Serveur d'exploration Stress et Covid

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COVID-19: Therapeutics and Their Toxicities

Identifieur interne : 000151 ( Pmc/Curation ); précédent : 000150; suivant : 000152

COVID-19: Therapeutics and Their Toxicities

Auteurs : Michael A. Chary [États-Unis] ; Alexander F. Barbuto [États-Unis] ; Sudeh Izadmehr [États-Unis] ; Bryan D. Hayes [États-Unis] ; Michele M. Burns [États-Unis]

Source :

RBID : PMC:7192319

Abstract

SARS-CoV-2 is a novel coronavirus that emerged in 2019 and is causing the COVID-19 pandemic. There is no current standard of care. Clinicians need to be mindful of the toxicity of a wide variety of possibly unfamiliar substances being tested or repurposed to treat COVID-19. The United States Food and Drug Administration (FDA) has provided emergency authorization for the use of chloroquine and hydroxychloroquine. These two medications may precipitate ventricular dysrhythmias, necessitating cardiac and electrolyte monitoring, and in severe cases, treatment with epinephrine and high-doses of diazepam. Recombinant protein therapeutics may cause serum sickness or immune complex deposition. Nucleic acid vaccines may introduce mutations into the human genome. ACE inhibitors and ibuprofen have been suggested to exacerbate the pathogenesis of COVID-19. Here, we review the use, mechanism of action, and toxicity of proposed COVID-19 therapeutics.


Url:
DOI: 10.1007/s13181-020-00777-5
PubMed: NONE
PubMed Central: 7192319

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PMC:7192319

Le document en format XML

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<p id="Par1">SARS-CoV-2 is a novel coronavirus that emerged in 2019 and is causing the COVID-19 pandemic. There is no current standard of care. Clinicians need to be mindful of the toxicity of a wide variety of possibly unfamiliar substances being tested or repurposed to treat COVID-19. The United States Food and Drug Administration (FDA) has provided emergency authorization for the use of chloroquine and hydroxychloroquine. These two medications may precipitate ventricular dysrhythmias, necessitating cardiac and electrolyte monitoring, and in severe cases, treatment with epinephrine and high-doses of diazepam. Recombinant protein therapeutics may cause serum sickness or immune complex deposition. Nucleic acid vaccines may introduce mutations into the human genome. ACE inhibitors and ibuprofen have been suggested to exacerbate the pathogenesis of COVID-19. Here, we review the use, mechanism of action, and toxicity of proposed COVID-19 therapeutics.</p>
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<label>2</label>
<institution-wrap>
<institution-id institution-id-type="GRID">grid.482852.1</institution-id>
<institution>Regional Center for Poison Control and Prevention Serving Massachusetts and Rhode Island,</institution>
</institution-wrap>
Boston, MA USA</aff>
<aff id="Aff3">
<label>3</label>
<institution-wrap>
<institution-id institution-id-type="GRID">grid.62560.37</institution-id>
<institution-id institution-id-type="ISNI">0000 0004 0378 8294</institution-id>
<institution>Department of Emergency Medicine,</institution>
<institution>Brigham and Women’s Hospital,</institution>
</institution-wrap>
Boston, MA USA</aff>
<aff id="Aff4">
<label>4</label>
<institution-wrap>
<institution-id institution-id-type="GRID">grid.59734.3c</institution-id>
<institution-id institution-id-type="ISNI">0000 0001 0670 2351</institution-id>
<institution>Division of Hematology and Medical Oncology,</institution>
<institution>Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai,</institution>
</institution-wrap>
New York, NY USA</aff>
<aff id="Aff5">
<label>5</label>
<institution-wrap>
<institution-id institution-id-type="GRID">grid.32224.35</institution-id>
<institution-id institution-id-type="ISNI">0000 0004 0386 9924</institution-id>
<institution>Department of Pharmacy, Department of Emergency Medicine,</institution>
<institution>Massachusetts General Hospital,</institution>
</institution-wrap>
Boston, MA USA</aff>
</contrib-group>
<author-notes>
<fn fn-type="com">
<p> Supervising Editor: Mark B. Mycyk, MD </p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>30</day>
<month>4</month>
<year>2020</year>
</pub-date>
<fpage>1</fpage>
<lpage>11</lpage>
<history>
<date date-type="received">
<day>24</day>
<month>3</month>
<year>2020</year>
</date>
<date date-type="rev-recd">
<day>9</day>
<month>4</month>
<year>2020</year>
</date>
<date date-type="accepted">
<day>9</day>
<month>4</month>
<year>2020</year>
</date>
</history>
<permissions>
<copyright-statement>© American College of Medical Toxicology 2020</copyright-statement>
<license>
<license-p>This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.</license-p>
</license>
</permissions>
<abstract id="Abs1">
<p id="Par1">SARS-CoV-2 is a novel coronavirus that emerged in 2019 and is causing the COVID-19 pandemic. There is no current standard of care. Clinicians need to be mindful of the toxicity of a wide variety of possibly unfamiliar substances being tested or repurposed to treat COVID-19. The United States Food and Drug Administration (FDA) has provided emergency authorization for the use of chloroquine and hydroxychloroquine. These two medications may precipitate ventricular dysrhythmias, necessitating cardiac and electrolyte monitoring, and in severe cases, treatment with epinephrine and high-doses of diazepam. Recombinant protein therapeutics may cause serum sickness or immune complex deposition. Nucleic acid vaccines may introduce mutations into the human genome. ACE inhibitors and ibuprofen have been suggested to exacerbate the pathogenesis of COVID-19. Here, we review the use, mechanism of action, and toxicity of proposed COVID-19 therapeutics.</p>
</abstract>
<kwd-group xml:lang="en">
<title>Keywords</title>
<kwd>COVID-19</kwd>
<kwd>SARS-CoV-2</kwd>
<kwd>Toxicity</kwd>
<kwd>Pandemic</kwd>
<kwd>Therapeutic</kwd>
</kwd-group>
<funding-group>
<award-group>
<funding-source>
<institution-wrap>
<institution-id institution-id-type="FundRef">http://dx.doi.org/10.13039/100000026</institution-id>
<institution>National Institute on Drug Abuse</institution>
</institution-wrap>
</funding-source>
<award-id>Loan Repayment Program</award-id>
<principal-award-recipient>
<name>
<surname>Chary</surname>
<given-names>Michael A.</given-names>
</name>
</principal-award-recipient>
</award-group>
</funding-group>
<funding-group>
<award-group>
<funding-source>
<institution-wrap>
<institution-id institution-id-type="FundRef">http://dx.doi.org/10.13039/100006108</institution-id>
<institution>National Center for Advancing Translational Sciences</institution>
</institution-wrap>
</funding-source>
<award-id>Loan Repayment Program</award-id>
<principal-award-recipient>
<name>
<surname>Izadmehr</surname>
<given-names>Sudeh</given-names>
</name>
</principal-award-recipient>
</award-group>
</funding-group>
</article-meta>
</front>
</pmc>
</record>

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