• 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

替加环素在日本患者中的疗效和安全性研究。

Study on the Efficacy and Safety of Tedizolid in Japanese Patients.

作者信息

Ishikawa Kazuhiro, Tsuda Yasumasa, Mori Nobuyoshi

机构信息

Department of Infectious Diseases, St. Luke's International Hospital, Tokyo 104-8560, Japan.

Department of Pharmacy, St. Luke's International Hospital, Chuo-ku, Tokyo 104-8560, Japan.

出版信息

Antibiotics (Basel). 2024 Dec 23;13(12):1237. doi: 10.3390/antibiotics13121237.

DOI:10.3390/antibiotics13121237
PMID:39766627
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11672433/
Abstract

: Tedizolid (TZD), an oxazolidinone, causes fewer adverse events than linezolid (LZD). However, studies on the long-term efficacy and safety of TZD, particularly in patients with hematological malignancies (HMs), remain limited. This study aimed to evaluate the safety of long-term TZD use in Japanese patients, including those with HM. : We retrospectively reviewed the medical records of patients aged 15 years and older who received TZD treatment at St. Luke's International Hospital between 2018 and 2023. Patient demographics, treatment duration, adverse events, and clinical outcomes were analyzed. : Data from 35 patients and 40 treatment episodes were analyzed, including 13 episodes in patients with HM, of whom 65.0% were male, with a median age of 69.0 years (IQR: 24.5 years). The median treatment duration was 13.5 days (IQR: 46.8), with a maximum of 203 days. TZD was switched from other anti-MRSA agents in 82.5% of cases, including 42.5% from LZD. One patient discontinued TZD due to liver dysfunction, attributed to concomitant medication use. Clinical cure rates were significantly higher in the non-HM group compared to the HM group (88.9% vs. 38.5%). The 90-day mortality rate differed notably between the HM and non-HM groups (69.2% and 3.7%). Despite 100% microbiological eradication, infection-related mortality rates were 3.7% in the non-HM and 38.5% in the HM group. No reported cases of optic neuritis, colitis, or major bleeding; : TZD appears to be safe for long-term use, regardless of HM status, with no major complications observed in this cohort.

摘要

替加环素(TZD)是一种恶唑烷酮类药物,与利奈唑胺(LZD)相比,其不良事件较少。然而,关于TZD长期疗效和安全性的研究,尤其是在血液系统恶性肿瘤(HM)患者中的研究仍然有限。本研究旨在评估日本患者(包括HM患者)长期使用TZD的安全性。

我们回顾性分析了2018年至2023年期间在圣路加国际医院接受TZD治疗的15岁及以上患者的病历。分析了患者的人口统计学特征、治疗持续时间、不良事件和临床结局。

分析了35例患者和40个治疗疗程的数据,其中包括13例HM患者的疗程,这些患者中65.0%为男性,中位年龄为69.0岁(四分位间距:24.5岁)。中位治疗持续时间为13.5天(四分位间距:46.8),最长为203天。82.5%的病例中TZD是从其他抗耐甲氧西林金黄色葡萄球菌(MRSA)药物转换而来,其中42.5%是从LZD转换而来。1例患者因肝功能障碍停用TZD,这归因于同时使用的药物。非HM组的临床治愈率显著高于HM组(88.9%对38.5%)。HM组和非HM组的90天死亡率有显著差异(69.2%和3.7%)。尽管微生物清除率为100%,但非HM组感染相关死亡率为3.7%,HM组为38.5%。未报告视神经炎、结肠炎或大出血病例。

无论HM状态如何,TZD长期使用似乎是安全的,该队列中未观察到重大并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e1f/11672433/480611eb46ff/antibiotics-13-01237-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e1f/11672433/480611eb46ff/antibiotics-13-01237-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e1f/11672433/480611eb46ff/antibiotics-13-01237-g001.jpg

相似文献

1
Study on the Efficacy and Safety of Tedizolid in Japanese Patients.替加环素在日本患者中的疗效和安全性研究。
Antibiotics (Basel). 2024 Dec 23;13(12):1237. doi: 10.3390/antibiotics13121237.
2
A Retrospective Study to Compare the Incidence of Hyponatremia after Administration between Linezolid and Tedizolid.一项比较利奈唑胺和替加环素给药后低钠血症发生率的回顾性研究。
Antibiotics (Basel). 2023 Feb 7;12(2):345. doi: 10.3390/antibiotics12020345.
3
Efficacy, safety and pharmacokinetics of tedizolid versus linezolid in patients with skin and soft tissue infections in Japan - Results of a randomised, multicentre phase 3 study.替加环素与利奈唑胺治疗日本皮肤和软组织感染患者的疗效、安全性及药代动力学——一项随机、多中心3期研究的结果
J Infect Chemother. 2018 Jun;24(6):434-442. doi: 10.1016/j.jiac.2018.01.010. Epub 2018 Mar 9.
4
Efficacy and safety of tedizolid for the treatment of ventilated gram-positive hospital-acquired or ventilator-associated bacterial pneumonia in Japanese patients: Results from a subgroup analysis of a phase 3, randomized, double-blind study comparing tedizolid and linezolid.替加环素治疗日本重症监护病房革兰阳性菌医院获得性或呼吸机相关性细菌性肺炎的疗效和安全性:一项比较替加环素和利奈唑胺的 3 期、随机、双盲研究的亚组分析结果。
J Infect Chemother. 2022 Sep;28(9):1235-1241. doi: 10.1016/j.jiac.2022.04.027. Epub 2022 Jun 16.
5
Antimicrobial and immunomodulatory effects of tedizolid against methicillin-resistant Staphylococcus aureus in a murine model of hematogenous pulmonary infection.替加环素在血源性肺部感染小鼠模型中对耐甲氧西林金黄色葡萄球菌的抗菌和免疫调节作用
Int J Med Microbiol. 2016 Sep;306(6):421-8. doi: 10.1016/j.ijmm.2016.05.010. Epub 2016 May 19.
6
Clinical efficacy and safety assessment of tedizolid using therapeutic drug monitoring.使用治疗药物监测评估替加环素的临床疗效和安全性
J Infect Chemother. 2025 Mar;31(3):102582. doi: 10.1016/j.jiac.2024.12.011. Epub 2024 Dec 10.
7
In vitro Susceptibility of Nontuberculous Mycobacteria to Tedizolid.非结核分枝杆菌对特地唑胺的体外敏感性
Infect Drug Resist. 2022 Aug 25;15:4845-4852. doi: 10.2147/IDR.S362583. eCollection 2022.
8
High-throughput and wide-range simultaneous determination of linezolid, daptomycin and tedizolid in human plasma using ultra-performance liquid chromatography coupled to tandem mass spectrometry.采用超高效液相色谱-串联质谱法高通量、宽范围同时测定人血浆中利奈唑胺、达托霉素和替加环素。
J Pharm Biomed Anal. 2021 Feb 5;194:113764. doi: 10.1016/j.jpba.2020.113764. Epub 2020 Nov 21.
9
Safety and Tolerability of More than Six Days of Tedizolid Treatment.连续使用泰地唑胺超过六天的安全性和耐受性。
Antimicrob Agents Chemother. 2020 Jun 23;64(7). doi: 10.1128/AAC.00356-20.
10
Comparative Efficacies of Linezolid vs. Tedizolid in an Experimental Murine Model of Vancomycin-Resistant Enterococcal (VRE) Bacteremia.利奈唑胺与特地唑胺在耐万古霉素肠球菌(VRE)菌血症实验小鼠模型中的疗效比较
Front Med (Lausanne). 2019 Feb 20;6:31. doi: 10.3389/fmed.2019.00031. eCollection 2019.

本文引用的文献

1
Comparison of Empiric Antibiotic Escalation Therapy with Vancomycin (VAN) versus Linezolid (LIN) in Patients with Febrile Neutropenia.发热性中性粒细胞减少症患者经验性抗生素升级治疗中万古霉素(VAN)与利奈唑胺(LIN)的比较
Mediterr J Hematol Infect Dis. 2022 May 1;14(1):e2022032. doi: 10.4084/MJHID.2022.032. eCollection 2022.
2
Real-World Use of Tedizolid Phosphate for 28 Days or More: A Case Series Describing Tolerability and Clinical Success.磷酸特地唑胺28天及以上的真实世界应用:描述耐受性和临床疗效的病例系列
Open Forum Infect Dis. 2022 May 23;9(6):ofac028. doi: 10.1093/ofid/ofac028. eCollection 2022 Jun.
3
Correction of thrombocytopenia caused by linezolid with scheduled sequential tedizolid use in patients with vertebral osteomyelitis by antibiotic resistant Gram-positive organisms.
采用替考拉宁序贯疗法纠正耐抗生素革兰阳性菌所致椎体骨髓炎患者的利奈唑胺引起的血小板减少症。
J Infect Chemother. 2022 Jul;28(7):1023-1028. doi: 10.1016/j.jiac.2022.04.003. Epub 2022 Apr 25.
4
Pharmacokinetics and Pharmacodynamics of Tedizolid.替加环素的药代动力学和药效学。
Clin Pharmacokinet. 2022 Apr;61(4):489-503. doi: 10.1007/s40262-021-01099-7. Epub 2022 Feb 7.
5
A Phase 3, Randomized, Double-Blind Study Comparing Tedizolid Phosphate and Linezolid for Treatment of Ventilated Gram-Positive Hospital-Acquired or Ventilator-Associated Bacterial Pneumonia.一项比较磷酸替加环素和利奈唑胺治疗有创性革兰阳性医院获得性或呼吸机相关性细菌性肺炎的 3 期、随机、双盲研究。
Clin Infect Dis. 2021 Aug 2;73(3):e710-e718. doi: 10.1093/cid/ciab032.
6
Efficacy, safety and pharmacokinetics of tedizolid versus linezolid in patients with skin and soft tissue infections in Japan - Results of a randomised, multicentre phase 3 study.替加环素与利奈唑胺治疗日本皮肤和软组织感染患者的疗效、安全性及药代动力学——一项随机、多中心3期研究的结果
J Infect Chemother. 2018 Jun;24(6):434-442. doi: 10.1016/j.jiac.2018.01.010. Epub 2018 Mar 9.
7
Management of febrile neutropaenia: ESMO Clinical Practice Guidelines.发热性中性粒细胞减少症的管理:ESMO临床实践指南
Ann Oncol. 2016 Sep;27(suppl 5):v111-v118. doi: 10.1093/annonc/mdw325.
8
Nonclinical and pharmacokinetic assessments to evaluate the potential of tedizolid and linezolid to affect mitochondrial function.评估替加环素和利奈唑胺影响线粒体功能可能性的非临床和药代动力学评估。
Antimicrob Agents Chemother. 2015 Jan;59(1):178-85. doi: 10.1128/AAC.03684-14. Epub 2014 Oct 20.
9
Platelet profile in patients with acute bacterial skin and skin structure infections receiving tedizolid or linezolid: findings from the Phase 3 ESTABLISH clinical trials.接受特地唑胺或利奈唑胺治疗的急性细菌性皮肤及皮肤结构感染患者的血小板情况:3期ESTABLISH临床试验结果
Antimicrob Agents Chemother. 2014 Dec;58(12):7198-204. doi: 10.1128/AAC.03509-14. Epub 2014 Sep 22.
10
Tedizolid for 6 days versus linezolid for 10 days for acute bacterial skin and skin-structure infections (ESTABLISH-2): a randomised, double-blind, phase 3, non-inferiority trial.替考拉宁治疗 6 天与利奈唑胺治疗 10 天治疗急性细菌性皮肤和皮肤结构感染(ESTABLISH-2):一项随机、双盲、III 期、非劣效性试验。
Lancet Infect Dis. 2014 Aug;14(8):696-705. doi: 10.1016/S1473-3099(14)70737-6. Epub 2014 Jun 5.