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1.
J Perinatol ; 37(1): 36-41, 2017 01.
Artigo em Inglês | MEDLINE | ID: mdl-27684425

RESUMO

OBJECTIVE: Oral colostrum priming (OCP) after birth in preterm infants is associated with improved weight gain and modification of the oral immunomicrobial environment. We hypothesized that OCP would modify salivary immune peptides and the oral microbiota in preterm infants. STUDY DESIGN: We conducted a prospective, randomized clinical trial to determine the effects of OCP on salivary immune peptide representation in preterm infants (<32 weeks completed gestation at birth). Saliva samples were collected before and after OCP. Salivary immune peptide representation was determined via mass spectroscopy. Oral microbiota representation was determined via sequencing of the 16S rRNA gene. RESULTS: Neonates who received OCP (n=48) had a 16-day reduction in the median length of hospitalization as compared with infants who did not receive OCP (n=51). No differences in salivary immune peptide sequence representation before OCP between groups were found. Longitudinal changes in peptides were detected (lysozyme C, immunoglobulin A, lactoferrin) but were limited to a single peptide difference (α-defensin 1) between primed and unprimed infants after OCP. We found no difference in microbial diversity between treatment groups at any time point, but diversity decreased significantly over time in both groups. OCP treatment marginally modified oral taxa with a decline in abundance of Streptococci in the OCP group at 30 days of life. CONCLUSIONS: OCP had neither an effect on the salivary peptides we examined nor on overall oral bacterial diversity and composition. Infants who received OCP had a reduced length of hospitalization and warrants further investigation.


Assuntos
Colostro/química , Hospitalização/estatística & dados numéricos , Microbiota , Boca/microbiologia , Saliva/imunologia , Administração Oral , Adulto , Bactérias/classificação , Colostro/imunologia , Feminino , Humanos , Imunoglobulina A/análise , Recém-Nascido , Recém-Nascido Prematuro/imunologia , Lactoferrina/análise , Tempo de Internação , Masculino , Muramidase/análise , Gravidez , Estudos Prospectivos , RNA Ribossômico 16S/genética , Saliva/química , Estados Unidos , Adulto Jovem
2.
J Perinatol ; 33(11): 847-50, 2013 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-23722974

RESUMO

OBJECTIVE: Earlier diagnosis and treatment of necrotizing enterocolitis (NEC) in preterm infants, before clinical deterioration, might improve outcomes. A monitor that measures abnormal heart rate characteristics (HRC) of decreased variability and transient decelerations was developed as an early warning system for sepsis. As NEC shares pathophysiologic features with sepsis, we tested the hypothesis that abnormal HRC occur before clinical diagnosis of NEC. STUDY DESIGN: Retrospective review of Bells stage II to III NEC cases among infants <34 weeks gestation enrolled in a prospective randomized clinical trial of HRC monitoring at three neonatal intensive care units. RESULT: Of 97 infants with NEC and HRC data, 33 underwent surgical intervention within 1 week of diagnosis. The baseline HRC index from 1 to 3 days before diagnosis was higher in patients who developed surgical vs medical NEC (2.06±1.98 vs 1.22±1.10, P=0.009). The HRC index increased significantly 16 h before the clinical diagnosis of surgical NEC and 6 h before medical NEC. At the time of clinical diagnosis, the HRC index was higher in patients with surgical vs medical NEC (3.3±2.2 vs 1.9±1.7, P<0.001). CONCLUSION: Abnormal HRC occur before clinical diagnosis of NEC, suggesting that continuous HRC monitoring may facilitate earlier detection and treatment.


Assuntos
Enterocolite Necrosante/diagnóstico , Enterocolite Necrosante/fisiopatologia , Frequência Cardíaca , Enterocolite Necrosante/terapia , Monitoramento Ambiental , Feminino , Humanos , Recém-Nascido , Doenças do Prematuro/diagnóstico , Doenças do Prematuro/fisiopatologia , Masculino , Estudos Prospectivos , Estudos Retrospectivos
3.
J Perinatol ; 30(7): 469-73, 2010 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20010613

RESUMO

OBJECTIVE: Our aim was to evaluate the safety of a silver-alginate-containing dressing to reduce peripherally inserted central catheter (PICC) infections in neonatal intensive care unit (NICU) patients. STUDY DESIGN: Patients were randomized 3:1 to receive a patch containing silver, alginate and maltodextrin or standard of care. Patches were placed under the regular transparent retention dressing at the PICC exit site at insertion and were replaced with every dressing change at least every 2 weeks until PICC discontinuation. All study infants were monitored for adverse skin reactions. RESULT: A total of 100 infants were followed up for 1922 person-days, including 75 subjects with 89 PICCs who received the patch. The median birth weight (1330 g) and median gestational age (30 weeks) was lower in the patch group when compared with the controls (P=0.001 and 0.005, respectively). Study patients received the patch with their PICC at a median age of 5 days; the patch stayed in place for a median of 13 days. We noted no adverse skin reactions and found no evidence that the patch alters the microbiology of PICC-associated infections. CONCLUSION: This pilot trial suggests that silver-alginate-coated dressings are skin safe and their inclusion in future trials aimed at reduction of PICC-associated bloodstream infections in the NICU should be considered.


Assuntos
Antibacterianos/administração & dosagem , Bandagens , Cateterismo Venoso Central/efeitos adversos , Cateteres de Demora/efeitos adversos , Sepse/prevenção & controle , Administração Cutânea , Alginatos/administração & dosagem , Feminino , Ácido Glucurônico/administração & dosagem , Ácidos Hexurônicos/administração & dosagem , Humanos , Recém-Nascido , Masculino , Projetos Piloto , Polissacarídeos/administração & dosagem , Prata/administração & dosagem , Resultado do Tratamento
4.
J Perinatol ; 28(6): 405-11, 2008 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-18185518

RESUMO

OBJECTIVE: Previous reports suggest a benefit of fluconazole prophylaxis in extremely low birth weight (ELBW) infants <1000 g. Our aim was to evaluate if limiting fluconazole prophylaxis to targeted highest risk infants effectively prevents invasive fungal infections, has no undesired side effects and limits unnecessary drug exposure. STUDY DESIGN: This nonrandomized retrospective pre-post intervention study compared two groups of infants: (1) Infants <26 weeks gestation and/or <750 g birth weight, requiring central vascular access and admitted to the Monroe Carell Jr Children's Hospital at Vanderbilt neonatal intensive care unit (NICU) prior to 5 days of age, who received fluconazole prophylaxis and (2) a matched control group from the year prior to prophylaxis. This target population was selected for fluconazole prophylaxis based on prior infection control data from our institution and a number needed to treat of <15 to prevent one episode of fungemia. Following implementation and integration through the institution's computerized physician order entry (CPOE) system, provider adherence to the protocol was assessed during the prophylaxis period. RESULT: A total of 86 patients were included in the study, 44 in the no-prophylaxis group and 42 in the prophylaxis group. In the targeted prophylaxis group, no invasive fungal infections were observed as compared to nine infants with invasive infections in the no-prophylaxis group (P=0.004). No significant adverse effects were recorded. Targeting the highest risk infants reduced the number of infants <1000 g requiring prophylaxis from 80 to 42 (48% reduction) with no preventable infection missed. Provider compliance was 91% following implementation of this protocol through the CPOE system using a standardized order set. CONCLUSION: Targeting the highest risk infants for fluconazole prophylaxis through CPOE can effectively prevent invasive fungal infections and limit drug exposure with no unwanted side effects.


Assuntos
Antifúngicos/uso terapêutico , Fluconazol/uso terapêutico , Doenças do Prematuro/prevenção & controle , Recém-Nascido de muito Baixo Peso , Humanos , Recém-Nascido , Recém-Nascido Prematuro , Sistemas de Registro de Ordens Médicas , Estudos Retrospectivos , Fatores de Risco
5.
J Perinatol ; 27(6): 392-4, 2007 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-17522689

RESUMO

Endogenous endophthalmitis is a rare complication of bacteremia. Proper intervention is critical, as the majority of affected patients lose vision in the infected eye. Treatment options include systemic antibiotics, intravitreous antibiotics and vitrectomy. We report a case of endogenous endophthalmitis presenting as leukocoria in a premature neonate with group B streptococcal meningitis.


Assuntos
Endoftalmite/diagnóstico , Recém-Nascido Prematuro , Infecções Estreptocócicas/diagnóstico , Streptococcus agalactiae , Gêmeos , Adulto , Antibacterianos/uso terapêutico , Diagnóstico Diferencial , Endoftalmite/patologia , Endoftalmite/cirurgia , Feminino , Humanos , Recém-Nascido , Masculino , Gravidez , Infecções Estreptocócicas/patologia , Infecções Estreptocócicas/cirurgia , Vancomicina/uso terapêutico , Vitrectomia
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