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Short bowel syndrome.

机译:短肠综合征。

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摘要

Short bowel syndrome is an uncommon disease that results from extensive intestinal resection. Short bowel patients develop severe malabsorption of macronutrients, micronutrients, electrolytes and water, and pose difficult management problems. This report describes a typical patient with the short bowel syndrome and how each component of the malabsorption syndrome is managed to maintain nutritional, electrolyte, and water balance. In practice, some short bowel patients become dependent on parenteral nutrition for life, while others become independent with time due to intestinal adaptation and can be managed on oral intake and supplementations. Short bowel patients are at risk of developing gallstones, oxalate kidney stones and, rarely, d-lactic acidosis, and the pathophysiology of these disease processes is outlined. A minority of short bowel patients may ultimately require intestinal transplantation due to irreversible complications, and the current status of this intervention is reviewed. Finally, growth factors that stimulate intestinal growth and, thus, enhance absorptive capacity, are currently being identified and may eventually be introduced in the treatment of these patients.
机译:短肠综合征是由广泛的肠切除术引起的罕见疾病。短肠患者会吸收大量营养素,微量营养素,电解质和水,严重吸收不良,并带来管理难题。该报告描述了典型的患有短肠综合征的患者,以及吸收不良综合征的各个组成部分如何进行管理以维持营养,电解质和水的平衡。在实践中,一些短肠患者终生依赖肠胃外营养,而其他人则由于肠道适应而随着时间的流逝而变得独立,可以通过口服和补充口服来治疗。短肠患者有发展胆结石,草酸盐肾结石的风险,极少出现d-乳酸性酸中毒,并且概述了这些疾病过程的病理生理学。少数短肠患者可能由于不可逆的并发症而最终需要肠移植,目前对该治疗的现状进行了回顾。最后,目前正在鉴定刺激肠生长并因此增强吸收能力的生长因子,并最终将其引入这些患者的治疗中。

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