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`Outcomes of Kahook Dual Blade Goniotomy with and without Phacoemulsification Cataract Extraction - 5cienceDirect
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`Ophthalmology Glaucoma
`Volume 1, Issue 1,July—August 2018, Pages 75-81
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`Original Article
`Outco mes of Kahook Dual Blade Gonioto my with and without
`Phacoe mulsification Cataract Extraction
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`Presented at: the American Glaucoma Society Annual Meeting, New York, NY, March 2018.
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`Erin G. Sieck MD 1, Rebecca S. Epstein MD 1, Jeffrey B. Kennedy MD 1, Jeffrey R. SooHoo MD 1, Mina B. Pantcheva MD
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`1, Jennifer L. Patnaik PhD 1, Brandie D. Wagner PhD 1' �, Anne M. Lynch MD 1, Malik Y. Kahook MD 1, Leonard K.
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`Seibold MD 1
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`Show more �r
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`https:��doi.org�10.1016�j.ogla.�018.06.006
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`Purpose
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`To determine the effectiveness and safety of Kahook Dual Blade (KDB) gonioto my in reducing
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`intraocular pressure (IOP) and medication need in glaucoma patients when comhined with
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`phacoe mulsification or as a standalone procedure.
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`Design
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`Retrospective study.
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`Participants
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`A total of 197 eyes fro m 143 patients were reviewed.
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`Methods
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`https://www.scienced irect.com/science/article/abs/pi i/S2589419618300413
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`Outcomes of Kahook Dual Blade Goniotomy with and without Phacoemulsification Cataract Extraction - 5cienceDirect
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`Thirty-two eyes underwent KDB goniotomy alone and 165 eyes underwent KDB goniotomy
`combined with phacoemulsification cataract surgery (phaco-KDB).
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`Main Outco me Measures
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`Surgical success, defined as IOP reduction of at least 20% from baseline at 12 months, and/or
`reduction of at least 1 glaucoma medication.
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`Results
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`At 12 months, the success rate was 71.8% for the phaco-KDB group and 68.8% for the KDB-alone
`group. In the phaco-KDB group at 12 months (n =124}, mean IOP was significantly reduced from
`16.7 {standard error [SE] 0.4) mmHg on 1.9 (SE 0.1) medications to 13.8 (SE 0.4) mmHg on 1.5 (SE
`0.1) medications. In the KDB-alone group at 12 months (n =1G), me an IOP was significantly
`reduced from 20.4 {SE 1.3) mmHg on 3.1 {SE 0.2} medications to 14.1 {SE 0.9} mmHg on 2.3 (SE
`0.4) medications. The most common complications were transient hyphema (17.3% at day 1} and
`IOP spike >10 mmHg from baseline at 1 week {10.2%). LogMAR visual acuity at 12 months was
`unch anged from baseline in the KDB -alone group (0.2].8 [SE 0.07] and 0.306 [5E 0.09], respectively,
`P = 0.244) and significantly improved in the phaco -KDB group {0.184 [SE 0.02] and 0.340 [SE 0.03],
`P < o.00l).
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`Conclusions
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`Goniotomy with the KDB has a favorable safety profile and is an effective procedure at reducing
`IOP and medication burden as a standalone procedure or combined with phacoemulsification.
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`Previous
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` Next
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`AbUreviations and Acrony ms
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`EVP, episclexal venous pxessuxe; IOP, intxaoculax pxessure ; KDB, Kahook Dual Blade ;
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`POAG, pri mary open-angle glauco ma; SE, standard error; TM, traUecular meshwork
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`Recom mended articles
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`Citing articles (0)
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`Financial Disclosure(s): The authors) have made the following disclosure(s): E.G.S.: Consultant New World Medical.
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`M.Y.K.: Patent Kahook Dual Blade, which is licensed by New World Medical. The University of Colorado receives
`royalties for the Kahook Dual Blade.
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`https://www.sciencedirect.comiscience/article/abslpiilS2589419618300413
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`Outcomes of Kahook Dual Blade Goniotomy with and without Phacoemulsification Cataract Extraction - 5cienceDirect
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`HUMAN SUBJECTS: Human subjects were included in this study. The Colorado Multiple Institutional Review Board
`approved this study. The study conformed to the tenets of the Declaration of Helsinki. Patients did not provide
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`consent as this was a retrospective chart review.
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`No animal subjects were used in this study.
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`Author Contributions:
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`Conception and design: Sieck, Epstein, Kennedy, Patnaik, Wagner, Lynch, Kahook, Seibold
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`Data collection: Sieck, Epstein, Kennedy, SooHoo, Pantcheva, Seibold
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`Analysis and interpretation: Sieck, Epstein, Kennedy, SooHoo, Pantcheva, Patnaik, Wagner, Lynch, Kahook, Seibold
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`Obtained funding: N�A
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`Overall responsibility: Sieck, Epstein, Kennedy, SooHoo, Pantcheva, Patnaik, Wagner, Lynch, Kahook, Seibold
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`View full text
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`© 2018 by the American Academy of Ophthalmology
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