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Your search keyword '"Ville de Goyet, Jean"' showing total 29 results
Start Over Author "Ville de Goyet, Jean" Publisher wiley
29 results on '"Ville de Goyet, Jean"'

3. Featured Cover

Author

de Ville de Goyet, Jean, primary, di Francesco, Fabrizio, additional, Cintorino, Davide, additional, Bici, Kejd, additional, Dona, Diletta, additional, Bonsignore, Pasquale, additional, and Gruttadauria, Salvatore, additional

Published
2024
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14. Focal congenital hyperinsulinism managed by medical treatment: a diagnostic algorithm based on molecular genetic screening

Author

Maiorana, Arianna, primary, Barbetti, Fabrizio, additional, Boiani, Arianna, additional, Rufini, Vittoria, additional, Pizzoferro, Milena, additional, Francalanci, Paola, additional, Faletra, Flavio, additional, Nichols, Colin G., additional, Grimaldi, Chiara, additional, de Ville de Goyet, Jean, additional, Rahier, Jacques, additional, Henquin, Jean-Claude, additional, and Dionisi-Vici, Carlo, additional

Published
2014
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20. Expert pediatric opinion on the Report of the Baveno IV Consensus Workshop on Methodology of Diagnosis and Therapy in Portal Hypertension

Author

Shneider, Benjamin, primary, Emre, Sukru, additional, Groszmann, Roberto, additional, Karani, John, additional, McKiernan, Patrick, additional, Sarin, Shiv, additional, Shashidhar, Harohalli, additional, Squires, Robert, additional, Superina, Riccardo, additional, de Ville de Goyet, Jean, additional, and de Franchis, Roberto, additional

Published
2006
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27. Unusual Tract and Complication of a Percutaneous Gastrostomy Tube.

Author

Adorisio O and de Ville de Goyet J

Subjects
Child, Endoscopy, Gastrointestinal methods, Enteral Nutrition adverse effects, Enteral Nutrition methods, Humans, Intubation, Gastrointestinal methods, Male, Endoscopy, Gastrointestinal adverse effects, Gastrostomy adverse effects, Intubation, Gastrointestinal adverse effects, Liver injuries
Published
2017
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28. Long-term outcome of home parenteral nutrition in patients with ultra-short bowel syndrome.

Author

Diamanti A, Conforti A, Panetta F, Torre G, Candusso M, Bagolan P, Papa RE, Grimaldi C, Fusaro F, Capriati T, Elia D, and De Ville de Goyet J

Subjects
Child, Child Development, Child, Preschool, Female, Follow-Up Studies, Humans, Infant, Infant, Newborn, Intestine, Small physiopathology, Male, Retrospective Studies, Short Bowel Syndrome physiopathology, Survival Rate, Time Factors, Liver Diseases etiology, Parenteral Nutrition, Home, Short Bowel Syndrome complications, Short Bowel Syndrome therapy
Abstract

Objective: The patients with ultra-short bowel syndrome (U-SBS) have been considered potential candidates for a preemptive/rehabilitative intestinal transplantation owing to the high risk of death from the underlying disease. We hypothesized that children with U-SBS, in the absence of intestinal failure-associated liver disease (IFALD), could also have a good rate of survival on home parenteral nutrition (HPN)., Methods: A prospective database from the "Bambino Gesù" Artificial Nutrition and Intestinal Failure Program was used to evaluate outcomes and morbidities of consecutive patients with ≤ 10 cm of small bowel enrolled since 2000., Results: Eleven patients were identified with a median bowel length of 7.5 (3-9) cm. Eight patients developed IFALD, which reversed in 7 of them; the IFALD progressively worsened in 1 patient until death. One patient underwent isolated intestinal transplantation and 1 patient is no longer receiving parenteral nutrition (PN) and both are fully enterally fed. The other patients remained at least partially dependent on HPN. The number of days of inpatient care decreased in all of the patients except for the 1 who had repeated episodes of central line infections., Conclusions: The survival of patients with U-SBS receiving HPN was good. Although IFALD was frequent, it had been manageable in most of the patients, but in a single complex case, it led to death. The multidisciplinary management warranted to these patients to approach the school age, to grow, and to maintain the oral intake. Patients with U-SBS are rare, and to better understand their long-term survival, further studies, including more large patient populations, are required.

Published
2014
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