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Record W1973748105 · doi:10.1136/bmj.e2809

Potential impact on estimated treatment effects of information lost to follow-up in randomised controlled trials (LOST-IT): systematic review

2012· review· en· W1973748105 on OpenAlexafffund
Elie A. Akl, Matthias Briel, John J. You, Xin Sun, Brad Johnston, Jason W. Busse, S. Mulla, François Lamontagne, Dirk Bassler, Claudio Vera, Mohamad Alshurafa, Christina M. Katsios, Qi Zhou, Tali Cukierman‐Yaffe, Azim S. Gangji, Edward J. Mills, Stephen D. Walter, Holger J. Schünemann, D. G. Altman, G. H. Guyatt

Bibliographic record

VenueBMJ · 2012
Typereview
Languageen
FieldDecision Sciences
TopicMeta-analysis and systematic reviews
Canadian institutionsUniversity of OttawaInstitute for Work & HealthInstitute for Clinical Evaluative SciencesSickKids FoundationHospital for Sick ChildrenUniversité de SherbrookeMcMaster University
FundersCanadian Institutes of Health ResearchHospital for Sick ChildrenCanadian Society of NephrologyCancer Research UKNational Natural Science Foundation of ChinaOntario Ministry of Health and Long-Term CareKidney Foundation of CanadaPfizer
KeywordsInterquartile rangeMedicineRandomized controlled trialRelative riskMEDLINEIntervention (counseling)Clinical trialIncidence (geometry)Confidence intervalSurgeryInternal medicinePsychiatry

Abstract

fetched live from OpenAlex

OBJECTIVE: To assess the reporting, extent, and handling of loss to follow-up and its potential impact on the estimates of the effect of treatment in randomised controlled trials. DESIGN: Systematic review. We calculated the percentage of trials for which the relative risk would no longer be significant under a number of assumptions about the outcomes of participants lost to follow-up. DATA SOURCES: Medline search of five top general medical journals, 2005-07. ELIGIBILITY CRITERIA: Randomised controlled trials that reported a significant binary primary patient important outcome. RESULTS: Of the 235 eligible reports identified, 31 (13%) did not report whether or not loss to follow-up occurred. In reports that did give the relevant information, the median percentage of participants lost to follow-up was 6% (interquartile range 2-14%). The method by which loss to follow-up was handled was unclear in 37 studies (19%); the most commonly used method was survival analysis (66, 35%). When we varied assumptions about loss to follow-up, results of 19% of trials were no longer significant if we assumed no participants lost to follow-up had the event of interest, 17% if we assumed that all participants lost to follow-up had the event, and 58% if we assumed a worst case scenario (all participants lost to follow-up in the treatment group and none of those in the control group had the event). Under more plausible assumptions, in which the incidence of events in those lost to follow-up relative to those followed-up is higher in the intervention than control group, results of 0% to 33% trials were no longer significant. CONCLUSION: Plausible assumptions regarding outcomes of patients lost to follow-up could change the interpretation of results of randomised controlled trials published in top medical journals.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.315
metaresearch head score (Gemma)0.376
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMetaresearch, Meta-epidemiology (narrow), Meta-epidemiology (broad), Insufficient payload (model declined to judge)
Consensus categoriesMetaresearch, Meta-epidemiology (narrow), Meta-epidemiology (broad), Insufficient payload (model declined to judge)
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Systematic review · Consensus signal: Systematic review
GenreCandidate signal: Review · Consensus signal: Review
Teacher disagreement score0.131
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.3150.376
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0930.026
Bibliometrics0.0020.003
Science and technology studies0.0000.000
Scholarly communication0.0010.000
Open science0.0020.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0040.020

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.534
GPT teacher head0.559
Teacher spread0.024 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; both teacher heads agree on what is shown here.

Study designSystematic review
Domainnot available
GenreReview

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations358
Published2012
Admission routes2
Has abstractyes

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