SCIN - Serviço de Cuidados Intensivos Neonatais
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Browsing SCIN - Serviço de Cuidados Intensivos Neonatais by Author "Carvalho, C."
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- Neonatal Hemophilia: A Rare PresentationPublication . Ferreira, N.; Proença, E.; Godinho, C.; Oliveira, D.; Guedes, A.; Morais, S.; Carvalho, C.Hemophilia A is a X-linked hereditary condition that lead to decreased factor VIII activity, occurs mainly in males. Decreased factor VIII activity leads to increased risk of bleeding events. During neonatal period, diagnosis is made after post-partum bleeding complication or unexpected bleeding after medical procedures. Subgaleal hemorrhage during neonatal period is a rare, severe extracranial bleeding with high mortality and usually related to traumatic labor or coagulation disorders. Subgaleal hemorrhage complications result from massive bleeding. We present a neonate with unremarkable family history and uneventful pregnancy with a vaginal delivery with no instrumentation, presenting with severe subgaleal bleeding at 52 hours of life. Aggressive support measures were implemented and bleeding managed. The unexpected bleeding lead to a coagulation study and the diagnosis of severe hemophilia A. There were no known sequelae. This case shows a rare hemophilia presentation reflecting the importance of coagulation studies when faced with unexplained severe bleeding.
- A Novel Noonan Syndrome RAF1 Mutation: Lethal Course in a Preterm InfantPublication . Ratola, A.; Silva, H.; Guedes, A.; Mota, C.; Braga, A.; Oliveira, D.; Alegria, A.; Carvalho, C.; Álvares, S.; Proença, E.Noonan syndrome is a relatively common and heterogeneous genetic disorder, associated with congenital heart defect in about 50% of the cases. If the defect is not severe, life expectancy is normal. We report a case of Noonan syndrome in a preterm infant with hypertrophic cardiomyopathy and lethal outcome associated to acute respiratory distress syndrome caused by Adenovirus pneumonia. A novel mutation in the RAF1 gene was identified: c.782C>G (p.Pro261Arg) in heterozygosity, not described previously in the literature. Consequently, the common clinical course in this mutation and its respective contribution to the early fatal outcome is unknown. No conclusion can be established regarding genotype/phenotype correlation.
- Prática ventilatória em recém-nascidos de extremo baixo pesoPublication . Ratola, A.; Silva, H.; Oliveira, D.; Carvalho, C.; Almeida, A.; Proença, E.Introdução: As práticas ventilatórias nos recém-nascidos de extremo baixo peso (RNEBP) têm vindo a alterar-se ao longo dos anos, havendo uma preocupação crescente em implementar estratégias protetoras do pulmão. O presente trabalho pretendeu caracterizar a prática ventilatória nos RNEBP numa unidade de cuidados intensivos neonatais. Métodos: Análise retrospetiva dos registos clínicos dos RNEBP, admitidos entre 01/09/2010 e 31/08/2013. Resultados: Foram admitidos 94 RNEBP (mediana peso 790 g), com idade gestacional de 23-32 semanas (mediana 27 semanas). Foi administrado pelo menos um ciclo de corticoide pré-natal em 65% e 69% receberam no mínimo uma dose de surfatante. Realizaram ventilação invasiva 74%, a maioria desde o nascimento, e 15% necessitaram de ventilação de alta frequência como resgate. Efetuaram ventilação não invasiva 70%, de forma exclusiva em 23% dos casos. Não precisaram de qualquer suporte ventilatório 3%. A mortalidade atingiu 31% (mediana idade gestacional 25 semanas), ocorrendo quase metade dos óbitos no primeiro dia de vida. Desenvolveram hemorragia pulmonar 7%, fuga aérea 5%, hemorragia intraperiventricular de grau III 22%, canal arterial hemodinamicamente significativo 23% e enterocolite necrosante 3%. O grupo que não realizou ventilação invasiva não apresentou hemorragia pulmonar, fuga aérea ou hemorragia intraperiventricular. Dos 65 sobreviventes, 20% desenvolveram displasia broncopulmonar moderada ou grave e 14% retinopatia da prematuridade (≥3/ doença plus). Discussão: O suporte ventilatório dos RNEBP tende a ser progressivamente mais protetor. No grupo analisado, a quase totalidade dos recém-nascidos necessitou de apoio ventilatório, mas cerca de um quarto realizou apenas ventilação não invasiva. A mortalidade global foi elevada, atingindo sobretudo os mais imaturos e em cerca de metade ocorreu no primeiro dia.
- Prenatal Diagnosis and Management of a Fetal Goiter Hypothyroidism due to DyshormonogenesisPublication . Figueiredo, C.; Falcão, I.; Vilaverde, J.; Freitas, J.; Oliveira, M.; Godinho, C.; Dores, J.; Rodrigues, M.; Carvalho, C.; Borges, T.Fetal goiter is a rare disorder not expected to be found during a healthy woman's pregnancy. It can be a prenatal manifestation of congenital hypothyroidism due to thyroid dyshormonogenesis and it can lead to serious perinatal complications. A vascularized fetal neck mass was detected at 29 weeks' gestation of a healthy primigravida. Magnetic resonance was suggestive of goiter causing airway deviation without polyhydramnios. Maternal thyroid function was normal and thyroid antibodies were negative. Two intra-amniotic levothyroxine infusions were performed at 32 and 33 weeks. Serial imaging control showed no progression of the mass. Elective caesarean section was performed at 38 weeks. The male newborn was admitted to the intensive care unit due to cardiorespiratory insufficiency with pulmonary hypertension. Hormonal assays revealed primary congenital hypothyroidism and ultrasonography confirmed diffuse goiter. Levothyroxine was started. Currently, he is 6 years old with adequate growth and normal psychomotor development. Genetic study found a heterozygous mutation in the TPO gene.