RESUMO
PURPOSE: To evaluate and compare the morbidity and mortality of neonates born to pregnant women with positive and negative cervical cultures. MATERIALS AND METHODS: The demographic and clinical features of mothers included in this study, along with details of the microorganisms isolated on maternal cervical cultures and the number of days between a positive cervical culture and delivery were recorded. Neonates were stratified into two groups based on cervical culture results of their mothers--Group 1, positive cervical culture; Group 2, negative cervical culture. RESULTS: A total of 216 women who delivered 242 infants were included in the study. Group 1 consisted of 90 neonates while Group 2 had 152 newborns. The difference between the groups with demographic characteristics was statistically insignificant. Mean levels of the acute phase reactants, CRP, and IL-6, obtained six hours after delivery were significantly higher in Group 1 compared to Group 2 (p < 0.05 for C-reactive protein (CRP) andp < 0.001 for IL-6). Although there was no difference between groups in terms of duration of respiratory support, mean duration of hospitalization, as well as mortality rate were significantly higher in Group 1 (p < 0.001, p < 0.05, respectively). CONCLUSIONS: Women diagnosed with a high-risk pregnancy should be treated with antibiotics immediately after a positive cervical culture result, and delivery should be delayed until the success of antibiotic treatment can be evaluated. Early initiation of maternal antibiotic therapy is associated with shorter durations of hospital stay for newborns. Close follow-up of mothers with high-risk pregnancies and extension of treatment duration are critical for determining prognosis in newborn infants.
Assuntos
Colo do Útero/microbiologia , Doenças do Prematuro/epidemiologia , Adulto , Antibacterianos/administração & dosagem , Corioamnionite/tratamento farmacológico , Corioamnionite/epidemiologia , Corioamnionite/microbiologia , Infecções por Escherichia coli/tratamento farmacológico , Infecções por Escherichia coli/epidemiologia , Feminino , Humanos , Recém-Nascido , Doenças do Prematuro/mortalidade , Masculino , Gravidez , Resultado da Gravidez , Gravidez de Alto Risco , Estudos Retrospectivos , Turquia/epidemiologiaAssuntos
Transtornos Cromossômicos/genética , Hérnias Diafragmáticas Congênitas/genética , Doenças do Recém-Nascido/genética , Microftalmia/genética , Trissomia/genética , Transtornos Cromossômicos/complicações , Cromossomos Humanos Par 13/genética , Hérnias Diafragmáticas Congênitas/etiologia , Humanos , Recém-Nascido , Masculino , Microftalmia/etiologia , Síndrome da Trissomia do Cromossomo 13RESUMO
OBJECTIVE: Leukocyte contamination during blood transfusion can cause many adverse effects. Filtration can be performed either at bedside during the transfusion or as pre-storage filtration. Pre-storage filtration is superior to bedside filtration because leukocytes are removed prior to storage, thus preventing further adverse effects associated with the storage of these cells. METHODS AND MATERIALS: One hundred and six infants were randomised into two groups: pre-storage filtration (group 1, n = 53) and bedside filtration (group 2, n = 53). C-reactive protein (CRP) and interleukin-6 (IL-6) levels were analysed within 24 h prior to the transfusion and 24 h after completion of the transfusion. RESULTS: In group 1, pre-transfusion median CRP and IL-6 levels were 2·95 (0·73-10·25) mg L(-1) and 8·59 (3·45-20·55) pg L(-1) , respectively, and post-transfusion median CRP and IL-6 levels were 2·28 (0·44-12·87) mg L(-1) and 6·62 (2·18-27·87) pg L(-1) , respectively. In group 2, pre-transfusion median CRP and IL-6 levels were 1·30 (0·40-7·84) mg L(-1) and 4·40 (2-17·12) pg L(-1) , respectively, and post-transfusion median CRP and IL-6 levels were 3·50 (0·50-7·85) mg L(-1) and 8·30 (3·48-23·75) pg L(-1) , respectively. There were no differences between pre-storage and post-storage leukoreduction average IL-6 and CRP levels in either group (P > 0·05 for both). Packed red blood cell (PRBC)-related necrotizing enterocolitis was detected in one infant in group 2. CONCLUSIONS: Because leukocytes in PRBC transfusions can be associated with many undesirable effects, leukoreduction is the best choice to prevent those effects. However, this method is still controversial. We demonstrated that using pre-storage and post-storage leukoreduction methods in erythrocyte transfusions did not change CRP or IL-6 levels, which are indicators of acute-phase response.
Assuntos
Preservação de Sangue , Proteína C-Reativa/análise , Transfusão de Eritrócitos , Recém-Nascido Prematuro , Interleucina-6/análise , Procedimentos de Redução de Leucócitos , Proteína C-Reativa/metabolismo , Feminino , Humanos , Recém-Nascido , Interleucina-6/sangue , Masculino , Distribuição AleatóriaAssuntos
Anormalidades Múltiplas/diagnóstico , Anormalidades Múltiplas/genética , Transtornos Cromossômicos/diagnóstico , Transtornos Cromossômicos/genética , Anormalidades Congênitas/diagnóstico , Anormalidades Congênitas/genética , Holoprosencefalia/diagnóstico , Holoprosencefalia/genética , Nariz/anormalidades , Trissomia/diagnóstico , Trissomia/genética , Cromossomos Humanos Par 13/genética , Evolução Fatal , Humanos , Recém-Nascido , Masculino , Fenótipo , Síndrome da Trissomia do Cromossomo 13Assuntos
Anormalidades Múltiplas/diagnóstico , Doenças Cerebelares/diagnóstico , Síndrome de Dandy-Walker/diagnóstico , Anormalidades do Olho/diagnóstico , Doenças Renais Císticas/diagnóstico , Retina/anormalidades , Cerebelo/anormalidades , Consanguinidade , Humanos , Recém-Nascido , Imageamento por Ressonância Magnética , MasculinoRESUMO
Fryns anophthalmia-plus syndrome is a rare syndrome with clinical diversity primarily including anophthalmia/microphthalmia, facial clefts, cleft lip/palate, ear and nasal deformities. Here we present two different cases of APS with anopthalmia/microphthalmia, cleft palate, low set ears, ventriculomegaly and one of which had intestinal non-fixation anomaly not described in the literature before.
Assuntos
Anormalidades Múltiplas/patologia , Anoftalmia/patologia , Ceco/anormalidades , Anormalidades Múltiplas/diagnóstico , Anoftalmia/diagnóstico , Ceco/cirurgia , Feminino , Humanos , Recém-NascidoRESUMO
Partial trisomy 4q is a rare chromosomal abnormality which results in variable clinical features, often including growth and developmental delay, mental retardation and dysmorphic features. We herein report a newborn with the diagnosis of partial trisomy 4q with Hirschsprung's disease who was monitored in neonatal intensive care unit. This is the first report of partial trisomy 4q27q35 with accompanying Hirschsprung's disease.
Assuntos
Anormalidades Múltiplas/patologia , Doença de Hirschsprung/patologia , Trissomia/patologia , Anormalidades Múltiplas/genética , Cromossomos Humanos Par 4/genética , Feminino , Doença de Hirschsprung/genética , Humanos , Recém-Nascido , Síndrome , Translocação Genética , Trissomia/genéticaRESUMO
PURPOSE: To identify the degree of perceived social support by mothers of infants hospitalized in neonatal intensive care unit (NICU) and to investigate effects depression and anxiety levels on the perceived social support. METHOD: The study included 50 mothers of infants hospitalized in NICU. Demographic and clinical characteristics of the mothers were collected using a personal data form designed by the study researchers via face-to-face interviews. The Multidimensional Scale of Perceived Social Support Scale (MSPSS) was used to evaluate the degree of perceived social support by the mothers and Hospital Anxiety and Depression (HAD) Scale was used to assess their anxiety and depression levels. RESULTS: The mean age of the mothers was 29.1 ± 4.2 years. There was a significant correlation between the scores of the anxiety and depression subscales (r=0.772; p<0.001), whereas these scores were not significantly correlated with MSPSS total score. The scores MSPSS subscales were significantly correlated with each other, as well as with MSPSS total score. Friend subscale score and depression subscale score were positively correlated with education level (r=0.295, p=0.038 and r=0.407, p=0.003, respectively). The family and spouse subscale scores and MSPSS total score were significantly higher assisted conception technique group compared with the spontaneous conception group (p=0.020, p=0.010 and p=0.016, respectively). The family and spouse subscale scores and MSPSS total score were significantly lower in the mothers with depression subscale score of ≥7 than in the mothers with depression subscale score of <7 (p=0.010, p=0.038 and p=0.018, respectively). In the linear regression model, only education level was found to be a significant factor affecting depression level (p=0.006). CONCLUSION: The mothers of infants hospitalized in the NICU with higher education levels had higher depression level and perceived social support from friends. Informing the family members and providing psychological support independent from the duration of gestation are of paramount importance.
RESUMO
Turkey is a country with intermediate endemicity for hepatitis B, and approximately 4% of the population are HBsAg-positive. A number of measures have been implemented to prevent hepatitis B infection. In 1998, hepatitis B antigen was included in the national immunisation programme, and infants have since been vaccinated with three doses. Catch-up strategies, vaccination for high risk groups and screening measures were also adopted. The aim of this study was to evaluate the impact of the prevention and control strategies on hepatitis B notification rates in Turkey in the period from 1990 to 2012, using data from the national surveillance system. Secular trends revealed that rates showed an initial increasing trend, followed by a steady decline from 2005. The most dramatic decline occurred among children younger than 15 years, highlighting the benefits of vaccination and catch-up strategies. However, vaccination cannot fully explain the decrease in this age group. Socioeconomic development, through interrupting the horizontal transmission may also have contributed. After 2005, a steady decline was achieved also among those 15 years and older. The rates in adults were higher, which indicates that stronger prevention measures are needed to target this group, particularly men.
Assuntos
Notificação de Doenças/estatística & dados numéricos , Vacinas contra Hepatite B/administração & dosagem , Hepatite B/epidemiologia , Hepatite B/prevenção & controle , Programas de Imunização/estatística & dados numéricos , Vacinação , Doença Aguda , Adulto , Distribuição por Idade , Criança , Pré-Escolar , Feminino , Hepatite B/transmissão , Antígenos de Superfície da Hepatite B/imunologia , Vacinas contra Hepatite B/imunologia , Humanos , Lactente , Masculino , Vigilância da População , Distribuição por Sexo , Fatores Socioeconômicos , Turquia/epidemiologiaAssuntos
Anormalidades Múltiplas/diagnóstico por imagem , Anormalidades Congênitas/diagnóstico por imagem , Permeabilidade do Canal Arterial/diagnóstico por imagem , Fêmur/anormalidades , Nefropatias/congênito , Rim/anormalidades , Síndrome de Pierre Robin/diagnóstico por imagem , Adulto , Diagnóstico Diferencial , Feminino , Fêmur/diagnóstico por imagem , Humanos , Recém-Nascido , Rim/diagnóstico por imagem , Nefropatias/diagnóstico por imagem , Masculino , Gravidez , Gravidez em Diabéticas , Radiografia , UltrassonografiaRESUMO
AIM: Evidence that oxidative stress plays a role in the development of bronchopulmonary dysplasia (BPD). There is a close relationship between oxidative stress and inflammation. In this study, it is aimed to investigate influences of hydrocortisone used in the treatment of BPD on anti-oxidant system in preterm infants with BPD. PATIENTS AND METHODS: The study enrolled 33 infants with severe BPD who were undergone inpatient treatment in neonatal intensive care unit (NICU) of our Hospital and received therapy with hydrocortisone. Total oxidant status (TOS) and total anti-oxidant capacity (TAC) levels of infants enrolled to the study before and one week after the hydrocortisone therapy were studies and oxidative stress index levels were calculated. Pre- and post-treatment TOS, TAC and OSI index levels were statistically compared. RESULTS: In preterm infants with BPD, who were enrolled into the study, TOS and OSI index were found high, whereas TAC values were low. Following the treatment with hydrocortisone, statistically significant decrease in TOS and OSI index and statistically significant elevation in TAC levels were found in comparison with pre-treatment levels. CONCLUSIONS: The treatment with hydrocortisone, which is used for BPD, improves anti-oxidant system and reduces oxidative stress in infants with BPD. There is need for further studies in order to clarify the physio-pathogenesis.
Assuntos
Displasia Broncopulmonar/tratamento farmacológico , Hidrocortisona/uso terapêutico , Estresse Oxidativo , Displasia Broncopulmonar/metabolismo , Feminino , Humanos , Recém-Nascido , MasculinoRESUMO
OBJECTIVES: Our aim was to investigate whether the maternal serum concentrations of first and second trimester serum analytes are altered in familial Mediterranean fever (FMF) pregnancies. MATERIALS AND METHODS: The screening tests were compared in a series of 16 serum samples from FMF pregnancies and in a cohort of 48 pregnant women with normal pregnancy. Serum samples were obtained between 11 and 13 weeks; 16 and 18 weeks gestation. RESULTS: Serum pregnancy-associated plasma protein-A (PAPP-A) levels, expressed as multiples of the median (0.9 ± 0.45 MoM) in the control group, were significantly higher than FMF patients (0.6 ± 0.3 MoM) (p = 0.027). Analyses of alpha-fetoprotein, human chorionic gonadotropin and oestriol levels showed no significant differences between FMF and normal pregnancies. CONCLUSIONS: Our study revealed that low levels of PAPP-A are associated with FMF.
Assuntos
Biomarcadores/análise , Febre Familiar do Mediterrâneo/metabolismo , Complicações na Gravidez/metabolismo , Primeiro Trimestre da Gravidez/fisiologia , Segundo Trimestre da Gravidez/fisiologia , Adulto , Estudos de Coortes , Feminino , Humanos , Gravidez , Proteína Plasmática A Associada à Gravidez/análiseRESUMO
BACKGROUND: Gastroesophageal reflux disease (GERD) may occur with poor weight gain, esophagitis, hematemesis and respiratory problems in an infant. Common treatment strategies include positioning, feeding thickeness, histamine2 receptor antagonists, antiacids, and prokinetics. Metoclopramide is a prokinetic drug used to treat GERD and it has been reported to be a most commonly prescribed medication in neonatal intensive care unit (NICU). This research involves a patient that was born at 30 weeks' gestation age and on the twentieth day of his admission, vomiting and gastric residuals were observed. All diseases which are related these symptoms were excluded. With no improvement observed following non-pharmacological interventions and metoclopramide was started with a dosage of 0.1 mg/kg, per dose 12 hours. After the second dose of metoclopramide, dystonic reactions occured. The premature infant was evaluated for differential diagnosis of the abnormal movements. No abnormal findings were reported. The dystonic reactions didn't recur after metoclopramide was stopped. CONCLUSIONS: The observed adverse effects of metoclopramide in the preterm infant might be due to an excessive serum concentration of the drug as a result of its prolonged plasma clearance in this age group. Attention is drawn to the serious adverse effects of metoclopramide in the neonate, particularly premature infant.
Assuntos
Antieméticos/efeitos adversos , Distonia/induzido quimicamente , Metoclopramida/efeitos adversos , Refluxo Gastroesofágico/tratamento farmacológico , Humanos , Recém-Nascido , Recém-Nascido Prematuro , Doenças do Prematuro/tratamento farmacológico , Unidades de Terapia Intensiva Neonatal , MasculinoRESUMO
OBJECTIVE: As scant information is present about the effect of water birth on newborns, we aimed to detect the fetal outcomes of water birth. MATERIALS AND METHODS: A hundred and ninety one among totally 220 newborns who were born by water birth were enrolled. The demographic and clinical features of the patients, birth complications, infection rates and rates of neonatal intensive care unit attendance were evaluated. RESULTS: The mean gestational week and birth weight were 39.2±1.3 weeks and 3326±409 g. 26% of the mothers was primiparous. Birth trauma was observed in three patients (1.6%) as one brachial nerve paralysis, one cord rupture and one cephal hematoma. Six of the patients (3.1%) were admitted to neonatal intensive care unit (NICU); four of whom had respiratory tract problems. CONCLUSIONS: Water birth is a safe method of delivery for the neonates when certain criteria are met.
Assuntos
Parto , Adolescente , Adulto , Infecções Bacterianas/epidemiologia , Feminino , Humanos , Recém-Nascido , Doenças do Recém-Nascido/epidemiologia , Unidades de Terapia Intensiva Neonatal , Masculino , Gravidez , Centros de Atenção Terciária , ÁguaRESUMO
BACKGROUND: Invasive fungal sepsis has become the third most common cause of late-onset infections in many neonatal intensive care units (NICU). The prevalence rate ranges from 2.6% to 16.7% among very-low-birth-weight infants and from 5.5% to 20% among extremely low-birth-weight infants. Despite the development of several new antifungal agents in the past few years, the management of serious fungal infections in the newborn continues to be problematic. MATERIALS, METHODS AND RESULTS: Voriconazole treatment was given to 17 newborns with invasive fungal sepsis, in initial doses of 2-3 mg/kg twice daily. In spite of the complications of cholestasis and liver function abnormality in 2, the dose regimen was 4-6 mg/kg (loading dose), followed by initial doses of 2-3 mg/kg twice daily. Drug cessation did not occur, and no permanent side effects were observed. In the end, 12 patients had been cured with antifungal treatment. CONCLUSIONS: Voriconazole at this dosage common with other antifungal agents or alone appears to be a safe and effective antifungal agent for neonatal invasive fungal sepsis. Based on relevant literature, to the best of our knowledge, ours is the largest case series to underline this issue. However, further studies are required to determine the pharmacokinetics (e.g. serum half-life, concentration, time of peak concentration, and distribution) of voriconazole use in newborns.
Assuntos
Antifúngicos/uso terapêutico , Ensaios de Uso Compassivo , Micoses/tratamento farmacológico , Pirimidinas/uso terapêutico , Sepse/tratamento farmacológico , Triazóis/uso terapêutico , Feminino , Humanos , Lactente , Recém-Nascido , Masculino , Sepse/microbiologia , VoriconazolRESUMO
INTRODUCTION: Neonatal sepsis remains an important clinical syndrome despite advances in neonatology. Current hematology analyzers can determine cell volume (V), conductivity for internal composition of cell (C) and light scatter for cytoplasmic granularity and nuclear structure (S), and standard deviations which are effective in the diagnosis of sepsis. Statistical models can be used to strengthen the diagnosis. Effective modeling of molecular activity (EMMA) uses combinatorial algorithm of the selection parameters for regression equation based on modified stepwise procedure. It allows obtaining different regression models with different combinations of parameters. METHODS: We investigated these parameters in screening of neonatal sepsis. We used LH780 hematological analyzer (Beckman Coulter, Fullerton, CA, USA). We combined these parameters with interleukin-6 (IL-6) and C-reactive protein (CRP) and developed models by EMMA. RESULTS: A total of 304 newborns, 76 proven sepsis, 130 clinical sepsis and 98 controls, were enrolled in the study. Mean neutrophil volume (MNV) and volume distribution width (VDW) were higher in both proven and clinical sepsis groups. We developed three models using MNV, VDW, IL-6, and CRP. These models gave more sensitivity and specificity than the usage of each marker alone. CONCLUSIONS: We suggest to use the combination of MNV and VDW with markers such as CRP and IL-6, and use diagnostic models created by EMMA.
Assuntos
Núcleo Celular/patologia , Grânulos Citoplasmáticos/patologia , Modelos Biológicos , Triagem Neonatal/métodos , Neutrófilos/patologia , Sepse/diagnóstico , Proteína C-Reativa/análise , Núcleo Celular/química , Forma do Núcleo Celular , Tamanho Celular , Grânulos Citoplasmáticos/química , Diagnóstico Precoce , Condutividade Elétrica , Feminino , Citometria de Fluxo , Humanos , Lactente , Recém-Nascido , Interleucina-6/sangue , Masculino , Neutrófilos/química , Reprodutibilidade dos Testes , Fatores de Risco , Sensibilidade e Especificidade , Sepse/sangue , Sepse/epidemiologia , Sepse/patologia , Turquia/epidemiologiaRESUMO
Jarcho-Levin syndrome (JLS) is a genetic disorder characterized by defects of spine formation, abnormal fusion of the ribs at the costovertebral and costochondral junction due to abnormal vertebral and costal segmentation. There are two subtypes associated with different distribution and severity of defects in JLS. While vertebral segmentation abnormalities are frequent in spondylo-thoracic subtype costal segmentation and fusion abnormalities are frequent in spondylo-costal subtype. Neural tube defects with severe hydrocephalus are rare findings in this syndrome. Herein we report three infants with severe hydrocephalus associated with Jarcho-Levin syndrome.
Assuntos
Cardiopatias Congênitas/complicações , Hérnia Diafragmática/complicações , Hidrocefalia/etiologia , Anormalidades Múltiplas/genética , Anormalidades Múltiplas/patologia , Feminino , Cardiopatias Congênitas/genética , Cardiopatias Congênitas/patologia , Hérnia Diafragmática/genética , Hérnia Diafragmática/patologia , Humanos , Hidrocefalia/genética , Hidrocefalia/patologia , Recém-Nascido , Masculino , Índice de Gravidade de DoençaRESUMO
Su Partial trisomy 3p and partial monosomy 11q are rare chromosomal disorders with a deletion of part of chromosome 11 combined with a duplication of part of chromosome 3. These are usually inherited from a parent who carries a balanced translocation involving chromosome 3, which can result in the unbalanced translocation trisomy 3p in a child. In this paper, we report a newborn who has dysmorphic facial features, double outlet right ventricle, hypotonia, hypospadias, neonatal thrombocytopenia, hydroureteronephrosis, talipes equinovarus and septum pellucidum et vergae. Cytogenetic investigation revealed 46,XY,der(11)t(3;11)(p22.2;q23.3) and the karyotype of his father showed a balanced translocation, 46XY,t(3;11)(p22.2;p23.3).