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1.
J Midwifery Womens Health ; 67(6): 753-758, 2022 11.
Artículo en Inglés | MEDLINE | ID: mdl-36433687

RESUMEN

The number of individuals choosing to give birth in a freestanding birth center has doubled since 2004. As many as half of all pregnant persons planning for a birth center birth ultimately develop medical complications and are unable to give birth outside of the hospital. Integrating birth centers into their regional perinatal health care system optimizes outcomes by establishing predetermined pathways for antepartum and intrapartum transfers of care and facilitates ongoing communication and cooperation among clinicians. The Vanderbilt Birth Center is a freestanding birth center that is operated by an academic medical center and partners with a hospital-based midwifery practice that cares for patients transferring from the birth center. Since the inception of the birth center in 2015, the entire perinatal team has worked to improve the process and experience of patient transfer from birth center to hospital care. This article will present strategies implemented through the ongoing collaboration between birth center and hospital health care providers. These include adopting a shared electronic health record, clinical practice guidelines that align across birth sites, preparing birth center patients prenatally for the possibility hospital transfer, the presentation of a united team across birth sites, clear and widely disseminated communication pathways for hospital admission and patient handoff, and ongoing opportunities for interteam communication, collaboration, and education. These strategies may benefit similar midwifery practice models as they seek to partner with larger health care systems and improve the transfer experience for their patients.


Asunto(s)
Centros de Asistencia al Embarazo y al Parto , Partería , Embarazo , Recién Nacido , Femenino , Humanos , Partería/educación , Parto , Centros Médicos Académicos , Transferencia de Pacientes
2.
AAPS PharmSciTech ; 15(6): 1439-46, 2014 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-24970586

RESUMEN

The α-ASTREE e-Tongue instrument uses seven sensors to characterize taste signals associated with a liquid sample. The instrument was used to study eight test preparations (comprised of a blank, four preparations corresponding to four known tastes and Sodium Topiramate in three concentrations known to have a bitter taste) and eight washes. Serially balanced residual effects designs were used to order the samples to estimate residual and main effects. The design provided for eight repeated measurements per test preparation. The experimental results suggested the following: (1) The seven sensors can be separated into three groups according to the ability to discriminate test preparations, and three of the sensors contributed little or no information. Further investigation suggested the lack of differentiability might be due to the age of the sensors. (2) The sensors discriminated known tastes from blank. The residual effect due to test preparations might appear after repeated usage. (3) Exploratory principal component analysis of the data indicated that nearly 90% of the total variability across the seven sensors could be explained by a single principal component. (4) The four standard taste preparations did not correspond to orthogonal dimensions in the principal component axes. (5) The three Sodium Topiramate test preparations could neither be associated with the corresponding known bitter taste sample nor could the three doses be shown to follow a quantitative dose-response relationship on the e-Tongue measurement scale. The practical interpretation of the results of the statistical analysis indicates only poor discriminative ability of the e-Tongue to distinguish clearly between increasing concentrations of a known bitter compound such as Sodium Topiramate. No apparent linear relationship could be discerned over increasing concentrations that would allow the quantification of bitterness.


Asunto(s)
Técnicas Biosensibles/instrumentación , Gusto , Lengua/fisiología , Transductores , Análisis por Conglomerados , Análisis Discriminante , Diseño de Equipo , Modelos Lineales , Modelos Estadísticos , Análisis de Componente Principal , Reproducibilidad de los Resultados , Procesamiento de Señales Asistido por Computador
3.
Int J Immunopathol Pharmacol ; 22(3): 787-93, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19822096

RESUMEN

Myelodysplastic Syndrome (MDS) cells present genetic instability and dysregulation of the gene C3ORF9, which was isolated from an MDS cDNA library and codes for a putative protein. We studied the expression of C3ORF9 in MDS syndromes to contribute to the understanding of the pathophysiology of MDS. One hundred and thirty-one patients and 35 healthy controls were involved in our study. Bone marrow aspirates and isolated CD34+ cells were used. Gene expression was estimated by quantitative PCR. C3ORF9 was found to be down-regulated in patients with CMML compared to the controls (p<0.01). There was no difference between RARS and the controls (p=0.1), while increased expression was found in RA, RAEB and RAEB-T (p<0.01 for all). No mutations or polymorphism were detected in our population. CD34+ cells expressed higher levels of C3ORF9 (p<0.01) in patients. The gene expression was correlated to the percentage of +cells in RAEB and RAEB-T (r=0.64). The altered C3ORF9 expression was possibly due to different gene regulation in these patients and/or to the increased CD34+ cells.


Asunto(s)
Células de la Médula Ósea/química , Síndromes Mielodisplásicos/genética , Proteínas/genética , Adulto , Anciano , Anciano de 80 o más Años , Antígenos CD34/análisis , Células de la Médula Ósea/inmunología , Estudios de Casos y Controles , Aberraciones Cromosómicas , Análisis Mutacional de ADN , Femenino , Regulación de la Expresión Génica , Glucosiltransferasas , Humanos , Cariotipificación , Masculino , Persona de Mediana Edad , Síndromes Mielodisplásicos/inmunología , Síndromes Mielodisplásicos/metabolismo , Proteínas/metabolismo , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa
4.
Dev Biol (Basel) ; 107: 71-6, 2002.
Artículo en Inglés | MEDLINE | ID: mdl-12079194

RESUMEN

The constrained four parameter logistic model has found wide application in describing dose response relationships across many assay systems. This discussion examines the basic model and its practical application to potency testing in the context of the 96 well plate. A two step procedure is recommended for the analysis: (i) the constrained logistic model to generate potency estimates, (ii) a linear mixed-effects model to account for within-plate and between plate variability for producing the final combined estimate of potency. The method is outlined in a case study. Design issues related to possible location effects on the plate may be ameliorated by use of a Latin square design.


Asunto(s)
Modelos Estadísticos , Bioensayo/métodos , Células Cultivadas , Replicación del ADN
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