TY - JOUR
T1 - Heart failure as an adverse effect of infliximab for Crohn's disease
T2 - A case report and review of the literature
AU - Grillo, Thais Gagno
AU - Almeida, Luciana Rocha
AU - Beraldo, Rodrigo Fedatto
AU - Marcondes, Mariana Barros
AU - Queiróz, Diego Aparecido Rios
AU - da Silva, Daniel Luiz
AU - Quera, Rodrigo
AU - Baima, Julio Pinheiro
AU - Saad-Hossne, Rogerio
AU - Sassaki, Ligia Yukie
N1 - Publisher Copyright:
© The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved.
PY - 2021/11/26
Y1 - 2021/11/26
N2 - Background Anti-tumor necrosis factor agents were the first biologic therapy approved for the management of Crohn's disease (CD). Heart failure (HF) is a rare but potential adverse effect of these medications. The objective of this report is to describe a patient with CD who developed HF after the use of infliximab. Case Summary A 50-year-old woman with a history of hypertension and diabetes presented with abdominal pain, diarrhea, and weight loss. Colonoscopy and enterotomography showed ulcerations, areas of stenosis and dilation in the terminal ileum, and thickening of the intestinal wall. The patient underwent ileocolectomy and the surgical specimen confirmed the diagnosis of stenosing CD. The patient started infliximab and azathioprine treatment to prevent post-surgical recurrence. At 6 mo after initiating infliximab therapy, the patient complained of dyspnea, orthopnea, and paroxysmal nocturnal dyspnea that gradually worsened. Echocardiography revealed biventricular dysfunction, moderate cardiac insufficiency, an ejection fraction of 36%, and moderate pericardial effusion, consistent with HF. The cardiac disease was considered an infliximab adverse effect and the drug was discontinued. The patient received treatment with diuretics for HF and showed improvement of symptoms and cardiac function. Currently, the patient is using Conclusion This reported case supports the need to investigate risk factors for HF in inflammatory bowel disease patients and to consider the risk-benefit of introducing infliximab therapy in such patients presenting with HF risk factors.
AB - Background Anti-tumor necrosis factor agents were the first biologic therapy approved for the management of Crohn's disease (CD). Heart failure (HF) is a rare but potential adverse effect of these medications. The objective of this report is to describe a patient with CD who developed HF after the use of infliximab. Case Summary A 50-year-old woman with a history of hypertension and diabetes presented with abdominal pain, diarrhea, and weight loss. Colonoscopy and enterotomography showed ulcerations, areas of stenosis and dilation in the terminal ileum, and thickening of the intestinal wall. The patient underwent ileocolectomy and the surgical specimen confirmed the diagnosis of stenosing CD. The patient started infliximab and azathioprine treatment to prevent post-surgical recurrence. At 6 mo after initiating infliximab therapy, the patient complained of dyspnea, orthopnea, and paroxysmal nocturnal dyspnea that gradually worsened. Echocardiography revealed biventricular dysfunction, moderate cardiac insufficiency, an ejection fraction of 36%, and moderate pericardial effusion, consistent with HF. The cardiac disease was considered an infliximab adverse effect and the drug was discontinued. The patient received treatment with diuretics for HF and showed improvement of symptoms and cardiac function. Currently, the patient is using Conclusion This reported case supports the need to investigate risk factors for HF in inflammatory bowel disease patients and to consider the risk-benefit of introducing infliximab therapy in such patients presenting with HF risk factors.
KW - Anti-tumor necrosis factor therapy
KW - Case report
KW - Crohn's disease
KW - Heart failure
KW - Inflammatory bowel disease
KW - Infliximab
UR - http://www.scopus.com/inward/record.url?scp=85120964335&partnerID=8YFLogxK
U2 - 10.12998/wjcc.v9.i33.10382
DO - 10.12998/wjcc.v9.i33.10382
M3 - Article
AN - SCOPUS:85120964335
SN - 2307-8960
VL - 9
SP - 10382
EP - 10391
JO - World Journal of Clinical Cases
JF - World Journal of Clinical Cases
IS - 33
ER -