Elsevier

Ophthalmology

Volume 113, Issue 11, November 2006, Pages 2026-2032
Ophthalmology

Original Article
Risk of Retinal Detachment after Cataract Extraction, 1980–2004: A Population-Based Study

Presented in part at: American Ophthalmological Society Annual Meeting, May 24, 2006, Half Moon Bay, California.
https://doi.org/10.1016/j.ophtha.2006.05.054Get rights and content

Purpose

To estimate the long-term cumulative risk of retinal detachment (RD) after cataract extraction (CE).

Design

Retrospective cohort study and nested case–control study.

Participants

All residents of Olmsted County, Minnesota who had CE from 1980 through 2004 (10 256 CEs in 7137 residents) and were diagnosed subsequently with RD in the same period. Two controls chosen from the primary cataract surgery cohort were matched to each RD case by age, gender, and duration of follow-up.

Methods

Cases were identified through the Rochester Epidemiology Project databases. Records were reviewed to confirm case status and ascertain risk factor information. The observed probability of RD after CE was estimated using the Kaplan–Meier method. A cumulative probability ratio of RD after CE was determined by comparing the observed probability of RD and the expected probability of RD in residents without CE. Logistic regression models assessed differences between cases and controls.

Main Outcome Measures

Probability of and risk factors associated with RD after CE.

Results

Eighty-two cases of RD were identified. The cumulative probability of RD increased in a nearly linear manner over the 25-year study period. At 1, 5, 10, 15, and 20 years after extracapsular CE (ECCE) and phacoemulsification, cumulative probabilities of RD were 0.27%, 0.71%, 1.23%, 1.58%, and 1.79%, respectively. There was no significant difference in the probability of RD after ECCE when compared with phacoemulsification (P = 0.13). The cumulative probability ratio of RD at 20 years after ECCE and phacoemulsification remained 4.0-fold (95% confidence interval, 2.6–5.4) higher than would be expected in a similar group of residents not undergoing CE (P<0.001). Male gender, younger age, myopia, increased axial length, and posterior capsular tear were associated significantly with RD (P<0.01).

Conclusions

The cumulative risk of RD after ECCE and phacoemulsification is increased for up to 20 years after surgery.

Section snippets

Materials and Methods

The institutional review board of Mayo Clinic College of Medicine approved the protocol for the study of this cohort.

Results

Medical record review identified 91 potential cases with a documented RD after CE. Exclusion of 9 nonresidents left 82 incident cases of pseudophakic RD in 79 residents. The mean age at RD diagnosis was 65±15 years (± standard deviation) (range, 11–93), with 40 of 82 cases (49%) in residents younger than 65. Among residents with a pseudophakic RD, the mean age at CE was 61±16, with 49 of 82 cases (60%) in residents younger than 65 at the time of cataract surgery. All residents were Caucasian.

Discussion

The findings of our population-based cohort study demonstrate that the risk of RD after ECCE and phacoemulsification increased in a nearly linear manner in the 25-year period 1980 through 2004. We report a cumulative probability of RD that increased from 0.27% at 1 year after CE to 1.79% at 20 years. At 20 years after ECCE and phacoemulsification, the risk of RD remained 4 times higher than would be expected in a comparable group of residents who did not have cataract surgery.

There is a lack of

References (27)

Cited by (74)

  • Genome-wide association meta-analysis of 88,250 individuals highlights pleiotropic mechanisms of five ocular diseases in UK Biobank

    2022, eBioMedicine
    Citation Excerpt :

    Close genetic relationship between AMD and DR is also reflected in their similar genetic correlations with several risk factors such as fat, insomnia, and lack of physical activity. The second group contained RD and myopia, with the highest genetic correlation estimate, have characterized by axial elongation.44,45 Overall, these results suggest significant pairwise genetic correlations among multiple ocular disorders and a higher level of genetic architecture that points to broader domains that underlie genetic risk for ocular pathology.

View all citing articles on Scopus

Manuscript no. 2006-406.

Supported in part by Research to Prevent Blindness, Inc., New York, New York, and the Mayo Foundation, Rochester, Minnesota.

No author has a financial or proprietary interest in any materials or methods mentioned.

View full text