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Paeds Casesendocrinology-diabetes-and-growth

Paeds Cases · endocrinology-diabetes-and-growth

Counselling a family starting recombinant growth hormone therapy — OSCE

OSCE communication and shared decision-making station: explaining to parents what a new growth hormone deficiency diagnosis means for their 6-year-old son, why the low growth velocity and delayed bone age were the clues, what the recombinant growth hormone therapy involves including the dose, route, monitoring and safety, what the long-term outlook is, and what the transition to adult care will mean — while addressing parental anxiety, injection burden, and the practicalities of daily therapy.

osce communication and shared decision-making2 min readVerification in progress

Target exams

MRCPCH ClinicalRACP DCERCPSC Pediatrics
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Target exams

MRCPCH ClinicalRACP DCERCPSC Pediatrics
Prompt
The parents of a 6-year-old boy sit with you in the paediatric endocrine clinic. He is the shortest in his class and his growth has been falling away from his peers. The work-up has confirmed growth hormone deficiency: a subnormal growth velocity, a delayed bone age, a low IGF-1, and a peak growth hormone of 4 ng/mL on two stimulation tests. The pituitary MRI is normal. You are about to start recombinant growth hormone therapy. The parents are worried about whether the treatment is safe, whether it will work, how they will manage a daily injection, and whether their son will reach a normal height. Counsel them.

A strong candidate frames the conversation around three questions the parents are really asking — what is wrong, what will we do, and what will happen — and addresses the practical and emotional burden of a daily injection honestly. The diagnosis is explained in plain language: the gland that produces the growth hormone signal is underactive, so the signal is too weak and the bones are not growing at the normal rate; the delayed bone age is good news because it means there is time to catch up. The therapy is a daily subcutaneous injection of recombinant growth hormone given at bedtime to mimic the body's natural overnight pulse, at a starting dose of around 0.045 to 0.050 mg/kg/day, with the dose adjusted to keep a blood test (the IGF-1) in the right range. [1] [2]

The safety discussion must be honest and balanced. The common side effects are minor and reversible — local injection-site reactions, occasional headache from a temporary rise in pressure inside the head that settles with dose adjustment, and a small increase in the risk of slipped hip and scoliosis that is caught by regular review. The long-term safety signal from the SAGhE mortality study is acknowledged with appropriate nuance: a possible small increase in all-cause and bone-tumour mortality in adults treated with growth hormone in childhood, with a very small absolute risk and substantial confounding, against which the benefit of treating a genuine growth hormone deficiency is clear. The candidate offers the parents written information and the contact details of the endocrine nurse specialist, and arranges a review of injection technique before the first dose is given at home. [4] [2]

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References3ShowHide
  1. [1]Collett-Solberg PF, et al. Diagnosis, genetics, and therapy of short stature in children: a Growth Hormone Research Society international perspective. Horm Res Paediatr, 2019.PMID 31514194
  2. [2]Grimberg A, et al. Guidelines for growth hormone and insulin-like growth factor-I treatment in children and adolescents. Horm Res Paediatr, 2016.PMID 27884013
  3. [4]Sävendahl L, et al. Long-term mortality and causes of death in isolated GHD, ISS, and SGA patients treated with recombinant growth hormone during childhood. J Clin Endocrinol Metab, 2012.PMID 22238393
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