Evidence map›Paper›PMID 37113607›Full record

ArticleFrontiers in medicine2023

The influence of immortal time bias in observational studies examining associations of antifibrotic therapy with survival in idiopathic pulmonary fibrosis: A simulation study.

Qiang Zheng, Petr Otahal, Ingrid A Cox, Barbara de Graaff, Julie A Campbell, Hasnat Ahmad, E Haydn Walters, Andrew J Palmer

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
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

6 citing papers in PubMed, 10 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

Qiang ZhengMenzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.
Petr OtahalMenzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.
Ingrid A CoxMenzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.
Barbara de GraaffMenzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.
Julie A CampbellMenzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.
Hasnat AhmadMenzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.
E Haydn WaltersMenzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.
Andrew J PalmerMenzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.
University of Tasmania · AUNational Health and Medical Research Council · AUAustralian Government · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Immortal time bias (ITB) has been overlooked in idiopathic pulmonary fibrosis (IPF). We aimed to identify the presence of ITB in observational studies examining associations between antifibrotic therapy and survival in patients with IPF and illustrate how ITB may affect effect size estimates of those associations. Methods: Immortal time bias was identified in observational studies using the ITB Study Assessment Checklist. We used a simulation study to illustrate how ITB may affect effect size estimates of antifibrotic therapy on survival in patients with IPF based on four statistical techniques including time-fixed, exclusion, time-dependent and landmark methods. Results: Of the 16 included IPF studies, ITB was detected in 14 studies, while there were insufficient data for assessment in two others. Our simulation study showed that use of time-fixed [hazard ratio (HR) 0.55, 95% confidence interval (CI) 0.47-0.64] and exclusion methods (HR 0.79, 95% CI 0.67-0.92) overestimated the effectiveness of antifibrotic therapy on survival in simulated subjects with IPF, in comparison of the time-dependent method (HR 0.93, 95% CI 0.79-1.09). The influence of ITB was mitigated using the 1 year landmark method (HR 0.69, 95% CI 0.58-0.81), compared to the time-fixed method. Conclusion: The effectiveness of antifibrotic therapy on survival in IPF can be overestimated in observational studies, if ITB is mishandled. This study adds to the evidence for addressing the influence of ITB in IPF and provides several recommendations to minimize ITB. Identifying the presence of ITB should be routinely considered in future IPF studies, with the time-dependent method being an optimal approach to minimize ITB.

Indexed as

idiopathic pulmonary fibrosisimmortal time biaslandmarkobservational researchtime–dependent

Identifiers

PMID37113607
PMCPMC10126672
OpenAlexW4364367846

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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.