Evidence map›Paper›PMID 32503523›Full record

ArticleBMC health services research2020

Chronic patients' satisfaction and priorities regarding medical care, information and services and quality of life: a French online patient community survey.

Apolline Adé, Frédérique Debroucker, Laura Delporte, Cécile De Monclin, Emmanuel Fayet, Pierre Legendre, Lise Radoszycki, Michael Chekroun

Abstract read
In one paragraph

Article in BMC health services research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  5. Virtual twin for healthcare management.Frontiers in digital health · 2023
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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.

Apolline AdéMedtronic, Boulogne-Billancourt, France.
Frédérique DebrouckerMedtronic, Boulogne-Billancourt, France.
Laura DelporteMedtronic, Boulogne-Billancourt, France.
Cécile De MonclinMedtronic, Boulogne-Billancourt, France.
Emmanuel FayetMedtronic, Boulogne-Billancourt, France.
Pierre LegendreCarenity, 1 Rue de Stockholm, 75008, Paris, France. pierre@carenity.com.
Lise RadoszyckiCarenity, 1 Rue de Stockholm, 75008, Paris, France.
Michael ChekrounCarenity, 1 Rue de Stockholm, 75008, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe French healthcare system is evolving to meet the challenges of an aging population, the growing prevalence of chronic diseases, the development of new technologies and the increasing involvement of patients in the management of their disease. The aim of this study is to assess the satisfaction and priorities of chronic patients regarding medical care, information and services and their quality of life.

methodsA cross-sectional study was conducted from February to March 2018 via the French Carenity platform. Adult patients enrolled in type 1 diabetes, heart failure or obesity communities were invited to answer an online questionnaire. A numeric scale from 0 (meaning not satisfied) to 5 was used to evaluate patients' satisfaction. Patients' priorities were assessed using a ranking question. Patients' satisfaction and priorities have been combined in a matrix to identify patients' expectations.

resultsSixty-seven respondents of each condition answered a questionnaire. The most important and least satisfactory items about medical care are availability and active listening from healthcare providers, as well as access to coordinated and multidisciplinary care. Regarding information and services, respondents mostly expect connected medical devices, in addition to lifestyle and dietary measures. As for the quality of life, respondents fear that their chronic condition will keep impacting their daily mood and ability to do physical activities.

conclusionsThis study shows that chronic patients want to be more actively involved in their care pathway. Patient training and therapeutic patient education programs could help them manage their chronic conditions within a patient-centred healthcare system.

Indexed as

AdolescentAdultAgedChronic DiseaseCross-Sectional StudiesFemaleFranceHealth Care SurveysHealth PrioritiesHumansInformation ServicesMaleMiddle AgedPatient SatisfactionQuality of LifeYoung AdultChronic conditionsInformationMedical carePatient communityPrioritiesQuality of lifeReal-word insightsSatisfactionServices

Identifiers

PMID32503523
PMCPMC7275411

What OpenQuestion holds

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Registered trials

None linked

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.