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1.
Adv Neonatal Care ; 10(5): 256-60, 2010 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-20838076

RESUMEN

One of the components of promoting good outcomes in high-risk neonates is supporting normal gas exchange while avoiding lung injury. Respiratory care in the first hour following birth plays an important role in stabilizing the infant with respiratory problems. The goal of this article is to review the causes of lung injury that can occur in the first hour and that could be prevented with careful respiratory support.


Asunto(s)
Enfermedades del Prematuro/prevención & control , Recien Nacido Prematuro/fisiología , Enfermedades Pulmonares/prevención & control , Lesión Pulmonar/prevención & control , Oxígeno/administración & dosificación , Oxígeno/efectos adversos , Intercambio Gaseoso Pulmonar/fisiología , Mecánica Respiratoria/fisiología , Salas de Parto , Humanos , Recién Nacido , Enfermedades del Prematuro/terapia , Enfermedades Pulmonares/terapia , Lesión Pulmonar/etiología
2.
J Pediatr ; 151(3): 260-5, 265.e1, 2007 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-17719934

RESUMEN

OBJECTIVE: To determine if INH-A21, an intravenous immune globulin (IGIV) derived from donors with high titers of antibody to surface adhesins of Staphylococcus epidermidis and S. aureus prevents late-onset sepsis (LOS) in very low birth weight (VLBW) infants. STUDY DESIGN: In this double-blind, placebo-controlled study, infants with birth weights 500 to 1250 g were randomized to receive up to four doses of INH-A21 (Veronate) or placebo. The primary objective was to determine the safety and efficacy of INH-A21 versus placebo for prevention of S. aureus LOS in VLBW infants. RESULTS: A total of 1983 infants from 95 neonatal intensive care units were randomized, and received at least one dose of study drug. S. aureus LOS developed in 50 of 989 (5%) and 60 of 994 (6%) infants who received placebo or INH-A21, respectively (P = .34). No differences were found in the frequencies of LOS caused by coagulase-negative staphylococci (CoNS), Candida spp, or overall mortality. No adverse events were statistically significantly associated with INH-A21 infusions compared with placebo. CONCLUSION: INH-A21 failed to reduce the incidence of staphylococcal LOS or candidemia in premature infants.


Asunto(s)
Infección Hospitalaria/prevención & control , Inmunoglobulinas Intravenosas/uso terapéutico , Factores Inmunológicos/uso terapéutico , Enfermedades del Prematuro/prevención & control , Sepsis/microbiología , Sepsis/prevención & control , Infecciones Estafilocócicas/prevención & control , Edad de Inicio , Comorbilidad , Método Doble Ciego , Femenino , Humanos , Recién Nacido , Recien Nacido Prematuro , Recién Nacido de muy Bajo Peso , Tiempo de Internación , Masculino , Sepsis/epidemiología , Factores de Tiempo
3.
Pediatr Infect Dis J ; 24(10): 858-66, 2005 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-16220082

RESUMEN

BACKGROUND: Prophylactic administration of intravenous immunoglobulin has been inconsistent in reducing the risk of sepsis in very low birth weight (VLBW) infants presumably because of varying titers of organism specific IgG antibodies. INH-A21 is an intravenous immunoglobulin from donors with high titers of antistaphylococcal antibodies. This dose-ranging study explored safety and preliminary activity of INH-A21 for prevention of staphylococcal sepsis in VLBW infants. METHODS: This was a multicenter, double blind, group-sequential study. Infants with birth weights 500-1250 g were randomized to receive up to 4 doses of placebo, 250 mg/kg, 500 mg/kg or 750 mg/kg INH-A21. Safety and frequencies of sepsis were compared across treatment groups. RESULTS: All treatment groups had similar mean gestational age, birth weight, Apgar score and maternal use of antibiotics. Randomizations to 250 mg/kg (N = 94) and 500 mg/kg (N = 96) doses were terminated after interim analyses demonstrated a low probability of finding a difference when compared with placebo. Infants randomized to the INH-A21 750 mg/kg group (N = 157) had fewer episodes of Staphylococcus aureus sepsis [relative risk (RR), 0.37; 95% confidence interval (CI), 0.12-1.12; P = 0.14], candidemia (RR 0.34; 95% CI 0.09-1.22; P = 0.09) and mortality (RR 0.64; 95% CI 0.25-1.61; P = 0.27) when compared with the placebo-treated cohort (N = 158). No dose-related trends were observed for adverse events or morbidities associated with prematurity. CONCLUSIONS: INH-A21 750 mg/kg demonstrated potential to reduce sepsis caused by S. aureus, candidemia and mortality in VLBW infants. Although statistical significance was not reached, based on the magnitude of the estimated differences, the efficacy and safety of INH-A21 750 mg/kg should be evaluated in an adequately powered, well-controlled study.


Asunto(s)
Infección Hospitalaria/prevención & control , Inmunoglobulinas Intravenosas/efectos adversos , Inmunoglobulinas Intravenosas/uso terapéutico , Enfermedades del Prematuro/prevención & control , Recién Nacido de muy Bajo Peso , Sepsis/prevención & control , Infección Hospitalaria/mortalidad , Método Doble Ciego , Femenino , Humanos , Inmunoglobulinas Intravenosas/administración & dosificación , Recién Nacido , Recien Nacido Prematuro , Enfermedades del Prematuro/etiología , Enfermedades del Prematuro/mortalidad , Masculino , Sepsis/etiología , Sepsis/mortalidad , Staphylococcus/inmunología , Resultado del Tratamiento
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