Kamm M A
St Mark's Hospital, London, UK.
Aliment Pharmacol Ther. 2004 Oct;20 Suppl 4:102-5. doi: 10.1111/j.1365-2036.2004.02052.x.
The clinical management of Crohn's disease can be considered in relation to the treatment of acute disease and the maintenance of remission. The medication used to achieve these two goals may or may not be the same. Some patients with mildly active disease may respond to high-dose (4 g/day) mesalazine (mesalamine), and 5-aminosalicylic acid may also be helpful in weaning a patient off steroids after treatment for a flare-up. However, the value of 5-aminosalicylic acid in maintaining remission in Crohn's disease remains controversial. Subgroups of patients may be helped: for example, patients with Crohn's disease who have experienced a relapse within the last 2 years may benefit. Steroids form the first-line therapy for acute episodes of inflammation but do not maintain remission. Azathioprine and mercaptopurine are the first-line drugs for the maintenance of remission in moderate to severe Crohn's disease, and by titrating the dose up from 2 mg/kg daily, some previously resistant patients will be brought into remission. One-half of patients who do not tolerate azathioprine will tolerate mercaptopurine. Methotrexate is effective in inducing and maintaining remission, and is useful for patients who fail azathioprine treatment. Thalidomide is not proven in controlled studies, but two open studies have demonstrated its efficacy. The optimal dose, however, remains to be defined. Purified liquid diets with food exclusion can induce remission in patients with active disease, but food exclusion is difficult to maintain long term. Infliximab can induce and maintain remission in patients resistant to other therapies, with two-thirds of patients initially responding to treatment. One-third go into remission and, of those who respond to a single treatment, approximately one-half maintain remission when treated regularly for a year. Infliximab is, however, associated with an increased risk of infection, and its effect on cancer incidence is uncertain. The development of antibodies against the drug is associated with a loss of effect and allergic infusion reactions. In summary, simple proven therapies should be used first, because of their safety and benefit in some patients. However, aggressive therapy should be used when needed.
克罗恩病的临床管理可从急性病治疗和缓解期维持两方面来考虑。用于实现这两个目标的药物可能相同,也可能不同。一些轻度活动性疾病患者可能对高剂量(4克/天)美沙拉嗪(5-氨基水杨酸)有反应,并且5-氨基水杨酸在治疗病情发作后帮助患者停用类固醇方面可能也有帮助。然而,5-氨基水杨酸在维持克罗恩病缓解方面的价值仍存在争议。部分患者亚组可能会从中受益:例如,在过去2年内经历过复发的克罗恩病患者可能会受益。类固醇是炎症急性发作的一线治疗药物,但不能维持缓解。硫唑嘌呤和巯嘌呤是中度至重度克罗恩病维持缓解的一线药物,通过将剂量从每日2毫克/千克逐步上调,一些先前耐药的患者会进入缓解期。一半不耐受硫唑嘌呤的患者会耐受巯嘌呤。甲氨蝶呤在诱导和维持缓解方面有效,对硫唑嘌呤治疗失败的患者有用。沙利度胺在对照研究中未得到证实,但两项开放性研究已证明其疗效。然而,最佳剂量仍有待确定。排除食物的纯化流质饮食可使活动期疾病患者诱导缓解,但长期维持食物排除很困难。英夫利昔单抗可使对其他疗法耐药的患者诱导并维持缓解,三分之二的患者最初对治疗有反应。三分之一进入缓解期,在对单次治疗有反应的患者中,约一半在接受一年定期治疗时维持缓解。然而,英夫利昔单抗会增加感染风险,其对癌症发病率的影响尚不确定。针对该药物产生抗体与疗效丧失和过敏输注反应有关。总之,应首先使用已证实的简单疗法,因为其安全性以及对一些患者有益。然而,必要时应采用积极治疗。
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