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1.
Med J Malaysia ; 68(1): 39-43, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23466765

RESUMEN

RetCam is an excellent screening tool for the detection of retinopathy of prematurity (ROP). However, affordability is a barrier when adopting the use of RetCam in developing countries. We aimed to describe different stages of ROP using ultrasonographic B-scan and to evaluate the association between funduscopic examinations and ultrasonographic B-scan findings in premature neonates with ROP in Malaysia. A descriptive cross sectional study was conducted in 90 eyes of 47 premature neonates with different stages of ROP in three tertiary hospitals in Malaysia. Experienced ophthalmologists performed detailed funduscopic examinations using binocular indirect ophthalmoscopy (BIO). A masked examiner performed a 10 MHz ultrasonographic B-scan evaluation with 12 meridian position images within 48 hours of clinical diagnosis. Data from the clinical examination and ultrasonographic findings were collected and analysed. We recruited 37 eyes (41.1%) with stage 1 ROP, 29 eyes (32.3%) with stage 2, 18 eyes (20.0%) with stage 3, and 3 eyes (3.3%) with stages 4 and 5 based on the clinical assessment. Ultrasonography correctly identified 3 (8.1%) stage 1 eyes, 17 (58.6%) stage 2 eyes, 13 (72.2%) stage 3 eyes, and 3 each (100%) of the stage 4 and 5 eyes. There was a significant association between the funduscopic signs and the ultrasound findings for stage 2 ROP and above (Fisher's exact test, p <0.001). In conclusion, all stages of ROP were detected and described with a 10 MHz ultrasonic B-scan system. A significant association was observed between funduscopic signs and ultrasonographic findings in premature Malaysian neonates with stage 2 ROP and above.


Asunto(s)
Oftalmoscopía , Retinopatía de la Prematuridad , Estudios Transversales , Humanos , Recién Nacido , Recién Nacido de muy Bajo Peso , Malasia , Sensibilidad y Especificidad
2.
Med J Malaysia ; 62(4): 343-4, 2007 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-18551944

RESUMEN

We report a three year follow up of a 35-year-old Indian gentleman who presented with sudden, painless blurring of left (L) eye vision with initial visual acuity (VA) of 6/60. Fundoscopy revealed (L) vitreous haemorrhage and subsequently confirmed a (L) inferotemporal capillary haemangioma. The adjacent area of capillary haemangioma was treated with barricade argon laser photocoagulation to prevent progression of exudative retinal detachment inferiorly. Subsequent follow up showed mild regression of capillary haemangioma with maintenance of (L) eye vision at 6/9.


Asunto(s)
Hemangioma Capilar/diagnóstico , Trastornos de la Visión/diagnóstico , Agudeza Visual , Enfermedad de von Hippel-Lindau/diagnóstico , Adulto , Hemangioma Capilar/fisiopatología , Humanos , Fotocoagulación/instrumentación , Masculino , Trastornos de la Visión/fisiopatología , Enfermedad de von Hippel-Lindau/fisiopatología
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