| Literature DB >> 29572456 |
Xiaoli Huang1, Zhengwei Zhang1, Jie Wang1, Xiaomei Meng1, Tiantian Chen1, Zhifeng Wu2.
Abstract
This retrospective consecutive case series aimed to evaluate spectral-domain optical coherence tomography (SD-OCT) for occult macular disease recognition preoperatively in patients scheduled for routine cataract surgery. All patients scheduled for cataract surgery underwent macular SD-OCT. Scans were reviewed for retinal, retinal pigment epithelium and vitreomacular interface abnormalities. For the subgroup analysis, the following information was collected: age; sex; and diabetes, hypertension, myopia, glaucoma, post intra-ocular surgery, endophotocoagulation, retinal vasculopathy and uveitis statuses. One-thousand-one-hundred-seventy-six consecutive scans were acquired from 1,176 patients. Macular pathology was found in 294 eyes. The most common macular disorders were an epiretinal membrane (n = 130), myopia atrophy (n = 61) and a dome-shaped macular with pathologic myopia (n = 32). One-hundred-thirty eyes (11.05%) presented macular epiretinal membranes not detected by dilated fundus examination, accounting for 44.22% of the abnormalities in diseased eyes and was higher than in previous Chinese studies. Some had multiple macular disorders. The most common ocular history was myopia, including high myopia. The pooled prevalence rate of macular diseases detected by OCT was 0.24 (95% CI 0.14-0.34) using meta-analysis. SD-OCT should be performed for routine cataract surgery patients to evaluate visual outcomes, especially in myopic patients and those considering advanced-technology intraocular lenses.Entities:
Mesh:
Year: 2018 PMID: 29572456 PMCID: PMC5865193 DOI: 10.1038/s41598-018-22807-7
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379
The number and frequency for the three cataract morphologies stratified by LOCS III grades.
| LOCS III | NO | C | P |
|---|---|---|---|
| ≤2.5 | 79 (10.6%) | 230 (25.8%) | 132 (45.5%) |
| 2.6–3.5 | 237 (31.7%) | 218 (24.4%) | 85 (29.3%) |
| 3.6–4.5 | 334 (44.7%) | 227 (25.4%) | 56 (19.3%) |
| 4.6–5.5 | 87 (11.6%) | 219 (24.6%) | 18 (6.2%) |
| >5.5 | 11 (1.5%) | NA | NA |
| Total | 748 | 894 | 291 |
NO = Nuclear opalescence; C = Cortical; P = Posterior subcapsular; NA = Not Available.
Figure 1Venn diagram describing 992 eligible subjects with nuclear, cortical, and PSC cataracts.
Figure 2Frequencies of macular pathologies using SD-OCT.
Figure 3Systemic and ocular history distributions.
Primary research in the literature and the present research.
| Author | Number of eyes | Abnormal number of eyes (%) | Device | Country | Publication year |
|---|---|---|---|---|---|
| Moreira Neto | 98 eyes | 21 (21.4%) | SD-OCT | Brazil | 2015 |
| Nino Hirnschall | 125 eyes | 65 (54.2%) | SD-OCT | Austria | 2016 |
| Betty R. Klein | 265 eyes | 35 (13.2%) | SD-OCT | USA | 2016 |
| Sidra Zafar | 155 eyes | 17 (10.9%) | SS-OCT | Pakistan | 2017 |
| present study | 1176 eyes | 294 (25.0%) | SD-OCT | China | NA |
SD-OCT = Spectral-domain optical coherence tomography; SS-OCT = Swept-source optical coherence tomography.
Figure 4The results of Meta-Analysis.
Figure 5(A) Epiretinal membrane (N3C3); (B) dome-shaped macula with pathologic myopia (N3C2P1); (C) macular hole (N3C2); (D) vitreomacular traction syndrome (N3C2); (E) macular retinoschisis (N3P1); (F) polypoidal choroidal vasculopathy (N3C3).