Evidence map›Paper›PMID 41493139›Full record

ArticleEndocrine connections2026

Continuous subcutaneous hydrocortisone infusion in pediatric primary adrenal insufficiency: a cohort study.

Khadidja Fouatih, Marie-Agathe Trouvin, Anne-Sophie Lambert, Anya Rothenbuhler, Tristan Verdelet, Anne-Lise Lecoq, Jérôme Bouligand, Lilia Laddada, Kenneth Chappell, Maureen Lopez and 7 more

Abstract read
In one paragraph

Article in Endocrine connections, 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

17 authors.

Khadidja FouatihAP-HP, Université Paris-Saclay, Service Endocrinologie et diabète de l'enfant, Centre de Référence des Maladies Rares du Développement Génital (CRMR DEVGEN), Hôpital Bicêtre Paris-Saclay, Le Kremlin-Bicêtre, France.ORCID https://orcid.org/0009-0009-8794-4138
Marie-Agathe TrouvinAP-HP, Université Paris-Saclay, Service Endocrinologie et diabète de l'enfant, Centre de Référence des Maladies Rares du Développement Génital (CRMR DEVGEN), Hôpital Bicêtre Paris-Saclay, Le Kremlin-Bicêtre, France.
Anne-Sophie LambertAP-HP, Université Paris-Saclay, Service Endocrinologie et diabète de l'enfant, Centre de Référence des Maladies Rares du Développement Génital (CRMR DEVGEN), Hôpital Bicêtre Paris-Saclay, Le Kremlin-Bicêtre, France.ORCID https://orcid.org/0000-0002-4232-3882
Anya RothenbuhlerAP-HP, Université Paris-Saclay, Service Endocrinologie et diabète de l'enfant, Centre de Référence des Maladies Rares du Développement Génital (CRMR DEVGEN), Hôpital Bicêtre Paris-Saclay, Le Kremlin-Bicêtre, France.
Tristan VerdeletAP-HP, Université Paris-Saclay, Service Endocrinologie et diabète de l'enfant, Centre de Référence des Maladies Rares du Développement Génital (CRMR DEVGEN), Hôpital Bicêtre Paris-Saclay, Le Kremlin-Bicêtre, France.
Anne-Lise LecoqINSERM, UMR-S U1185, Physiologie et Physiopathologie Endocriniennes, Le Kremlin Bicêtre, France.
Jérôme BouligandINSERM, UMR-S U1185, Physiologie et Physiopathologie Endocriniennes, Le Kremlin Bicêtre, France.
Lilia LaddadaAP-HP, Université Paris-Saclay, Service de Médecine Génomique et Pharmacogénomique, Hôpital Bicêtre Paris-Saclay, Le Kremlin Bicêtre, France.
Kenneth ChappellINSERM, UMR-S U1185, Physiologie et Physiopathologie Endocriniennes, Le Kremlin Bicêtre, France.
Maureen LopezAP-HP, Université Paris-Saclay, Service de Médecine Génomique et Pharmacogénomique, Hôpital Bicêtre Paris-Saclay, Le Kremlin Bicêtre, France.
Mohammed BouyacoubAP-HP, Université Paris-Saclay, Service de Biochimie, Hormonologie, Pharmaco-Toxicologie, UF Hormonologie, Hôpital Bicêtre Paris-Saclay, Le Kremlin Bicêtre, France.
Azza YahiaAP-HP, Université Paris-Saclay, Service de Biochimie, Hormonologie, Pharmaco-Toxicologie, UF Hormonologie, Hôpital Bicêtre Paris-Saclay, Le Kremlin Bicêtre, France.
Hazar HaidarAP-HP, Université Paris-Saclay, Service de Biochimie, Hormonologie, Pharmaco-Toxicologie, UF Hormonologie, Hôpital Bicêtre Paris-Saclay, Le Kremlin Bicêtre, France.
Séverine TrabadoINSERM, UMR-S U1185, Physiologie et Physiopathologie Endocriniennes, Le Kremlin Bicêtre, France.
Agnès LinglartAP-HP, Université Paris-Saclay, Service Endocrinologie et diabète de l'enfant, Centre de Référence des Maladies Rares du Développement Génital (CRMR DEVGEN), Hôpital Bicêtre Paris-Saclay, Le Kremlin-Bicêtre, France.
Claire BouvattierAP-HP, Université Paris-Saclay, Service Endocrinologie et diabète de l'enfant, Centre de Référence des Maladies Rares du Développement Génital (CRMR DEVGEN), Hôpital Bicêtre Paris-Saclay, Le Kremlin-Bicêtre, France.
Abd El Kader Ait TayebINSERM, UMR-S U1185, Physiologie et Physiopathologie Endocriniennes, Le Kremlin Bicêtre, France.ORCID https://orcid.org/0000-0001-6432-1098

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Primary adrenal insufficiency (PAI) in children, most commonly caused by congenital adrenal hyperplasia (CAH), is challenging to treat due to the short half-life of hydrocortisone and the difficulty in mimicking the physiological rhythm of cortisol. Continuous subcutaneous hydrocortisone infusion (CSHI) has shown benefits in CAH adults but remains poorly studied in children. The aim of our study was to evaluate the feasibility, safety, and clinical efficacy of CSHI in pediatric patients under oral treatment with poorly controlled PAI. Methods: We conducted a retrospective monocentric study including 13 children and adolescents with PAI who were switched from oral hydrocortisone to CSHI between 2017 and 2024 due to a lack of disease control. Hormonal and clinical parameters were monitored over a median follow-up of 48 months. Results: The median age at CSHI initiation was 11.08 (7.75-14.08) years. Eleven patients (84.6%) had CAH. The median duration of CSHI was 48 (6-54) months. Biochemical control improved, morning cortisol increased, while ACTH, 17-OHP, androstenedione, and testosterone levels decreased during follow-up. Growth velocity and BMI remained stable. In one patient with prior and recurrent adrenal crises, these events ceased. In boys with testicular adrenal rest tumors, tumor volume decreased or resolved. One adolescent girl with amenorrhea resumed regular menstrual cycles under CSHI. CSHI was well tolerated with no major complications. Conclusion: CSHI offers a promising therapeutic alternative for children with PAI who are poorly controlled on oral therapy. It provides more physiological cortisol delivery, improves hormonal control, and appears safe during long-term pediatric use. Larger prospective studies are needed to confirm these findings and evaluate quality-of-life outcomes.

Indexed as

congenital adrenal hyperplasiacontinuous subcutaneous hydrocortisone infusionprimary adrenal insufficiency

Identifiers

PMID41493139
PMCPMC12811715

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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.