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1.
Am J Transplant ; 20(3): 739-751, 2020 03.
Artigo em Inglês | MEDLINE | ID: mdl-31652392

RESUMO

We conducted an adaptive design single-center pilot trial between October 2017 and November 2018 to determine the safety and efficacy of ultra-short-term perioperative pangenotypic direct acting antiviral (DAA) prophylaxis for deceased hepatitis C virus (HCV)-nucleic acid test (NAT) positive donors to HCV negative kidney recipients (D+/R-). In Group 1, 10 patients received one dose of SOF/VEL (sofusbuvir/velpatasvir) pretransplant and one dose on posttransplant Day 1. In Group 2A (N = 15) and the posttrial validation (Group 2B; N = 25) phase, patients received two additional SOF/VEL doses (total 4) on Days 2 and 3 posttransplant. Development of posttransplant HCV transmission triggered 12-week DAA therapy. For available donor samples (N = 27), median donor viral load was 1.37E + 06 IU/mL (genotype [GT]1a: 70%; GT2: 7%; GT3: 23%). Overall viral transmission rate was 12% (6/50; Group 1:30% [3/10]; Group 2A:13% [2/15]; Group 2B:4% [1/25]). For the 6 viremic patients, 5 (83%) achieved sustained virologic response (3 with first-line DAA therapy; and two after retreatment with second-line DAA). At a median follow-up of 8 months posttransplant, overall patient and allograft survivals were 98%, respectively. The 4-day strategy reduced viral transmission to 7.5% (3/40; 95% confidence interval [CI]: 1.8%-20.5%) and could result in avoidance of prolonged posttransplant DAA therapy for most D+/R - transplants.


Assuntos
Hepatite C Crônica , Hepatite C , Transplante de Rim , Antivirais/uso terapêutico , Hepacivirus , Hepatite C/tratamento farmacológico , Hepatite C/prevenção & controle , Hepatite C Crônica/tratamento farmacológico , Humanos , Transplante de Rim/efeitos adversos , Transplantados
2.
J La State Med Soc ; 161(2): 97, 99-102, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19489390

RESUMO

This report presents autopsy trends in Louisiana for 1999-2006 data and provides some comparison with national data for 2003. Mortality data for Louisiana was collected from the field 'autopsy' on the Certificate of Death from 1999-2006 and compared with national data for the year 2003. The overall autopsy rate was 9.3% in Louisiana versus 7.7% in the United States (U.S.) in 2003. Autopsy rates were higher than those of the U.S. in almost all categories of personal factors (gender, race and age group). Louisiana's autopsy levels were generally greater for both natural disease (3.7% versus 3.5% for the U.S.) and the high autopsy rate group (61.1% versus 54.3% for the U.S.).


Assuntos
Autopsia/estatística & dados numéricos , Mortalidade/tendências , Adolescente , Adulto , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Causas de Morte , Criança , Pré-Escolar , Atestado de Óbito , Etnicidade , Feminino , Humanos , Lactente , Recém-Nascido , Modelos Logísticos , Louisiana , Masculino , Pessoa de Meia-Idade , Gravidez , Grupos Raciais , Fatores Sexuais , Estados Unidos
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