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Target Trial Emulation Using Hospital-Based Observational Data: Demonstration and Application in Covid-19 Publisher



Martinuka O1 ; Cube MV1 ; Hazard D1 ; Marateb HR2, 3 ; Mansourian M3, 4 ; Sami R5 ; Hajian MR5 ; Ebrahimi S6 ; Wolkewitz M1
Authors
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Authors Affiliations
  1. 1. Institute of Medical Biometry and Statistics, Faculty of Medicine and Medical Centre, University of Freiburg, Freiburg, 79104, Germany
  2. 2. Biomedical Engineering Department, Engineering Faculty, University of Isfahan, Isfahan, 81746-73441, Iran
  3. 3. Biomedical Engineering Research Centre (CREB), Automatic Control Department (ESAII), Universitat Politecnica de Catalunya-Barcelona Tech (UPC) Building H, Floor 4, Av. Diagonal 647, Barcelona, 08028, Spain
  4. 4. Department of Epidemiology and Biostatistics, School of Health, Isfahan University of Medical Sciences, Isfahan, 81746-73461, Iran
  5. 5. Department of Internal Medicine, School of Medicine, Isfahan University of Medical Sciences, Isfahan, 81746-73461, Iran
  6. 6. Alzahra Research Institute, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, 81746-75731, Iran

Source: Life Published:2023


Abstract

Methodological biases are common in observational studies evaluating treatment effectiveness. The objective of this study is to emulate a target trial in a competing risks setting using hospital-based observational data. We extend established methodology accounting for immortal time bias and time-fixed confounding biases to a setting where no survival information beyond hospital discharge is available: a condition common to coronavirus disease 2019 (COVID-19) research data. This exemplary study includes a cohort of 618 hospitalized patients with COVID-19. We describe methodological opportunities and challenges that cannot be overcome applying traditional statistical methods. We demonstrate the practical implementation of this trial emulation approach via clone–censor–weight techniques. We undertake a competing risk analysis, reporting the cause-specific cumulative hazards and cumulative incidence probabilities. Our analysis demonstrates that a target trial emulation framework can be extended to account for competing risks in COVID-19 hospital studies. In our analysis, we avoid immortal time bias, time-fixed confounding bias, and competing risks bias simultaneously. Choosing the length of the grace period is justified from a clinical perspective and has an important advantage in ensuring reliable results. This extended trial emulation with the competing risk analysis enables an unbiased estimation of treatment effects, along with the ability to interpret the effectiveness of treatment on all clinically important outcomes. © 2023 by the authors.