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ArticleSupportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer2025

Improving transparency and empowerment for cancer patients by accessing their full online personal medical records.

Gwenaelle Gravis, Rajae Touzani, Thérèse Aurran, Aude Charbonnier, Domitille Dano, Anne Madroszyk, Slimane Dermeche, Anthony Gonçalves, Marie Le Morvan, Sabrina Ettoubi and 3 more

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Article in Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

13 authors.

Gwenaelle GravisInstitut Paoli-Calmettes, Department of Medical Oncology, Aix Marseille Univ, INSERM, CNRS, CRCM, Immunity and Cancer Team, Marseille, France.
Rajae TouzaniInstitut Paoli-Calmettes, SESSTIM, Aix-Marseille Univ, INSERM, IRD, Marseille, France.
Thérèse AurranInstitut Paoli Calmettes, Departement of Hematology, SESSTIM, Aix-Marseille Univ, INSERM, IRD, Marseille, France.
Aude CharbonnierInstitut Paoli Calmettes, Departement of Hematology, Marseille, France.
Domitille DanoInstitut Paoli-Calmettes, Department of Medical Oncology, Marseille, France.
Anne MadroszykInstitut Paoli-Calmettes, Department of Medical Oncology, Marseille, France.
Slimane DermecheInstitut Paoli-Calmettes, Department of Medical Oncology, Marseille, France.
Anthony GonçalvesAix-Marseille Univ, U1068 Inserm, UMR7258 CNRS, Department of Medical Oncology, Institut Paoli-Calmettes, Cancer Research Center of Marseille (CRCM), Marseille, France.
Marie Le MorvanInstitut Paoli Calmettes, Department of Digital Transformation, Marseille, France.
Sabrina EttoubiInstitut Paoli Calmettes, Department of Digital Transformation, Marseille, France.
Camille JauffretInstitut Paoli-Calmettes, Department of Surgical Oncology, Marseille, France.
Lorène SeguinAix-Marseille Univ, CNRS, INSERM, Institut Paoli-Calmettes, Department of Medical Oncology, CRCM, Marseille, France.
Patricia MarinoInstitut Paoli-Calmettes, SESSTIM, Aix-Marseille Univ, INSERM, IRD, Marseille, France. patricia.marino@inserm.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeOnline medical records are becoming increasingly accessible to patients, but real-time access could increase anxiety in cancer patients whose prognosis may be life-threatening. This study assessed cancer patients' experience of full access to medical records using an application (app), and the impact on their anxiety.

methodsWe conducted a cross-sectional study in a comprehensive cancer center in June 2023. Patients completed a paper-based questionnaire investigating their perceptions of the app (e.g., usefulness, information available, access to medical records), anxiety (HADS), quality of life (EQ5D) and health literacy (HLQ). Factors associated with access to medical records were analyzed adjusting for patients' characteristics.

results340/560 patients completed the questionnaire. For the 10% who lacked access to the app, 80.8% wanted access. Overall, 94.9% of users were satisfied with the app. Frequent users found information easy to access (p<0.001), useful (p=0.028), and understandable (p=0.022). They felt it improved their care (p=0.011), involvement (p=0.006), discussions with doctors (p=0.044) and loved ones (p=0.046), understanding of their illness (p=0.035). Access was more frequent among patients under treatment (OR=2.32, p=0.007), those searching health information online (OR=3.8, p<0.001), and those who found information easily (OR=2.68, p=0.002). Anxiety about the medical information, patients' level of anxiety (HADS), QOL and health literacy were not associated with frequency of use.

conclusionPatients were satisfied with the app and real-time access to medical records did not increase their anxiety. Few patients regretted accessing their medical records. As patients become more informed and involved, doctors will have to adapt the way they communicate.

Indexed as

Electronic Health RecordsEmpowermentHealth Records, PersonalNeoplasmsPatient Access to RecordsAccess to InformationAdultAgedAnxietyCross-Sectional StudiesFemaleHealth LiteracyHumansMaleMiddle AgedMobile ApplicationsAnxietyCancerDigital applicationPatients’ experiencePersonal medical records

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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.