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1.
J Pediatr ; 211: 39-45.e2, 2019 08.
Artículo en Inglés | MEDLINE | ID: mdl-31113718

RESUMEN

OBJECTIVE: To evaluate the effect of blood sampling from the placental end of the umbilical cord compared with initial blood sampling from neonates, on the need for first packed red blood cell transfusion in extremely preterm infants. We hypothesized that cord blood sampling could delay the time to first blood transfusion. STUDY DESIGN: In this single-center, assessor blind, randomized controlled trial, we included extremely low birth weight neonates <28 weeks of gestational age at birth. Five milliliter of blood for initial laboratory investigations was collected either from the placental end of the umbilical cord (study group) or from the neonate upon neonatal intensive care unit admission (control group). Both groups received similar anemia prevention strategies. The primary outcome was the time (in days) to the first packed red blood cell transfusion, and was compared using survival analysis. RESULTS: Eighty neonates were enrolled. The time to first transfusion was significantly delayed in the cord sampling group (30 vs 14 days, hazard ratio: 0.44, [95% CI 0.27-0.72], P < .001). Fewer neonates in the cord sampling group were transfused in the first 28 days of life (30% vs 75%, P < .001). Overall transfusion requirements and other clinical outcomes were similar in the groups. CONCLUSIONS: Initial blood sampling from placental end of umbilical cord, when combined with anemia prevention strategies, significantly prolonged the time to first transfusion and reduced the need for early transfusions among extremely premature neonates. TRIAL REGISTRATION: Ctri.nic.in/ (CTRI/2017/04/008320).


Asunto(s)
Recolección de Muestras de Sangre , Transfusión Sanguínea , Cordocentesis , Sangre Fetal/trasplante , Placenta/irrigación sanguínea , Transfusión de Eritrocitos , Eritropoyetina/sangre , Femenino , Edad Gestacional , Humanos , Lactante , Recien Nacido Extremadamente Prematuro , Recién Nacido de Bajo Peso/sangre , Recién Nacido , Masculino , Embarazo , Modelos de Riesgos Proporcionales , Resultado del Tratamiento , Cordón Umbilical
2.
Clin Transl Sci ; 7(1): 48-51, 2014 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-24118988

RESUMEN

The human skin not only provides passive protection as a physical barrier against external injury, but also mediates active surveillance via epidermal cell surface receptors that recognize and respond to potential invaders. Primary keratinocytes and immortalized cell lines, the commonly used sources to investigate immune responses of cutaneous epithelium are often difficult to obtain and/or potentially exhibit changes in cellular genetic make-up. Here we investigated the possibility of using salivary epithelial cells (SEC) to evaluate the host response to cutaneous microbes. Elevated secretion of IFN-γ and IL-12 was observed in the SEC stimulated with Staphylococcus aureus, a transient pathogen of the skin, as mono species biofilm as compared to SEC stimulated with a commensal microbe, the Staphylococcus epidermidis. Co-culture of the SEC with both microbes as dual species biofilm elicited maximum cytokine response. Stimulation with S. aureus alone but not with S. epidermidis alone induced maximum toll-like receptor-2 (TLR-2) expression in the SEC. Exposure to dual species biofilm induced a sustained upregulation of TLR-2 in the SEC for up to an hour. The data support novel application of the SEC as efficient biospecimen that may be used to investigate personalized response to cutaneous microflora.


Asunto(s)
Saliva/citología , Saliva/inmunología , Piel/inmunología , Piel/microbiología , Staphylococcus aureus/inmunología , Staphylococcus aureus/patogenicidad , Biopelículas/crecimiento & desarrollo , Células Cultivadas , Citocinas/biosíntesis , Células Epiteliales/inmunología , Células Epiteliales/microbiología , Interacciones Huésped-Patógeno/inmunología , Humanos , Vigilancia Inmunológica , Queratinocitos/inmunología , Queratinocitos/microbiología , Modelos Inmunológicos , Mucosa Bucal/inmunología , Mucosa Bucal/microbiología , Saliva/microbiología , Infecciones Cutáneas Estafilocócicas/inmunología , Staphylococcus epidermidis/inmunología , Staphylococcus epidermidis/patogenicidad , Simbiosis/inmunología , Receptor Toll-Like 2/metabolismo , Investigación Biomédica Traslacional
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