The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Evaluation of growth hormone stimulation testing in children
Abstract
Summary: Objective: To evaluate the use and interpretation of growth hormone (GH) stimulation tests used across the UK for diagnosing GH deficiency. Background: Previous studies show poor consensus on the use of GH stimulation tests. Sex steroid priming and retesting in the transition period are areas not previously surveyed. Design: Data were collected from tertiary paediatric endocrinologists, paediatricians with a specialist interest in endocrinology and biochemists across the UK over 6 months through distributing electronic surveys. Results: At least three different GH stimulation tests were used by 33% of departments. Glucagon and insulin doses varied most, and sampling frequency varied most using insulin. All laboratories use a recommended chemiluminescence immunoassay with an acceptable coefficient of variability. The GH peak for diagnosing GH deficiency varied from 6 to 8 μg/l. A wide range of clinical scenarios prompted retesting in the transition period, suggesting nonstandardized current practice. Seventy‐five per cent of departments use sex steroid priming, but follow criteria variously combining bone age, chronological age and pubertal stage, together with variations in steroid type and dose. Conclusions: Although a contentious diagnostic test, GH stimulation tests remain the gold standard for diagnosing GH deficiency. Our data suggest that together with variation in indication, protocol and interpretation, there is considerable variation in current practices pertaining to priming and retesting in transition. Given the current financial climate and the need for careful resource management, this study emphasizes the considerable need for consensus in the investigation, diagnosis and long‐term follow‐up of these children, at least nationally if not internationally.
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“A 2016 survey of 48 pediatric departments and 57 biochemistry departments in the UK found that the cutoff values used to diagnose GHD in children ranged from 5 to 10 mg/L, with the overwhelming majority using a cutoff of ,7 mg/L (28).”
From Diagnosis of GH Deficiency as a Late Effect of Radiotherapy in Survivors of Childhood Cancers (2018) · cites this paper as [28]
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Molitch, M. E., Clemmons, D. R., Malozowski, S., Merriam, G. R., & Vance, M. L. (2011) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2011-0179 · Cited by 1,047
Consensus statement on the management of the GH-treated adolescent in the transition to adult care
Clayton, P. E., Cuneo, R. C., Juul, A., Monson, J. P., Shalet, S. M., & Tauber, M. (2005) · European Journal of Endocrinology · doi:10.1530/eje.1.01829 · Cited by 270
Research works printed but not linked: 31
- 10.1210/jc.2011-1995 · DOI · Paper page
- 10.1210/jc.2011-2882 · DOI
- 10.1007/s40124-013-0009-5 · DOI
- National Institute for Heath and Clinical Excellence, 2010, Human growth hormone (somatropin) for the treatment of growth failure in children (Technology Appraisal Guidance 188)
- 10.1210/jc.85.11.3990 · doi:10.1210/jc.85.11.3990 · Paper page
- National Institute for Heath and Clinical Excellence, 2002, Guidance on the use of growth hormone (somatropin) in children with growth failure (Technology Appraisal Guidance 42)
- 10.1136/jcp.2002.002238 · doi:10.1136/jcp.2002.002238
- 10.1159/000066265 · DOI
- 10.4158/EP.9.1.64 · DOI
- 10.1159/000284396 · DOI
- 10.1210/jc.85.11.4168 · DOI
- 10.1515/JPEM.2008.21.3.257 · doi:10.1515/jpem.2008.21.3.257
- 10.1515/JPEM.2004.17.1.77 · DOI
- 10.4274/jcrpe.v1i5.205 · DOI
- 10.1210/jc.2007-0167 · DOI
- Vught A.J., 2009, Pharmacological and physiological growth hormone stimulation tests to predict successful GH therapy in children, Journal of Pediatric Endocrinology and Metabolism, 22, 679
- Paediatric Formulary Committee, 2015, BNF for Children
- 10.1210/jc.83.5.1615 · DOI · Paper page
- 10.1210/jc.81.9.3323 · DOI · Paper page
- 10.1016/j.ghir.2013.06.002 · DOI
- 10.1373/clinchem.2010.150631 · DOI · Paper page
- 10.1515/CCLM.2011.201 · DOI
- 10.1136/adc.82.3.266k · doi:10.1136/adc.82.3.266k
- 10.1007/s12098-009-0115-0 · doi:10.1007/s12098-009-0115-0
- 10.1136/adc.80.5.443 · doi:10.1136/adc.80.5.443
- 10.1530/EJE-07-0631 · DOI · Paper page
- 10.1210/jc.2008-1333 · DOI
- De Sanctis V., 2014, Is priming with sex steroids useful for defining patients who will benefit from GH treatment?, Pediatric Endocrinology Reviews, 11, 284
- 10.1016/j.tem.2004.06.004 · doi:10.1016/j.tem.2004.06.004
- 10.1016/j.ghir.2003.11.003 · DOI
- 10.1210/er.2013-1067 · DOI · Paper page
Cited by
Diagnosis of GH Deficiency as a Late Effect of Radiotherapy in Survivors of Childhood Cancers
Sfeir, J. G., Kittah, N. E. N., Tamhane, S. U., Jasim, S., Chemaitilly, W., Cohen, L. E., & Murad, M. H. (2018) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2018-01204 · Cited by 35
QSOX2 Deficiency-induced short stature, gastrointestinal dysmotility and immune dysfunction
Maharaj, A. V., Ishida, M., Rybak, A., Elfeky, R., Andrews, A., Joshi, A., Elmslie, F., Joensuu, A., Kantojärvi, K., Jia, R. Y., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-52587-w · Cited by 9
Metadata
- Authors
- Chesover, A. D., & Dattani, M. T.
- Affiliations
- Department of Paediatrics Luton and Dunstable University Hospital NHS Foundation Trust Luton UK
- Department of Paediatric Endocrinology UCL Institute of Child Health/Great Ormond Street Hospital for Children/UCL Hospitals London UK
- Venue
- Clinical Endocrinology
- Publisher
- Wiley
- Published
- 2016-02-25
- Volume
- 84
- Issue
- 5
- Pages
- 708-714
- ISSN
- 0300-0664
- 1365-2265
- Cited by
- 47
- References
- 2
- Language
- en
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