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Drug interventions for prevention of COVID-19 progression to severe disease in outpatients : a systematic review with meta-analyses and trial sequential analyses (The LIVING Project)

Petersen, Johanne Juul ; Jørgensen, Caroline Kamp ; Faltermeier, Pascal ; Siddiqui, Faiza ; Feinberg, Joshua ; Nielsen, Emil Eik ; Torp Kristensen, Andreas ; Juul, Sophie ; Holgersson, Johan LU and Nielsen, Niklas LU , et al. (2023) In BMJ Open 13(6).
Abstract

Objectives To assess the effects of interventions authorised by the European Medicines Agency (EMA) or the US Food and Drug Administration (FDA) for prevention of COVID-19 progression to severe disease in outpatients. Setting Outpatient treatment. Participants Participants with a diagnosis of COVID-19 and the associated SARS-CoV-2 virus irrespective of age, sex and comorbidities. Interventions Drug interventions authorised by EMA or FDA. Primary outcome measures Primary outcomes were all-cause mortality and serious adverse events. Results We included 17 clinical trials randomising 16 257 participants to 8 different interventions authorised by EMA or FDA. 15/17 of the included trials (88.2%) were assessed at high risk of bias. Only... (More)

Objectives To assess the effects of interventions authorised by the European Medicines Agency (EMA) or the US Food and Drug Administration (FDA) for prevention of COVID-19 progression to severe disease in outpatients. Setting Outpatient treatment. Participants Participants with a diagnosis of COVID-19 and the associated SARS-CoV-2 virus irrespective of age, sex and comorbidities. Interventions Drug interventions authorised by EMA or FDA. Primary outcome measures Primary outcomes were all-cause mortality and serious adverse events. Results We included 17 clinical trials randomising 16 257 participants to 8 different interventions authorised by EMA or FDA. 15/17 of the included trials (88.2%) were assessed at high risk of bias. Only molnupiravir and ritonavir-boosted nirmatrelvir seemed to improve both our primary outcomes. Meta-analyses showed that molnupiravir reduced the risk of death (relative risk (RR) 0.11, 95% CI 0.02 to 0.64; p=0.0145, 2 trials; very low certainty of evidence) and serious adverse events (RR 0.63, 95% CI 0.47 to 0.84; p=0.0018, 5 trials; very low certainty of evidence). Fisher's exact test showed that ritonavir-boosted nirmatrelvir reduced the risk of death (p=0.0002, 1 trial; very low certainty of evidence) and serious adverse events (p<0.0001, 1 trial; very low certainty of evidence) in 1 trial including 2246 patients, while another trial including 1140 patients reported 0 deaths in both groups. Conclusions The certainty of the evidence was very low, but, from the results of this study, molnupiravir showed the most consistent benefit and ranked highest among the approved interventions for prevention of COVID-19 progression to severe disease in outpatients. The lack of certain evidence should be considered when treating patients with COVID-19 for prevention of disease progression. PROSPERO registration number CRD42020178787.

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organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
COVID-19, epidemiology, general medicine (see internal medicine), primary care, public health, quality in health care
in
BMJ Open
volume
13
issue
6
article number
e064498
publisher
BMJ Publishing Group
external identifiers
  • pmid:37339844
  • scopus:85163921350
ISSN
2044-6055
DOI
10.1136/bmjopen-2022-064498
language
English
LU publication?
yes
id
d8e0bafc-8995-4cd7-98c3-5e15cd3fbbe8
date added to LUP
2023-09-13 09:04:32
date last changed
2024-04-20 04:19:32
@article{d8e0bafc-8995-4cd7-98c3-5e15cd3fbbe8,
  abstract     = {{<p>Objectives To assess the effects of interventions authorised by the European Medicines Agency (EMA) or the US Food and Drug Administration (FDA) for prevention of COVID-19 progression to severe disease in outpatients. Setting Outpatient treatment. Participants Participants with a diagnosis of COVID-19 and the associated SARS-CoV-2 virus irrespective of age, sex and comorbidities. Interventions Drug interventions authorised by EMA or FDA. Primary outcome measures Primary outcomes were all-cause mortality and serious adverse events. Results We included 17 clinical trials randomising 16 257 participants to 8 different interventions authorised by EMA or FDA. 15/17 of the included trials (88.2%) were assessed at high risk of bias. Only molnupiravir and ritonavir-boosted nirmatrelvir seemed to improve both our primary outcomes. Meta-analyses showed that molnupiravir reduced the risk of death (relative risk (RR) 0.11, 95% CI 0.02 to 0.64; p=0.0145, 2 trials; very low certainty of evidence) and serious adverse events (RR 0.63, 95% CI 0.47 to 0.84; p=0.0018, 5 trials; very low certainty of evidence). Fisher's exact test showed that ritonavir-boosted nirmatrelvir reduced the risk of death (p=0.0002, 1 trial; very low certainty of evidence) and serious adverse events (p&lt;0.0001, 1 trial; very low certainty of evidence) in 1 trial including 2246 patients, while another trial including 1140 patients reported 0 deaths in both groups. Conclusions The certainty of the evidence was very low, but, from the results of this study, molnupiravir showed the most consistent benefit and ranked highest among the approved interventions for prevention of COVID-19 progression to severe disease in outpatients. The lack of certain evidence should be considered when treating patients with COVID-19 for prevention of disease progression. PROSPERO registration number CRD42020178787.</p>}},
  author       = {{Petersen, Johanne Juul and Jørgensen, Caroline Kamp and Faltermeier, Pascal and Siddiqui, Faiza and Feinberg, Joshua and Nielsen, Emil Eik and Torp Kristensen, Andreas and Juul, Sophie and Holgersson, Johan and Nielsen, Niklas and Bentzer, Peter and Thabane, Lehana and Kwasi Korang, Steven and Klingenberg, Sarah and Gluud, Christian and Jakobsen, Janus C.}},
  issn         = {{2044-6055}},
  keywords     = {{COVID-19; epidemiology; general medicine (see internal medicine); primary care; public health; quality in health care}},
  language     = {{eng}},
  number       = {{6}},
  publisher    = {{BMJ Publishing Group}},
  series       = {{BMJ Open}},
  title        = {{Drug interventions for prevention of COVID-19 progression to severe disease in outpatients : a systematic review with meta-analyses and trial sequential analyses (The LIVING Project)}},
  url          = {{http://dx.doi.org/10.1136/bmjopen-2022-064498}},
  doi          = {{10.1136/bmjopen-2022-064498}},
  volume       = {{13}},
  year         = {{2023}},
}