# Enhanced Treatment in Severe-Critical COVID-19 With Tocilizumab, Remdesivir, Dexamethasone: A Jordanian Cohort Study

**Authors:** Abdel-Hameed W Al-Mistarehi, Shadi El-Akawi, Khalid A Kheirallah, Ehab M Bani Ata, Khaled J Zaitoun, Ahmad B Khassawneh, Abdullah Jarrah, Hamed M Alzoubi, Sayer Al-Azzam, Reema A Karasneh, Rana B Altawalbeh, Basheer Khassawneh

PMC · DOI: 10.7759/cureus.67467 · 2024-08-22

## TL;DR

This study found that combining tocilizumab, remdesivir, and dexamethasone reduced mortality and ICU stays in severe COVID-19 patients in Jordan.

## Contribution

The study provides evidence for the combined efficacy of tocilizumab, remdesivir, and dexamethasone in treating severe COVID-19.

## Key findings

- TCZ+RDV group had the lowest mortality rate (32.1%) compared to RDV (40.6%) and standard therapy (47.1%).
- ICU stays and invasive ventilation durations were significantly shorter in the TCZ+RDV group.
- Among ICU patients, TCZ+RDV showed significantly lower mortality (51.1%) compared to other groups.

## Abstract

Background: Several medications have been proposed to manage COVID-19, with controversial data regarding their clinical benefits. We aimed to investigate the clinical efficacy of using remdesivir (RDV) with and without tocilizumab (TCZ) and standard therapy in treating severe COVID-19.

Methods: This retrospective cohort study was conducted in a Jordanian tertiary hospital (September 26th, 2020 - August 28th, 2021) and included adult COVID-19 patients requiring oxygen support. Patients were categorized into three groups based on treatment: TCZ+RDV and standard therapy; RDV and standard therapy; and standard therapy alone, which included dexamethasone, vitamins, anticoagulants, and ceftriaxone.

Results: Of 1,556 screened, 1,244 patients (mean age 62.33, 60.8% men) were included. Distribution was 106 in TCZ+RDV, 520 in RDV, and 618 in standard therapy. No significant differences were observed in age, gender, or BMI. Mortality was lowest in TCZ+RDV (32.1%), followed by RDV (40.6%) and standard therapy (47.1%) (p=0.005). Among ICU patients, TCZ+RDV showed significantly lower mortality (51.1%) compared to RDV (75%) and standard therapy (85.8%) (p<0.001). The ICU stays and invasive mandatory ventilation (IMV) durations were significantly shorter with TCZ+RDV (4.30 and 2.69 days, respectively) compared to RDV (7.61 and 4.52 days) and standard therapy (7.98 and 5.32 days) (p<0.001 for ICU stays, p=0.025 for IMV durations).

Conclusions: Combining TCZ, RDV, and dexamethasone shows promise in reducing mortality and ICU/IMV duration for severe COVID-19.

## Linked entities

- **Chemicals:** remdesivir (PubChem CID 121304016), dexamethasone (PubChem CID 5743), ceftriaxone (PubChem CID 5479530)
- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Diseases:** COVID-19 (MESH:D000086382)
- **Chemicals:** Dexamethasone (MESH:D003907), RDV (MESH:C000606551), ceftriaxone (MESH:D002443), oxygen (MESH:D010100), TCZ (MESH:C502936)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11417280/full.md

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Source: https://tomesphere.com/paper/PMC11417280