Visual outcome and associated risk factors in patients following small incision cataract surgery at the National Referral Hospital, Bhutan

Abstract

Purpose To evaluate small incision cataract surgery visual outcomes and associated risk factors in a tertiary eye care center in Bhutan.

Methods This was a hospital-based prospective longitudinal study. A total of 310 patients who met the eligibility criteria were included in the study.

Results The mean age of the patients was 68.36 (SD: 12.74 years), and 157 (50.6%) were male. 285 (91.94%) of the cataract-operated eyes had best-corrected vision greater than 6/60, while 25 (8.06%) of the eyes had vision less than 6/60. 47 individuals (15.16%) had pre-existing ocular co-morbidity. Intraoperative complications were seen in 19 eyes (6%). At the 6-week follow-up visit, based on best-corrected visual acuity (BCVA), 90.65% had a good visual outcome. Analysis of multiple logistic regression showed that patients with preoperative ocular comorbidities (OR 50.92; 95% CI 10.23, 253.37) and those with operative complications (OR 16.59; 95% CI 3.54, 77.70) were significantly associated with poor visual outcome.

Conclusions This study shows that cataract surgery can restore good visual acuity. However, patients should be followed up on for a longer period, and greater emphasis should be given to monitoring outcomes after cataract surgery.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

Yes

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Institutional Review Board (IRB), Khesar Gyalpo University of Medical Sciences of Bhutan (KGUMSB)

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All Data are stored in the hard drive and can be made available on requirement and can be shared.

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