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Table 1 Baseline clinical, laboratory and echocardiographic parameters of the study groups

From: Telmisartan versus EnalapRil In heart failure with redUced ejection fraction patients with Moderately impaired kidney Functions; randomized controlled trial: “TRIUMF trial

 

Total (n = 107)

Telmisartan (n = 54)

Enalapril (n = 53)

P-value*

Age (years)

59.3 ± 9.9

60.13 ± 10.1

58.42 ± 9.7

0.38

Male sex

72 (67.9%)

35 (64.8%)

37 (69.8%)

0.485

Height (cm)

163.98 ± 6.5

163.76 ± 6.1

164.21 ± 6.8

0.725

Weight (kg)

77.21 ± 9.2

76.72 ± 9.6

77.87 ± 8.6

0.736

BMI (Kg/m2)

29.04 ± 6.6

29.33 ± 7.4

28.74 ± 5.6

0.654

NYHA

0.204

 I–II

64 (59.8%)

35 (64.8%)

29 (54.7%)

 III

25 (23.4%)

11 (20.4%)

14 (26.4%)

 IV

18 (16.8)

8 (14.8%)

10 (18.9%)

Baseline 6MWT

112.88 ± 74.83

104.91 ± 10.3

121.01 ± 10.1

0.268

Baseline Serum Cr. (mg/dl)

1.68 ± 0.46

1.72 ± 0.4

1.65 ± 0.4

0.441

Baseline eGFR (ml/min/1.73 m2)

49.7 ± 7.63

47.91 ± 7.4

51.55 ± 7.5

0.013

Baseline serum K (mEq/L)

4.22 ± 0.59

4.27 ± 0.5

4.16 ± 0.6

0.332

Baseline serum albumin

3.4 ± 0.43

3.4 ± 0.5

3.4 ± 0.4

0.529

LV Ejection fraction

32.05 ± 2.2

32.31 ± 2.1

31.77 ± 2.4

0.656

LV EDD

6.34 ± 0.6

6.33 ± 0.6

6.26 ± 0.7

0.626

LV ESD

5.37 ± 0.8

5.27 ± 0.8

5.20 ± 0.9

0.659

TR-Vmax (m/s)

2.70 ± 0.7

2.82 ± 0.7

2.52 ± 0.7

0.162

Starting diuretic dose†

107 ± 117

100 ± 99

108 ± 104

0.503

Starting BB dose ‡

25% ± 22.6

22% ± 20

28% ± 25

0.134

Starting MRA dose ‡

61% ± 26

59% ± 22

63% ± 30

0.548

Starting RAASi dose ‡

50% [50–50]

50% [50–50]

50% [50–50]

0.09

  1. Bold refers to statistically significant p value
  2. 6MWT—Six-minute walk test; BMI—body mass index; Cr.—creatinine; EDD—end diastolic diameter; eGFR—estimated glomerular filtration rate (by MDRD-4 formula); ESD—end systolic diameter; K—potassium; LV—left ventricular; NYHA—New York heart association; TR-Vmax—Tricuspid regurgitation jet maximum velocity
  3. *Representing the comparison of distribution between Telmisartan versus Enalapril groups
  4. Expressed in mean ± standard deviation (SD) of Frusemide equivalents, considering 20 mg of Torsemide, 1 mg of Bumetanide and 40 mg of Frusemide as equivalents
  5. Expressed as either mean ± SD or median [IQR] percentage of the guidelines recommended target dose