<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(21)</volume><submitter>Mahana I</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Our objective was to assess real-world outcomes and health care use associated with commercial mavacamten use in patients with obstructive hypertrophic cardiomyopathy.&lt;h4>Methods&lt;/h4>We used the Symphony Dataverse to study patients receiving mavacamten between May 25, 2022 and June 30, 2024. Safety outcomes were prespecified.&lt;h4>Results&lt;/h4>We included 2440 patients and 18 494 mavacamten dispenses (63% women, median age 66 years [interquartile range {IQR}, 55-73]). Patients were followed for a median of 3037.0 days (IQR, 2808-3221) before mavacamten initiation and for 240 days (IQR, 117-407) on mavacamten. Atrial fibrillation or flutter (AF/AFL) at baseline were present in 536 (22%) of patients, whereas new-onset AF/AFL requiring therapy occurred in 125 patients (5%) and</pubmed_abstract><journal>Journal of the American Heart Association</journal><pagination>e042488</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12684520</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Characteristics and Outcomes of Mavacamten Use in 2440 Patients With Obstructive Hypertrophic Cardiomyopathy.</pubmed_title><pmcid>PMC12684520</pmcid><pubmed_authors>Mahana I</pubmed_authors><pubmed_authors>Kamna D</pubmed_authors><pubmed_authors>Nguyen O</pubmed_authors><pubmed_authors>Masri A</pubmed_authors><pubmed_authors>Elman MR</pubmed_authors><pubmed_authors>Chen H</pubmed_authors><pubmed_authors>Mejia AT</pubmed_authors><pubmed_authors>Volk H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Characteristics and Outcomes of Mavacamten Use in 2440 Patients With Obstructive Hypertrophic Cardiomyopathy.</name><description>&lt;h4>Background&lt;/h4>Our objective was to assess real-world outcomes and health care use associated with commercial mavacamten use in patients with obstructive hypertrophic cardiomyopathy.&lt;h4>Methods&lt;/h4>We used the Symphony Dataverse to study patients receiving mavacamten between May 25, 2022 and June 30, 2024. Safety outcomes were prespecified.&lt;h4>Results&lt;/h4>We included 2440 patients and 18 494 mavacamten dispenses (63% women, median age 66 years [interquartile range {IQR}, 55-73]). Patients were followed for a median of 3037.0 days (IQR, 2808-3221) before mavacamten initiation and for 240 days (IQR, 117-407) on mavacamten. Atrial fibrillation or flutter (AF/AFL) at baseline were present in 536 (22%) of patients, whereas new-onset AF/AFL requiring therapy occurred in 125 patients (5%) and</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-06-05T23:55:26.97Z</modification><creation>2026-05-23T03:13:48.033Z</creation></dates><accession>S-EPMC12684520</accession><cross_references><pubmed>41147368</pubmed><doi>10.1161/JAHA.125.042488</doi></cross_references></HashMap>