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Table 3 Haemodynamics and response to adenosine

From: A comparison of standard and high dose adenosine protocols in routine vasodilator stress cardiovascular magnetic resonance: dosage affects hyperaemic myocardial blood flow in patients with severe left ventricular systolic impairment

 

CAD

n = 20

HF LVEF ≥ 40%

n = 16

HF LVEF < 40%

n = 24

Comparison between groups (p)

 

Standard dose

High dose

p

Standard dose

High dose

p

Standard dose

High dose

p

Standard dose

High dose

Rest HR (bpm)

62 ± 10

63 ± 9

0.534

65 ± 14

65 ± 13

1.000

75 ± 12

77 ± 14

0.547

0.002

0.001

Rest SBP (mmHg)

132 ± 17

131 ± 16

0.735

124 ± 16

124 ± 17

0.320

119 ± 16

119 ± 16

0.526

0.066

0.089

Stress HR (bpm)

75 ± 13‡

78 ± 13‡

0.027*

79 ± 20‡

80 ± 17‡

0.659

87 ± 16‡

90 ± 18‡

0.418

0.039

0.038

Stress SBP (mmHg)

124 ± 15

121 ± 12

0.219

124 ± 11

120 ± 13

0.005**

122 ± 18

124 ± 19

0.391

0.597

0.970

Change in HR (bpm)

12 ± 10

15 ± 8

0.112

14 ± 14

15 ± 9

0.637

12 ± 12

13 ± 19

0.751

0.875

0.889

Change in SBP

− 2 ± 10

− 6 ± 11

0.455

− 2 ± 13

− 2 ± 11

0.139

2 ± 8

3 ± 13

0.700

0.377

0.072

Non-responders (< 10 bpm) (%)

8 (40%)

4 (20%)

0.168

6 (38%)

3 (19%)

0.433

10 (42%)

11 (46%)

0.771

0.966

0.097

Failed splenic switch off (%)

2 (10%)

0

0.487

1 (6%)

0

1

2 (8%)

2 (8%)

1

1.0

0.334

  1. Resting HR was significantly higher in the moderate-severe heart failure (HF) group, no difference was seen between groups in rate of non-responders or absolute measures of haemodynamic response to adenosine
  2. Data given as mean ± standard deviation or n (%)
  3. HR heart rate, SBP systolic blood pressure
  4. *Significant difference between adenosine doses, p < 0.05, **significant difference between adenosine doses, p < 0.01, ‡significant difference from rest value, p < 0.01. Group 1—Patients with coronary artery disease and left ventricular ejection fraction (LVEF) > 40%. Group 2 – Mild to moderate heart failure, LVEF ≥ 40% and no evidence of coronary artery disease. Group 3—moderate to severe heart failure, LVEF < 40% and no evidence of coronary artery disease. Standard dose—140 µg/kg/min. High dose—210 µg/kg/min.