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1.
J Pediatr ; 264: 113780, 2024 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-37852434

RESUMO

OBJECTIVE: To evaluate in the Netherlands the national outcomes in providing cause of and insights into sudden and unexplained child deaths among children via the Postmortem Evaluation of Sudden Unexplained Death in Youth (PESUDY) procedure. STUDY DESIGN: Children aged 0-18 years in the Netherlands who died suddenly were included in the PESUDY procedure if their death was unexplained and their parents gave consent. The PESUDY procedure consists of pediatric and forensic examination, biochemical, and microbiological tests; radiologic imaging; autopsy; and multidisciplinary discussion. Data on history, modifiable factors, previous symptoms, performed diagnostics, and cause of death were collected between October 2016 and December 2021. RESULTS: In total, 212 cases (median age 11 months, 56% boys, 33% comorbidity) were included. Microbiological, toxicological, and metabolic testing was performed in 93%, 34%, and 32% of cases. In 95% a computed tomography scan or magnetic resonance imaging was done and in 62% an autopsy was performed. The cause of death was explained in 58% of cases and a plausible cause was identified in an additional 13%. Most children died from infectious diseases. Noninfectious cardiac causes were the second leading cause of death found. Modifiable factors were identified in 24% of non-sudden infant death syndrome/unclassified sudden infant death cases and mostly involved overlooked alarming symptoms. CONCLUSIONS: The PESUDY procedure is valuable and effective for determining the cause of death in children with sudden unexplained deaths and for providing answers to grieving parents and involved health care professionals.


Assuntos
Morte Súbita do Lactente , Lactente , Masculino , Adolescente , Criança , Humanos , Feminino , Morte Súbita do Lactente/diagnóstico , Morte Súbita do Lactente/epidemiologia , Morte Súbita do Lactente/etiologia , Autopsia , Imageamento por Ressonância Magnética , Países Baixos/epidemiologia , Causas de Morte
2.
JPEN J Parenter Enteral Nutr ; 36(5): 538-50, 2012 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22549765

RESUMO

BACKGROUND: We previously showed that parenteral nutrition (PN) compared with formula feeding results in hepatic insulin resistance and steatosis in neonatal pigs. The current aim was to test whether the route of feeding (intravenous [IV] vs enteral) rather than other feeding modalities (diet, pattern) had contributed to the outcome. METHODS: Neonatal pigs were fed enterally or parenterally for 14 days with 1 of 4 feeding modalities as follows: (1) enteral polymeric formula intermittently (FORM), (2) enteral elemental diet (ED) intermittently (IEN), (3) enteral ED continuously (CEN), and (4) parenteral ED continuously (PN). Subgroups of pigs underwent IV glucose tolerance tests (IVGTT) and hyperinsulinemic-euglycemic clamps (CLAMP). Following CLAMP, pigs were euthanized and tissues collected for further analysis. RESULTS: Insulin secretion during IVGTT was significantly higher and glucose infusion rates during CLAMP were lower in CEN and PN than in FORM and IEN. Endogenous glucose production rate was suppressed to zero in all groups during CLAMP. In the fed state, plasma glucose-dependent insulinotropic polypeptide (GIP), glucagon-like peptide (GLP)-1, and GLP-2 were different between feeding modalities. Insulin receptor phosphorylation in liver and muscle was decreased in IEN, CEN, and PN compared with FORM. Liver weight was highest in PN. Steatosis and myeloperoxidase (MPO) activity tended to be highest in PN and CEN. Enterally fed groups had higher plasma GLP-2 and jejunum weight compared with PN. CONCLUSIONS: PN and enteral nutrition (EN) when given continuously as an elemental diet reduces insulin sensitivity and the secretion of key gut incretins. The intermittent vs continuous pattern of EN produced the optimal effect on metabolic function.


Assuntos
Nutrição Enteral/métodos , Doenças Metabólicas/etiologia , Nutrição Parenteral/métodos , Administração Intravenosa , Animais , Animais Recém-Nascidos , Glicemia/análise , Determinação de Ponto Final , Nutrição Enteral/efeitos adversos , Fígado Gorduroso/fisiopatologia , Feminino , Alimentos Formulados , Peptídeo 1 Semelhante ao Glucagon/metabolismo , Peptídeo 2 Semelhante ao Glucagon/metabolismo , Incretinas/metabolismo , Inflamação/fisiopatologia , Insulina/sangue , Insulina/metabolismo , Resistência à Insulina , Secreção de Insulina , Intestino Delgado/efeitos dos fármacos , Intestino Delgado/crescimento & desenvolvimento , Fígado/efeitos dos fármacos , Fígado/metabolismo , Doenças Metabólicas/fisiopatologia , Dinâmica não Linear , Tamanho do Órgão/efeitos dos fármacos , Nutrição Parenteral/efeitos adversos , Suínos
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