Half Open Regimen
Mostrando 1-12 de 13 artigos, teses e dissertações.
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1. Em busca do convívio social: o regime semi-aberto no Instituto Penal Oscar Stevenson / In search of the social conviviality: the half-open regimen in the Criminal Institute Oscar Stevenson
O presente trabalho tem como objetivo central analisar o Sistema Penitenciário do Estado do Rio de Janeiro a partir do regime semi-aberto, tendo como campo de análise o Instituto Penal Oscar Stevenson, situado em Benfica, no município do Rio de Janeiro, voltado para um público carcerário feminino. Buscou-se verificar, sob o enfoque das presas, a expecta
Publicado em: 2010
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2. Interação farmacocinetica entre o acetato de medroxiprogesterona de deposito e a terapia anti-retroviral
Primary Objective: To evaluate the interaction between antiretroviral therapy and hormonal contraceptives. Secondary Objectives: 1- To review the knowledge about hormonal contraceptive use by HIV-infected women under antiretroviral therapy; 2- To compare pharmacokinetic (PK) profile of depot-medroxyprogesterone acetate (DMPA) in HIV-infected women treated wi
Publicado em: 2007
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3. Dimensões fundacionais da luta pela anistia
This article analyses the meaning of the struggle for the General Amnesty in Brazil, undertaken by the Brazilian Amnesty Commitees (CBAs) - with the Womens Movement for Amnesty (MFPA), the exiles and the political prisoners - in the second half of the 1970 decade, and its political effects in the last twenty years. Three questions constitute the starting-poi
Publicado em: 1903
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4. Pilot study of azithromycin in the treatment of genital donovanosis.
OBJECTIVES: To determine the effectiveness of azithromycin, an azalide antibiotic with long tissue half-life, in a pilot study of patients with genital donovanosis in the Northern Territory, Australia. DESIGN: Patients with histologically confirmed donovanosis were randomised to receive one of two open-label azithromycin dosage regimens: Regimen A--1.0 g onc
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5. A pilot study of the efficacy and safety of bolus administration of alteplase in acute myocardial infarction.
OBJECTIVE--To examine the efficacy, safety, and the pharmacokinetic profile of a bolus dose administration regimen of alteplase in the treatment of acute myocardial infarction. DESIGN--An open pilot study. SETTING--District general hospital. PATIENTS--33 suitable consecutive patients presenting within six hours of the onset of symptoms who satisfied the elec
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6. Open-label crossover study to determine pharmacokinetics and penetration of two dose regimens of levofloxacin into inflammatory fluid.
Two levofloxacin administration regimens were used for six healthy male volunteers. They received either 500 mg of levofloxacin orally every 12 h for five doses or 500 mg every 24 h for three doses, and then 6 weeks later they received the other course. The concentrations of the drug in plasma, cantharidin-induced inflammatory fluid, and urine were measured
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7. Multiple-dose pharmacokinetics of the monobactam azthreonam (SQ 26,776) in healthy subjects.
Azthreonam, a monocyclic beta-lactam highly active against aerobic gram-negative bacteria in vitro, was administered to four groups of nine healthy male volunteers in the following four regimens: 500 mg intravenously (i.v.) over 2 min every 8 h, 1,000 mg i.v. over 2 min every 8 h, 500 mg intramuscularly (i.m.) every 8 h, and 1,000 mg i.m. every 8 h for 7 day
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8. Pharmacokinetics of Two Multiple-Dosing Regimens of D0870 in Human Immunodeficiency Virus-Positive Patients: a Phase I Study
D0870 is a triazole with a broad antifungal spectrum, and it has been shown to have both in vitro and in vivo activities against wild-type and fluconazole-resistant strains of Candida albicans. Twenty-two human immunodeficiency virus (HIV)-positive male subjects were enrolled in an open, nonrandomized trial investigating the pharmacokinetics of two different
American Society for Microbiology.
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9. Cefotaxime and desacetylcefotaxime pharmacokinetics in infants and children with meningitis.
The pharmacokinetics and cerebrospinal fluid (CSF) penetration of cefotaxime (Ctx) and desacetylcefotaxime (dCtx) were evaluated in 13 infants and children with meningitis after dose 6 of Ctx in a multiple-dose intermittent intravenous infusion regimen (50 mg/kg every 6 h). Model-dependent and noncompartmental pharmacokinetic parameters were determined and w
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10. Single- and multiple-dose pharmacokinetics of pipemidic acid in normal human volunteers.
The pharmacokinetic profile of pipemidic acid was studied in two groups of young healthy volunteers by using a new, sensitive, high-pressure liquid chromatography procedure for quantitation of pipemidic acid in biological fluids. After oral or intravenous administration, the disposition of pipemidic acid may be described as a one- or a two-compartment open m
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11. Safety, Pharmacokinetics, and Pharmacodynamics of Cyclodextrin Itraconazole in Pediatric Patients with Oropharyngeal Candidiasis
The safety, pharmacokinetics, and pharmacodynamics of cyclodextrin itraconazole (CD-ITRA) oral suspension were investigated in an open sequential dose escalation study with 26 human immunodeficiency virus (HIV)-infected children and adolescents (5 to 18 years old; mean CD4+-cell count, 128/μl) with oropharyngeal candidiasis (OPC). Patients received CD-ITRA
American Society for Microbiology.
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12. Teicoplanin in cardiac surgery: intraoperative pharmacokinetics and concentrations in cardiac and mediastinal tissues.
The concentrations of teicoplanin in the sera and mediastinal and heart tissues of 23 patients undergoing cardiac surgery were measured after two regimens of teicoplanin administration. Intraoperative pharmacokinetic parameters were also obtained. Patients were randomized into two groups. Those in group 1 were given teicoplanin at 6 mg x kg(-1) intravenously