beam. Results The volume of light and number of beads observed increased significantly as the slit-beam widened. Additionally, 3 separate biomicroscopes of identical make and model were found to produce different levels of luminance at the same aperture dial settings, influencing the number of beads observed, with the brighter biomicroscope yielding higher bead counts. Conclusions Ability to count beads and perhaps the ability to count inflammatory cells in an inflamed eye depend on a number of factors, including the level of illumination and width of the slit-beam. This study demonstrated that the brighter the illumination and the wider the beam, the more beads were observed. This illustrates the importance of standardizing biomicroscopy, particularly where consecutive observations are used to make clinical decisions and in cases of multicenter clinical trials where clinical data are evaluated across different facilities.
AbstractList To determine how a biomicroscope illumination system affects the grading of anterior chamber (AC) inflammation. Laboratory investigation. An artificial AC was designed to replicate optically a human AC and was filled with 5-μm polystyrene beads suspended in ethanol. A high-definition video eyepiece camera recorded the moving beads. Using image processing software, the main outcomes measures determined were the average number of beads in a 1 × 1-mm field at varying widths of the slit-beam. The volume of light and number of beads observed increased significantly as the slit-beam widened. Additionally, 3 separate biomicroscopes of identical make and model were found to produce different levels of luminance at the same aperture dial settings, influencing the number of beads observed, with the brighter biomicroscope yielding higher bead counts. Ability to count beads and perhaps the ability to count inflammatory cells in an inflamed eye depend on a number of factors, including the level of illumination and width of the slit-beam. This study demonstrated that the brighter the illumination and the wider the beam, the more beads were observed. This illustrates the importance of standardizing biomicroscopy, particularly where consecutive observations are used to make clinical decisions and in cases of multicenter clinical trials where clinical data are evaluated across different facilities.
PURPOSETo determine how a biomicroscope illumination system affects the grading of anterior chamber (AC) inflammation.DESIGNLaboratory investigation.METHODSAn artificial AC was designed to replicate optically a human AC and was filled with 5-mum polystyrene beads suspended in ethanol. A high-definition video eyepiece camera recorded the moving beads. Using image processing software, the main outcomes measures determined were the average number of beads in a 1 x 1-mm field at varying widths of the slit-beam.RESULTSThe volume of light and number of beads observed increased significantly as the slit-beam widened. Additionally, 3 separate biomicroscopes of identical make and model were found to produce different levels of luminance at the same aperture dial settings, influencing the number of beads observed, with the brighter biomicroscope yielding higher bead counts.CONCLUSIONSAbility to count beads and perhaps the ability to count inflammatory cells in an inflamed eye depend on a number of factors, including the level of illumination and width of the slit-beam. This study demonstrated that the brighter the illumination and the wider the beam, the more beads were observed. This illustrates the importance of standardizing biomicroscopy, particularly where consecutive observations are used to make clinical decisions and in cases of multicenter clinical trials where clinical data are evaluated across different facilities.
To determine how a biomicroscope illumination system affects the grading of anterior chamber (AC) inflammation. Laboratory investigation. An artificial AC was designed to replicate optically a human AC and was filled with 5-μm polystyrene beads suspended in ethanol. A high-definition video eyepiece camera recorded the moving beads. Using image processing software, the main outcomes measures determined were the average number of beads in a 1 × 1-mm field at varying widths of the slit-beam. The volume of light and number of beads observed increased significantly as the slit-beam widened. Additionally, 3 separate biomicroscopes of identical make and model were found to produce different levels of luminance at the same aperture dial settings, influencing the number of beads observed, with the brighter biomicroscope yielding higher bead counts. Ability to count beads and perhaps the ability to count inflammatory cells in an inflamed eye depend on a number of factors, including the level of illumination and width of the slit-beam. This study demonstrated that the brighter the illumination and the wider the beam, the more beads were observed. This illustrates the importance of standardizing biomicroscopy, particularly where consecutive observations are used to make clinical decisions and in cases of multicenter clinical trials where clinical data are evaluated across different facilities.
Purpose To determine how a biomicroscope illumination system affects the grading of anterior chamber (AC) inflammation. Design Laboratory investigation. Methods An artificial AC was designed to replicate optically a human AC and was filled with 5-μm polystyrene beads suspended in ethanol. A high-definition video eyepiece camera recorded the moving beads. Using image processing software, the main outcomes measures determined were the average number of beads in a 1 × 1-mm field at varying widths of the slit-beam. Results The volume of light and number of beads observed increased significantly as the slit-beam widened. Additionally, 3 separate biomicroscopes of identical make and model were found to produce different levels of luminance at the same aperture dial settings, influencing the number of beads observed, with the brighter biomicroscope yielding higher bead counts. Conclusions Ability to count beads and perhaps the ability to count inflammatory cells in an inflamed eye depend on a number of factors, including the level of illumination and width of the slit-beam. This study demonstrated that the brighter the illumination and the wider the beam, the more beads were observed. This illustrates the importance of standardizing biomicroscopy, particularly where consecutive observations are used to make clinical decisions and in cases of multicenter clinical trials where clinical data are evaluated across different facilities.
To determine how a biomicroscope illumination system affects the grading of anterior chamber (AC) inflammation. Laboratory investigation. An artificial AC was designed to replicate optically a human AC and was filled with 5-mum polystyrene beads suspended in ethanol. A high-definition video eyepiece camera recorded the moving beads. Using image processing software, the main outcomes measures determined were the average number of beads in a 1 x 1-mm field at varying widths of the slit-beam. The volume of light and number of beads observed increased significantly as the slit-beam widened. Additionally, 3 separate biomicroscopes of identical make and model were found to produce different levels of luminance at the same aperture dial settings, influencing the number of beads observed, with the brighter biomicroscope yielding higher bead counts. Ability to count beads and perhaps the ability to count inflammatory cells in an inflamed eye depend on a number of factors, including the level of illumination and width of the slit-beam. This study demonstrated that the brighter the illumination and the wider the beam, the more beads were observed. This illustrates the importance of standardizing biomicroscopy, particularly where consecutive observations are used to make clinical decisions and in cases of multicenter clinical trials where clinical data are evaluated across different facilities.
Author Vargas-Martín, Fernando
Wong, Ira G
Nugent, Alex K
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Cites_doi 10.1364/OE.15.016561
10.1016/j.ajo.2005.03.057
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References Henson (bib5) 1996
Rasband (bib3)
Bohren (bib4) 1995
Yurkin, Semyanov, Maltsev, Hoekstra (bib1) 2007; 15
Jabs, Nussenblatt, Rosenbaum (bib2) 2005; 140
Yurkin (10.1016/j.ajo.2009.04.027_bib1) 2007; 15
Rasband (10.1016/j.ajo.2009.04.027_bib3)
Bohren (10.1016/j.ajo.2009.04.027_bib4) 1995
Jabs (10.1016/j.ajo.2009.04.027_bib2) 2005; 140
Henson (10.1016/j.ajo.2009.04.027_bib5) 1996
References_xml – start-page: 6.1
  year: 1995
  end-page: 6.21
  ident: bib4
  article-title: Scattering by particles
  publication-title: Handbook of Optics Volume I: Fundamentals, Techniques, and Design
  contributor:
    fullname: Bohren
– ident: bib3
  article-title: ImageJ Image Processing and Analysis in Java, United States National Institutes of Health website
  contributor:
    fullname: Rasband
– volume: 140
  start-page: 509
  year: 2005
  end-page: 516
  ident: bib2
  article-title: Standardization of Uveitis Nomenclature for reporting clinical data
  publication-title: Am J Ophthalmol
  contributor:
    fullname: Rosenbaum
– start-page: 138
  year: 1996
  end-page: 154
  ident: bib5
  article-title: Slit-lamps
  publication-title: Optometric Instrumentation
  contributor:
    fullname: Henson
– volume: 15
  start-page: 16561
  year: 2007
  end-page: 16580
  ident: bib1
  article-title: Discrimination of granulocyte subtypes from light scattering: theoretical analysis using a granulated sphere model
  publication-title: Opt Express
  contributor:
    fullname: Hoekstra
– volume: 15
  start-page: 16561
  year: 2007
  ident: 10.1016/j.ajo.2009.04.027_bib1
  article-title: Discrimination of granulocyte subtypes from light scattering: theoretical analysis using a granulated sphere model
  publication-title: Opt Express
  doi: 10.1364/OE.15.016561
  contributor:
    fullname: Yurkin
– start-page: 6.1
  year: 1995
  ident: 10.1016/j.ajo.2009.04.027_bib4
  article-title: Scattering by particles
  contributor:
    fullname: Bohren
– volume: 140
  start-page: 509
  year: 2005
  ident: 10.1016/j.ajo.2009.04.027_bib2
  article-title: Standardization of Uveitis Nomenclature for reporting clinical data
  publication-title: Am J Ophthalmol
  doi: 10.1016/j.ajo.2005.03.057
  contributor:
    fullname: Jabs
– start-page: 138
  year: 1996
  ident: 10.1016/j.ajo.2009.04.027_bib5
  article-title: Slit-lamps
  contributor:
    fullname: Henson
– ident: 10.1016/j.ajo.2009.04.027_bib3
  contributor:
    fullname: Rasband
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Snippet Purpose To determine how a biomicroscope illumination system affects the grading of anterior chamber (AC) inflammation. Design Laboratory investigation....
To determine how a biomicroscope illumination system affects the grading of anterior chamber (AC) inflammation. Laboratory investigation. An artificial AC was...
To determine how a biomicroscope illumination system affects the grading of anterior chamber (AC) inflammation. Laboratory investigation. An artificial AC was...
PURPOSETo determine how a biomicroscope illumination system affects the grading of anterior chamber (AC) inflammation.DESIGNLaboratory investigation.METHODSAn...
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SubjectTerms Anterior Chamber - pathology
Biological and medical sciences
Clinical medicine
Clinical trials
Colleges & universities
Digital cameras
Digital video
Ethanol
Humans
Inflammation - classification
Light
Lighting
Lymphocytes - pathology
Macrophages - pathology
Medical sciences
Microscopy - instrumentation
Microspheres
Miscellaneous
Models, Anatomic
Ophthalmology
University colleges
Uveitis, Anterior - classification
Title The Effect of Biomicroscope Illumination System on Grading Anterior Chamber Inflammation
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