ESE audit on management of adult growth hormone deficiency in clinical practice


Por: Martel-Duguech, L, Jorgensen, JOL, Korbonits, M, Johannsson, G, Webb, SM, ESE AGHD Study Grp Pan-European Au

Publicada: 1 feb 2021
Resumen:
Guidelines recommend adults with pituitary disease in whom GH therapy is contemplated, to be tested for GH deficiency (AGHD); however, clinical practice is not uniform. Aims: (1) To record current practice of AGHD management throughout Europe and benchmark it against guidelines; (2) To evaluate educational status of healthcare professionals about AGHD. Design: Online survey in endocrine centres throughout Europe. Patients and methods: Endocrinologists voluntarily completed an electronic questionnaire regarding AGHD patients diagnosed or treated in 2017-2018. Results: Twenty-eight centres from 17 European countries participated, including 2139 AGHD patients, 28% of childhood-onset GHD. Aetiology was most frequently non-functioning pituitary adenoma (26%), craniopharyngioma (13%) and genetic/congenital midline malformations (13%). Diagnosis of GHD was confirmed by a stimulation test in 52% (GHRH+arginine: 45%; insulin-tolerance: 42%, glucagon: 6%; GHRH alone and clonidine tests: 7%); in the remaining, >= 3 pituitary deficiencies and low serum IGF-I were diagnostic. Initial GH dose was lower in older patients, but only women <26 years were prescribed a higher dose than men; dose titration was based on normal serum IGF-I, tolerance and side-effects. In one country, AGHD treatment was not approved. Full public reimbursement was not available in four countries and only in childhood-onset GHD in another. AGHD awareness was low among non-endocrine professionals and healthcare administrators. Postgraduate AGHD curriculum training deserves being improved. Conclusion: Despite guideline recommendations, GH replacement in AGHD is still not available or reimbursed in all European countries. Knowledge among professionals and health administrators needs improvement to optimise the care of adults with GHD.

Filiaciones:
Martel-Duguech, L:
 Univ Autonoma Barcelona, Hosp St Pau, IIB St Pau, Barcelona, Catalunya, Spain

 Univ Autonoma Barcelona, Hosp St Pau, Dept Endocrinol Med, Barcelona, Catalunya, Spain

 ISCIII, Ctr Invest Biomed Red Enfermedades Raras CIBER ER, Unit 747, Barcelona, Catalunya, Spain

Jorgensen, JOL:
 European Soc Endocrinol, Pituitary & Neuroendocrinol, Starling House, Bristol, Avon, England

 Dept Endocrinol & Diabet, Dept Clin Med, Aarhus, Denmark

Korbonits, M:
 Endo ERN Res & Sci Workpackage, Leiden, Netherlands

 Endo ERN Pituitary Themat Grp, Leiden, Netherlands

 Queen Mary Univ London, Barts & London Sch Med & Dent, William Harvey Res Inst, Endocrinol, Charterhouse Sq, London, England

Johannsson, G:
 Endo ERN Growth & Genet Obes Syndrome Themat Grp, Leiden, Netherlands

 Univ Gothenburg, Sahlgrenska Acad, Inst Med, Gothenburg, Sweden

Webb, SM:
 Univ Autonoma Barcelona, Hosp St Pau, IIB St Pau, Barcelona, Catalunya, Spain

 Univ Autonoma Barcelona, Hosp St Pau, Dept Endocrinol Med, Barcelona, Catalunya, Spain

 ISCIII, Ctr Invest Biomed Red Enfermedades Raras CIBER ER, Unit 747, Barcelona, Catalunya, Spain
ISSN: 08044643
Editorial
BIOSCIENTIFICA LTD, STARLING HOUSE, 1600 BRISTOL PARKWAY N, BRISTOL, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 184 Número: 2
Páginas: 323-334
WOS Id: 000608421100017
ID de PubMed: 33320830
imagen Green Published, hybrid, Green Submitted

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