Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/99123
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dc.contributorSchool of Optometryen_US
dc.creatorYuan, Yen_US
dc.creatorWang, Wen_US
dc.creatorXiong, Ren_US
dc.creatorZhang, Jen_US
dc.creatorLi, Cen_US
dc.creatorYang, Sen_US
dc.creatorFriedman, DSen_US
dc.creatorFoster, PJen_US
dc.creatorHe, Men_US
dc.date.accessioned2023-06-23T09:10:20Z-
dc.date.available2023-06-23T09:10:20Z-
dc.identifier.issn0161-6420en_US
dc.identifier.urihttp://hdl.handle.net/10397/99123-
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rights© 2023 by the American Academy of Ophthalmology. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).en_US
dc.rightsThe following publication Yuan, Y., Wang, W., Xiong, R., Zhang, J., Li, C., Yang, S., Friedman, D. S., Foster, P. J., & He, M. (2023). Fourteen-Year Outcome of Angle-Closure Prevention with Laser Iridotomy in the Zhongshan Angle-Closure Prevention Study: Extended Follow-up of a Randomized Controlled Trial. Ophthalmology, 130(8), 786-794 is available at https://doi.org/10.1016/j.ophtha.2023.03.024.en_US
dc.subjectExtended follow-upen_US
dc.subjectLaser peripheral iridotomyen_US
dc.subjectPrimary angle closureen_US
dc.titleFourteen-year outcome of angle-closure prevention with laser iridotomy in the Zhongshan Angle-Closure Prevention Study : extended follow-up of a randomized controlled trialen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage786en_US
dc.identifier.epage794en_US
dc.identifier.volume130en_US
dc.identifier.issue8en_US
dc.identifier.doi10.1016/j.ophtha.2023.03.024en_US
dcterms.abstractPurpose: This study aimed to evaluate the efficacy of laser peripheral iridotomy (LPI) prophylaxis for patients with primary angle-closure suspect (PACS) after 14 years and to identify risk factors for the conversion from PACS to primary angle closure (PAC).en_US
dcterms.abstractDesign: Extended follow-up of the Zhongshan Angle-Closure Prevention Study.en_US
dcterms.abstractParticipants: Eight hundred eighty-nine Chinese patients 50 to 70 years of age with bilateral PACS.en_US
dcterms.abstractMethods: Each patient received LPI in 1 randomly selected eye, with the fellow untreated eye serving as a control. Because the risk of glaucoma was low and acute angle closure (AAC) occurred only rarely, the follow-up was extended to 14 years despite substantial benefits of LPI reported after the 6-year visit.en_US
dcterms.abstractMain Outcome Measures: Incidence of PAC, a composite end point including peripheral anterior synechiae, intraocular pressure (IOP) of > 24 mmHg, or AAC.en_US
dcterms.abstractResults: During the 14 years, 390 LPI-treated eyes and 388 control eyes were lost to follow-up. A total of 33 LPI-treated eyes and 105 control eyes reached primary end points (P < 0.01). Within them, 1 LPI-treated eye and 5 control eyes progressed to AAC. Primary angle-closure glaucoma was found in 2 LPI-treated eyes and 4 control eyes. The hazard ratio for progression to PAC was 0.31 (95% confidence interval, 0.21–0.46) in LPI-treated eyes compared with control eyes. At the 14-year visit, LPI-treated eyes showed more severe nuclear cataract, higher IOP, and larger angle width and limbal anterior chamber depth (LACD) than control eyes. Higher IOP, shallower LACD, and greater central anterior chamber depth (CACD) were associated with an increased risk of end points developing in control eyes. In the treated group, eyes with higher IOP, shallower LACD, or less IOP elevation after the darkroom prone provocative test (DRPPT) were more likely to demonstrate PAC after LPI.en_US
dcterms.abstractConcluions: Despite a two-third decrease in PAC occurrence after LPI, the cumulative risk of progression was relatively low in the community-based PACS population over 14 years. Apart from IOP, IOP elevation after DRPPT, CACD, and LACD, more risk factors are needed to achieve precise prediction of PAC occurrence and to guide clinical practice.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationOphthalmology, Aug. 2023, v. 130, no. 8, p. 786-794en_US
dcterms.isPartOfOphthalmologyen_US
dcterms.issued2023-08-
dc.identifier.pmid37030454-
dc.description.validate202306 bckwen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera2178-n01-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe Natural Science Foundation of Guangdong Province (China); The National Natural Science Foundation of China; The Sun Yat-sen University; The Fight for Sight UK; The National Institute for Health Research Biomedical Research Centre at Moorfields Eye Hospital, London, United Kingdom; The Richard Desmond Charitable Foundation (via Fight for Sight UK)en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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