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. 2013 Sep 20;4(4):247–257. doi: 10.1007/s13539-013-0115-9

Table 2.

Comorbidities of 84 MHD patients in AIONID study

All (N = 84) Group A (N = 19) Group B (N = 22) Group C (N = 22) Group D (N = 21) P value
(%) ONS + PTX ONS PTX placebo
Hypertension 16 (19) 3 (16) 3 (14) 5 (23) 5 (24) 0.79
Coronary artery disease 10 (11) 3 (16) 4 (18) 1 (5) 2 (10) 0.50
Coronary artery disease (post-CABG) 3 (4) 0 (0) 1 (5) 0 (0) 2 (10) 0.29
Congestive heart failure 19 (23) 3 (16) 5 (23) 6 (27) 5 (24) 0.85
Cerebrovascular disease 7 (8) 0 (0) 3 (14) 3 (14) 1 (5) 0.30
Peripheral vascular disease 12 (14) 4 (21) 4 (18) 2 (9) 2 (10) 0.60
COPD 11 (13) 3 (16) 5 (23) 2 (9) 1 (5) 0.32
Peptic ulcer 6 (7) 2 (11) 1 (5) 2 (9) 1 (5) 0.84
Moderate to severe liver disease 2 (2) 1 (5) 0 (0) 0 (0) 1 (5) 0.52
Depression 9 (11) 1 (5) 3 (14) 2 (9) 3 (14) 0.77
Cancer 1 (1) 0 (0) (0) 0 (0) 1 (5) 0.39
Hepatitis C 7 (8) 2 (11) 0 (0) 2 (9) 3 (14) 0.38
Hepatitis B carrier 1 (1) 0 (0) 0 (0) 1 (5) 0 (0) 0.41

ONS oral nutrition supplements, consisting of a high (19 g) protein supplement (Nepro®, 8 oz/day) combined with a concentrated anti-inflammatory and anti-oxidant module (fish oil, borage oil, beta-carotene, vitamins C and E, zinc, and selenium, 2 oz/day); PTX pentoxifylline (400 mg/day). The supplements and pills for the same day and the following day (6 days/week) were provided to the patients during each thrice-weekly hemodialysis treatment; COPD chronic obstructive pulmonary disease; CABG coronary artery bypass graft