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2.
Air Med J ; 25(1): 26-34, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16413424

RESUMO

INTRODUCTION: This study examined the epidemiology of winter resort injuries presenting to regional trauma centers by helicopter (HEMS) or ground (GEMS) ambulance. METHODS: Five hundred seventy-five patients (GEMS 289; HEMS 286) were identified from trauma registries and HEMS transport records. Demographic data, hospital interventions, and discharge status were examined. RESULTS: HEMS patients had a significantly lower Glasgow coma score (GCS) and trauma score (TS), longer intensive care unit (ICU) length of stay (LOS), and more deaths than did GEMS patients (P < 0.05). Despite this, significantly more HEMS patients were discharged home from the emergency department (24.5% vs. 4.8%; P < 0.001). HEMS patients had more isolated head/facial injuries and multiple injuries, with less isolated extremity injuries than did GEMS patients (P < 0.05). Regardless of transport mode, patients with multiple injuries, thoracoabdominal injuries, or head injuries with a GCS < or = 13 were more likely to require immediate interventions (intubation, chest tube, blood products). Patients with isolated extremity injuries rarely needed immediate care. CONCLUSION: HEMS patients had a higher acuity and different injury pattern when compared to GEMS patients. Approximately 24.5% of HEMS patients were discharged home from the ED. This reflects significant overtriage of patients to HEMS. A prospective study examining the initial triage of patients injured at winter resorts would help to determine which subset of patients are best served by HEMS transport.


Assuntos
Resgate Aéreo , Temperatura Baixa , Estações do Ano , Transporte de Pacientes , Ferimentos e Lesões/epidemiologia , Adolescente , Adulto , Feminino , Humanos , Atividades de Lazer , Masculino , Estudos Retrospectivos , Utah/epidemiologia , Ferimentos e Lesões/classificação
3.
Toxicol Appl Pharmacol ; 211(3): 245-60, 2006 Mar 15.
Artigo em Inglês | MEDLINE | ID: mdl-16040073

RESUMO

Strategies were developed for the estimation of systemically available daily doses of chemicals, diurnal variations in blood levels, and rough elimination rates in subchronic feeding/drinking water studies, utilizing a minimal number of blood samples. Systemic bioavailability of chemicals was determined by calculating area under the plasma concentration curve over 24 h (AUC-24 h) using complete sets of data (> or =5 data points) and also three, two, and one selected time points. The best predictions of AUC-24 h were made when three time points were used, corresponding to Cmax, a mid-morning sample, and C(min). These values were found to be 103 +/- 10% of the original AUC-24 h, with 13 out of 17 values ranging between 96 and 105% of the original. Calculation of AUC-24 h from two samples (Cmax and Cmin) or one mid-morning sample afforded slightly larger variations in the calculated AUC-24 h (69-136% of the actual). Following drinking water exposure, prediction of AUC-24 h using 3 time points (Cmax, mid-morning, and Cmin) was very close to actual values (80-100%) among mice, while values for rats were only 63% of the original due to less frequent drinking behavior of rats during the light cycle. Collection and analysis of 1-3 blood samples per dose may provide insight into dose-proportional or non-dose-proportional differences in systemic bioavailability, pointing towards saturation of absorption or elimination or some other phenomenon warranting further investigation. In addition, collection of the terminal blood samples from rats, which is usually conducted after 18 h of fasting, will be helpful in rough estimation of blood/plasma half-life of the compound. The amount of chemical(s) and/or metabolite(s) in excreta and their possible use as biomarkers in predicting the daily systemic exposure levels are also discussed. Determining these parameters in the early stages of testing will provide critical information to improve the appropriate design of other longer-term toxicity studies.


Assuntos
Ácido 2,4-Diclorofenoxiacético/farmacocinética , Clorpirifos/farmacocinética , Projetos de Pesquisa , Testes de Toxicidade Crônica , Ácido 2,4-Diclorofenoxiacético/sangue , Ácido 2,4-Diclorofenoxiacético/toxicidade , Administração Oral , Animais , Área Sob a Curva , Disponibilidade Biológica , Clorpirifos/sangue , Clorpirifos/toxicidade , Ingestão de Líquidos , Inativação Metabólica , Masculino , Ratos , Ratos Endogâmicos F344 , Fatores de Tempo , Testes de Toxicidade Crônica/normas
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