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Transient Leukopenia Induced by Combination Therapy for Severe SARS-CoV-2 Pneumonia
Treatment strategies for patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continue to be heavily researched and ever-changing. Recent data has suggested that combination therapy with dexamethasone, remdesivir and baricitinib could decrease the severity and length of illness...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SMC Media Srl
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9678126/ https://www.ncbi.nlm.nih.gov/pubmed/36415839 http://dx.doi.org/10.12890/2022_003636 |
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author | Sullivan, Sierra Leelaviwat, Natnicha Davalos, Jesus Evans, Abbie Abdelnabi, Mahmoud Mittal, Neha |
author_facet | Sullivan, Sierra Leelaviwat, Natnicha Davalos, Jesus Evans, Abbie Abdelnabi, Mahmoud Mittal, Neha |
author_sort | Sullivan, Sierra |
collection | PubMed |
description | Treatment strategies for patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continue to be heavily researched and ever-changing. Recent data has suggested that combination therapy with dexamethasone, remdesivir and baricitinib could decrease the severity and length of illness in patients with severe SARS-CoV-2. However; the data regarding the safety and side effects related to this combination therapy are limited to case reports. The purpose of this case report is to highlight a potentially life-threatening side effect of one or all medications mentioned above. LEARNING POINTS: Current National Institutes of Health treatment guidelines recommend remdesivir for patients with a high risk of progression. In patients requiring minimal supplemental oxygen, remdesivir or dexamethasone monotherapy is recommended, while in patients requiring high-flow oxygen or non-invasive ventilation, dexamethasone monotherapy or dexamethasone plus remdesivir is recommended. Baricitinib or tocilizumab can be added in patients requiring oxygen supplementation. Clinicians should be aware of transient leukocytopenia that can be induced with combination therapy of dexamethasone, remdesivir and baricitinib during the early phase of treatment of SARS-CoV-2 patients. The evaluation approach for leukopenia should consider autoimmune disorders, inflammatory diseases, infections, malignancy, and medication and toxin exposure. |
format | Online Article Text |
id | pubmed-9678126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SMC Media Srl |
record_format | MEDLINE/PubMed |
spelling | pubmed-96781262022-11-21 Transient Leukopenia Induced by Combination Therapy for Severe SARS-CoV-2 Pneumonia Sullivan, Sierra Leelaviwat, Natnicha Davalos, Jesus Evans, Abbie Abdelnabi, Mahmoud Mittal, Neha Eur J Case Rep Intern Med Articles Treatment strategies for patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continue to be heavily researched and ever-changing. Recent data has suggested that combination therapy with dexamethasone, remdesivir and baricitinib could decrease the severity and length of illness in patients with severe SARS-CoV-2. However; the data regarding the safety and side effects related to this combination therapy are limited to case reports. The purpose of this case report is to highlight a potentially life-threatening side effect of one or all medications mentioned above. LEARNING POINTS: Current National Institutes of Health treatment guidelines recommend remdesivir for patients with a high risk of progression. In patients requiring minimal supplemental oxygen, remdesivir or dexamethasone monotherapy is recommended, while in patients requiring high-flow oxygen or non-invasive ventilation, dexamethasone monotherapy or dexamethasone plus remdesivir is recommended. Baricitinib or tocilizumab can be added in patients requiring oxygen supplementation. Clinicians should be aware of transient leukocytopenia that can be induced with combination therapy of dexamethasone, remdesivir and baricitinib during the early phase of treatment of SARS-CoV-2 patients. The evaluation approach for leukopenia should consider autoimmune disorders, inflammatory diseases, infections, malignancy, and medication and toxin exposure. SMC Media Srl 2022-10-25 /pmc/articles/PMC9678126/ /pubmed/36415839 http://dx.doi.org/10.12890/2022_003636 Text en © EFIM 2022 https://creativecommons.org/licenses/by-nc-nd/4.0/This article is licensed under a Commons Attribution Non-Commercial 4.0 License (https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Articles Sullivan, Sierra Leelaviwat, Natnicha Davalos, Jesus Evans, Abbie Abdelnabi, Mahmoud Mittal, Neha Transient Leukopenia Induced by Combination Therapy for Severe SARS-CoV-2 Pneumonia |
title | Transient Leukopenia Induced by Combination Therapy for Severe SARS-CoV-2 Pneumonia |
title_full | Transient Leukopenia Induced by Combination Therapy for Severe SARS-CoV-2 Pneumonia |
title_fullStr | Transient Leukopenia Induced by Combination Therapy for Severe SARS-CoV-2 Pneumonia |
title_full_unstemmed | Transient Leukopenia Induced by Combination Therapy for Severe SARS-CoV-2 Pneumonia |
title_short | Transient Leukopenia Induced by Combination Therapy for Severe SARS-CoV-2 Pneumonia |
title_sort | transient leukopenia induced by combination therapy for severe sars-cov-2 pneumonia |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9678126/ https://www.ncbi.nlm.nih.gov/pubmed/36415839 http://dx.doi.org/10.12890/2022_003636 |
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