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病例报告:己酮可可碱治疗显微镜下结肠炎

Case report: Pentoxifylline treatment in microscopic colitis.

作者信息

Cotter Thomas G, Kamboj Amrit K, Hicks Stephen Bradley, Tremaine William J, Loftus Edward V, Pardi Darrell S

机构信息

aDepartment of Internal Medicine bDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.

出版信息

Medicine (Baltimore). 2017 Nov;96(46):e8355. doi: 10.1097/MD.0000000000008355.

Abstract

RATIONALE

Microscopic colitis is a common cause of diarrhea. Pentoxifylline, a xanthine derivative with anti-tumor necrosis factor-alpha properties, is prescribed for intermittent claudication and other disorders. Our goal was to evaluate the outcomes of patients with microscopic colitis treated with pentoxifylline.

PATIENT CONCERNS

Nine patients with microscopic colitis (8 collagenous colitis and 1 lymphocytic colitis) seen at Mayo Clinic, Rochester, between January 1, 1997 and November 30, 2016, were included. The median age was 56.9 years (range 51.6-60.2), 8 were female (89%), and the median disease duration was 64.8 months (range 60-109). The indications for treatment were budesonide refractoriness in 7 patients, budesonide dependence in 1 patient, and budesonide intolerance in 1 patient.

DIAGNOSES

A histological diagnosis of microscopic colitis was confirmed in all patients.

INTERVENTIONS

Pentoxifylline 400 mg three times a day was used for a median of 3 months (range 2.5-8.3).

OUTCOMES

Complete response occurred in 1 patient (11%) and partial response in 3 patients (33%). The patient who achieved complete response was treated with pentoxifylline due to budesonide intolerance, and completed 43 months of successful maintenance therapy. There were no adverse effects reported.

LESSONS

The majority of budesonide-experienced patients with active microscopic colitis did not respond to pentoxifylline. However, it was well-tolerated, with 1 patient achieving long-term remission and one-third of the cohort having a partial response. Larger controlled studies are required to evaluate the efficacy of pentoxifylline and predictors of response in microscopic colitis. In particular, patients who are not budesonide-refractory may be more likely to respond.

摘要

理论依据

显微镜下结肠炎是腹泻的常见病因。己酮可可碱是一种具有抗肿瘤坏死因子-α特性的黄嘌呤衍生物,常用于治疗间歇性跛行和其他疾病。我们的目标是评估接受己酮可可碱治疗的显微镜下结肠炎患者的治疗效果。

患者情况

纳入了1997年1月1日至2016年11月30日期间在罗切斯特梅奥诊所就诊的9例显微镜下结肠炎患者(8例胶原性结肠炎和1例淋巴细胞性结肠炎)。中位年龄为56.9岁(范围51.6 - 60.2岁),8例为女性(89%),中位病程为64.8个月(范围60 - 109个月)。治疗指征为7例患者对布地奈德难治,1例患者对布地奈德依赖,1例患者对布地奈德不耐受。

诊断

所有患者均经组织学确诊为显微镜下结肠炎。

干预措施

使用己酮可可碱,每日3次,每次400mg,中位治疗时间为3个月(范围2.5 - 8.3个月)。

治疗效果

1例患者(11%)完全缓解,3例患者(33%)部分缓解。因对布地奈德不耐受而接受己酮可可碱治疗的患者实现了完全缓解,并完成了43个月的成功维持治疗。未报告不良反应。

经验教训

大多数有布地奈德治疗经历的活动性显微镜下结肠炎患者对己酮可可碱无反应。然而,其耐受性良好,1例患者实现长期缓解,三分之一的患者有部分反应。需要更大规模的对照研究来评估己酮可可碱在显微镜下结肠炎中的疗效及反应预测因素。特别是,对布地奈德并非难治的患者可能更易产生反应。

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