Patterns of Uveitis at the Tertiary Eye Care Clinic of Kinshasa, Democratic Republic of Congo

Research Article

J Ophthalmol & Vis Sci. 2021; 6(4): 1058.

Patterns of Uveitis at the Tertiary Eye Care Clinic of Kinshasa, Democratic Republic of Congo

Nsiangani LN* and Kaimbo KD

Department of Ophthalmology, Teaching Hospital, University of Kinshasa, Democratic Republic of Congo

*Corresponding author: Nadine Nsiangani Lusambo, Department of Ophthalmology, Teaching Hospital, University of Kinshasa, Democratic Republic of Congo

Received: August 30, 2021; Accepted: October 21, 2021; Published: October 28, 2021

Abstract

Purpose: To describe the clinical characteristics and the etiology of uveitis in a retrospective series of patients referred to the Tertiary Eye Care Clinic of Kinshasa, Democratic Republic of Congo.

Methods: We performed a retrospective analysis of the medical records of all patients who presented to consultation between January 2010 and December 2012. The time of follow-up ranged from 6 months to 4 years. Each patient underwent an ophthalmic and general clinical examination, and an etiological assessment according to the diagnostic hypotheses was carried out.

Results: 115 cases of uveitis were diagnosed, giving a prevalence of 0.6% of all diagnoses at the hospital. Men represented 51.3% of patients, with a sex ratio of 1:1. The mean age of the patient at presentation ± SD was 42.4 ± 18.3 years (Range: 8-80 years). At the initial consultation, 53% of patients had visual impairment (VA <6/18). Anterior (50.4%) and posterior (26.1%) uveitis were the most frequent anatomical types of uveitis among patients. The etiology of uveitis could not be determined in 58 patients (50.4%). Uveitis from infectious causes accounted for 44.3% and non-infectious causes 5.2%. During follow-up, 34.8% of patients developed a complication; cataracts (27.8%) and retinal detachment (8.7%) were the most common complications.

Conclusion: Infectious causes account for most cases on most studies of uveitis in the Sub-Saharan. Visual impairment and complications are frequent among patients. Limitations in diagnostic techniques and financial resources impose a challenge for etiological diagnosis and patient care.

Keywords: Uveitis; Pattern; Etiology; Africa; RD Congo

Introduction

Uveitis refers to inflammation of the uvea, the middle vascular layer of the eye. It is the most common cause of inflammatory eye disease and is a significant cause of blindness and visual impairment worldwide. Uveitis leads to 5% to 20% of legal blindness in the United States and Europe and approximately 25% in developing countries [1,2]. Because uveitis typically affects young adults in their productive years of life, this sight-threatening disease’s personal and populational burden is substantial [2]. Genetic, geographic, social, and environmental factors affect the distribution of the types, clinical associations, and causes of uveitis in different populations [2,3].

There is a lack of studies on uveitis in Sub-Saharan African countries [4-7]. These studies are necessary to determine the distribution of the types and causes of uveitis in order to guide a focused approach to investigation, diagnosis, and management of this condition [1,2].

Therefore, this study aimed to describe the clinical characteristics and etiology of uveitis in a retrospective series of patients referred to the Department of Ophthalmology of the University Hospital of Kinshasa and compare the findings with previously published studies from other Sub-Saharan African countries to identify similarities and differences.

Materials and Methods

We performed a retrospective analysis of the medical records of all patients who presented to the Tertiary Eye Care Clinic of Kinshasa in the Democratic Republic of Congo from January 2010 to December 2012. The time of follow-up ranged from 6 months to 4 years.

The inclusion criteria were a diagnosis of uveitis. Exclusion criteria were a diagnosis of masquerade syndromes (ocular irritation after surgery, trauma, retinal detachment, posterior vitreous detachment, vitreous hemorrhage, or malignancies).

Each patient underwent an ophthalmological examination that consisted of visual acuity, slit-lamp examination, tonometry, and indirect ophthalmoscopy. We based our diagnostic criteria, anatomic classification, and course of uveitis on the Standardization of Uveitis Nomenclature (SUN) workshop and International Uveitis Study Group criteria [8]. The visual acuity of the patients was classified according to WHO criteria [9].

An Internal Medicine specialist performed a general clinical examination on each patient, and an etiological assessment according to the diagnostic hypotheses was carried out.

Results

During the study period, 115 cases of uveitis were diagnosed, giving a prevalence of 0.6%. Men represented 51.3% of patients, with a sex ratio of 1:1. The mean age of the patients at presentation ± SD was 42.4 ± 18.3 years (range: 8-80 years). Children represented 5.2% of patients. Uveitis was unilateral in 67 patients (58.3%). Decreased visual acuity (69.6%), pain (40.9%), and eye redness (24.3%) were the most common complaints. At the initial consultation, 53% of patients (78/163 eyes = 47.8%) had a visual impairment (VA <6/18); low vision (3/60 ≤ VA< 6/18) and blindness (VA < 3/60) affecting respectively 37 eyes (22.7%) and 41 eyes (25.1%) (Table 1). The course of the disease was chronic in 66.1% of cases and acute in 28.7 %. Anterior (50.4%) and posterior (26.1%) uveitis were the most frequent anatomical types of uveitis among patients. The etiology of uveitis could not be determined in 58 patients (50.4%). Uveitis from infectious causes accounted for 44.3% and non-infectious causes 5.2%. Among the infectious causes, ocular toxoplasmosis (27%) and viral uveitis (14.8%) were the most encountered etiologies. Spondyloarthritis was the most frequent cause of non-infectious uveitis among our patients (4.3 %). During follow-up, 34.8% of patients developed a complication. Cataracts (27.8%), retinal detachment (8.7%), and secondary glaucoma (7.8%) were the most common complications (Table 2).