Higher persistence in newly diagnosed nonvalvular atrial fibrillation patients treated with dabigatran versus warfarin.
| dc.contributor.author | Zalesak, Martin | |
| dc.contributor.author | Siu, Kimberly | |
| dc.contributor.author | Francis, Kevin | |
| dc.contributor.author | Yu, Chen | |
| dc.contributor.author | Alvrtsyan, Hasmik | |
| dc.contributor.author | Rao, Yajing | |
| dc.contributor.author | Walker, David | |
| dc.contributor.author | Sander, Stephen | |
| dc.contributor.author | Miyasato, Gavin | |
| dc.contributor.author | Matchar, David | |
| dc.contributor.author | Sanchez, Herman | |
| dc.date.accessioned | 2021-05-11T07:40:20Z | |
| dc.date.available | 2021-05-11T07:40:20Z | |
| dc.date.issued | 2013-09 | |
| dc.date.updated | 2021-05-11T07:40:18Z | |
| dc.description.abstract | BackgroundOral anticoagulation therapy is the primary tool in reducing stroke risk in patients with nonvalvular atrial fibrillation but is underused. Patients nonpersistent with therapy contribute to this underuse. The objective of this study was to compare persistence rates in newly diagnosed nonvalvular atrial fibrillation patients treated with warfarin versus dabigatran as their oral anticoagulation.Methods and resultsUS Department of Defense administrative claims were used to identify patients receiving warfarin or dabigatran between October 28, 2010, and June 30, 2012. Patient records were examined for a minimum of 12 months before index date to restrict the analyses to those newly diagnosed with nonvalvular atrial fibrillation and naive-to-treatment, identifying 1775 on warfarin and 3370 on dabigatran. Propensity score matching was used to identify 1745 matched pairs. Persistence was defined as time on therapy to discontinuation. Kaplan-Meier curves were used to depict persistence over time. Cox proportional hazards model was used to determine the factors significantly associated with persistence. Using a 60-day permissible medication gap, the persistence rates were higher for dabigatran than for warfarin at both 6 months (72% versus 53%) and 1 year (63% versus 39%). Patients on dabigatran with a low-to-moderate risk of stroke (CHADS2<2) or with a higher bleed risk (HEMORR2HAGES>3) had a higher likelihood of nonpersistence (hazard ratios, 1.37; 95% confidence interval, 1.17-1.60; P<0.001; and hazard ratios, 1.24; 95% confidence interval, 1.04-1.47; P=0.016).ConclusionsPatients who initiated dabigatran treatment were more persistent than patients who began warfarin treatment. Within each cohort, patients with lower stroke risk were more likely to discontinue therapy. | |
| dc.identifier | CIRCOUTCOMES.113.000192 | |
| dc.identifier.issn | 1941-7713 | |
| dc.identifier.issn | 1941-7705 | |
| dc.identifier.uri | ||
| dc.language | eng | |
| dc.publisher | Ovid Technologies (Wolters Kluwer Health) | |
| dc.relation.ispartof | Circulation. Cardiovascular quality and outcomes | |
| dc.relation.isversionof | 10.1161/circoutcomes.113.000192 | |
| dc.subject | Humans | |
| dc.subject | Atrial Fibrillation | |
| dc.subject | Hemorrhage | |
| dc.subject | Benzimidazoles | |
| dc.subject | Warfarin | |
| dc.subject | beta-Alanine | |
| dc.subject | Antithrombins | |
| dc.subject | Anticoagulants | |
| dc.subject | Treatment Outcome | |
| dc.subject | Multivariate Analysis | |
| dc.subject | Logistic Models | |
| dc.subject | Proportional Hazards Models | |
| dc.subject | Odds Ratio | |
| dc.subject | Risk Factors | |
| dc.subject | Chi-Square Distribution | |
| dc.subject | Retrospective Studies | |
| dc.subject | Time Factors | |
| dc.subject | Aged | |
| dc.subject | Aged, 80 and over | |
| dc.subject | Middle Aged | |
| dc.subject | Female | |
| dc.subject | Male | |
| dc.subject | Stroke | |
| dc.subject | Medication Adherence | |
| dc.subject | Propensity Score | |
| dc.subject | Kaplan-Meier Estimate | |
| dc.subject | Dabigatran | |
| dc.title | Higher persistence in newly diagnosed nonvalvular atrial fibrillation patients treated with dabigatran versus warfarin. | |
| dc.type | Journal article | |
| duke.contributor.orcid | Matchar, David|0000-0003-3020-2108 | |
| pubs.begin-page | 567 | |
| pubs.end-page | 574 | |
| pubs.issue | 5 | |
| pubs.organisational-group | School of Medicine | |
| pubs.organisational-group | Duke Clinical Research Institute | |
| pubs.organisational-group | Duke Global Health Institute | |
| pubs.organisational-group | Pathology | |
| pubs.organisational-group | Medicine, General Internal Medicine | |
| pubs.organisational-group | Duke | |
| pubs.organisational-group | Institutes and Centers | |
| pubs.organisational-group | University Institutes and Centers | |
| pubs.organisational-group | Institutes and Provost's Academic Units | |
| pubs.organisational-group | Clinical Science Departments | |
| pubs.organisational-group | Medicine | |
| pubs.publication-status | Published | |
| pubs.volume | 6 |
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