Suppr超能文献

经皮影像引导下腹盆腔脓肿引流的光动力治疗的安全性和可行性:1 期试验。

Safety and Feasibility of Photodynamic Therapy for Percutaneous Image-guided Abdominopelvic Abscess Drainage: Phase 1 Trial.

机构信息

From the Department of Imaging Sciences (T.M.B., D.A.B., L.C., E.L., M.D.F., T.H.F., A.K.S.) and Clinical & Translational Science Institute (E.L.), University of Rochester Medical Center, 601 Elmwood Ave, Box 648, Rochester, NY 14642; and Department of Biomedical Engineering and Institute of Optics, University of Rochester, Rochester, NY (T.M.B.).

出版信息

Radiology. 2024 Mar;310(3):e232667. doi: 10.1148/radiol.232667.

Abstract

Background Standard-of-care abscess management includes image-guided percutaneous drainage and antibiotics; however, cure rates vary, and concern for antibiotic-resistant bacteria is growing. Photodynamic therapy (PDT), which uses light-activated dyes to generate cytotoxic reactive oxygen species, could complement the standard of care by sterilizing the abscess at the time of drainage. Purpose To evaluate safety and feasibility of PDT with methylene blue (hereafter, MB-PDT) at the time of percutaneous abscess drainage. Materials and Methods This prospective, open-label, dose-escalation, first-in-humans, registered phase 1 clinical study of MB-PDT included participants who underwent percutaneous abdominal or pelvic abscess drainage with CT or US guidance from January 2015 to March 2020 and September 2022 to September 2023. Following drainage, MB-PDT was performed with laser illumination at a fluence rate of 20 mW/cm, with fluence groups of 6, 12, 18, 24, 30, and 36 J/cm ( = 3 each). The primary outcome was safety, indicated by absence of fat embolism, MB escape, abscess wall damage, and need for surgery to remove optical fibers. Preliminary efficacy end points included the time to drainage catheter removal, drainage catheter output volume, and clinical symptom and fever duration. Relationships between fluence and outcomes were analyzed with Spearman correlation and linear regression analyses, and ordinary one-way analysis of variance was used for group comparisons. Results MB-PDT was safe and feasible in all 18 participants (mean age, 60.1 years ± 18.3 [SD]; 10 female), with no negative safety outcomes observed for any participant. No study-related adverse events were encountered, and the procedure did not increase reported pain ( = .1). Clinical symptom and fever duration was shorter in participants receiving higher fluences (30 and 36 J/cm vs 6 J/cm) ( = .03). The presence of antibiotic-resistant bacteria was not predictive of clinical symptom and fever duration (β = 0.13, = .37). Conclusion MB-PDT was a safe and feasible adjunct to image-guided percutaneous abscess drainage. Clinical measures indicated a dose-dependent response to PDT. ClinicalTrials.gov registration no.: NCT02240498 © RSNA, 2024 See also the editorial by Johnston and Goldberg in this issue.

摘要

背景 标准的脓肿处理包括影像引导下经皮引流和抗生素治疗;然而,治愈率各不相同,对抗生素耐药菌的担忧也在增加。光动力疗法(PDT)利用光激活染料产生细胞毒性活性氧,可通过在引流时对脓肿进行杀菌,补充标准治疗。目的 评估经皮脓肿引流时使用亚甲蓝(MB)的 PDT(MB-PDT)的安全性和可行性。 材料与方法 这是一项前瞻性、开放性、剂量递增、首例人体、已注册的 1 期临床研究,纳入了 2015 年 1 月至 2020 年 3 月和 2022 年 9 月至 2023 年 9 月期间接受 CT 或 US 引导的经皮腹部或骨盆脓肿引流的参与者。引流后,使用激光以 20 mW/cm 的辐照率进行 MB-PDT,辐照剂量分别为 6、12、18、24、30 和 36 J/cm(每组各 3 例)。主要结果是安全性,表现为无脂肪栓塞、MB 逸出、脓肿壁损伤和需要手术取出光纤。初步疗效终点包括引流导管拔除时间、引流导管输出量以及临床症状和发热持续时间。使用 Spearman 相关和线性回归分析评估剂量与结果之间的关系,并用普通单向方差分析进行组间比较。 结果 18 名参与者(平均年龄 60.1 岁±18.3[标准差];10 名女性)均接受了 MB-PDT,所有参与者均未出现任何负面的安全性结果。未发生与研究相关的不良事件,该程序并未增加报告的疼痛( =.1)。接受较高剂量(30 和 36 J/cm)的参与者的临床症状和发热持续时间更短( =.03)。抗生素耐药菌的存在与临床症状和发热持续时间无关(β=0.13, =.37)。 结论 MB-PDT 是影像引导下经皮脓肿引流的一种安全可行的辅助治疗方法。临床指标表明 PDT 有剂量依赖性反应。ClinicalTrials.gov 注册号:NCT02240498 ©RSNA,2024 详见本期 Johnston 和 Goldberg 的社论。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验