Assessing Safety of Direct Thrombin Inhibitors, Direct Factor Xa Inhibitors and Vitamin K Antagonists in Patients with Atrial Fibrillation: A Nation-Wide Propensity Score Matched Cohort from Sweden.

PURPOSE: To evaluate associations between first-time use of direct oral anticoagulants or vitamin K antagonists and bleeding risk or mortality in the elderly with atrial fibrillation in a real-world setting in Sweden. PATIENTS AND METHODS: The study population comprises first-time users, above age 60, of dabigatran, apixaban, rivaroxaban, or warfarin, with first atrial fibrillation occurrence within 6 months before dispensing (2012-2016). Outcomes were gastrointestinal, any, or intracranial bleeding, and mortality. Exposure started at first dispensing of a study drug. Follow-up continued until outcome, end of drug supply, dispensing of another study drug, death or end of study (December 2016). We conducted a propensity score matched, nationwide register-based cohort study including three treatment groups: direct thrombin inhibitors, direct factor Xa inhibitors and vitamin K antagonists, each compared to the other two, focusing on subgroups of age and sex. Cox proportional hazard models adjusted for CHA2DS2VASc and HAS-BLED scores provided hazard ratios with 95% confidence intervals.
RESULTS: The matched study populations consisted of 7,264 patients for the direct thrombin inhibitors vs vitamin K antagonists comparison, 12,566 patients for the direct factor Xa inhibitors vs vitamin K antagonists comparison and 6,606 patients for the direct factor Xa inhibitors vs direct thrombin inhibitors comparison, in total 26,436 patients. Numerically high, but imprecise, hazard ratios for gastrointestinal bleeding were observed for women aged 75-80, 80-85, or above 85 years, eg 6.00 (1.02, 113.47) for direct thrombin inhibitors vs vitamin K antagonists. For both sexes, numerically high hazard ratios for any bleeding were observed in ages 80-85, or above 85 years, eg 2.90 (1.01, 10.41) for direct thrombin inhibitors vs vitamin K antagonists. Numerically high HRs for intracranial bleeding were observed for women aged 75-80 or 80-85 years, eg 2.70 (0.65, 18.19) for direct factor Xa inhibitors vs vitamin K antagonists. Excess mortality was observed in both sexes, across age groups, for naive and experienced anticoagulant users.
CONCLUSION: The observed increased gastrointestinal bleeding risk in first-time users of direct thrombin inhibitors or direct factor Xa inhibitors is consistent with previous studies. The possible risk of excess mortality merits further studies.

Introduction

Atrial fibrillation (AF) is a potent risk factor for stroke and an important cause of mortality. The prevalence of AF in Sweden was 2.9% in 2010 for ages 20 years and above, rising with age, up to 14.3% by age 84 years.1 Lindberg et al found the prevalence of AF to be 4.9% among a cohort aged 60 years or older.2

Earlier, warfarin was the most common treatment in patients with AF for the prevention of stroke, but nowadays the direct oral anticoagulants (DOACs) have gained use. The direct thrombin inhibitor (DTI) dabigatran has been available for stroke prevention in AF in Sweden since December 2011. The direct factor Xa inhibitors (Xabans) rivaroxaban and apixaban have been available since September 2008 and May 2012, respectively.

There are several benefits with DOACs such as its simple fixed-dose regimen, no routine laboratory monitoring due to reduced variability in the anticoagulation effect, and potentially fewer drug interactions.3–5 However, there are reports on major bleedings, more specifically gastrointestinal bleedings associated with DOACs, especially in elderly users and users with renal impairment.6–9 Further, real-world data regarding bleeding risks have been conflicting.7,10–12

The randomized evaluation of long-term anticoagulation therapy (RE-LY) study found that compared to warfarin, dabigatran 150 mg was superior with respect to stroke and systemic embolism and similar with respect to major bleedings, and that dabigatran 110 mg was similar with respect to stroke and systemic embolism and superior with respect to major bleedings.13 In the Apixaban for Reduction in Stroke and Other Thromboembolic Events in Atrial Fibrillation (ARISTOTLE) trial, it was found that apixaban was superior to warfarin with respect to stroke, systemic embolism, bleedings, and mortality.14 In the Rivaroxaban Once Daily Oral Direct Factor Xa Inhibition Compared with Vitamin K Antagonism for Prevention of Stroke and Embolism Trial in Atrial Fibrillation (ROCKET AF), it was demonstrated that rivaroxaban was noninferior to warfarin for stroke and systemic embolism, and no significant difference of major bleedings was found.15

The aim of the current study was to evaluate the association between first-time use of DOACs or vitamin K antagonists (VKAs) and the risk for bleedings and all-cause mortality in elderly patients diagnosed with AF, in a real-world clinical setting in Sweden.

Patients and Methods

Data Sources

The study population was derived through linkage of national population-based registers, enabled via the unique identification number assigned to each citizen.16 In 2016 the Swedish population comprised almost 10 million people.

The Swedish patient register (NPR) started in 1964. The inpatient part of the register gained full coverage from 1987 and information from outpatients was included starting from 2001. The validity of the register is high with positive predictive values generally 85–95% for the majority of diagnoses.17 From NPR (using inpatient data from 1997 and outpatient data from 2001) information about AF, bleeding outcomes, comorbidities, CHA2DS2VASc, and HAS-BLED scores () were retrieved using the International Classification of Diseases 10th revision (ICD-10). Hospitalization days and the number of visits to specialized care were also obtained from NPR.

The Swedish prescribed drug register (PDR) started in July 2005 and contains all community pharmacy dispensed medicines recorded by the Anatomic Therapeutic Chemical Classification system (ATC).18 Using PDR we retrieved dispensing data on dabigatran (ATC: B01AE07), apixaban (ATC: B01AF02), rivaroxaban (ATC: B01AF01), warfarin (ATC: B01AA03), other anticoagulants and other drugs ( and ). We also retrieved data on dispensing county, private clinic prescriber, and urban area living from PDR. The Swedish cancer register provided information on any cancer (ICDO2/3 codes: C00-D48) from 1997 onwards. From the Swedish register of care and social services for the elderly and for persons with impairments, we retrieved information on certain municipal services. Level of education was retrieved from the Swedish education register and the date of death was retrieved from the Swedish cause of death register.

Study Design and Population

We conducted a propensity score matched, nationwide register-based cohort study in Sweden with data covering 1 December 1997 to 31 December 2016. Essentially, in Sweden 2012–2016, VKAs equal warfarin, DTIs equal dabigatran etexilate and Xabans equal rivaroxaban and apixaban. The study population comprised first-time users, above the age of 60, of DTIs, Xabans, or VKAs, with the first-time occurrence of AF (ICD-10: I48) within 6 months before dispensing date (January 2012 – November 2016). Exclusion criteria were: hip or knee surgery (surgical codes NF and NG) within 5 weeks before dispensing, or any of the following conditions: stroke (I61-I64), deep vein thrombosis (I80.2) pulmonary embolism (I26), bleedings (), inherited or acquired bleeding disorders (D564, D58, D66, D67, D680, D681, D682, D684, D685), any cancer within 6 months before dispensing, or hospitalized at dispensing.

Exposure

Start of exposure was the date of the first dispensing of either dabigatran, apixaban, rivaroxaban, or warfarin (index date). Patients were followed until the occurrence of an outcome, end of the supply of the index drug, dispensing of another study drug, death or end of study (31 December 2016). Duration of each dispensing was calculated as the dispensing date plus the number of days supplied according to the WHO defined daily dose.19 For a subsequent dispensing to count as continuous supply, a maximum gap of 75 days, capturing 90% of all refills, was allowed between two dispensing dates, overlapping duration was cut short.

Outcomes

The primary outcome was gastrointestinal bleeding. Secondary outcomes were intracranial bleeding, any bleeding (a composite of other bleeding, gastrointestinal bleeding and intracranial bleeding) and all-cause mortality ().

Statistical Analysis

The main analysis was subgrouped by age and sex simultaneously. We also performed analyses for one-way subgroupings: sex, age or previous use of other anticoagulants (experienced: within 2 years, naïve: more than 2 years). Baseline characteristics were reported by means and standard deviations for quantitative characteristics and with frequencies and proportions for qualitative characteristics.

We included three treatment groups; DTIs, Xabans and VKAs. Each group was compared to the other two, resulting in DTIs vs VKAs, Xabans vs VKAs and Xabans vs DTIs. In order to assure balanced characteristics, separate propensity score (PS) 1:1 matching was employed for each of the three comparisons before analyzing. Patients were matched selected randomly with no replacement using PS matching based on a greedy matching algorithm with 0.09 as the largest distance between matches.20 PS was obtained from logistic regression models with the following baseline information (recorded ever before dispensing date) included: age (60–74, 75–79, 80–84 and 85+ years), dispensing county (21 counties), urban city living (yes/no), education (9-year compulsory school, high school, tertiary education and missing), dispensing period (quarters 2012–2016), private clinic (yes/no), number of hospitalization days (1–3, 4–10, >10), number of visits in specialized care (1–3, 4–10, >10), granted hours of municipal services (<45, 45–90, >90), indicators of vascular disease, congestive heart failure, transient ischemic attack, embolism, diabetes, hypertension, alcohol abuse, renal disease, abnormal renal and hepatic function, staying at a nursing home, simultaneous intake of more than five other drugs (), indicators (yes/no) of aspirin, clopidogrel, non-steroidal anti-inflammatory, antidepressant, antibiotic and antiarrhythmic drugs. The PS matching was evaluated by standardized distances between the matched groups and judged to be nonequivalent if the difference was greater than 0.25 standard deviations.

Cox proportional hazard models adjusted for CHA2DS2VASc and HAS-BLED scores were used to calculate hazard ratios (HR) with 95% confidence intervals (CI) corresponding to a 5% significance level with days since index date as time-scale. The assumption of proportional hazards was tested through an interaction term between the logarithm of time to the event and the exposure. All analyses were performed with SAS® Enterprise Guide, Version 7.1 (SAS Institute Inc., Cary, NC, USA)

Ethical Approval

The current research was performed by employees at the Swedish National Board of Health and Welfare (NBHW) in collaboration with employees at Karolinska Institutet. NBHW is a government agency and may, in accordance with Swedish law, use population-based registers to follow and analyze health and social conditions among the population without the requirement of ethical permission.

Results

The eligible population comprised 4,384 first time DTI users, 21,944 first time VKA users and 19,349 first time Xabans users. The matched study populations consisted of 7,264 patients for the DTIs vs VKAs comparison, 12,566 patients for the Xabans vs VKAs comparison and 6,606 patients for the Xabans vs DTIs comparison (Figure 1), in total 26,436 patients.

Figure 1

Flow chart of the study population. All patients were 60 years of age or older and with a diagnosis of atrial fibrillation within 6 months before start of treatment with dabigatran, direct factor Xa inhibitors or with warfarin.

Characteristics of the Study Populations

Table 1 presents the baseline characteristics of first-time users of DTIs, Xabans and VKAs. Standardized differences are presented in .

Table 1

Baseline Characteristics for All Included, Matched Individuals by Propensity Score Matched Cohorts and Index Drug. All Patients Were 60 Years of Age or Older and with a Diagnosis of Atrial Fibrillation Within 6 Months Before Start of Treatment with Direct Thrombin Inhibitors, Direct Factor Xa Inhibitors or with Vitamin K Antagonists

Characteristics	Direct Thrombin Inhibitors vs Vitamin K Antagonists		Direct Factor Xa Inhibitors vs Direct Thrombin Inhibitors		Direct Factor Xa Inhibitors vs Vitamin K Antagonists
	DTI	VKA	XAB	DTI	XAB	VKA
Total, n	3632	3632	3303	3303	6283	6283
Age, mean (SD)	72.8 (7.7)	73.1 (7.8)	73.0 (7.7)	72.7 (7.7)	75.6 (8.5)	75.6 (8.3)
Female, n (%)	1705 (46.9%)	1714 (47.2%)	1545 (46.8%)	1557 (47.1%)	3120 (49.7%)	3125 (49.7%)
CHA2DS2VASc,a mean (SD)	3.0 (1.5)	3.0 (1.5)	2.9 (1.5)	2.9 (1.5)	3.4 (1.6)	3.4 (1.6)
Modified HAS-BLED,b mean (SD)	2.2 (1.0)	2.2 (1.0)	2.1 (1.0)	2.1 (1.0)	2.4 (1.1)	2.4 (1.1)
Hospitalization (days), mean (SD)	0.9 (3.1)	0.9 (3.3)	0.9 (2.9)	0.9 (3.1)	1.4 (4.0)	1.4 (4.0)
Municipal services (hours), mean (SD)	1.3 (10.2)	1.1 (9.2)	1.1 (8.6)	1.4 (10.1)	2.6 (14.5)	2.7 (14.9)
Number of simultaneous drugs, mean (SD)	5.3 (2.9)	5.4 (3.0)	5.2 (2.9)	5.3 (2.9)	5.9 (3.1)	6.0 (3.2)
Number of visits in specialized care, mean (SD)	1.3 (2.0)	1.3 (2.0)	1.1 (1.9)	1.1 (1.9)	1.0 (1.9)	1.0 (1.9)
Private clinic, n (%)	100 (2.8%)	93 (2.6%)	131 (4.0%)	126 (3.8%)	64 (1.0%)	58 (0.9%)
Urban living, n (%)	1818 (50.1%)	1819 (50.1%)	1602 (48.5%)	1620 (49.0%)	2906 (46.3%)	2830 (45.0%)
Education
9-year compulsory, n (%)	1134 (31.2%)	1121 (30.9%)	967 (29.3%)	996 (30.2%)	2379 (37.9%)	2362 (37.6%)
High school, n (%)	1361 (37.5%)	1393 (38.4%)	1272 (38.5%)	1255 (38.0%)	2492 (39.7%)	2440 (38.8%)
Tertiary education, n (%)	1092 (30.1%)	1067 (29.4%)	1019 (30.9%)	1015 (30.7%)	1341 (21.3%)	1396 (22.2%)
Missing, n (%)	45 (1.2%)	51 (1.4%)	45 (1.4%)	37 (1.1%)	71 (1.1%)	85 (1.4%)
Comorbidities
Abnormal renal function, n (%)	68 (1.9%)	63 (1.7%)	45 (1.4%)	55 (1.7%)	344 (5.5%)	328 (5.2%)
Abnormal hepatic function, n (%)	6 (0.2%)	7 (0.2%)	7 (0.2%)	6 (0.2%)	23 (0.4%)	16 (0.3%)
Alcohol intake, n (%)	121 (3.3%)	125 (3.4%)	105 (3.2%)	104 (3.1%)	170 (2.7%)	158 (2.5%)
Bleedings, n (%)	446 (12.3%)	451 (12.4%)	434 (13.1%)	418 (12.7%)	938 (14.9%)	948 (15.1%)
Congestive heart failure, n (%)	755 (20.8%)	763 (21.0%)	629 (19.0%)	638 (19.3%)	1697 (27.0%)	1667 (26.5%)
Diabetes, n (%)	496 (13.7%)	485 (13.4%)	423 (12.8%)	427 (12.9%)	1023 (16.3%)	1015 (16.2%)
Disorders of thyroid gland, n (%)	330 (9.1%)	330 (9.1%)	288 (8.7%)	299 (9.1%)	597 (9.5%)	590 (9.4%)
Embolism, n (%)	27 (0.7%)	32 (0.9%)	23 (0.7%)	25 (0.8%)	64 (1.0%)	61 (1.0%)
Hepatic disease, n (%)	61 (1.7%)	61 (1.7%)	50 (1.5%)	51 (1.5%)	124 (2.0%)	107 (1.7%)
Hypertension, n (%)	2409 (66.3%)	2428 (66.9%)	2108 (63.8%)	2132 (64.5%)	4483 (71.4%)	4498 (71.6%)
Ischemic stroke, n (%)	151 (4.2%)	137 (3.8%)	129 (3.9%)	133 (4.0%)	328 (5.2%)	317 (5.0%)
Peripheral arterial disease, n (%)	132 (3.6%)	141 (3.9%)	126 (3.8%)	110 (3.3%)	328 (5.2%)	324 (5.2%)
Renal disease, n (%)	64 (1.8%)	56 (1.5%)	40 (1.2%)	49 (1.5%)	328 (5.2%)	313 (5.0%)
Transient ischemic attack, n (%)	160 (4.4%)	163 (4.5%)	137 (4.1%)	142 (4.3%)	335 (5.3%)	343 (5.5%)
Vascular disease, n (%)	317 (8.7%)	323 (8.9%)	289 (8.7%)	282 (8.5%)	817 (13.0%)	810 (12.9%)
Comedication
Antiarrhythmics, n (%)	84 (2.3%)	87 (2.4%)	64 (1.9%)	59 (1.8%)	189 (3.0%)	212 (3.4%)
Antibiotics, n (%)	1 (0.0%)	2 (0.1%)	0 (0.0%)	1 (0.0%)	1 (0.0%)	2 (0.0%)
Antidepressants, n (%)	194 (5.3%)	204 (5.6%)	186 (5.6%)	180 (5.4%)	396 (6.3%)	385 (6.1%)
Antimycotics, n (%)	1 (0.0%)	0 (0.0%)	0 (0.0%)	1 (0.0%)	1 (0.0%)	0 (0.0%)
Low dose acetylsalicylic acid, n (%)	1243 (34.2%)	1257 (34.6%)	1005 (30.4%)	998 (30.2%)	2232 (35.5%)	2223 (35.4%)
Clopidogrel, n (%)	110 (3.0%)	103 (2.8%)	95 (2.9%)	89 (2.7%)	281 (4.5%)	287 (4.6%)
NSAIDs,c n (%)	204 (5.6%)	194 (5.3%)	180 (5.4%)	185 (5.6%)	302 (4.8%)	301 (4.8%)
Other previous anticoagulants, n (%)	1725 (47.5%)	1749 (48.2%)	1470 (44.5%)	1444 (43.7%)	3252 (51.8%)	3283 (52.3%)
Steroids, n (%)	142 (3.9%)	144 (4.0%)	141 (4.3%)	124 (3.8%)	304 (4.8%)	311 (4.9%)

Notes: aScore based on congestive heart failure, hypertension, age, diabetes, stroke, vascular disease and sex. bScore based on hypertension, abnormal renal function, abnormal hepatic function, stroke, bleedings, age, medicines and alcohol intake. cAnti-inflammatory and antirheumatic products, non-steroids.

Abbreviations: DTI, direct thrombin inhibitors; VKA, vitamin K antagonists; XAB, direct factor Xa inhibitors.

Analytical results

We analyzed one primary and three secondary outcomes, each for DTIs vs VKAs, Xabans vs DTIs and Xabans vs VKAs. The main analysis was subgrouped by sex and age category simultaneously, Table 2. Additional analyses were subgrouped by sex, age category or user status (naïve, experienced), . All results are given as HRs with 95% CIs. Only results from the main analysis for comparisons with VKAs are listed as text.

Table 2

Hazard Ratios with 95% Confidence Intervals, for Each Outcome and Comparison, by Sex and Age. All Patients Were 60 Years of Age or Older and with a Diagnosis of Atrial Fibrillation Within 6 Months Before Start of Treatment with Direct Thrombin Inhibitors, Direct Factor Xa Inhibitors or with Vitamin K Antagonists

Outcome	Comparison	Men				Women
		60–74	75–79	80–84	85+	60–74	75–79	80–84	85+
Bleedings	DTI vs VKA	0.76 (0.53, 1.09)	0.62 (0.37, 1.05)	2.90* (1.01, 10.41)	2.42 (0.72, 10.94)	0.88 (0.52, 1.50)	1.45 (0.72, 3.05)	1.13 (0.47, 2.73)	0.84 (0.33, 2.10)
	XAB vs VKA	0.75 (0.53, 1.04)	0.89 (0.57, 1.38)	1.40 (0.79, 2.56)	1.28 (0.74, 2.25)	0.85 (0.55, 1.33)	1.62 (0.90, 3.02)	1.89* (1.03, 3.65)	0.99 (0.63, 1.56)
	XAB vs DTI	1.03 (0.68, 1.57)	1.27 (0.66, 2.49)	1.31 (0.56, 3.22)	1.68 (0.64, 4.80)	1.25 (0.64, 2.48)	1.24 (0.66, 2.39)	1.17 (0.54, 2.62)	1.70 (0.64, 4.97)
Gastro-intestinal bleeding	DTI vs VKA	0.80 (0.35, 1.79)	0.55 (0.17, 1.70)	0.95 (0.11, 7.93)	1.60 (0.15, 34.46)	1.97 (0.90, 4.60)	2.29 (0.67, 10.40)	6.00* (1.02, 113.47)	1.52 (0.25, 11.58)
	XAB vs VKA	0.65 (0.31, 1.30)	0.72 (0.31, 1.65)	1.96 (0.65, 7.20)	0.89 (0.32, 2.55)	0.67 (0.27, 1.63)	3.19* (1.01, 14.02)	1.30 (0.48, 3.86)	1.34 (0.65, 2.93)
	XAB vs DTI	0.90 (0.40, 2.02)	1.04 (0.29, 3.74)	1.61 (0.28, 12.30)	0.59 (0.03, 6.18)	0.39 (0.11, 1.18)	0.98 (0.36, 2.69)	0.54 (0.14, 1.90)	2.16 (0.60, 10.05)
Intracranial bleeding	DTI vs VKA	0.65 (0.24, 1.71)	0.14* (0.01, 0.84)	NE	NE	0.47 (0.02, 4.91)	1.22 (0.29, 6.09)	0.76 (0.03, 19.45)	0.37 (0.02, 3.97)
	XAB vs VKA	0.47 (0.20, 1.03)	0.95 (0.31, 2.97)	1.04 (0.23, 5.33)	0.86 (0.22, 3.50)	1.01 (0.37, 2.84)	1.22 (0.37, 4.71)	2.70 (0.65, 18.19)	0.68 (0.23, 2.01)
	XAB vs DTI	0.92 (0.17, 5.00)	3.03 (0.39, 61.27)	0.84 (0.03, 21.23)	0.96 (0.04, 24.33)	NE	1.18 (0.20, 9.02)	1.53 (0.14, 33.05)	NE
Death	DTI vs VKA	2.85* (1.20, 7.83)	0.57 (0.23, 1.37)	1.36 (0.22, 10.39)	1.37 (0.45, 4.55)	6.71* (1.20, 125.51)	2.55 (0.73, 11.74)	6.24* (1.03, 119.90)	2.05 (0.66, 7.57)
	XAB vs VKA	1.99* (1.11, 3.76)	1.51 (0.75, 3.24)	1.21 (0.64, 2.33)	2.91* (1.55, 5.96)	1.70 (0.76, 4.17)	1.15 (0.47, 2.95)	1.84 (0.85, 4.41)	2.03* (1.31, 3.26)
	XAB vs DTI	0.83 (0.41, 1.65)	1.10 (0.39, 3.16)	4.57* (1.16, 30.31)	1.10 (0.40, 3.15)	1.60 (0.53, 5.31)	0.88 (0.28, 2.71)	1.41 (0.49, 4.62)	1.81 (0.81, 4.42)

Note: *Statistically significant at the 5% significance level.

Abbreviations: DTI, direct thrombin inhibitors; VKA, vitamin K antagonists; XAB, direct factor Xa inhibitors; NE, not estimable.

Gastrointestinal Bleeding

In general, the numerically highest HRs were observed for women in the age categories; 75–80, 80–85 and above 85 years of age. In particular, for DTIs vs VKAs, the numerically highest HRs were seen for women in the age groups below 75, 75–80 and 80–85; 1.97 (0.90, 4.60), 2.29 (0.67, 10.40) and 6.00 (1.02, 113.47), respectively. Conversely, the numerically lowest HR was observed for men 75–80 years, 0.55 (0.17, 1.70). For Xabans vs VKAs, the numerically highest HRs were observed for women 75–80 years and for men 80–85 years; 3.19 (1.01, 14.02) and 1.96 (0.65, 7.20), respectively. The numerically lowest HR 0.65 (0.31, 1.30) was seen for men 60–75 years.

Any Bleeding

In general, the numerically highest HRs were observed in the highest age groups 80–85 and above 85 years for both sexes. In particular, for DTIs vs VKAs, the numerically highest HRs were observed for men in the age groups 80–85 and above 85 years; 2.90 (1.01, 10.41) and 2.42 (0.72, 10.94), respectively. Conversely, the numerically lowest HR 0.62 (0.37, 1.05) was seen for men 75–80 years. For Xabans vs VKAs, the numerically highest HRs were observed for women in the age groups 75–80 and 80–85, 1.62 (0.90, 3.02) and 1.89 (1.03, 3.65), respectively.

Intracranial Bleeding

In general, the numerically highest HRs were observed for women in the higher age categories; 75–80 and 80–85 years of age. In particular, for DTIs vs VKAs, a numerically low HR 0.14 (0.01, 0.84) was observed for men 75–80 years of age. For Xabans vs VKAs, a numerically high HR 2.70 (0.65, 18.19) was observed for women 80–85 years and a numerically low HR 0.47 (0.20, 1.03) for men 60–75 years.

Mortality

For mortality, no general pattern was observed. In particular, for DTIs vs VKAs, numerically high, but imprecise, HRs were seen for women 60–75 and 80–85 years of age; 6.71 (1.20, 125.51) and 6.24 (1.03, 119.90), respectively. Also, a numerically low HR 0.57 (0.23, 1.37) was observed for men 75–80 years. For Xabans vs VKAs, a numerically high HR 2.91 (1.55, 5.96) was observed for men above 85 years.

Discussion

Even though there are a plethora of studies on DOACs already published, few comprise large, Nordic, unselected populations of patients with AF from nationwide registers including all available DOACs simultaneously to compare bleeding outcomes between each DOAC class and VKAs, additionally describing sex and age differences. In this observational nationwide register study, we found the following statistically significant associations of increased risk at the 5% level when comparing DTIs or Xabans with VKAs: gastrointestinal bleeding in women, overall and in age groups 75–80 and 80–85; any bleeding in both men and women 80–85 years of age, and also overall for the age group 80–85 years; all-cause mortality in both sexes, across different age groups and for both naive and experienced users. However, part of the risks may be attributed to the patient characteristics and could be a consequence of confounding by indication.21 The differences between the reported results in this and previous studies may also lie in different methodological approaches.

Case reports have raised awareness about the risk of gastrointestinal bleedings associated with dabigatran.6,8,22 For apixaban and rivaroxaban, there are less reports on gastrointestinal bleedings.23,24 A meta-analysis including 43 randomized controlled trials showed an increased risk for gastrointestinal bleedings in patients treated with new oral anticoagulants for venous thromboembolism or acute coronary syndrome.25 A French nationwide propensity matched cohort study showed no difference in bleeding or other outcomes between VKAs and DOACs, suggesting equal caution to be exercised by physicians in both groups.12 However, a retrospective study of commercially insured people in the US found no significant risk for gastrointestinal bleedings when comparing dabigatran or rivaroxaban with warfarin. They noted that the excess risk of gastrointestinal bleedings with dabigatran relative to warfarin reported in other studies may be age dependent and concentrated among the oldest, a population that was not well represented in their study.10 Similarly, a retrospective propensity matched study based on administrative claims data in the US showed similar gastrointestinal bleeding risks in dabigatran or rivaroxaban and warfarin.26 A Danish study, with a similar design to ours, showed no risk of gastrointestinal bleedings associated with low- or high-dose dabigatran use.11 This could be due to differing administrations of DOACs or due to the underreporting of adverse events of the new oral anticoagulants, though a third Danish nationwide cohort study described that oral anticoagulant naïve dabigatran users initiated proton pump inhibitors more often than those treated with warfarin.27 A Food and Drug Administration study of Medicare beneficiaries found an increased risk of gastrointestinal bleedings in new users of dabigatran compared to warfarin in elderly patients with non-valvular atrial fibrillation.7 The present study found more than two-fold risks for gastrointestinal bleedings associated with DTIs or Xabans as compared to VKAs among female patients aged 75–80 or 80–85 years with AF. Graham et al also reported a two-fold increased risk of gastrointestinal bleedings in women aged 85 years and older.7 A meta-analysis including eight studies comprising 9,417 patients concluded that women suffer more bleeding complications compared to men when using a DOAC for venous thromboembolism.28 This indicates that greater attention should be given in DOAC treated women with non-valvular AF.

The present study could not find any elevated bleeding risk with respect to user status (naïve or experienced). A short-term observational Danish study among patients with AF indicated an association between bleeding risk and VKA experience status for the 110 mg dose of dabigatran.29 A sub-study of the RE-LY trial found no difference in bleeding risk when comparing VKA-experienced with VKA-naïve users.30 Nevertheless, another Danish register study showed an increased risk of gastrointestinal bleedings among VKA initiators of warfarin, but no excess risk of bleedings when comparing dabigatran to warfarin users irrespective of VKA experience.31

Nathan et al performed reviews of case reports of bleeding events involving dabigatran, Xabans and warfarin in the food and drug administration adverse event reporting system and found a signal between DOAC use and life-threatening or serious bleeding.32 The present study found a more than two-fold risk of any bleeding for men 80–85 or 85 and above years of age.

Eikelboom et al found that dabigatran compared to warfarin had lower risks of intracranial bleeding.33 In our study, we found a protective effect of dabigatran over warfarin for men 75–80 years of age. On the other hand, we found a more than two-fold risk of intracranial bleeding associated with Xabans as compared to VKAs in women 80–85 years of age.

The Medicare study noted a significant 87% risk of all-cause mortality in patients more than or equal to 75 years in association with dabigatran use. In a large meta-analysis, the new oral anticoagulants were significantly associated with a lower risk of mortality.34 The current study found excess risks of mortality for both DTIs and Xabans as compared to VKAs in both sexes and varying age groups.

The current study used nationwide data from well-characterized registers precluding recall bias. It only included first-time users of DTIs, Xabans or VKAs, given the potential risk of channeling toward DTIs or Xabans due to previous compliance problems or adverse effects with VKAs. We compared DTIs and Xaban users separately and did not combine the two classes since they might have different risk profiles. The use of propensity scores enabled well-balanced comparison groups.

This was a real-world study using national registers; therefore, residual confounding cannot be ruled out. There is no information available in the national registers on time in therapeutic range (TTR) for warfarin users. Lack of knowledge on TTR precludes analyses of good and poorly controlled warfarin users and their bleeding risk. It has been shown that high values of TTR correlate with a reduction in complications such as bleeding and thrombosis.35 However, it has been reported that TTR of warfarin users in Sweden is high (mean value 76.2%) compared to TTR in some clinical trials.13,35,36 We did not have access to the prescribed dose and prescriptions may be guided by the patients bleeding risk and hence other doses than the recommended may be used as presented in a French study.12 The definition of diseases relied on ICD-10 codes from hospital care and since some diseases are diagnosed in primary care (not included in NPR) the study might have missed milder cases of AF. However, it has been shown that only 12% of the AF diagnoses in Stockholm county council (2006–2010) are covered exclusively by primary care, ie 88% of the diagnoses were captured.37 For hypertension, it has been shown that the specificity defined through the prescription of at least two classes of antihypertensive drugs was almost 95%.38 The CHA2DS2VASc and HAS-BLED scores were based on recorded diagnoses and may be underestimated. However, this approach has been used successfully in previous studies and was adopted for comparative reasons.11,27,31,39 We investigated the objectives in an incident cohort and have not estimated risks in switchers, also we compared only drug classes, not specific drugs. The study did not have information on some lifestyle factors related to the outcomes, such as body mass index, smoking, physical activity, hemoglobin levels and alcohol consumption. Lastly, the present results are based on filled prescriptions assuming adherence.

Conclusion

The results are consistent with previous studies showing an increased risk in mainly gastrointestinal bleedings in first-time users of DTIs and Xabans. The risks of all-cause mortality merit further studies and a special attention from care-providers to vulnerable groups.