Real-life GH dosing patterns in children with GHD, TS or born SGA: a report from the NordiNet® International Outcome Study
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, multicentrická studie
PubMed
28522645
PubMed Central
PMC5488395
DOI
10.1530/eje-16-1055
PII: EJE-16-1055
Knihovny.cz E-zdroje
- MeSH
- dítě MeSH
- hypofyzární nanismus diagnóza farmakoterapie epidemiologie MeSH
- hypotrofický novorozenec * MeSH
- internacionalita * MeSH
- lidé MeSH
- lidský růstový hormon aplikace a dávkování MeSH
- mladiství MeSH
- následné studie MeSH
- poruchy růstu diagnóza farmakoterapie epidemiologie MeSH
- předškolní dítě MeSH
- prospektivní studie MeSH
- průřezové studie MeSH
- Turnerův syndrom diagnóza farmakoterapie epidemiologie MeSH
- výsledek terapie MeSH
- výzkumná zpráva * MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- předškolní dítě MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- Geografické názvy
- Česká republika epidemiologie MeSH
- Francie epidemiologie MeSH
- Německo epidemiologie MeSH
- Spojené království epidemiologie MeSH
- Názvy látek
- lidský růstový hormon MeSH
OBJECTIVE: To describe real-life dosing patterns in children with growth hormone deficiency (GHD), born small for gestational age (SGA) or with Turner syndrome (TS) receiving growth hormone (GH) and enrolled in the NordiNet International Outcome Study (IOS; Nbib960128) between 2006 and 2016. DESIGN: This non-interventional, multicentre study included paediatric patients diagnosed with GHD (isolated (IGHD) or multiple pituitary hormone deficiency (MPHD)), born SGA or with TS and treated according to everyday clinical practice from the Czech Republic (IGHD/MPHD/SGA/TS: n = 425/61/316/119), France (n = 1404/188/970/206), Germany (n = 2603/351/1387/411) and the UK (n = 259/60/87/35). METHODS: GH dosing was compared descriptively across countries and indications. Proportions of patients by GH dose group (low/medium/high) or GH dose change (decrease/increase/no change) during years 1 and 2 were also evaluated across countries and indications. RESULTS: In the Czech Republic, GH dosing was generally within recommended levels. In France, average GH doses were higher for patients with IGHD, MPHD and SGA than in other countries. GH doses in TS tended to be at the lower end of the recommended label range, especially in Germany and the UK; the majority of patients were in the low-dose group. A significant inverse association between baseline height standard deviation score and GH dose was shown (P < 0.05); shorter patients received higher doses. Changes in GH dose, particularly increases, were more common in the second (40%) than in the first year (25%). CONCLUSIONS: GH dosing varies considerably across countries and indications. In particular, almost half of girls with TS received GH doses below practice guidelines and label recommendations.
2nd Faculty of Medicine Charles University and University Hospital Motol Prague Czech Republic
Alder Hey Children's NHS Foundation Trust Liverpool UK
Department of Paediatric Endocrinology Hôpital des Enfants Toulouse France
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ClinicalTrials.gov
NCT00960128