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1.
Minerva Pediatr ; 62(4): 411-7, 2010 Aug.
Artigo em Italiano | MEDLINE | ID: mdl-20940674

RESUMO

Congenital chylothorax is a rare condition characterized by the accumulation of lymph fluid in the pleural space that causes respiratory and circulatory dysfunctions, immune deficiencies, hypoalbuminemia, electrolyte imbalance and alterations of the coagulation. Mortality rates are elevated and can rise to 50%. Therapy consists in conservative treatment based on thoracic drainage combined with total parenteral nutrition or use of low-fat high-protein diet supplemented with medium chain triglycerides. In case of failure surgical intervention may be considered. During the last years some authors have experienced the use of octreotide with doubtful results. In no case the drug impact on insulin, GH and cortisol secretion in neonatal age has been investigated and only in one case the effect on thyroid hormones has been assessed. We report the case of a 36-week baby with congenital chylothorax treated with octreotide for 42 days. The drug was well tolerated but hormonal level measurements showed a deep depression of insulin secretion unaccompanied by alterations of glucose levels. Levels of GH and TSH showed only a transitory decrease. ACTH and cortisol remained normal. At 5 months, the measurements of hormonal levels did not show significant alterations. It is not possible to determine if such a drug played an essential role in the solution of the pleural effusion, but it is important to emphasize that a prolonged treatment with octreotide has not caused, in our case, persistent hormonal alterations.


Assuntos
Biomarcadores/sangue , Quilotórax/sangue , Quilotórax/tratamento farmacológico , Hormônios/sangue , Octreotida/administração & dosagem , Hormônio Adrenocorticotrópico/sangue , Quilotórax/congênito , Quilotórax/diagnóstico , Hormônio do Crescimento Humano/sangue , Humanos , Lactente , Insulina/sangue , Fator de Crescimento Insulin-Like I/metabolismo , Masculino , Octreotida/efeitos adversos , Tireotropina/sangue , Tireotropina/metabolismo , Tiroxina/sangue , Resultado do Tratamento , Tri-Iodotironina/sangue
2.
Minerva Pediatr ; 62(1): 29-41, 2010 Feb.
Artigo em Italiano | MEDLINE | ID: mdl-20212396

RESUMO

AIM: The aim of this study was to evaluate survival rates in a single Neonatal Intensive Care Unit (NICU) (period 2002-2007), with a special focus on the survival data and outcome at one-year of corrected age for infants born at 23-25 weeks of gestation. METHODS: All infants who had evidence of heart activity at birth were actively resuscitated, regardless of birth weight or gestational age. Survival rate was calculated as a function of the following variables: birth weight and gestational category; gender in infants of birth weight < or = 1000 g ; appropriate (AGA) or small (SGA) weight for gestational age; inborn or outborn. Twenty-eight newborns (23-25 weeks of gestation) completed follow-up at one-year of corrected age. RESULTS: During the examined period, no infants died in the delivery room; 833 newborns were admitted to the NICU. Overall survival rates were as following: <500 g (37%), 501-750 g (59%), 751-1,000 g (82%), 1,001-1,250 g (96%), 1251-1,500 g (97%), 1,501-2,000 g (100%), 2,001-2,500 g (98%), >2,500 g (99%); 23-25 weeks of gestation (50%); 26-27 weeks (77%), 28-32 weeks (90%); males < or = 1,000 g (68%), females < or = 1,000 g (68%); AGA < or = 1,000 g (63%), SGA < or = 1,000 g (79%), AGA < or =28 weeks (63%), SGA < or = 28 weeks (67%); inborn (54%), outborn (25%). A fraction of 64% (infants of 23-25 weeks of gestation) did not show handicap at one-year of corrected age, while 25% presented severe, 7% moderate, and 4% mild handicaps. CONCLUSION: High rate of survival without handicap at one-year of corrected age at extremely low gestational age and the chance of improvements in neonatal care for newborn < or = 24 weeks, indicate the appropriateness for our strategy of resuscitating all newborns with evidence of heart activity in the delivery room.


Assuntos
Recém-Nascido Prematuro/crescimento & desenvolvimento , Sistema Nervoso/crescimento & desenvolvimento , Feminino , Idade Gestacional , Humanos , Recém-Nascido , Unidades de Terapia Intensiva Neonatal , Masculino , Taxa de Sobrevida
3.
Pediatr Med Chir ; 20(5): 341-3, 1998.
Artigo em Italiano | MEDLINE | ID: mdl-10068984

RESUMO

The formation of biliary sludge and cholelithiasis after ceftriaxone administration is not uncommon. Prompt resolution of sludge has been demonstrated with discontinuation of the drug. Despite this, cholecystectomy has been performed in symptomatic patients. Ceftriaxone is popular drug in pediatrics, but the complication is not widely appreciated in the gastroenterology and surgical literature. For this adverse effect and for cost ceftriaxone should be used with more caution. We describe two cases of children with ceftriaxone induced cholelithiasis.


Assuntos
Ceftriaxona/efeitos adversos , Cefalosporinas/efeitos adversos , Colelitíase/induzido quimicamente , Criança , Colelitíase/diagnóstico por imagem , Feminino , Seguimentos , Humanos , Masculino , Fatores de Tempo , Ultrassonografia
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