Table 2 Association between baseline characteristics and choice of reduced dose at first prescription in 927,523 NOAC treatments in AIFA Registry (2013–2018).

From: Starting dose and dose adjustment of non-vitamin K antagonist oral anticoagulation agents in a nationwide cohort of patients with atrial fibrillation

 

OR (95% CI) Dabigatran

OR (95% CI) Rivaroxaban

OR (95% CI) Apixaban

OR (95% CI) Edoxaban

Sex—Females vs Males

1.25 (1.19–1.31)

1.25 (1.21–1.29)

1.47 (1.42–1.52)

1.82 (1.7–1.95)

 ≥ 65 and < 75 vs < 65 years

1.8 (1.69–1.91)

1.74 (1.63–1.85)

1.57 (1.46–1.7)

2.05 (1.82–2.32)

 ≥ 75 and < 85 vs < 65 years

12.42 (11.32–13.63)

6.29 (5.81–6.82)

7.42 (6.78–8.12)

6.94 (5.91–8.14)

 ≥ 85 vs < 65 years

180.41 (160.24–203.13)

24.82 (22.88–26.93)

38.2 (34.86–41.86)

32.78 (27.88–38.55)

CHA2DS2-VASc Score1 vs 0

0.74 (0.63–0.87)

1.22 (0.94–1.59)

0.63 (0.47–0.85)

1.21 (0.75–1.93)

CHA2DS2-VASc Score2 vs 0

0.82 (0.69–0.98)

1.73 (1.33–2.26)

0.64 (0.48–0.87)

1.37 (0.85–2.22)

CHA2DS2-VASc Score 3 vs 0

0.96 (0.79–1.16)

2.16 (1.64–2.84)

0.72 (0.53–0.98)

1.58 (0.96–2.61)

CHA2DS2-VASc Score 4 vs 0

1.07 (0.85–1.33)

2.45 (1.84–3.25)

0.8 (0.58–1.1)

1.71 (1.01–2.89)

CHA2DS2-VASc Score 5 vs 0

1.14 (0.89–1.47)

2.56 (1.9–3.45)

0.81 (0.58–1.12)

1.76 (1.01–3.07)

CHA2DS2-VASc Score 6 + vs 0

1.34 (0.99–1.82)

2.69 (1.96–3.69)

0.84 (0.59–1.19)

1.84 (1.01–3.37)

HAS-BLED Score1 vs 0

1.28 (1.16–1.4)

1.58 (1.37–1.82)

1.56 (1.3–1.87)

0.87 (0.72–1.07)

HAS-BLED Score 2 vs 0

1.38 (1.25–1.52)

1.77 (1.52–2.05)

1.9 (1.58–2.28)

0.91 (0.74–1.12)

HAS-BLED Score 3 vs 0

1.32 (1.18–1.47)

1.83 (1.57–2.14)

2 (1.66–2.42)

0.84 (0.67–1.05)

HAS-BLED Score 4 + vs 0

1.04 (0.91–1.18)

1.7 (1.44–2.01)

1.91 (1.56–2.33)

0.69 (0.54–0.9)

Diabetes history vs None

0.92 (0.88–0.96)

0.98 (0.95–1.01)

0.95 (0.92–0.99)

0.94 (0.88–1.01)

Hypertension history vs None

0.88 (0.83–0.93)

0.88 (0.84–0.92)

0.74 (0.71–0.78)

0.81 (0.75–0.88)

Stroke/TIA/Thromboembolism history vs None

0.85 (0.78–0.93)

0.89 (0.84–0.95)

0.88 (0.83–0.94)

1 (0.88–1.14)

Vascular disease history vs None

1.29 (1.23–1.35)

1.13 (1.09–1.17)

1.2 (1.16–1.24)

1.13 (1.06–1.22)

CHF history vs None

1.18 (1.12–1.24)

1.35 (1.31–1.4)

1.45 (1.4–1.49)

1.4 (1.31–1.5)

Alcohol use vs None

0.74 (0.7–0.78)

0.69 (0.65–0.72)

0.61 (0.58–0.64)

0.8 (0.73–0.87)

Liver disease vs None

1.57 (1.41–1.74)

1.06 (0.96–1.17)

1.35 (1.23–1.49)

1.48 (1.22–1.78)

Renal diseasea vs None

3.23 (2.98–3.51)

9.86 (9.33–10.41)

6.26 (5.97–6.56)

11.81 (10.66–13.08)

Prior major bleeding or predisposition to bleeding vs None

2.22 (2.12–2.33)

1.53 (1.47–1.59)

1.75 (1.69–1.82)

1.81 (1.68–1.94)

Labile INR vs No

1.17 (1.12–1.22)

1.04 (0.99–1.08)

1.13 (1.08–1.19)

1.1 (1–1.2)

Prior anticoagulant treatment (AVK) vs None

1.01 (0.98–1.04)

0.83 (0.8–0.85)

0.73 (0.7–0.75)

0.8 (0.75–0.85)

Medication usage predisposing to bleeding vs None

2.09 (2.01–2.18)

1.28 (1.24–1.33)

1.14 (1.1–1.19)

1.24 (1.15–1.32)

Prior NOAC treatment (switch) vs None

1.52 (1.42–1.62)

1.6 (1.55–1.66)

1.59 (1.54–1.64)

1.98 (1.88–2.08)

  1. Data are expressed as odds ratio and confidence intervals for the baseline characteristics for each NOAC.
  2. aRenal disease = renal transplantation or dialysis or plasma creatinin > 200 µmol/L.