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特发性胆汁酸吸收不良:定性和定量临床特征及对考来烯胺的反应

Idiopathic bile acid malabsorption: qualitative and quantitative clinical features and response to cholestyramine.

作者信息

Sinha L, Liston R, Testa H J, Moriarty K J

机构信息

Department of Gastroenterology, Bolton General Hospital, Farnworth, UK.

出版信息

Aliment Pharmacol Ther. 1998 Sep;12(9):839-44. doi: 10.1046/j.1365-2036.1998.00388.x.

Abstract

BACKGROUND

Idiopathic bile acid malabsorption is a poorly recognized cause of chronic diarrhoea. The SeHCAT (75Selenium HomotauroCholic Acid Test) can accurately diagnose this condition.

AIM

To identify patients with idiopathic bile acid malabsorption, to describe their clinical features, both qualitatively and quantitatively, and to assess the response to cholestyramine.

METHOD

Idiopathic bile acid malabsorption was considered in all patients complaining of chronic diarrhoea. They were included in the study if their SeHCATs were positive (< 15% retention) and secondary causes of bile acid malabsorption were excluded. The response to therapy with cholestyramine was assessed.

RESULTS

Nine patients were diagnosed with idiopathic bile acid malabsorption (median SeHCAT retention 8%, range 3-12.6). Their median daily faecal weight was 285 g (range 85-676) and median faecal fat output was 17 mmol/24 h (range 8.3-38.8). Six patients had an immediate response to cholestyramine. There was a marked reduction in stool frequency (median stool frequency pre-treatment 5/day vs. 2/day post-treatment, P = 0.03). Five patients had large volume diarrhoea (faecal weight > 200 g/day) and three had steatorrhoea.

CONCLUSIONS

Idiopathic bile acid malabsorption, once suspected, especially by documenting true 'large volume' watery diarrhoea or steatorrhoea, is easily diagnosed and response to therapy is often very good. There is often a previous history of gastrointestinal infection and this condition should be considered in patients with chronic diarrhoea of undetermined origin, especially before they are labelled as having irritable bowel syndrome.

摘要

背景

特发性胆汁酸吸收不良是慢性腹泻的一个鲜为人知的病因。硒-同型牛磺胆酸试验(SeHCAT)可准确诊断该病。

目的

识别特发性胆汁酸吸收不良患者,定性和定量描述其临床特征,并评估对考来烯胺的反应。

方法

所有主诉慢性腹泻的患者均被考虑患有特发性胆汁酸吸收不良。若其SeHCAT试验结果为阳性(潴留<15%)且排除胆汁酸吸收不良的继发原因,则纳入本研究。评估考来烯胺治疗的反应。

结果

9例患者被诊断为特发性胆汁酸吸收不良(SeHCAT潴留中位数为8%,范围3%-12.6%)。他们的每日粪便重量中位数为285克(范围85-676克),粪便脂肪排出量中位数为17毫摩尔/24小时(范围8.3-38.8毫摩尔/24小时)。6例患者对考来烯胺立即产生反应。大便频率显著降低(治疗前大便频率中位数为5次/天,治疗后为2次/天,P=0.03)。5例患者有大量腹泻(粪便重量>200克/天),3例有脂肪泻。

结论

特发性胆汁酸吸收不良一旦被怀疑,尤其是通过记录真正的“大量”水样腹泻或脂肪泻,很容易诊断,且对治疗的反应通常非常好。患者常有胃肠道感染史,对于病因不明的慢性腹泻患者,尤其是在被诊断为肠易激综合征之前,应考虑此病。

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