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ArticleQuality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation2018

Developing a patient-reported outcome measure for HIV care on perceived barriers to antiretroviral adherence: assessing the needs of HIV clinicians through qualitative analysis.

Isabelle Toupin, Kim Engler, David Lessard, Leo Wong, Andràs Lènàrt, Bruno Spire, François Raffi, Bertrand Lebouché

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Article in Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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  8. Evaluation of a project to engage patients in the development of a patient-reported measure for HIV care (the I-Score Study).Health expectations : an international journal of public participation in health care and health policy · 2019
    Article
  9. Developing a patient-reported outcome measure for HIV care on perceived barriers to antiretroviral adherence: assessing the needs of HIV clinicians through qualitative analysis.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2018
    Article
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.

Isabelle ToupinDepartment of Family Medicine, McGill University, Montreal, Canada. isabelle.toupin.1@gmail.com.
Kim EnglerDepartment of Family Medicine, McGill University, Montreal, Canada.
David LessardDepartment of Family Medicine, McGill University, Montreal, Canada.
Leo WongCentre for Outcomes Research & Evaluation, Research Institute of the McGill University Health Centre, 5252 Boul de Maisonneuve, 3C.35, Montreal, QC, H4A 3S5, Canada.
Andràs LènàrtDepartment of Family Medicine, McGill University, Montreal, Canada.
Bruno SpireSESSTIM, Université Aix-Marseille, Marseille, France.
François RaffiDepartment of Infectious Diseases, CHU de Nantes and CIC 1413, INSERM, Nantes, France.
Bertrand LebouchéDepartment of Family Medicine, McGill University, Montreal, Canada.

Funding

CIHR's HIV Clinical Trials Network CTN 283Mentorship Chair in Innovative Clinical Trials awarded by the Canadian Institutes of Health Research 383427Merck Canada Inc IISP-53538Mitacs Accelerate Postdoctoral Internship award 05857
6 · The paper itself

Abstract

purposeTo identify HIV clinicians' needs for the clinical use of a new patient-reported outcome measure (PRO) on barriers to antiretroviral therapy (ART) adherence.

methodsIn 2015, five focus groups with 31 clinicians from France were transcribed, coded with Atlas.ti, and submitted to a typological analysis.

resultsThe analysis identified seven patient profiles, each tied to distinct barriers to adherence and to specific needs for the PRO's content, data collection and transmission. Clinicians preferred, for the patient who is: (1) 'passive,' that the PRO collect information on ART knowledge, to ensure that the prescription's instructions are being respected; (2) 'misleading,' that it be able to detect adherence to ART and socially desirable responses; (3) 'stoic,' that questions challenge the patient to recognize treatment-specific side effects; (4) 'hedonistic,' that the PRO contains content on lifestyle and risk-taking; (5) 'obsessive,' that the PRO captures quality of life and stressful life events; (6) 'overburdened,' that the PRO provides information on the person's home environment, socioeconomic status and cultural constraints. For all or most patient profiles, the clinicians wished that the PRO be completed, minimally, prior to the medical consultation and to receive alerts, under varying conditions, when problematic scores were detected. Depending on the profile, there was preference for the inclusion of open-ended questions and transmission of cross-sectional, periodic or longitudinal PRO data.

conclusionOverall, this study's findings suggest that to support the clinical management of ART adherence, our PRO must meet the needs of a wide variety of patients and must perform multiple functions.

Indexed as

Patient Reported Outcome MeasuresAnti-HIV AgentsCross-Sectional StudiesFemaleFocus GroupsHIV InfectionsHumansMaleMedication AdherencePhysiciansQuality of LifeAnti-HIV AgentsAntiretroviral therapy adherenceHIV careHIV patient profilesPatient-reported outcome measure, HIV clinicians’ needsQualitative analysis

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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.