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Guidance on Minimizing Risk of Drug-Induced Ventricular Arrhythmia During Treatment of COVID-19: A Statement from the Canadian Heart Rhythm Society.
Sapp, John L; Alqarawi, Wael; MacIntyre, Ciorsti J; Tadros, Rafik; Steinberg, Christian; Roberts, Jason D; Laksman, Zachary; Healey, Jeff S; Krahn, Andrew D.
  • Sapp JL; Dalhousie University and Queen Elizabeth II Health Sciences Centre, Halifax, Nova Scotia, Canada. Electronic address: john.sapp@nshealth.ca.
  • Alqarawi W; University of Ottawa Heart Institute, Ottawa, Ontario, Canada.
  • MacIntyre CJ; Dalhousie University and Queen Elizabeth II Health Sciences Centre, Halifax, Nova Scotia, Canada.
  • Tadros R; Cardiovascular Genetics Centre, Montréal Heart Institute, Montréal, Québec, Canada.
  • Steinberg C; Institut Universitaire de Cardiologie et Pneumologie de Québec, Université Laval, Québec, Québec, Canada.
  • Roberts JD; Western University, London, Ontario, Canada.
  • Laksman Z; University of British Columbia, Vancouver, British Columbia, Canada.
  • Healey JS; Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
  • Krahn AD; University of British Columbia, Vancouver, British Columbia, Canada.
Can J Cardiol ; 36(6): 948-951, 2020 06.
Article in English | MEDLINE | ID: covidwho-77139
ABSTRACT
The COVID-19 pandemic has led to efforts at rapid investigation and application of drugs which may improve prognosis but for which safety and efficacy are not yet established. This document attempts to provide reasonable guidance for the use of antimicrobials which have uncertain benefit but may increase risk of QT interval prolongation and ventricular proarrhythmia, notably, chloroquine, hydroxychloroquine, azithromycin, and lopinavir/ritonavir. During the pandemic, efforts to reduce spread and minimize effects on health care resources mandate minimization of unnecessary medical procedures and testing. We recommend that the risk of drug proarrhythmia be minimized by 1) discontinuing unnecessary medications that may also increase the QT interval, 2) identifying outpatients who are likely to be at low risk and do not need further testing (no history of prolonged QT interval, unexplained syncope, or family history of premature sudden cardiac death, no medications that may prolong the QT interval, and/or a previous known normal corrected QT interval [QTc]), and 3) performing baseline testing in hospitalized patients or those who may be at higher risk. If baseline electrocardiographic testing reveals a moderately prolonged QTc, optimization of medications and electrolytes may permit therapy. If the QTc is markedly prolonged, drugs that further prolong it should be avoided, or expert consultation may permit administration with mitigating precautions. These recommendations are made while there are no known effective treatments for COVID-19 and should be revisited when further data on efficacy and safety become available.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Arrhythmias, Cardiac / Risk Management / Long QT Syndrome / Coronavirus Infections / Azithromycin / Ritonavir / Pandemics / Hydroxychloroquine Type of study: Diagnostic study / Observational study / Prognostic study Topics: Long Covid Limits: Humans Country/Region as subject: North America Language: English Journal: Can J Cardiol Journal subject: Cardiology Year: 2020 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Arrhythmias, Cardiac / Risk Management / Long QT Syndrome / Coronavirus Infections / Azithromycin / Ritonavir / Pandemics / Hydroxychloroquine Type of study: Diagnostic study / Observational study / Prognostic study Topics: Long Covid Limits: Humans Country/Region as subject: North America Language: English Journal: Can J Cardiol Journal subject: Cardiology Year: 2020 Document Type: Article