Table 3.
Disease-modifying treatment (DMT) as a risk factor for severe COVID-19 outcome in multiple sclerosis patients.a
Univariate analysis, (n=332) | Multivariate analysis, (n=332) | |||
---|---|---|---|---|
DMT | OR (95% CI) | p value | OR (95% CI) | p value |
Interferon | 0.39 (0.17–0.81) | 0.02 | 0.72 (0.34–1.40) | 0.26 |
Glatiramer acetate | 0.36 (0.14–0.79) | 0.01 | 0.81 (0.42–1.83) | 0.42 |
Teriflunomide | 0.54 (0.29–1.17) | 0.82 | 0.83 (0.39–1.97) | 0.67 |
Fumaratesb | 0.47 (0.17–0.79) | 0.01 | 1.08 (0.49–2.09) | 0.74 |
S1P modulatorsc | 0.57 (0.21–0.96) | 0.04 | 1.12 (0.52–2.34) | 0.85 |
Natalizumab | 0.42 (0.18–0.62) | 0.01 | 1.18 (0.53–2.10) | 0.76 |
Anti-CD20d | 0.81 (0.63–1.23) | 0.14 | 2.18 (1.53–4.58) | 0.01 |
Other | 0.41 (0.22–1.07) | 0.07 | 1.24 (0.36–2.22) | 0.80 |
No therapye | 1 (ref) | 1 (ref) |
Abbreviations: CI, confidence interval; COVID-19, corona virus disease 2019; OR, odds ratio.
Intensive care unit admission, mechanical ventilation, and/or death.
Dimethyl fumarate, diroximel fumarate, or monomethyl fumarate.
Fingolimod, siponimod, or ozanimod.
Ocrelizumab or rituximab.
The no therapy group was used as the reference category.