Evidence map›Paper›PMID 28583149›Full record

SynthesisCritical care (London, England)2017

Effect sizes in ongoing randomized controlled critical care trials.

Elliott E Ridgeon, Rinaldo Bellomo, Scott K Aberegg, Rob Mac Sweeney, Rachel S Varughese, Giovanni Landoni, Paul J Young

Abstract readSystematic Review
In one paragraph

Synthesis in Critical care (London, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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

19 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Review
  6. Sample size requirements and intra-cluster correlations for stepped wedge cluster randomised trials in intensive care medicine: A practical guide.Critical care and resuscitation : journal of the Australasian Academy of Critical Care Medicine · 2026
    Article
  7. Review
  8. INCEPT: The Intensive Care Platform Trial-Design and protocol.Acta anaesthesiologica Scandinavica · 2025
    Article
  9. The importance of plausibility.Intensive care medicine · 2023
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Opportunities and challenges of clustering, crossing over, and using registry data in the PEPTIC trial.Critical care and resuscitation : journal of the Australasian Academy of Critical Care Medicine · 2020
    Article
  16. Article
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  18. Article
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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

7 authors.

Elliott E RidgeonMedical Research Institute of New Zealand, Wellington, New Zealand.
Rinaldo BellomoAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia.
Scott K AbereggDivision of Pulmonary and Critical Care Medicine, University of Utah School of Medicine, Salt Lake City, UT, USA.
Rob Mac SweeneyIntensive Care Unit, Royal Victoria Hospital, Belfast, UK.
Rachel S VarugheseMedical Research Institute of New Zealand, Wellington, New Zealand.
Giovanni LandoniDepartment of Anesthesia and Intensive Care, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), San Raffaele Scientific Institute, Milan, Italy.
Paul J YoungIntensive Care Unit, Wellington Regional Hospital, Wellington, New Zealand. paul.young@ccdhb.org.nz.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAn important limitation of many critical care trial designs is that they hypothesize large, and potentially implausible, reductions in mortality. Interpretation of trial results could be improved by systematic assessment of the plausibility of trial hypotheses; however, such assessment has not been attempted in the field of critical care medicine. The purpose of this study was to determine clinicians' views about prior probabilities and plausible effect sizes for ongoing critical care trials where the primary endpoint is landmark mortality.

methodsWe conducted a systematic review of clinical trial registries in September 2015 to identify ongoing critical care medicine trials where landmark mortality was the primary outcome, followed by a clinician survey to obtain opinions about ten large trials. Clinicians were asked to estimate the probability that each trial would demonstrate a mortality effect equal to or larger than that used in its sample size calculations.

resultsEstimates provided by individual clinicians varied from 0% to 100% for most trials, with a median estimate of 15% (IQR 10-20%). The median largest absolute mortality reduction considered plausible was 4.5% (IQR 3.5-5%), compared with a median absolute mortality reduction used in sample size calculations of 5% (IQR 3.6-10%) (P = 0.27).

conclusionsFor some of the largest ongoing critical care trials, many clinicians regard prior probabilities as low and consider that plausible effects on absolute mortality are less than 5%. Further work is needed to determine whether pooled estimates obtained by surveying clinicians are replicable and accurate or whether other methods of estimating prior probability are preferred.

Indexed as

Hospital MortalityPatient SelectionCritical Care OutcomesHumansRandomized Controlled Trials as TopicRegistriesResearch DesignStatistics, NonparametricSurveys and QuestionnairesClinical trial designCritical careIntensive careIntensive care unitRandomized clinical trial

Identifiers

PMID28583149
PMCPMC5460326

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.