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Hormone replacement therapy in morphine-induced hypogonadic male chronic pain patients

BACKGROUND: In male patients suffering from chronic pain, opioid administration induces severe hypogonadism, leading to impaired physical and psychological conditions such as fatigue, anaemia and depression. Hormone replacement therapy is rarely considered for these hypogonadic patients, notwithstan...

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Autores principales: Aloisi, Anna Maria, Ceccarelli, Ilaria, Carlucci, Maria, Suman, Annalisa, Sindaco, Gianfranco, Mameli, Sergio, Paci, Valentina, Ravaioli, Laura, Passavanti, Giandomenico, Bachiocco, Valeria, Pari, Gilberto
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3049183/
https://www.ncbi.nlm.nih.gov/pubmed/21332999
http://dx.doi.org/10.1186/1477-7827-9-26
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author Aloisi, Anna Maria
Ceccarelli, Ilaria
Carlucci, Maria
Suman, Annalisa
Sindaco, Gianfranco
Mameli, Sergio
Paci, Valentina
Ravaioli, Laura
Passavanti, Giandomenico
Bachiocco, Valeria
Pari, Gilberto
author_facet Aloisi, Anna Maria
Ceccarelli, Ilaria
Carlucci, Maria
Suman, Annalisa
Sindaco, Gianfranco
Mameli, Sergio
Paci, Valentina
Ravaioli, Laura
Passavanti, Giandomenico
Bachiocco, Valeria
Pari, Gilberto
author_sort Aloisi, Anna Maria
collection PubMed
description BACKGROUND: In male patients suffering from chronic pain, opioid administration induces severe hypogonadism, leading to impaired physical and psychological conditions such as fatigue, anaemia and depression. Hormone replacement therapy is rarely considered for these hypogonadic patients, notwithstanding the various pharmacological solutions available. METHODS: To treat hypogonadism and to evaluate the consequent endocrine, physical and psychological changes in male chronic pain patients treated with morphine (epidural route), we tested the administration of testosterone via a gel formulation for one year. Hormonal (total testosterone, estradiol, free testosterone, DHT, cortisol), pain (VAS and other pain questionnaires), andrological (Ageing Males' Symptoms Scale - AMS) and psychological (POMS, CES-D and SF-36) parameters were evaluated at baseline (T0) and after 3, 6 and 12 months (T3, T6, T12 respectively). RESULTS: The daily administration of testosterone increased total and free testosterone and DHT at T3, and the levels remained high until T12. Pain rating indexes (QUID) progressively improved from T3 to T12 while the other pain parameters (VAS, Area%) remained unchanged. The AMS sexual dimension and SF-36 Mental Index displayed a significant improvement over time. CONCLUSIONS: In conclusion, our results suggest that a constant, long-term supply of testosterone can induce a general improvement of the male chronic pain patient's quality of life, an important clinical aspect of pain management.
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spelling pubmed-30491832011-03-07 Hormone replacement therapy in morphine-induced hypogonadic male chronic pain patients Aloisi, Anna Maria Ceccarelli, Ilaria Carlucci, Maria Suman, Annalisa Sindaco, Gianfranco Mameli, Sergio Paci, Valentina Ravaioli, Laura Passavanti, Giandomenico Bachiocco, Valeria Pari, Gilberto Reprod Biol Endocrinol Research BACKGROUND: In male patients suffering from chronic pain, opioid administration induces severe hypogonadism, leading to impaired physical and psychological conditions such as fatigue, anaemia and depression. Hormone replacement therapy is rarely considered for these hypogonadic patients, notwithstanding the various pharmacological solutions available. METHODS: To treat hypogonadism and to evaluate the consequent endocrine, physical and psychological changes in male chronic pain patients treated with morphine (epidural route), we tested the administration of testosterone via a gel formulation for one year. Hormonal (total testosterone, estradiol, free testosterone, DHT, cortisol), pain (VAS and other pain questionnaires), andrological (Ageing Males' Symptoms Scale - AMS) and psychological (POMS, CES-D and SF-36) parameters were evaluated at baseline (T0) and after 3, 6 and 12 months (T3, T6, T12 respectively). RESULTS: The daily administration of testosterone increased total and free testosterone and DHT at T3, and the levels remained high until T12. Pain rating indexes (QUID) progressively improved from T3 to T12 while the other pain parameters (VAS, Area%) remained unchanged. The AMS sexual dimension and SF-36 Mental Index displayed a significant improvement over time. CONCLUSIONS: In conclusion, our results suggest that a constant, long-term supply of testosterone can induce a general improvement of the male chronic pain patient's quality of life, an important clinical aspect of pain management. BioMed Central 2011-02-18 /pmc/articles/PMC3049183/ /pubmed/21332999 http://dx.doi.org/10.1186/1477-7827-9-26 Text en Copyright ©2011 Aloisi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Aloisi, Anna Maria
Ceccarelli, Ilaria
Carlucci, Maria
Suman, Annalisa
Sindaco, Gianfranco
Mameli, Sergio
Paci, Valentina
Ravaioli, Laura
Passavanti, Giandomenico
Bachiocco, Valeria
Pari, Gilberto
Hormone replacement therapy in morphine-induced hypogonadic male chronic pain patients
title Hormone replacement therapy in morphine-induced hypogonadic male chronic pain patients
title_full Hormone replacement therapy in morphine-induced hypogonadic male chronic pain patients
title_fullStr Hormone replacement therapy in morphine-induced hypogonadic male chronic pain patients
title_full_unstemmed Hormone replacement therapy in morphine-induced hypogonadic male chronic pain patients
title_short Hormone replacement therapy in morphine-induced hypogonadic male chronic pain patients
title_sort hormone replacement therapy in morphine-induced hypogonadic male chronic pain patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3049183/
https://www.ncbi.nlm.nih.gov/pubmed/21332999
http://dx.doi.org/10.1186/1477-7827-9-26
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