ReviewBMJ (Clinical research ed.)2020
Potential impact of missing outcome data on treatment effects in systematic reviews: imputation study.
Review in BMJ (Clinical research ed.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers, 5 of them syntheses that pooled 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.
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.
Who cites it
16 citing papers in PubMed, 5 syntheses or guidelines pooled it.
- Shuxuetong injection for ischemic stroke: an overview of systematic reviews using different methodological quality assessment tools.Frontiers in pharmacology · 2026Pooled it
- Methodological survey of missing outcome data in an alteplase for ischemic stroke meta-analysis.Acta neurologica Scandinavica · 2022Pooled it
- Oral anticoagulation in people with cancer who have no therapeutic or prophylactic indication for anticoagulation.The Cochrane database of systematic reviews · 2021Pooled it
- Antithrombotic therapy for ambulatory patients with multiple myeloma receiving immunomodulatory agents.The Cochrane database of systematic reviews · 2021Pooled it
- Anticoagulation for the long-term treatment of venous thromboembolism in people with cancer.The Cochrane database of systematic reviews · 2018Pooled it
- X-CircuiT and conventional exercise in home-based cardiac rehabilitation for patients with coronary artery disease and risk factors: a randomized controlled non-inferiority trial.Annals of medicine · 2025Trial
- Clinical and Molecular Findings After Autologous Stem Cell Transplantation or Cyclophosphamide for Scleroderma: Handling Missing Longitudinal Data.Arthritis care & research · 2023Trial
- Telitacicept for pediatric Henoch-Schönlein purpura nephritis: analytical populations and safety monitoring.Clinical rheumatology · 2026Article
- Review
- The Effect of Consuming Caffeine Before Late Afternoon/Evening Training or Competition on Sleep: A Systematic Review with Meta-Analysis.Sports (Basel, Switzerland) · 2025Review
- Time to resolution of symptoms and recovery after mild traumatic brain injury: protocol for a systematic review and meta-analysis.BMJ open · 2024Article
- Influence of lack of blinding on the estimation of medication-related harms: a retrospective cohort study of randomized controlled trials.BMC medicine · 2024Article
- Informative missingness: What can we learn from patterns in missing laboratory data in the electronic health record?Journal of biomedical informatics · 2023Article
- Validity of data extraction in evidence synthesis practice of adverse events: reproducibility study.BMJ (Clinical research ed.) · 2022Article
- How robust are findings of pairwise and network meta-analysis in the presence of missing participant outcome data?BMC medicine · 2021Article
- Utilization of the evidence from studies with no events in meta-analyses of adverse events: an empirical investigation.BMC medicine · 2021Article
Corrections and comments
- Erratum issued
Authors and funding
17 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveTo assess the risk of bias associated with missing outcome data in systematic reviews.
designImputation study.
settingSystematic reviews. POPULATION: 100 systematic reviews that included a group level meta-analysis with a statistically significant effect on a patient important dichotomous efficacy outcome.
main outcome measuresMedian percentage change in the relative effect estimate when applying each of the following assumption (four commonly discussed but implausible assumptions (best case scenario, none had the event, all had the event, and worst case scenario) and four plausible assumptions for missing data based on the informative missingness odds ratio (IMOR) approach (IMOR 1.5 (least stringent), IMOR 2, IMOR 3, IMOR 5 (most stringent)); percentage of meta-analyses that crossed the threshold of the null effect for each method; and percentage of meta-analyses that qualitatively changed direction of effect for each method. Sensitivity analyses based on the eight different methods of handling missing data were conducted.
results100 systematic reviews with 653 randomised controlled trials were included. When applying the implausible but commonly discussed assumptions, the median change in the relative effect estimate varied from 0% to 30.4%. The percentage of meta-analyses crossing the threshold of the null effect varied from 1% (best case scenario) to 60% (worst case scenario), and 26% changed direction with the worst case scenario. When applying the plausible assumptions, the median percentage change in relative effect estimate varied from 1.4% to 7.0%. The percentage of meta-analyses crossing the threshold of the null effect varied from 6% (IMOR 1.5) to 22% (IMOR 5) of meta-analyses, and 2% changed direction with the most stringent (IMOR 5).
conclusionEven when applying plausible assumptions to the outcomes of participants with definite missing data, the average change in pooled relative effect estimate is substantive, and almost a quarter (22%) of meta-analyses crossed the threshold of the null effect. Systematic review authors should present the potential impact of missing outcome data on their effect estimates and use this to inform their overall GRADE (grading of recommendations assessment, development, and evaluation) ratings of risk of bias and their interpretation of the results.
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Registered trials
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.