RESUMO
BACKGROUND: Extremely low birth weight (ELBW) infants are at risk of impaired postnatal growth. Impaired postnatal growth has been reported to be associated with delayed cognitive and motor development. AIMS: To describe postnatal growth patterns of appropriate and small for gestational age (AGA and SGA) ELBW children in relation to their cognitive and motor outcome at age 5.5. STUDY DESIGN: Retrospective cohort study. SUBJECTS: One hundred one children with a BW ≤ 750g, born between 1996 and 2005 in the University Hospital Utrecht, The Netherlands. OUTCOME MEASURES: Height (Ht), weight (Wt), occipital-frontal circumference (OFC) at birth, 15 months and 2 years corrected age and 3.5 and 5.5 years. Cognitive and motor outcome at 5.5 years of age, classified as normal (Z-score ≥-1), mildly delayed (-2≤Z-score <-1) or severely delayed (Z-score <-2). AGA (Ht, Wt or OFC at birth ≥-2 SDS) infants were compared with SGA (Ht, Wt or OFC at birth <-2 SDS) infants. RESULTS: Between birth and 5.5 years catch-up growth in Ht, weight for height (Wt/Ht), Wt and OFC was seen in 72.2%, 55.2%, 28.6% and 68.9% respectively of the SGA infants. For AGA infants we found substantial catch-down growth in Ht (15.4%) and Wt (33.8%). Cognitive and motor outcome was normal in 76.2% and 41.6% of the 101 children. A significantly higher percentage of normal cognitive outcome was found in AGA infants with Wt growth remaining at ≥-2 SDS compared to AGA infants with catch-down growth (83% vs 63%). Next, SGA infants who caught-up in OFC had a higher prevalence of normal cognitive outcome compared to SGA infants who did not catch-up in OFC. Furthermore, a higher percentage of severely delayed motor outcome was found in SGA infants without catch-up growth in Wt compared to SGA infants who caught-up in Wt (61.5% vs 32.2%). CONCLUSIONS: Catch-up growth in Ht, Wt/Ht and OFC occurred in the majority of the SGA infants with a BW ≤ 750 g, but was less common in Wt. AGA children who remained their Wt at ≥-2 SDS have a better cognitive and motor developmental outcome at 5.5 years of age. Catch-up growth in OFC was associated with a better cognitive outcome at 5.5 years of age.
Assuntos
Desenvolvimento Infantil/fisiologia , Recém-Nascido de Peso Extremamente Baixo ao Nascer/crescimento & desenvolvimento , Recém-Nascido Prematuro/crescimento & desenvolvimento , Recém-Nascido Pequeno para a Idade Gestacional/crescimento & desenvolvimento , Estatura/fisiologia , Peso Corporal/fisiologia , Pré-Escolar , Estudos de Coortes , Feminino , Cabeça/anatomia & histologia , Humanos , Recém-Nascido , Masculino , Países Baixos , Estudos Retrospectivos , Estatísticas não ParamétricasRESUMO
BACKGROUND: Extremely low birth weight (ELBW) infants are at risk of cognitive impairment and follow-up is therefore of major importance. The age at which their neurodevelopmental outcome (NDO) can reliably be predicted differs in the literature. AIMS: To describe NDO at 2, 3.5 and 5.5 years in an ELBW cohort. To examine the value of NDO at 2 years corrected age (CA) for prediction of NDO at 3.5 and 5.5 years. STUDY DESIGN: A retrospective cross-sectional and longitudinal cohort study. SUBJECTS: 101 children with a BW≤750 g, born between 1996 and 2005, who survived NICU admission and were included in a follow-up program. OUTCOME MEASURES: NDO, measured with different tests for general development and intelligence, depending on age of assessment and classified as normal (Z-score≥-1), mildly delayed (-2≤Z-score<-1) or severely delayed (Z-score<-2). RESULTS: At 2, 3.5 and 5.5 years 74.3, 82.2 and 76.2% had a normal NDO. A normal NDO at 2 years CA predicted a normal NDO at 3.5 and 5.5 years in 92% and 84% respectively. Of the children with a mildly or severely delayed NDO at 2 years CA the majority showed an improved NDO at 3.5 (69.2%) and 5.5 years (65.4%) respectively. CONCLUSIONS: The majority of the children with a BW≤750 g had a normal NDO at all ages. A normal NDO at 2 years CA is a good predictor for normal outcome at 3.5 and 5.5 years, whereas a delayed NDO at 2 years CA is subject to change with the majority of the children showing a better NDO at 3.5 and 5.5 years.
Assuntos
Desenvolvimento Infantil/fisiologia , Cognição/fisiologia , Deficiências do Desenvolvimento/fisiopatologia , Recém-Nascido de muito Baixo Peso/fisiologia , Distribuição de Qui-Quadrado , Estudos de Coortes , Estudos Transversais , Feminino , Seguimentos , Humanos , Recém-Nascido , Recém-Nascido Prematuro , Recém-Nascido de muito Baixo Peso/psicologia , Estudos Longitudinais , Valor Preditivo dos Testes , GravidezRESUMO
OBJECTIVES: To describe 2-year neurodevelopmental outcome (NDO) in a cohort of extremely low birthweight infants, and compare NDO between two consecutive 5-year periods and between appropriate (AGA, ≥p10) and small for gestational age (SGA,
Assuntos
Deficiências do Desenvolvimento/etiologia , Recém-Nascido Prematuro/psicologia , Peso ao Nascer , Métodos Epidemiológicos , Feminino , Idade Gestacional , Humanos , Cuidado do Lactente/métodos , Recém-Nascido , Recém-Nascido Pequeno para a Idade Gestacional/psicologia , Recém-Nascido de muito Baixo Peso/psicologia , Unidades de Terapia Intensiva Neonatal , Masculino , Prognóstico , PsicometriaRESUMO
Albinism is an autosomal recessive disorder that is caused by a defective synthesis of melanin, resulting in a generalized reduction of pigmentation in the skin, hair and eyes, and leading to an increased risk of skin cancer and vision problems. We report a case of a 22-year-old primigravida of Negroid origin who delivered dichorial diamniotic twins: two daughters were born with a totally different appearance. The first child had a light brown skin, black curly hair and brown eyes, whereas the second had a striking white skin, red-blond curly hair and blue eyes. Oculocutaneous albinism (OCA) and heteropaternal superfecundation were considered in the differential diagnosis. Genetic testing confirmed the diagnosis of OCA type 2 in the second child. The diagnosis of albinism has clinical implications and must be considered when a black and white twin is born.
Assuntos
Albinismo Oculocutâneo/diagnóstico , População Negra , Doenças em Gêmeos/diagnóstico , Gêmeos Dizigóticos , Albinismo Oculocutâneo/genética , Doenças em Gêmeos/genética , Feminino , Humanos , Recém-Nascido , Proteínas de Membrana Transportadoras/genética , Mutação , Gêmeos Dizigóticos/genética , Adulto JovemRESUMO
BACKGROUND: Improvement in perinatal and neonatal care has resulted in increased survival of extremely low birth weight (ELBW) infants. OBJECTIVES: To describe survival and neonatal morbidity in a cohort of ELBW infants, to compare two consecutive 5-year periods, and compare appropriate (AGA) with small for gestational age (SGA) infants (AGA ≥p10, and SGA Assuntos
Recém-Nascido de Peso Extremamente Baixo ao Nascer
, Doenças do Prematuro/epidemiologia
, Doenças do Prematuro/mortalidade
, Adulto
, Algoritmos
, Peso ao Nascer/fisiologia
, Estudos de Coortes
, Feminino
, Idade Gestacional
, Humanos
, Mortalidade Infantil
, Recém-Nascido
, Recém-Nascido Pequeno para a Idade Gestacional
, Terapia Intensiva Neonatal/estatística & dados numéricos
, Morbidade
, Gravidez
, Estudos Retrospectivos
, Análise de Sobrevida
, Adulto Jovem