Susan M. Protheroe MRCP (Specialist Registrar), Deirdre A. Kelly MD, FRCPI, FRCP (Consultant Paediatric Hepatologist Reader in Paediatric Hepatology University of Birmingham)
{"title":"10 Cholestasis and end-stage liver disease","authors":"Susan M. Protheroe MRCP (Specialist Registrar), Deirdre A. Kelly MD, FRCPI, FRCP (Consultant Paediatric Hepatologist Reader in Paediatric Hepatology University of Birmingham)","doi":"10.1016/S0950-3528(98)90010-0","DOIUrl":null,"url":null,"abstract":"<div><p>Protein-energy malnutrition is an inevitable consequence of chronic liver disease, particularly in the developing infant. Severe malnutrition with loss of fat stores and muscle wasting affects between 60% and 80% of infants with liver disease (<span>Beath, 1993a</span>; <span>Holt et al, 1997</span>). Reduced energy intake secondary to anorexia, vomiting and fat malabsorption, in association with a disordered metabolism of carbohydrate and protein, increased energy requirements and vitamin and mineral deficiencies, contributes towards growth failure. Reversal of malnutrition is one of the key aims of liver transplantation and is achieved in the majority of long-term survivors. The aetiology of persistent growth failure posttransplantation is multifactorial and is related to pre-operative malnutrition, glucocorticoid administration, feeding problems and post-operative complications. Strategies to prevent pre- and post-transplant growth failure include early referral for liver transplantation and a multidisciplinary approach to nutritional support, which may increase survival and improve the quality of life and outcome of liver transplantation.</p></div>","PeriodicalId":77028,"journal":{"name":"Bailliere's clinical gastroenterology","volume":"12 4","pages":"Pages 823-841"},"PeriodicalIF":0.0000,"publicationDate":"1998-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0950-3528(98)90010-0","citationCount":"14","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bailliere's clinical gastroenterology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0950352898900100","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 14
Abstract
Protein-energy malnutrition is an inevitable consequence of chronic liver disease, particularly in the developing infant. Severe malnutrition with loss of fat stores and muscle wasting affects between 60% and 80% of infants with liver disease (Beath, 1993a; Holt et al, 1997). Reduced energy intake secondary to anorexia, vomiting and fat malabsorption, in association with a disordered metabolism of carbohydrate and protein, increased energy requirements and vitamin and mineral deficiencies, contributes towards growth failure. Reversal of malnutrition is one of the key aims of liver transplantation and is achieved in the majority of long-term survivors. The aetiology of persistent growth failure posttransplantation is multifactorial and is related to pre-operative malnutrition, glucocorticoid administration, feeding problems and post-operative complications. Strategies to prevent pre- and post-transplant growth failure include early referral for liver transplantation and a multidisciplinary approach to nutritional support, which may increase survival and improve the quality of life and outcome of liver transplantation.
蛋白质能量营养不良是慢性肝病不可避免的后果,特别是在发育中的婴儿。60%至80%患有肝病的婴儿患有严重营养不良、脂肪储存减少和肌肉萎缩(Beath, 1993年a;Holt et al ., 1997)。厌食症、呕吐和脂肪吸收不良引起的能量摄入减少,与碳水化合物和蛋白质代谢紊乱、能量需求增加以及维生素和矿物质缺乏有关,是导致生长衰竭的原因。逆转营养不良是肝移植的主要目标之一,大多数长期幸存者都能实现这一目标。移植后持续生长衰竭的病因是多因素的,与术前营养不良、糖皮质激素的使用、喂养问题和术后并发症有关。预防移植前和移植后生长衰竭的策略包括肝移植的早期转诊和多学科的营养支持方法,这可能会增加生存率,改善肝移植的生活质量和预后。