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1.
Semin Pediatr Surg ; 33(3): 151424, 2024 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-38830311

RESUMEN

Lymphatic disorders presenting in the first year of life are difficult to identify and manage given the broad range of underlying etiologies. Neonatal lymphatic disease arising from congenital or acquired conditions results in the abnormal accumulation of lymph fluid in the pleura (chylothorax), peritoneum (chylous ascites) and skin (edema/anasarca). There is also increasing recognition of lymphatic losses through the intestine resulting in protein-losing enteropathy (PLE). While the incidence of lymphatic disorders in neonates is unclear, advances in genetic testing and lymphatic imaging are improving our understanding of the underlying pathophysiology. Despite these advancements, medical management of neonatal lymphatic disorders remains challenging and variable among clinicians.


Asunto(s)
Enfermedades Linfáticas , Humanos , Recién Nacido , Enfermedades Linfáticas/diagnóstico , Enfermedades Linfáticas/terapia , Enfermedades Linfáticas/etiología , Enteropatías Perdedoras de Proteínas/diagnóstico , Enteropatías Perdedoras de Proteínas/terapia , Enteropatías Perdedoras de Proteínas/etiología , Linfedema/terapia , Linfedema/diagnóstico , Linfedema/etiología , Quilotórax/terapia , Quilotórax/diagnóstico , Quilotórax/etiología
3.
J Pediatr ; 178: 309-310, 2016 11.
Artículo en Inglés | MEDLINE | ID: mdl-27522441
4.
J Pediatr ; 173: 50-55.e1, 2016 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-27004673

RESUMEN

OBJECTIVE: To determine differences in the incidence of bronchopulmonary dysplasia (BPD) or death in extremely low birth weight infants managed on high flow nasal cannula (HFNC) vs continuous positive airway pressure (CPAP). STUDY DESIGN: This is a retrospective data analysis from the Alere Neonatal Database for infants born between January 2008 and July 2013, weighing ≤1000 g at birth, and received HFNC or CPAP. Baseline demographics, clinical characteristics, and neonatal outcomes were compared between the infants who received CPAP and HFNC, or HFNC ± CPAP. Multivariable regression analysis was performed to control for the variables that differ in bivariate analysis. RESULTS: A total of 2487 infants met the inclusion criteria (941 CPAP group, 333 HFNC group, and 1546 HFNC ± CPAP group). The primary outcome of BPD or death was significantly higher in the HFNC group (56.8%) compared with the CPAP group (50.4%, P < .05). Similarly, adjusted odds of developing BPD or death was greater in the HFNC ± CPAP group compared with the CPAP group (OR 1.085, 95% CI 1.035-1.137, P = .001). The number of ventilator days, postnatal steroid use, days to room air, days to initiate or reach full oral feeds, and length of hospitalization were significantly higher in the HFNC and HFNC ± CPAP groups compared with the CPAP group. CONCLUSIONS: In this retrospective study, use of HFNC in extremely low birth weight infants is associated with a higher risk of death or BPD, increased respiratory morbidities, delayed oral feeding, and prolonged hospitalization. A large clinical trial is needed to evaluate long-term safety and efficacy of HFNC in preterm infants.


Asunto(s)
Displasia Broncopulmonar/epidemiología , Recien Nacido con Peso al Nacer Extremadamente Bajo , Tiempo de Internación/estadística & datos numéricos , Terapia por Inhalación de Oxígeno/efectos adversos , Terapia por Inhalación de Oxígeno/métodos , Presión de las Vías Aéreas Positiva Contínua , Utilización de Medicamentos , Femenino , Glucocorticoides/uso terapéutico , Mortalidad Hospitalaria , Humanos , Lactante , Recién Nacido , Unidades de Cuidado Intensivo Neonatal , Masculino , Estudios Retrospectivos , Factores de Tiempo , Estados Unidos/epidemiología
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