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1.
Pediatr Emerg Care ; 28(10): 971-6, 2012 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-23023460

RESUMEN

OBJECTIVES: The goals of this study were to (1) conduct a cost-benefit analysis, from a hospital's perspective, of using a pediatrician in triage (PIT) in the emergency department (ED) and (2) assess the impact of a physician in triage on provider satisfaction. METHODS: This was a prospective, controlled trial of PIT (intervention) versus conventional registered nurse-driven triage (control), at an urban, academic, tertiary level pediatric ED, which led to a cost-benefit analysis by looking at the effect that PIT has on length of stay (LOS) and thus on ED revenue. Provider satisfaction was assessed through surveys. RESULTS: During the 8-week study period, a total of 6579 patients were triaged: 3242 in the PIT group and 3337 in the control group. The 2 groups were similar in age, sex, admission rate, left-without-being-seen rate, and level of acuity. The mean LOS in the PIT group was 24.3 minutes shorter than in the control group. The costs of PIT seem to be increased and are not offset by savings; the net margin (total revenue minus costs) was $42,883 per year lower in the PIT than in the control group. Sensitivity analysis showed that if the LOS were reduced by more than 98.4 minutes, the cost savings would favor PIT. Most of the physicians and nurses (67%) reported that PIT facilitated their job. CONCLUSIONS: Placement of a PIT during periods of peak census resulted in shorter stay and notable provider satisfaction but at an incremental cost of $42,883 per year.


Asunto(s)
Servicio de Urgencia en Hospital/economía , Hospitalización/economía , Triaje/economía , Preescolar , Análisis Costo-Beneficio , Femenino , Estudios de Seguimiento , Humanos , Masculino , Estudios Prospectivos , Estados Unidos
3.
Rapid Commun Mass Spectrom ; 16(24): 2278-85, 2002.
Artículo en Inglés | MEDLINE | ID: mdl-12478572

RESUMEN

Single nucleotide polymorphisms (SNPs) and mutations were genotyped for both homozygous and heterozygous PCR products of p53, a tumor suppressor gene, and K-ras, an oncogene, using electrospray ionization (ESI) quadrupole time-of-flight (Q-TOF) mass spectrometry (MS) and ESI-quadrupole MS analysis. Mass accuracy was adequate for both instruments to detect genetic changes in homozygous PCR products, including the most difficult to distinguish (adenine [A] --> thymine [T] transversion). However, for the detection of A --> T shifts (9.0 Da difference) in heterozygous PCR products, the increased resolution of ESI-Q-TOFMS proved essential. Although, greater mass differences in heterozygotes (e.g. cytosine [C] <--> T or guanine [G] <--> A) can be discriminated using ESI-quadrupole MS analysis.


Asunto(s)
Genes p53/genética , Genes ras/genética , Espectrometría de Masas/métodos , Mutación Puntual/genética , Reacción en Cadena de la Polimerasa/métodos , Espectrometría de Masa por Ionización de Electrospray/métodos , Secuencia de Bases , Genotipo , Humanos , Datos de Secuencia Molecular , Análisis de Secuencia de ADN
4.
Rapid Commun Mass Spectrom ; 17(24): 2755-62, 2003.
Artículo en Inglés | MEDLINE | ID: mdl-14673823

RESUMEN

A computer-based method is described for automated detection of peaks in product ion spectra that allows discrimination of structurally related polymerase chain reaction (PCR) products. PCR products of K-ras mutants having single nucleotide substitutions and isomeric sequence changes in positions 1 and 2 of codon 12 (e.g. TGT and GTT) were used as a model system. SpecDiff, a tool for differentiating pairs of mass spectra by identifying peaks that either differ in relative intensity between spectra or only appear in one of a pair of spectra, was created to help automate detection. This program was demonstrated to have great utility in detection of mutations and could also be useful as a general tool for differentiating other molecules of closely related structure.


Asunto(s)
Algoritmos , Oligonucleótidos/análisis , Oligonucleótidos/química , Reconocimiento de Normas Patrones Automatizadas , Reacción en Cadena de la Polimerasa/métodos , Alineación de Secuencia/métodos , Análisis de Secuencia de ADN/métodos , Espectrometría de Masa por Ionización de Electrospray/métodos , Secuencia de Bases , Análisis por Conglomerados , Codón/análisis , Codón/química , Datos de Secuencia Molecular , Reproducibilidad de los Resultados , Sensibilidad y Especificidad
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