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An evaluation of inverse probability weighting using the propensity score for baseline covariate adjustment in smaller population randomised controlled trials with a continuous outcome.
Raad, Hanaya; Cornelius, Victoria; Chan, Susan; Williamson, Elizabeth; Cro, Suzie.
Affiliation
  • Raad H; Imperial Clinical Trials Unit, Imperial College London, Stadium House, 68 Wood Lane, London, W12 7RH, UK.
  • Cornelius V; Imperial Clinical Trials Unit, Imperial College London, Stadium House, 68 Wood Lane, London, W12 7RH, UK.
  • Chan S; Children's Allergy, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom, London, SE1 7EH, UK.
  • Williamson E; King's College London School of Life Course Sciences & School of Immunology & Microbial Sciences, King's Health Partners, London, UK.
  • Cro S; Department of Medical Statistics, Faculty of Epidemiology and population health, London School of Hygiene and Tropical Medicine, London, WC1E 7HT, UK.
BMC Med Res Methodol ; 20(1): 70, 2020 03 23.
Article in En | MEDLINE | ID: mdl-32293286
ABSTRACT

BACKGROUND:

It is important to estimate the treatment effect of interest accurately and precisely within the analysis of randomised controlled trials. One way to increase precision in the estimate and thus improve the power for randomised trials with continuous outcomes is through adjustment for pre-specified prognostic baseline covariates. Typically covariate adjustment is conducted using regression analysis, however recently, Inverse Probability of Treatment Weighting (IPTW) using the propensity score has been proposed as an alternative method. For a continuous outcome it has been shown that the IPTW estimator has the same large sample statistical properties as that obtained via analysis of covariance. However the performance of IPTW has not been explored for smaller population trials (< 100 participants), where precise estimation of the treatment effect has potential for greater impact than in larger samples.

METHODS:

In this paper we explore the performance of the baseline adjusted treatment effect estimated using IPTW in smaller population trial settings. To do so we present a simulation study including a number of different trial scenarios with sample sizes ranging from 40 to 200 and adjustment for up to 6 covariates. We also re-analyse a paediatric eczema trial that includes 60 children.

RESULTS:

In the simulation study the performance of the IPTW variance estimator was sub-optimal with smaller sample sizes. The coverage of 95% CI's was marginally below 95% for sample sizes < 150 and ≥ 100. For sample sizes < 100 the coverage of 95% CI's was always significantly below 95% for all covariate settings. The minimum coverage obtained with IPTW was 89% with n = 40. In comparison, regression adjustment always resulted in 95% coverage. The analysis of the eczema trial confirmed discrepancies between the IPTW and regression estimators in a real life small population setting.

CONCLUSIONS:

The IPTW variance estimator does not perform so well with small samples. Thus we caution against the use of IPTW in small sample settings when the sample size is less than 150 and particularly when sample size < 100.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Propensity Score Type of study: Clinical_trials / Diagnostic_studies / Health_economic_evaluation / Prognostic_studies Limits: Child / Humans Language: En Journal: BMC Med Res Methodol Journal subject: MEDICINA Year: 2020 Type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Propensity Score Type of study: Clinical_trials / Diagnostic_studies / Health_economic_evaluation / Prognostic_studies Limits: Child / Humans Language: En Journal: BMC Med Res Methodol Journal subject: MEDICINA Year: 2020 Type: Article Affiliation country: United kingdom