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1.
Mali Med ; 22(3): 1-4, 2007.
Artículo en Francés | MEDLINE | ID: mdl-19434985

RESUMEN

The national policy of assumption of responsibility of the PVVIH decided to put 80% of new inclusions under Triomune, 1st therapeutic line made up of 3TC + D4T + Nevirapine. The use of Nevirapine among patients VIH+ plays a very important part in improvement of the quality of their life. The goal of this study was to evaluate the clinical and biological tolerance of Nevirapine at the PVVIH under treatment ARV and having Nevirapine in their diagram. We had collected 102 files of patients. The average age was 38 years. Association Lamivudine + Stavudine + Nevirapine was the diagram most frequently prescribed (82.4%). The skin, mucous and neurological signs, digestive disorders, muscular signs, cardiopulmonary signs were frequently observed in the first month of the treatment but these symptoms became less frequent in the third month and disappeared at the 6th month. We observed disorders in hepatic and renal functional parameters, rise in the lymphocytes. We obtained a considerable increase in the rate of CD4 between the beginning of the treatment and the 6th month. The treatment schema of 3TC + D4T + Nevirapine gives an excellent clinical and biological tolerance. But, the study must continue to confirm these results over a longer period.


Asunto(s)
Síndrome de Inmunodeficiencia Adquirida/tratamiento farmacológico , Fármacos Anti-VIH/administración & dosificación , Nevirapina/administración & dosificación , Adulto , Quimioterapia Combinada , Femenino , Humanos , Lamivudine/administración & dosificación , Masculino , Persona de Mediana Edad , Estavudina/administración & dosificación , Resultado del Tratamiento
2.
Bull Soc Pathol Exot Filiales ; 81(2): 260-70, 1988.
Artículo en Francés | MEDLINE | ID: mdl-3046772

RESUMEN

In a double blind study Ivermectin has been compared to a placebo in 234 male and female with onchocerciasis who had more than 20 microfilariae per milligram of skin and moderate ocular involvement. Patient was randomized to receive a simple oral dose of Ivermectin 100, 150 and 200 micrograms/kg or placebo. The following was 12 months. The decrease of microfilarodermia since to the 3rd day was from 72.8 to 79.3% of initial rate. At six months it was more than 91% and more than 87% in 12 months. Ocular microfilariae, initially between 12 and 23 stay lower than 2 at 12 months. Punctuated keratitis disappear and did not recidive still 6 months in patients with persistent microfilariae. Ivermectin produce only few side effects. Negative waves have been observed on ECG but without any clinical signs. The Power efficient dose seen to be 100 micrograms/kg.


Asunto(s)
Ivermectina/uso terapéutico , Oncocercosis/tratamiento farmacológico , Ensayos Clínicos como Asunto , Método Doble Ciego , Electrocardiografía , Femenino , Humanos , Queratitis/tratamiento farmacológico , Masculino , Malí , Distribución Aleatoria , Recurrencia , Piel/parasitología
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