Skip to main content

Table 1 Demographic and baseline characteristics

From: Oral dabigatran etexilate versus enoxaparin for venous thromboembolism prevention after total hip arthroplasty: pooled analysis of two phase 3 randomized trials

 

Dabigatran 220 mg

Enoxaparin 40 mg

(n = 2,156)

(n = 2,157)

Number of treated patients

2,156

2,157

 Age, yr

63 ± 11

63 ± 11

 Females, n (%)

1177 (54.6)

1152 (53.4)

 Weight, kg

79 ± 16

79 ± 16

 Body mass indexa

27.8 ± 4.7

27.6 ± 4.6

 Previous VTE, n (%)

65 (3.0)

54 (2.5)

 Creatinine clearanceb, mL/min

92 ± 31

93 ± 31

Racec, n (%)

  

 White

2,051 (95.1)

2,052 (95.1)

 Asian

96 (4.4)

88 (4.1)

 Black

5 (0.2)

12 (0.6)

 Other

4 (0.2)

5 (0.2)

Geographical region, n (%)

  

 Western Europe

1,282 (59.5)

1,291 (59.9)

 Central Europe

474 (22.0)

470 (21.8)

 North America

170 (7.9)

168 (7.8)

 India

91 (9.0)

88 (4.1)

 Australia/New Zealand/South Africa

139 (6.4)

140 (6.5)

Patients treated and operated, n (%)

2,138 (99.2)

2,134 (98.9)

Anesthesiad, n (%)

  

 General alone

525 (24.4)

503 (22.3)

 Neuraxial alonee

1,461 (67.8)

1,486 (65.8)

 Combinationf

149 (6.9)

144 (6.4)

Mean duration of surgery ± SD, min

85.4 ± 30.2

85. ±30.4

Study treatment

  

 Mean time to first subcutaneous injectiong,h in relation to surgery, hr

–15.6 ± 20.7

–15.2 ± 13.5

 Mean time to first oral dose postsurgeryh, hr

3.1 ± 2.6

3.2 ± 2.7g

 Median (range) duration of hospital stayi, d

8.5 (3–51)

8.5 (3–26)

 Median (range) treatment duration, d

31.6 (1–89)

31.7 (1–49)

  1. Data are given as mean ± SD except where indicated
  2. SD standard deviation, VTE Venous thromboembolism
  3. aBody mass index was defined as weight in kilograms divided by square of height in meters; bCreatinine clearance rates were calculated using the Cockcroft–Gault formula; cAs reported by the investigator; dPatients may have had more than one type of anesthetic; eIncludes spinal and epidural anesthesia; fPeripheral nerve block plus general or neuraxial anesthesia; g26 patients in RE-NOVATE II group received their first dose postsurgery; hIncludes both active treatment and placebo; iTime from surgery until day of discharge, data available in RE-NOVATE for 1,136 and 1,140 patients, respectively