Impact of Socioeconomic Status on Clinical Features and Outcomes of Bacterial Keratitis: The Midlands Infectious Keratitis Study

ABSTRACT

Background/Aims To evaluate the impact of socioeconomic deprivation on clinical presentation and outcomes of bacterial keratitis (BK) in the United Kingdom.

Methods A retrospective multicentre cohort study of 320 patients with BK presenting to two UK tertiary ophthalmic centres. Demographic, clinical and microbiological data were extracted from electronic health records. Socioeconomic status was assigned using residential postcodes mapped to the 2019 English Index of Multiple Deprivation (IMD) and grouped into quintiles (Q1 most deprived; Q5 least deprived). Presenting severity and outcomes were compared across IMD quintiles.

Results The mean age was 54.0±20.9 years; 50.6% were male and 83.4% were White. Mean presenting CDVA was 1.10±1.01 logMAR and time to presentation was a median of 3 days (IQR 1–6). Most cases had a small infiltrate (<3Lmm; 68.4%), small epithelial defect (<3Lmm; 63.4%) and no hypopyon (72.5%). Hospitalisation was required in 50.0%, and 17.5% underwent surgery. Culture positivity was 36.3%. There were no significant differences in presenting CDVA, time to presentation, clinical severity, admission, microbiological profile, surgical intervention or final CDVA across IMD quintiles (all p>0.05). Final CDVA improved to 0.75±0.96 logMAR (p<0.001). On multivariable analysis, poorer final CDVA was associated with worse presenting CDVA, increasing age and Gram-positive organisms, but not IMD.

Conclusion Socioeconomic deprivation did not influence the clinical presentation or outcomes in BK. Clinical severity at presentation and microbiological profile were the principal determinants of outcome. In this acute, painful sight-threatening condition, deprivation-related disparities may be attenuated by prompt presentation and universal access to emergency ophthalmic care.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

Funding support from the Medical Research Council Clinician Scientist Fellowship (UKRI2441) and Birmingham Health Partners (BHP) Clinician Scientist Fellowship.

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:

The study was approved by the clinical governance team of both institutions as a clinical audit (BMEC Ref: 2444; QMC Ref: 19-265C) and was conducted in accordance with the tenets of Declaration of Helsinki. Ethics approval was not required as this clinical audit only involved retrospective study of anonymised data that were collected during the process of standard clinical care.

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).

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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

Footnotes

Funding/support: DSJT acknowledges funding support from the Medical Research Council Clinician Scientist Fellowship (UKRI2441) and Birmingham Health Partners (BHP) Clinician Scientist Fellowship.

Conflict of interest: None

Data Availability

All data produced in the present study are available upon reasonable request to the authors

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