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1.
J Infect Dis ; 220(220 Suppl 3): S116-S125, 2019 10 08.
Artigo em Inglês | MEDLINE | ID: mdl-31593600

RESUMO

Approximately 3.6 million cases of active tuberculosis (TB) go potentially undiagnosed annually, partly due to limited access to confirmatory diagnostic tests, such as molecular assays or mycobacterial culture, in community and primary healthcare settings. This article provides guidance for TB triage test evaluations. A TB triage test is designed for use in people with TB symptoms and/or significant risk factors for TB. Triage tests are simple and low-cost tests aiming to improve ease of access and implementation (compared with confirmatory tests) and decrease the proportion of patients requiring more expensive confirmatory testing. Evaluation of triage tests should occur in settings of intended use, such as community and primary healthcare centers. Important considerations for triage test evaluation include study design, population, sample type, test throughput, use of thresholds, reference standard (ideally culture), and specimen flow. The impact of a triage test will depend heavily on issues beyond accuracy, primarily centered on implementation.


Assuntos
Bioensaio/normas , Testes Diagnósticos de Rotina/normas , Mycobacterium tuberculosis/isolamento & purificação , Guias de Prática Clínica como Assunto , Triagem/métodos , Tuberculose Pulmonar/diagnóstico , Adulto , Bioensaio/economia , Biomarcadores/sangue , Biomarcadores/urina , Hemocultura/normas , Criança , Estudos de Coortes , Estudos Transversais , Testes Diagnósticos de Rotina/economia , Humanos , Mycobacterium tuberculosis/patogenicidade , Mycobacterium tuberculosis/fisiologia , Padrões de Referência , Projetos de Pesquisa , Fatores de Risco , Sensibilidade e Especificidade , Escarro/microbiologia , Triagem/economia , Triagem/normas , Tuberculose Pulmonar/microbiologia , Tuberculose Pulmonar/fisiopatologia , Organização Mundial da Saúde
2.
PLoS One ; 14(2): e0211027, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-30726247

RESUMO

Access to therapeutic oxygen remains a challenge in the effort to reduce pneumonia mortality among children in low- and middle-income countries. The use of oxygen concentrators is common, but their effectiveness in delivering uninterrupted oxygen is gated by reliability of the power grid. Often cylinders are employed to provide continuous coverage, but these can present other logistical challenges. In this study, we examined the use of a novel, low-pressure oxygen storage system to capture excess oxygen from a concentrator to be delivered to patients during an outage. A prototype was built and tested in a non-clinical trial in Jinja, Uganda. The trial was carried out at Jinja Regional Referral Hospital over a 75-day period. The flow rate of the unit was adjusted once per week between 0.5 and 5 liters per minute. Over the trial period, 1284 power failure episodes with a mean duration of 3.1 minutes (range 0.08 to 1720 minutes) were recorded. The low-pressure system was able to deliver oxygen over 56% of the 4,295 power outage minutes and cover over 99% of power outage events over the course of the study. These results demonstrate the technical feasibility of a method to extend oxygen availability and provide a basis for clinical trials.


Assuntos
Emergências , Sistemas de Medicação no Hospital , Oxigênio/administração & dosagem , Pneumonia/terapia , Centros de Atenção Terciária/organização & administração , Países em Desenvolvimento , Armazenamento de Medicamentos/métodos , Equipamentos e Provisões Hospitalares , Estudos de Viabilidade , Recursos em Saúde/provisão & distribuição , Humanos , Oxigênio/provisão & distribuição , Reprodutibilidade dos Testes , Uganda
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