Evidence map›Paper›PMID 42390109›Full record

ArticleAnesthesia and analgesia2026

Patients' Perspectives and Experiences of Participating in Anesthesia Research: A Qualitative Study.

Bethany R Tellor Pennington, Allison M Janda, Shayna Rosen, Nora Alrubaie, Jennifer Percich, Sathish Kumar, Sachin Kheterpal, Michael S Avidan, Mary C Politi

Abstract read
In one paragraph

Article in Anesthesia and analgesia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Bethany R Tellor PenningtonFrom the Department of Anesthesiology, Washington University School of Medicine, St. Louis, Missouri.ORCID 0000-0003-1571-6434
Allison M JandaDepartment of Anesthesiology, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0001-5080-5630
Shayna RosenFrom the Department of Anesthesiology, Washington University School of Medicine, St. Louis, Missouri.
Nora AlrubaieDepartment of Anesthesiology, University of Michigan, Ann Arbor, Michigan.
Jennifer PercichFrom the Department of Anesthesiology, Washington University School of Medicine, St. Louis, Missouri.
Sathish KumarDepartment of Anesthesiology, University of Michigan, Ann Arbor, Michigan.
Sachin KheterpalDepartment of Anesthesiology, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0002-6546-0273
Michael S AvidanFrom the Department of Anesthesiology, Washington University School of Medicine, St. Louis, Missouri.ORCID 0000-0001-6248-044
Mary C PolitiBursky School of Public Health, Washington University in St. Louis, Missouri.ORCID 0000-0001-9103-6495

Funding

PHEnylephrine versus NOrepinephrine in Major NONcardiac surgery (PHENOMeNON): Foundational Studies for a Pragmatic Randomized Clinical Trial.K23HL166685 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Allison Mary Janda · 2023 to 2026
$689k
NHLBI NIH HHS K23 HL166685
6 · The paper itself

Abstract

backgroundExploring participants' experiences in comparative effectiveness anesthesia clinical trials offers valuable insights for improving trial design, conduct, and outcome measures while identifying factors that may hinder trial success. The challenges and opportunities of conducting comparative effectiveness trials are distinct from classic explanatory trials. To optimize and conduct a full-scale comparative effectiveness trial, we interviewed patients to identify barriers and facilitators to study participation and offer strategies to improve the recruitment and retention of participants in anesthesia comparative effectiveness clinical trials.

methodsWe conducted qualitative semi-structured interviews using constructs from the Consolidated Framework for Implementation Research. Interviews assessed barriers and facilitators to study participation in an anesthesia clinical trial comparing outcomes after receiving either total intravenous anesthesia (TIVA) or inhaled volatile anesthesia (INVA). Interview guides were co-developed with a multidisciplinary team, including patient partners, and addressed study participation, acceptability of the study procedures, and prior experiences with anesthesia. Participants were recruited at two large academic medical centers. Two coders used a standardized codebook to code each interview, achieving > 95% agreement. Interview transcripts were analyzed using thematic analysis.

resultsNinety-one patients were approached, 43 agreed to participate, and 35 interviews were conducted until we reached thematic saturation. Patients found participation in the anesthesia research study to be positive, straightforward, and non-intrusive. Study-related barriers to enrollment and participation included survey language, blinding, randomization, and concerns for breach of confidentiality. Patient-related barriers included fear and mistrust of research and discomfort with technology. Study-related facilitators included the safety and non-experimental nature of both general anesthesia techniques, use of digital technology, minimal time burden, trust and clear communication by the study staff, and compensation. Patients were motivated to participate by altruistic values. Adaptable barriers were addressed, and solutions were implemented to improve study procedures and staff responsibilities, aimed at enhancing participation and ensuring positive experiences for patients in future anesthesia comparative effectiveness clinical trials.

conclusionsKey elements to consider when designing and conducting a comparative effectiveness anesthesia trial include promoting participant comfort and trust, ensuring clear communication, highlighting the safety and clinical equipoise of the trial comparators, supportive behaviors from the clinical team, minimizing time burden, and using simple-to-learn digital technology. Findings of this study were used to refine the full-scale pragmatic, comparative effectiveness, randomized controlled trial evaluating patient experiences with TIVA and INVA.

Identifiers

PMID42390109
PMCPMC13336238

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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.