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Modified 30 G needle trypan blue staining technique under air for a uniform and consistent anterior capsule staining
PURPOSE: To describe a trypan blue dye staining technique under air, a modification of the previously described 30 G needle under-air technique. DESIGN: This is a prospective, randomized study of 1,000 eyes of 952 patients undergoing phacoemulsification in a private practice setting from January 201...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608478/ https://www.ncbi.nlm.nih.gov/pubmed/29075093 http://dx.doi.org/10.2147/OPTH.S147510 |
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author | Om Parkash, Rohit Mahajan, Shruti Om Parkash, Tushya |
author_facet | Om Parkash, Rohit Mahajan, Shruti Om Parkash, Tushya |
author_sort | Om Parkash, Rohit |
collection | PubMed |
description | PURPOSE: To describe a trypan blue dye staining technique under air, a modification of the previously described 30 G needle under-air technique. DESIGN: This is a prospective, randomized study of 1,000 eyes of 952 patients undergoing phacoemulsification in a private practice setting from January 2015 to August 2016. Three variants as a modification of the previously known 30 G needle technique are described. In our technique, after injecting one drop of the dye under air, the needle is kept in the anterior chamber (AC) for 15 seconds. In the second variation, along with the additional hold time, 0.05 mL air is injected prior to dye injection to deepen the AC in eyes with shallow ACs or in cases with increased posterior pressure. The third variation is the selective painting approach in which more than one drop is injected for a homogenous staining. MAIN OUTCOME MEASURES: The main outcome measures were safety and reproducibility of the technique along with homogeneity and uniformity of the anterior capsule staining. RESULTS: AC remained stable during the hold time of 15 seconds with no egress of air. No iatrogenic trauma occurred in any of the cases. All cases had a homogeneously stained anterior capsule. The staining intensity was excellent in 80.8% of the eyes and good in 19.2% of the eyes. CONCLUSION: This is a safe, simple, and cost-effective technique which achieves consistent, uniform, and reproducible staining. It overcomes the shortcomings of the known 30 G needle technique. |
format | Online Article Text |
id | pubmed-5608478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56084782017-10-26 Modified 30 G needle trypan blue staining technique under air for a uniform and consistent anterior capsule staining Om Parkash, Rohit Mahajan, Shruti Om Parkash, Tushya Clin Ophthalmol Original Research PURPOSE: To describe a trypan blue dye staining technique under air, a modification of the previously described 30 G needle under-air technique. DESIGN: This is a prospective, randomized study of 1,000 eyes of 952 patients undergoing phacoemulsification in a private practice setting from January 2015 to August 2016. Three variants as a modification of the previously known 30 G needle technique are described. In our technique, after injecting one drop of the dye under air, the needle is kept in the anterior chamber (AC) for 15 seconds. In the second variation, along with the additional hold time, 0.05 mL air is injected prior to dye injection to deepen the AC in eyes with shallow ACs or in cases with increased posterior pressure. The third variation is the selective painting approach in which more than one drop is injected for a homogenous staining. MAIN OUTCOME MEASURES: The main outcome measures were safety and reproducibility of the technique along with homogeneity and uniformity of the anterior capsule staining. RESULTS: AC remained stable during the hold time of 15 seconds with no egress of air. No iatrogenic trauma occurred in any of the cases. All cases had a homogeneously stained anterior capsule. The staining intensity was excellent in 80.8% of the eyes and good in 19.2% of the eyes. CONCLUSION: This is a safe, simple, and cost-effective technique which achieves consistent, uniform, and reproducible staining. It overcomes the shortcomings of the known 30 G needle technique. Dove Medical Press 2017-09-14 /pmc/articles/PMC5608478/ /pubmed/29075093 http://dx.doi.org/10.2147/OPTH.S147510 Text en © 2017 Om Parkash et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Om Parkash, Rohit Mahajan, Shruti Om Parkash, Tushya Modified 30 G needle trypan blue staining technique under air for a uniform and consistent anterior capsule staining |
title | Modified 30 G needle trypan blue staining technique under air for a uniform and consistent anterior capsule staining |
title_full | Modified 30 G needle trypan blue staining technique under air for a uniform and consistent anterior capsule staining |
title_fullStr | Modified 30 G needle trypan blue staining technique under air for a uniform and consistent anterior capsule staining |
title_full_unstemmed | Modified 30 G needle trypan blue staining technique under air for a uniform and consistent anterior capsule staining |
title_short | Modified 30 G needle trypan blue staining technique under air for a uniform and consistent anterior capsule staining |
title_sort | modified 30 g needle trypan blue staining technique under air for a uniform and consistent anterior capsule staining |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608478/ https://www.ncbi.nlm.nih.gov/pubmed/29075093 http://dx.doi.org/10.2147/OPTH.S147510 |
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