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. 2017 Sep 11;12(10):1569–1577. doi: 10.2215/CJN.00670117

Table 3.

Clinical measures after randomization in participants assigned to receive dietary potassium restriction or standard care

Variables Control Potassium Restriction P Value
Change in eGFR,a ml/min per 1.73 m2 −5.4±8.5 −5.2±7.9 0.91
Final eGFR, ml/min per 1.73 m2 31±11 28±11 0.94
Change in systolic BP,a mmHg 2±17 −5±18 0.25
Change in weight,a kg −1.8±3.8 −1.1±6.0 0.65
Received sodium polystyrene sulfonate, n/N (%) 2/21 (9.5) 10/21 (47.6) 0.02
Time on sodium polystyrene sulfonate,b mo 1.5±0.7 19.5±5.4
Sodium polystyrene sulfonate dose,b g/d 11.3±5.3 19.8±7.8
Potassium data
 Mean serum potassium,c mEq/L 4.8±0.4 4.6±0.5 0.03
 Change in serum potassium,a mEq/L 0.1±0.7 −0.1±0.8 0.40
 Serum potassiumd <4.5 mEq/L n/N (%) 14/76 (21) 32/65 (42) 0.002
 Change in 24-h urinary potassium,a mEq/24 h 2.3 (−46–65) −7.9 (−40–29) 0.24
Dietary nutrient data
 Mean dietary potassium,c,e mg/d 3874 (2769–4812) 3272 (2524–3954) 0.001
 Change in dietary potassium,a,e mg/d −343 (−999–153) −854 (−1606–0) 0.35
 Change in dietary sodium,a mg/d −115.6±1444.6 −768.3±1426.5 0.15
 Change in protein,a mg/d −17.3±41.0 −11.4±30.6 0.60
 Change in energy,a kJ/d 1230±3859 1506±3442 0.81

Continuous variables are summarized as mean±SD.

a

Change refers to analysis of the change from baseline to final value.

b

Average months and dose of sodium polystyrene sulfonate among participants who received the drug (n=2 control; n=10 intervention).

c

Group mean data were assessed at 6-month intervals and are expressed as raw unadjusted means, with P values from generalized linear model analyses adjusted for baseline value.

d

Proportions are over postrandomization visits assessed at 6-month intervals. P values are from a generalized linear model adjusting for baseline and account for the correlation within a patient over time.

e

Indicates variables that are not normally distributed and are summarized as median (interquartile range).