Growth should be monitored on age- and sex-appropriate growth charts. On average, puberty contributes 20 to 25 cm of height in females and 25 to 30 cm in males, and this is dependent upon adequate GH and insulin-like growth factor 1 (IGF1) concentrations. Monitoring of patients with an acquired cause of GHD (e.g., tumors, radiation, and infiltrative disorders) will depend upon the individual condition. All patients on GH treatment need to be monitored and continue receiving treatment until final height or epiphyseal closure is achieved.[61]Rappaport R, Mugnier E, Limoni C, et al; French Serono Study Group. A 5-year prospective study of growth hormone (GH)-deficient children treated with GH before the age of 3 years. J Clin Endocrinol Metab. 1997 Feb;82(2):452-6.
https://academic.oup.com/jcem/article/82/2/452/2823284
http://www.ncbi.nlm.nih.gov/pubmed/9024235?tool=bestpractice.com
Endocrine reassessment should be undertaken after completion of growth and puberty in patients with idiopathic isolated GHD and GHD with only one additional pituitary hormone deficit to identify adults with ongoing GHD and ascertain the need for adult GH replacement.[42]Grimberg A, DiVall SA, Polychronakos C, et al. Guidelines for growth hormone and insulin-like growth factor-I treatment in children and adolescents: growth hormone deficiency, idiopathic short stature, and primary insulin-like growth factor-I deficiency. Horm Res Paediatr. 2016;86(6):361-97.
https://www.karger.com/Article/FullText/452150
http://www.ncbi.nlm.nih.gov/pubmed/27884013?tool=bestpractice.com
[79]Ho KK, 2007 GH Deficiency Consensus Workshop Participants. Consensus guidelines for the diagnosis and treatment of adults with GH deficiency II: a statement of the GH Research Society in association with the European Society for Pediatric Endocrinology, Lawson Wilkins Society, European Society of Endocrinology, Japan Endocrine Society, and Endocrine Society of Australia. Eur J Endocrinol. 2007 Dec;157(6):695-700.
https://eje.bioscientifica.com/view/journals/eje/157/6/695.xml
http://www.ncbi.nlm.nih.gov/pubmed/18057375?tool=bestpractice.com
[97]Molitch ME, Clemmons DR, Malozowski S, et al. Evaluation and treatment of adult growth hormone deficiency: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2011 Jun;96(6):1587-609.
https://academic.oup.com/jcem/article/96/6/1587/2833853
http://www.ncbi.nlm.nih.gov/pubmed/21602453?tool=bestpractice.com
In 25% to 75% of patients, the GH response to provocation is in the normal range.[98]de Boer H, van der Veen EA. Why retest young adults with childhood-onset growth hormone deficiency? J Clin Endocrinol Metab. 1997 Jul;82(7):2032-6.
https://academic.oup.com/jcem/article/82/7/2032/2865881
http://www.ncbi.nlm.nih.gov/pubmed/9215268?tool=bestpractice.com
The reasons for this reversal of GHD are unclear. For patients with GHD due to acquired hypothalamo-pituitary damage (e.g., from a craniopharyngioma), known genetic mutations causing hypopituitarism, widespread midline structural brain defects, or ≥3 other pituitary hormone deficits, retesting may not be mandatory.
Pituitary hormone deficiencies can evolve with time, so regular monitoring, both clinically and with regular biochemical investigations, is needed.