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Event Videos
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https://www.ncbi.nlm.nih.gov/pubmed/27663215 Usatin D, Fernandes M, Allen IE, Perito ER, Ostroff J, Heyman MB. J Pediatr. 2016 Dec;179:160-165.e3. doi: 10.1016/j.jpeds.2016.08.046. Abstract OBJECTIVES: To systematically review risks and summarize reported complication rates associated with the performance of endoscopic retrograde cholangiopancreatography (ERCP) in children during the past 2 decades. STUDY DESIGN: Published on:
Dec-2016
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https://www.ncbi.nlm.nih.gov/pubmed/27749391 Lungren MP, Lindquester WS, Seidel FG, Kothary N, Monroe EJ, Shivaram G, Gill AE, Hawkins MC. J Pediatr Gastroenterol Nutr. 2016 Dec;63(6):e147-e151 Abstract OBJECTIVES: The aim of the study was to describe and assess the technical success and safety of ultrasound-guided liver biopsy with gelatin sponge pledget tract embolization technique in infants <10 kg across 3 tertiary pediatric hospitals. MATERIALS AND METHODS: Published on:
Dec-2016
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https://www.ncbi.nlm.nih.gov/pubmed/26910645 Liver transplantation Prytula A, Vandekerckhove K, Raes A, De Wolf D, Dehoorne J, Vande Walle J, De Bruyne R. J Pediatr Gastroenterol Nutr. 2016 Dec;63(6):616-623. Abstract BACKGROUND: The aim of the study was to analyze the incidence of hypertension in pediatric liver transplantation (LT) recipients using ambulatory blood pressure measurements (ABPM) and to identify factors associated with hypertension. We also investigated whether hypertension or tacrolimus predose concentration (TAC C0) was associated with increased left ventricular (LV) wall thickness. PATIENTS AND METHODS: Published on:
Nov-2016
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https://www.ncbi.nlm.nih.gov/pubmed/27569726 Schwimmer JB, Lavine JE, Wilson LA, Neuschwander-Tetri BA, Xanthakos SA, Kohli R, Barlow SE, Vos MB, Karpen SJ, Molleston JP, Whitington PF, Rosenthal P, Jain AK, Murray KF, Brunt EM, Kleiner DE, Van Natta ML, Clark JM, Tonascia J, Doo E; NASH CRN. Gastroenterology. 2016 Dec;151(6):1141-1154.e9. doi: 10.1053/j.gastro.2016.08.027. Abstract BACKGROUND & AIMS: No treatment for nonalcoholic fatty liver disease (NAFLD) has been approved by regulatory agencies. We performed a randomized controlled trial to determine whether 52 weeks of cysteamine bitartrate delayed release (CBDR) reduces the severity of liver disease in children with NAFLD. METHODS: Published on:
Dec-2016
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https://www.ncbi.nlm.nih.gov/pubmed/27130505 Alam S, Sood V. Indian J Pediatr. 2016 Nov;83(11):1321-1333. Published on:
Nov-2016
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https://www.ncbi.nlm.nih.gov/pubmed/28027587 Wang KS, Tiao G, Bass LM, Hertel PM, Mogul D, Kerkar N, Clifton M, Azen C, Bull L, Rosenthal P, Stewart D, Superina R, Arnon R, Bozic M, Brandt ML, Dillon PA, Fecteau A, Iyer K, Kamath B, Karpen S, Karrer F, Loomes KM, Mack C, Mattei P, Miethke A, Soltys K, Turmelle YP, West K, Zagory J, Goodhue C, Shneider BL; the Childhood Liver Disease Research Network (ChiLDReN).. Hepatology. 2016 Dec 27. doi: 10.1002/hep.29019. Abstract Published on:
Dec-2016
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https://www.ncbi.nlm.nih.gov/pubmed/27504812 Valentino PL, Wiggins S, Harney S, Raza R, Lee CK, Jonas MM. J Pediatr Gastroenterol Nutr. 2016 Dec;63(6):603-609. Abstract OBJECTIVES: Data regarding pediatric primary sclerosing cholangitis (PSC) natural history are limited. We describe a large pediatric PSC cohort with longitudinal follow-up. METHODS: The present study records review of pediatric patients with PSC diagnosed between 1984 and 2014. RESULTS: Published on:
Nov-2016
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https://www.ncbi.nlm.nih.gov/pubmed/28045774 Sood V, Rawat D, Khanna R, Sharma S, Gupta PK, Alam S, Sarin SK. J Pediatr Gastroenterol Nutr. 2016 Dec 30. doi: 10.1097/MPG.0000000000001510. Abstract OBJECTIVES: Fatty acid oxidation defects (FAODs) may underlie or modify the course of acute liver failure (ALF). Overall significance of carnitine/acylcarnitine and aminoacid profile in ALF is similarly undetermined. Thus, this study was undertaken to study the abnormalities in carnitine/acylcarnitine and aminoacid profile in ALF. PATIENTS AND METHODS: A prospective study was performed including all cases of ALF and detailed evaluation including metabolic testing was done. RESULTS: Published on:
Dec-2016
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https://www.ncbi.nlm.nih.gov/pubmed/27504812 Valentino PL, Wiggins S, Harney S, Raza R, Lee CK, Jonas MM. J Pediatr Gastroenterol Nutr. 2016 Dec;63(6):603-609. Abstract OBJECTIVES: Data regarding pediatric primary sclerosing cholangitis (PSC) natural history are limited. We describe a large pediatric PSC cohort with longitudinal follow-up. METHODS: The present study records review of pediatric patients with PSC diagnosed between 1984 and 2014. RESULTS: Published on:
Nov-2016
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