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口服他克莫司(FK506)治疗复杂性近端小肠及瘘管性克罗恩病的初步报告

Preliminary report on the use of oral tacrolimus (FK506) in the treatment of complicated proximal small bowel and fistulizing Crohn's disease.

作者信息

Sandborn W J

机构信息

Inflammatory Bowel Disease Clinic, Division of Gastroenterology, Mayo Clinic and Mayo Foundation, Rochester, Minnesota 55905, USA.

出版信息

Am J Gastroenterol. 1997 May;92(5):876-9.

PMID:9149205
Abstract

BACKGROUND

Tacrolimus (FK506) has a mechanism of action similar to cyclosporine. Unlike standard oral cyclosporine, tacrolimus is well absorbed orally, even from diseased small bowel mucosa.

OBJECTIVE

To report the use of oral tacrolimus in three patients with complicated proximal small bowel or fistulizing Crohn's disease as a "bridge" to methotrexate or 6-mercaptopurine.

CASE REPORTS

Oral tacrolimus was started at doses of 0.15-0.29 mg/kg/day and adjusted to a whole blood tacrolimus concentration range of 10-20 ng/ml. Case 1: Gastroenterostomy for gastroduodenal Crohn's disease complicated by recurrent gastrointestinal hemorrhage from persistent duodenal ulceration. Case 2: Diffuse jejunoileal Crohn's disease, seven prior stricturoplasties, and a postoperative small intestinal fistula causing an abdominal abscess. Case 3: Perianal and pouch-vaginal fistulae after colectomy and ileal pouch-anal anastomosis in a patient with Crohn's disease. All three patients had good oral absorption of tacrolimus, rapid clinical improvement of their Crohn's disease, and began long-term remission maintenance treatment with either methotrexate (n = 2) or 6-mercaptopurine (n = 1). Dose dependent side effects resulting from tacrolimus therapy occurred in all three patients (nephrotoxicity, hyperkalemia, diarrhea, nausea, flushing, headache, tremor, paresthesias, and insomnia).

CONCLUSIONS

Oral tacrolimus (0.15-0.29 mg/kg/day) is well absorbed in patients with Crohn's disease with proximal small bowel involvement or fistulae and appears to be of clinical benefit as a rapidly acting "bridge" to long-term therapy with methotrexate or 6-mercaptopurine.

摘要

背景

他克莫司(FK506)的作用机制与环孢素相似。与标准口服环孢素不同,他克莫司口服吸收良好,即使是从患病的小肠黏膜也能有效吸收。

目的

报告口服他克莫司在3例患有复杂近端小肠病变或瘘管性克罗恩病患者中作为甲氨蝶呤或6-巯基嘌呤的“桥梁”的应用情况。

病例报告

口服他克莫司起始剂量为0.15 - 0.29mg/kg/天,并调整至全血他克莫司浓度范围为10 - 20ng/ml。病例1:胃十二指肠克罗恩病行胃肠吻合术,并发持续性十二指肠溃疡反复胃肠道出血。病例2:弥漫性空回肠克罗恩病,既往行7次狭窄成形术,术后小肠瘘导致腹腔脓肿。病例3:克罗恩病患者在结肠切除术后回肠储袋肛管吻合术后出现肛周和储袋 - 阴道瘘。所有3例患者他克莫司口服吸收良好,克罗恩病临床症状迅速改善,并开始用甲氨蝶呤(n = 2)或6-巯基嘌呤(n = 1)进行长期缓解维持治疗。所有3例患者均出现他克莫司治疗引起的剂量依赖性副作用(肾毒性、高钾血症、腹泻、恶心、潮红、头痛、震颤、感觉异常和失眠)。

结论

口服他克莫司(0.15 - 0.29mg/kg/天)在患有近端小肠受累或瘘管的克罗恩病患者中吸收良好,作为甲氨蝶呤或6-巯基嘌呤长期治疗的快速起效“桥梁”似乎具有临床益处。

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