Early cessation and non-response are important and possibly related problems in growth hormone therapy: an OZGROW analysis
Abstract
Objective To investigate growth hormone (GH) treatment and treatment cessation with respect to efficacy and efficiency. To identify factors that best classify or predict cessation type: completed treatment (CT), early cessation (EC), or non-response (NR).Design Observational study (1990-2013) of the Australian GH Program comparing CT, EC, and NR groups with respect to demographic, clinical, and response criteria. All patients treated for GH deficiency (GHD; 909), short stature and slow growth (SSSG; 2144), and Turner Syndrome (TS; 626) were included. Information was retrieved from the OZGROW database.Results 51.9% of patients were EC, 40.7% CT and 7.4% NR.Median treatment durations for NR patients were often longer than patients who completed treatment. EC and NR groups were both associated with poor growth response with males overrepresented.Socioeconomic status differentiated NR (higher) and EC (lower) groups.Conclusions EC was observed at very high rates and appears, generally, to be a little-recognised but frequent problem in GH therapy.EC and delayed recognition of NR may be interrelated being differentiated by the decision to cease or continue treatment following poor response.Poor treatment compliance is likely a major causal factor in EC.Strategies to address poor response and compliance have been developed, however, given the scale of these problems, it may be that long acting GH formulations or individualized treatment need consideration.
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Poor adherence and early treatment discontinuation may result in lower height gain.
“Poor adherence189 to prescribed doses and early treatment discontinuation190 may also result in lower height gain.”
From Clinical practice guidelines for the care of girls and women with Turner syndrome. (2024) · cites this paper as [190]
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Clinical practice guidelines for the care of girls and women with Turner syndrome.
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- Authors
- Hughes, I. P., Choong, C., Rath, S., Atkinson, H., Cotterill, A., Cutfield, W., Hofman, P., & Harris, M.
- Affiliations
- The University of Queensland (AU)
- The University of Western Australia (AU)
- Children's Health Queensland Hospital and Health Service (AU)
- University of Auckland (NZ)
- Corresponding author
- Hughes, Ian P.
- ORCID
- Venue
- Growth Hormone & IGF Research
- Publisher
- Elsevier BV
- Published
- 2016-08
- Volume
- 29
- Pages
- 63-70
- ISSN
- 1096-6374 (ISSN-L)
- OpenAlex
- W2343383102
- Cited by
- 32
- References
- 40
- Citations by year
- 2026: 7 · 2025: 3 · 2024: 5 · 2023: 2 · 2022: 6 · 2021: 2 · 2019: 1 · 2018: 3 · 2017: 1 · 2016: 2
- FWCI
- 2.34
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Growth Hormone & IGF Research (publishedVersion)
- PubMed (publishedVersion)
- UWA Profiles and Research Repository (UWA) (submittedVersion)
- eSpace (Curtin University) (submittedVersion)
- ResearchSpace (University of Auckland) (submittedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Growth Hormone and Insulin-like Growth Factors
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pituitary Gland Disorders and Treatments
- Health Sciences › Medicine › Reproductive Medicine › Hypothalamic control of reproductive hormones
- Keywords
- growth hormone therapy, treatment non-response, growth hormone deficiency, Turner syndrome, medication adherence, socioeconomic status, treatment duration
- MeSH terms
- Adolescent, Australia, Child, Child, Preschool, Female, Growth Disorders, Humans, Hypopituitarism, Male, Social Class, Time Factors, Turner Syndrome, Databases, Factual, Treatment Outcome, Treatment Failure, Human Growth Hormone, Medication Adherence
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