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1.
J Surg Res ; 212: 229-237, 2017 05 15.
Artigo em Inglês | MEDLINE | ID: mdl-28550912

RESUMO

BACKGROUND: This pilot study focuses on regional tissue oxygenation (rSO2) in patients with infantile hypertrophic pyloric stenosis in a perioperative setting. To investigate the influence of enhanced metabolic alkalosis (MA) on cerebral (c-rSO2) and renal (r-rSO2) tissue oxygenation, two-site near-infrared spectroscopy (NIRS) technology was applied. MATERIALS AND METHODS: Perioperative c-rSO2, r-rSO2, capillary blood gases, and electrolytes from 12 infants were retrospectively compared before and after correction of MA at admission (T1), before surgery (T2), and after surgery (T3). RESULTS: Correction of MA was associated with an alteration of cerebral oxygenation without affecting renal oxygenation. When compared to T1, 5-min mean (± standard deviation) c-rSO2 increased after correction of MA at T2 (72.74 ± 4.60% versus 77.89 ± 5.84%; P = 0.058), reaching significance at T3 (80.79 ± 5.29%; P = 0.003). Furthermore, relative 30-min c-rSO2 values at first 3 h of metabolic compensation were significantly lowered compared with postsurgical states at 16 and 24 h. Cerebral oxygenation was positively correlated with levels of sodium (r = 0.37; P = 0.03) and inversely correlated with levels of bicarbonate (r = -0.34; P = 0.05) and base excess (r = -0.36; P = 0.04). Analysis of preoperative and postoperative cerebral and renal hypoxic burden yielded no differences. However, a negative correlation (r = -0.40; P = 0.03) regarding hematocrite and mean r-rSO2, indirectly indicative of an increased renal blood flow under hemodilution, was obtained. CONCLUSIONS: NIRS seems suitable for the detection of a transiently impaired cerebral oxygenation under state of pronounced MA in infants with infantile hypertrophic pyloric stenosis. Correction of MA led to normalization of c-rSO2. NIRS technology constitutes a promising tool for optimizing perioperative management, especially in the context of a possible diminished neurodevelopmental outcome after pyloromyotomy.


Assuntos
Alcalose/metabolismo , Encéfalo/metabolismo , Rim/metabolismo , Oxigênio/metabolismo , Estenose Pilórica Hipertrófica/fisiopatologia , Alcalose/etiologia , Alcalose/terapia , Biomarcadores/metabolismo , Feminino , Humanos , Lactente , Recém-Nascido , Masculino , Período Perioperatório , Projetos Piloto , Estenose Pilórica Hipertrófica/cirurgia , Estudos Retrospectivos , Espectroscopia de Luz Próxima ao Infravermelho
3.
J Pediatr Surg ; 45(10): 2064-7, 2010 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-20920732

RESUMO

We report the case of a newborn baby with a large congenital skull defect owing to Adams-Oliver syndrome. An initial attempt at conservative treatment failed and led to disruption of the leptomeningeal membrane and prolapse of the brain. After local debridement, delayed and stepwise surgical closure was complicated by cerebrospinal fluid leakage, which required the insertion of a cerebrospinal fluid shunt. This case report highlights the potential serious risks of nonsurgical management of largely extended congenital skull defects.


Assuntos
Displasia Ectodérmica/patologia , Displasia Ectodérmica/terapia , Encefalocele/patologia , Encefalocele/terapia , Crânio/anormalidades , Vazamento de Líquido Cefalorraquidiano , Rinorreia de Líquido Cefalorraquidiano/cirurgia , Derivações do Líquido Cefalorraquidiano/métodos , Displasia Ectodérmica/diagnóstico por imagem , Encefalocele/diagnóstico por imagem , Humanos , Recém-Nascido , Deformidades Congênitas dos Membros/diagnóstico por imagem , Deformidades Congênitas dos Membros/patologia , Deformidades Congênitas dos Membros/terapia , Imageamento por Ressonância Magnética , Necrose/patologia , Radiografia , Couro Cabeludo/anormalidades , Couro Cabeludo/patologia , Dermatoses do Couro Cabeludo/congênito , Dermatoses do Couro Cabeludo/diagnóstico por imagem , Dermatoses do Couro Cabeludo/patologia , Dermatoses do Couro Cabeludo/terapia , Crânio/patologia
4.
J Pediatr Surg ; 44(8): 1646-8, 2009 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-19635321

RESUMO

We report a unique combination of an esophageal atresia without fistula associated with a tubular noncommunicating esophageal duplication. The diagnosis was made at delayed repair and led to a successful outcome.


Assuntos
Atresia Esofágica/diagnóstico , Atresia Esofágica/cirurgia , Esôfago/anormalidades , Anastomose Cirúrgica , Humanos , Recém-Nascido , Masculino
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