Prevalence of Corneal Dystrophies in the United States: Estimates from Claims Data

被引:80
作者
Musch, David C. [1 ,2 ]
Niziol, Leslie M.
Stein, Joshua D.
Kamyar, Roheena M. [3 ]
Sugar, Alan
机构
[1] Univ Michigan, Sch Med, Dept Ophthalmol & Visual Sci, Kellogg Eye Ctr, Ann Arbor, MI 48105 USA
[2] Univ Michigan, Dept Epidemiol, Ann Arbor, MI 48105 USA
[3] Univ Pittsburgh, Ctr Eye, Pittsburgh, PA USA
关键词
RISK-FACTORS; GUTTATA; POPULATION; JAPAN;
D O I
10.1167/iovs.11-7771
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. To estimate the prevalence of corneal dystrophies. METHODS. Records of almost 8 million enrollees in a national managed-care network throughout the United States who had an eye care visit in 2001 to 2009 were searched for a recording of corneal dystrophy on a claim submitted by an ophthalmologist or optometrist from January 1, 2001, through December 31, 2007. RESULTS. Unique individuals (n = 27,372) received two or more diagnoses of any type of corneal dystrophy, for an overall corneal dystrophy prevalence rate of 897 per million (106) covered lives. Endothelial and anterior corneal dystrophies accounted for most of the reported dystrophies, and granular corneal dystrophy was the least common, being reported in 167 enrollees. Age, sex, and race variations among the various corneal dystrophies were observed. The mean age of those with macular corneal dystrophy (47.3 years) was 15 years younger than the age of those with endothelial dystrophy (62.9 years), and females were most highly represented (68.5%) among those with lattice corneal dystrophy. Hispanics and blacks were underrepresented relative to enrollees undergoing eye care for reasons other than corneal dystrophy. Keratoplasty was most frequently coded among those with lattice dystrophy. CONCLUSIONS. Although caveats must be considered in using claims data to estimate prevalence in a population, these data provide an indication of corneal dystrophy's prevalence within insured subjects across the United States. Variations in age, sex, and race, within and between the different types of corneal dystrophies, raise questions that warrant further study. (Invest Ophthalmol Vis Sci. 2011;52:6959-6963) DOI:10.1167/iovs.11-7771
引用
收藏
页码:6959 / 6963
页数:5
相关论文
共 16 条
[1]  
[Anonymous], 2006, PHYS INT CLASSIFICAT
[2]  
[Anonymous], 2006, CURRENT PROCEDURAL T
[3]  
[Anonymous], 2006, PHYS INT CLASSIFICAT, V2
[4]  
*AUSTR CORN GRAFT, 2007, REP ACT
[5]   E2-2 Protein and Fuchs's Corneal Dystrophy [J].
Baratz, Keith H. ;
Tosakulwong, Nirubol ;
Ryu, Euijung ;
Brown, William L. ;
Branham, Kari ;
Chen, Wei ;
Tran, Khoa D. ;
Schmid-Kubista, Katharina E. ;
Heckenlively, John R. ;
Swaroop, Anand ;
Abecasis, Goncalo ;
Bailey, Kent R. ;
Edwards, Albert O. .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (11) :1016-1024
[6]   Use of insurance claims databases to evaluate the outcomes of ophthalmic surgery [J].
Coleman, AL ;
Morgenstern, H .
SURVEY OF OPHTHALMOLOGY, 1997, 42 (03) :271-278
[7]  
DUKEELDER S, 1965, SYSTEM OPHTHALMOLOGY, V8, P921
[8]   Posterior polymorphous corneal dystrophy in Czech families maps to chromosome 20 and excludes the VSX1 gene [J].
Gwilliam, R ;
Liskova, P ;
Filipec, M ;
Kmoch, S ;
Jirsova, K ;
Huckle, EJ ;
Stables, CL ;
Bhattacharya, SS ;
Hardcastle, AJ ;
Deloukas, P ;
Ebenezer, ND .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2005, 46 (12) :4480-4484
[9]   Prevalence of and Risk Factors for Cornea Guttata in a Population-Based Study in a Southwestern Island of Japan The Kumejima Study [J].
Higa, Akiko ;
Sakai, Hiroshi ;
Sawaguchi, Shoichi ;
Iwase, Aiko ;
Tomidokoro, Atsuo ;
Amano, Shiro ;
Araie, Makoto .
ARCHIVES OF OPHTHALMOLOGY, 2011, 129 (03) :332-336
[10]   Macular corneal dystrophy in Iceland - A clinical, genealogic, and immunohistochemical study of 28 patients [J].
Jonasson, F ;
Oshima, E ;
Thonar, EJMA ;
Smith, CF ;
Johannsson, JH ;
Klintworth, GK .
OPHTHALMOLOGY, 1996, 103 (07) :1111-1117