Bilateral Venous Access for Cardiac Resynchronization Therapy in a Hemodialysis Patient With Cabozantinib-associated Heart Failure.

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
In vivo Pub Date : 2025-05-01 DOI:10.21873/invivo.13973
Amane Otoi, Akinori Higaki, Noriyoshi Miura, Keisho Kurokawa, Kohei Yoshimoto, Tomoaki Nishikawa, Rikako Horie, Arisa Abe, Yasuhisa Nakao, Tomoki Fujisawa, Shigehiro Miyazaki, Yusuke Akazawa, Toru Miyoshi, Hiroshi Kawakami, Haruhiko Higashi, Shunsuke Tamaki, Kazuhisa Nishimura, Katsuji Inoue, Shuntaro Ikeda, Osamu Yamaguchi
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引用次数: 0

Abstract

Background: Cabozantinib, a multi-targeted tyrosine kinase inhibitor, is widely used for the treatment of renal and hepatic cancers. While cabozantinib-associated cardiotoxicity is rare, it has been documented in several cases. In most instances, cancer therapeutics-related cardiac dysfunction (CTRCD) is managed by discontinuing cabozantinib and initiating cardioprotective agents. In this report, we present the case of a 63-year-old male with cabozantinib-induced heart failure (HF) with reduced ejection fraction (EF) and complete left bundle branch block (CLBBB).

Case report: The patient, undergoing hemodialysis for chronic kidney disease, had limited therapeutic options due to prior treatment failures. Despite six months of standard HF therapy, symptoms persisted, prompting cardiac resynchronization therapy (CRT) implantation without interrupting cabozantinib. Due to the presence of a dialysis shunt in the patient's left arm, the right subclavian vein was selected for venous access to minimize the risk of lead-related complications. Using a tunneling tool, the left ventricular lead was placed via the contralateral vasculature to the ipsilateral generator. Six months post-CRT, echocardiography showed significant reverse remodeling with improved EF and reduced left ventricular end-diastolic diameter, alongside clinical symptom relief.

Conclusion: This case highlights the utility of bilateral venous access with a tunneling tool in cardiac resynchronization therapy, particularly for patients with hemodialysis shunts.

卡博赞替尼相关性心力衰竭血液透析患者心脏再同步化治疗的双侧静脉通路。
背景:卡博赞替尼是一种多靶点酪氨酸激酶抑制剂,广泛用于治疗肾癌和肝癌。虽然卡博赞替尼相关的心脏毒性是罕见的,但它已被记录在几个病例。在大多数情况下,癌症治疗相关的心功能障碍(CTRCD)是通过停用卡博赞替尼和启动心脏保护剂来管理的。在本报告中,我们报告了一例63岁男性卡博替尼诱发心力衰竭(HF)伴射血分数降低(EF)和完全性左束支阻滞(CLBBB)的病例。病例报告:患者,接受血液透析慢性肾脏疾病,有限的治疗选择,由于先前的治疗失败。尽管标准HF治疗6个月,症状持续存在,促使心脏再同步化治疗(CRT)植入而不中断卡博赞替尼。由于患者左臂存在透析分流,因此选择右锁骨下静脉进行静脉通路,以尽量减少铅相关并发症的风险。使用隧道工具,左心室导线通过对侧脉管系统放置到同侧发生器。crt后6个月,超声心动图显示明显的反向重构,EF改善,左室舒张末期内径减小,同时临床症状缓解。结论:本病例强调了双侧静脉通道隧道工具在心脏再同步化治疗中的应用,特别是对血液透析分流患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
In vivo
In vivo 医学-医学:研究与实验
CiteScore
4.20
自引率
4.30%
发文量
330
审稿时长
3-8 weeks
期刊介绍: IN VIVO is an international peer-reviewed journal designed to bring together original high quality works and reviews on experimental and clinical biomedical research within the frames of physiology, pathology and disease management. The topics of IN VIVO include: 1. Experimental development and application of new diagnostic and therapeutic procedures; 2. Pharmacological and toxicological evaluation of new drugs, drug combinations and drug delivery systems; 3. Clinical trials; 4. Development and characterization of models of biomedical research; 5. Cancer diagnosis and treatment; 6. Immunotherapy and vaccines; 7. Radiotherapy, Imaging; 8. Tissue engineering, Regenerative medicine; 9. Carcinogenesis.
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