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

**Authors:** Magdalena Karasek, Maciej Majcherek, Bartłomiej Kuszczak, Agnieszka Szeremet, Olga Chyrko, Tomasz Wróbel, Anna Czyż

PMC · DOI: 10.46989/001c.94362 · Clinical Hematology International · 2024-03-04

## TL;DR

A small percentage of patients receiving cyclosporine A after a stem cell transplant may develop sinus bradycardia, but switching to tacrolimus can resolve it without complications.

## Contribution

This study reports a rare adverse effect of cyclosporine A—sinus bradycardia—in patients after allogeneic stem cell transplantation.

## Key findings

- Sinus bradycardia occurred in 2.9% of patients receiving cyclosporine A after stem cell transplantation.
- Switching from cyclosporine A to tacrolimus resolved bradycardia without cardiac complications.
- Most patients with bradycardia had pre-existing cardiovascular conditions.

## 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.

## Linked entities

- **Chemicals:** cyclosporine A (PubChem CID 5284373), tacrolimus (PubChem CID 445643), atropine (PubChem CID 3661)
- **Diseases:** graft-versus-host disease (MONDO:0013730)

## Full-text entities

- **Diseases:** Sinus bradycardia (MESH:D012804), myeloid malignancies (MESH:D009369), aggressive lymphoma (MESH:D008223), cardiovascular disorders (MESH:D002318), tachycardia (MESH:D013610), cardiac complications (MESH:D006331), GvHD (MESH:D006086), bradycardia (MESH:D001919)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC11087002/full.md

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Source: https://tomesphere.com/paper/PMC11087002