<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Buch MH</submitter><funding>Pfizer Inc</funding><pagination>e003912</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11029242</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(2)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>Compare the risk of extended major adverse cardiovascular (CV) event (MACE) composite outcomes and component events in patients with rheumatoid arthritis (RA) treated with tofacitinib versus tumour necrosis factor inhibitors (TNFi) in Oral Rheumatoid Arthritis Trial (ORAL) Surveillance.&lt;h4>Methods&lt;/h4>Patients with RA aged ≥50 years and with ≥1 additional CV risk factor received tofacitinib 5 mg or 10 mg two times per day or TNFi. MACE (non-fatal myocardial infarction (MI), non-fatal stroke or CV death (MACE-3)) was extended by sequential addition of CV events (hospitalisation for unstable angina (MACE-4), coronary revascularisation (MACE-5), transient ischaemic attack (MACE-6), peripheral vascular disease (MACE-7)), heart failure (HF) hospitalisation (MACE-8) and venous</pubmed_abstract><journal>RMD open</journal><pubmed_title>Risk of extended major adverse cardiovascular event endpoints with tofacitinib versus TNF inhibitors in patients with rheumatoid arthritis: a post hoc analysis of a phase 3b/4 randomised safety study.</pubmed_title><pmcid>PMC11029242</pmcid><funding_grant_id>N/A</funding_grant_id><pubmed_authors>Giles JT</pubmed_authors><pubmed_authors>Mikuls T</pubmed_authors><pubmed_authors>Buch MH</pubmed_authors><pubmed_authors>Nagy E</pubmed_authors><pubmed_authors>Jo H</pubmed_authors><pubmed_authors>Kwok K</pubmed_authors><pubmed_authors>Charles-Schoeman C</pubmed_authors><pubmed_authors>Yndestad A</pubmed_authors><pubmed_authors>Connell CA</pubmed_authors><pubmed_authors>Koch GG</pubmed_authors><pubmed_authors>Ytterberg S</pubmed_authors><pubmed_authors>Masri KR</pubmed_authors><pubmed_authors>Bhatt DL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Risk of extended major adverse cardiovascular event endpoints with tofacitinib versus TNF inhibitors in patients with rheumatoid arthritis: a post hoc analysis of a phase 3b/4 randomised safety study.</name><description>&lt;h4>Objectives&lt;/h4>Compare the risk of extended major adverse cardiovascular (CV) event (MACE) composite outcomes and component events in patients with rheumatoid arthritis (RA) treated with tofacitinib versus tumour necrosis factor inhibitors (TNFi) in Oral Rheumatoid Arthritis Trial (ORAL) Surveillance.&lt;h4>Methods&lt;/h4>Patients with RA aged ≥50 years and with ≥1 additional CV risk factor received tofacitinib 5 mg or 10 mg two times per day or TNFi. MACE (non-fatal myocardial infarction (MI), non-fatal stroke or CV death (MACE-3)) was extended by sequential addition of CV events (hospitalisation for unstable angina (MACE-4), coronary revascularisation (MACE-5), transient ischaemic attack (MACE-6), peripheral vascular disease (MACE-7)), heart failure (HF) hospitalisation (MACE-8) and venous</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2026-06-08T06:02:13.613Z</modification><creation>2026-06-08T03:14:14.567Z</creation></dates><accession>S-EPMC11029242</accession><cross_references><pubmed>38609322</pubmed><doi>10.1136/rmdopen-2023-003912</doi></cross_references></HashMap>