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Association of Nonsteroidal Anti-inflammatory Drug Use and Adverse Outcomes Among Patients Hospitalized With Influenza.

Identifieur interne : 000788 ( Main/Exploration ); précédent : 000787; suivant : 000789

Association of Nonsteroidal Anti-inflammatory Drug Use and Adverse Outcomes Among Patients Hospitalized With Influenza.

Auteurs : Lars Christian Lund [Danemark] ; Mette Reilev [Danemark] ; Jesper Hallas [Danemark] ; Kasper Bruun Kristensen [Danemark] ; Reimar Wernich Thomsen [Danemark] ; Christian Fynbo Christiansen [Danemark] ; Henrik Toft S Rensen [Danemark, États-Unis] ; Nanna Borup Johansen [Danemark] ; Nikolai Constantin Brun [Danemark] ; Marianne Voldstedlund [Danemark] ; Henrik St Vring [Danemark] ; Marianne Kragh Thomsen [Danemark] ; Steffen Christensen [Danemark] ; Anton Potteg Rd [Danemark]

Source :

RBID : pubmed:32609352

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English descriptors

Abstract

Importance

During the ongoing coronavirus disease 2019 pandemic, case reports have suggested that the use of nonsteroidal anti-inflammatory drugs (NSAIDs) may lead to adverse outcomes.

Objective

To study the association of NSAID use with adverse outcomes in patients hospitalized with influenza or influenza pneumonia.

Design, Setting, and Participants

This cohort study used propensity score matching among 7747 individuals aged 40 years or older who were hospitalized with influenza, confirmed by polymerase chain reaction or antigen testing, between 2010 and 2018. Data were collected using Danish nationwide registers. All analyses reported were performed on May 29, 2020.

Exposures

Prescription fill of an NSAID within 60 days before admission.

Main Outcomes and Measures

Risk ratio (RR) and risk difference (RD) with 95% CIs for intensive care unit admission and death within 30 days of admission.

Results

A total of 7747 patients (median [interquartile range] age, 71 [59-80] years, 3980 [51.4%] men) with confirmed influenza were identified. Of these, 520 (6.7%) were exposed to NSAIDs. In the unmatched cohorts, 104 of 520 patients (20.0%) who used NSAIDs and 958 of 7227 patients (13.3%) who did not use NSAIDs were admitted to the intensive care unit. For death within 30 days of admission, we observed 37 events (7.1%) among those who used NSAIDs compared with 563 events (7.8%) among those who did not. Current NSAID use was associated with intensive care unit admission (RR, 1.51; 95% CI, 1.26 to 1.81; RD, 6.7%; 95% CI, 3.2% to 10.3%), while NSAID use was not associated with death (RR, 0.91; 95% CI, 0.66 to 1.26; RD, -0.7%; 95% CI, -3.0% to 1.6%). In the matched cohorts, risks were unchanged for patients who used NSAIDs, while 83 ICU admissions (16.0%) and 36 deaths (6.9%) were observed among matched individuals who did not use NSAIDs. Matched (ie, adjusted) analyses yielded attenuated risk estimates for intensive care unit admission (RR, 1.25; 95% CI, 0.95 to 1.63; RD, 4.0%; 95% CI, -0.6% to 8.7%) and death (RR, 1.03; 95% CI, 0.66 to 1.60; RD, 0.2%; 95% CI, -2.9% to 3.3%). Associations were more pronounced among patients who used NSAIDs for a longer period (eg, for intensive care unit admission: RR, 1.90; 95% CI, 1.19 to 3.06; RD, 13.4%; 95% CI, 4.0% to 22.8%).

Conclusions and Relevance

In this cohort study of adult patients hospitalized with influenza, the use of NSAIDs was not associated with 30-day intensive care unit admission or death in adjusted analyses. There was an association between long-term use of NSAIDs and intensive care unit admission.


DOI: 10.1001/jamanetworkopen.2020.13880
PubMed: 32609352
PubMed Central: PMC7330719


Affiliations:


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<name sortKey="Kristensen, Kasper Bruun" sort="Kristensen, Kasper Bruun" uniqKey="Kristensen K" first="Kasper Bruun" last="Kristensen">Kasper Bruun Kristensen</name>
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<name sortKey="Thomsen, Reimar Wernich" sort="Thomsen, Reimar Wernich" uniqKey="Thomsen R" first="Reimar Wernich" last="Thomsen">Reimar Wernich Thomsen</name>
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<name sortKey="Christiansen, Christian Fynbo" sort="Christiansen, Christian Fynbo" uniqKey="Christiansen C" first="Christian Fynbo" last="Christiansen">Christian Fynbo Christiansen</name>
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<nlm:affiliation>Department of Clinical Epidemiology, Aarhus University Hospital, Aarhus, Denmark.</nlm:affiliation>
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<name sortKey="S Rensen, Henrik Toft" sort="S Rensen, Henrik Toft" uniqKey="S Rensen H" first="Henrik Toft" last="S Rensen">Henrik Toft S Rensen</name>
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<nlm:affiliation>Department of Clinical Epidemiology, Aarhus University Hospital, Aarhus, Denmark.</nlm:affiliation>
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<nlm:affiliation>Center for Population Health and Sciences, Stanford University, Stanford, California.</nlm:affiliation>
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<name sortKey="Voldstedlund, Marianne" sort="Voldstedlund, Marianne" uniqKey="Voldstedlund M" first="Marianne" last="Voldstedlund">Marianne Voldstedlund</name>
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<name sortKey="St Vring, Henrik" sort="St Vring, Henrik" uniqKey="St Vring H" first="Henrik" last="St Vring">Henrik St Vring</name>
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<name sortKey="Christensen, Steffen" sort="Christensen, Steffen" uniqKey="Christensen S" first="Steffen" last="Christensen">Steffen Christensen</name>
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<wicri:regionArea>Department of Anaesthesia and Intensive Care Medicine, Aarhus University Hospital, Aarhus</wicri:regionArea>
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<name sortKey="Potteg Rd, Anton" sort="Potteg Rd, Anton" uniqKey="Potteg Rd A" first="Anton" last="Potteg Rd">Anton Potteg Rd</name>
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<nlm:affiliation>Hospital Pharmacy Funen, Odense University Hospital, Odense, Denmark.</nlm:affiliation>
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<title level="j">JAMA network open</title>
<idno type="eISSN">2574-3805</idno>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Adult (MeSH)</term>
<term>Aged (MeSH)</term>
<term>Aged, 80 and over (MeSH)</term>
<term>Anti-Inflammatory Agents, Non-Steroidal (adverse effects)</term>
<term>Anti-Inflammatory Agents, Non-Steroidal (pharmacology)</term>
<term>Betacoronavirus (MeSH)</term>
<term>COVID-19 (MeSH)</term>
<term>Cohort Studies (MeSH)</term>
<term>Coronavirus Infections (complications)</term>
<term>Coronavirus Infections (drug therapy)</term>
<term>Coronavirus Infections (mortality)</term>
<term>Coronavirus Infections (virology)</term>
<term>Denmark (epidemiology)</term>
<term>Female (MeSH)</term>
<term>Hospitalization (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Influenza, Human (MeSH)</term>
<term>Intensive Care Units (MeSH)</term>
<term>Male (MeSH)</term>
<term>Middle Aged (MeSH)</term>
<term>Odds Ratio (MeSH)</term>
<term>Pandemics (MeSH)</term>
<term>Pneumonia (MeSH)</term>
<term>Pneumonia, Viral (complications)</term>
<term>Pneumonia, Viral (drug therapy)</term>
<term>Pneumonia, Viral (mortality)</term>
<term>Pneumonia, Viral (virology)</term>
<term>SARS-CoV-2 (MeSH)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Adulte (MeSH)</term>
<term>Adulte d'âge moyen (MeSH)</term>
<term>Anti-inflammatoires non stéroïdiens (effets indésirables)</term>
<term>Anti-inflammatoires non stéroïdiens (pharmacologie)</term>
<term>Betacoronavirus (MeSH)</term>
<term>Danemark (épidémiologie)</term>
<term>Femelle (MeSH)</term>
<term>Grippe humaine (MeSH)</term>
<term>Hospitalisation (MeSH)</term>
<term>Humains (MeSH)</term>
<term>Infections à coronavirus (complications)</term>
<term>Infections à coronavirus (mortalité)</term>
<term>Infections à coronavirus (traitement médicamenteux)</term>
<term>Infections à coronavirus (virologie)</term>
<term>Mâle (MeSH)</term>
<term>Odds ratio (MeSH)</term>
<term>Pandémies (MeSH)</term>
<term>Pneumopathie infectieuse (MeSH)</term>
<term>Pneumopathie virale (complications)</term>
<term>Pneumopathie virale (mortalité)</term>
<term>Pneumopathie virale (traitement médicamenteux)</term>
<term>Pneumopathie virale (virologie)</term>
<term>Sujet âgé (MeSH)</term>
<term>Sujet âgé de 80 ans ou plus (MeSH)</term>
<term>Unités de soins intensifs (MeSH)</term>
<term>Études de cohortes (MeSH)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="adverse effects" xml:lang="en">
<term>Anti-Inflammatory Agents, Non-Steroidal</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en">
<term>Anti-Inflammatory Agents, Non-Steroidal</term>
</keywords>
<keywords scheme="MESH" type="geographic" qualifier="epidemiology" xml:lang="en">
<term>Denmark</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en">
<term>Coronavirus Infections</term>
<term>Pneumonia, Viral</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en">
<term>Coronavirus Infections</term>
<term>Pneumonia, Viral</term>
</keywords>
<keywords scheme="MESH" qualifier="effets indésirables" xml:lang="fr">
<term>Anti-inflammatoires non stéroïdiens</term>
<term>Infections à coronavirus</term>
<term>Pneumopathie virale</term>
</keywords>
<keywords scheme="MESH" qualifier="mortality" xml:lang="en">
<term>Coronavirus Infections</term>
<term>Pneumonia, Viral</term>
</keywords>
<keywords scheme="MESH" qualifier="mortalité" xml:lang="fr">
<term>Infections à coronavirus</term>
<term>Pneumopathie virale</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr">
<term>Anti-inflammatoires non stéroïdiens</term>
</keywords>
<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr">
<term>Infections à coronavirus</term>
<term>Pneumopathie virale</term>
</keywords>
<keywords scheme="MESH" qualifier="virologie" xml:lang="fr">
<term>Infections à coronavirus</term>
<term>Pneumopathie virale</term>
</keywords>
<keywords scheme="MESH" qualifier="virology" xml:lang="en">
<term>Coronavirus Infections</term>
<term>Pneumonia, Viral</term>
</keywords>
<keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr">
<term>Danemark</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Adult</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Betacoronavirus</term>
<term>COVID-19</term>
<term>Cohort Studies</term>
<term>Female</term>
<term>Hospitalization</term>
<term>Humans</term>
<term>Influenza, Human</term>
<term>Intensive Care Units</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Odds Ratio</term>
<term>Pandemics</term>
<term>Pneumonia</term>
<term>SARS-CoV-2</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Betacoronavirus</term>
<term>Femelle</term>
<term>Grippe humaine</term>
<term>Hospitalisation</term>
<term>Humains</term>
<term>Mâle</term>
<term>Odds ratio</term>
<term>Pandémies</term>
<term>Pneumopathie infectieuse</term>
<term>Sujet âgé</term>
<term>Sujet âgé de 80 ans ou plus</term>
<term>Unités de soins intensifs</term>
<term>Études de cohortes</term>
</keywords>
<keywords scheme="Wicri" type="geographic" xml:lang="fr">
<term>Danemark</term>
</keywords>
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</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p>
<b>Importance</b>
</p>
<p>During the ongoing coronavirus disease 2019 pandemic, case reports have suggested that the use of nonsteroidal anti-inflammatory drugs (NSAIDs) may lead to adverse outcomes.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Objective</b>
</p>
<p>To study the association of NSAID use with adverse outcomes in patients hospitalized with influenza or influenza pneumonia.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Design, Setting, and Participants</b>
</p>
<p>This cohort study used propensity score matching among 7747 individuals aged 40 years or older who were hospitalized with influenza, confirmed by polymerase chain reaction or antigen testing, between 2010 and 2018. Data were collected using Danish nationwide registers. All analyses reported were performed on May 29, 2020.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Exposures</b>
</p>
<p>Prescription fill of an NSAID within 60 days before admission.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Main Outcomes and Measures</b>
</p>
<p>Risk ratio (RR) and risk difference (RD) with 95% CIs for intensive care unit admission and death within 30 days of admission.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Results</b>
</p>
<p>A total of 7747 patients (median [interquartile range] age, 71 [59-80] years, 3980 [51.4%] men) with confirmed influenza were identified. Of these, 520 (6.7%) were exposed to NSAIDs. In the unmatched cohorts, 104 of 520 patients (20.0%) who used NSAIDs and 958 of 7227 patients (13.3%) who did not use NSAIDs were admitted to the intensive care unit. For death within 30 days of admission, we observed 37 events (7.1%) among those who used NSAIDs compared with 563 events (7.8%) among those who did not. Current NSAID use was associated with intensive care unit admission (RR, 1.51; 95% CI, 1.26 to 1.81; RD, 6.7%; 95% CI, 3.2% to 10.3%), while NSAID use was not associated with death (RR, 0.91; 95% CI, 0.66 to 1.26; RD, -0.7%; 95% CI, -3.0% to 1.6%). In the matched cohorts, risks were unchanged for patients who used NSAIDs, while 83 ICU admissions (16.0%) and 36 deaths (6.9%) were observed among matched individuals who did not use NSAIDs. Matched (ie, adjusted) analyses yielded attenuated risk estimates for intensive care unit admission (RR, 1.25; 95% CI, 0.95 to 1.63; RD, 4.0%; 95% CI, -0.6% to 8.7%) and death (RR, 1.03; 95% CI, 0.66 to 1.60; RD, 0.2%; 95% CI, -2.9% to 3.3%). Associations were more pronounced among patients who used NSAIDs for a longer period (eg, for intensive care unit admission: RR, 1.90; 95% CI, 1.19 to 3.06; RD, 13.4%; 95% CI, 4.0% to 22.8%).</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Conclusions and Relevance</b>
</p>
<p>In this cohort study of adult patients hospitalized with influenza, the use of NSAIDs was not associated with 30-day intensive care unit admission or death in adjusted analyses. There was an association between long-term use of NSAIDs and intensive care unit admission.</p>
</div>
</front>
</TEI>
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<Year>2020</Year>
<Month>09</Month>
<Day>09</Day>
</DateCompleted>
<DateRevised>
<Year>2020</Year>
<Month>12</Month>
<Day>18</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">2574-3805</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>3</Volume>
<Issue>7</Issue>
<PubDate>
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<Month>07</Month>
<Day>01</Day>
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</JournalIssue>
<Title>JAMA network open</Title>
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<ArticleTitle>Association of Nonsteroidal Anti-inflammatory Drug Use and Adverse Outcomes Among Patients Hospitalized With Influenza.</ArticleTitle>
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<Abstract>
<AbstractText Label="Importance">During the ongoing coronavirus disease 2019 pandemic, case reports have suggested that the use of nonsteroidal anti-inflammatory drugs (NSAIDs) may lead to adverse outcomes.</AbstractText>
<AbstractText Label="Objective">To study the association of NSAID use with adverse outcomes in patients hospitalized with influenza or influenza pneumonia.</AbstractText>
<AbstractText Label="Design, Setting, and Participants">This cohort study used propensity score matching among 7747 individuals aged 40 years or older who were hospitalized with influenza, confirmed by polymerase chain reaction or antigen testing, between 2010 and 2018. Data were collected using Danish nationwide registers. All analyses reported were performed on May 29, 2020.</AbstractText>
<AbstractText Label="Exposures">Prescription fill of an NSAID within 60 days before admission.</AbstractText>
<AbstractText Label="Main Outcomes and Measures">Risk ratio (RR) and risk difference (RD) with 95% CIs for intensive care unit admission and death within 30 days of admission.</AbstractText>
<AbstractText Label="Results">A total of 7747 patients (median [interquartile range] age, 71 [59-80] years, 3980 [51.4%] men) with confirmed influenza were identified. Of these, 520 (6.7%) were exposed to NSAIDs. In the unmatched cohorts, 104 of 520 patients (20.0%) who used NSAIDs and 958 of 7227 patients (13.3%) who did not use NSAIDs were admitted to the intensive care unit. For death within 30 days of admission, we observed 37 events (7.1%) among those who used NSAIDs compared with 563 events (7.8%) among those who did not. Current NSAID use was associated with intensive care unit admission (RR, 1.51; 95% CI, 1.26 to 1.81; RD, 6.7%; 95% CI, 3.2% to 10.3%), while NSAID use was not associated with death (RR, 0.91; 95% CI, 0.66 to 1.26; RD, -0.7%; 95% CI, -3.0% to 1.6%). In the matched cohorts, risks were unchanged for patients who used NSAIDs, while 83 ICU admissions (16.0%) and 36 deaths (6.9%) were observed among matched individuals who did not use NSAIDs. Matched (ie, adjusted) analyses yielded attenuated risk estimates for intensive care unit admission (RR, 1.25; 95% CI, 0.95 to 1.63; RD, 4.0%; 95% CI, -0.6% to 8.7%) and death (RR, 1.03; 95% CI, 0.66 to 1.60; RD, 0.2%; 95% CI, -2.9% to 3.3%). Associations were more pronounced among patients who used NSAIDs for a longer period (eg, for intensive care unit admission: RR, 1.90; 95% CI, 1.19 to 3.06; RD, 13.4%; 95% CI, 4.0% to 22.8%).</AbstractText>
<AbstractText Label="Conclusions and Relevance">In this cohort study of adult patients hospitalized with influenza, the use of NSAIDs was not associated with 30-day intensive care unit admission or death in adjusted analyses. There was an association between long-term use of NSAIDs and intensive care unit admission.</AbstractText>
</Abstract>
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<ForeName>Lars Christian</ForeName>
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</AffiliationInfo>
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<LastName>Reilev</LastName>
<ForeName>Mette</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Clinical Pharmacology and Pharmacy, Department of Public Health, University of Southern Denmark, Odense, Denmark.</Affiliation>
</AffiliationInfo>
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<LastName>Hallas</LastName>
<ForeName>Jesper</ForeName>
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<AffiliationInfo>
<Affiliation>Clinical Pharmacology and Pharmacy, Department of Public Health, University of Southern Denmark, Odense, Denmark.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Clinical Biochemistry and Clinical Pharmacology, Odense University Hospital, Odense, Denmark.</Affiliation>
</AffiliationInfo>
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<ForeName>Kasper Bruun</ForeName>
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</AffiliationInfo>
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<LastName>Thomsen</LastName>
<ForeName>Reimar Wernich</ForeName>
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<Affiliation>Department of Clinical Epidemiology, Aarhus University Hospital, Aarhus, Denmark.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Christiansen</LastName>
<ForeName>Christian Fynbo</ForeName>
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<Affiliation>Department of Clinical Epidemiology, Aarhus University Hospital, Aarhus, Denmark.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Sørensen</LastName>
<ForeName>Henrik Toft</ForeName>
<Initials>HT</Initials>
<AffiliationInfo>
<Affiliation>Department of Clinical Epidemiology, Aarhus University Hospital, Aarhus, Denmark.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Center for Population Health and Sciences, Stanford University, Stanford, California.</Affiliation>
</AffiliationInfo>
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<ForeName>Nanna Borup</ForeName>
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</AffiliationInfo>
</Author>
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<LastName>Brun</LastName>
<ForeName>Nikolai Constantin</ForeName>
<Initials>NC</Initials>
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</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Voldstedlund</LastName>
<ForeName>Marianne</ForeName>
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</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Støvring</LastName>
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<AffiliationInfo>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Public Health-Biostatistics, Aarhus University, Aarhus, Denmark.</Affiliation>
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<Author ValidYN="Y">
<LastName>Thomsen</LastName>
<ForeName>Marianne Kragh</ForeName>
<Initials>MK</Initials>
<AffiliationInfo>
<Affiliation>Department of Clinical Microbiology, Aarhus University Hospital, Aarhus, Denmark.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Christensen</LastName>
<ForeName>Steffen</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>Department of Anaesthesia and Intensive Care Medicine, Aarhus University Hospital, Aarhus, Denmark.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Pottegård</LastName>
<ForeName>Anton</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Clinical Pharmacology and Pharmacy, Department of Public Health, University of Southern Denmark, Odense, Denmark.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Hospital Pharmacy Funen, Odense University Hospital, Odense, Denmark.</Affiliation>
</AffiliationInfo>
</Author>
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