Visual Status of Patients with Retinitis Pigmentosa: A Multicenter Study.

AIM: To determine the degree of visual loss associated with retinitis pigmentosa (RP) in Nigerians at first ophthalmic clinic presentation METHODOLOGY: Multicenter, prospective, cross-sectional study in four collaborating retina clinics within Nigeria between January and December 2018. The primary outcome measure was the World Health Organization's visual status classification at presentation. Clinical examination, including a Snellen's visual acuity, refraction, anterior segment examination using a slit lamp biomicroscope, and dilated fundus examination using a +90D or +78D, was done in all consecutive RP patients. We analyzed the data using SPSS (version 22), P < 0.05. RESULTS: Of 8614 patients seen within the study period, fiftyfour eyes of 27 patients diagnosed to have RP with a mean age of 44.1years ± 17.6 years (ranging between 5­73 years) constituted the study population. Eighteen (66.7%) were males and 9 (33.3%) females. The hospital-based prevalence of RP was 0.31%. Ten patients (37.0%) presented with myopia. RP was bilateral in all cases and non-syndromic. Bilateral low vision and blindness were noted in 44.4% and 22.2% of patients respectively. CONCLUSION: About a quarter of patients with RP presenting to the retina clinics would have some degree of visual morbidity. Educating eye care providers and patients about the disease would improve understanding, encourage early clinic visits, manage visual morbidity and enhance rehabilitation when necessary.

OBJECTIF: Déterminer le degré de perte visuelle associée à la rétinite pigmentaire (RP) chez les Nigérians lors de la première présentation en clinique ophtalmique MÉTHODOLOGIE: Étude multicentrique, prospective et transversale dans quatre cliniques de rétine collaboratrices au Nigeria entre janvier et décembre 2018. Le principal critère de jugement était la classification de l'état visuel de l'Organisation mondiale de la santé à la présentation. Un examen clinique, comprenant une acuité visuelle de Snellen, une réfraction, un examen du segment antérieur à l'aide d'un biomicroscope à lampe à fente et un examen du fond d'œil dilaté à l'aide d'un +90D ou +78D, a été effectué chez tous les patients consécutifs atteints de RP. Nous avons analysé les données à l'aide du SPSS (version 22), P < 0,05 RÉSULTATS: Sur les 8614 patients examinés pendant la période d'étude, 54 yeux de 27 patients diagnostiqués comme ayant une RP et âgés en moyenne de 44,1 ans ± 17,6 ans (entre 5 et 73 ans) ont constitué la population étudiée. Dix-huit (66,7 %) étaient des hommes et 9 (33,3 %) des femmes. La prévalence de la RP dans les hôpitaux était de 0,31 %. Dix patients (37,0 %) présentaient une myopie. La RP était bilatérale dans tous les cas et non syndromique. Une basse vision et une cécité bilatérales ont été constatées chez 44,4 % et 22,2 % des patients respectivement. CONCLUSION: Environ un quart des patients atteints de RP se présentant dans les cliniques de la rétine auraient un certain degré de morbidité visuelle. L'éducation des prestataires de soins ophtalmologiques et des patients sur la maladie permettrait d'améliorer la compréhension, d'encourager les visites précoces dans les cliniques, de gérer la morbidité visuelle et d'améliorer la réadaptation si nécessaire. Mots clés: Rétinite pigmentaire, Nigeria, basse vision, cécité.

Polypoidal Choroidal Vasculopathy Amongst Nigerians; A Multicenter Study.

OBJECTIVE: To investigate the prevalence and presentation of polypoidal choroidal vasculopathy (PCV) in Nigerians. METHODS: A cross-sectional, multicenter, hospital-based, descriptive study. Data were collected prospectively between January and December 2018, from consecutive patients diagnosed to have a retina disease at the general outpatient and retinal clinics of four eye departments in Nigeria. All participants had visual acuity, refraction, intraocular pressure, anterior segment examination, and dilated fundus examination. Some patients had fundus fluorescein angiography, optical coherence tomography (OCT), and OCT angiography (OCTA). Systemic comorbidity was determined by medical history and systemic evaluation. Diagnosis of PCV was based on clinical findings, and in some patients using OCT. RESULTS: A total of 8,614 patients were seen and 15 patients (18 eyes) were diagnosed to have PCV giving a yearly hospital-based prevalence of 0.17%. The mean age at presentation was 63.27 ± 11.5 years (range 44-84 years). There were nine females (60%). The male: female ratio was 1.5:1. Twelve (66.7%) of the 18 eyes were blind, 16.7% had severe visual impairment while 11.1% had mild visual impairment. Seven eyes (38.9%) had vitreous hemorrhage. Of the 12 blind eyes, 50% had vitreous hemorrhage (P = 0.463). Nine patients (60%) had systemic hypertensive as comorbidity (P = 0.016). CONCLUSION: PCV is a cause of vision loss among Nigerians. Majority of the eyes were blind and 50% of blind eyes had vitreous hemorrhage. Since Indocyanine Green Angiography is the most appropriate imaging technology and is mostly unavailable in Nigeria, efforts should be made to address this need and improve the diagnostic accuracy.