{"title":"Transarterial Embolization Using Imipenem/Cilastatin for Chronic Painful Achilles Tendinopathy Refractory to Conservative Management.","authors":"Neeraj Kumar, Niraj Nirmal Pandey, Sanjeev Kumar, Aprateem Mukherjee, Vikrant Manhas, Priya Jagia","doi":"10.1016/j.jvir.2025.10.009","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate the feasibility, safety, and efficacy of transarterial embolization (TAE) for painful chronic Achilles tendinopathy (AT) refractory to conservative management.</p><p><strong>Materials and methods: </strong>This prospective study included 20 limbs in 18 patients (7 males, mean age: 45.89 ± 9.97 years) with painful chronic AT, not responding to conservative management for ≥3 months. Superselective cannulation of branches from the posterior tibial artery or the peroneal artery supplying the point of maximal pain in the Achilles tendon was performed. Branches showing hypervascular staining were embolized using a suspension of 500mg of imipenem/ cilastatin sodium in 5mL of iodinated contrast agent. Visual analogue scale (VAS) and Victorian Institute of Sports Assessment-Achilles questionnaire (VISA-A) scores were used to assess pain and function at baseline, 1 day, 1 week, 1 month, 3 months, 6 months, 9 months, and 12 months post-procedure.</p><p><strong>Results: </strong>Hypervascular staining at the point of maximal pain was seen in all patients. Branches from the posterior tibial artery or the peroneal artery supplying the area of hypervascular staining could be superselectively embolized in 18/20 limbs, indicating 90% technical success. Significant decrease in VAS score (Median (IQR): 7(7-8) vs. 1(1-2); p<0.0001) and significant increase in VISA-A score (Median (IQR): 29.5(24-33) vs. 68(56-76); p=0.0001) were noted on day 1 post-procedure which persisted through one year of follow-up. Clinical success, defined as a >50% reduction in VAS score, was achieved in 94.44% (17/18) of procedures.</p><p><strong>Conclusions: </strong>TAE is a feasible, safe and effective treatment for alleviating pain associated with chronic AT refractory to conservative management, with a low risk of adverse events.</p>","PeriodicalId":49962,"journal":{"name":"Journal of Vascular and Interventional Radiology","volume":" ","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Vascular and Interventional Radiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.jvir.2025.10.009","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PERIPHERAL VASCULAR DISEASE","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: To evaluate the feasibility, safety, and efficacy of transarterial embolization (TAE) for painful chronic Achilles tendinopathy (AT) refractory to conservative management.
Materials and methods: This prospective study included 20 limbs in 18 patients (7 males, mean age: 45.89 ± 9.97 years) with painful chronic AT, not responding to conservative management for ≥3 months. Superselective cannulation of branches from the posterior tibial artery or the peroneal artery supplying the point of maximal pain in the Achilles tendon was performed. Branches showing hypervascular staining were embolized using a suspension of 500mg of imipenem/ cilastatin sodium in 5mL of iodinated contrast agent. Visual analogue scale (VAS) and Victorian Institute of Sports Assessment-Achilles questionnaire (VISA-A) scores were used to assess pain and function at baseline, 1 day, 1 week, 1 month, 3 months, 6 months, 9 months, and 12 months post-procedure.
Results: Hypervascular staining at the point of maximal pain was seen in all patients. Branches from the posterior tibial artery or the peroneal artery supplying the area of hypervascular staining could be superselectively embolized in 18/20 limbs, indicating 90% technical success. Significant decrease in VAS score (Median (IQR): 7(7-8) vs. 1(1-2); p<0.0001) and significant increase in VISA-A score (Median (IQR): 29.5(24-33) vs. 68(56-76); p=0.0001) were noted on day 1 post-procedure which persisted through one year of follow-up. Clinical success, defined as a >50% reduction in VAS score, was achieved in 94.44% (17/18) of procedures.
Conclusions: TAE is a feasible, safe and effective treatment for alleviating pain associated with chronic AT refractory to conservative management, with a low risk of adverse events.
目的:评价经动脉栓塞(TAE)治疗难以保守治疗的疼痛性慢性跟腱病(AT)的可行性、安全性和有效性。材料与方法:本前瞻性研究纳入18例20肢疼痛性慢性AT患者(男性7例,平均年龄45.89±9.97岁),保守治疗无效≥3个月。从胫骨后动脉或供应最大疼痛点的腓骨动脉的分支进行超选择性插管。用500mg亚胺培南/西司他汀钠混悬液在5mL碘化造影剂中栓塞显示血管增生的分支。采用视觉模拟量表(VAS)和victoria Institute of Sports Assessment-Achilles questionnaire (VISA-A)评分,分别在术后基线、1天、1周、1个月、3个月、6个月、9个月和12个月评估疼痛和功能。结果:所有患者最大疼痛点均可见高血管染色。在18/20的肢体中,供应高血管染色区域的胫骨后动脉或腓动脉分支可以超选择性栓塞,表明90%的技术成功率。VAS评分显著降低(Median (IQR): 7(7-8) vs. 1(1-2);94.44%(17/18)的手术达到VAS评分降低50%。结论:TAE是一种可行、安全、有效的治疗方法,可缓解顽固性慢性AT患者的疼痛,不良事件风险低。
期刊介绍:
JVIR, published continuously since 1990, is an international, monthly peer-reviewed interventional radiology journal. As the official journal of the Society of Interventional Radiology, JVIR is the peer-reviewed journal of choice for interventional radiologists, radiologists, cardiologists, vascular surgeons, neurosurgeons, and other clinicians who seek current and reliable information on every aspect of vascular and interventional radiology. Each issue of JVIR covers critical and cutting-edge medical minimally invasive, clinical, basic research, radiological, pathological, and socioeconomic issues of importance to the field.