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. 2009 Feb 27;4(2):e4644. doi: 10.1371/journal.pone.0004644

Table 6. Characteristics of subjects recruited in the PeriOperative Epidural Trial Pilot Study.

Descriptor Epidural Group (n = 49) IV Group (n = 49)
Mean age±SD, year 70.9±7.6 70.3±8.6
Sex, n (%)
Female 12 (24.5) 15 (30.6)
Male 38 (77.6) 36 (73.5)
Comorbid conditions, n (%)
Coronary artery disease 14 (28.6) 12 (24.5)
Peripheral vascular disease 13 (26.5) 11 (22.4)
Stroke/transient ischemic attack 1 (2.0) 4 (8.2)
Congestive heart failure 2 (4.1) 0 (0.0)
Hypertension 34 (69.4) 31 (63.3)
Diabetes mellitus 11 (22.4) 14 (28.6)
Chronic renal dysfunction 2 (4.1) 0 (0.0)
Smoker
 Former 18 (36.7) 24 (49.0)
 Current 11 (22.4) 7 (14.3)
Chronic obstructive pulmonary disease 4 (8.2) 7 (14.3)
Medication history, n (%)
Aspirin 16 (32.6) 21 (42.8)
Clopidogrel/ticlopidine 2 (4.1) 2 (4.1)
Warfarin 1 (2.0) 2 (4.1)
Heparins 1 (2.0) 2 (4.1)
Statins 26 (53.1) 22 (44.9)
Nitrates 2 (4.1) 4 (8.2)
Diuretics 15 (30.6) 15 (30.6)
ACE inhibitors/angiotensin II receptor blockers 23 (46.9) 19 (38.8)
Beta-adrenergic blockers 16 (32.6) 21 (42.8)
Calcium channel blockers 8 (16.3) 17 (34.7)
Digoxin 2 (4.1) 3 (6.1)
Amiodarone 1 (2.0) 2 (4.1)
Beta-agonist bronchodilators 1 (2.0) 1 (2.0)
Inhaled steroids 3 (6.1) 1 (2.0)

Abbreviation: ACE, angiotensin converting enzyme; SD, standard deviation.