Serveur d'exploration COVID et hydrochloroquine

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Compassionate use of hydroxychloroquine in clinical practice for patients with mild to severe Covid-19 in a French university hospital.

Identifieur interne : 001376 ( Main/Corpus ); précédent : 001375; suivant : 001377

Compassionate use of hydroxychloroquine in clinical practice for patients with mild to severe Covid-19 in a French university hospital.

Auteurs : Olivier Paccoud ; Florence Tubach ; Amandine Baptiste ; Alexandre Bleibtreu ; David Hajage ; Gentiane Monsel ; Gianpiero Tebano ; David Boutolleau ; Elise Klement ; Nagisa Godefroy ; Romain Palich ; Oula Itani ; Antoine Fayssal ; Marc-Antoine Valantin ; Roland Tubiana ; Sonia Burrel ; Vincent Calvez ; Eric Caumes ; Anne-Geneviève Marcelin ; Valérie Pourcher

Source :

RBID : pubmed:32556143

Abstract

BACKGROUND

Data from non-randomized studies have suggested that hydroxychloroquine could be an effective therapeutic agent against Covid-19.

METHODS

We conducted an observational, retrospective cohort study involving hospitalized adult patients with confirmed, mild to severe Covid-19 in a French university hospital. Patients who received hydroxychloroquine (200mg tid dosage for 10 days) on a compassionate basis in addition to SOCwere compared to patients without contraindications to hydroxychloroquine who received SOCalone. A propensity score-weighted analysis was performed to control for confounders: age, sex, time between symptom onset and admission ≤ 7 days, Charlson comorbidity index, medical history of arterial hypertension, and obesity, NEWS2 score at admission, and pneumonia severity. The primary endpoint was time to unfavorable outcome, defined as: death, admission to an intensive care unit, or decision to withdraw or withhold life-sustaining treatments, whichever came first.

RESULTS

Data from 89 patients with laboratory-confirmed Covid-19 were analyzed, 84 of whom were considered in the primary analysis; 38 patients treated with hydroxychloroquine and 46 patients treated with SOCalone. At admission, the mean age of patients was 66 years, the median Charlson comorbidity index was 3, and the median NEWS2 severity score was 3. After propensity score weighting, treatment with hydroxycholoroquine was not associated with a significantly reduced risk of unfavorable outcome (HR 0.90 [0.38; 2.1], p = 0.81). Overall survival was not significantly different between the two groups (HR 0.89 [0.23; 3.47], p = 1).

CONCLUSION

In hospitalized adults with Covid-19, no significant reduction of the risk of unfavorable outcomes was observed with hydroxychloroquine in comparison to standard of care. Unmeasured confounders may however have persisted despite careful propensity-weighted analysis and the study might be underpowered. Ongoing controlled trials in patients with varying degrees of initial severity on a larger scale will help determine whether there is a place for hydroxychloroquine in the treatment of Covid-19.


DOI: 10.1093/cid/ciaa791
PubMed: 32556143
PubMed Central: PMC7337663

Links to Exploration step

pubmed:32556143

Le document en format XML

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<name sortKey="Calvez, Vincent" sort="Calvez, Vincent" uniqKey="Calvez V" first="Vincent" last="Calvez">Vincent Calvez</name>
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<name sortKey="Caumes, Eric" sort="Caumes, Eric" uniqKey="Caumes E" first="Eric" last="Caumes">Eric Caumes</name>
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<name sortKey="Marcelin, Anne Genevieve" sort="Marcelin, Anne Genevieve" uniqKey="Marcelin A" first="Anne-Geneviève" last="Marcelin">Anne-Geneviève Marcelin</name>
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<nlm:affiliation>Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière - Charles Foix, laboratoire de virologie, Paris, France.</nlm:affiliation>
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<name sortKey="Pourcher, Valerie" sort="Pourcher, Valerie" uniqKey="Pourcher V" first="Valérie" last="Pourcher">Valérie Pourcher</name>
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<title xml:lang="en">Compassionate use of hydroxychloroquine in clinical practice for patients with mild to severe Covid-19 in a French university hospital.</title>
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<name sortKey="Tubach, Florence" sort="Tubach, Florence" uniqKey="Tubach F" first="Florence" last="Tubach">Florence Tubach</name>
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<nlm:affiliation>Sorbonne Université, INSERM UMR 1136, Département de Santé Publique, Unité de Recherche Clinique Pitié Salpêtrière - Charles Foix, Centre de Pharmaco-épidémiologie de l'AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, Paris, France.</nlm:affiliation>
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<nlm:affiliation>Sorbonne Université, INSERM UMR 1136, Département de Santé Publique, Unité de Recherche Clinique Pitié Salpêtrière - Charles Foix, Centre de Pharmaco-épidémiologie de l'AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, Paris, France.</nlm:affiliation>
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<name sortKey="Hajage, David" sort="Hajage, David" uniqKey="Hajage D" first="David" last="Hajage">David Hajage</name>
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<nlm:affiliation>Sorbonne Université, INSERM UMR 1136, Département de Santé Publique, Unité de Recherche Clinique Pitié Salpêtrière - Charles Foix, Centre de Pharmaco-épidémiologie de l'AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, Paris, France.</nlm:affiliation>
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<name sortKey="Monsel, Gentiane" sort="Monsel, Gentiane" uniqKey="Monsel G" first="Gentiane" last="Monsel">Gentiane Monsel</name>
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<nlm:affiliation>Assistance Publique - Hôpitaux de Paris, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, Service de Maladies infectieuses et Tropicales, 75013, Paris, France.</nlm:affiliation>
</affiliation>
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<name sortKey="Tebano, Gianpiero" sort="Tebano, Gianpiero" uniqKey="Tebano G" first="Gianpiero" last="Tebano">Gianpiero Tebano</name>
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<nlm:affiliation>Assistance Publique - Hôpitaux de Paris, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, Service de Maladies infectieuses et Tropicales, 75013, Paris, France.</nlm:affiliation>
</affiliation>
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<name sortKey="Boutolleau, David" sort="Boutolleau, David" uniqKey="Boutolleau D" first="David" last="Boutolleau">David Boutolleau</name>
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<nlm:affiliation>Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière - Charles Foix, laboratoire de virologie, Paris, France.</nlm:affiliation>
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<nlm:affiliation>Sorbonne Université, INSERM 1136, Institut Pierre Louis d'Epidémiologie et de Santé Publique, Paris, France.</nlm:affiliation>
</affiliation>
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<name sortKey="Klement, Elise" sort="Klement, Elise" uniqKey="Klement E" first="Elise" last="Klement">Elise Klement</name>
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<nlm:affiliation>Assistance Publique - Hôpitaux de Paris, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, Service de Maladies infectieuses et Tropicales, 75013, Paris, France.</nlm:affiliation>
</affiliation>
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<name sortKey="Godefroy, Nagisa" sort="Godefroy, Nagisa" uniqKey="Godefroy N" first="Nagisa" last="Godefroy">Nagisa Godefroy</name>
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<name sortKey="Palich, Romain" sort="Palich, Romain" uniqKey="Palich R" first="Romain" last="Palich">Romain Palich</name>
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</affiliation>
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<name sortKey="Itani, Oula" sort="Itani, Oula" uniqKey="Itani O" first="Oula" last="Itani">Oula Itani</name>
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<nlm:affiliation>Assistance Publique - Hôpitaux de Paris, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, Service de Maladies infectieuses et Tropicales, 75013, Paris, France.</nlm:affiliation>
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<name sortKey="Fayssal, Antoine" sort="Fayssal, Antoine" uniqKey="Fayssal A" first="Antoine" last="Fayssal">Antoine Fayssal</name>
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<nlm:affiliation>Assistance Publique - Hôpitaux de Paris, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, Service de Maladies infectieuses et Tropicales, 75013, Paris, France.</nlm:affiliation>
</affiliation>
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<name sortKey="Valantin, Marc Antoine" sort="Valantin, Marc Antoine" uniqKey="Valantin M" first="Marc-Antoine" last="Valantin">Marc-Antoine Valantin</name>
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<name sortKey="Tubiana, Roland" sort="Tubiana, Roland" uniqKey="Tubiana R" first="Roland" last="Tubiana">Roland Tubiana</name>
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</affiliation>
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<name sortKey="Burrel, Sonia" sort="Burrel, Sonia" uniqKey="Burrel S" first="Sonia" last="Burrel">Sonia Burrel</name>
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<nlm:affiliation>Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière - Charles Foix, laboratoire de virologie, Paris, France.</nlm:affiliation>
</affiliation>
<affiliation>
<nlm:affiliation>Sorbonne Université, INSERM 1136, Institut Pierre Louis d'Epidémiologie et de Santé Publique, Paris, France.</nlm:affiliation>
</affiliation>
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<author>
<name sortKey="Calvez, Vincent" sort="Calvez, Vincent" uniqKey="Calvez V" first="Vincent" last="Calvez">Vincent Calvez</name>
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<nlm:affiliation>Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière - Charles Foix, laboratoire de virologie, Paris, France.</nlm:affiliation>
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<affiliation>
<nlm:affiliation>Sorbonne Université, INSERM 1136, Institut Pierre Louis d'Epidémiologie et de Santé Publique, Paris, France.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Caumes, Eric" sort="Caumes, Eric" uniqKey="Caumes E" first="Eric" last="Caumes">Eric Caumes</name>
<affiliation>
<nlm:affiliation>Assistance Publique - Hôpitaux de Paris, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, Service de Maladies infectieuses et Tropicales, 75013, Paris, France.</nlm:affiliation>
</affiliation>
<affiliation>
<nlm:affiliation>Sorbonne Université, INSERM 1136, Institut Pierre Louis d'Epidémiologie et de Santé Publique, Paris, France.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Marcelin, Anne Genevieve" sort="Marcelin, Anne Genevieve" uniqKey="Marcelin A" first="Anne-Geneviève" last="Marcelin">Anne-Geneviève Marcelin</name>
<affiliation>
<nlm:affiliation>Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière - Charles Foix, laboratoire de virologie, Paris, France.</nlm:affiliation>
</affiliation>
<affiliation>
<nlm:affiliation>Sorbonne Université, INSERM 1136, Institut Pierre Louis d'Epidémiologie et de Santé Publique, Paris, France.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Pourcher, Valerie" sort="Pourcher, Valerie" uniqKey="Pourcher V" first="Valérie" last="Pourcher">Valérie Pourcher</name>
<affiliation>
<nlm:affiliation>Assistance Publique - Hôpitaux de Paris, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, Service de Maladies infectieuses et Tropicales, 75013, Paris, France.</nlm:affiliation>
</affiliation>
<affiliation>
<nlm:affiliation>Sorbonne Université, INSERM 1136, Institut Pierre Louis d'Epidémiologie et de Santé Publique, Paris, France.</nlm:affiliation>
</affiliation>
</author>
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<series>
<title level="j">Clinical infectious diseases : an official publication of the Infectious Diseases Society of America</title>
<idno type="eISSN">1537-6591</idno>
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<date when="2020" type="published">2020</date>
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<front>
<div type="abstract" xml:lang="en">
<p>
<b>BACKGROUND</b>
</p>
<p>Data from non-randomized studies have suggested that hydroxychloroquine could be an effective therapeutic agent against Covid-19.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>We conducted an observational, retrospective cohort study involving hospitalized adult patients with confirmed, mild to severe Covid-19 in a French university hospital. Patients who received hydroxychloroquine (200mg tid dosage for 10 days) on a compassionate basis in addition to SOCwere compared to patients without contraindications to hydroxychloroquine who received SOCalone. A propensity score-weighted analysis was performed to control for confounders: age, sex, time between symptom onset and admission ≤ 7 days, Charlson comorbidity index, medical history of arterial hypertension, and obesity, NEWS2 score at admission, and pneumonia severity. The primary endpoint was time to unfavorable outcome, defined as: death, admission to an intensive care unit, or decision to withdraw or withhold life-sustaining treatments, whichever came first.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>Data from 89 patients with laboratory-confirmed Covid-19 were analyzed, 84 of whom were considered in the primary analysis; 38 patients treated with hydroxychloroquine and 46 patients treated with SOCalone. At admission, the mean age of patients was 66 years, the median Charlson comorbidity index was 3, and the median NEWS2 severity score was 3. After propensity score weighting, treatment with hydroxycholoroquine was not associated with a significantly reduced risk of unfavorable outcome (HR 0.90 [0.38; 2.1], p = 0.81). Overall survival was not significantly different between the two groups (HR 0.89 [0.23; 3.47], p = 1).</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSION</b>
</p>
<p>In hospitalized adults with Covid-19, no significant reduction of the risk of unfavorable outcomes was observed with hydroxychloroquine in comparison to standard of care. Unmeasured confounders may however have persisted despite careful propensity-weighted analysis and the study might be underpowered. Ongoing controlled trials in patients with varying degrees of initial severity on a larger scale will help determine whether there is a place for hydroxychloroquine in the treatment of Covid-19.</p>
</div>
</front>
</TEI>
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<PMID Version="1">32556143</PMID>
<DateRevised>
<Year>2021</Year>
<Month>05</Month>
<Day>19</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Electronic">1537-6591</ISSN>
<JournalIssue CitedMedium="Internet">
<PubDate>
<Year>2020</Year>
<Month>Jun</Month>
<Day>18</Day>
</PubDate>
</JournalIssue>
<Title>Clinical infectious diseases : an official publication of the Infectious Diseases Society of America</Title>
<ISOAbbreviation>Clin Infect Dis</ISOAbbreviation>
</Journal>
<ArticleTitle>Compassionate use of hydroxychloroquine in clinical practice for patients with mild to severe Covid-19 in a French university hospital.</ArticleTitle>
<ELocationID EIdType="pii" ValidYN="Y">ciaa791</ELocationID>
<ELocationID EIdType="doi" ValidYN="Y">10.1093/cid/ciaa791</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Data from non-randomized studies have suggested that hydroxychloroquine could be an effective therapeutic agent against Covid-19.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">We conducted an observational, retrospective cohort study involving hospitalized adult patients with confirmed, mild to severe Covid-19 in a French university hospital. Patients who received hydroxychloroquine (200mg tid dosage for 10 days) on a compassionate basis in addition to SOCwere compared to patients without contraindications to hydroxychloroquine who received SOCalone. A propensity score-weighted analysis was performed to control for confounders: age, sex, time between symptom onset and admission ≤ 7 days, Charlson comorbidity index, medical history of arterial hypertension, and obesity, NEWS2 score at admission, and pneumonia severity. The primary endpoint was time to unfavorable outcome, defined as: death, admission to an intensive care unit, or decision to withdraw or withhold life-sustaining treatments, whichever came first.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Data from 89 patients with laboratory-confirmed Covid-19 were analyzed, 84 of whom were considered in the primary analysis; 38 patients treated with hydroxychloroquine and 46 patients treated with SOCalone. At admission, the mean age of patients was 66 years, the median Charlson comorbidity index was 3, and the median NEWS2 severity score was 3. After propensity score weighting, treatment with hydroxycholoroquine was not associated with a significantly reduced risk of unfavorable outcome (HR 0.90 [0.38; 2.1], p = 0.81). Overall survival was not significantly different between the two groups (HR 0.89 [0.23; 3.47], p = 1).</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">In hospitalized adults with Covid-19, no significant reduction of the risk of unfavorable outcomes was observed with hydroxychloroquine in comparison to standard of care. Unmeasured confounders may however have persisted despite careful propensity-weighted analysis and the study might be underpowered. Ongoing controlled trials in patients with varying degrees of initial severity on a larger scale will help determine whether there is a place for hydroxychloroquine in the treatment of Covid-19.</AbstractText>
<CopyrightInformation>© The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.</CopyrightInformation>
</Abstract>
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<LastName>Paccoud</LastName>
<ForeName>Olivier</ForeName>
<Initials>O</Initials>
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<Affiliation>Assistance Publique - Hôpitaux de Paris, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, Service de Maladies infectieuses et Tropicales, 75013, Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Tubach</LastName>
<ForeName>Florence</ForeName>
<Initials>F</Initials>
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<Affiliation>Sorbonne Université, INSERM UMR 1136, Département de Santé Publique, Unité de Recherche Clinique Pitié Salpêtrière - Charles Foix, Centre de Pharmaco-épidémiologie de l'AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, Paris, France.</Affiliation>
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<LastName>Pourcher</LastName>
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<AffiliationInfo>
<Affiliation>Sorbonne Université, INSERM 1136, Institut Pierre Louis d'Epidémiologie et de Santé Publique, Paris, France.</Affiliation>
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<Language>eng</Language>
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<Year>2020</Year>
<Month>06</Month>
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<RefSource>Clin Infect Dis. 2021 May 4;72(9):e440-e441</RefSource>
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