医学文献 >>
  • 检索发现
  • 增强检索
知识库 >>
  • 临床诊疗知识库
  • 中医药知识库
评价分析 >>
  • 机构
  • 作者
默认
×
热搜词:
换一批
论文 期刊
取消
高级检索

检索历史 清除

乌司奴单抗双静脉诱导治疗复杂性肛瘘型克罗恩病的疗效分析

Analysis on the efficacy of dual vein induction therapy of Ustekinumab in complex perianal fistulizing Crohn′s disease

摘要目的:分析乌司奴单抗(UST)双静脉诱导治疗复杂性肛瘘型克罗恩病(PFCD)的疗效。方法:回顾性分析2022年1月至2023年3月就诊于温州医科大学附属第二医院并确诊为复杂性PFCD患者的临床资料。所有患者分别于第0、8周给予足量UST(6 mg/kg)单次静脉输注后,每隔8周单次皮下注射UST 90 mg维持治疗。第8、16、22~26周采用肛周疾病活动指数(PDAI)评估肛瘘临床结局,Harvey-Bradshaw指数(HBI)评估整体活动度。第22~26周采用Van Assche指数(VAI)评估肛瘘影像结局,简化克罗恩病内镜评分(SES-CD)评估肠道结局事件。比较UST治疗前后上述指标的差异。依据是否采用UST一线治疗将PFCD患者分为一线UST治疗组与非一线UST治疗组,比较两组之间肛瘘应答率和缓解率、肠道应答率和缓解率以及整体活动度应答率和缓解率的差异。结果:共纳入60例PFCD患者,男46例,女14例,年龄[ M( Q1, Q3)]25.0(20.8,30.0)岁。第8、16、22~26周的肛瘘临床应答率[41.7%(25/60)、55.0%(33/60)、63.3%(38/60), P=0.056]和肛瘘临床缓解率[21.7%(13/60)、31.7%(19/60)和43.3%(26/60), P=0.002]逐渐增高;整体活动度应答率[53.3%(32/60)、70.0%(42/60)、83.3%(50/60), P=0.040]和整体活动度缓解率[41.7%(25/60)、61.7%(37/60)、75.0%(45/60), P=0.001]亦逐渐增高。第22~26周时,肛瘘影像学部分应答率和瘘管愈合率分别为45.0%(27/60)和38.3%(23/60);内镜应答率和内镜缓解率分别为73.7%(44/60)和45.0%(27/60)。一线UST治疗组[男23例,女8例,年龄22.0(21.0,39.0)岁]的内镜应答率高于非一线UST治疗组[男23例,女6例,年龄26.5(20.0,30.0)岁](87.1%比58.6%, P=0.013)。 结论:UST双静脉诱导治疗能有效改善复杂性PFCD患者的临床疗效。

更多

abstractsObjectives:To analyze the efficacy of dual vein induction therapy of Ustekinumab (UST) in complex perianal fistulizing Crohn′s disease (PFCD).Methods:Clinical data of patients diagnosed with complex PFCD in the Second Affiliated Hospital of Wenzhou Medical University from January 2022 to March 2023 were retrospectively analyzed. After sufficient single intravenous infusion of UST (6 mg/kg) at week 0 and 8, every patient received single subcutaneous injection of UST 90 mg every 8 weeks for maintenance treatment. At week 8, 16, and 22-26, clinical outcomes of anal fistula were evaluated using perianal disease activity index (PDAI), and overall activity of the patients was evaluated using Harvey Bradshaw index (HBI). At week 22-26, Van Assche Index (VAI) was used to evaluate imaging outcome of anal fistula, and simplified endoscopic score of Crohn′s disease (SES-CD) was employed to assess intestinal outcome events. The above indexes were compared in the patients before and after UST treatment. PFCD patients were divided into first-line UST treatment group and non first-line UST treatment group according to whether first-line UST treatment was used, the differences in anal fistula response rate and remission rate, intestinal response rate and remission rate as well as overall activity response rate and remission rate were compared between the two groups.Results:A total of 60 PFCD patients were included, including 46 males and 14 females, aged [ M ( Q1, Q3)] 25.0 (20.8, 30.0) years old. The clinical response rates of anal fistula [41.7% (25/60), 55.0% (33/60) and 63.3% (38/60), respectively, P=0.056] and the clinical remission rates of anal fistula [21.7% (13/60), 31.7% (19/60) and 43.3% (26/60), respectively, P=0.002] gradually increased at week 8, 16, 22-26. The overall activity response rates [53.3% (32/60), 70.0% (42/60), 83.3% (50/60), respectively, P=0.040] and the overall activity response rates [41.7% (25/60), 61.7% (37/60), 75.0% (45/60), respectively, P=0.001] also gradually increased at week 8, 16, 22-26. At week 22-26, the partial response rate and fistula healing rate of anal fistula imaging were 45.0% (27/60) and 38.3% (23/60), respectively. The endoscopic response rate and endoscopic response rate were 73.7% (44/60) and 45.0% (27/60), respectively. The endoscopic response rate of patients receiving first-line UST treatment [23 males and 8 females, aged 22.0 (21.0, 39.0) years] was higher than that of patients receiving non first-line UST treatment[23 males and 6 females, aged 26.5 (20.0, 30.0) years,87.1% vs 58.6%, P=0.013]. Conclusion:The dual vein induction therapy of UST could effectively improve the clinical efficacy in patients with complex PFCD.

More
广告
  • 浏览91
  • 下载2
中华医学杂志

中华医学杂志

2023年103卷41期

3301-3306页

MEDLINEISTICPKUCSCDCA

加载中!

相似文献

  • 中文期刊
  • 外文期刊
  • 学位论文
  • 会议论文

加载中!

加载中!

加载中!

加载中!

扩展文献

特别提示:本网站仅提供医学学术资源服务,不销售任何药品和器械,有关药品和器械的销售信息,请查阅其他网站。

  • 客服热线:4000-115-888 转3 (周一至周五:8:00至17:00)

  • |
  • 客服邮箱:yiyao@wanfangdata.com.cn

  • 违法和不良信息举报电话:4000-115-888,举报邮箱:problem@wanfangdata.com.cn,举报专区

官方微信
万方医学小程序
new医文AI 翻译 充值 订阅 收藏 移动端

官方微信

万方医学小程序

使用
帮助
Alternate Text
调查问卷