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1.
Child Care Health Dev ; 50(2): e13239, 2024 03.
Artículo en Inglés | MEDLINE | ID: mdl-38413377

RESUMEN

BACKGROUND: Preterm children are at increased risk of cognitive and language delay compared with term-born children. While many perinatal factors associated with prematurity are well established, there is limited research concerning the influence of the socio-familial environment on the development of preterm children. This study aims to assess the relative impact of perinatal and socio-familial risk factors on cognitive and language development at 2 years corrected age (CA). METHOD: This retrospective cross-sectional study included preterm infants with a gestational age <32 weeks and/or a birth weight <1500 g, who underwent neurodevelopmental assessment at 2 years CA. Cognitive and language scores were assessed using the Bayley Scales of Infant-Toddler Development, third edition. Adjusted odds ratios (aORs) with 95% confidence intervals (CIs) were calculated using a multivariable model to examine the relationship between developmental delays and perinatal and socio-familial factors. RESULT: The prevalence of language delay was negatively associated with daycare attendance (aOR: 0.25, 95% CI: 0.07-0.85, p < 0.05) and high maternal educational levels (aOR: 0.24, 95% CI: 0.05-0.93, p < 0.05) and positively associated with bilingual environments (aOR: 5.62, 95% CI: 1.46-24.3, p < 0.05). Perinatal and postnatal risk factors did not show a significant impact on cognitive or language development. CONCLUSION: The development of language appears to be more influenced by the socio-familial environment than by early perinatal and postnatal factors associated with prematurity. These findings highlight the importance of considering socio-familial factors in the early identification and intervention of language delay among preterm children.


Asunto(s)
Recien Nacido Extremadamente Prematuro , Trastornos del Desarrollo del Lenguaje , Lactante , Embarazo , Femenino , Niño , Recién Nacido , Humanos , Recien Nacido Extremadamente Prematuro/psicología , Discapacidades del Desarrollo/epidemiología , Estudios Retrospectivos , Estudios Transversales , Desarrollo del Lenguaje , Desarrollo Infantil , Edad Gestacional , Trastornos del Desarrollo del Lenguaje/etiología , Trastornos del Desarrollo del Lenguaje/complicaciones , Cognición , Recién Nacido de muy Bajo Peso
2.
Nutrients ; 13(11)2021 Nov 16.
Artículo en Inglés | MEDLINE | ID: mdl-34836364

RESUMEN

Neonatal vitamin K prophylaxis is essential to prevent vitamin K deficiency bleeding (VKDB) with a clear benefit compared to placebo. Various routes (intramuscular (IM), oral, intravenous (IV)) and dosing regimens were explored. A literature review was conducted to compare vitamin K regimens on VKDB incidence. Simultaneously, information on practices was collected from Belgian pediatric and neonatal departments. Based on the review and these practices, a consensus was developed and voted on by all co-authors and heads of pediatric departments. Today, practices vary. In line with literature, the advised prophylactic regimen is 1 or 2 mg IM vitamin K once at birth. In the case of parental refusal, healthcare providers should inform parents of the slightly inferior alternative (2 mg oral vitamin K at birth, followed by 1 or 2 mg oral weekly for 3 months when breastfed). We recommend 1 mg IM in preterm <32 weeks, and the same alternative in the case of parental refusal. When IM is perceived impossible in preterm <32 weeks, 0.5 mg IV once is recommended, with a single additional IM 1 mg dose when IV lipids are discontinued. This recommendation is a step towards harmonizing vitamin K prophylaxis in all newborns.


Asunto(s)
Enfermedades del Recién Nacido/prevención & control , Neonatología/normas , Sangrado por Deficiencia de Vitamina K/prevención & control , Vitamina K/administración & dosificación , Vitaminas/administración & dosificación , Bélgica/epidemiología , Consenso , Femenino , Humanos , Incidencia , Recién Nacido , Enfermedades del Recién Nacido/epidemiología , Recien Nacido Prematuro , Masculino , Nacimiento a Término , Vitamina K/normas , Sangrado por Deficiencia de Vitamina K/epidemiología , Vitaminas/normas
3.
Int J Gynaecol Obstet ; 155(3): 490-495, 2021 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-34358338

RESUMEN

OBJECTIVE: To examine the impact of the coronavirus disease 2019 (COVID-19) pandemic and the resulting isolation measures on the risk of postpartum depression (PPD) after preterm birth. METHODS: This is a cross-sectional study of mothers of extreme and early preterm infants who completed the Edinburgh Postnatal Depression Scale (EPDS) at the standardized 3-6 months follow-up consultation for preterm infants. Mothers assessed during the COVID-19 pandemic (n = 34; from April 1, 2020 to March 31, 2021) were compared with an antecedent control group (n = 108; from January 1, 2017 to December 31, 2019). A multivariable logistic regression model was used to examine the relationship between the pandemic and the risk of PPD (EPDS score ≥13). RESULTS: The prevalence of depressive symptoms was significantly higher in the COVID-19 study group (26% versus 12%, P = 0.043). The multivariable logistic regression model showed a significant association between the COVID-19 pandemic and the risk of PPD (adjusted odds ratio 3.60, 95% confidence interval 1.06-12.59, P = 0.040). CONCLUSION: Among mothers of extreme and early preterm infants, the COVID-19 pandemic was independently associated with a higher risk of PPD. This confirms the need for a close and long-term follow up of maternal psychological health after preterm birth.


Asunto(s)
COVID-19 , Depresión Posparto , Nacimiento Prematuro , Estudios Transversales , Depresión , Depresión Posparto/epidemiología , Femenino , Humanos , Lactante , Recién Nacido , Recien Nacido Prematuro , Madres , Pandemias , Embarazo , Nacimiento Prematuro/epidemiología , Factores de Riesgo , SARS-CoV-2
4.
Pediatr Nephrol ; 21(7): 1037-40, 2006 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-16773420

RESUMEN

Pseudo-Bartter syndrome presents the same clinical and biological characteristics as Bartter syndrome but without primary renal tubule abnormalities. We relate the case of a premature baby presenting at birth with severe hypokalemic metabolic alkalosis associated with hyponatremia and hypochloremia. Maternal blood at the time of delivery showed the same electrolyte perturbations. The baby's mother had suffered from anorexia and vomiting during pregnancy. A few weeks after birth the baby's blood abnormalities had almost returned to normal. Chloride depletion is at the origin of both maternal and fetal hypokalemic alkalosis.


Asunto(s)
Síndrome de Bartter/diagnóstico , Feto/patología , Adulto , Alcalosis/diagnóstico , Alcalosis/genética , Síndrome de Bartter/genética , Femenino , Feto/metabolismo , Humanos , Hipopotasemia/diagnóstico , Hipopotasemia/genética , Recién Nacido , Madres , Embarazo , Simportadores del Cloruro de Sodio/metabolismo , Desequilibrio Hidroelectrolítico
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