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Transient diabetes insipidus in critically ill COVID19 patients

PURPOSE: Vasopressin has become an important vasopressor drug while treating a critically ill patient to maintain adequate mean arterial pressure. Diabetes insipidus (DI) is a rare syndrome characterized by the excretion of a large volume of diluted urine, inappropriate for water homeostasis. We not...

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Autores principales: Statlender, Liran, Fishman, Guy, Hellerman, Moran, Kagan, Ilya, Bendavid, Itai, Gorfil, Dan, Kaptzon, Shani, Singer, Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828890/
https://www.ncbi.nlm.nih.gov/pubmed/36630859
http://dx.doi.org/10.1016/j.jcrc.2022.154211
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author Statlender, Liran
Fishman, Guy
Hellerman, Moran
Kagan, Ilya
Bendavid, Itai
Gorfil, Dan
Kaptzon, Shani
Singer, Pierre
author_facet Statlender, Liran
Fishman, Guy
Hellerman, Moran
Kagan, Ilya
Bendavid, Itai
Gorfil, Dan
Kaptzon, Shani
Singer, Pierre
author_sort Statlender, Liran
collection PubMed
description PURPOSE: Vasopressin has become an important vasopressor drug while treating a critically ill patient to maintain adequate mean arterial pressure. Diabetes insipidus (DI) is a rare syndrome characterized by the excretion of a large volume of diluted urine, inappropriate for water homeostasis. We noticed that several COVID19 patients developed excessive polyuria suggestive of DI, with a concomitant plasma sodium-level increase and/or low urine osmolality. We noticed a temporal relationship between vasopressin treatment cessation and polyuria periods. We reviewed those cases to better describe this phenomenon. METHODS: We retrospectively collected COVID19 ECMO patients' (from July 6, 2020, to November 30, 2021) data from the electronic medical records. By examining urine output, urine osmolality (if applicable), plasma sodium level, and plasma osmolality, we set DI diagnosis. We described the clinical course of DI episodes and compared baseline characteristics between patients who developed DI and those who did not. RESULTS: Out of 37 patients, 12 had 18 episodes of DI. These patients were 7 years younger and had lower severity scores (APACHE-II and SOFA). Mortality difference was not seen between groups. 17 episodes occurred after vasopressin discontinuation; 14 episodes were treated with vasopressin reinstitution. DI lasted for a median of 21 h, with a median increase of 14 mEq/L of sodium. CONCLUSIONS: Temporary DI prevalence after vasopressin discontinuation in COVID19 ECMO patients might be higher than previously described for vasopressin-treated patients.
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spelling pubmed-98288902023-01-10 Transient diabetes insipidus in critically ill COVID19 patients Statlender, Liran Fishman, Guy Hellerman, Moran Kagan, Ilya Bendavid, Itai Gorfil, Dan Kaptzon, Shani Singer, Pierre J Crit Care Article PURPOSE: Vasopressin has become an important vasopressor drug while treating a critically ill patient to maintain adequate mean arterial pressure. Diabetes insipidus (DI) is a rare syndrome characterized by the excretion of a large volume of diluted urine, inappropriate for water homeostasis. We noticed that several COVID19 patients developed excessive polyuria suggestive of DI, with a concomitant plasma sodium-level increase and/or low urine osmolality. We noticed a temporal relationship between vasopressin treatment cessation and polyuria periods. We reviewed those cases to better describe this phenomenon. METHODS: We retrospectively collected COVID19 ECMO patients' (from July 6, 2020, to November 30, 2021) data from the electronic medical records. By examining urine output, urine osmolality (if applicable), plasma sodium level, and plasma osmolality, we set DI diagnosis. We described the clinical course of DI episodes and compared baseline characteristics between patients who developed DI and those who did not. RESULTS: Out of 37 patients, 12 had 18 episodes of DI. These patients were 7 years younger and had lower severity scores (APACHE-II and SOFA). Mortality difference was not seen between groups. 17 episodes occurred after vasopressin discontinuation; 14 episodes were treated with vasopressin reinstitution. DI lasted for a median of 21 h, with a median increase of 14 mEq/L of sodium. CONCLUSIONS: Temporary DI prevalence after vasopressin discontinuation in COVID19 ECMO patients might be higher than previously described for vasopressin-treated patients. Elsevier Inc. 2023-04 2023-01-09 /pmc/articles/PMC9828890/ /pubmed/36630859 http://dx.doi.org/10.1016/j.jcrc.2022.154211 Text en © 2022 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Statlender, Liran
Fishman, Guy
Hellerman, Moran
Kagan, Ilya
Bendavid, Itai
Gorfil, Dan
Kaptzon, Shani
Singer, Pierre
Transient diabetes insipidus in critically ill COVID19 patients
title Transient diabetes insipidus in critically ill COVID19 patients
title_full Transient diabetes insipidus in critically ill COVID19 patients
title_fullStr Transient diabetes insipidus in critically ill COVID19 patients
title_full_unstemmed Transient diabetes insipidus in critically ill COVID19 patients
title_short Transient diabetes insipidus in critically ill COVID19 patients
title_sort transient diabetes insipidus in critically ill covid19 patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828890/
https://www.ncbi.nlm.nih.gov/pubmed/36630859
http://dx.doi.org/10.1016/j.jcrc.2022.154211
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