Central Serous Chorioretinopathy and Ocular Comorbidities

被引:0
|
作者
Samanta, Anindya [1 ]
Driban, Matthew [2 ]
Sahoo, Niroj [3 ]
Parameswarappa, Deepika [3 ]
Singh, Sumit Randhir [4 ]
Caplash, Sonny [2 ]
Mishra, Pranjal [5 ]
Agrawal, Rohit [5 ]
Venkatesh, Ramesh [5 ]
Maltsev, Dmitrii S. [6 ]
Chhablani, Jay [2 ]
机构
[1] Baylor Coll Med, Dept Ophthalmol, Houston, TX 77030 USA
[2] Univ Pittsburgh, UPMC Eye Ctr, Pittsburgh, PA 15261 USA
[3] LV Prasade Eye Inst, Kallam Anji Reddy Campus,LV Prasad Marg,Opp PVR,Pk, Hyderabad 500034, India
[4] Akhand Jyoti Eye Hosp, CoE Mastichak, Dept Vitreoretina, Saran 841219, India
[5] Narayana Nethralaya, 121-C Chord Rd,1st R Block, Bangalore 560010, India
[6] Mil Med Acad, 21 Botkinskaya Str, St Petersburg 194044, Russia
关键词
Central serous chorioretinopathy; ocular comorbidities; retinal detachment; CSCR; RISK;
D O I
10.3390/jcm14030720
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Objectives: Central serous chorioretinopathy (CSCR) is a common retinopathy that can present with other concurrent diseases; thus, further research into the prevalence of other ocular comorbidities in eyes with CSCR is required. Methods: This retrospective, multicentric, cross-sectional observational study reviewed the charts of 9157 patients. Of them, 579 (6.32%) patients and 766 eyes had an additional ocular comorbidity, in addition to CSCR, in at least one subject eye. Results: The baseline best-corrected visual acuity (BCVA) of the subjects eyes was 0.49 +/- 0.36 logMAR. The average BCVA of subject eyes with coexisting macular diseases was 0.50 logMAR, while the corresponding BCVA of subject eyes with coexisting peripheral disease was 0.55 logMAR. The most prevalent coexisting macular diseases were non-proliferative diabetic retinopathy (26.8%), non-exudative age-related macular degeneration (AMD) (7.6%) and hypertensive retinopathy (3.0%). The most prevalent coexisting non-macular diseases were lattice degeneration (8.9%), optic atrophy (5.1%), rhegmatogenous retinal detachment (1.70%) and optic disc pit (1.7%). The odds of having a comorbid disease in the same eye as CSCR were statistically significant for branch retinal vein occlusion (OR 11.56, p-value = 0.02) and non-exudative AMD (OR 2.06; p-value = 0.01); additionally, there was a trend towards significance for idiopathic polypoidal choroidal vasculopathy (OR 4.43; p-value = 0.05) when compared to the eyes without CSCR. Conclusions: Certain diseases are more likely to coexist in eyes with CSCR. Additionally, eyes with CSCR may have statistically significant odds of certain diseases when compared to eyes without CSCR.
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