Evidence map›Paper›PMID 36983933›Full record

ArticleLife (Basel, Switzerland)2023

Target Trial Emulation Using Hospital-Based Observational Data: Demonstration and Application in COVID-19.

Oksana Martinuka, Maja von Cube, Derek Hazard, Hamid Reza Marateb, Marjan Mansourian, Ramin Sami, Mohammad Reza Hajian, Sara Ebrahimi, Martin Wolkewitz

Abstract read
In one paragraph

Article in Life (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from 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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Oksana MartinukaInstitute of Medical Biometry and Statistics, Faculty of Medicine and Medical Centre, University of Freiburg, 79104 Freiburg, Germany.ORCID 0000-0003-0874-7670
Maja von CubeInstitute of Medical Biometry and Statistics, Faculty of Medicine and Medical Centre, University of Freiburg, 79104 Freiburg, Germany.ORCID 0000-0003-3088-3513
Derek HazardInstitute of Medical Biometry and Statistics, Faculty of Medicine and Medical Centre, University of Freiburg, 79104 Freiburg, Germany.
Hamid Reza MaratebBiomedical Engineering Department, Engineering Faculty, University of Isfahan, Isfahan 81746-73441, Iran.ORCID 0000-0003-4408-2397
Marjan MansourianBiomedical Engineering Research Centre (CREB), Automatic Control Department (ESAII), Universitat Politècnica de Catalunya-Barcelona Tech (UPC) Building H, Floor 4, Av. Diagonal 647, 08028 Barcelona, Spain.
Ramin SamiDepartment of Internal Medicine, School of Medicine, Isfahan University of Medical Sciences, Isfahan 81746-73461, Iran.
Mohammad Reza HajianDepartment of Internal Medicine, School of Medicine, Isfahan University of Medical Sciences, Isfahan 81746-73461, Iran.
Sara EbrahimiAlzahra Research Institute, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan 81746-75731, Iran.
Martin WolkewitzInstitute of Medical Biometry and Statistics, Faculty of Medicine and Medical Centre, University of Freiburg, 79104 Freiburg, Germany.

Funding

Deutsche Forschungsgemeinschaft WO 1746/5-1
6 · The paper itself

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.

Indexed as

competing eventsCOVID-19methodologyobservational datatarget trial emulation

Identifiers

PMID36983933
PMCPMC10053871

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Registered trials

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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.