Buurman Dorien J, De Monchy Jan G R, Schellekens Reinout C A, van der Waaij Laurens A, Kleibeuker Jan H, Dijkstra Gerard
Department of Gastroenterology and Hepatology, University Medical Center Groningen, University of Groningen , Groningen , The Netherlands.
Scand J Gastroenterol. 2015 Apr;50(4):399-405. doi: 10.3109/00365521.2014.962608. Epub 2015 Jan 29.
Mesalazine is a key drug in the treatment of ulcerative colitis (UC). Intolerance to mesalazine has been described, including fever and gastrointestinal symptoms. Several case reports reported successful desensitization of patients with mesalazine intolerance. The aim was to assess the number of UC patients who are persistently intolerant to mesalazine after single-blinded rechallenge and to test the effectiveness of a rapid desensitization protocol in UC patients demonstrated mesalazine intolerance.
This is a prospective, single-blind randomized study in UC patients who discontinued mesalazine because of intolerance. Patients with severe reactions were excluded. Eligible patients underwent a skin patch test with mesalazine followed by a single-blinded randomized crossover rechallenge with 500 mg mesalazine or placebo. Patients with symptoms upon rechallenge were admitted to the hospital for 3 days oral desensitization.
Nine of the 37 identified UC patients who discontinued mesalazine because of intolerance were included. All nine patients had negative patch tests, seven patients had symptoms (fever, nausea, vomiting and diarrhea) within 2 h upon rechallenge. Four of these seven patients participated in the desensitization protocol and in none a successful desensitization could be performed. All four had an inflammatory intolerance reaction with rise in C-reactive protein. There were no elevations in serum tryptase or urinary-methylhistamine levels observed and no signs of immediate type allergic reactions, like urticaria, bronchial obstruction or anaphylaxis.
We recommend not to rechallenge UC patients with an inflammatory response upon mesalazine and these patients will not benefit from a rapid desensitization protocol.
美沙拉嗪是治疗溃疡性结肠炎(UC)的关键药物。已报道了对美沙拉嗪的不耐受情况,包括发热和胃肠道症状。几例病例报告显示对美沙拉嗪不耐受的患者脱敏成功。目的是评估在单盲再激发后持续对美沙拉嗪不耐受的UC患者数量,并测试快速脱敏方案在已证明对美沙拉嗪不耐受的UC患者中的有效性。
这是一项针对因不耐受而停用美沙拉嗪的UC患者的前瞻性、单盲随机研究。排除有严重反应的患者。符合条件的患者接受美沙拉嗪皮肤斑贴试验,随后用500mg美沙拉嗪或安慰剂进行单盲随机交叉再激发。再激发时出现症状的患者入院进行3天的口服脱敏。
37例因不耐受而停用美沙拉嗪的UC患者中有9例被纳入研究。所有9例患者斑贴试验均为阴性,7例患者在再激发后2小时内出现症状(发热、恶心、呕吐和腹泻)。这7例患者中有4例参与了脱敏方案,但均未成功进行脱敏。所有4例患者均有炎症性不耐受反应,C反应蛋白升高。未观察到血清类胰蛋白酶或尿甲基组胺水平升高,也没有立即型过敏反应的迹象,如荨麻疹、支气管阻塞或过敏反应。
我们建议不对美沙拉嗪激发后有炎症反应的UC患者进行再激发,这些患者不会从快速脱敏方案中获益。