Serveur d'exploration COVID et hydrochloroquine

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Positive impact of oral hydroxychloroquine and povidone-iodine throat spray for COVID-19 prophylaxis: An open-label randomized trial.

Identifieur interne : 000100 ( Main/Corpus ); précédent : 000099; suivant : 000101

Positive impact of oral hydroxychloroquine and povidone-iodine throat spray for COVID-19 prophylaxis: An open-label randomized trial.

Auteurs : Raymond Chee Seong Seet ; Amy May Lin Quek ; Delicia Shu Qin Ooi ; Sharmila Sengupta ; Satish Ramapatna Lakshminarasappa ; Chieh Yang Koo ; Jimmy Bok Yan So ; Boon Cher Goh ; Kwok Seng Loh ; Dale Fisher ; Hock Luen Teoh ; Jie Sun ; Alex R. Cook ; Paul Anantharajah Tambyah ; Mikael Hartman

Source :

RBID : pubmed:33864917

Abstract

BACKGROUND

We examined whether existing licensed pharmacotherapies could reduce the spread of coronavirus disease 2019 (COVID-19).

METHODS

An open-label parallel randomized controlled trial was performed among healthy migrant workers quarantined in a large multi-storey dormitory in Singapore. Forty clusters (each defined as individual floors of the dormitory) were randomly assigned to receive a 42-day prophylaxis regimen of either oral hydroxychloroquine (400 mg once, followed by 200 mg/day), oral ivermectin (12 mg once), povidone-iodine throat spray (3 times/day, 270 μg/day), oral zinc (80 mg/day)/vitamin C (500 mg/day) combination, or oral vitamin C, 500 mg/day. The primary outcome was laboratory evidence of SARS-CoV-2 infection as shown by either: (1) a positive serologic test for SARS-CoV-2 antibody on day 42, or (2) a positive PCR test for SARS-CoV-2 at any time between baseline and day 42.

RESULTS

A total of 3037 asymptomatic participants (mean age, 33.0 years; all men) who were seronegative to SARS-CoV-2 at baseline were included in the primary analysis. Follow-up was nearly complete (99.6%). Compared with vitamin C, significant absolute risk reductions (%, 98.75% confidence interval) were observed for oral hydroxychloroquine (21%, 2-42%) and povidone-iodine throat spray (24%, 7-39%). No statistically significant differences were observed with oral zinc/vitamin C combination (23%, -5 to +41%) and ivermectin (5%, -10 to +22%). Interruptions due to side effects were highest among participants who received zinc/vitamin C combination (6.9%), followed by vitamin C (4.7%), povidone-iodine (2.0%), and hydroxychloroquine (0.7%).

CONCLUSIONS

Chemoprophylaxis with either oral hydroxychloroquine or povidone-iodine throat spray was superior to oral vitamin C in reducing SARS-CoV-2 infection in young and healthy men.


DOI: 10.1016/j.ijid.2021.04.035
PubMed: 33864917
PubMed Central: PMC8056783

Links to Exploration step

pubmed:33864917

Le document en format XML

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<name sortKey="Teoh, Hock Luen" sort="Teoh, Hock Luen" uniqKey="Teoh H" first="Hock Luen" last="Teoh">Hock Luen Teoh</name>
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<name sortKey="Sun, Jie" sort="Sun, Jie" uniqKey="Sun J" first="Jie" last="Sun">Jie Sun</name>
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<name sortKey="Cook, Alex R" sort="Cook, Alex R" uniqKey="Cook A" first="Alex R" last="Cook">Alex R. Cook</name>
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<name sortKey="Tambyah, Paul Anantharajah" sort="Tambyah, Paul Anantharajah" uniqKey="Tambyah P" first="Paul Anantharajah" last="Tambyah">Paul Anantharajah Tambyah</name>
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<name sortKey="Hartman, Mikael" sort="Hartman, Mikael" uniqKey="Hartman M" first="Mikael" last="Hartman">Mikael Hartman</name>
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<name sortKey="Ooi, Delicia Shu Qin" sort="Ooi, Delicia Shu Qin" uniqKey="Ooi D" first="Delicia Shu Qin" last="Ooi">Delicia Shu Qin Ooi</name>
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<name sortKey="Lakshminarasappa, Satish Ramapatna" sort="Lakshminarasappa, Satish Ramapatna" uniqKey="Lakshminarasappa S" first="Satish Ramapatna" last="Lakshminarasappa">Satish Ramapatna Lakshminarasappa</name>
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<name sortKey="Koo, Chieh Yang" sort="Koo, Chieh Yang" uniqKey="Koo C" first="Chieh Yang" last="Koo">Chieh Yang Koo</name>
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<name sortKey="So, Jimmy Bok Yan" sort="So, Jimmy Bok Yan" uniqKey="So J" first="Jimmy Bok Yan" last="So">Jimmy Bok Yan So</name>
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</affiliation>
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<name sortKey="Teoh, Hock Luen" sort="Teoh, Hock Luen" uniqKey="Teoh H" first="Hock Luen" last="Teoh">Hock Luen Teoh</name>
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<nlm:affiliation>Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; Division of Neurology, Department of Medicine, National University Hospital, Singapore.</nlm:affiliation>
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<name sortKey="Sun, Jie" sort="Sun, Jie" uniqKey="Sun J" first="Jie" last="Sun">Jie Sun</name>
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<nlm:affiliation>Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore.</nlm:affiliation>
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<name sortKey="Cook, Alex R" sort="Cook, Alex R" uniqKey="Cook A" first="Alex R" last="Cook">Alex R. Cook</name>
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<nlm:affiliation>Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore.</nlm:affiliation>
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<name sortKey="Tambyah, Paul Anantharajah" sort="Tambyah, Paul Anantharajah" uniqKey="Tambyah P" first="Paul Anantharajah" last="Tambyah">Paul Anantharajah Tambyah</name>
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<nlm:affiliation>Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; Division of Infectious Diseases, Department of Medicine, National University Hospital, Singapore.</nlm:affiliation>
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<name sortKey="Hartman, Mikael" sort="Hartman, Mikael" uniqKey="Hartman M" first="Mikael" last="Hartman">Mikael Hartman</name>
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<p>
<b>BACKGROUND</b>
</p>
<p>We examined whether existing licensed pharmacotherapies could reduce the spread of coronavirus disease 2019 (COVID-19).</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>An open-label parallel randomized controlled trial was performed among healthy migrant workers quarantined in a large multi-storey dormitory in Singapore. Forty clusters (each defined as individual floors of the dormitory) were randomly assigned to receive a 42-day prophylaxis regimen of either oral hydroxychloroquine (400 mg once, followed by 200 mg/day), oral ivermectin (12 mg once), povidone-iodine throat spray (3 times/day, 270 μg/day), oral zinc (80 mg/day)/vitamin C (500 mg/day) combination, or oral vitamin C, 500 mg/day. The primary outcome was laboratory evidence of SARS-CoV-2 infection as shown by either: (1) a positive serologic test for SARS-CoV-2 antibody on day 42, or (2) a positive PCR test for SARS-CoV-2 at any time between baseline and day 42.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>A total of 3037 asymptomatic participants (mean age, 33.0 years; all men) who were seronegative to SARS-CoV-2 at baseline were included in the primary analysis. Follow-up was nearly complete (99.6%). Compared with vitamin C, significant absolute risk reductions (%, 98.75% confidence interval) were observed for oral hydroxychloroquine (21%, 2-42%) and povidone-iodine throat spray (24%, 7-39%). No statistically significant differences were observed with oral zinc/vitamin C combination (23%, -5 to +41%) and ivermectin (5%, -10 to +22%). Interruptions due to side effects were highest among participants who received zinc/vitamin C combination (6.9%), followed by vitamin C (4.7%), povidone-iodine (2.0%), and hydroxychloroquine (0.7%).</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>Chemoprophylaxis with either oral hydroxychloroquine or povidone-iodine throat spray was superior to oral vitamin C in reducing SARS-CoV-2 infection in young and healthy men.</p>
</div>
</front>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">We examined whether existing licensed pharmacotherapies could reduce the spread of coronavirus disease 2019 (COVID-19).</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">An open-label parallel randomized controlled trial was performed among healthy migrant workers quarantined in a large multi-storey dormitory in Singapore. Forty clusters (each defined as individual floors of the dormitory) were randomly assigned to receive a 42-day prophylaxis regimen of either oral hydroxychloroquine (400 mg once, followed by 200 mg/day), oral ivermectin (12 mg once), povidone-iodine throat spray (3 times/day, 270 μg/day), oral zinc (80 mg/day)/vitamin C (500 mg/day) combination, or oral vitamin C, 500 mg/day. The primary outcome was laboratory evidence of SARS-CoV-2 infection as shown by either: (1) a positive serologic test for SARS-CoV-2 antibody on day 42, or (2) a positive PCR test for SARS-CoV-2 at any time between baseline and day 42.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">A total of 3037 asymptomatic participants (mean age, 33.0 years; all men) who were seronegative to SARS-CoV-2 at baseline were included in the primary analysis. Follow-up was nearly complete (99.6%). Compared with vitamin C, significant absolute risk reductions (%, 98.75% confidence interval) were observed for oral hydroxychloroquine (21%, 2-42%) and povidone-iodine throat spray (24%, 7-39%). No statistically significant differences were observed with oral zinc/vitamin C combination (23%, -5 to +41%) and ivermectin (5%, -10 to +22%). Interruptions due to side effects were highest among participants who received zinc/vitamin C combination (6.9%), followed by vitamin C (4.7%), povidone-iodine (2.0%), and hydroxychloroquine (0.7%).</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Chemoprophylaxis with either oral hydroxychloroquine or povidone-iodine throat spray was superior to oral vitamin C in reducing SARS-CoV-2 infection in young and healthy men.</AbstractText>
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<ForeName>Amy May Lin</ForeName>
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</AffiliationInfo>
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<LastName>Lakshminarasappa</LastName>
<ForeName>Satish Ramapatna</ForeName>
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<Affiliation>Department of Anatomy, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.</Affiliation>
</AffiliationInfo>
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<Affiliation>Department of Cardiology, National University Heart Centre, Singapore.</Affiliation>
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<ForeName>Jimmy Bok Yan</ForeName>
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<Author ValidYN="Y">
<LastName>Teoh</LastName>
<ForeName>Hock Luen</ForeName>
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<Affiliation>Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; Division of Neurology, Department of Medicine, National University Hospital, Singapore.</Affiliation>
</AffiliationInfo>
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<Affiliation>Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore.</Affiliation>
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<ForeName>Alex R</ForeName>
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<Affiliation>Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore.</Affiliation>
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<LastName>Tambyah</LastName>
<ForeName>Paul Anantharajah</ForeName>
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<AffiliationInfo>
<Affiliation>Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore; Division of Infectious Diseases, Department of Medicine, National University Hospital, Singapore.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Hartman</LastName>
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<Initials>M</Initials>
<AffiliationInfo>
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