Elsevier

Ophthalmology

Volume 118, Issue 7, July 2011, Pages 1429-1434
Ophthalmology

Original article
The Predisposing Pathology and Clinical Characteristics in the Scottish Retinal Detachment Study

https://doi.org/10.1016/j.ophtha.2010.11.031Get rights and content

Purpose

To describe the predisposing pathology and clinical features of all incident cases of rhegmatogenous retinal detachment (RRD) recruited in Scotland during a 2-year period.

Design

Prospective surveillance study of incident cases of RRD.

Participants

All incident cases of RRD recruited as part of the Scottish Retinal Detachment Study.

Methods

During a 2-year period, we coordinated a comprehensive system in which every case of primary RRD presenting to 1 of 6 vitreoretinal surgical sites in Scotland was examined and approached for study inclusion.

Main Outcome Measures

Rhegmatogenous retinal detachment incidence, predisposing features, and clinical characteristics.

Results

A total of 1202 cases were recruited. Detailed clinical information was available on 1130 (94%) of cases. By causative break, the proportions of RRD were horseshoe tear (HST) associated with posterior vitreous detachment (PVD) in 86.2%, giant retinal tear (GRT) and PVD in 1.3%, non-PVD round hole (RH) in 4.9%, retinal dialysis in 5.9%, and retinoschisis RRD in 1.6%. One in 10 cases reported significant ocular trauma. One in 5 cases were pseudophakic. Round hole RRD more frequently presented with multiple retinal breaks compared with HST RRD (67.8% vs. 48.7%; P = 0.003). In PVD-associated RRD, 56.1% (95% confidence interval [CI], 53.8–58.3) of breaks were identified in the superotemporal retina. In non-PVD RRD, 54.6% (95% CI, 47.9–61.1) of breaks were inferotemporal, followed by superotemporal in 34.9% (95% CI, 28.7–41.5). Lattice degeneration was present in 18.7% of affected eyes and more common in RH RRD (35.7%) than in HST RRD (19.3%) (P = 0.003). Seven percent reported an affected first-degree relative, and these cases were significantly more myopic than nonfamilial cases.

Conclusions

More than 85% of RRD cases are associated with PVD and related tractional tears. Non-PVD RH RRD occurred in younger and more myopic individuals. The majority of cases are caused by more than 1 retinal break, and the macula is affected in more than 50% at presentation. Ocular trauma, previous cataract surgery, family history, and lattice degeneration are important predisposing features.

Financial Disclosure(s)

The author(s) have no proprietary or commercial interest in any materials discussed in this article.

Section snippets

Materials and Methods

The Scottish Retinal Detachment study was a prospectively recruited epidemiology study, the methodology of which has been described in detail.4 Between November 1, 2007, and October 31, 2009, we established a comprehensive system in which each primary RRD case presenting to 1 of the 6 vitreoretinal surgical centers in Scotland was approached for study inclusion. The study adhered to the tenets of the Declaration of Helsinki and was approved by the Multicenter Research and Ethics Committee

Results

A total of 1202 incident cases of primary RRD were recruited in Scotland over the 2-year study period. In 1130 cases, data were available on the clinical features of RRD. In total, PVD was present in 87.6% of cases (990/1130), with single or multiple HST RRD accounting for 98.5% of this group (975/990) and GRT RRD accounting for 1.5% of this group (15/990). Posterior vitreous detachment was absent in 12.4% of cases (140/1130), and these comprised RH RRD in 40% (56/140), retinal dialysis in

Discussion

This study represents some of the most extensive and detailed data ever compiled on the epidemiology of RRD and provides important clinical information for vitreoretinal surgeons and useful data for healthcare resource planning.

In our series, both PVD-present and PVD-absent RRD were more common in men. Rhegmatogenous retinal detachment associated with PVD demonstrated a higher proportion of right eyes affected and a peak incidence in the sixth decade of life. Rhegmatogenous retinal detachment

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    Manuscript no. 2010-929.

    Financial Disclosure(s): The author(s) have no proprietary or commercial interest in any materials discussed in this article.

    This study was supported by a major Ophthalmology grant from the Royal College of Surgeons Edinburgh, the Royal Blind School Edinburgh/Scottish War Blinded, the W.H. Ross Foundation for the Prevention of Blindness and the Chief Scientist Office Scotland (CZB/4/705). The authors received (a proportion of their) financial support from the Department of Health through the award made by the National Institute for Health Research to Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology for a Specialist Biomedical Research Centre for Ophthalmology. The views expressed in this publication are those of the authors and not necessarily those of the Department of Health.

    Competing interests: None declared.

    A list of members of the Scottish RD Study Group is available at http://aaojournal.org.

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