ArticleBMC medical research methodology2018
Multiple imputation for patient reported outcome measures in randomised controlled trials: advantages and disadvantages of imputing at the item, subscale or composite score level.
Article in BMC medical research methodology, 2018. 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 49 papers, 2 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
49 citing papers in PubMed, 2 syntheses or guidelines pooled it.
- Measuring patient disability in the peri-operative period using the WHODAS 2.0 questionnaire: a systematic review.Anaesthesia · 2026Pooled it
- Handling Missing Data in Health Economics and Outcomes Research (HEOR): A Systematic Review and Practical Recommendations.PharmacoEconomics · 2023Pooled it
- Trial
- Imputing longitudinal PROM data at the item and score level in clinical trials.BMC medical research methodology · 2026Article
- Missing Data in Trial-Based Cost-Effectiveness Analysis: The Journey Continues.PharmacoEconomics · 2026Review
- Feasibility and acceptability of a joint employee-manager workplace intervention to support mental health and job retention (MENTOR 2.0).BMC public health · 2026Article
- When patients' voices aren't heard: estimands and statistical methods for handling missing patient-reported outcomes in oncology studies.BMC medical research methodology · 2026Article
- Missing data considerations for patient reported outcome measures in randomized controlled trials.Journal of patient-reported outcomes · 2026Article
- How to Analyze Longitudinal Patient-Reported Outcomes in Populations With High Mortality Rates.Journal of the American Geriatrics Society · 2026Article
- A brief universal parenting program for recently settled immigrants in Sweden: a feasibility study.BMC psychology · 2026Article
- Impact of missing patient report outcomes in clinical trials for ulcerative colitis: Should we always assume treatment failure?Crohn's & colitis 360 · 2026Article
- Comparison of different approaches in handling missing data in longitudinal multiple-item patient-reported outcomes: a simulation study.Health and quality of life outcomes · 2025Article
- Handling of missing component information for common composite score outcomes used in axial spondyloarthritis research when complete-case analysis is unbiased.BMC medical research methodology · 2025Article
- Balancing efficacy and computational burden: weighted mean, multiple imputation, and inverse probability weighting methods for item non-response in reliable scales.Journal of the American Medical Informatics Association : JAMIA · 2024Article
- Robotic versus laparoscopic hepatectomy for liver malignancies (ROC'N'ROLL): a single-centre, randomised, controlled, single-blinded clinical trial.The Lancet regional health. Europe · 2024Article
- PROPOSE. Development and validation of a prediction model for shared decision making for patients with lumbar spinal stenosis.North American Spine Society journal · 2024Article
- Sleep Disorders, Sleep Medication Use, and Predictors of Sleep Disturbance in Children with Persistent Tic Disorders.Children's health care : journal of the Association for the Care of Children's Health · 2024Article
- Efficacy and safety of transcranial pulse stimulation in young adolescents with attention-deficit/hyperactivity disorder: a pilot, randomized, double-blind, sham-controlled trial.Frontiers in neurology · 2024Article
- HIV knowledge and protective factors among racial-ethnic minority youth: Moderation by Ethnic identity and LGBQ+ identity.Journal of LGBT youth · 2024Article
- The Joint Awareness Score: A Shortened, Simplified, Improved Alternative to the Forgotten Joint Score.Arthroplasty today · 2023Article
Corrections and comments
- Erratum issued
Authors and funding
5 authors.
Funding
Abstract
backgroundMissing data can introduce bias in the results of randomised controlled trials (RCTs), but are typically unavoidable in pragmatic clinical research, especially when patient reported outcome measures (PROMs) are used. Traditionally applied to the composite PROMs score of multi-item instruments, some recent research suggests that multiple imputation (MI) at the item level may be preferable under certain scenarios. This paper presents practical guidance on the choice of MI models for handling missing PROMs data based on the characteristics of the trial dataset. The comparative performance of complete cases analysis, which is commonly used in the analysis of RCTs, is also considered.
methodsRealistic missing at random data were simulated using follow-up data from an RCT considering three different PROMs (Oxford Knee Score (OKS), EuroQoL 5 Dimensions 3 Levels (EQ-5D-3L), 12-item Short Form Survey (SF-12)). Data were multiply imputed at the item (using ordinal logit and predicted mean matching models), sub-scale and score level; unadjusted mean outcomes, as well as treatment effects from linear regression models were obtained for 1000 simulations. Performance was assessed by root mean square errors (RMSE) and mean absolute errors (MAE).
resultsConvergence problems were observed for MI at the item level. Performance generally improved with increasing sample sizes and lower percentages of missing data. Imputation at the score and subscale level outperformed imputation at the item level in small sample sizes (n ≤ 200). Imputation at the item level is more accurate for high proportions of item-nonresponse. All methods provided similar results for large sample sizes (≥500) in this particular case study.
conclusionsMany factors, including the prevalence of missing data in the study, sample size, the number of items within the PROM and numbers of levels within the individual items, and planned analyses need consideration when choosing an imputation model for missing PROMs data.
Indexed as
Identifiers
What OpenQuestion holds
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.