Abstract

Objective: To identify patient characteristics predictive of all-cause healthcare costs among individuals with newly diagnosed non-valvular atrial fibrillation (NVAF) who initiated oral anticoagulant therapy with dabigatran or warfarin. 

Study Design: Retrospective analysis of administrative claims data of patients with newly diagnosed NVAF. 

Methods: Dabigatran and warfarin cohorts were identified by first claim (index date) during 10/1/2010 to 11/30/2012. Episode-based costs (all-cause) were determined using Episode Treatment Group (ETG) methodology and computed as per-patient-per-month. Baseline predictors of cost included baseline characteristics and baseline Episode Risk Group (ERG) risk score, which was grouped into 6 categories. To assess cohort differences in subgroups of patients, predictor variables representing the interaction of treatment cohort with patient characteristics were of primary interest. Cost ratios were then computed for subgroups of patients with different characteristics. 

Results: Cohorts included 4150 dabigatran- and 11,032 warfarin-treated patients. Compared with warfarin, dabigatran patients were younger (mean age: 67.3 vs. 72.5 years; P<0.001) and had lower mean ERG risk scores (4.1 vs. 5.6, P<0.001). Treatment cohort was not a statistically significant predictor of costs. Compared with warfarin, dabigatran was associated with higher cost at ERG risk scores of 2.1 to 4.0 and lower cost at scores of 6.1 to 8.0. 

Conclusions: Adding to existing evidence that treatment with dabigatran (vs warfarin) for NVAF would not incur higher all-cause healthcare costs, this study found that differences in all-cause healthcare costs did not follow a trend across subgroups of patients with NVAF based on different ERG risk score categories, favoring either therapy.


                                                                                         Am J Pharm Benefits. 2018;10(1)22-30

Atrial fibrillation (AF) confers a 4- to 5-fold higher risk of stroke, resulting in great morbidity and substantial healthcare costs.1-3 Oral anticoagulant (OAC) therapy is recommended to reduce risk of stroke among patients with AF at moderate-to-high risk of stroke.4,5 Warfarin has historically been the mainstay of OAC therapy. However, since 2010, therapeutic options have expanded with the introduction of dabigatran6 and other novel OACs indicated for nonvalvular AF (NVAF).7 In the Randomized Evaluation of Long-Term Anticoagulant Therapy clinical trial, dabigatran was associated with lower rates of stroke and systemic embolism compared with dose-adjusted warfarin.8

Real-world economic comparisons of dabigatran and warfarin among patients with NVAF initiating OAC therapy have recently been conducted. These retrospective claims analyses of all-cause healthcare costs suggest that dabigatran is cost-neutral relative to warfarin.9-12 In these studies, costs were reported for overall patient samples13 and did not examine whether subgroups of patients with similar demographic/clinical profiles might incur different costs when initiated on dabigatran versus warfarin.

Clinical characteristics, including disease severity, have been studied widely as risk factors that, when adjusted for, enable more accurate assessment of healthcare costs. The importance of incorporating patient heterogeneity into economic evaluations is also recognized.14 Patients with AF are a clinically heterogeneous population5,13 and initiation on appropriate OAC therapy has the potential to improve clinical outcomes and reduce resource use and costs. The Affordable Care Act, which reimburses services based on clinical episodes, rather than on a fee-for-service basis,15 has created opportunity to explore the episode-based approach for examining differences in costs among patients with different comorbidities undergoing treatment for their conditions. One such approach is Episode Treatment Group (ETG), a condition classification methodology that defines episodes of care for measurement of associated healthcare costs.16 ETG methodology has been vetted in actuarial science17-19 and in health economics and outcomes research.20 Episode Risk Group (ERG) is a medically meaningful metric to account for patient heterogeneity, which assesses risks of incurring costs according to comorbidities and medical complications.16

Given the gap in current literature regarding subgroups of real-world patients with NVAF who may incur different healthcare costs following initiation of dabigatran versus warfarin, we conducted exploratory modeling to assess whether ERG risk score and other patient characteristics were predictive of differential all-cause healthcare costs computed on an episode basis using ETG methodology among these 2 cohorts. We also examined traditional predictors of costs, namely patient demographics and Charlson Comorbidity Index (CCI) score, using a non–episode-based approach.

METHODS
Study Design and Data Source
This was a retrospective cohort study of commercial and Medicare Advantage with Part D enrollees. The study utilized administrative claims data from a large national US health plan from April 1, 2009, through November 30, 2013 (study period). All data were accessed in accordance with the Health Insurance Portability and Accountability Act rules.

Patient Identification and Study Cohorts
Patients with evidence of newly diagnosed NVAF initiating therapy with either dabigatran or warfarin were identified using enrollment data and medical and pharmacy claims from October 1, 2010, through November 30, 2012. Patients were selected for inclusion in a sequential manner:

1. Evidence of AF defined as at least 1 inpatient stay, 2 physician office visits, 2 emergency department (ED) visits, or a combination of office visit and ED visit on distinct service dates, with a diagnosis code for AF (International Classification of Diseases, Ninth Revision, Clinical Modification diagnosis code 427.31, in any position) from October 1, 2010, through August 31, 2012 (identification period).21 The AF index date was the date of the first qualifying claim with a diagnosis code for AF. Patients were aged ≥18 years as of AF index date, had 12 months continuous enrollment (no gaps >45 days) with medical and pharmacy benefits prior to AF index date, and had no medical claims with a diagnosis code for AF within 12 months prior to AF index date. 

2. Excluded were patients with ≥1 medical claim with evidence of valvular heart disease or hyperthyroidism (reversible cause of AF22) prior to AF index date, and patients with evidence of transient AF within 3 months prior to AF index date.  

3. Newly initiating OAC therapy with dabigatran or warfarin by meeting all of the following criteria: ≥1 pharmacy claim for warfarin or dabigatran on the AF index date or during the 3-month period following AF index date; the date of the first claim was defined as the OAC index date; continuous enrollment during the period of AF index date through OAC index date; and no pharmacy claims for any OAC for 12 months prior to OAC index date (baseline period).  

4. Remaining patients were required to have ≥30 days follow-up after OAC index date. The follow-up period began on the OAC index date and ended at the earliest occurrence of the following: (a) end of study period; (b) death; (c) switch to another OAC without a claim for ischemic stroke and/or bleed; (d) discontinuation of index OAC with a gap >30 days from the run-out of the last fill without a claim for ischemic stroke and/or bleed; (e) end of continuous enrollment in health plan; or (f) greater than 364 days following OAC index date. Twelve months follow-up is similar to recent studies comparing resource utilization and costs between dabigatran and warfarin cohorts;12,21 it also aligns with year budget allocation cycle by different payers and providers across the United States.

Patients were then assigned to 2 mutually exclusive study cohorts according to index OAC. Relevant codes for conditions used in patient selection are shown in eAppendix Table 1A (eAppendices available at AJPB.com).

Model Variables
Follow-up Healthcare Costs
Two measures of all-cause healthcare costs (combined health plan and patient paid amounts) were computed during the variable length of follow-up period: (a) episode-based total costs (all-cause medical and pharmacy) were determined using ETG methodology16 and included episode-based predictors of healthcare costs; (b) all-claims total costs (all-cause medical and pharmacy) were computed and only included non–episode-based predictors of healthcare costs. Both measures of costs were computed as per-patient per-month (PPPM) costs to adjust for variable length of follow-up. Costs were adjusted to 2013 US dollars using the annual medical care component of the Consumer Price Index to account for inflation between 2009 and 2013.23

Predictors of Healthcare Costs
Patient severity was captured using 2 measures: baseline CCI score for all-cause claims cost analysis and baseline ERG risk score for all-cause episode-based cost analysis. The CCI score24-26 is a proxy for likelihood of mortality according to the burden of comorbidity; scores were grouped as 0, 1-2, 3-4, and ≥5. The ERG risk score assesses the prospective risk of healthcare utilization and costs according to comorbidities and medical complications. ERG risk scores were determined using ETG methodology, which defines episode of care for measurement of healthcare costs using diagnosis, procedure, and revenue codes; and National Drug Code numbers to formulate clinically homogeneous episodes of care (eAppendix Figure 1A).16 The ETG methodology allows for case-mix adjustment, clinical homogeneity, episode building, concurrent and recurrent episodes, and shifting episodes.27 ETGs are then mapped to ERGs for each patient. Next, individual ERG risk scores are computed by summing weights assigned to each ERG and to the patient’s demographic and healthcare resource utilization profile.28 The ETG/ERG methodology is used by several health plans29-35 and allows for customized categorization of ERG scores, but there is no guidance in current literature on grouping ERG risk score into specific categories. For this study, scores were grouped, a priori, into 6 categories: ≤2.0; 2.1 to 4.0; 4.1 to 6.0; 6.1 to 8.0; 8.1 to 10.0; and >10.0. A score of 1.0 indicates risk comparable with that of the overall population, while a score of 2.0 or greater indicates a 2-fold or greater risk of higher healthcare resource utilization and costs.

Additional variables considered for inclusion as predictors in multivariable modeling of follow-up costs were age, sex, geographic region, health plan type, baseline healthcare costs, and durations of treatment delay and follow-up for the all-claim cost analysis. For the episode-based cost analysis, all but age, gender, and baseline healthcare costs were included because ERG risk score accounts for these measures.

Statistical Analysis
Between-cohort comparisons of baseline characteristics, durations of follow-up and treatment delay, and follow-up unadjusted healthcare costs were examined with t tests (for continuous variables) and χ2 tests (for categorical variables). Two predictive models of healthcare costs were developed: (1) the all-claims costs model, and (2) the episode-based costs model. To assess cohort differences in subgroups of patients, predictor variables representing interactions of cohort with patient characteristics were examined. Based on an a priori specified variables list, variables were entered using stepwise selection; P value thresholds of .15 and .20 were used for variable entry and exit into the model, respectively. There were 2 exceptions to the stepwise selection of variables: (1) cohort indicator was forced into models, and (2) if an interaction term (with cohort) satisfied P value thresholds for selection, the corresponding main effect (ie, noninteraction term) was also forced into models. For the all-claims model, predictor variables subject to stepwise selection were as follows (“*” denotes interaction): age group, cohort*age group, baseline CCI score group, cohort*baseline CCI score group, gender, cohort*gender, geographic region, cohort*geographic region, health plan type, cohort*health plan type, baseline healthcare costs group, cohort*baseline healthcare costs group, duration of treatment delay, cohort*duration of treatment delay, duration of follow-up period, and cohort*duration of follow-up period. For the episode-based costs model, predictor variables subject to stepwise selection were baseline ERG risk score category, cohort*baseline ERG risk score category, geographic region, cohort*geographic region, health plan type, cohort*health plan type, duration of treatment delay, cohort*duration of treatment delay, duration of follow-up period, and cohort*duration of follow-up period.

Development and validation of predictive models utilized bootstrap methods. Using N of study sample, 100 bootstrapped samples (random samples with replacement) were used to run generalized linear models with gamma distribution and log-link function.36,37 The concordance (c) index was computed to assess how well each model’s predicted costs agreed with actual costs. A c-index of 0.50 indicates that model prediction is no better than chance; a value >0.50 indicates that the model has predictive value; and a value <0.50 indicates that the model’s predictive value is worse than chance.

Statistically significant interactions with cohort (P <.05) were examined to determine patient characteristics predictive of differential costs between the 2 cohorts. Durations of treatment delay and follow-up (and their corresponding interactions with cohort) were entered into models using stepwise selection, though only for the purpose of model adjustment. Parameter estimates, 95% CIs, and P values were presented for predictors of each model. Estimated cost ratios (CRs) were derived from exponentiated parameter estimates. The Global Wald test was used to examine overall significance of polychotomous covariates and interaction terms. Statistical analyses were performed using SAS version 9.4 (SAS Institute Inc; Cary, North Carolina).

RESULTS
Patient Identification and Characteristics
A total of 15,182 patients with evidence of newly diagnosed NVAF who initiated OAC with dabigatran (n = 4150) or warfarin (n = 11,032) were included. Compared with the dabigatran cohort, the warfarin cohort was older (72.5 years vs 67.3 years), had higher mean CCI score (2.0 vs 1.4), and higher mean ERG risk score (5.6 vs 4.1) (all P <.001). Mean all-cause costs during baseline were also 59.1% higher ($26,240 vs $16,497; P <.001) among the warfarin cohort (Table 1).

Follow-Up All-Cause Episodes and Unadjusted Healthcare Costs
The total count of episodes was 31,906 in the dabigatran cohort and 100,502 in the warfarin cohort.
Unadjusted costs during follow-up did not differ between cohorts (eAppendix Table 1B). Mean PPPM costs were $3003 for the dabigatran cohort and $3223 for the warfarin cohort (P = .108); mean episode-based PPPM costs were $2807 for the dabigatran cohort and $2905 for the warfarin cohort (P = .412).

Cost Predictors
Predictors retained in the all-claims model and their associated cost ratios are shown in Table 2. The main effect for cohort was not a statistically significant predictor of follow-up PPPM costs (P = .635). Further, no interaction terms between cohort and patient characteristics were statistically significant. Statistically significant main effect variables predictive of lower costs were female gender and groups aged 65 and older. The adjusted c-index for the model was 0.64.

The main effect for cohort was also not a statistically significant predictor of PPPM costs (P = .208) in the episode-based model (Table 2). However, 3 interaction terms were statistically significant, indicating that costs differed between treatment cohorts depending on the characteristics of patients: cohort*baseline ERG risk score category (P = .017), cohort*geographic region (P = .047), and cohort*health plan type (P = .034). The adjusted c-index for the model was 0.60.

Further analysis of the association between cohort and all-cause costs within each ERG category (Table 3) revealed that compared with warfarin, the dabigatran cohort was associated with higher costs for ERG risk scores of 2.1 to 4.0 (CR, 1.14) and lower costs for risk scores of 6.1 to 8.0 (CR, 0.78). There were no statistically significant differences among cohorts for remaining ERG risk score categories.

DISCUSSION
Previous studies demonstrated that patients with newly diagnosed NVAF have similar average healthcare costs following initiation on dabigatran versus warfarin,9-12 wherein higher average medical resource utilization by patients on warfarin may offset their lower average pharmacy cost.38 However, current literature lacks guidance on identifying subgroups of patients with NVAF who may incur lower costs when initiated on these medications. This retrospective analysis explored the role of patient characteristics as predictors of differential healthcare costs in patients with NVAF who initiated therapy with dabigatran versus warfarin. Specifically, we explored subgroups of patients based on ERG risk scores or CCI scores that may influence all-cause costs for patients initiated on dabigatran versus warfarin. Compared with dabigatran patients, those initiated on warfarin were older, had greater risk of mortality (per CCI score), and higher baseline prospective risk of healthcare utilization (per ERG risk score). This finding suggests that, in a US managed care population, warfarin is more likely to be prescribed to older patients and to patients at higher risk for needing healthcare services and who, therefore, incur higher health-related costs. With the lower cost of warfarin, it is possible that older patients with Medicare coverage, taking several medications for multiple comorbidities, intend to minimize risk of entering a prescription drug plan coverage gap by managing pharmacy expenses. In addition, incentives provided by drug companies that often bring patients’ monthly drug cost to a minimum is only available for patients with commercial insurance, not those with Medicare and may, therefore, favor the use of drugs with lower costs among Medicare patients. However, this interpretation cannot be validated with the study because the claims database used does not capture relevant information.

This exploratory study adds to the body of literature examining characteristics of newly diagnosed patients with NVAF in clinical practice. First, both cost models found that main treatment effect for cohort was not statistically significant in predicting difference in total all-cause healthcare costs. Second, neither model found any trend in differences in all-cause costs across CCI score groups or ERG risk score categories favoring either cohort. While there were no statistically significant interactions among cohort and variables of interest in the all-claims model, in the episode-based model, dabigatran was associated with higher costs among patients with ERG risk score 2.1 to 4.0 and with lower costs with ERG risk score 6.1 to 8.0, compared with warfarin, indicating no linear trend in cost differences among cohorts across all 6 ERG risk score categories. As such, the possibility remains that newly diagnosed patients with NVAF, regardless of their CCI score or the ERG risk score subgroups to which they belong, may not incur different costs if treated with dabigatran versus warfarin. Interactions between treatment cohort and geographic region and, separately, health plan type, were also significant in the episode-based model. These interactions lend support to the possibility of differential cost profiles for dabigatran versus warfarin among subsets of patients.

Patient characteristics predictive of costs in cardiovascular disease have been well studied,39,40,41 and our study contributes to this body of research by examining the utility of ERG and CCI scores in predicting all-cause costs among newly diagnosed patients with NVAF who are initiated on dabigatran or warfarin. As a meaningful risk measure for incurring costs, ERG risk score may be a useful tool for identifying patients who could benefit from more aggressive disease and/or medical therapy management.35 However, application to specific diseases/therapies is a unique perspective in this study, and it has not been validated. Separately, the mix of medical comorbidities present in the dabigatran cohort versus the warfarin cohort may differ even when the ERG risk score categorization is the same. The authors recommend that the results of this study be emphasized as hypothesis-generating, and this application must be further validated with other OAC treatments (ie, rivaroxaban, apixaban), other retrospective populations, and prospective populations with randomization.

Limitations
The results of this study should be considered in the context of several limitations. ERG risk scores were grouped into 6 distinct categories; however, this categorization scheme is not an established methodology. ETG/ERG methodology relies on the accuracy and completeness of claims submitted for reimbursement. Missing or incorrect codes for important comorbidities would underestimate ERG risk score. The same would apply to diseases that were not coded but are included in CCI score (eg, liver disease, chronic pulmonary disease). Claims data lack certain clinical assessments that also may be important risk factors for healthcare utilization. For example, an important measure in determining congestive heart failure risk is left ventricular ejection fraction, which is not captured in claims data. Lab-based parameters such as time within therapeutic range, which measures the patient’s level of anticoagulation, can be calculated based on merging laboratory results data with administrative claims; however, missing data is frequently an issue. This lab-based measure is currently used to monitor and manage the risk of stroke and/or bleed with different therapeutic options in long-term care of patients with NVAF. However, the study intended to provide different perspectives in managing these patients with consideration of a prospective risk of healthcare costs that is easier to track and measure consistently across large patient populations by payers, integrated delivery networks, and accountable care organizations. It is likely that increasing ERG risk score would serve as a proxy marker for increased difficulty with warfarin management. As comorbidity burden increases, the capacity to maintain international normalized ratio (INR) within a therapeutic range decreases. Different clinical practice methods—lab practice in particular—may be applied to improve the safety and efficacy of warfarin therapy (ie, use of home monitoring devices for INR, use of dedicated anticoagulation management clinicians). These practices may have an underlying role among the subgroups as specified for ERG risk score categorization. The authors of the ROCKET AF study42 (a randomized trial of rivaroxaban versus warfarin that was designed to demonstrate noninferiority of rivaroxaban) conducted a post hoc analysis of their data to account for the variation in warfarin dosing that might have resulted from using home monitoring devices for INR by group of patients; the device was systematically undermeasuring INR and thus potentially introducing bias into the rates of bleeding complications in the warfarin group. Similar factors may have been at play that were missed in the current analysis; this is an inherent limitation of claims-based retrospective cohort study design.

The creation of predictors that were derived from a patient’s medical history relied on 1 year of baseline data only; conditions occurring outside baseline were not included in ERG risk score or CCI score. The a priori grouping of ERG risk scores into 6 categories might have limited the model in identifying the linear relationship in difference of costs across ERG risk categories.

There may have also been other, unmeasured factors (eg, patient behavioral/ socioeconomic characteristics, clinical practice) that may have influenced costs. Claims data do not indicate whether the patient took medications as prescribed. Although follow-up ended if there were gaps in index OAC supply for more than 30 days, measures of medication possession ratio during follow-up were not evaluated. Despite these limitations, the findings provide insight about ERG risk and CCI categories in predicting all-cause healthcare costs and establish the basis for future research in identifying newly diagnosed patients with NVAF who would incur differential all-cause healthcare costs following initiation of dabigatran versus warfarin.

CONCLUSIONS
This retrospective cohort study, based on a real-world sample of US patients with newly diagnosed NVAF, offers evidence for comparing dabigatran versus warfarin for different subgroups of ERG risk score. Adding to existing literature on this topic, the findings indicated that there was no definitive evidence of a trend in difference of total all-cause costs favoring dabigatran or warfarin across 6 ERG risk score categories employed in this study.  

1Health Economics & Outcomes Research, Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT; 2Health Economics and Outcomes Research, Optum, Inc, Eden Prairie, MN

Corresponding author: Sabyasachi Ghosh, MS Health Economics & Outcomes Research, Manager Boehringer Ingelheim Pharmaceuticals, Inc
900 Ridgebury Road, Ridgefield, CT 06877 Tel: (800) 243-0127 Fax: (203) 791-6234 E-mail: tito.ghosh@boehringer-ingelheim.com
Disclosure: Support for this work was provided by Boehringer Ingelheim Pharmaceuticals, Inc (BIPI). Drs Swindle and White were employees of Optum, Inc, which was contracted by BIPI to perform the study; employment was not contingent on this funding. Mr Ghosh, Dr Sander, and Dr Wang were employees of BIPI at the time of this study.


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Appendix A
Table 1. Codes and Descriptions Used to Identify Conditions and Procedures for Sample selection for Patients with Newly Diagnosed Non-valvular Atrial Fibrillation Initiating Treatment with Dabigatran or Warfarin. Optum Research Database, April 1, 2009 - November 30, 2013
Description Codes
 Valvular heart disease ICD-9-CM Diagnosis Codes
Mitral stenosis 394.0x
Mitral stenosis with insufficiency 394.2
Mitral valve stenosis and aortic valve stenosis 396
Mitral valve stenosis and aortic valve insufficiency 396.1
  ICD-9-CM Procedure Codes
Open and other replacement of unspecified heart valve 35.2
Open and other replacement of aortic valve 35.22
Open and other replacement of mitral valve 35.24
Open and other replacement of pulmonary valve 35.26
Open and other replacement of tricuspid valve 35.28
  CPT Codes
Unlisted procedure, cardiac surgery 33999
Implantation of catheter-delivered prosthetic aortic heart valve; open thoracic approach 0257T
Transthoracic cardiac exposure (e.g., sternotomy, thoracotomy, subxiphoid) for catheter-delivered aortic valve replacement; without cardiopulmonary bypass 0258T
Transthoracic cardiac exposure (e.g., sternotomy, thoracotomy, subxiphoid) for catheter-delivered aortic valve replacement; with cardiopulmonary bypass 0259T
Replacement, aortic valve, with cardiopulmonary bypass; with prosthetic valve other than homograft or stentless valve 33405
Valvuloplasty, mitral valve, with cardiopulmonary bypass 33425
Valvuloplasty, mitral valve, with cardiopulmonary bypass; with prosthetic ring 33426
Valvuloplasty, mitral valve, with cardiopulmonary bypass; radical reconstruction, with or without ring 33427
Replacement, mitral valve, with cardiopulmonary bypass 33430
Implantation of catheter-delivered prosthetic pulmonary valve, endovascular approach 0262T
Replacement, pulmonary valve 33475
Valvectomy, tricuspid valve, with cardiopulmonary bypass 33460
Valvuloplasty, tricuspid valve; without ring insertion 33463
Valvuloplasty, tricuspid valve; with ring insertion 33464
Replacement, tricuspid valve, with cardiopulmonary bypass 33465
  ICD-9-CM Diagnosis Codes
Hyperthyroidism 242.x
Ischemic stroke 433.x1, 434.x1, 436
(first-listed position only)
Major bleed  
Intracranial hemorrhage 430.xx, 431.xx, 432.xx, 852.0x, 852.2x, 852.4x, 853.0
(any position)
Gastrointestinal bleeding 455.2, 455.5, 455.8, 456.0, 456.20,459.0, 530.7, 530.82, 531.0, 531.2, 531.4, 531.6, 532.0, 532.2, 532.4, 532.6, 533.0, 533.2, 533.4, 533.6, 534.0, 534.2, 534.4, 534.6, 535.01, 535.11, 535.21, 535.31, 535.41, 535.51, 535.61, 537.83, 562.02, 562.03, 562.12, 562.13, 568.81, 569.3, 569.85, 578
(first-listed position only)
Other bleeding 599.7, 719.1x, 786.3, 423.0, 593.81, 784.7, 784.8
(first-listed position only)

CPT = Current Procedural Terminology; ICD-9-CM = International Classification of Diseases Ninth Revision Clinical Modification


Figure 1. Assignment of Episode Risk Score using Episode Treatment Group/Episode Risk Group methodology

















ERG=Episode Risk Group; ETG=Episode Treatment Group

Appendix B
Table 1. Unadjusted Per-patient-per-month (PPPM) All-claims and Episode-based Costs of Patients with Newly Diagnosed Non-Valvular Atrial Fibrillation Initiating Treatment with Dabigatran or Warfarin
  All Patients
(n=15,182)
Dabigatran
(n=4,150)
Warfarin
(n=11,032)
P-valuea
Follow-up PPPM all-claims healthcare costs, $        
Mean (SD) 3,163 (7,749) 3,003 (7,398) 3,223 (7,877) 0.108
Median 1,174 1,182 1,170 <0.001
Follow-up PPPM episode-based healthcare costs,$,         
Mean (SD) 2,878 (6,230) 2,807 (6,810) 2,905 (5,998) 0.412
Median 1,099 1,101 1,098 0.005
a By t-test for means and Wilcoxon test for medians