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      Prophylaxis against covid-19: living systematic review and network meta-analysis

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      1 , * , 1 , * , , 1 , * , 1 , * , 1 , * , 2 , * , 3 , 1 , 4 , 1 , 5 , 1 , 6 , 1 , 7 , 4 , 1 , 1 , 1 , 8 , 9 , 10 , 11 , 1 , 7 , 1 , 7 , 12 , 13 , 1 , 14 , 15 , 7 , 16 , 17 , 18 , 19 , 1 , 7 , 1 , 20 , 1 , 21 , 22 , 23 , 18 , 24 , 1 , 1 , 1 , 1 , 7 , 1
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          Abstract

          Objective

          To determine and compare the effects of drug prophylaxis on SARS-CoV-2 infection and covid-19.

          Design

          Living systematic review and network meta-analysis.

          Data sources

          World Health Organization covid-19 database, a comprehensive multilingual source of global covid-19 literature to 25 March 2021, and six additional Chinese databases to 20 February 2021.

          Study selection

          Randomised trials of people at risk of covid-19 who were assigned to receive prophylaxis or no prophylaxis (standard care or placebo). Pairs of reviewers independently screened potentially eligible articles.

          Methods

          Random effects bayesian network meta-analysis was performed after duplicate data abstraction. Included studies were assessed for risk of bias using a modification of the Cochrane risk of bias 2.0 tool, and certainty of evidence was assessed using the grading of recommendations assessment, development, and evaluation (GRADE) approach.

          Results

          The first iteration of this living network meta-analysis includes nine randomised trials—six of hydroxychloroquine (n=6059 participants), one of ivermectin combined with iota-carrageenan (n=234), and two of ivermectin alone (n=540), all compared with standard care or placebo. Two trials (one of ramipril and one of bromhexine hydrochloride) did not meet the sample size requirements for network meta-analysis. Hydroxychloroquine has trivial to no effect on admission to hospital (risk difference 1 fewer per 1000 participants, 95% credible interval 3 fewer to 4 more; high certainty evidence) or mortality (1 fewer per 1000, 2 fewer to 3 more; high certainty). Hydroxychloroquine probably does not reduce the risk of laboratory confirmed SARS-CoV-2 infection (2 more per 1000, 18 fewer to 28 more; moderate certainty), probably increases adverse effects leading to drug discontinuation (19 more per 1000, 1 fewer to 70 more; moderate certainty), and may have trivial to no effect on suspected, probable, or laboratory confirmed SARS-CoV-2 infection (15 fewer per 1000, 64 fewer to 41 more; low certainty). Owing to serious risk of bias and very serious imprecision, and thus very low certainty of evidence, the effects of ivermectin combined with iota-carrageenan on laboratory confirmed covid-19 (52 fewer per 1000, 58 fewer to 37 fewer), ivermectin alone on laboratory confirmed infection (50 fewer per 1000, 59 fewer to 16 fewer) and suspected, probable, or laboratory confirmed infection (159 fewer per 1000, 165 fewer to 144 fewer) remain very uncertain.

          Conclusions

          Hydroxychloroquine prophylaxis has trivial to no effect on hospital admission and mortality, probably increases adverse effects, and probably does not reduce the risk of SARS-CoV-2 infection. Because of serious risk of bias and very serious imprecision, it is highly uncertain whether ivermectin combined with iota-carrageenan and ivermectin alone reduce the risk of SARS-CoV-2 infection.

          Systematic review registration

          This review was not registered. The protocol established a priori is included as a supplement.

          Readers’ note

          This article is a living systematic review that will be updated to reflect emerging evidence. Updates may occur for up to two years from the date of original publication.

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          Most cited references32

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          RoB 2: a revised tool for assessing risk of bias in randomised trials

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            The PRISMA extension statement for reporting of systematic reviews incorporating network meta-analyses of health care interventions: checklist and explanations.

            The PRISMA statement is a reporting guideline designed to improve the completeness of reporting of systematic reviews and meta-analyses. Authors have used this guideline worldwide to prepare their reviews for publication. In the past, these reports typically compared 2 treatment alternatives. With the evolution of systematic reviews that compare multiple treatments, some of them only indirectly, authors face novel challenges for conducting and reporting their reviews. This extension of the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-analyses) statement was developed specifically to improve the reporting of systematic reviews incorporating network meta-analyses. A group of experts participated in a systematic review, Delphi survey, and face-to-face discussion and consensus meeting to establish new checklist items for this extension statement. Current PRISMA items were also clarified. A modified, 32-item PRISMA extension checklist was developed to address what the group considered to be immediately relevant to the reporting of network meta-analyses. This document presents the extension and provides examples of good reporting, as well as elaborations regarding the rationale for new checklist items and the modification of previously existing items from the PRISMA statement. It also highlights educational information related to key considerations in the practice of network meta-analysis. The target audience includes authors and readers of network meta-analyses, as well as journal editors and peer reviewers.
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              A Randomized Trial of Hydroxychloroquine as Postexposure Prophylaxis for Covid-19

              Abstract Background Coronavirus disease 2019 (Covid-19) occurs after exposure to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). For persons who are exposed, the standard of care is observation and quarantine. Whether hydroxychloroquine can prevent symptomatic infection after SARS-CoV-2 exposure is unknown. Methods We conducted a randomized, double-blind, placebo-controlled trial across the United States and parts of Canada testing hydroxychloroquine as postexposure prophylaxis. We enrolled adults who had household or occupational exposure to someone with confirmed Covid-19 at a distance of less than 6 ft for more than 10 minutes while wearing neither a face mask nor an eye shield (high-risk exposure) or while wearing a face mask but no eye shield (moderate-risk exposure). Within 4 days after exposure, we randomly assigned participants to receive either placebo or hydroxychloroquine (800 mg once, followed by 600 mg in 6 to 8 hours, then 600 mg daily for 4 additional days). The primary outcome was the incidence of either laboratory-confirmed Covid-19 or illness compatible with Covid-19 within 14 days. Results We enrolled 821 asymptomatic participants. Overall, 87.6% of the participants (719 of 821) reported a high-risk exposure to a confirmed Covid-19 contact. The incidence of new illness compatible with Covid-19 did not differ significantly between participants receiving hydroxychloroquine (49 of 414 [11.8%]) and those receiving placebo (58 of 407 [14.3%]); the absolute difference was −2.4 percentage points (95% confidence interval, −7.0 to 2.2; P=0.35). Side effects were more common with hydroxychloroquine than with placebo (40.1% vs. 16.8%), but no serious adverse reactions were reported. Conclusions After high-risk or moderate-risk exposure to Covid-19, hydroxychloroquine did not prevent illness compatible with Covid-19 or confirmed infection when used as postexposure prophylaxis within 4 days after exposure. (Funded by David Baszucki and Jan Ellison Baszucki and others; ClinicalTrials.gov number, NCT04308668.)
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                Author and article information

                Contributors
                Role: methodologist
                Role: methodologist, internist
                Role: methodologist
                Role: methodologist
                Role: methodologist
                Role: methodologist
                Role: methodologist
                Role: assistant professor
                Role: methodologist, internist
                Role: methodologist, internist
                Role: methodologist, immunologist
                Role: librarian
                Role: methodologist
                Role: methodologist
                Role: methodologist
                Role: methodologist, critical care physician
                Role: methodologist, internist
                Role: data analyst
                Role: methodologist, critical care physician
                Role: methodologist, infectious disease physician
                Role: methodologist, internist
                Role: methodologistRole: assistant professor
                Role: methodologist
                Role: clinical associate professor, paediatric critical care, infectious diseases physician
                Role: methodologist, nephrologist
                Role: methodologist, internist
                Role: methodologist
                Role: methodologist
                Role: methodologist, critical care physician
                Role: methodologist
                Role: methodologist
                Role: professor
                Role: methodologist, internist
                Role: methodologist
                Role: methodologist
                Role: methodologist, pharmacist
                Role: methodologist
                Role: methodologist, pharmacist
                Role: methodologist, internist
                Role: methodologist
                Journal
                BMJ
                BMJ
                BMJ-UK
                bmj
                The BMJ
                BMJ Publishing Group Ltd.
                0959-8138
                1756-1833
                2021
                26 April 2021
                : 373
                : n949
                Affiliations
                [1 ]Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada
                [2 ]Evidence Based Social Science Research Center, School of Public Health, Lanzhou University, Lanzhou, Gansu, China
                [3 ]Department of Preventive Medicine, College of Medicine, Chosun University, Gwangju, Republic of Korea
                [4 ]Department of Anesthesia, McMaster University, Hamilton, ON, Canada
                [5 ]Department of Medicine, University of Toronto, Toronto, ON, Canada
                [6 ]Division of General Internal Medicine & Division of Clinical Epidemiology, University Hospitals of Geneva, Geneva, Switzerland
                [7 ]Department of Medicine, McMaster University, Hamilton, ON, Canada
                [8 ]Department of Medicine, Western University, London, ON, Canada
                [9 ]Servicio de Clinica Médica del Hospital Alemán, Buenos Aires, Argentina
                [10 ]Wolfson Palliative Care Research Centre, Hull York Medical School, York, UK
                [11 ]Department of Medicine and Centre de recherche du CHU de Sherbrooke, Sherbrooke, QC, Canada
                [12 ]Schwartz/Reisman Emergency Medicine Institute, Sinai Health, Toronto, ON, Canada
                [13 ]Department of Family and Community Medicine, University of Toronto, Toronto, ON, Canada
                [14 ]Department of Pediatrics, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada
                [15 ]Department of Medicine, University of Kansas Medical Center, Kansas City, MO, USA
                [16 ]Iberoamerican Cochrane Centre, Sant Pau Biomedical Research Institute (IIB Sant Pau), Barcelona, Spain
                [17 ]CIBER de Epidemiología y Salud Pública (CIBERESP), Barcelona, Spain
                [18 ]Epistemonikos Foundation, Santiago, Chile
                [19 ]C Evidence Center, Cochrane Chile Associated Center, Pontificia Universidad Católica de Chile, Santiago, Chile
                [20 ]School of Public Health and Preventative Medicine, Monash University, Melbourne, Australia
                [21 ]Institute of Health and Society, University of Oslo, Oslo, Norway
                [22 ]Department of Nephrology and Hypertension, University Medical Center Utrecht, Utrecht, Netherlands
                [23 ]Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands
                [24 ]Centro de Investigación de Salud Pública y Epidemiología Clínica (CISPEC), Facultad de Ciencias de la Salud Eugenio Espejo, Universidad UTE, Quito, Ecuador
                [* ]Joint first authors
                Author notes
                Correspondence to: R A C Siemieniuk McMaster University Medical Centre 1280 Main Street West 2C Area Hamilton, ON, L8S 4K1, Canada reed.siemieniuk@ 123456medportal.ca (or @rsiemieniuk on Twitter)
                Author information
                https://orcid.org/0000-0002-3725-3031
                Article
                barj064893
                10.1136/bmj.n949
                8073806
                33903131
                fc7903f5-a63d-4312-b9e7-90f3c46c41e5
                © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

                This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 07 April 2021
                Categories
                Research
                2474

                Medicine
                Medicine

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