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Approach to the Patient: Management of Pituitary Hormone Replacement Through Transition

Hypopituitarism in childhood is a rare, complex disorder that can present with highly variable phenotypes, which may continue into adult life. Pituitary deficits can evolve over time, with unpredictable patterns resulting in significant morbidity and mortality. Hypopituitarism and hypothalamic dysfu...

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Autores principales: Cerbone, Manuela, Katugampola, Harshini, Simpson, Helen L, Dattani, Mehul T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9202712/
https://www.ncbi.nlm.nih.gov/pubmed/35262704
http://dx.doi.org/10.1210/clinem/dgac129
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author Cerbone, Manuela
Katugampola, Harshini
Simpson, Helen L
Dattani, Mehul T
author_facet Cerbone, Manuela
Katugampola, Harshini
Simpson, Helen L
Dattani, Mehul T
author_sort Cerbone, Manuela
collection PubMed
description Hypopituitarism in childhood is a rare, complex disorder that can present with highly variable phenotypes, which may continue into adult life. Pituitary deficits can evolve over time, with unpredictable patterns resulting in significant morbidity and mortality. Hypopituitarism and hypothalamic dysfunction may be associated with challenging comorbidities such as obesity, learning difficulties, behavioral issues, sleep disturbance, and visual impairment. Transition is the purposeful planned movement of adolescents and young adults with chronic conditions from child-centered to adult-oriented health care systems with a shift from parent- to patient-focused care. To achieve effective transition within a health care setting, the inherent challenges involved in the evolution from a dependent child to an independent adult must be recognized. Transition is a critical time medically for patients with hypopituitarism. Complex issues with respect to puberty, attainment of optimal stature, adherence to treatment, and acceptance of the need for life-sustaining medications need to be addressed. For health care professionals, transition is an opportunity for reassessment of the pituitary deficits and the need for lifelong replacement therapies, often against a background of complex psychological issues. We present 4 illustrative cases of hypopituitarism of differing etiologies with diverse clinical presentations. Diagnostic and management processes from clinical presentation to young adulthood are discussed, with a particular focus on needs and outcomes through transition.
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spelling pubmed-92027122022-06-21 Approach to the Patient: Management of Pituitary Hormone Replacement Through Transition Cerbone, Manuela Katugampola, Harshini Simpson, Helen L Dattani, Mehul T J Clin Endocrinol Metab Approach to the Patient Hypopituitarism in childhood is a rare, complex disorder that can present with highly variable phenotypes, which may continue into adult life. Pituitary deficits can evolve over time, with unpredictable patterns resulting in significant morbidity and mortality. Hypopituitarism and hypothalamic dysfunction may be associated with challenging comorbidities such as obesity, learning difficulties, behavioral issues, sleep disturbance, and visual impairment. Transition is the purposeful planned movement of adolescents and young adults with chronic conditions from child-centered to adult-oriented health care systems with a shift from parent- to patient-focused care. To achieve effective transition within a health care setting, the inherent challenges involved in the evolution from a dependent child to an independent adult must be recognized. Transition is a critical time medically for patients with hypopituitarism. Complex issues with respect to puberty, attainment of optimal stature, adherence to treatment, and acceptance of the need for life-sustaining medications need to be addressed. For health care professionals, transition is an opportunity for reassessment of the pituitary deficits and the need for lifelong replacement therapies, often against a background of complex psychological issues. We present 4 illustrative cases of hypopituitarism of differing etiologies with diverse clinical presentations. Diagnostic and management processes from clinical presentation to young adulthood are discussed, with a particular focus on needs and outcomes through transition. Oxford University Press 2022-03-09 /pmc/articles/PMC9202712/ /pubmed/35262704 http://dx.doi.org/10.1210/clinem/dgac129 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Approach to the Patient
Cerbone, Manuela
Katugampola, Harshini
Simpson, Helen L
Dattani, Mehul T
Approach to the Patient: Management of Pituitary Hormone Replacement Through Transition
title Approach to the Patient: Management of Pituitary Hormone Replacement Through Transition
title_full Approach to the Patient: Management of Pituitary Hormone Replacement Through Transition
title_fullStr Approach to the Patient: Management of Pituitary Hormone Replacement Through Transition
title_full_unstemmed Approach to the Patient: Management of Pituitary Hormone Replacement Through Transition
title_short Approach to the Patient: Management of Pituitary Hormone Replacement Through Transition
title_sort approach to the patient: management of pituitary hormone replacement through transition
topic Approach to the Patient
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9202712/
https://www.ncbi.nlm.nih.gov/pubmed/35262704
http://dx.doi.org/10.1210/clinem/dgac129
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