首页> 外文期刊>Acta gastro-enterologica Belgica >Safety and cost of infliximab for the treatment of belgian pediatric patients with Crohn's disease
【24h】

Safety and cost of infliximab for the treatment of belgian pediatric patients with Crohn's disease

机译:英夫利昔单抗治疗比利时克罗恩病儿科患者的安全性和费用

获取原文
获取原文并翻译 | 示例
           

摘要

Biologicals have become an important component in the treatment of Crohn's disease in children. Their increased and long term use raises safety concerns. We describe safety and cost of infliximab in Belgian pediatric Crohn's disease patients. All patients on infliximab as part of the present or past treatment for Crohn's Disease until January 1st 2011 were selected from an existing database. Information on disease phenotype, medication and adverse events were extracted. Adverse events occurred in 25.9% of patients exposed to infliximab of which 29.6% were severe. In total 31.7% of patients stopped infliximab therapy. The main reasons for discontinuation were adverse events in 45.4% and loss of response in 30.3%. No malignancies or lethal complications occurred over this 241 patient year observation period. Immuno - modulators were concomitant medication in 75% of patients and were discontinued subsequently in 38.4% of them. The cost of infliximab infusions per treated patient per year in the Belgian health care setting is approximately 9 474 euro, including only medication and hospital related costs. Even though infliximab is relatively safe in pediatric CD on the short term, close follow-up and an increased awareness of the possible adverse reactions is highly recommended. Adverse reactions appeared in 25.9% of all patients and were the main reason for discontinuation. Treatment cost has to be balanced against efficacy and modifications in disease course. In the Belgian health care system, the medication is available to all patients with moderate to severe CD.
机译:生物制剂已成为治疗儿童克罗恩氏病的重要组成部分。它们的长期使用增加了安全隐患。我们描述了英夫利昔单抗在比利时小儿克罗恩病患者中的安全性和费用。从现有数据库中选择直到2011年1月1日为止,作为当前或过去克罗恩病治疗的一部分使用英夫利昔单抗治疗的所有患者。提取有关疾病表型,药物和不良事件的信息。暴露于英夫利昔单抗的患者中有25.9%发生不良事件,其中29.6%的患者为严重事件。共有31.7%的患者停止了英夫利昔单抗治疗。停药的主要原因是不良事件占45.4%,反应丧失占30.3%。在这241个患者年的观察期内,未发生任何恶性肿瘤或致死性并发症。免疫调节剂在75%的患者中同时用药,随后在38.4%的患者中停用。在比利时的医疗机构中,每位接受治疗的患者每年注射英夫利昔单抗的费用约为9 474欧元,仅包括药物和医院相关费用。尽管英夫利昔单抗短期内在儿科CD中相对安全,但仍强烈建议密切随访并提高对可能出现的不良反应的认识。不良反应发生在所有患者中的25.9%,是停药的主要原因。治疗成本必须与功效和疾病过程中的调整相平衡。在比利时的医疗保健系统中,所有中度至重度CD患者均可使用该药物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号