Serveur d'exploration COVID et hydrochloroquine

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COVID-SAFER: Deprescribing Guidance for Hydroxychloroquine Drug Interactions in Older Adults.

Identifieur interne : 001613 ( Main/Corpus ); précédent : 001612; suivant : 001614

COVID-SAFER: Deprescribing Guidance for Hydroxychloroquine Drug Interactions in Older Adults.

Auteurs : Sydney B. Ross ; Marnie Goodwin Wilson ; Louise Papillon-Ferland ; Sarah Elsayed ; Peter E. Wu ; Kiran Battu ; Sandra Porter ; Babak Rashidi ; Robyn Tamblyn ; Louise Pilote ; James Downar ; Andre Bonnici ; Allen Huang ; Todd C. Lee ; Emily G. Mcdonald

Source :

RBID : pubmed:32441771

English descriptors

Abstract

BACKGROUND/OBJECTIVES

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection causes high morbidity and mortality in older adults with chronic illnesses. Several trials are currently underway evaluating the antimalarial drug hydroxychloroquine as a potential treatment for acute infection. However, polypharmacy predisposes patients to increased risk of drug-drug interactions with hydroxychloroquine and may render many in this population ineligible to participate in trials. We aimed to quantify the degree of polypharmacy and burden of potentially inappropriate medications (PIMs) that older hospitalized adults are taking that would interact with hydroxychloroquine.

METHODS

We reanalyzed data from the cohort of patients 65 years and older enrolled in the MedSafer pilot study. We first identified patients taking medications with potentially harmful drug-drug interactions with hydroxychloroquine that might exclude them from participation in a typical 2019 coronavirus disease (COVID-19) therapeutic trial. Next, we identified medications that were flagged by MedSafer as potentially inappropriate and crafted guidance around medication management if contemplating the use of hydroxychloroquine.

RESULTS

The cohort contained a total of 1,001 unique patients with complete data on their home medications at admission. Of these 1,001 patients, 590 (58.9%) were receiving one or more home medications that could potentially interact with hydroxychloroquine, and of these, 255 (43.2%) were flagged as potentially inappropriate by the MedSafer tool. Common classes of PIMs observed were antipsychotics, cardiac medications, and antidiabetic agents.

CONCLUSION

The COVID-19 pandemic highlights the importance of medication optimization and deprescribing PIMs in older adults. By acting now to reduce polypharmacy and use of PIMs, we can better prepare this vulnerable population for inclusion in trials and, if substantiated, pharmacologic treatment or prevention of COVID-19. J Am Geriatr Soc 68:1636-1646, 2020.


DOI: 10.1111/jgs.16623
PubMed: 32441771
PubMed Central: PMC7280600

Links to Exploration step

pubmed:32441771

Le document en format XML

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<name sortKey="Rashidi, Babak" sort="Rashidi, Babak" uniqKey="Rashidi B" first="Babak" last="Rashidi">Babak Rashidi</name>
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<nlm:affiliation>Division of General Internal Medicine, McGill University Health Centre, Montreal, Quebec, Canada.</nlm:affiliation>
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<name sortKey="Downar, James" sort="Downar, James" uniqKey="Downar J" first="James" last="Downar">James Downar</name>
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<nlm:affiliation>Division of Palliative Medicine, The Ottawa Hospital, Ottawa, Ontario, Canada.</nlm:affiliation>
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<name sortKey="Huang, Allen" sort="Huang, Allen" uniqKey="Huang A" first="Allen" last="Huang">Allen Huang</name>
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<term>Aged (MeSH)</term>
<term>Aged, 80 and over (MeSH)</term>
<term>Betacoronavirus (MeSH)</term>
<term>COVID-19 (MeSH)</term>
<term>Clinical Trials as Topic (MeSH)</term>
<term>Coronavirus Infections (drug therapy)</term>
<term>Deprescriptions (MeSH)</term>
<term>Female (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Hydroxychloroquine (administration & dosage)</term>
<term>Male (MeSH)</term>
<term>Pandemics (MeSH)</term>
<term>Patient Selection (MeSH)</term>
<term>Pilot Projects (MeSH)</term>
<term>Pneumonia, Viral (drug therapy)</term>
<term>Polypharmacy (MeSH)</term>
<term>Potentially Inappropriate Medication List (standards)</term>
<term>SARS-CoV-2 (MeSH)</term>
</keywords>
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<term>Hydroxychloroquine</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en">
<term>Coronavirus Infections</term>
<term>Pneumonia, Viral</term>
</keywords>
<keywords scheme="MESH" qualifier="standards" xml:lang="en">
<term>Potentially Inappropriate Medication List</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Betacoronavirus</term>
<term>COVID-19</term>
<term>Clinical Trials as Topic</term>
<term>Deprescriptions</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Pandemics</term>
<term>Patient Selection</term>
<term>Pilot Projects</term>
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<front>
<div type="abstract" xml:lang="en">
<p>
<b>BACKGROUND/OBJECTIVES</b>
</p>
<p>Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection causes high morbidity and mortality in older adults with chronic illnesses. Several trials are currently underway evaluating the antimalarial drug hydroxychloroquine as a potential treatment for acute infection. However, polypharmacy predisposes patients to increased risk of drug-drug interactions with hydroxychloroquine and may render many in this population ineligible to participate in trials. We aimed to quantify the degree of polypharmacy and burden of potentially inappropriate medications (PIMs) that older hospitalized adults are taking that would interact with hydroxychloroquine.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>We reanalyzed data from the cohort of patients 65 years and older enrolled in the MedSafer pilot study. We first identified patients taking medications with potentially harmful drug-drug interactions with hydroxychloroquine that might exclude them from participation in a typical 2019 coronavirus disease (COVID-19) therapeutic trial. Next, we identified medications that were flagged by MedSafer as potentially inappropriate and crafted guidance around medication management if contemplating the use of hydroxychloroquine.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>The cohort contained a total of 1,001 unique patients with complete data on their home medications at admission. Of these 1,001 patients, 590 (58.9%) were receiving one or more home medications that could potentially interact with hydroxychloroquine, and of these, 255 (43.2%) were flagged as potentially inappropriate by the MedSafer tool. Common classes of PIMs observed were antipsychotics, cardiac medications, and antidiabetic agents.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSION</b>
</p>
<p>The COVID-19 pandemic highlights the importance of medication optimization and deprescribing PIMs in older adults. By acting now to reduce polypharmacy and use of PIMs, we can better prepare this vulnerable population for inclusion in trials and, if substantiated, pharmacologic treatment or prevention of COVID-19. J Am Geriatr Soc 68:1636-1646, 2020.</p>
</div>
</front>
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<DateCompleted>
<Year>2020</Year>
<Month>08</Month>
<Day>31</Day>
</DateCompleted>
<DateRevised>
<Year>2021</Year>
<Month>05</Month>
<Day>15</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Electronic">1532-5415</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>68</Volume>
<Issue>8</Issue>
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<Year>2020</Year>
<Month>Aug</Month>
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<Title>Journal of the American Geriatrics Society</Title>
<ISOAbbreviation>J Am Geriatr Soc</ISOAbbreviation>
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<ArticleTitle>COVID-SAFER: Deprescribing Guidance for Hydroxychloroquine Drug Interactions in Older Adults.</ArticleTitle>
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</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1111/jgs.16623</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND/OBJECTIVES" NlmCategory="OBJECTIVE">Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection causes high morbidity and mortality in older adults with chronic illnesses. Several trials are currently underway evaluating the antimalarial drug hydroxychloroquine as a potential treatment for acute infection. However, polypharmacy predisposes patients to increased risk of drug-drug interactions with hydroxychloroquine and may render many in this population ineligible to participate in trials. We aimed to quantify the degree of polypharmacy and burden of potentially inappropriate medications (PIMs) that older hospitalized adults are taking that would interact with hydroxychloroquine.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">We reanalyzed data from the cohort of patients 65 years and older enrolled in the MedSafer pilot study. We first identified patients taking medications with potentially harmful drug-drug interactions with hydroxychloroquine that might exclude them from participation in a typical 2019 coronavirus disease (COVID-19) therapeutic trial. Next, we identified medications that were flagged by MedSafer as potentially inappropriate and crafted guidance around medication management if contemplating the use of hydroxychloroquine.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The cohort contained a total of 1,001 unique patients with complete data on their home medications at admission. Of these 1,001 patients, 590 (58.9%) were receiving one or more home medications that could potentially interact with hydroxychloroquine, and of these, 255 (43.2%) were flagged as potentially inappropriate by the MedSafer tool. Common classes of PIMs observed were antipsychotics, cardiac medications, and antidiabetic agents.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">The COVID-19 pandemic highlights the importance of medication optimization and deprescribing PIMs in older adults. By acting now to reduce polypharmacy and use of PIMs, we can better prepare this vulnerable population for inclusion in trials and, if substantiated, pharmacologic treatment or prevention of COVID-19. J Am Geriatr Soc 68:1636-1646, 2020.</AbstractText>
<CopyrightInformation>© 2020 The American Geriatrics Society.</CopyrightInformation>
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<LastName>Ross</LastName>
<ForeName>Sydney B</ForeName>
<Initials>SB</Initials>
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<Affiliation>Division of Experimental Medicine, Faculty of Medicine, McGill University, Montreal, Quebec, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Centre for Outcomes Research and Evaluation, McGill University Health Centre, Montreal, Quebec, Canada.</Affiliation>
</AffiliationInfo>
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</AffiliationInfo>
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</AffiliationInfo>
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</AffiliationInfo>
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<Affiliation>Division of General Internal Medicine, University Health Network, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
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<LastName>Battu</LastName>
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<Affiliation>Department of Pharmacy, University Health Network, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
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<LastName>Porter</LastName>
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<Affiliation>Department of Pharmacy, University Health Network, Toronto, Ontario, Canada.</Affiliation>
</AffiliationInfo>
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<AffiliationInfo>
<Affiliation>Division of General Internal Medicine, The Ottawa Hospital, Ottawa, Ontario, Canada.</Affiliation>
</AffiliationInfo>
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<AffiliationInfo>
<Affiliation>Centre for Outcomes Research and Evaluation, McGill University Health Centre, Montreal, Quebec, Canada.</Affiliation>
</AffiliationInfo>
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<ForeName>Louise</ForeName>
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<Affiliation>Centre for Outcomes Research and Evaluation, McGill University Health Centre, Montreal, Quebec, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Division of General Internal Medicine, McGill University Health Centre, Montreal, Quebec, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Downar</LastName>
<ForeName>James</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Division of Palliative Medicine, The Ottawa Hospital, Ottawa, Ontario, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Bonnici</LastName>
<ForeName>Andre</ForeName>
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<AffiliationInfo>
<Affiliation>Department of Pharmacy, McGill University Health Centre, Montreal, Quebec, Canada.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y">
<LastName>Huang</LastName>
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