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Handling Poor Accrual in Pediatric Trials

A Simulation Study Using a Bayesian Approach

Bibliographic Data

ID15468004
AuthorsDanila Azzolina (0000-0002-8185-5742, Università degli Studi del Piemonte Orientale “Amedeo Avogadro”), Giulia Lorenzoni (0000-0003-1771-4686, University of Padua), Silvia Bressan (0000-0002-6736-5392, University of Padua), Liviana Da Dalt (0000-0003-2977-3907, University of Padua), Ileana Baldi (0000-0002-8578-9164, University of Padua), Dario Gregori (0000-0001-7906-0580, University of Padua, corresponding author)
Year2021
Volume18
Issue4
Pages2095-2095
Publication date2021-02-21
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueInternational Journal of Environmental Research and Public Health (JOURNAL)
Journal identifiersISSN: 1661-7827 • E-ISSN: 1660-4601
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/ijerph18042095
PMID33669985
OpenAlexW3129706294
LanguageEN
References cited47

In the conduction of trials, a common situation is related to potential difficulties in recruiting the planned sample size as provided by the study design. A Bayesian analysis of such trials might provide a framework to combine prior evidence with current evidence, and it is an accepted approach by regulatory agencies. However, especially for small trials, the Bayesian inference may be severely conditioned by the prior choices. The Renal Scarring Urinary Infection (RESCUE) trial, a pediatric trial that was a candidate for early termination due to underrecruitment, served as a motivating example to investigate the effects of the prior choices on small trial inference. The trial outcomes were simulated by assuming 50 scenarios combining different sample sizes and true absolute risk reduction (ARR). The simulated data were analyzed via the Bayesian approach using 0%, 50%, and 100% discounting factors on the beta power prior. An informative inference (0% discounting) on small samples could generate data-insensitive results. Instead, the 50% discounting factor ensured that the probability of confirming the trial outcome was higher than 80%, but only for an ARR higher than 0.17. A suitable option to maintain data relevant to the trial inference is to define a discounting factor based on the prior parameters. Nevertheless, a sensitivity analysis of the prior choices is highly recommended

Bayesian inference · Bayesian probability · Clinical trial · Discounting · Econometrics · Economics · Inference · Randomized controlled trial · Sample size determination · Statistics · Advanced Causal Inference Techniques · Computer Science · Health Systems, Economic Evaluations, Quality of Life · Mathematics · Medicine · Statistical Methods in Clinical Trials · Artificial Intelligence · Internal Medicine

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