Evidence map›Paper›PMID 35114767›Full record

ArticlePediatric endocrinology, diabetes, and metabolism2021

Effectiveness, economical and safety aspects of growth hormone (GH) therapy in growth promoting doses in patients with isolated GH deficiency after the attainment of near-final height. Is there a need to modify the criteria of therapy withdrawal?

Joanna Smyczyńska, Maciej Hilczer, Andrzej Lewinski, Urszula Smyczyńska, Renata Stawerska

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Article in Pediatric endocrinology, diabetes, and metabolism, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Joanna SmyczyńskaDepartment of Pediatrics, Diabetology Endocrinology and Nephrology, Medical University of Lodz, Poland.
Maciej HilczerDepartment of Endocrinology and Metabolic Diseases, Polish Mother's Memorial Hospital - Research Institute in Lodz, Poland.
Andrzej LewinskiDepartment of Endocrinology and Metabolic Diseases, Polish Mother's Memorial Hospital - Research Institute in Lodz, Poland.
Urszula SmyczyńskaDepartment of Biostatistics and Translational Medicine, Medical University of Lodz, Poland.
Renata StawerskaDepartment of Endocrinology and Metabolic Diseases, Polish Mother's Memorial Hospital - Research Institute in Lodz, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionApart from growth promotion, growth hormone (GH) has important metabolic effects. Patients with severe GH deficiency (GHD) should be treated with GH throughout life. Current criteria for growth promoting therapy withdrawal in Poland differ from the latest recommendations. Aim of the study To assess cost-effectiveness and safety of continuation of GH therapy in growth promoting doses in patients with isolated GHD after the attainment of near-final height (near-FH) and the incidence of persistent GHD after the therapy withdrawal. MATERIAL AND

methods160 children with isolated GHD (height < 3 centile, GH peak < 10.0 µg/l), who continued GH therapy for growth promotion after the attainment of near-FH (height velocity   2.0) at near-FH and incidence of severe GHD in retesting (performed in 62 patients).

resultsHeight gain after near-FH was 1.1 ±0.8 cm in boys and 1.0 ±0.8 in girls. Increase of height by 1.0 cm required on average 487 mg of GH (264 injections). IGF-1 concentrations at near-FH were increased in 39 patients, with no clinical side effects. None of the patients retested had GH peak   10.0 µg/l.

conclusionsThere is no rationale to continue GH therapy in growth promoting doses in the patients with isolated GHD after fulfilling the criteria of near-FH.

Indexed as

Dwarfism, PituitaryHuman Growth HormoneBody HeightChildCost-Benefit AnalysisFemaleHumansMalePolandHuman Growth Hormonefinal height.growth hormone deficiencyinsulin-like growth factor-1recombinant growth hormonetreatment efficacy

Identifiers

PMID35114767
PMCPMC10226357

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