<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Barrett CD</submitter><funding>NHLBI NIH HHS</funding><pagination>e12669</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8935535</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(2)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Few therapies exist to treat severe COVID-19 respiratory failure once it develops. Given known diffuse pulmonary microthrombi on autopsy studies of COVID-19 patients, we hypothesized that tissue plasminogen activator (tPA) may improve pulmonary function in COVID-19 respiratory failure.&lt;h4>Methods&lt;/h4>A multicenter, retrospective, observational study of patients with confirmed COVID-19 and severe respiratory failure who received systemic tPA (alteplase) was performed. Seventy-nine adults from seven medical centers were included in the final analysis after institutional review boards' approval; 23 were excluded from analysis because tPA was administered for pulmonary macroembolism or deep venous thrombosis. The primary outcome was improvement in the PaO&lt;sub>2&lt;/sub>/FiO&lt;sub>2&lt;/sub> ratio from baseline to 48 h after tPA. Linear mixed modeling was used for analysis.&lt;h4>Results&lt;/h4>tPA was associated with significant PaO&lt;sub>2&lt;/sub>/FiO&lt;sub>2&lt;/sub> improvement at 48 h (estimated paired difference = 23.1 ± 6.7), which was sustained at 72 h (interaction term &lt;i>p &lt;/i>&lt; 0.00). tPA administration was also associated with improved National Early Warning Score 2 scores at 24, 48, and 72 h after receiving tPA (interaction term &lt;i>p &lt;/i>= 0.00). D-dimer was significantly elevated immediately after tPA, consistent with lysis of formed clot. Patients with declining respiratory status preceding tPA administration had more marked improvement in PaO&lt;sub>2&lt;/sub>/FiO&lt;sub>2&lt;/sub> ratios than those who had poor but stable (not declining) respiratory status. There was one intracranial hemorrhage, which occurred within 24 h following tPA administration.&lt;h4>Conclusions&lt;/h4>These data suggest tPA is associated with significant improvement in pulmonary function in severe COVID-19 respiratory failure, especially in patients whose pulmonary function is in decline, and has an acceptable safety profile in this patient population.</pubmed_abstract><journal>Research and practice in thrombosis and haemostasis</journal><pubmed_title>MUlticenter STudy of tissue plasminogen activator (alteplase) use in COVID-19 severe respiratory failure (MUST COVID): A retrospective cohort study.</pubmed_title><pmcid>PMC8935535</pmcid><funding_grant_id>R00 HL151887</funding_grant_id><pubmed_authors>Barrett CD</pubmed_authors><pubmed_authors>Shaefi S</pubmed_authors><pubmed_authors>Wright FL</pubmed_authors><pubmed_authors>Yaffe MB</pubmed_authors><pubmed_authors>Yacoub M</pubmed_authors><pubmed_authors>Moore EE</pubmed_authors><pubmed_authors>Jhunjhunwala R</pubmed_authors><pubmed_authors>Banner-Goodspeed V</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Ramdeo R</pubmed_authors><pubmed_authors>Hajizadeh N</pubmed_authors><pubmed_authors>Capers K</pubmed_authors><pubmed_authors>Nemec H</pubmed_authors><pubmed_authors>Moore HB</pubmed_authors><pubmed_authors>Hussain S</pubmed_authors><pubmed_authors>Moore PK</pubmed_authors><pubmed_authors>Nonnemacher C</pubmed_authors><pubmed_authors>Baedorf-Kassis EN</pubmed_authors><pubmed_authors>Sauaia A</pubmed_authors><pubmed_authors>Moraco A</pubmed_authors><pubmed_authors>Bull T</pubmed_authors><pubmed_authors>McIntyre R</pubmed_authors><pubmed_authors>Hattar L</pubmed_authors><pubmed_authors>Talmor DS</pubmed_authors><pubmed_authors>Benjamin Christie D</pubmed_authors><pubmed_authors>Espinal A</pubmed_authors><pubmed_authors>Rajcooar N</pubmed_authors><pubmed_authors>Orfanos S</pubmed_authors><pubmed_authors>Anez-Bustillos L</pubmed_authors><pubmed_authors>Guevara A</pubmed_authors><pubmed_authors>Thomas Buchanan J</pubmed_authors><pubmed_authors>Al-Shammaa A</pubmed_authors></additional><is_claimable>false</is_claimable><name>MUlticenter STudy of tissue plasminogen activator (alteplase) use in COVID-19 severe respiratory failure (MUST COVID): A retrospective cohort study.</name><description>&lt;h4>Background&lt;/h4>Few therapies exist to treat severe COVID-19 respiratory failure once it develops. Given known diffuse pulmonary microthrombi on autopsy studies of COVID-19 patients, we hypothesized that tissue plasminogen activator (tPA) may improve pulmonary function in COVID-19 respiratory failure.&lt;h4>Methods&lt;/h4>A multicenter, retrospective, observational study of patients with confirmed COVID-19 and severe respiratory failure who received systemic tPA (alteplase) was performed. Seventy-nine adults from seven medical centers were included in the final analysis after institutional review boards' approval; 23 were excluded from analysis because tPA was administered for pulmonary macroembolism or deep venous thrombosis. The primary outcome was improvement in the PaO&lt;sub>2&lt;/sub>/FiO&lt;sub>2&lt;/sub> ratio from baseline to 48 h after tPA. Linear mixed modeling was used for analysis.&lt;h4>Results&lt;/h4>tPA was associated with significant PaO&lt;sub>2&lt;/sub>/FiO&lt;sub>2&lt;/sub> improvement at 48 h (estimated paired difference = 23.1 ± 6.7), which was sustained at 72 h (interaction term &lt;i>p &lt;/i>&lt; 0.00). tPA administration was also associated with improved National Early Warning Score 2 scores at 24, 48, and 72 h after receiving tPA (interaction term &lt;i>p &lt;/i>= 0.00). D-dimer was significantly elevated immediately after tPA, consistent with lysis of formed clot. Patients with declining respiratory status preceding tPA administration had more marked improvement in PaO&lt;sub>2&lt;/sub>/FiO&lt;sub>2&lt;/sub> ratios than those who had poor but stable (not declining) respiratory status. There was one intracranial hemorrhage, which occurred within 24 h following tPA administration.&lt;h4>Conclusions&lt;/h4>These data suggest tPA is associated with significant improvement in pulmonary function in severe COVID-19 respiratory failure, especially in patients whose pulmonary function is in decline, and has an acceptable safety profile in this patient population.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2026-04-08T17:23:24.314Z</modification><creation>2025-04-19T22:38:23.173Z</creation></dates><accession>S-EPMC8935535</accession><cross_references><pubmed>35341072</pubmed><doi>10.1002/rth2.12669</doi></cross_references></HashMap>