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炎症性肠病的药物治疗

Drug therapy of inflammatory bowel disease.

作者信息

Sack D M, Peppercorn M A

出版信息

Pharmacotherapy. 1983 May-Jun;3(3):158-76. doi: 10.1002/j.1875-9114.1983.tb03245.x.

Abstract

Although the etiology of inflammatory bowel disease is unknown and specific therapy is unavailable, enough information on existing empiric agents is available to allow rational therapy. These agents include sulfasalazine, steroids, immunosuppressive drugs, metronidazole and cholestyramine. Sulfasalazine is a two-part molecule that depends on bacterial cleavage in the colon to deliver locally acting 5-aminosalicylate, whose mechanism of action may relate to inhibition of prostaglandin synthesis. The other half of the molecule, sulfapyridine, is responsible for most of the side effects of the drug. While the efficacy of sulfasalazine in the treatment and prevention of attacks of ulcerative colitis is well established, its use in Crohn's disease appears to be limited to patients with active colitis and ileo-colitis. Sulfasalazine is of major benefit in preventing relapses in patients with ulcerative colitis in remission. New formulations of 5-aminosalicylate may allow delivery of the apparently active moiety to the small bowel and colon without concomitant sulfapyridine toxicity. Corticosteroids are highly effective in acute attacks of ulcerative colitis and Crohn's ileitis and ileo-colitis; the mechanism of antiinflammatory action remains speculative. However, maintenance therapy with steroids is ineffective in preventing relapses or recurrent attacks of either ulcerative colitis or Crohn's disease. Steroid enemas allow topical administration to patients with distal colitis and proctitis with few systemic side effects. In children with growth failure associated with active Crohn's disease, amelioration by steroid therapy may actually restore normal growth. Immunosuppressive agents such as azathioprine and 6-mercaptopurine are of little value in active Crohn's disease when administered alone; however, in combination with other agents they may help diminish steroid dose, close fistulae and prevent relapse. Their mode of action likely depends on long-term cytostatic effects on immune effector cells. Concern for leukopenia and the development of late malignancy has limited their use to patients not responding to other therapies. Metronidazole, an antimicrobial agent that is effective against anaerobes, has recently been shown useful in Crohn's disease involving the colon and perianal area. Its mechanism of action is uncertain, but may be related to its antibacterial actions on anaerobes. Cholestyramine can be successfully used to control bile salt-induced diarrhea in Crohn's patients with terminal ileal resections. Effective drug therapy of inflammatory bowel disease is only part of a total program of management including reassurance, frequent explanation, well-timed use of surgery, and an understanding physician.

摘要

尽管炎症性肠病的病因不明且尚无特效疗法,但关于现有经验性用药的信息已足够,可据此进行合理治疗。这些药物包括柳氮磺胺吡啶、类固醇、免疫抑制药、甲硝唑和考来烯胺。柳氮磺胺吡啶是一种双分子药物,依赖结肠内细菌裂解来释放具有局部作用的5-氨基水杨酸,其作用机制可能与抑制前列腺素合成有关。该分子的另一半,即磺胺吡啶,是该药大多数副作用的根源。虽然柳氮磺胺吡啶在治疗和预防溃疡性结肠炎发作方面的疗效已得到充分证实,但其在克罗恩病中的应用似乎仅限于患有活动性结肠炎和回结肠型克罗恩病的患者。柳氮磺胺吡啶对预防处于缓解期的溃疡性结肠炎患者复发有很大益处。新型5-氨基水杨酸制剂可能使活性部分送达小肠和结肠,而无磺胺吡啶毒性。皮质类固醇对溃疡性结肠炎、克罗恩病的回肠炎和回结肠型克罗恩病的急性发作非常有效;其抗炎作用机制仍属推测。然而,用类固醇进行维持治疗对预防溃疡性结肠炎或克罗恩病的复发或反复发作为无效。类固醇灌肠剂可局部用于患有远端结肠炎和直肠炎的患者,且几乎无全身副作用。在患有与活动性克罗恩病相关的生长发育迟缓的儿童中,类固醇治疗改善病情实际上可能恢复正常生长。免疫抑制药如硫唑嘌呤和6-巯基嘌呤单独用于活动性克罗恩病时价值不大;然而,与其他药物联合使用时,它们可能有助于减少类固醇剂量、闭合瘘管并预防复发。其作用方式可能取决于对免疫效应细胞长期的细胞生长抑制作用。对白细胞减少症和晚期恶性肿瘤发生的担忧限制了它们仅用于对其他治疗无反应的患者。甲硝唑是一种对厌氧菌有效的抗菌剂,最近已显示对涉及结肠和肛周区域的克罗恩病有用。其作用机制尚不确定,但可能与其对厌氧菌的抗菌作用有关。考来烯胺可成功用于控制患有末端回肠切除的克罗恩病患者中胆盐引起的腹泻。炎症性肠病的有效药物治疗只是整个治疗方案的一部分,该方案还包括安慰、经常解释、适时进行手术以及一位善解人意的医生。

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