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Severe ARDS due to Ruxolitinib discontinuation syndrome: case presentation and literature review
OBJECTIVE: Discontinuation of Ruxolitinib (RUX), a JAK1/JAK2 inhibitor, can induce symptom-relapse and even life-threatening adverse events. Due to increasing use of RUX, this so-called RUX discontinuation syndrome (RDS) is becoming more prevalent. To create better awareness for this potentially fat...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720527/ https://www.ncbi.nlm.nih.gov/pubmed/36478803 http://dx.doi.org/10.1016/j.heliyon.2022.e11782 |
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author | Houthuys, Jona F. Wilmer, Alexander P. Peetermans, Marijke Meersseman, Philippe Devos, Timothy |
author_facet | Houthuys, Jona F. Wilmer, Alexander P. Peetermans, Marijke Meersseman, Philippe Devos, Timothy |
author_sort | Houthuys, Jona F. |
collection | PubMed |
description | OBJECTIVE: Discontinuation of Ruxolitinib (RUX), a JAK1/JAK2 inhibitor, can induce symptom-relapse and even life-threatening adverse events. Due to increasing use of RUX, this so-called RUX discontinuation syndrome (RDS) is becoming more prevalent. To create better awareness for this potentially fatal syndrome, we present a case of an adult male who developed a fatal RDS. RESULTS: Our case presented with acute respiratory failure and a shock-like syndrome, with the need for mechanical ventilation, venovenous-extracorporeal membrane oxygenation (ECMO) and vasopressors. Respiratory symptoms quickly improved after initiation of corticosteroids, but disease course was complicated with a spontaneous spleen rupture leading to hemorrhagic shock and eventually death. CONCLUSION: This case report is the first case of severe RDS necessitating vv-ECMO and complicated with spleen rupture. Clinicians should be aware of this potentially lethal syndrome as it can present acutely but be effectively treated with corticosteroids and/or restarting JAK-inhibitors. |
format | Online Article Text |
id | pubmed-9720527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-97205272022-12-06 Severe ARDS due to Ruxolitinib discontinuation syndrome: case presentation and literature review Houthuys, Jona F. Wilmer, Alexander P. Peetermans, Marijke Meersseman, Philippe Devos, Timothy Heliyon Case Report OBJECTIVE: Discontinuation of Ruxolitinib (RUX), a JAK1/JAK2 inhibitor, can induce symptom-relapse and even life-threatening adverse events. Due to increasing use of RUX, this so-called RUX discontinuation syndrome (RDS) is becoming more prevalent. To create better awareness for this potentially fatal syndrome, we present a case of an adult male who developed a fatal RDS. RESULTS: Our case presented with acute respiratory failure and a shock-like syndrome, with the need for mechanical ventilation, venovenous-extracorporeal membrane oxygenation (ECMO) and vasopressors. Respiratory symptoms quickly improved after initiation of corticosteroids, but disease course was complicated with a spontaneous spleen rupture leading to hemorrhagic shock and eventually death. CONCLUSION: This case report is the first case of severe RDS necessitating vv-ECMO and complicated with spleen rupture. Clinicians should be aware of this potentially lethal syndrome as it can present acutely but be effectively treated with corticosteroids and/or restarting JAK-inhibitors. Elsevier 2022-11-28 /pmc/articles/PMC9720527/ /pubmed/36478803 http://dx.doi.org/10.1016/j.heliyon.2022.e11782 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Houthuys, Jona F. Wilmer, Alexander P. Peetermans, Marijke Meersseman, Philippe Devos, Timothy Severe ARDS due to Ruxolitinib discontinuation syndrome: case presentation and literature review |
title | Severe ARDS due to Ruxolitinib discontinuation syndrome: case presentation and literature review |
title_full | Severe ARDS due to Ruxolitinib discontinuation syndrome: case presentation and literature review |
title_fullStr | Severe ARDS due to Ruxolitinib discontinuation syndrome: case presentation and literature review |
title_full_unstemmed | Severe ARDS due to Ruxolitinib discontinuation syndrome: case presentation and literature review |
title_short | Severe ARDS due to Ruxolitinib discontinuation syndrome: case presentation and literature review |
title_sort | severe ards due to ruxolitinib discontinuation syndrome: case presentation and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720527/ https://www.ncbi.nlm.nih.gov/pubmed/36478803 http://dx.doi.org/10.1016/j.heliyon.2022.e11782 |
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