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广泛小肠切除术后短肠综合征的管理

Management of the short bowel syndrome after extensive small bowel resection.

作者信息

Keller Jutta, Panter Heidi, Layer Peter

机构信息

Israelitic Hospital, Orchideenstieg 14, 22297 Hamburg, Germany.

出版信息

Best Pract Res Clin Gastroenterol. 2004 Oct;18(5):977-92. doi: 10.1016/j.bpg.2004.05.002.

Abstract

Short bowel syndrome (SBS) is a global malabsorption syndrome that results from extensive intestinal resections. It used to be a typical complication of repetitive bowel resections in patients with Crohn's disease. However, due to improved medical and surgical therapies for these patients it currently occurs more frequently as a consequence of vascular disorders in adults (intestinal infarction) and congenital aberrations in children, respectively. Adequate therapy depends on the degree of (small) bowel losses and on resulting functional disturbances. Moreover, it must be adjusted to the postoperative adaptation process, which consists of three phases: The immediate acute phase lasts less than 4 weeks and serves to stabilise the patient. The subsequent year should be used to induce maximal adaptation by gradually increasing nutrient exposure. When maximal stimulation of nutrient absorption has been achieved, permanent maintenance nutrition treatment should be defined individually, dependent on extent and quality of nutritive deficits. In patients with Crohn's disease, optimal treatment of the underlying disease is of pivotal importance in order to avoid a further reduction of absorptive capacity or other complications. Current investigations aim at improving the adaptation process by administration of specific diets and growth hormones. With these, it appears possible to treat even some patients with very short bowel, i.e. less than 50 cm of small intestine left, with oral nutrition, only. Still, a considerable proportion of patients will need long-term parenteral nutrition. If young patients experience intolerable complications of parenteral nutrition, intestinal transplantation may be considered as a high risk therapy of last choice.

摘要

短肠综合征(SBS)是一种由于广泛肠道切除导致的全身性吸收不良综合征。它曾是克罗恩病患者反复肠道切除的典型并发症。然而,由于针对这些患者的内科和外科治疗方法有所改进,目前该综合征在成人中更常见于血管疾病(肠梗死),在儿童中则更常见于先天性畸形。适当的治疗取决于(小肠)丢失的程度以及由此产生的功能障碍。此外,治疗必须根据术后适应过程进行调整,该过程包括三个阶段:即刻急性期持续不到4周,目的是使患者病情稳定。随后的一年应通过逐渐增加营养接触来诱导最大程度的适应。当实现营养吸收的最大刺激后,应根据营养缺乏的程度和性质,为患者个体化确定长期维持营养治疗方案。对于克罗恩病患者,为避免吸收能力进一步下降或出现其他并发症,对基础疾病进行最佳治疗至关重要。目前的研究旨在通过给予特定饮食和生长激素来改善适应过程。通过这些方法,似乎甚至有可能仅通过口服营养来治疗一些小肠非常短(即剩余小肠不足50厘米)的患者。尽管如此,仍有相当一部分患者需要长期肠外营养。如果年轻患者出现难以耐受的肠外营养并发症,可考虑将肠道移植作为最后选择的高风险治疗方法。

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