2020
DOI: 10.1111/imj.14929
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COVID‐19 pandemic and the tension between the need to act and the need to know

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Cited by 7 publications
(10 citation statements)
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“…As mentioned earlier, a pandemic as serious as COVID-19 will compel some clinicians and patients to try unproven therapies based on theory, in vitro data, animal models, clinical anecdotes, observational studies and uncontrolled trials that may later be shown to be misleading [ 40 ]. This leads to multiple small, non-controlled and non-randomised trials that would not generate the strong evidence needed to determine the relative effectiveness of potential treatments [ 41 ].…”
Section: Discussionmentioning
confidence: 99%
“…As mentioned earlier, a pandemic as serious as COVID-19 will compel some clinicians and patients to try unproven therapies based on theory, in vitro data, animal models, clinical anecdotes, observational studies and uncontrolled trials that may later be shown to be misleading [ 40 ]. This leads to multiple small, non-controlled and non-randomised trials that would not generate the strong evidence needed to determine the relative effectiveness of potential treatments [ 41 ].…”
Section: Discussionmentioning
confidence: 99%
“…Although the rapid translation of COVID-related medical research is essential, it is balanced by the ‘false promise of rushed science [ 33 ▪▪ ].’ There are already several hundred COVID-19 trials registered across the world, and this number is increasing exponentially. The increase in preprint publication servers allows for dissemination of nonpeer-reviewed research, which can be publicized and reported prior to appropriate scrutiny of results and conclusions.…”
Section: Be a Critical Readermentioning
confidence: 99%
“…The increase in preprint publication servers allows for dissemination of nonpeer-reviewed research, which can be publicized and reported prior to appropriate scrutiny of results and conclusions. Concerns have been raised about publication of small case series, or randomized controlled trials that have small samples from a single center, which ‘at any other time would be hypothesis generating’ now receiving significant weight and attention [ 33 ▪▪ ].…”
Section: Be a Critical Readermentioning
confidence: 99%
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“…Some adaptive designs may improve efficiency, confer health benefits to trial participants, or in some cases achieve both (Burnett et al, 2020;Pallmann et al, 2018), including in the context of COVID-19 treatment trials (Stallard et al, 2020) and of vaccine trials (Kahn et al, 2021). Response-adaptive randomisation (RAR), in which the proportion of people randomised to a particular trial arm is modified based on accumulated data observed at an interim analysis, has been suggested (Kahn et al, 2021;Scott, 2020) to have the potential to balance the competing objectives of health benefits to the trial participants, power and time until A c c e p t e d M a n u s c r i p t a conclusion is reached. Brueckner et al (2018) compared different RAR designs for trials of treatments during an epidemic.…”
Section: Introductionmentioning
confidence: 99%