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. 2017 Oct 11;46(4):323–332. doi: 10.1159/000481270

Table 2.

Demographics and clinical characteristics

Patiromer treatment group
p value*
without food (n = 57) with food (n = 55)
Age, years, mean (SD) 66.8 (13.5) 66.3 (10.3) 0.832
Age ≥65 years, n (%) 38 (66.7) 35 (63.6) 0.843
Male, n (%) 40 (70.2) 33 (60.0) 0.322
Race, n (%)
 White 48 (84.2) 44 (80.0) 0.864
 Black 6 (l0.5) 8 (l4.5)
 Other 3 (5.3) 3 (5.4)
Ethnicity, n (%)
 Hispanic/Latino 33 (57.9) 30 (54.5) 0.849
 Non-Hispanic/Latino 24 (42.l) 25 (45.5)
Serum K+, mEq/L, mean (SD) 5.4 (0.4) 5.3 (0.4) 0.166
 <5.5, n (%) 32 (56.1) 34 (61.8) 0.570
 ≥5.5, n (%) 25 (43.9) 21 (38.2)
CKD (all stages), n (%) 44 (77.2) 41 (74.5) 0.827
 CKD stages 1–3a 9 (l5.8) 7 (l2.7) 0.785
 CKD stages 3b–5 35 (61.4) 34 (61.8)
Diabetes mellitus, n (%) 48 (84.2) 44 (80.0) 0.627
Heart failure, n (%) 5 (8.8) 5 (9.1) 1.000
Hypertension, n (%) 55 (96.5) 50 (90.9) 0.267
RAAS inhibitors, n (%) 35 (61.4) 31 (56.4) 0.701
Beta-blocking agents, n (%) 28 (49.1) 30 (54.5) 0.577
Non-RAAS inhibitor diuretic, n (%) 18 (31.6) 22 (40.0) 0.431

CKD, chronic kidney disease; K+, potassium; RAAS, renin-angiotensin aldosterone system.

*

p values for age and serum K+ were based on 2-sample t tests and all other p values were based on Fisher's exact tests.

Baseline serum K+ is defined as the mean of serum K+ from the central laboratory on 2 consecutive days (day −1 and day 1) immediately prior to the first dose of patiromer.

All non-RAAS inhibitor diuretics were potassium-wasting.