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Adherence To NOAC Therapy: A Case Study

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DISCUSSION
The analysis found higher adherence to NOAC therapy as compared to warfarin over 1-year period. This result was consistent over short and long term when examined at 3, 6, 9 and 12-month interval. The adherence decreased over time in both the cohorts (NOAC vs Warfarin).
Unadjusted estimates suggested age, insurance type, region, CHA2DS2VASC score, statin, ARB-inhibitors and beta-blocker use were associated with the adherence to the therapy. For multivariate analysis controlling for the covariates, increase in age, drug cost, less co-morbidities and statin use led to better adherence whereas low risk CHA2DS2VASC led to lower adherence. It was interesting to know that CHA2DS2VASC score and region was significantly associated with …show more content…

INR values, ventricular ejection fraction, body mass index) were not included in the dataset, clinical determinants such as CHA2DS2VASC and CCI helped to control for disease severity by considering hypertension, prior cardiovascular disease, diabetes and other co-morbidities. Furthermore, adherence assessment based on 3, 6, 9, and 12 month windows might lead to truncation of the data, therefore the windows were kept close at every 3 months. It is also important to understand dosing of warfarin is variable and frequently adjusted. We also looked at the distribution of days of supply to explore a potential bias. The distribution of the days of supply for warfarin and NOAC was primarily around 30 and 60 day dosing which substantiated that the therapies might be comparable. Prior use of anti-hypertensive drugs was also accounted and selection of the drugs was based on recommended AF therapy by American Heart Association.(AHA). These drugs were also used as covariates to understand the individual effects in the dabigatran and rivaroxaban pivotal trials. However, aspirin use was not comprehensively captured in claims database due to its availability as OTC drug. Differences in the descriptive charaterstics might be explained by the fact that NOACs might be prescribed to patients who have unmet need after warfarin therapy, this might lead to potential channeling or selection bias, in our study we did not control the selection bias using propensity

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