Isfahan University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! On (X network) By
Delayed Myocardial Infarction Associated With Rituximab Infusion: A Case Report and Literature Review Publisher Pubmed



Mehrpooya M1 ; Vaseghi G2 ; Eshraghi A3 ; Eslami N4
Authors
Show Affiliations
Authors Affiliations
  1. 1. Clinical Pharmacy Department, Hamedan University of Medical Sciences, Hamadan, Iran
  2. 2. Applied Physiology Research Center, Isfahan Cardiovascular Research Institute, Department of Pharmacology, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran
  3. 3. Department of Clinical Pharmacy, Faculty of Pharmacy-International Campus, Iran University of Medical Sciences, P.O. Box: 14155-6153, Tehran, Iran
  4. 4. Faculty of Pharmacy, Lorestan University of Medical Sciences, Khorramabad, Iran

Source: American Journal of Therapeutics Published:2016


Abstract

To report a case of delayed myocardial infraction after rituximab infusion. A 52-year-old woman with history of refractory idiopathic thrombocytopenic purpura had hypertension, seizure, and mild coronary artery disease and received rituximab; after 24 hours, she returned back with chest pain, nausea, and vomiting. Her electrocardiogram showed a ST-elevation in the II, III, aVF, and aVR lead and ST depression in I and aVL lead; after another complementary test, the myocardial infraction was confirmed. The patient was sent to the intensive care unit, and after 8-day hospitalization, she was discharged. Based on the Naranjo Probability Scale, the likelihood of rituximab-induced acute myocardial infarction in this case was probable. Rituximab is generally well tolerated; however, cardiovascular effects of this drug can be fatal. The side effects usually occur during or a short time after infusion; this case demonstrated that rituximab side effects may occur with delay. This case demonstrates, although a rare phenomenon, myocardial infraction may occur after 24 hours and clinicians should be aware of this fatal effect even after a period of time in patients receiving rituximab, especially in patients with history of coronary artery disease. Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved.