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1.
Adv Emerg Nurs J ; 40(3): 183-193, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30059373

RESUMO

Within emergency care settings, rapid sequence intubation (RSI) is frequently used to secure a definitive airway (i.e., endotracheal tube) to provide optimal oxygenation and ventilation in critically ill patients of all ages. For providers in these settings, a deeper understanding of the indications, associated medications, and adjunctive techniques may maximize success with this common procedure. Identification of difficult airways, using mnemonics and standardized criteria prior to the procedure allows, the clinician additional time for assimilation of additional resources and tools to increase the likelihood of first-pass success with intubation. This article describes tools for the procedure of RSI, including the "7 Ps" checklist of intubation.


Assuntos
Estado Terminal , Serviço Hospitalar de Emergência , Intubação Intratraqueal/métodos , Humanos
2.
Science ; 321(5897): 1837-41, 2008 Sep 26.
Artigo em Inglês | MEDLINE | ID: mdl-18818360

RESUMO

Almost two decades after CFTR was identified as the gene responsible for cystic fibrosis (CF), we still lack answers to many questions about the pathogenesis of the disease, and it remains incurable. Mice with a disrupted CFTR gene have greatly facilitated CF studies, but the mutant mice do not develop the characteristic manifestations of human CF, including abnormalities of the pancreas, lung, intestine, liver, and other organs. Because pigs share many anatomical and physiological features with humans, we generated pigs with a targeted disruption of both CFTR alleles. Newborn pigs lacking CFTR exhibited defective chloride transport and developed meconium ileus, exocrine pancreatic destruction, and focal biliary cirrhosis, replicating abnormalities seen in newborn humans with CF. The pig model may provide opportunities to address persistent questions about CF pathogenesis and accelerate discovery of strategies for prevention and treatment.


Assuntos
Regulador de Condutância Transmembrana em Fibrose Cística/genética , Fibrose Cística , Modelos Animais de Doenças , Suínos , Animais , Animais Recém-Nascidos , Cloretos/metabolismo , Fibrose Cística/genética , Fibrose Cística/patologia , Fibrose Cística/fisiopatologia , Regulador de Condutância Transmembrana em Fibrose Cística/metabolismo , Feminino , Vesícula Biliar/patologia , Íleus/patologia , Íleus/fisiopatologia , Intestinos/patologia , Transporte de Íons , Fígado/patologia , Cirrose Hepática Biliar/patologia , Pulmão/patologia , Masculino , Pâncreas Exócrino/patologia , Recombinação Genética
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