Evidence map›Paper›PMID 37286384›Full record

ArticleJournal of cystic fibrosis : official journal of the European Cystic Fibrosis Society2023

Potential implicit bias in attribution of adverse events in randomized controlled trials in cystic fibrosis.

Ranjani Somayaji, Madeline E Wessels, Tijana Milinic, Kathleen J Ramos, Nicole Mayer-Hamblett, Bonnie W Ramsey, Sonya Heltshe, Umer Khan, Christopher H Goss

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 38% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Ranjani SomayajiDepartment of Medicine, University of Calgary, Calgary, Canada.
Madeline E WesselsSeattle Children's Research Institute, Seattle, WA USA.
Tijana MilinicDepartment of Medicine, University of Washington, Seattle, WA USA.
Kathleen J RamosDepartment of Medicine, University of Washington, Seattle, WA USA.
Nicole Mayer-HamblettSeattle Children's Research Institute, Seattle, WA USA; Department of Pediatrics, Division of Pulmonary, University of Washington, Seattle, WA USA.
Bonnie W RamseySeattle Children's Research Institute, Seattle, WA USA; Department of Pediatrics, Division of Pulmonary, University of Washington, Seattle, WA USA.
Sonya HeltsheSeattle Children's Research Institute, Seattle, WA USA; Department of Pediatrics, Division of Pulmonary, University of Washington, Seattle, WA USA.
Umer KhanSeattle Children's Research Institute, Seattle, WA USA.
Christopher H GossSeattle Children's Research Institute, Seattle, WA USA; Department of Medicine, University of Washington, Seattle, WA USA; Department of Pediatrics, Division of Pulmonary, University of Washington, Seattle, WA USA. Electronic address: goss@uw.edu.
University of Washington · USUniversity of Calgary · CA

Funding

Translational Research Center to Expedite Novel Therapies in Cystic FibrosisP30DK089507 · NIDDK · SEATTLE CHILDREN'S HOSPITAL · PI Christopher Hooper Goss, Lucas R Hoffman · 2010 to 2026
$21.4M
Proof of Principle Evaluation of IV Gallium Nitrate in Patients with CFUM1HL119073 · NHLBI · UNIVERSITY OF WASHINGTON · PI GOSS, CHRISTOPHER HOOPER, SINGH, PRADEEP K · 2013 to 2017
$4.8M
Investigating treatment resistance mechanisms in chronic bacterial infectionsR01AI101307 · NIAID · UNIVERSITY OF WASHINGTON · PI BRUCE, JAMES EDWARD, MANOIL, COLIN · 2012 to 2016
$2.9M
Regulation of host inflammatory responses and outcome in melioidosis by TLR5R01HL113382 · NHLBI · UNIVERSITY OF WASHINGTON · PI WEST, TIMOTHY EOIN · 2012 to 2016
$2.6M
NHLBI NIH HHS R01 HL113382NHLBI NIH HHS UM1 HL119073NIAID NIH HHS R01 AI101307NIDDK NIH HHS P30 DK089507
6 · The paper itself

Abstract

introductionAlthough work to date in cystic fibrosis (CF) has elucidated frequencies and characteristics of adverse events, the accuracy of attribution of relatedness to study drug by investigators has not been assessed. We aimed to determine whether there was an association of attribution by group allocation in CF clinical trials.

methodsWe conducted a secondary analysis from 4 CF trials of all persons who experienced an AE. Our primary outcome was the odds of an AE related to active study drug and predictor of interest was the treatment allocation. We constructed a multivariable generalized estimating equation model allowing for repeated measures.

resultsA total of 785 subjects (47.5% female, mean age 12 years) had 11,974 AEs, of which 430 were serious. AE attribution was greater with receipt of active study drug as compared to placebo but did not reach statistical significance (OR 1.38, 95% CI 0.98-1.82). Significantly associated factors included female sex (OR 0.58, 95% 0.39-0.87), age (OR 1.24, 95% CI 1.06-1.46) and baseline lung function (per 10%, OR 1.16, 95% CI 1.05-1.28).

conclusionIn our large study, there was a non-significant but greater odds of AE attribution (a key element of clinical trial reporting) to active study drug based on assigned treatment to study drug or control which suggests that there is a trend in physicians to attribute blinded safety data to the active drug. Interestingly, females were less likely to have AE attribution to study drug and warrants further work in development and validation of monitoring guidelines and processes.

Indexed as

Cystic FibrosisBias, ImplicitChildFemaleHumansMaleRandomized Controlled Trials as TopicResearch DesignAdverse eventBiasClinical trialCystic fibrosisFemale sexSafety monitoring

Identifiers

PMID37286384
PMCPMC10529796
OpenAlexW4379389267

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.