Safety profile of intravenous digoxin in Chinese patients with acute heart failure with reduced ejection fraction: a small-scale prospective cohort study

Background: Adverse effects of intravenous digoxin vary from patients and disease status, which should be closely monitored.Aims: To explore the safety profile of intravenous digoxin in acute heart failure with reduced ejection fraction (HFrEF) among Chinese patients.Methods: A clinical prospective,...

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Main Authors: Xintian Liu, Haojie Zhang, Wenlin Cheng, Qingkun Fan, Zhibing Lu, Xuan Zheng, Gangcheng Zhang
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-11-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2023.1291896/full
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author Xintian Liu
Xintian Liu
Haojie Zhang
Wenlin Cheng
Qingkun Fan
Zhibing Lu
Xuan Zheng
Gangcheng Zhang
author_facet Xintian Liu
Xintian Liu
Haojie Zhang
Wenlin Cheng
Qingkun Fan
Zhibing Lu
Xuan Zheng
Gangcheng Zhang
author_sort Xintian Liu
collection DOAJ
description Background: Adverse effects of intravenous digoxin vary from patients and disease status, which should be closely monitored.Aims: To explore the safety profile of intravenous digoxin in acute heart failure with reduced ejection fraction (HFrEF) among Chinese patients.Methods: A clinical prospective, single-center, single-arm, open-label exploratory clinical trial was performed in patients with acute HFrEF at Wuhan Asia Heart Hospital. A fixed dose of 0.5 mg digoxin was used intravenously once per day for 3 days. The normalized dosage of digoxin (NDD), toxic serum digoxin concentration (SDC), and adverse reactions of intravenous digoxin were recorded.Results: A total of 40 patients were recruited in the study. The SDC increased from 1.03 ± 0.34 ng/mL to 1.95 ± 0.52 ng/mL during treatment. 50% (20/40) patients reached a toxic SDC of 2.0 ng/mL, and toxic effects were seen in 30% (12/40) patients. Estimated glomerular filtration rate (eGFR) < 60 mL/min [HR: 5.269; 95% CI: 1.905–14.575, p = 0.001], NDD ≥7 μg/kg [HR: 3.028; 95% CI: 1.119–8.194, p = 0.029], and ischemic cardiomyopathy [HR: 2.658; 95% CI: 1.025–6.894, p = 0.044] were independent risk factors for toxic SDC. Toxic SDC was effectively identified [area under the receiver operating characteristic (ROC) curve = 0.85, p < 0.001] using this model, and patients would have a higher risk of toxicity with more risk factors.Conclusion: Intravenous digoxin of 0.5 mg was safe and effective for initial dose but not suitable for maintenance treatment in Chinese patients with acute HFrEF. Patients who had lower eGFR, received higher NDD, and had ischemic cardiomyopathy should be closely monitored to avoid digoxin toxicity.
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spelling doaj.art-b87cc03745664a0090445ba43f20998d2023-11-14T02:15:31ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122023-11-011410.3389/fphar.2023.12918961291896Safety profile of intravenous digoxin in Chinese patients with acute heart failure with reduced ejection fraction: a small-scale prospective cohort studyXintian Liu0Xintian Liu1Haojie Zhang2Wenlin Cheng3Qingkun Fan4Zhibing Lu5Xuan Zheng6Gangcheng Zhang7Center of Structural Heart Disease, Zhongnan Hospital of Wuhan University, Wuhan, ChinaDepartment of Cardiology, Zhongnan Hospital of Wuhan University, Wuhan, ChinaCenter of Structural Heart Disease, Zhongnan Hospital of Wuhan University, Wuhan, ChinaDepartment of Cardiology, Zhongnan Hospital of Wuhan University, Wuhan, ChinaLaboratory Medicine, Wuhan Asia Heart Hospital, Wuhan University of Science and Technology, Wuhan, ChinaDepartment of Cardiology, Zhongnan Hospital of Wuhan University, Wuhan, ChinaCenter of Structural Heart Disease, Zhongnan Hospital of Wuhan University, Wuhan, ChinaCenter of Structural Heart Disease, Zhongnan Hospital of Wuhan University, Wuhan, ChinaBackground: Adverse effects of intravenous digoxin vary from patients and disease status, which should be closely monitored.Aims: To explore the safety profile of intravenous digoxin in acute heart failure with reduced ejection fraction (HFrEF) among Chinese patients.Methods: A clinical prospective, single-center, single-arm, open-label exploratory clinical trial was performed in patients with acute HFrEF at Wuhan Asia Heart Hospital. A fixed dose of 0.5 mg digoxin was used intravenously once per day for 3 days. The normalized dosage of digoxin (NDD), toxic serum digoxin concentration (SDC), and adverse reactions of intravenous digoxin were recorded.Results: A total of 40 patients were recruited in the study. The SDC increased from 1.03 ± 0.34 ng/mL to 1.95 ± 0.52 ng/mL during treatment. 50% (20/40) patients reached a toxic SDC of 2.0 ng/mL, and toxic effects were seen in 30% (12/40) patients. Estimated glomerular filtration rate (eGFR) < 60 mL/min [HR: 5.269; 95% CI: 1.905–14.575, p = 0.001], NDD ≥7 μg/kg [HR: 3.028; 95% CI: 1.119–8.194, p = 0.029], and ischemic cardiomyopathy [HR: 2.658; 95% CI: 1.025–6.894, p = 0.044] were independent risk factors for toxic SDC. Toxic SDC was effectively identified [area under the receiver operating characteristic (ROC) curve = 0.85, p < 0.001] using this model, and patients would have a higher risk of toxicity with more risk factors.Conclusion: Intravenous digoxin of 0.5 mg was safe and effective for initial dose but not suitable for maintenance treatment in Chinese patients with acute HFrEF. Patients who had lower eGFR, received higher NDD, and had ischemic cardiomyopathy should be closely monitored to avoid digoxin toxicity.https://www.frontiersin.org/articles/10.3389/fphar.2023.1291896/fullacute heart failure with reduced ejection fractionintravenous digoxindigoxin toxicityserum digoxin concentration (SDC)safety evaluation
spellingShingle Xintian Liu
Xintian Liu
Haojie Zhang
Wenlin Cheng
Qingkun Fan
Zhibing Lu
Xuan Zheng
Gangcheng Zhang
Safety profile of intravenous digoxin in Chinese patients with acute heart failure with reduced ejection fraction: a small-scale prospective cohort study
Frontiers in Pharmacology
acute heart failure with reduced ejection fraction
intravenous digoxin
digoxin toxicity
serum digoxin concentration (SDC)
safety evaluation
title Safety profile of intravenous digoxin in Chinese patients with acute heart failure with reduced ejection fraction: a small-scale prospective cohort study
title_full Safety profile of intravenous digoxin in Chinese patients with acute heart failure with reduced ejection fraction: a small-scale prospective cohort study
title_fullStr Safety profile of intravenous digoxin in Chinese patients with acute heart failure with reduced ejection fraction: a small-scale prospective cohort study
title_full_unstemmed Safety profile of intravenous digoxin in Chinese patients with acute heart failure with reduced ejection fraction: a small-scale prospective cohort study
title_short Safety profile of intravenous digoxin in Chinese patients with acute heart failure with reduced ejection fraction: a small-scale prospective cohort study
title_sort safety profile of intravenous digoxin in chinese patients with acute heart failure with reduced ejection fraction a small scale prospective cohort study
topic acute heart failure with reduced ejection fraction
intravenous digoxin
digoxin toxicity
serum digoxin concentration (SDC)
safety evaluation
url https://www.frontiersin.org/articles/10.3389/fphar.2023.1291896/full
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