Subject(s)
COVID-19 , Channelopathies , Ion Channels/metabolism , Long QT Syndrome , Muscle Cells , SARS-CoV-2 , COVID-19/complications , COVID-19/metabolism , COVID-19/physiopathology , Channelopathies/metabolism , Channelopathies/physiopathology , Channelopathies/prevention & control , Channelopathies/virology , Heart Conduction System/metabolism , Heart Conduction System/virology , Host Microbial Interactions , Host-Derived Cellular Factors/metabolism , Humans , Long QT Syndrome/etiology , Long QT Syndrome/metabolism , Long QT Syndrome/prevention & control , Long QT Syndrome/virology , Muscle Cells/physiology , Muscle Cells/virology , SARS-CoV-2/pathogenicity , SARS-CoV-2/physiologySubject(s)
Chloroquine/adverse effects , Coronavirus Infections/drug therapy , Hydroxychloroquine/adverse effects , Long QT Syndrome/prevention & control , Pneumonia, Viral/drug therapy , Antiviral Agents/adverse effects , Arrhythmias, Cardiac/chemically induced , Arrhythmias, Cardiac/diagnosis , Arrhythmias, Cardiac/physiopathology , Arrhythmias, Cardiac/prevention & control , Azithromycin/adverse effects , COVID-19 , Cardiotoxicity/diagnosis , Cardiotoxicity/etiology , Cardiotoxicity/physiopathology , Cardiotoxicity/prevention & control , Coronavirus Infections/complications , Dehydration/complications , Drug Interactions , Electrocardiography , Humans , Long QT Syndrome/chemically induced , Long QT Syndrome/diagnosis , Long QT Syndrome/physiopathology , Pandemics , Pneumonia, Viral/complications , Risk Assessment , Water-Electrolyte Imbalance/complicationsSubject(s)
Antiviral Agents/therapeutic use , Azithromycin/therapeutic use , COVID-19 Drug Treatment , Hydroxychloroquine/therapeutic use , SARS-CoV-2/drug effects , Anti-Bacterial Agents/therapeutic use , Antimalarials/therapeutic use , COVID-19/virology , Clinical Trials as Topic , Drug Combinations , Drug Interactions , Drug Repositioning , Drug Synergism , Electrocardiography , Humans , Long QT Syndrome/prevention & control , Monitoring, Physiologic , Patient Safety , RNA, Viral/antagonists & inhibitors , RNA, Viral/genetics , SARS-CoV-2/genetics , SARS-CoV-2/pathogenicity , Treatment OutcomeSubject(s)
Antiviral Agents/therapeutic use , Azithromycin/therapeutic use , COVID-19 Drug Treatment , Hydroxychloroquine/therapeutic use , SARS-CoV-2/drug effects , Anti-Bacterial Agents/therapeutic use , Antimalarials/therapeutic use , COVID-19/virology , Clinical Trials as Topic , Drug Combinations , Drug Interactions , Drug Repositioning , Drug Synergism , Electrocardiography , Humans , Hyperkalemia/prevention & control , Hypokalemia/prevention & control , Long QT Syndrome/prevention & control , Magnesium/administration & dosage , Patient Safety , RNA, Viral/antagonists & inhibitors , RNA, Viral/genetics , SARS-CoV-2/genetics , SARS-CoV-2/pathogenicity , Treatment OutcomeSubject(s)
Antiviral Agents/therapeutic use , Azithromycin/therapeutic use , COVID-19 Drug Treatment , Hydroxychloroquine/therapeutic use , SARS-CoV-2/pathogenicity , Anti-Bacterial Agents/therapeutic use , Antimalarials/therapeutic use , COVID-19/virology , Clinical Trials as Topic , Drug Combinations , Drug Interactions , Drug Repositioning , Drug Synergism , Electrocardiography , Humans , Hyperkalemia/prevention & control , Hypokalemia/prevention & control , Long QT Syndrome/prevention & controlABSTRACT
INTRODUCTION AND AIM: Hydroxychloroquine alone or in combination with azithromycin has been increasingly used for patients with coronavirus disease 2019, in both children and adults. Drugs are generally well tolerated in clinical practice; however, both can cause corrected QT prolongation. We aimed to report our experience of QT interval evaluation associated with the use of hydroxychloroquine with concurrent azithromycin among children testing positive for coronavirus disease 2019. METHODS: Our single-centre; retrospective, study evaluated children with coronavirus disease 2019 disease admitted to the Pediatric Department at Sancaktepe Training and Research Hospital Istanbul, Turkey from 10 March, 2020 to 10 April, 2020. The data including demographics, clinical symptoms, co-morbid diseases, laboratory, radiological findings as well as electrocardiographs of the patients were obtained from our records. Electrocardiograms were evaluated before, one day after and at the termination of the treatment. RESULTS: 21 patients aged 9 to 18 years were evaluated. The median age was 170 months (range 112-214), 51.1% of them were girls and 48.9% were boys. Their laboratory results did not reveal any abnormalities. None of them needed intensive care. We did not detect QT prolongation during or at the termination of the treatment. CONCLUSION: We did not detect QT prolongation during or at the termination of the treatment in our patients due to the fact that they were not severely affected by the disease. Patients were treated in our inpatient clinic and none of them required intensive care. Laboratory results were also insignificant. Furthermore, they did not need other medications.
Subject(s)
Azithromycin , Coronavirus Infections/drug therapy , Electrocardiography/methods , Hydroxychloroquine , Long QT Syndrome , Pneumonia, Viral/drug therapy , Adolescent , Anti-Infective Agents/administration & dosage , Anti-Infective Agents/adverse effects , Azithromycin/administration & dosage , Azithromycin/adverse effects , COVID-19 , Child , Coronavirus Infections/diagnosis , Coronavirus Infections/epidemiology , Female , Hospitalization/statistics & numerical data , Humans , Hydroxychloroquine/administration & dosage , Hydroxychloroquine/adverse effects , Long QT Syndrome/chemically induced , Long QT Syndrome/diagnosis , Long QT Syndrome/prevention & control , Male , Outcome and Process Assessment, Health Care , Pandemics , Pneumonia, Viral/diagnosis , Pneumonia, Viral/epidemiology , Retrospective Studies , Turkey/epidemiologyABSTRACT
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), responsible for coronavirus disease 19 (COVID-19), has rapidly spread since December 2019 to become the focus of healthcare systems worldwide. Its highly contagious nature and significant mortality has led to its prioritization as a public health issue. The race to prevent and treat this disease has led to "off-label" prescribing of medications such as hydroxychloroquine, azithromycin, and Kaletra (lopinavir/ritonavir). Currently, there is no robust clinical evidence for the use of these drugs in the treatment of COVID-19, with most, if not all of these medications associated with the potential for QT interval prolongation, torsades de pointes, and resultant drug-induced sudden cardiac death. The aim of this document is to help healthcare providers mitigate the potential deleterious effects of drug-induced QTc prolongation.
Subject(s)
Anti-Bacterial Agents/adverse effects , Antiviral Agents/adverse effects , Azithromycin/adverse effects , COVID-19 Drug Treatment , Hydroxychloroquine/adverse effects , Long QT Syndrome/chemically induced , Lopinavir/adverse effects , Ritonavir/adverse effects , Torsades de Pointes/chemically induced , Drug Combinations , Electrocardiography , Enzyme Inhibitors/adverse effects , Humans , Long QT Syndrome/blood , Long QT Syndrome/diagnosis , Long QT Syndrome/prevention & control , Magnesium/blood , Pandemics , Potassium/blood , Practice Guidelines as Topic , Risk Assessment , Risk Factors , SARS-CoV-2Subject(s)
Coronavirus Infections , Drug-Related Side Effects and Adverse Reactions , Hydroxychloroquine , Long QT Syndrome , Pandemics , Pneumonia, Viral , Antimalarials/administration & dosage , Antimalarials/adverse effects , Betacoronavirus/drug effects , COVID-19 , Clinical Trials as Topic , Coronavirus Infections/drug therapy , Coronavirus Infections/epidemiology , Drug-Related Side Effects and Adverse Reactions/etiology , Drug-Related Side Effects and Adverse Reactions/prevention & control , Humans , Hydroxychloroquine/administration & dosage , Hydroxychloroquine/adverse effects , Long QT Syndrome/chemically induced , Long QT Syndrome/prevention & control , Observational Studies as Topic , Pneumonia, Viral/drug therapy , Pneumonia, Viral/epidemiology , SARS-CoV-2 , COVID-19 Drug TreatmentSubject(s)
Antiviral Agents/pharmacology , Coronavirus Infections/drug therapy , Long QT Syndrome , Mental Disorders/drug therapy , Pneumonia, Viral/drug therapy , Psychotropic Drugs/pharmacology , Betacoronavirus , COVID-19 , Comorbidity , Coronavirus Infections/complications , Coronavirus Infections/epidemiology , Drug Interactions , Drug Therapy, Combination/methods , Humans , Long QT Syndrome/chemically induced , Long QT Syndrome/prevention & control , Mental Disorders/epidemiology , Pandemics , Pneumonia, Viral/epidemiology , Risk Adjustment/methods , SARS-CoV-2 , COVID-19 Drug TreatmentSubject(s)
Antiviral Agents/adverse effects , Betacoronavirus , Coronavirus Infections/drug therapy , Hydroxychloroquine/adverse effects , Hypokalemia/chemically induced , Long QT Syndrome/chemically induced , Lopinavir/adverse effects , Pandemics , Pneumonia, Viral/drug therapy , Ritonavir/adverse effects , Antiviral Agents/pharmacology , COVID-19 , Coronavirus Infections/blood , Drug Combinations , Drug Monitoring , Heart Conduction System/drug effects , Humans , Hydroxychloroquine/pharmacology , Hypokalemia/drug therapy , Hypokalemia/physiopathology , Long QT Syndrome/blood , Long QT Syndrome/prevention & control , Lopinavir/pharmacology , Magnesium/blood , Magnesium/therapeutic use , Pneumonia, Viral/blood , Potassium/blood , Potassium/therapeutic use , Retrospective Studies , Ritonavir/pharmacology , SARS-CoV-2 , COVID-19 Drug TreatmentABSTRACT
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.