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Intravenous Immunoglobulin-Induced Bradycardia in a Patient with Idiopathic Thrombocytopenic Purpura

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Abstract

Intravenous immunoglobulin (IVIG) is a plasma-derived product and one of the most effective choices in the treatment of immune thrombocytopenic purpura. Various cardiovascular complications such as hypotension, bradycardia, supraventricular tachycardia, and even acute myocardial infarction (MI) have been reported following IVIG infusion so far. Most of these patients had pre-existing cardiac underlying risk factors. In this article, we report a 30-year-old woman with no history of cardiac disease who developed severe symptomatic bradycardia during IVIG infusion. Bradycardia was initially managed with atropine injections and administration of theophylline oral solution. Despite this adverse effect, IVIG infusion was resumed for two more days and the therapy courses were finished.

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Data Availability

The data that support the findings of this study are available from the corresponding author, (MM), upon reasonable request.

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Acknowledgements

We would like to thank Ms. Rose Naderi of Duke University Trinity College of Arts and Sciences for English proofreading the manuscript.

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G.A. and M.M. contributed to data collection, writing, drafting of the manuscript, and critical appraisal of the manuscript. M.E. contributed to scientific writing and final revision

Corresponding author

Correspondence to Masoud Mortezazadeh.

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In this study, no additional costs and procedures were imposed on the patient. We reported the standard treatment process of the patient retrograde. We maintained the patient’s privacy, and her written consent was obtained.

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The patient has consented to the participation of this case report.

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The participant has consented to the publication of this case report.

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The authors declare no competing interests.

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Esfandbod, M., Mortezazadeh, M. & Alavian, G. Intravenous Immunoglobulin-Induced Bradycardia in a Patient with Idiopathic Thrombocytopenic Purpura. SN Compr. Clin. Med. 3, 1789–1792 (2021). https://doi.org/10.1007/s42399-021-00937-w

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  • DOI: https://doi.org/10.1007/s42399-021-00937-w

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