Evidence map›Paper›PMID 40827106›Full record

ArticleClinical endocrinology2025

Sucessful Transition in Rare Endocrine Diseases: Patient Experiences in a French Reference Centre.

Karine Aouchiche, Thierry Brue, Emeline Marquant, Gilbert Simonin, Sarah Castets, Rachel Reynaud, Frederique Albarel

Abstract read
In one paragraph

Article in Clinical endocrinology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Karine AouchicheDepartment of Paediatrics, Assistance Publique-Hôpitaux de Marseille (APHM), Paediatric Endocrinology Unit, CHU Timone Enfants, Marseille, France.ORCID https://orcid.org/0009-0008-5550-9636
Thierry BrueINSERM, MMG, UMR 1251, Institut MarMaRa, Aix Marseille Univ, Marseille, France.
Emeline MarquantDepartment of Paediatrics, Assistance Publique-Hôpitaux de Marseille (APHM), Paediatric Endocrinology Unit, CHU Timone Enfants, Marseille, France.ORCID https://orcid.org/0000-0002-9094-7382
Gilbert SimoninDepartment of Paediatrics, Assistance Publique-Hôpitaux de Marseille (APHM), Paediatric Endocrinology Unit, CHU Timone Enfants, Marseille, France.
Sarah CastetsDepartment of Paediatrics, Assistance Publique-Hôpitaux de Marseille (APHM), Paediatric Endocrinology Unit, CHU Timone Enfants, Marseille, France.
Rachel ReynaudDepartment of Paediatrics, Assistance Publique-Hôpitaux de Marseille (APHM), Paediatric Endocrinology Unit, CHU Timone Enfants, Marseille, France.
Frederique AlbarelDepartment of Endocrinology, Centre de Référence des Maladies Rare de l'Hypophyse HYPO, Assistance Publique-Hôpitaux de Marseille (APHM), La Conception University Hospital, Marseille, France.

Funding

The authors received no specific funding for this work.
6 · The paper itself

Abstract

objectiveThis study aimed to evaluate the experiences of patients who had a joint endocrinology consultation for transition to adult care at Marseille university hospitals between 2010 and 2020, focusing on patient follow-up, satisfaction, difficulties, and expectations.

methodsA healthcare transition questionnaire was designed and administered to patients several years after transition to adult care.

resultsOne hundred and fifteen patients with rare endocrine disorders were included, with a mean age of 18.8 years at the transition consultation. Ninety-six percent (110/115) continued adult care after the first joint consultation, and 75% were still in follow-up when completing the questionnaire (mean follow-up, 4.5 years). Of the 81 respondents, 89% were satisfied with the transition, and 64% reported no difficulties. The most common difficulties were psychological, logistical, and medical. Fifty-three out of 74 respondents (72%) felt the transition occurred at the right time, 17 (24%) thought it was too early, and 4 (5%) felt it was too late. The main concern was the transmission of medical information between doctors. Suggestions for improvement included more joint consultations and personalized transition pathways.

conclusionIn this group of rare endocrine disease patients, a transition pathway based on a joint pediatric-adult consultation was associated with high patient satisfaction and long-term follow-up rates. Patients' suggestions and reported difficulties highlight issues to be addressed and complementary strategies to develop.

Indexed as

Endocrine System DiseasesRare DiseasesTransition to Adult CareAdolescentAdultChildFemaleFranceHumansMaleMiddle AgedPatient SatisfactionReferral and ConsultationSurveys and QuestionnairesYoung Adultbrain tumourcongenital pituitary deficiencyendocrine disordersexperiencegrowth hormone deficiency, corticotropic deficiencyhypopituitarismjoint consultationrare diseasetransition to adult care

Identifiers

PMID40827106
PMCPMC12583310

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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.