Risk Factors for Blindness in Children With Primary Congenital Glaucoma - Follow-up of a Registry Cohort

被引:6
作者
Alshigari, Rayan [1 ]
Freidi, Alia [2 ]
Souru, Ches [1 ]
Edward, Deepak P. [1 ,3 ]
Malik, Rizwan [1 ]
机构
[1] King Khalid Eye Specialist Hosp, Glaucoma Div, Riyadh 12329, Saudi Arabia
[2] Lebanese Int Univ, Dept Math, Beirut, Lebanon
[3] Univ Illinois, Coll Med, Dept Ophthalmol & Visual Sci, Chicago, IL USA
关键词
CYP1B1; MUTATIONS; SAUDI-ARABIA; AMBLYOPIA; GENOTYPE; OUTCOMES; SURGERY; RIYADH; GENE;
D O I
10.1016/j.ajo.2020.12.014
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE: To evaluate the baseline features associated with blindness in a cohort of children with primary congenital glaucoma (PCG) from a hospital registry. DESIGN: Retrospective clinical cohort study. METHODS: SETTING: Observational cohort study. STUDY POPULATION: The registry included all children who presented to our tertiary care institute between 1995 and 2014 with a diagnosis of childhood glaucoma. OBSERVATION PROCEDURE: Baseline characteristics at initial presentation of children with PCG in the registry who were blind at the last follow-up were compared with those who were not blind, using bivariate and then multivariate regressions to account for potential confounders. MAIN OUTCOME MEASURES: Blindness was defined as a best-corrected visual acuity of 3/60 (20/400) or worse in the better eye at the final follow-up. RESULTS: The eligible sample consisted of 196 children with a mean age of 9.54 +/- 22.44 months at presentation. After a mean +/- standard deviation follow-up of 8.49 +/- 3.85 years, 20 (10.2%) children were blind. The baseline demographic factors, intraocular pressure, horizontal corneal diameter, spherical equivalent, axial length, and corneal thickness, were similar for the ``blind'' and "not blind'' groups (P>.05). In the multivariate regression, only the severity of corneal opacification remained significantly (P<.001) associated with the risk of blindness (odds ratio[ 4.05; 95% confidence interval: 1.89-8.85). CONCLUSION: Corneal clouding is a predictor of future blindness in children with PCG. Children with severe corneal clouding may need more aggressive intraocular pressure control, closer follow-up, and earlier counseling. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:238 / 245
页数:8
相关论文
共 39 条
[1]  
Abu-Amero KK, 2011, MOL VIS, V17, P2911
[2]   Primary and Secondary Congenital Glaucoma: Baseline Features From a Registry at King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia [J].
Alanazi, Farhan F. ;
Song, Jonathan C. ;
Mousa, Ahmed ;
Morales, Jose ;
Al Shahwan, Sami ;
Alodhayb, Sami ;
Al Jadaan, Ibrahim ;
Al-Turkmani, Shahira ;
Edward, Deepak P. .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 2013, 155 (05) :882-889
[3]   Functional Visual Ability and Quality of Life in Children With Glaucoma [J].
Aldarrab, Abdulrahman ;
Al Qurashi, Mohannad ;
Al Thiabi, Saad ;
Khandekar, Rajiv ;
Edward, Deepak P. .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 2019, 200 :95-99
[4]   Quality of Life of Caregivers of Children With Glaucoma in an Arab Population: A Cross-Sectional Study [J].
AlQurashi, Mohannad ;
Mocan, Mehmet C. ;
AlDarrab, Abdulrahman ;
Al Thiabi, Saad ;
Khandekar, Rajiv ;
Ahmad, Khabir ;
Edward, Deepak P. .
JOURNAL OF GLAUCOMA, 2019, 28 (11) :965-968
[5]   CYP1B1 mutations in patients with primary congenital glaucoma from Saudi Arabia [J].
Badeeb, Osama M. ;
Micheal, Shazia ;
Koenekoop, Robert K. ;
den Hollander, Anneke I. ;
Hedrawi, Manal T. .
BMC MEDICAL GENETICS, 2014, 15
[6]   GONIOTOMY FOR THE RELIEF OF CONGENITAL GLAUCOMA [J].
BARKAN, O .
BRITISH JOURNAL OF OPHTHALMOLOGY, 1948, 32 (09) :701-728
[7]  
Beck AD, 2013, CHILDHOOD GLAUCOMA C, V9
[8]   Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia [J].
Bejjani, BA ;
Lewis, RA ;
Tomey, KF ;
Anderson, KL ;
Dueker, DK ;
Jabak, M ;
Astle, WF ;
Otterud, B ;
Leppert, M ;
Lupski, JR .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (02) :325-333
[9]  
BIGLAN AW, 1979, J PEDIAT OPHTH STRAB, V16, P377
[10]  
Chandna Arvind, 2010, Community Eye Health, V23, P1