RESUMEN
Exposure keratopathy is a sight-threatening complication which can occur in patients admitted to intensive care units. This is a prospective study over a period of 5 months in the intensive care unit of the specialty hospital of the IBN SINA medical center, with a capacity of 8 beds. The purpose of our study was to determine the incidence of and risk factors for exposure keratopathy in intensive care settings. Forty-two percent of patients developed exposure keratopathy, 48% exhibited chemosis, and 40% showed lagophthalmos with the cornea visible in 30% of cases. The frequency of keratopathy was significantly higher in patients with chemosis and lagophthalmos (P<0.0001). Lagophthalmos was significantly related to chemosis (P<0.0001). Chemosis in the ventilated patient, also known as "ventilator eye," is a serious complication leading to the risk of keratopathy. The risk factors for keratopathy found in our series were chemosis (OR=25.28, 95% CI=[3.339-191.52] P-value=0.002), lagophthalmos (OR=40.8, 95% CI=[4.347-383.666] P-value=0.001) and length of stay in intensive care (OR=12.28, 95% CI=[1.476-102.230] P-value=0.020). Several methods might be used and adapted to each case for prevention of exposure keratopathy, and we found that raising nursing staff awareness is of paramount importance.
Asunto(s)
Enfermedades de la Conjuntiva , Enfermedades de la Córnea , Enfermedades de los Párpados , Queratoconjuntivitis , Humanos , Incidencia , Estudios Prospectivos , Unidades de Cuidados Intensivos , Enfermedades de la Córnea/epidemiología , Enfermedades de la Córnea/etiología , Enfermedades de la Conjuntiva/complicaciones , Queratoconjuntivitis/complicaciones , Factores de Riesgo , Enfermedades de los Párpados/complicacionesAsunto(s)
Desplazamiento del Cristalino , Subluxación del Cristalino , Cristalino , Adulto , Humanos , Desplazamiento del Cristalino/complicaciones , Desplazamiento del Cristalino/diagnóstico , Desplazamiento del Cristalino/cirugía , Subluxación del Cristalino/complicaciones , Subluxación del Cristalino/diagnóstico , Cristalino/diagnóstico por imagen , Cristalino/cirugíaRESUMEN
INTRODUCTION: Behçet's disease is a systemic disease of unknown etiology. Its ocular manifestations are multiple and polymorphic, with uveitis at the top of the list. Classically, uveitis in Behçet's disease does not cause elevation of intraocular pressure. However, this may be found in 10 to 20% of cases, secondary to trabeculitis, trabecular obstruction by inflammatory cells, anterior or posterior synechiae, or induced by prolonged use of corticosteroids. Its occurrence is a major complication, the management of which is especially delicate when glaucoma occurs. The purpose of this study was to study the factors predictive of glaucoma in Behçet's disease. MATERIALS AND METHODS: This is a retrospective study of all the charts of patients consecutively hospitalized for Behçet's disease over a period of 8years in the ophthalmology A department of the specialty hospital of Rabat university medical center. RESULTS: Fifty patients were treated for Behçet's disease during the study period. There were 41 men (82%), and 9 women (18%). Glaucoma was diagnosed in 11 patients (22%). The mean age of this subgroup was 31years, with a gender ratio of 6 women/5 men. The glaucoma was associated with anterior synechiae in 4 cases, primary open-angle glaucoma in 5 cases, neovascular glaucoma in 1 case and seclusio pupillae in 1 case. Therapeutically, all patients were on glaucoma eye drops, and five underwent filtering surgery. Statistically, on univariate analysis, ocular hypertension was observed particularly in patients with low initial visual acuity (less than 1/10) (P=0.001), with severe posterior segment involvement, especially retinal vasculitis (29% vs. 6%, P=0.04), macular edema (40% vs. 4%, P=0.001), and optic disc edema (50% vs. 15%, P=0.02). A high number of recurrences was also associated with glaucoma (1.0 vs. 3.0, P<0.0001). On multivariate analysis, low baseline visual acuity, presence of retinal vasculitis, and high number of recurrences were independent risk factors for ocular hypertension in our patients followed for Behçet's disease. CONCLUSION: Glaucoma can complicate the management of Behçet's disease. This glaucoma will be more difficult to manage in this delicate pathological context. It requires special vigilance in patients with severe posterior segment inflammation, to institute effective management to avoid its potentially blinding complications.
Asunto(s)
Síndrome de Behçet/complicaciones , Síndrome de Behçet/epidemiología , Glaucoma/epidemiología , Glaucoma/etiología , Uveítis/epidemiología , Uveítis/etiología , Corticoesteroides/uso terapéutico , Adulto , Síndrome de Behçet/tratamiento farmacológico , Femenino , Glaucoma/tratamiento farmacológico , Humanos , Inmunosupresores/uso terapéutico , Masculino , Marruecos/epidemiología , Prevalencia , Estudios Retrospectivos , Uveítis/tratamiento farmacológico , Visión Ocular/efectos de los fármacos , Adulto JovenAsunto(s)
Coroides/anomalías , Coloboma/diagnóstico , Retina/anomalías , Ambliopía/diagnóstico , Ambliopía/etiología , Ambliopía/patología , Preescolar , Coroides/diagnóstico por imagen , Coroides/patología , Coloboma/complicaciones , Coloboma/patología , Humanos , Masculino , Marruecos , Retina/diagnóstico por imagen , Retina/patologíaAsunto(s)
Ceguera/diagnóstico , Ceguera/etiología , Neoplasias del Plexo Coroideo/complicaciones , Neoplasias del Plexo Coroideo/diagnóstico , Diagnóstico Tardío , Adulto , Ceguera/cirugía , Neoplasias del Plexo Coroideo/patología , Neoplasias del Plexo Coroideo/cirugía , Diagnóstico Diferencial , Servicios Médicos de Urgencia , Femenino , Cefalea/diagnóstico , Cefalea/etiología , Cefalea/cirugía , Humanos , Hidrocefalia/diagnóstico , Hidrocefalia/etiología , Hidrocefalia/cirugía , Procedimientos Neuroquirúrgicos , Factores de Riesgo , Carga TumoralAsunto(s)
Traumatismos del Nervio Óptico/diagnóstico , Corticoesteroides/uso terapéutico , Niño , Descompresión Quirúrgica , Equimosis/diagnóstico , Equimosis/tratamiento farmacológico , Equimosis/etiología , Equimosis/cirugía , Lesiones Oculares/complicaciones , Lesiones Oculares/diagnóstico , Lesiones Oculares/tratamiento farmacológico , Lesiones Oculares/cirugía , Enfermedades de los Párpados/complicaciones , Enfermedades de los Párpados/diagnóstico , Enfermedades de los Párpados/tratamiento farmacológico , Enfermedades de los Párpados/cirugía , Humanos , Masculino , Traumatismos del Nervio Óptico/tratamiento farmacológico , Traumatismos del Nervio Óptico/etiología , Traumatismos del Nervio Óptico/cirugía , Papiledema/diagnóstico , Papiledema/tratamiento farmacológico , Papiledema/etiología , Papiledema/cirugía , Desprendimiento de Retina/diagnóstico , Desprendimiento de Retina/tratamiento farmacológico , Desprendimiento de Retina/etiología , Desprendimiento de Retina/cirugía , Hemorragia Retiniana/diagnóstico , Hemorragia Retiniana/tratamiento farmacológico , Hemorragia Retiniana/etiología , Hemorragia Retiniana/cirugía , Adulto JovenRESUMEN
PURPOSE: To analyze clinical, therapeutic and prognostic features of pediatric Vogt-Koyanagi-Harada (VKH) disease. MATERIAL AND METHODS: This retrospective study included 16 eyes of 8 children diagnosed with VKH disease followed at a teaching hospital over a 10 year period. Diagnosis was based on the revised criteria of VKH disease. All data were analyzed using SPSS® software. RESULTS: There were 62.5% girls and 37.5% boys. The mean age (years) was 14.6±4.4. The mean follow-up (months) was 38.7±28.7. The mean initial visual acuity (VA) (LogMAR) was 1.4 with 68.8% of eyes presenting with severe visual loss at admission. The median time (days) required for resorption of the serous retinal detachment was 10 [8.25-25]. Extraocular signs were present in 62.5% of cases. The mean time until initiation of treatment was 25.6 days. 62.5% of patients received corticosteroids alone, and 37.5% of patients received a combination of corticosteroids and immunosuppressive therapy. Final VA was 0.4 [0.1-2.3]. In our study, the time until consultation, low initial VA and recurrences were statistically associated with severe visual loss (P≤0.05). CONCLUSION: Life expectancy in pediatric cases of VKH disease justifies the early initiation of immunosuppressive treatment or even biological therapy to achieve better steroid sparing and preserve visual function.