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Central diabetes insipidus and pain medications – a risky combination
BACKGROUND: Central Diabetes Insipidus (CDI) results from decreased production of antidiuretic hormone (ADH) leading to an inability to concentrate urine. CDI is treated with desmopressin (DDAVP). Rarely reported in the literature, opioids and non-steroidal anti-inflammatories (NSAIDs) can induce hy...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207735/ https://www.ncbi.nlm.nih.gov/pubmed/34134784 http://dx.doi.org/10.1186/s40842-021-00124-9 |
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author | Pinto, Teresa E. Mokashi, Arati Cummings, Elizabeth A. |
author_facet | Pinto, Teresa E. Mokashi, Arati Cummings, Elizabeth A. |
author_sort | Pinto, Teresa E. |
collection | PubMed |
description | BACKGROUND: Central Diabetes Insipidus (CDI) results from decreased production of antidiuretic hormone (ADH) leading to an inability to concentrate urine. CDI is treated with desmopressin (DDAVP). Rarely reported in the literature, opioids and non-steroidal anti-inflammatories (NSAIDs) can induce hyponatremia in individuals treated for CDI. CASE PRESENTATION: A 10-year-old boy with septo-optic dysplasia and CDI was treated with DDAVP 1.6 mg orally TID maintaining normal sodium levels. Post admission for a femur fracture, he was discharged on ibuprofen and hydromorphone. Sodium was 136 mmol/l two days before discharge. He returned to the ED after having a seizure at home. He was euvolemic and mildly lethargic. Sodium was low at 108 mmol/l. DDAVP and hydromorphone were held and he was fluid restricted, but the sodium remained low. Sodium began to rise when Ibuprofen was stopped. Intermittent small doses of DDAVP were given to facilitate gradual correction of hyponatremia. At discharge, sodium had normalized. CONCLUSION: Hyponatremia has occasionally been described as a side effect of opioids and rarely of NSAIDs in patients with CDI. Stimulation of the thirst centre may play a role with opioids while a decrease in urine output may be the mechanism with NSAIDs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40842-021-00124-9. |
format | Online Article Text |
id | pubmed-8207735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82077352021-06-16 Central diabetes insipidus and pain medications – a risky combination Pinto, Teresa E. Mokashi, Arati Cummings, Elizabeth A. Clin Diabetes Endocrinol Case Report BACKGROUND: Central Diabetes Insipidus (CDI) results from decreased production of antidiuretic hormone (ADH) leading to an inability to concentrate urine. CDI is treated with desmopressin (DDAVP). Rarely reported in the literature, opioids and non-steroidal anti-inflammatories (NSAIDs) can induce hyponatremia in individuals treated for CDI. CASE PRESENTATION: A 10-year-old boy with septo-optic dysplasia and CDI was treated with DDAVP 1.6 mg orally TID maintaining normal sodium levels. Post admission for a femur fracture, he was discharged on ibuprofen and hydromorphone. Sodium was 136 mmol/l two days before discharge. He returned to the ED after having a seizure at home. He was euvolemic and mildly lethargic. Sodium was low at 108 mmol/l. DDAVP and hydromorphone were held and he was fluid restricted, but the sodium remained low. Sodium began to rise when Ibuprofen was stopped. Intermittent small doses of DDAVP were given to facilitate gradual correction of hyponatremia. At discharge, sodium had normalized. CONCLUSION: Hyponatremia has occasionally been described as a side effect of opioids and rarely of NSAIDs in patients with CDI. Stimulation of the thirst centre may play a role with opioids while a decrease in urine output may be the mechanism with NSAIDs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40842-021-00124-9. BioMed Central 2021-06-16 /pmc/articles/PMC8207735/ /pubmed/34134784 http://dx.doi.org/10.1186/s40842-021-00124-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Pinto, Teresa E. Mokashi, Arati Cummings, Elizabeth A. Central diabetes insipidus and pain medications – a risky combination |
title | Central diabetes insipidus and pain medications – a risky combination |
title_full | Central diabetes insipidus and pain medications – a risky combination |
title_fullStr | Central diabetes insipidus and pain medications – a risky combination |
title_full_unstemmed | Central diabetes insipidus and pain medications – a risky combination |
title_short | Central diabetes insipidus and pain medications – a risky combination |
title_sort | central diabetes insipidus and pain medications – a risky combination |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207735/ https://www.ncbi.nlm.nih.gov/pubmed/34134784 http://dx.doi.org/10.1186/s40842-021-00124-9 |
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