Sinus bradycardia as a rare adverse event in patients receiving cyclosporine A after allogeneic hematopoietic stem cell transplantation.

M. Karasek, Maciej Majcherek, Bartłomiej Kuszczak, A. Szeremet, Olga Chyrko, Tomasz Wróbel, A. Czyż
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Abstract

Cyclosporine A (CSA) is a commonly used immunosuppressive agent for the prophylaxis of graft-versus-host disease following allogeneic hematopoietic stem cell transplantation (alloHSCT). While tachycardia is a known adverse effect of CSA, bradycardia remains a phenomenon rarely described in the literature. We conducted a retrospective evaluation of the incidence of bradycardia in patients after alloHSCT treated with CSA between January 2020 and February 2023 at our center. Out of 206 patients, sinus bradycardia following the administration of CSA was observed in 6 (2.9%), comprising 3 women and 3 men, with the median age of 55 years (range: 20-65). The underlying diseases were myeloid malignancies in 4 and aggressive lymphoma in 2 patients. The patients received grafts from a matched unrelated (n=5) or a haploidentical family donor (n=1) following various conditioning regimens. Coexisting cardiovascular disorders were found in 5 of the 6 patients. All patients experienced symptomatic bradycardia within 1-4 days (median 2 days) after CSA introduction, which persisted until CSA withdrawal. One patient required treatment with atropine. All patients continued their immunosuppressive therapy with tacrolimus, which was well-tolerated Our study indicates CSA as a causative factor of sinus bradycardia in a small percentage of alloHSCT patients receiving CSA as graft-versus host disease (GvHD) prophylaxis. Importantly, these patients did not experience any cardiac complications when switched to tacrolimus. Although further research on the effects of CSA on heart automatation is needed, our single-center experience can help prompt diagnosis and therapeutic intervention in daily clinical practice.
窦性心动过缓是异体造血干细胞移植后接受环孢素 A 患者的一种罕见不良反应。
环孢素A(CSA)是异基因造血干细胞移植(alloHSCT)后预防移植物抗宿主疾病的常用免疫抑制剂。心动过速是CSA的已知不良反应,而心动过缓仍然是文献中极少描述的现象。我们对本中心2020年1月至2023年2月期间接受CSA治疗的alloHSCT患者心动过缓的发生率进行了回顾性评估。在 206 名患者中,有 6 人(2.9%)在使用 CSA 后出现窦性心动过缓(包括 3 名女性和 3 名男性),中位年龄为 55 岁(20-65 岁)。4名患者的基础疾病是骨髓恶性肿瘤,2名患者是侵袭性淋巴瘤。这些患者在接受不同的调理方案后,接受了来自匹配的非亲缘供体(5 人)或单倍体家族供体(1 人)的移植物。6 名患者中有 5 人同时患有心血管疾病。所有患者在引入 CSA 后 1-4 天内(中位数为 2 天)都出现了症状性心动过缓,这种症状一直持续到撤除 CSA。一名患者需要使用阿托品治疗。我们的研究表明,CSA 是一小部分接受 CSA 作为移植物抗宿主病(GvHD)预防药物的异体肝移植患者出现窦性心动过缓的致病因素。重要的是,这些患者在改用他克莫司治疗后没有出现任何心脏并发症。尽管还需要进一步研究 CSA 对心脏自动调节的影响,但我们的单中心经验有助于在日常临床实践中及时诊断和治疗干预。
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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