Suppr超能文献

短肠综合征患儿长期随访中的营养与免疫状态

Nutrition and immunological status in long-term follow up of children with short bowel syndrome.

作者信息

González Horacio F, Pérez Néstor B, Malpeli Agustina, Martínez María I, Del Buono Beatriz, Viteri Fernando E

机构信息

Instituto de Desarrollo e Investigaciones Pediátricas, Hospital de Niños Sor María Ludovica, Calle 16 No 1069 1900, La Plata, Argentina.

出版信息

JPEN J Parenter Enteral Nutr. 2005 May-Jun;29(3):186-91. doi: 10.1177/0148607105029003186.

Abstract

BACKGROUND

Little is known about the long-term evolution, nutrition status, growth, and eventual deficiencies of patients with short bowel syndrome (SBS) adapted to oral feeding after parenteral nutrition (PN). Because there are not absolute criteria for weaning from parenteral or enteral nutrition to oral feeding, new nutrient deficiencies may develop. Subtle nutrition deficits could induce subclinical immune deficiencies; therefore, we studied long-term growth, nutrition status, and the state of the immune system in 10 patients with SBS after weaning PN for at least 2 years.

METHODS

Ten children with SBS (3-12 years old; mean, 7.4 years) who had not received PN for at least 2 years were studied. Anthropometric measurements, hemoglobin values, and indicators of iron, zinc, copper, folate and vitamin B(12) nutrition status were evaluated, along with immunoglobulins, lymphocyte subpopulations, and polymorphonuclear candidicidal activity.

RESULTS

Weight-for-height was normal in 8 children; height-for-age was low in 5 children whose SBS was established early in life. Fat body mass was also low in 5 subjects. Four children presented macrocytosis, 2 with anemia. Low serum levels of vitamin B(12) (1 child), folates (4 children), and ferritin (2 children) were observed. Diminished candidicidal activity (4 children) was the only remarkable immunological abnormality.

CONCLUSION

Many biologic and growth deficiencies are frequently seen in patients with SBS, even in children adapted to enteral feeding. This finding and the existence of previously unreported decreased candidicidal activity in some patients with SBS deserve long-term clinical and biologic follow up.

摘要

背景

对于经肠外营养(PN)后适应口服喂养的短肠综合征(SBS)患者的长期演变、营养状况、生长及最终出现的营养缺乏情况,人们了解甚少。由于从肠外或肠内营养过渡到口服喂养尚无绝对标准,可能会出现新的营养缺乏。细微的营养缺乏可能会引发亚临床免疫缺陷;因此,我们研究了10例经肠外营养撤机至少2年的短肠综合征患者的长期生长、营养状况及免疫系统状态。

方法

研究了10例年龄在3至12岁(平均7.4岁)且已停用肠外营养至少2年的短肠综合征患儿。评估了人体测量指标、血红蛋白值、铁、锌、铜、叶酸和维生素B12营养状况指标,以及免疫球蛋白、淋巴细胞亚群和多形核白细胞杀念珠菌活性。

结果

8名儿童的身高体重比正常;5名早年确诊短肠综合征的儿童年龄别身高较低。5名受试者的体脂量也较低。4名儿童出现大细胞性贫血,其中2名伴有贫血。观察到1名儿童血清维生素B12水平低,4名儿童叶酸水平低,2名儿童铁蛋白水平低。杀念珠菌活性降低(4名儿童)是唯一显著的免疫异常。

结论

短肠综合征患者常出现多种生物学和生长方面的缺乏,即使是适应肠内喂养的儿童也不例外。这一发现以及部分短肠综合征患者存在此前未报道的杀念珠菌活性降低情况,值得进行长期临床和生物学随访。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验