| Literature DB >> 33732466 |
Nophol Leelayuwatanakul1, Napplika Kongpolprom1, Thitiwat Sriprasart1, Vorakamol Phoophiboon1, Vorawut Thanthitaweewat1, Sarita Thawanaphong1, Worawan Sirichana1, Naricha Chirakalwasan1, Kamon Kawkitinarong1, Chanchai Sittipunt1, Opass Putcharoen2,3, Leilani Paitoonpong2,3, Gompol Suwanpimolkul2,3, Watsamon Jantarabenjakul3,4, Nattachai Srisawat5, Monvasi Pachinburavan1.
Abstract
Cytokine release syndrome (CRS) is known to be associated with severe coronavirus disease 2019 (COVID-19). Multiple anti-inflammatory therapies such as tocilizumab, corticosteroids, intravenous immunoglobulin (IVIG), and haemoadsorption or haemoperfusion have been used to combat this life-threatening condition. However, immunocompromised hosts are often omitted from research studies, and knowledge on the clinical efficacy of these therapies in immunocompromised patients is therefore limited. We report two cases of immunocompromised patients with severe COVID-19-related CRS requiring mechanical ventilation who were treated with multimodality treatment consisting of tocilizumab, IVIG, and haemoperfusion. Within 48 h, both patients showed clinical improvement with PaO2:FiO2 ratio and haemodynamic stability. Both survived to discharge. There were no adverse events following these therapies. In conclusion, combined therapeutic modalities, possibly tailored to individual inflammatory profiles, are promising treatment for severe COVID-19 infection in the immunocompromised host. Timely administration of adjunctive therapies that alleviate overwhelming inflammation may provide the best outcome.Entities:
Keywords: COVD‐19; IVIG; SARS‐CoV‐2; haemoperfusion; tocilizumab
Year: 2021 PMID: 33732466 PMCID: PMC7938208 DOI: 10.1002/rcr2.733
Source DB: PubMed Journal: Respirol Case Rep ISSN: 2051-3380