TY - JOUR
T1 - Tocilizumab
T2 - A retrospective multi-center cohort study of critically ill patients with COVID-19
AU - Villatoro Santos, Claudia R.
AU - Bhargava, Ashish
AU - Coyle, Meredith
AU - Szpunar, Susan
AU - Saravolatz, Louis D.
N1 - Publisher Copyright:
© 2021 Dustri-Verlag Dr. Karl Feistle. All rights reserved.
PY - 2021/11
Y1 - 2021/11
N2 - Background: Coronavirus disease 19 (COVID-19) can have a severe presentation characterized by a dysregulated immune response requiring admission to the intensive care unit (ICU). Immunomodulatory treatments like tocilizumab were found to improve inflammatory markers and lung injury over time. We aim to evaluate the effectiveness of tocilizumab treatment on critically ill patients with severe COVID-19. Materials and methods: We conducted a multi-center retrospective cohort study of 154 adult patients admitted to the ICU for severe COVID-19 pneumonia between March 15 and May 8, 2020. Data were obtained by electronic medical record (EMR) review. The primary outcome of interest was mortality. Results: Of 154 patients, 34 (21.4%) received tocilizumab. Compared to the non-treated group, the treated group was significantly younger, had fewer comorbidities, lower creatinine and procalcitonin levels, and higher alanine aminotransferase levels on admission. The treated group was more likely to receive supportive measures in the context of critical illness. The overall case fatality rate was 71.4%, and it was significantly lower in the treated than the nontreated (52.9 vs. 76.7%, p = 0.007). In multivariable survival analysis, tocilizumab treatment was associated with a 2.1 times lower hazard of mortality when compared to those who were not treated (hazard ratio: 0.47; 95% CI: 0.27, 0.83; p = 0.009). The prevalence of secondary infection was higher in the treated group compared to the non-treated without significant difference (p = 0.17). Conclusion: Tocilizumab treatment for critically ill patients with COVID-19 resulted in a lower likelihood of mortality.
AB - Background: Coronavirus disease 19 (COVID-19) can have a severe presentation characterized by a dysregulated immune response requiring admission to the intensive care unit (ICU). Immunomodulatory treatments like tocilizumab were found to improve inflammatory markers and lung injury over time. We aim to evaluate the effectiveness of tocilizumab treatment on critically ill patients with severe COVID-19. Materials and methods: We conducted a multi-center retrospective cohort study of 154 adult patients admitted to the ICU for severe COVID-19 pneumonia between March 15 and May 8, 2020. Data were obtained by electronic medical record (EMR) review. The primary outcome of interest was mortality. Results: Of 154 patients, 34 (21.4%) received tocilizumab. Compared to the non-treated group, the treated group was significantly younger, had fewer comorbidities, lower creatinine and procalcitonin levels, and higher alanine aminotransferase levels on admission. The treated group was more likely to receive supportive measures in the context of critical illness. The overall case fatality rate was 71.4%, and it was significantly lower in the treated than the nontreated (52.9 vs. 76.7%, p = 0.007). In multivariable survival analysis, tocilizumab treatment was associated with a 2.1 times lower hazard of mortality when compared to those who were not treated (hazard ratio: 0.47; 95% CI: 0.27, 0.83; p = 0.009). The prevalence of secondary infection was higher in the treated group compared to the non-treated without significant difference (p = 0.17). Conclusion: Tocilizumab treatment for critically ill patients with COVID-19 resulted in a lower likelihood of mortality.
KW - ARDS
KW - coronavirus disease 19
KW - mechanical ventilation
KW - tocilizumab
UR - http://www.scopus.com/inward/record.url?scp=85121957991&partnerID=8YFLogxK
U2 - 10.5414/CP203954
DO - 10.5414/CP203954
M3 - Article
C2 - 34448693
AN - SCOPUS:85121957991
SN - 0946-1965
VL - 59
SP - 705
EP - 712
JO - International Journal of Clinical Pharmacology and Therapeutics
JF - International Journal of Clinical Pharmacology and Therapeutics
IS - 11
ER -