• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

对于失去对英夫利昔单抗反应的克罗恩病患者,基于检测的策略比经验性剂量递增更具成本效益。

A test-based strategy is more cost effective than empiric dose escalation for patients with Crohn's disease who lose responsiveness to infliximab.

机构信息

Division of Gastroenterology and Hepatology, University of California, San Francisco, California 94115, USA.

出版信息

Clin Gastroenterol Hepatol. 2013 Jun;11(6):654-66. doi: 10.1016/j.cgh.2012.12.035. Epub 2013 Jan 26.

DOI:10.1016/j.cgh.2012.12.035
PMID:23357488
Abstract

BACKGROUND & AIMS: Patients with Crohn's disease who become unresponsive to therapy with tumor necrosis factor antagonists are managed initially with either empiric dose escalation or testing-based strategies. The comparative cost effectiveness of these 2 strategies is unknown. We investigated whether a testing-based strategy is more cost effective than an empiric dose-escalation strategy.

METHODS

A decision analytic model that simulated 2 cohorts of patients with Crohn's disease compared outcomes for the 2 strategies over a 1-year time period. The incremental cost-effectiveness ratio of the empiric strategy was expressed as cost per quality-adjusted life-year (QALY) gained, compared with the testing-based strategy. We performed 1-way, probabilistic, and prespecified secondary analyses.

RESULTS

The testing strategy yielded similar QALYs compared with the empiric strategy (0.801 vs 0.800, respectively) but was less expensive ($31,870 vs $37,266, respectively). In sensitivity analyses, the incremental cost-effectiveness ratio of the empiric strategy ranged from $500,000 to more than $5 million per QALY gained. Similar rates of remission (63% vs 66%) and response (28% vs 26%) were achieved through differential use of available interventions. The testing-based strategy resulted in a higher percentage of surgeries (48% vs 34%) and lower percentage use of high-dose biological therapy (41% vs 54%).

CONCLUSIONS

A testing-based strategy is a cost-effective alternative to the current strategy of empiric dose escalation for managing patients with Crohn's disease who have lost responsiveness to infliximab. The basis for this difference is lower cost at similar outcomes.

摘要

背景与目的

对于肿瘤坏死因子拮抗剂治疗无应答的克罗恩病患者,最初采用经验性剂量升级或基于检测的策略进行治疗。这两种策略的比较成本效益尚不清楚。我们研究了基于检测的策略是否比经验性剂量升级策略更具成本效益。

方法

一个决策分析模型模拟了两组克罗恩病患者,在 1 年的时间内比较了这两种策略的结果。经验性策略的增量成本效益比表示为每获得一个质量调整生命年(QALY)的成本,与基于检测的策略相比。我们进行了单向、概率和预设的二次分析。

结果

与经验性策略相比,检测策略的 QALY 相似(分别为 0.801 和 0.800),但成本较低(分别为 31870 美元和 37266 美元)。在敏感性分析中,经验性策略的增量成本效益比范围从每获得一个 QALY 的 50 万美元到超过 500 万美元。通过不同地使用现有干预措施,实现了相似的缓解率(63%比 66%)和应答率(28%比 26%)。基于检测的策略导致更高比例的手术(48%比 34%)和较低比例的高剂量生物治疗(41%比 54%)。

结论

对于肿瘤坏死因子拮抗剂治疗无应答的克罗恩病患者,基于检测的策略是经验性剂量升级策略的一种具有成本效益的替代方案。这种差异的基础是相似结果下的更低成本。

相似文献

1
A test-based strategy is more cost effective than empiric dose escalation for patients with Crohn's disease who lose responsiveness to infliximab.对于失去对英夫利昔单抗反应的克罗恩病患者,基于检测的策略比经验性剂量递增更具成本效益。
Clin Gastroenterol Hepatol. 2013 Jun;11(6):654-66. doi: 10.1016/j.cgh.2012.12.035. Epub 2013 Jan 26.
2
Infliximab dose escalation vs. initiation of adalimumab for loss of response in Crohn's disease: a cost-effectiveness analysis.英夫利昔单抗剂量递增与阿达木单抗起始治疗用于克罗恩病反应丧失的比较:一项成本效益分析
Aliment Pharmacol Ther. 2007 Dec;26(11-12):1509-20. doi: 10.1111/j.1365-2036.2007.03548.x. Epub 2007 Oct 11.
3
Strategies for the prevention of postoperative recurrence in Crohn's disease: results of a decision analysis.克罗恩病术后复发预防策略的决策分析结果。
Am J Gastroenterol. 2011 Nov;106(11):2009-17. doi: 10.1038/ajg.2011.237. Epub 2011 Jul 26.
4
Individualised therapy is more cost-effective than dose intensification in patients with Crohn's disease who lose response to anti-TNF treatment: a randomised, controlled trial.在对 TNF 治疗应答丧失的克罗恩病患者中,个体化治疗比剂量强化更具成本效益:一项随机对照试验。
Gut. 2014 Jun;63(6):919-27. doi: 10.1136/gutjnl-2013-305279. Epub 2013 Jul 22.
5
Cost-utility analysis of biologic treatments for moderate-to-severe Crohn's disease.生物制剂治疗中重度克罗恩病的成本效用分析。
Pharmacotherapy. 2012 Jun;32(6):515-26. doi: 10.1002/j.1875-9114.2011.01053.x. Epub 2012 Apr 23.
6
Risks and benefits of infliximab for the treatment of Crohn's disease.英夫利昔单抗治疗克罗恩病的风险与益处
Clin Gastroenterol Hepatol. 2006 Aug;4(8):1017-24; quiz 976. doi: 10.1016/j.cgh.2006.05.020. Epub 2006 Jul 14.
7
Health-economic analysis: cost-effectiveness of scheduled maintenance treatment with infliximab for Crohn's disease--modelling outcomes in active luminal and fistulizing disease in adults.卫生经济分析:英夫利昔单抗定期维持治疗克罗恩病的成本效益——对成人活动性肠腔和瘘管性疾病的建模结果
Aliment Pharmacol Ther. 2008 Jul;28(1):76-87. doi: 10.1111/j.1365-2036.2008.03709.x. Epub 2008 Apr 11.
8
Can mucosal healing be a cost-effective endpoint for biologic therapy in Crohn's disease? A decision analysis.黏膜愈合能否成为克罗恩病生物治疗的一种具有成本效益的终点?一项决策分析。
Inflamm Bowel Dis. 2013 Jan;19(1):37-44. doi: 10.1002/ibd.22951.
9
The Cost-effectiveness of Initial Immunomodulators or Infliximab Using Modern Optimization Strategies for Crohn's Disease in the Biosimilar Era.生物类似药时代中,采用现代优化策略的初始免疫调节剂或英夫利昔单抗治疗克罗恩病的成本效益分析。
Inflamm Bowel Dis. 2020 Feb 11;26(3):369-379. doi: 10.1093/ibd/izz159.
10
The Cost-effectiveness of Biological Therapy Cycles in the Management of Crohn's Disease.生物治疗周期在克罗恩病管理中的成本效益。
J Crohns Colitis. 2019 Sep 27;13(10):1323-1333. doi: 10.1093/ecco-jcc/jjz063.

引用本文的文献

1
Annual Therapeutic Drug Monitoring in Patients with Inflammatory Bowel Disease During Infliximab Maintenance Therapy: Balancing Efficacy with Risk of Pharmacokinetic Failure.英夫利昔单抗维持治疗期间炎症性肠病患者的年度治疗药物监测:平衡疗效与药代动力学失败风险
Dig Dis Sci. 2025 Apr 29. doi: 10.1007/s10620-025-09032-9.
2
Attitudes, perceptions and barriers in implementing therapeutic drug monitoring for anti-TNFs in inflammatory bowel disease: a survey from the Middle East.炎症性肠病中抗 TNF 药物治疗药物监测实施中的态度、认知与障碍:一项来自中东地区的调查
Therap Adv Gastroenterol. 2024 Feb 24;17:17562848241230902. doi: 10.1177/17562848241230902. eCollection 2024.
3
A Review of Therapeutic Drug Monitoring in Patients with Inflammatory Bowel Disease Receiving Combination Therapy.
炎症性肠病患者联合治疗中治疗药物监测的综述
J Clin Med. 2023 Oct 17;12(20):6577. doi: 10.3390/jcm12206577.
4
Infliximab Pricing in International Economic Evaluations in Inflammatory Bowel Disease to Inform Biologic and Biosimilar Access Policies: A Systematic Review.英夫利昔单抗在炎症性肠病国际经济评估中的定价以指导生物制剂和生物类似药的准入政策:一项系统评价
MDM Policy Pract. 2023 Feb 24;8(1):23814683231156433. doi: 10.1177/23814683231156433. eCollection 2023 Jan-Jun.
5
Multi-utility of therapeutic drug monitoring in inflammatory bowel diseases.治疗药物监测在炎症性肠病中的多种用途。
Front Med (Lausanne). 2022 Jul 28;9:864888. doi: 10.3389/fmed.2022.864888. eCollection 2022.
6
Management of Non-response and Loss of Response to Anti-tumor Necrosis Factor Therapy in Inflammatory Bowel Disease.炎症性肠病中抗肿瘤坏死因子治疗无应答及应答丧失的管理
Front Med (Lausanne). 2022 Jun 15;9:897936. doi: 10.3389/fmed.2022.897936. eCollection 2022.
7
Delaying an infliximab infusion by more than 3 days is associated with a significant reduction in trough levels but not with clinical worsening.英夫利昔单抗输注延迟超过3天与谷浓度显著降低相关,但与临床病情恶化无关。
Therap Adv Gastroenterol. 2022 Mar 14;15:17562848221083395. doi: 10.1177/17562848221083395. eCollection 2022.
8
Cost-Effectiveness of Therapeutic Drug Monitoring of Anti-TNF Therapy in Inflammatory Bowel Disease: A Systematic Review.炎症性肠病中抗TNF治疗药物监测的成本效益:一项系统评价
Pharmaceutics. 2022 May 7;14(5):1009. doi: 10.3390/pharmaceutics14051009.
9
Therapeutic drug monitoring for biological medications in inflammatory bowel disease.炎症性肠病生物药物的治疗药物监测。
Saudi J Gastroenterol. 2022 Sep-Oct;28(5):322-331. doi: 10.4103/sjg.sjg_3_22.
10
Objective disease activity assessment and therapeutic drug monitoring prior to biologic therapy changes in routine inflammatory bowel disease clinical practice: TARGET-IBD.目标疾病活动评估和生物治疗前的治疗药物监测在常规炎症性肠病临床实践中的变化:TARGET-IBD。
BMC Gastroenterol. 2022 Feb 19;22(1):71. doi: 10.1186/s12876-022-02143-x.