Neodymium:YAG Lasers: An FDA Report

Walter J. Stark; David Worthen; Jack T. Holladay; George Murray

doi:10.1016/S0161-6420(85)34051-4

Neodymium:YAG Lasers: An FDA Report

Walter J. Stark, David Worthen, Jack T. Holladay, George Murray

School of Medicine

Research output: Contribution to journal › Article › peer-review

127 Scopus citations

Abstract

Analysis of data from four neodymium:YAG laser manufacturers submitted to the Food and Drug Administration (FDA) on over 17,000 cases indicate the procedure is safe and effective for cutting opaque posterior lens capsules. A successful opening in the pupillary membrane was achieved in 98% of the cases, and vision improved in 84% of the cases. Clinically significant risks include: a rise in intraocular pressure two to four hours after treatment, damage to the intraocular lens, and rupture of the anterior hyaloid face.

Original language	English (US)
Pages (from-to)	209-212
Number of pages	4
Journal	Ophthalmology
Volume	92
Issue number	2
DOIs	https://doi.org/10.1016/S0161-6420(85)34051-4
State	Published - Jan 1 1985

Keywords

FDA
cystoid macular edema
glaucoma
intraocular lens
neodymium:YAG laser
posterior capsule opacification

ASJC Scopus subject areas

Ophthalmology

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10.1016/S0161-6420(85)34051-4

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title = "Neodymium:YAG Lasers: An FDA Report",

abstract = "Analysis of data from four neodymium:YAG laser manufacturers submitted to the Food and Drug Administration (FDA) on over 17,000 cases indicate the procedure is safe and effective for cutting opaque posterior lens capsules. A successful opening in the pupillary membrane was achieved in 98% of the cases, and vision improved in 84% of the cases. Clinically significant risks include: a rise in intraocular pressure two to four hours after treatment, damage to the intraocular lens, and rupture of the anterior hyaloid face.",

keywords = "FDA, cystoid macular edema, glaucoma, intraocular lens, neodymium:YAG laser, posterior capsule opacification",

author = "Stark, {Walter J.} and David Worthen and Holladay, {Jack T.} and George Murray",

year = "1985",

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AB - Analysis of data from four neodymium:YAG laser manufacturers submitted to the Food and Drug Administration (FDA) on over 17,000 cases indicate the procedure is safe and effective for cutting opaque posterior lens capsules. A successful opening in the pupillary membrane was achieved in 98% of the cases, and vision improved in 84% of the cases. Clinically significant risks include: a rise in intraocular pressure two to four hours after treatment, damage to the intraocular lens, and rupture of the anterior hyaloid face.

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KW - glaucoma

KW - intraocular lens

KW - neodymium:YAG laser

KW - posterior capsule opacification

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Neodymium:YAG Lasers: An FDA Report

Abstract

Keywords

ASJC Scopus subject areas

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