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2.
Am J Crit Care ; 14(2): 113-20, 2005 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-15728953

RESUMO

BACKGROUND: Accurate documentation of time is essential in critical care for treatments, interventions, research, and medicolegal and quality improvement activities. OBJECTIVES: To assess use of timepieces in critical care and to determine practical methods for improving their accuracy. METHODS: Providers were surveyed to identify timepieces used during routine and emergency care. Times displayed on standard unit and personal timepieces were compared with coordinated universal time. Four models of atomic clocks were assessed for drift for 6 weeks and for resynchronization for 1 week. Bedside monitors were manually synchronized to coordinated universal time and were assessed for drift. RESULTS: Survey response was 78% (149/190). Nurses (n = 93), physicians (n = 32), and respiratory therapists (n = 24) use wall clocks (50%) and personal timepieces (46%) most frequently during emergencies. The difference from coordinated universal time was a median of -4 minutes (range, -5 minutes to +2 min) for wall clocks, -2.5 minutes (-90 minutes to -1 minute) for monitors, and 0 minutes (-22 minutes to +12 minutes) for personal timepieces. Kruskal-Wallis testing indicated significant variations for all classes of timepieces (P<.001) and for personal timepieces grouped by discipline (P=.02). Atomic clocks were accurate to 30 seconds of coordinated universal time for 6 weeks when manually set but could not be synchronized by radiofrequency signal. Drift of bedside monitors was 1 minute. CONCLUSIONS: Timepieces used in critical care are highly variable and inaccurate. Manually synchronizing timepieces to coordinated universal time improved accuracy for several weeks, but the feasibility of synchronizing all timepieces is undetermined.


Assuntos
Cuidados Críticos , Tempo , Coleta de Dados , Equipe de Assistência ao Paciente , Estados Unidos
3.
Environ Pollut ; 123(1): 21-9, 2003.
Artigo em Inglês | MEDLINE | ID: mdl-12663202

RESUMO

Ecological risk assessment (ERA) guidance recommends that field-truthing efforts proceed when modeled hazard quotients (HQs) suggest that toxicological effects are occurring to site receptors. To date, no field methods have been proposed by the regulatory community that can lead to definitive determinations of acceptable or unacceptable risk for birds and mammals, the two terrestrial classes of receptors that are commonly assessed using the HQ method. This paper describes rodent sperm analysis (RSA) as a viable method to be applied in the field at sites with historical contamination. RSA is capable of detecting biological differences that bear on reproduction, a highly regarded toxicological endpoint of concern in USEPA Superfund-type ERAs. The results of RSA's first application at a study site are reported and discussed. The paper also provides the rationale for RSA's efficacy in the context of Superfund and other environmental cleanup programs, where limited time and money are available to determine and evaluate the field condition.


Assuntos
Ecologia , Monitoramento Ambiental/métodos , Poluição Ambiental , Roedores/fisiologia , Espermatozoides/fisiologia , Animais , Arvicolinae , Masculino , Camundongos , Peromyscus , Projetos Piloto , Modelos de Riscos Proporcionais , Ratos , Medição de Risco , Contagem de Espermatozoides , Motilidade dos Espermatozoides , Espermatozoides/patologia
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