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Prevalence of Refractive Errors among School Children Aged 5 to 15 Years Old at CHU-IOTA
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作者 Kadiatou Ba Aichata Tall +19 位作者 Mory coulibaly Cheick Sogodogo Zoumana Bagayogo Aoua Ibrahim Toure Ousmane Toure brainima coulibaly Fatoumata Tata Sidibe Aly Konipo Roucky Sangare Seydou Diallo Moro Sidibe Oumar Diallo Assiatou Simaga Gounon Saye Modibo Sissoko Mamadou Kole Sidibe Sidi Diarra Nouhoum Guirou Abdoulaye Napo Adama Guindo 《Surgical Science》 2024年第8期480-491,共12页
Introduction: Undetected refractive errors constitute a health problem among school children who cannot take advantage of educational opportunities. The authors studied the prevalence of refractive errors in school ch... Introduction: Undetected refractive errors constitute a health problem among school children who cannot take advantage of educational opportunities. The authors studied the prevalence of refractive errors in school children aged 5 to 15 at CHU-IOTA. Patients and Method: This is a prospective, descriptive cross-sectional study carried out in the ophthalmic-pediatrics department of CHU-IOTA, from October to November 2023. Results: We received 340 school children aged 5 to 15, among whom 111 presented ametropia, i.e. a prevalence of 32.65%. The average age was 11.42 ± 2.75 years and a sex ratio of 0.59. The average visual acuity was 4/10 (range 1/10 and 10/10). We found refractive defects: astigmatism 73.87%, hyperopia 23.87% of cases and myopia 2.25%. The decline in distance visual acuity was the most common functional sign. Ocular abnormalities associated with ametropia were dominated by allergic conjunctivitis (26.13%) and papillary excavation (6.31%) in astigmatics;allergic conjunctivitis (9.01%) and papillary excavation (7.20%) in hyperopic patients;turbid vitreous (0.90%), myopic choroidosis (0.45%) and allergic conjunctivitis (0.45%) in myopes. Conclusion: Refractive errors constitute a reality and a major public health problem among school children. 展开更多
关键词 Refractive Errors PREVALENCE CHILD CHU-IOTA
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Prevalence of Ocular Trauma at the Reference Health Center (CSREF) of Kati
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作者 Kadiatou Ba Aichata Tall +18 位作者 brainima coulibaly Sadio Cissoko Bakary Danfaga Moro Sidibe Seydou Diallo Oumar Diallo Fatoumata Tata Sidibe Aly Konipo Mory coulibaly Ousmane Touré Aoua I. Touré Cheick Sogodogo Ibrahim Bamenta Gounon Saye Modibo Sissoko Mamadou Kole Sidibe Sidi Diarra Nouhoum Guirou Lamine Traoré 《Surgical Science》 2024年第5期371-380,共10页
Introduction: The authors wanted to study the prevalence of ocular trauma in the ophthalmology unit of the CSREF of Kati. Patients and method: This is a retrospective study, covering the period from January to Decembe... Introduction: The authors wanted to study the prevalence of ocular trauma in the ophthalmology unit of the CSREF of Kati. Patients and method: This is a retrospective study, covering the period from January to December 2015, carried out in the ophthalmology unit of the CSREF in Kati. Results: The sample consisted of 568 patients, or 6.82% of ophthalmological consultations. Children aged 0 to 14 years accounted for 154 (27.11%) of the trauma cases. Bruises constitute the main circumstance (58.1%) of eye trauma, followed by domestic accidents (15.6%). Closed globe ocular trauma was the main type of trauma (61.6%), followed by ocular adnexal trauma (30.1%) and open globe trauma (8.3%) in which the penetrating wound was the lesion, the least common (2.6%) but the most serious. Medical treatment was the most used therapeutic modality in 82.4% of cases, followed by surgery with 17.6% of cases. The evolution of the lesions after treatment was favorable in 85.6% of cases and unfavorable in 14.4% of cases. Complications were observed in 5.8% of cases and sequelae in 8.6% of cases. Conclusion: Ocular trauma constitutes an important reason for ophthalmological consultation at the CSREF of Kati. The severity of some of these lesions requires frequent recourse to surgery. The complexity of the treatment should encourage us to favor preventive measures. 展开更多
关键词 Eye Trauma PREVALENCE CSREF Kati
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Morning Glory Syndrome in Two (02) Malians: Case Report from IOTA-University Hospital
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作者 Seydou Bakayoko brainima coulibaly +5 位作者 Mohamed Kolé Sidibe Elien Gyrr Modibo Sissoko Gounon Saye Marcel Tembely Fatoumata Sylla 《Open Journal of Ophthalmology》 2020年第3期265-269,共5页
<strong>Background:</strong><span style="font-family:;" "=""><span style="font-family:Verdana;"> First described by Handmann in 1929, the “Morning Glory Synd... <strong>Background:</strong><span style="font-family:;" "=""><span style="font-family:Verdana;"> First described by Handmann in 1929, the “Morning Glory Syndrome” is a rare congenital anomaly of the optic papilla whose notable ophthalmoscopic sign is papillary excavation associated with other ocular and/or non-ocular anomalies. </span><b><span style="font-family:Verdana;">Purpose:</span></b><span style="font-family:Verdana;"> The main purpose of this study is to report 2 cases of this rare congenital papilla anomaly in 2 young Malian adults diagnosed in the IOTA-University Hospital respectively in January and May 2020. </span><b><span style="font-family:Verdana;">Materials and methods:</span></b><span style="font-family:Verdana;"> In our study, we have included two cases of </span><span style="font-family:Verdana;">male</span><span style="font-family:Verdana;"> gender. </span><b><span style="font-family:Verdana;">Results:</span></b><span style="font-family:Verdana;"> In the 1</span><sup><span style="font-family:Verdana;">st</span></sup><span style="font-family:Verdana;"> case the defect concerned both papillae. It </span><span style="font-family:Verdana;">is also associated with other ocular malformations (bilateral macular reshaping</span><span style="font-family:Verdana;"> and unilateral cataract), without associated cerebral defects. In the 2</span><sup><span style="font-family:Verdana;">nd</span></sup><span style="font-family:Verdana;"> case, only one papilla was affected by the malformation and there was an absence of associated malformations of other ocular and cerebral structures. </span><b><span style="font-family:Verdana;">Discussion:</span></b><span style="font-family:Verdana;"> The Morning Glory Syndrome is part of the group of congenital defects of the optic nerve. It is often referred to as ectasia coloboma of the optical papilla or bindweed flower-like optical papilla because of its similarity to the tropical flower known as “bindweed”. Its exact pathogenesis remains unknown, but it is linked to the poor development of the posterior sclera and lamina </span><span style="font-family:Verdana;">cribrosa</span><span style="font-family:Verdana;"> during gestation. </span><b><span style="font-family:Verdana;">Conclusion:</span></b><span style="font-family:Verdana;"> Morning Glory Syndrome through papillary excavation and other associated ocular and/or cerebral malformations may be a threat to vision.</span></span> 展开更多
关键词 Morning Glory Syndrome Congenital Papilla Defects BAMAKO
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