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1.
Indian J Pathol Microbiol ; 2011 Jan-Mar 54(1): 121-123
Artículo en Inglés | IMSEAR | ID: sea-141930

RESUMEN

Parasitic gastrointestinal infections are a major cause of morbidity and mortality in the developing world, with stool microscopy being the mainstay of diagnostic practice. Both direct microscopy and concentration techniques can be utilized; direct microscopy may be time consuming and tedious; however clinical laboratories in developing countries lack trained staff who can effectively use concentration methods. In our practice we used the Parasep O and P filter concentrator tubes (manufactured by DiaSys Ltd, Berkshire, England. Product Code 146000) along with direct microscopic techniques and found that Parasep filters enhanced the ability to detect intestinal parasites that would have been missed on routine microscopy. We found the Parasep filter concentration method to be easy, cost-effective and reliable for routine stool examinations.


Asunto(s)
Animales , Técnicas de Laboratorio Clínico/economía , Técnicas de Laboratorio Clínico/métodos , Heces/parasitología , Humanos , Parasitosis Intestinales/diagnóstico , Microscopía , Parásitos/aislamiento & purificación , Parasitología/economía , Parasitología/métodos , Sensibilidad y Especificidad , Manejo de Especímenes/economía , Manejo de Especímenes/métodos
2.
Southeast Asian J Trop Med Public Health ; 2006 Nov; 37(6): 1187-95
Artículo en Inglés | IMSEAR | ID: sea-34054

RESUMEN

Early and rapid diagnosis of tuberculosis is necessary for both treatment and control of the disease. This study evaluated two microcolony observation techniques based on liquid and solid media and a mycobacteriophage assay, to evaluate their effectiveness in the diagnosis of pulmonary TB compared with a standard culture (BACTEC 460 and LJ medium). Middlebrook7H9 (M7H9) broth based on microcolony determination detected 57/61 positives cultures (n = 200) with a sensitivity of 93.4% and a specificity of 87.1%. M7H11 agar detected 57/62 positive cultures (n = 198) with a sensitivity of 91.9% and a specificity of 89.7%. The mycobacteriophage assay detected 98/143 (68.5%) of positive samples. The time to positivity was 48 hours in the mycobacteriophage assay versus 7 days in both the M7H9 broth and M7H11 agar. The costs in comparison with the culture (BACTEC 460 and LJ) were 33% and 48% for the microcolony and mycobacteriophage methods, respectively. Microcolony methods were rapid and cost effective compared to standard cultures. The mycobacteriophage assay, despite its lower sensitivity, has a short turn around time, and may be recommended as a screening test in countries with a low prevalence of tuberculosis.


Asunto(s)
Técnicas Bacteriológicas/métodos , Bioensayo , Recuento de Colonia Microbiana , Humanos , Micobacteriófagos/clasificación , Mycobacterium tuberculosis/aislamiento & purificación , Esputo/microbiología , Tuberculosis Pulmonar/diagnóstico
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