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1.
Pathog Glob Health ; 109(6): 275-82, 2015 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-26260354

RESUMO

We conducted a randomised single-blinded clinical trial of 100 cholera patients in Port-au-Prince, Haiti to determine if the probiotic Saccharomyces cerevisiae var. boulardii and the anti-diarrhoeal drug bismuth subsalicylate (BS) were able to reduce the duration and severity of cholera. Subjects received either: S. boulardii 250 mg, S. boulardii 250 mg capsule plus BS 524 mg tablet, BS 524 mg, or two placebo capsules every 6 hours alongside standard treatment for cholera. The length of hospitalisation plus the number and volume of emesis, stool and urine were recorded every 6 hours until the study subject was discharged (n = 83), left against medical advice (n = 11), or requested removal from the study (n = 6). There were no reported deaths or adverse study-related events. There were no statistically significant differences between the study arms and the outcomes of interest.


Assuntos
Antibacterianos/uso terapêutico , Bismuto/uso terapêutico , Cólera/tratamento farmacológico , Cólera/terapia , Diarreia/prevenção & controle , Serviços Médicos de Emergência/métodos , Compostos Organometálicos/uso terapêutico , Probióticos/uso terapêutico , Saccharomyces , Salicilatos/uso terapêutico , Vibrio cholerae/efeitos dos fármacos , Adulto , Antibacterianos/economia , Anticorpos Antibacterianos , Cólera/economia , Cólera/epidemiologia , Surtos de Doenças/economia , Serviços Médicos de Emergência/economia , Fezes/microbiologia , Feminino , Hidratação/economia , Haiti/epidemiologia , Humanos , Tempo de Internação/economia , Tempo de Internação/estatística & dados numéricos , Masculino , Índice de Gravidade de Doença , Resultado do Tratamento
2.
J Emerg Med ; 45(3): 433-40, 2013 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-23871326

RESUMO

BACKGROUND: Bedbug infestations are increasing across North America and Europe, with more people presenting to Emergency Departments for treatment. Physicians cannot provide substantive treatment for people affected by bedbugs. STUDY OBJECTIVE: To determine if ivermectin, a relatively inexpensive and safe, long-acting oral anti-parasitic drug is able to cause bedbug morbidity and mortality. METHODS: We evaluated the effects of ivermectin on bedbugs using an artificial feeding membrane and mice and humans. Bedbug morbidity, mortality, and nymph molting was recorded. RESULTS: Using an artificial feeding membrane, bedbug mortality was 98% (n = 81) for 260 ng/mL ivermectin and 0% for 0 ng/mL ivermectin (control; n = 90) after 13 days. Mortality for bedbugs fed on mice injected with the human equivalent of 200 µg/kg ivermectin was 86% (n = 22), vs. 0% in the 0 µg/kg ivermectin (control; n = 21). Of the surviving nymphs, 0% exposed to ivermectin molted by day 75, vs. 80% in the control group by day 8. Bedbugs that fed once on human study subjects 3 h after consuming 200 µg/kg of oral ivermectin had a 63% (n = 24) 20-day mortality rate, vs. 8% (n = 24) in the control group. Of the surviving nymphs, 0% (n = 5) in the 3-h ivermectin group molted, vs. 80% (n = 10) of the control group. CONCLUSIONS: It may be possible that ivermectin could help eradicate, suppress, or prevent a bedbug infestation.


Assuntos
Percevejos-de-Cama/efeitos dos fármacos , Mordeduras e Picadas de Insetos/prevenção & controle , Inseticidas/farmacologia , Ivermectina/farmacologia , Adulto , Animais , Feminino , Humanos , Inseticidas/administração & dosagem , Ivermectina/administração & dosagem , Masculino , Camundongos , Ninfa/efeitos dos fármacos , Adulto Jovem
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