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1.
Early Hum Dev ; 168: 105573, 2022 05.
Artículo en Inglés | MEDLINE | ID: mdl-35468574

RESUMEN

BACKGROUND: Exposure to pain in early life was associated with long term consequences, therefore strategies for minimizing painful procedures in newborns should be employed. The utility and reliability of cord blood CBC was demonstrated before, however data regarding use of cord blood in healthy infants at risk for polycythemia are lacking. METHODS: A single-center, paired-sampling prospective laboratory study including all healthy asymptomatic infants born after 36 weeks gestation who were SGA (<2500 g), LGA (>4000 g), or born to mothers with diabetes in pregnancy. Blood count indices were compared between umbilical and neonatal capillary or venous blood samples. In order to predict cut-off values for neonatal polycythemia using umbilical hematocrit, receiver operator curves (ROC) were plotted. RESULTS: Paired samples were collected from 433 infants. Mean gestational age and birth-weight were 39.0 ± 1.3 weeks and 3489 ± 682 g. Hemoglobin, hematocrit and WBC values were lower in cord blood compared to neonatal, but PLT count was higher. Pearson r showed only modest correlation between peripheral capillary and umbilical or venous Hct - 0.35 (p < 0.001), and 0.44 (p < 0.001), respectively. In order to try and capture clinically significant polycythemia ROC was plotted for hematocrit >70% and <40%. In our cohort, using the calculated cutoff values (>51% and <35%) could have resulted in a decrease of 72% of neonatal blood draws. CONCLUSION: This analysis should be interpreted with caution, as currently it cannot support the routine use of umbilical samples' hematocrits for making treatment decision in newborns at risk for polycythemia. Further larger studies are needed.


Asunto(s)
Policitemia , Femenino , Sangre Fetal , Hematócrito , Humanos , Recién Nacido , Dolor , Policitemia/diagnóstico , Embarazo , Estudios Prospectivos , Reproducibilidad de los Resultados , Cordón Umbilical
2.
J Clin Virol ; 138: 104798, 2021 05.
Artículo en Inglés | MEDLINE | ID: mdl-33770655

RESUMEN

BACKGROUND: Most infants with congenital cytomegalovirus (cCMV) have no overt manifestations at birth, yet may later develop CMV-related sensorineural hearing loss (SNHL). With targeted screening, many asymptomatic neonates are missed and lose the opportunity for timely anti-viral treatment to ameliorate SNHL. Saliva is the preferred screening specimen given its ease of collection. OBJECTIVES: Assess a pooled saliva CMV DNA detection technique for cCMV screening of healthy full-term neonates. STUDY DESIGN: We conducted a prospective laboratory CMV PCR screening study in a secondary hospital from March-June 2019. Saliva specimens were obtained from 1000 newborns two-four hours after birth. Specimens were analyzed for CMV DNA with a real-time PCR platform (Altona) in pools of 10 and individually (40 µL and 400 µL, respectively). Neonates with positive saliva CMV DNA detection required urine CMV PCR testing to confirm cCMV diagnosis. RESULTS: From the 1000 saliva samples, there were 6 urine-confirmed cCMV cases, yielding a prevalence rate of 0.6 %. The specificity was high for both pooled and individual saliva sampling (99.9 % and 98.1 %, respectively). The positive predictive value of the pooled sample was 85.7 %, compared to 24.0 % for a single saliva sample. CONCLUSIONS: Pooling saliva of healthy newborns appears to be a reliable method to identify asymptomatic cCMV infection when positive results are confirmed by urine CMV DNA. Pooling in sizes appropriate to the cCMV prevalence rate may improve the laboratory workflow and decrease costs. Further studies should evaluate the clinical implications of this widespread cCMV pooled screening technique.


Asunto(s)
Infecciones por Citomegalovirus , Saliva , Citomegalovirus/genética , Infecciones por Citomegalovirus/diagnóstico , Infecciones por Citomegalovirus/epidemiología , ADN Viral , Humanos , Lactante , Recién Nacido , Laboratorios , Tamizaje Neonatal , Estudios Prospectivos , Reacción en Cadena en Tiempo Real de la Polimerasa
3.
Neonatology ; 110(1): 75-82, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27058608

RESUMEN

BACKGROUND: Phototherapy has been reported to alter blood flow to various tissues. We hypothesized that during phototherapy the coronary blood flow will decrease because of a 'steal effect' to the periphery. OBJECTIVES: To evaluate the effects of phototherapy on coronary blood flow in healthy, jaundiced, term neonates. METHODS: Flow velocity [peak diastolic velocity (Vd)] and flow measures [diastolic time velocity integral (TVId) and flow index (FI)] in the left main (LM) and left anterior descending (LAD) coronary arteries were prospectively studied with 2D/pulsed Doppler ultrasound before, during and after phototherapy in 19 healthy term, jaundiced neonates (study group) and in matched nonjaundiced controls (25 neonates). Significance was set at p < 0.05. RESULTS: The neonates' characteristics were comparable in both groups. Sequential studies in the study group showed no significant decrease in measures of velocity and flow during phototherapy; however, there was a significant increase in some of these measures (Vd and TVId in the LM coronary artery, and Vd in the LAD coronary artery) after phototherapy. Velocity (Vd) and flow measures (TVId and FI) in the LAD coronary artery, but not in the LM coronary artery, were significantly lower when comparing the study group during phototherapy with the controls. In a multivariate model, phototherapy was an independent variable affecting Vd and TVId in LAD coronary arteries. Measures of cardiac output did not change significantly throughout the study. CONCLUSIONS: While part of our findings may suggest a modestly lower flow in coronary arteries during phototherapy, we conclude that no clinically significant alteration in coronary arterial flow occurs during phototherapy in healthy term neonates.


Asunto(s)
Circulación Coronaria , Vasos Coronarios/diagnóstico por imagen , Ictericia Neonatal/terapia , Fototerapia/métodos , Velocidad del Flujo Sanguíneo , Estudios de Casos y Controles , Diástole , Ecocardiografía Doppler , Humanos , Recién Nacido , Israel , Ictericia Neonatal/sangre , Análisis Multivariante , Proyectos Piloto , Nacimiento a Término
4.
Breastfeed Med ; 9(9): 430-7, 2014 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-25290824

RESUMEN

OBJECTIVE: This study explored clinical implications of tongue-tie (TT) on breastfeeding from the mothers' perspective and evaluated the assistance provided. MATERIALS AND METHODS: This was a single-center observational study using a structured survey. All newborns with TT born in 2005-2010 were identified; two controls without TT were assigned for each. Mothers were interviewed using a uniform structured questionnaire regarding breastfeeding experience, challenges, lactation consultation, and frenotomy, if performed. RESULTS: One hundred eighty-three TT mothers and 314 controls were interviewed. Although the overall rates of breastfeeding problems in the first month were similar (59% vs. 52%, respectively), TT mothers reported significantly more problems with latching, prolonged breastfeeding, and infant's exhaustion during feedings, but not pain or sore nipples. Breastfeeding rates at 6 months were similar. TT mothers more frequently used pumped breastmilk to supplement breastfeeding. Significantly more TT mothers sought consultation after discharge, and a significantly greater proportion of them felt that lactation consultation helped. Eighty-seven percent of the mothers were aware of their children's TT, yet only 50% associated it with breastfeeding problems. Of the TT infants at 2 years of age or older, 11.9% were reported to have speech problems. The possibility of frenotomy was mentioned to 69% of mothers, and it was performed in 35% of cases. Procedure satisfaction was generally poor, except for when done to solve breastfeeding problems. CONCLUSIONS: TT infants had significantly more breastfeeding problems in the first month, but similar rates and durations of breastfeeding. Early diagnosis and lactation consultation may assist mother-infant dyads substantially. Mothers whose infants underwent frenotomies for breastfeeding more frequently found the procedure alleviated breastfeeding problems.


Asunto(s)
Lactancia Materna , Frenillo Lingual/anomalías , Madres , Anomalías de la Boca/fisiopatología , Adulto , Anquiloglosia , Lactancia Materna/psicología , Consejo Dirigido , Diagnóstico Precoz , Femenino , Humanos , Recién Nacido , Lactancia , Frenillo Lingual/cirugía , Masculino , Madres/psicología , Anomalías de la Boca/diagnóstico , Anomalías de la Boca/cirugía , Pezones , Dolor , Satisfacción del Paciente , Embarazo , Estudios Retrospectivos , Conducta en la Lactancia , Encuestas y Cuestionarios , Resultado del Tratamiento
5.
Am J Perinatol ; 31(3): 203-8, 2014 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-23616073

RESUMEN

OBJECTIVE: To study the influence of policy changes in the evaluation of neonatal hyperbilirubinemia on discharge process from the nursery. Changes included early assessment of risk factors by universal umbilical blood sampling for blood type, Coombs test, and glucose-6-phosphate dehydrogenase (G6PD) and universal noninvasive transcutaneous bilirubinometry at discharge. STUDY DESIGN: The 1,569 newborns (≥ 36 weeks' gestation) admitted after the implementation of changes were compared with the 1,822 born before. RESULTS: Policy changes improved the diagnosis of G6PD deficiency and ABO incompatibility and decreased the number of referrals from the community for jaundice follow-up. The average number of needlesticks per baby as well as the time required for the analysis of serum bilirubin levels on discharge day decreased. Changes did not significantly increase costs. CONCLUSION: Changes seem to have improved the quality of medical care, including early identification of risk factors and better follow-up of neonatal hyperbilirubinemia with reduction of pain and increased efficiency.


Asunto(s)
Deficiencia de Glucosafosfato Deshidrogenasa/diagnóstico , Hiperbilirrubinemia Neonatal/diagnóstico , Ictericia Neonatal/etiología , Tamizaje Neonatal , Bilirrubina/sangre , Prueba de Coombs , Sangre Fetal/química , Deficiencia de Glucosafosfato Deshidrogenasa/complicaciones , Humanos , Recién Nacido , Israel , Tamizaje Neonatal/métodos , Tamizaje Neonatal/tendencias , Guías de Práctica Clínica como Asunto , Estudios Retrospectivos , Factores de Riesgo
6.
Am J Perinatol ; 30(6): 499-504, 2013 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-23147081

RESUMEN

OBJECTIVE: Evaluate the need for urine culture in early neonatal sepsis workup of term and late preterm infants. STUDY DESIGN: Urine culture by suprapubic aspiration or catheter was included in early sepsis evaluations of 173 term and late preterm newborns (mean gestational age 38.6 ± 2.0 weeks) during a 6-month study period. A historic control group included 182 newborns (38.6 ± 2.9 weeks) who had sepsis evaluations without routine urine cultures a year earlier. RESULTS: Urine cultures were sampled in 106 (61%) of the study group, No significant differences were found between study and control groups in the rate of bacteremia (1.73% versus 2.2%) or urinary tract infection (UTI; 0.94% versus 1.1%), which was low. Early UTIs were not accompanied by bacteremia or structural anomalies and were associated with exacerbation of neonatal jaundice in two of three infants. CONCLUSIONS: There seems to be no justification for routine urine culture in early neonatal sepsis workup of term and late preterm infants, unless there are accompanying clinical symptoms, usually related to neonatal jaundice.


Asunto(s)
Enfermedades del Prematuro/diagnóstico , Sepsis/diagnóstico , Toma de Muestras de Orina/estadística & datos numéricos , Enfermedades Asintomáticas , Bacteriemia/diagnóstico , Humanos , Recién Nacido , Ictericia Neonatal/diagnóstico , Nacimiento Prematuro , Factores de Riesgo , Sepsis/epidemiología , Nacimiento a Término , Infecciones Urinarias/diagnóstico
7.
J Pediatr ; 161(2): 191-6.e1, 2012 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-22459229

RESUMEN

OBJECTIVE: To characterize the occurrence of glucose-6-phosphate dehydrogenase (G6PD) deficiency and its association with neonatal hyperbilirubinemia. STUDY DESIGN: This study involved an evaluation of G6PD data for 2656 newborns from a universal newborn screening program. RESULTS: Mean G6PD activity was 14.2 ± 3.3 U/g Hb. Some 2.71% of the newborns were G6PD-deficient, and 1.77% had borderline G6PD activity, with male and female predominance, respectively. G6PD deficiency was more prevalent in newborns of Sephardic Jew and Muslim Arab backgrounds. The infants with G6PD deficiency had higher bilirubin levels at the time of discharge from the nursery. Infants with low and borderline G6PD activity were more likely to require phototherapy (22.2% and 25.5%, respectively, vs 7.6% of infants with normal G6PD activity; P < .005) and to have more referrals for exacerbation of jaundice (15.3% and 14.9%, respectively, vs 6.1%; P < .005). Mean G6PD activity was higher in preterm infants born at 27-34 weeks gestational age compared with those born later (16.3 ± 1.8 U/g Hb vs 14.8 ± 2.0 U/g Hb). Based on sex distribution and theoretical genetic calculations for the rate of heterozygous females, we propose that the range of borderline G6PD activity should be 2-10 U/g Hb rather than the currently accepted range of 2-7 U/g Hb. CONCLUSIONS: There is association between G6PD deficiency and significant neonatal hyperbilirubinemia. Increased risk is also associated with borderline G6PD activity. The suggested new range for borderline G6PD activity should enhance the identification of females at risk. G6PD activity is higher in preterm infants.


Asunto(s)
Deficiencia de Glucosafosfato Deshidrogenasa/complicaciones , Hiperbilirrubinemia Neonatal/etiología , Árabes , Femenino , Deficiencia de Glucosafosfato Deshidrogenasa/diagnóstico , Deficiencia de Glucosafosfato Deshidrogenasa/etnología , Humanos , Hiperbilirrubinemia Neonatal/etnología , Recién Nacido , Judíos , Masculino , Tamizaje Neonatal
9.
J Pediatr ; 152(6): 782-7, 787.e1-2, 2008 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-18492516

RESUMEN

OBJECTIVE: To assess the reliability of visual assessment of bilirubin levels (BiliEye) in newborns as a screening tool to detect significant neonatal hyperbilirubinemia. STUDY DESIGN: 5 neonatologists and 17 nurses estimated 3,532 BiliEye in 1,129 term and late preterm (> or = 35 weeks) infants before discharge from the nursery, at 62 +/- 24 hours. Total serum bilirubin (TSB) levels were measured concomitantly. RESULTS: Mean TSB and BiliEye were 6.7 +/- 2.9 mg/dL (range, 0.4-18.2 mg/dL) and 6.6 +/- 3.2 mg/dL (range, 0.0-17.2 mg/dL), respectively, with good correlation (Pearson's r = 0.752, P < .0001), but other measures of agreement were poor. 61.5% of the 109 babies with TSB levels in high-risk zones were clinically misclassified. The area under curve (AUC) of the receiver-operating characteristics plotted for these high-risk zones was 0.825, but became low for early discharge (< or = 36 hours; AUC = 0.638) and late preterm (35-37 weeks; AUC = 0.613). There was significant interobserver variation (low weighted kappa, 0.363). CONCLUSIONS: Although there was good correlation between BiliEye and actual TSB level, visual assessment was unreliable as a screening tool to detect significant neonatal hyperbilirubinemia before discharge. Babies with TSB levels within high-risk zones may be clinically misdiagnosed as low-risk, resulting in inadequate follow-up.


Asunto(s)
Ictericia Neonatal/diagnóstico , Adulto , Bilirrubina/sangre , Femenino , Humanos , Recién Nacido , Ictericia Neonatal/sangre , Masculino , Tamizaje Neonatal/métodos , Examen Físico/métodos , Reproducibilidad de los Resultados
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