Association of hydroxychloroquine and cardiac arrhythmia in patients with systemic lupus erythematosus: A population-based case control study

Hydroxychloroquine is widely used to treat certain viral and rheumatic diseases including systemic lupus erythematosus. Cardiac arrhythmia is an important safety issue with hydroxychloroquine. The aim of this study was to investigate whether hydroxychloroquine increases new-onset arrhythmia among pa...

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Veröffentlicht in:PloS one 2021-05, Vol.16 (5), p.e0251918-e0251918
Hauptverfasser: Lo, Chien-Hsien, Wang, Yu-Hsun, Tsai, Chin-Feng, Chan, Kuei-Chuan, Li, Li-Ching, Lo, Tse-Hsien, Wei, James Cheng-Chung, Su, Chun-Hung
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creator Lo, Chien-Hsien
Wang, Yu-Hsun
Tsai, Chin-Feng
Chan, Kuei-Chuan
Li, Li-Ching
Lo, Tse-Hsien
Wei, James Cheng-Chung
Su, Chun-Hung
description Hydroxychloroquine is widely used to treat certain viral and rheumatic diseases including systemic lupus erythematosus. Cardiac arrhythmia is an important safety issue with hydroxychloroquine. The aim of this study was to investigate whether hydroxychloroquine increases new-onset arrhythmia among patients with systemic lupus erythematosus. This was a nested case-control study using data from the Longitudinal Health Insurance Database of Taiwan. A conditional logistic regression model was used to analyse differences in the risk of arrhythmia between systemic lupus erythematosus patients with and without hydroxychloroquine treatment after controlling for related variables. A total of 2499 patients with newly diagnosed systemic lupus erythematosus were identified (81% females), of whom 251 were enrolled in the new-onset arrhythmia group (mean age 50.4 years) and 251 in the non-arrhythmia group (mean age 49.1 years). There was no significantly increased risk of cardiac arrhythmia (adjusted odds ratio = 1.49, 95% confidence interval: 0.98-2.25) or ventricular arrhythmia (adjusted odds ratio = 1.02, 95% confidence interval: 0.19-5.41) between the patients with and without hydroxychloroquine treatment. In addition, there were no significant differences in the risk of arrhythmia between those receiving hydroxychloroquine treatment for
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Cardiac arrhythmia is an important safety issue with hydroxychloroquine. The aim of this study was to investigate whether hydroxychloroquine increases new-onset arrhythmia among patients with systemic lupus erythematosus. This was a nested case-control study using data from the Longitudinal Health Insurance Database of Taiwan. A conditional logistic regression model was used to analyse differences in the risk of arrhythmia between systemic lupus erythematosus patients with and without hydroxychloroquine treatment after controlling for related variables. A total of 2499 patients with newly diagnosed systemic lupus erythematosus were identified (81% females), of whom 251 were enrolled in the new-onset arrhythmia group (mean age 50.4 years) and 251 in the non-arrhythmia group (mean age 49.1 years). There was no significantly increased risk of cardiac arrhythmia (adjusted odds ratio = 1.49, 95% confidence interval: 0.98-2.25) or ventricular arrhythmia (adjusted odds ratio = 1.02, 95% confidence interval: 0.19-5.41) between the patients with and without hydroxychloroquine treatment. In addition, there were no significant differences in the risk of arrhythmia between those receiving hydroxychloroquine treatment for &lt;180 days or ≥180 days, with a drug adherence rate of &lt;50% or ≥50%, and receiving a daily dose of &lt;400 mg or ≥400 mg. In patients with systemic lupus erythematosus, hydroxychloroquine treatment did not significantly increase the risk of cardiac arrhythmia or life-threatening ventricular arrhythmia regardless of the different hydroxychloroquine treatment duration, drug adherence rate, or daily dose.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0251918</identifier><identifier>PMID: 34015030</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Alcoholism ; Antimalarial agents ; Arrhythmia ; Arthritis ; Autoimmune diseases ; Biology and Life Sciences ; Cardiac arrhythmia ; Cardiology ; Cardiovascular disease ; Cardiovascular diseases ; Chronic conditions ; Chronic obstructive pulmonary disease ; Complications and side effects ; Congestive heart failure ; Coronary artery disease ; Coronaviruses ; COVID-19 ; Diabetes mellitus ; Disease transmission ; Drug abuse ; Drug dosages ; Drug therapy ; Health insurance ; Health risks ; Heart diseases ; Heart failure ; Hospitals ; Hydroxychloroquine ; Hyperlipidemia ; Hypertension ; Immunomodulators ; Inflammatory diseases ; Internal medicine ; Kidney diseases ; Liver diseases ; Lung diseases ; Lupus ; Medical research ; Medical treatment ; Medicine ; Medicine and Health Sciences ; Obstructive lung disease ; Patients ; Population ; Population studies ; Population-based studies ; Regression analysis ; Rheumatoid arthritis ; Risk factors ; Severe acute respiratory syndrome coronavirus 2 ; Statistics ; Stroke ; Systemic lupus erythematosus</subject><ispartof>PloS one, 2021-05, Vol.16 (5), p.e0251918-e0251918</ispartof><rights>COPYRIGHT 2021 Public Library of Science</rights><rights>2021 Lo et al. 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One</addtitle><date>2021-05-20</date><risdate>2021</risdate><volume>16</volume><issue>5</issue><spage>e0251918</spage><epage>e0251918</epage><pages>e0251918-e0251918</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Hydroxychloroquine is widely used to treat certain viral and rheumatic diseases including systemic lupus erythematosus. Cardiac arrhythmia is an important safety issue with hydroxychloroquine. The aim of this study was to investigate whether hydroxychloroquine increases new-onset arrhythmia among patients with systemic lupus erythematosus. This was a nested case-control study using data from the Longitudinal Health Insurance Database of Taiwan. A conditional logistic regression model was used to analyse differences in the risk of arrhythmia between systemic lupus erythematosus patients with and without hydroxychloroquine treatment after controlling for related variables. A total of 2499 patients with newly diagnosed systemic lupus erythematosus were identified (81% females), of whom 251 were enrolled in the new-onset arrhythmia group (mean age 50.4 years) and 251 in the non-arrhythmia group (mean age 49.1 years). There was no significantly increased risk of cardiac arrhythmia (adjusted odds ratio = 1.49, 95% confidence interval: 0.98-2.25) or ventricular arrhythmia (adjusted odds ratio = 1.02, 95% confidence interval: 0.19-5.41) between the patients with and without hydroxychloroquine treatment. In addition, there were no significant differences in the risk of arrhythmia between those receiving hydroxychloroquine treatment for &lt;180 days or ≥180 days, with a drug adherence rate of &lt;50% or ≥50%, and receiving a daily dose of &lt;400 mg or ≥400 mg. In patients with systemic lupus erythematosus, hydroxychloroquine treatment did not significantly increase the risk of cardiac arrhythmia or life-threatening ventricular arrhythmia regardless of the different hydroxychloroquine treatment duration, drug adherence rate, or daily dose.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>34015030</pmid><doi>10.1371/journal.pone.0251918</doi><tpages>e0251918</tpages><orcidid>https://orcid.org/0000-0003-4003-008X</orcidid><orcidid>https://orcid.org/0000-0001-5729-5928</orcidid><oa>free_for_read</oa></addata></record>
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subjects Alcoholism
Antimalarial agents
Arrhythmia
Arthritis
Autoimmune diseases
Biology and Life Sciences
Cardiac arrhythmia
Cardiology
Cardiovascular disease
Cardiovascular diseases
Chronic conditions
Chronic obstructive pulmonary disease
Complications and side effects
Congestive heart failure
Coronary artery disease
Coronaviruses
COVID-19
Diabetes mellitus
Disease transmission
Drug abuse
Drug dosages
Drug therapy
Health insurance
Health risks
Heart diseases
Heart failure
Hospitals
Hydroxychloroquine
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Systemic lupus erythematosus
title Association of hydroxychloroquine and cardiac arrhythmia in patients with systemic lupus erythematosus: A population-based case control study
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