Treatment burden, adherence, and quality of life in children with daily GH treatment in France.

growth hormone deficiency patient-reported outcomes quality of life recombinant growth hormone treatment burden

Journal

Endocrine connections
ISSN: 2049-3614
Titre abrégé: Endocr Connect
Pays: England
ID NLM: 101598413

Informations de publication

Date de publication:
01 Apr 2023
Historique:
received: 02 03 2023
accepted: 03 03 2023
medline: 4 3 2023
pubmed: 4 3 2023
entrez: 3 3 2023
Statut: epublish

Résumé

The objective of this study was to describe in a real-life setting the treatment burden and adherence and quality of life (QOL) of children treated with daily injections of growth hormone and their relationship with treatment duration. This non-interventional, multicenter, cross-sectional French study involved children aged 3-17 years treated with daily growth hormone injections. Based on a recent validated dyad questionnaire, the mean overall life interference total score (100 = most interference) was described, with treatment adherence and QOL, using the Quality of Life of Short Stature Youth questionnaire (100 = best). All analyses were performed according to treatment duration prior to inclusion. Among the 275/277 analyzed children, 166 (60.4%) had only growth hormone deficiency (GHD). In the GHD group, the mean age was 11.7 ± 3.2 years; median treatment duration was 3.3 years (interquartile range 1.8-6.4). The mean overall life interference total score was 27.7 ± 20.7 (95% CI (24.2; 31.2)), with non-significant correlation with treatment duration (P = 0.1925). Treatment adherence was good (95.0% of children reported receiving >80% of planned injections over the last month); it slightly decreased with treatment duration (P = 0.0364). Children's overall QOL was good (81.5 ± 16.6 and 77.6 ± 18.7 according to children and parents, respectively), but subscores of the coping and treatment impact domains were <50. Similar results were observed in all patients independently of the condition requiring treatment. This real-life French cohort confirms the treatment burden of daily growth hormone injections, as previously reported in an interventional study.

Identifiants

pubmed: 36866786
doi: 10.1530/EC-22-0464
pii: EC-22-0464
pmc: PMC10083659
doi:
pii:

Types de publication

Journal Article

Langues

eng

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Auteurs

Régis Coutant (R)

Department of Pediatric Endocrinology and Diabetology, Reference Center for Rare Pituiatry Diseases, University Hospital of Angers, Angers, France.

Maithé Tauber (M)

Reference Center for the Prader-Willi syndrome and other rare obesities with feeding disorders (PRADORT), Children Hospital, CHU Toulouse, Toulouse, France.
Pediatric team of the Clinical Investigation Center 9302/INSERM, Hospital of Children, Toulouse, France.
Institut Toulousain des Maladies Infectieuses et Inflammatoires (Infinity), INSERM UMR1291 - CNRS UMR5051 - Université Toulouse III, Toulouse, France.

Béatrice Demaret (B)

GRANDIR - French Growth Disorders Association, Asnières-sur-Seine, France.

Yves Brault (Y)

Pfizer France, Paris France.

Olivier Chassany (O)

Health Economics Clinical Trial Unit (URC-ECO), Hospital of Hotel-Dieu, AP-HP, Paris, France.
Patient-Reported Outcomes Unit (PROQOL), UMR 1123, University Paris Cité, INSERM, Paris, France.

Michel Polak (M)

Hôpital Universitaire Necker Enfants Malades, Pediatric Endocrinology, Gynecology and Diabetology, Imagine Institute, INSERM U1163, Cochin Institute, INSERM U1016, Centre de référence des pathologies endocriniennes rares de la croissance et du développement, Université de Paris Cité, Paris, France.

Classifications MeSH