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Case Reports
. 2021 Mar 7;9(4):e0733.
doi: 10.1002/rcr2.733. eCollection 2021 Apr.

Multimodality treatment in immunocompromised patients with severe COVID-19: the role of IL-6 inhibitor, intravenous immunoglobulin, and haemoperfusion

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Case Reports

Multimodality treatment in immunocompromised patients with severe COVID-19: the role of IL-6 inhibitor, intravenous immunoglobulin, and haemoperfusion

Nophol Leelayuwatanakul et al. Respirol Case Rep. .

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.

Keywords: COVD‐19; IVIG; SARS‐CoV‐2; haemoperfusion; tocilizumab.

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Figures

Figure 1
Figure 1
Summary of mode of oxygen therapy and adjunctive treatments given in each patient in time sequence.
Figure 2
Figure 2
Laboratory investigations of each patient in time sequence.
Figure 3
Figure 3
Chest radiographs on initial presentation, on the day before each adjunctive therapy, and on discharge date.

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