<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>67</volume><submitter>Maghbooli Z</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>This study aimed to consider the main risk factors related to adverse clinical outcomes in MS patients with COVID-19.&lt;h4>Methods&lt;/h4>Using the electronic health records systems, this is a cross-sectional study of two years of hospital admissions in terms of COVID-19 in Iran from March 2019 to August 2021. The severities of COVID-19 outcomes were admitted to ICU, hospitalization days, and in-hospital mortality.&lt;h4>Results&lt;/h4>A total of 1634 hospitalized MS patients with a definite diagnosis of COVID-19 based on PCR were recorded in the electronic health systems. MS patients had a 7% increased risk for longer hospitalization, a 3% increased risk for the need to the ICU, and no increased risk of mortality compared with the general population. MS patients who were taking immunosuppressive (IS)-disease modifying therapies (DMT) had longer hospitalization (adjusted OR=2.06, 95%CI: 1.48, 2.86) and higher mortality risk (adjusted OR=2.05, 95%CI: 1.52, 6.29) compared to patients were under the immunomodulatory (IM)-DMT. There was not any significant association between the types of DMT and ICU (12.2% vs. 12.7%). Besides, MS patients who were vaccinated against COVID-19 before admission had shorter hospitalization (adjusted OR=0.40, 95% CI: 0.18, 0.92).&lt;h4>Conclusions&lt;/h4>The current data suggest that MS healthcare providers should consider specific risks of severe COVID-19 infection before starting IS-DMT.</pubmed_abstract><journal>Multiple sclerosis and related disorders</journal><pagination>104067</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9306262</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Association between disease-modifying therapies and adverse clinical outcomes in multiple sclerosis patients with COVID-19 infection.</pubmed_title><pmcid>PMC9306262</pmcid><pubmed_authors>Fattahi MR</pubmed_authors><pubmed_authors>Hosseinpour H</pubmed_authors><pubmed_authors>Varzandi T</pubmed_authors><pubmed_authors>Sahraian MA</pubmed_authors><pubmed_authors>Aghababaei Y</pubmed_authors><pubmed_authors>Hamtaeigashi S</pubmed_authors><pubmed_authors>Maghbooli Z</pubmed_authors><pubmed_authors>Mohammad-Nabi S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association between disease-modifying therapies and adverse clinical outcomes in multiple sclerosis patients with COVID-19 infection.</name><description>&lt;h4>Background&lt;/h4>This study aimed to consider the main risk factors related to adverse clinical outcomes in MS patients with COVID-19.&lt;h4>Methods&lt;/h4>Using the electronic health records systems, this is a cross-sectional study of two years of hospital admissions in terms of COVID-19 in Iran from March 2019 to August 2021. The severities of COVID-19 outcomes were admitted to ICU, hospitalization days, and in-hospital mortality.&lt;h4>Results&lt;/h4>A total of 1634 hospitalized MS patients with a definite diagnosis of COVID-19 based on PCR were recorded in the electronic health systems. MS patients had a 7% increased risk for longer hospitalization, a 3% increased risk for the need to the ICU, and no increased risk of mortality compared with the general population. MS patients who were taking immunosuppressive (IS)-disease modifying therapies (DMT) had longer hospitalization (adjusted OR=2.06, 95%CI: 1.48, 2.86) and higher mortality risk (adjusted OR=2.05, 95%CI: 1.52, 6.29) compared to patients were under the immunomodulatory (IM)-DMT. There was not any significant association between the types of DMT and ICU (12.2% vs. 12.7%). Besides, MS patients who were vaccinated against COVID-19 before admission had shorter hospitalization (adjusted OR=0.40, 95% CI: 0.18, 0.92).&lt;h4>Conclusions&lt;/h4>The current data suggest that MS healthcare providers should consider specific risks of severe COVID-19 infection before starting IS-DMT.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-04T03:06:13.369Z</modification><creation>2025-04-04T03:06:13.369Z</creation></dates><accession>S-EPMC9306262</accession><cross_references><pubmed>35933755</pubmed><doi>10.1016/j.msard.2022.104067</doi></cross_references></HashMap>