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Pituitary function within the first year after traumatic brain injury or subarachnoid haemorrhage
PURPOSE: Reports on long-term variations in pituitary function after traumatic brain injury (TBI) and subarachnoid haemorrhage (SAH) diverge. The aim of the current study was to evaluate the prevalence and changes in pituitary function during the first year after moderate and severe TBI and SAH and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5269462/ https://www.ncbi.nlm.nih.gov/pubmed/27671168 http://dx.doi.org/10.1007/s40618-016-0546-1 |
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author | Tölli, A. Borg, J. Bellander, B.-M. Johansson, F. Höybye, C. |
author_facet | Tölli, A. Borg, J. Bellander, B.-M. Johansson, F. Höybye, C. |
author_sort | Tölli, A. |
collection | PubMed |
description | PURPOSE: Reports on long-term variations in pituitary function after traumatic brain injury (TBI) and subarachnoid haemorrhage (SAH) diverge. The aim of the current study was to evaluate the prevalence and changes in pituitary function during the first year after moderate and severe TBI and SAH and to explore the relation between pituitary function and injury variables. METHODS: Adults with moderate and severe TBI or SAH were evaluated at 10 days, 3, 6 and 12 months post-injury/illness. Demographic, clinical, radiological, laboratory, including hormonal data were collected. RESULTS: A total of 91 adults, 56 (15 women/41 men) with TBI and 35 (27 women/8 men) with SAH were included. Perturbations in pituitary function were frequent early after the event but declined during the first year of follow-up. The most frequent deficiency was hypogonadotrope hypogonadism which was seen in approximately 25 % of the patients. Most of the variations were transient and without clinical significance. At 12 months, two patients were on replacement with hydrocortisone, four men on testosterone and one man on replacement with growth hormone. No relations were seen between hormonal levels and injury variables. CONCLUSIONS: Perturbations in pituitary function continue to occur during the first year after TBI and SAH, but only a few patients need replacement therapy. Our study could not identify a marker of increased risk of pituitary dysfunction that could guide routine screening. However, data demonstrate the need for systematic follow-up of pituitary function after moderate or severe TBI or SAH. |
format | Online Article Text |
id | pubmed-5269462 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-52694622017-02-09 Pituitary function within the first year after traumatic brain injury or subarachnoid haemorrhage Tölli, A. Borg, J. Bellander, B.-M. Johansson, F. Höybye, C. J Endocrinol Invest Original Article PURPOSE: Reports on long-term variations in pituitary function after traumatic brain injury (TBI) and subarachnoid haemorrhage (SAH) diverge. The aim of the current study was to evaluate the prevalence and changes in pituitary function during the first year after moderate and severe TBI and SAH and to explore the relation between pituitary function and injury variables. METHODS: Adults with moderate and severe TBI or SAH were evaluated at 10 days, 3, 6 and 12 months post-injury/illness. Demographic, clinical, radiological, laboratory, including hormonal data were collected. RESULTS: A total of 91 adults, 56 (15 women/41 men) with TBI and 35 (27 women/8 men) with SAH were included. Perturbations in pituitary function were frequent early after the event but declined during the first year of follow-up. The most frequent deficiency was hypogonadotrope hypogonadism which was seen in approximately 25 % of the patients. Most of the variations were transient and without clinical significance. At 12 months, two patients were on replacement with hydrocortisone, four men on testosterone and one man on replacement with growth hormone. No relations were seen between hormonal levels and injury variables. CONCLUSIONS: Perturbations in pituitary function continue to occur during the first year after TBI and SAH, but only a few patients need replacement therapy. Our study could not identify a marker of increased risk of pituitary dysfunction that could guide routine screening. However, data demonstrate the need for systematic follow-up of pituitary function after moderate or severe TBI or SAH. Springer International Publishing 2016-09-26 2017 /pmc/articles/PMC5269462/ /pubmed/27671168 http://dx.doi.org/10.1007/s40618-016-0546-1 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Tölli, A. Borg, J. Bellander, B.-M. Johansson, F. Höybye, C. Pituitary function within the first year after traumatic brain injury or subarachnoid haemorrhage |
title | Pituitary function within the first year after traumatic brain injury or subarachnoid haemorrhage |
title_full | Pituitary function within the first year after traumatic brain injury or subarachnoid haemorrhage |
title_fullStr | Pituitary function within the first year after traumatic brain injury or subarachnoid haemorrhage |
title_full_unstemmed | Pituitary function within the first year after traumatic brain injury or subarachnoid haemorrhage |
title_short | Pituitary function within the first year after traumatic brain injury or subarachnoid haemorrhage |
title_sort | pituitary function within the first year after traumatic brain injury or subarachnoid haemorrhage |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5269462/ https://www.ncbi.nlm.nih.gov/pubmed/27671168 http://dx.doi.org/10.1007/s40618-016-0546-1 |
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