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1.
J Forensic Sci ; 65(3): 823-832, 2020 May.
Artigo em Inglês | MEDLINE | ID: mdl-31703160

RESUMO

Elevators are mechanical transportation devices used to move vertically between different levels of a building. When first developed, elevators lacked the safety features. When safety mechanisms were developed, elevators became a common feature of multistory buildings. Despite their well-regarded safety record, elevators are not without the potential for danger of injury or death. Persons at-risk for elevator-related death include maintenance and construction workers, other employees, and those who are prone to risky behavior. Deaths may be related to asphyxia, blunt force, avulsion injuries, and various forms of environmental trauma. In this review, we report on 48 elevator-related deaths that occurred in nine different medicolegal death investigation jurisdictions within the United States over an approximately 30-year period. The data represents a cross-section of the different types of elevator-related deaths that may be encountered. The review also presents an overview of preventive strategies for the purpose of avoiding future elevator-related fatalities.


Assuntos
Causas de Morte , Elevadores e Escadas Rolantes , Acidentes por Quedas/mortalidade , Acidentes Domésticos/mortalidade , Acidentes de Trabalho/mortalidade , Adolescente , Adulto , Distribuição por Idade , Idoso , Idoso de 80 Anos ou mais , Asfixia/mortalidade , Criança , Lesões por Esmagamento/mortalidade , Afogamento/mortalidade , Traumatismos por Eletricidade/mortalidade , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Traumatismo Múltiplo/mortalidade , Saúde Ocupacional , Assunção de Riscos , Distribuição por Sexo , Transtornos Relacionados ao Uso de Substâncias/complicações , Adulto Jovem
3.
Diagn Microbiol Infect Dis ; 94(2): 109-112, 2019 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-30696609

RESUMO

Diagnosing Clostridioides (Clostridium) difficile infection is challenged by lack of a clear gold standard. We sought to determine if the two-step algorithm (screening GDH and toxin lateral flow assay followed by tcdB PCR) would have adequate clinical performance at a tertiary care center. Of 486 patients, 310 (63.8%) were immunocompromised. Of 150 PCR-positive specimens, 52 (34.7%) were toxin-positive and 126 (84.0%) were GDH positive. Positive GDH or toxin results corresponded to lower PCR cycle threshold values (P < 0.01). PCR-positive patients had more frequently documented antibiotic usage (78.4% vs 66.9%, P = 0.05) and diarrhea (91.0% vs. 79.4%, P < 0.01) and less frequent alternate etiologies of diarrhea (27.3% vs. 41.1%, P = 0.004) or laxative use (24.6% vs 36.1%, P = 0.02). Toxin positivity was associated with antibiotic use (P < 0.01), but not with neutropenia, diarrhea, malignancy, or chemotherapy (P > 0.05). The application of the 2-step algorithm should be thoroughly evaluated in immunocompromised patient populations before implementation.


Assuntos
Infecções por Clostridium/diagnóstico , Testes Diagnósticos de Rotina/métodos , Imunoensaio/métodos , Programas de Rastreamento/métodos , Idoso , Toxinas Bacterianas/análise , Toxinas Bacterianas/genética , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Reação em Cadeia da Polimerase/métodos , Desidrogenase do Álcool de Açúcar/análise , Desidrogenase do Álcool de Açúcar/genética , Centros de Atenção Terciária
4.
Clin Vaccine Immunol ; 21(11): 1481-9, 2014 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-25165027

RESUMO

Detection of immunoglobulin M (IgM) antibodies has long been used as an important diagnostic tool for identifying active viral infections, but their relevance in later stages has not been clearly defined in vivo. In this study, we followed the kinetics, longevity, and function of influenza virus-specific IgM antibodies for 2 years following sublethal infection of mice with live mouse-adapted A/PR/8/34 virus or immunization with formalin-inactivated virus. These groups mounted robust protective immune responses and survived lethal challenges with 50 × 50% lethal dose (LD50) mouse-adapted A/PR/8/34 virus 600 days after the primary exposure. Surprisingly, the virus-specific IgM antibodies persisted along with IgG antibodies, and we found a significantly higher number of IgM-positive (IgM(+)) virus-specific plasma cells than IgG(+) plasma cells that persisted for at least 9 months postexposure. The IgM antibodies were functional as they neutralized influenza virus in the presence of complement just as well as IgG antibodies did.


Assuntos
Anticorpos Antivirais/sangue , Imunoglobulina M/sangue , Vírus da Influenza A/imunologia , Vacinas contra Influenza/imunologia , Infecções por Orthomyxoviridae/prevenção & controle , Animais , Anticorpos Neutralizantes/sangue , Proteínas do Sistema Complemento/imunologia , Modelos Animais de Doenças , Feminino , Vacinas contra Influenza/administração & dosagem , Camundongos Endogâmicos BALB C , Testes de Neutralização , Plasmócitos/imunologia , Análise de Sobrevida , Vacinas de Produtos Inativados/administração & dosagem , Vacinas de Produtos Inativados/imunologia
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