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Treatment of severe steroid refractory ulcerative colitis 被引量:1
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作者 Gert Van Assche Séverine Vermeire Paul Rutgeerts 《World Journal of Gastroenterology》 SCIE CAS CSCD 2008年第36期5508-5511,共4页
Although systemic steroids are highly efficacious in ulcerative colitis (UC), failure to respond to steroids still poses an important challenge to the surgeon and physician alike. Even if the life time risk of a fulmi... Although systemic steroids are highly efficacious in ulcerative colitis (UC), failure to respond to steroids still poses an important challenge to the surgeon and physician alike. Even if the life time risk of a fulminant UC flare is only 20%, this condition is potentially life threatening and should be managed in hospital. If patients fail 3 to 5 d of intravenous corticosteroids and optimal supportive care, they should be considered for any of three options: intravenous cyclosporine (2 mg/kg for 7 d, and serum level controlled), infliximab (5 mg/kg Ⅳ, 0-2-6 wk) or total colectomy. The choice between these three options is a medical- surgical decision based on clinical signs, radiological and endoscopic findings and blood analysis (CRP, serum albumin). Between 65 and 85% of patients will initially respond to cyclosporine and avoid colectomy on the short term. Over 5 years only 50% of initial responders avoid colectomy and outcomes are better in patients naive to azathioprine (bridging strategy). The data on infliximab as a medical rescue in fulminant colitis are more limited although the efficacy of this anti tumor necrosis factor (TNF) monoclonal antibody has been demonstrated in a controlled trial. Controlled data on the comparative efficacy of cyclosporine and infliximab are not available at this moment. Both drugs are immunosuppressants and are used in combination with steroids and azathioprine, which infers a risk of serious, even fatal, opportunistic infections. Therefore, patients not responding to these agents within 5-7 d should be considered for colectomy and responders should be closely monitored for infections. 展开更多
关键词 Ulcerative colitis STEROIDS CORTICOSTEROIDS AZATHIOPRINE CYCLOSPORINE INFLIXIMAB Imrnunosuppressants
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支气管哮喘患儿红细胞免疫状态研究 被引量:1
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作者 滕小军 陈卫珍 江利国 《中国医师杂志》 CAS 2001年第12期903-904,906,共3页
目的 探讨支气管哮喘患儿红细胞免疫粘附功能的变化及糖皮质激素对哮喘患儿红细胞免疫粘附功能的影响。方法 采用酵母菌花环法对 42例支气管哮喘患儿 ,2 8例哮喘缓解期患儿及 2 0例健康儿童进行红细胞C3b受体花环率 (RBC -C3breceptor... 目的 探讨支气管哮喘患儿红细胞免疫粘附功能的变化及糖皮质激素对哮喘患儿红细胞免疫粘附功能的影响。方法 采用酵母菌花环法对 42例支气管哮喘患儿 ,2 8例哮喘缓解期患儿及 2 0例健康儿童进行红细胞C3b受体花环率 (RBC -C3breceptorrosetterate,RBC -C3bRR)及红细胞免疫复合物花环率 (RBC -Immuno complexrosseterate,RBC -ICR)检测 ,同时检测 2 8例哮喘患儿缓解期应用激素吸入治疗 1月及 6月后的RBC -C3bRR及RBC -ICR。结果 哮喘发作组RBC -C3bRR较缓解组和对照组均明显下降 (P <0 0 5 ,P <0 0 1)。RBC -ICR较对照组升高 (P <0 0 5 )。哮喘患儿缓解期应用激素吸入治疗 1月后 ,RBC -C3bRR较未用药组高 ,差异有显著意义 (P <0 0 5 )。两组RBC -ICR差异无显著性 (P >0 0 5 )。激素治疗 6月后 ,RBC -C3bRR较未用药组明显升高 ,差异有高度显著性 (P <0 0 1)。两组RBC -ICR差异无显著意义 (P >0 0 5 )。结论 支气管哮喘患儿红细胞免疫粘附功能下降。 展开更多
关键词 哮喘 红细胞免疫 皮质类甾醇类 治疗 儿童
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