低剂量短疗程地塞米松治疗原发性肝癌经导管动脉化疗栓塞后栓塞后综合征的新疗法:回顾性病例对照研究

Meng Yb, Cheng Sm, Y. M, Xu Xw, C. L, Zhu Xj, Du J
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引用次数: 0

摘要

目的:地塞米松(DEX)被认为是栓塞后综合征(PES)的有效治疗方法。但目前常用的DEX疗程长,用量大,副作用大。本研究旨在评价低剂量短疗程DEX预防PES的疗效和安全性,建立新的治疗疗程。方法:采用回顾性队列研究,观察右美托咪唑治疗原发性肝癌经导管动脉化疗栓塞(Transcatheter Arterial Chemoembolization, TACE)患者PES的疗效。根据患者意愿选择DEX,将患者分为两组。实验组,52例患者从TACE当日开始,每日静脉注射DEX 5mg和托司司琼5mg。其余52例患者(对照组)每日仅使用5mg托哌司琼。记录呕吐、腹痛和发热的发生率和程度。行血常规及c反应蛋白(CRP)检测,评估肝肾功能,评估TACE前后凝血指数及东部肿瘤合作组(ECOG)表现状态。结果:呕吐、发热、腹痛等不良反应严重程度评分;2级和3级不良反应发生率;实验组CRP、ECOG评分均显著低于对照组(P< 0.05)。两组患者TACE前后血常规、肝肾功能、凝血指标比较,差异均无统计学意义(P> 0.05)。结论:TACE术后低剂量短疗程DEX治疗可有效减轻PES的严重程度,且无不良反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low-Dose and Short-Course Dexamethasone Treatment as a New Therapy against the Post-Embolization Syndrome after Transcatheter Arterial Chemoembolization in Primary Liver Cancer: A Retrospective Case-Control Study
Objective: Dexamethasone (DEX) is considered an effective treatment for Post-Embolization Syndrome (PES). However, the current commonly used DEX treatment course is long and involves a large amount of DEX and thus causes substantial side effects. This study aimed to evaluate the efficacy and safety of low-dose shortcourse DEX treatment in the prevention of PES to establish a new treatment course. Methods: A retrospective cohort study was conducted to observe the efficacy of DEX in treating PES on patients with primary liver cancer who underwent Transcatheter Arterial Chemoembolization (TACE). DEX was selected according to the wishes of the patients, who were subsequently divided into two groups. In the experimental group, 52 patients daily received an intravenous injection of 5 mg DEX and 5 mg tropisetron, starting on the day of TACE. The remaining 52 patients (control group) were treated with only 5 mg tropisetron daily. Incidence and degree of vomiting, abdominal pain, and fever were recorded. Routine blood tests and the C-Reactive Protein (CRP) test were performed, liver and kidney functions were evaluated, and the coagulation index and Eastern Cooperative Oncology Group (ECOG) performance status were assessed before and after TACE. Results: Severity scores of adverse reactions, such as vomiting, fever, and abdominal pain; incidence of grade 2 and 3 adverse reactions; and CRP and ECOG scores were significantly lower in the experimental group than in the control group (P< 0.05). There was no significant difference in routine blood parameters, liver and kidney functions, or coagulation between the two groups before or after TACE (P> 0.05). Conclusion: Low-dose and short-course DEX treatment after TACE can effectively reduce the severity of PES without side effects.
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