Risk factors
Most RRDs are associated with retinal tear formation at the time of PVD.13 The risk of tear formation is increased in people with areas of pre-existing retinal thinning such as lattice degeneration, which is also associated with abnormal vitreoretinal adhesion. RRDs can also occur without PVD in people with pre-existing retinal lesions, such as atrophic retinal holes, lattice degeneration and retinal dialyses which can be due to previous blunt trauma or idiopathic.14 15 Approximately 7%–8% of the normal population have areas of lattice degeneration, but only a small proportion will progress to RRD, although higher than the non-lattice degeneration population.16 17 Asymptomatic retinal dialysis is thought to have a high risk of progression to RD, especially after trauma.18
There is an increased risk of RRD in myopic patients, with an up to 10-fold increase in myopia over three dioptres (D).15 This is an important consideration amid the increasing incidence of high myopia (greater than −6D) worldwide, with the prevalence in school-aged children in Asia as high as 80%.19 20 RRD risk also varies by gender and ethnicity with men, and Caucasian and Asian populations are at relatively higher risk.21 22
People who previously had cataract surgery also have a higher incidence of RRD, with approximately one in five RRDs in the UK being pseudophakic.1 About 0.5%–0.6% of people experience RRD after phacoemulsification, with the risk increasing year on year to at least 10 years. Posterior capsule rupture increases the risk substantially by up to 15–20 times.22–24 Several other factors are associated with pseudophakic RRD, including (in order of decreasing effect) increasing axial length, younger age and male sex.22
Risk to fellow eye
The fellow eye in patients with RRD is at a higher risk. The Scottish Retinal Detachment Study found a prevalence of bilateral RRD of 7%.25 Interestingly, in the same cohort, retinal tears were found in 8% of fellow eyes in patients with primary RRD, which underscores the need for a thorough dilated fundal examination of the fellow eye. A UK study by Fajgenbaum et al found that the risk of fellow-eye RRD was highest during the early postoperative period and declined over the years.26 Specifically, the probability (hazard rate) of RRD in the fellow eye was 3% in the first year, and declined to 0.3% over 10 years; the cumulative risk of RRD in the fellow eye was 8% over 15 years.26
Prevention: prophylactic treatment to fellow eye following RRD
Although RRD may develop in a fellow eye from pre-existing retinal lesions, most subsequent RRDs (at least 50% and possibly as high as 80%–90%) in the fellow eye will occur from ophthalmoscopically normal areas of retina,27 therefore, prophylactic treatment with either laser or cryotherapy to funduscopically abnormal areas does not completely reduce the incidence of fellow-eye RRD. However, in one large UK study only 6% of eyes treated prophylactically developed RRD.25 It should also be noted that 30% of patients with symptomatic retinal tears or holes, will develop RRD if untreated.28
Diagnosis: rules for detecting retinal breaks
The cornerstone of RRD examination is the search for retinal break(s). For over 40 years, the seminal paper by Lincoff and Giese,29 gave rise to the ubiquitously cited ‘Lincoff rules’ for identifying the location of the primary or causative retinal break in RRD (figure 2). There are RRDs that do not obey these rules that present clinical challenges. Although not yet validated, but based on long experience, David Wong cited six new rules that illustrate the locations of retinal breaks in RRDs that do not obey Lincoff’s rule, during the 2018 British and Eire Association of Vitreoretinal Surgeons meeting (figure 3) (D.Wong, personal communication). He described that a retinal break in the upper temporal quadrant would recruit SRF and gradually result in a subtotal RD, higher on the temporal side and bullous inferiorly (rule 1). Similarly, a retinal break in the same location could result in an acute bullous superior RD overhanging the posterior pole and macula (rule 2). This last configuration is thought to be due to vitreous separation and collapse, which in turn is responsible for rapid onset and the bullous overhanging nature of the RD. Areas of thin retina in the detached retina point to where the break is (rule 3). In fundus-obscuring vitreous haemorrhage the ophthalmologist should suspect multiple retinal breaks (rule 4). In case of RRD involving the posterior retina but limited in extent inferiorly and peripherally, the primary break is likely located at the posterior pole (rule 5). Finally, in inferior bullous RRD, the retinal breaks should be on the concave as opposed to the convex side, and this can be appreciated by alternately rolling the patient on each side (rule 6). Further work needs to be undertaken to determine if these rules hold.
Figure 2Lincoff Rules. Summary of ‘Lincoff Rules’ to aid the identification and position of a retinal break in RRD. RRD, rhegmatogenous retinal detachment.
Figure 3Six new rules presented at BEAVRS 2018 by David Wong. Not validated. BEAVRS, British and Eire Association of Vitreoretinal Surgeons.
Surgical management of RRD
Aim of intervention
The main target of RRD management is to achieve retinal reattachment. Although the benefit for treatment of asymptomatic (chronic) RRD remains unclear, symptomatic RRD is a clear indication for surgery. On presentation, RRD is usually divided into ‘macula-on’ where the foveal centre is not involved, and ‘macula-off’ where the fovea is detached.30 People with macula-on RRD typically have good initial best-corrected visual acuity (BCVA) and a better visual prognosis with successful surgery. Macula-off RRDs have lower initial BCVA and worse visual prognosis even with successful reattachment of the retina. However, in macula-off RRDs postoperative BCVA is better in patients with 1–3 days of visual loss compared with 4–6 days, and hence these patients also need to be treated as a matter of urgency.31 Indeed it is likely that prognosis reduces linearly for every day that the macula remains detached.
Optical coherence tomography (OCT) is not routinely required to assess macular status, as this can be established by BCVA and clinical examination, with preoperative BCVA determining potential postoperative BCVA. However, OCT and ultrasound imaging may be useful in assessing the presence of PVD, as this can influence the surgical approach.