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. 2016 Apr 7;82(1):83–91. doi: 10.1111/bcp.12917

Table 4.

Parameters obtained by pharmacokinetic–pharmacodynamic analysis (inhibitory E max model) relating the plasma concentrations of the d‐nebivolol enantiomer as a function of the heart rate variation induced by isometric handgrip exercise, including all investigated patients classified as extensive metabolizers of cytochrome P450 2D6 (n = 43). Data are expressed as mean (95% confidence interval)

Parameters Control group (n = 22) CKD group (n = 12) Haemodialysis (n = 10)
E max (bpm) 11.87 (7.78, 21.09) 15.53 (11.19, 23.80) 11.62 (9.16, 17.43)
EC 50 (pg ml –1 ) 1411.29 (1071.22, 2166.66) 1656.11 (966.98, 3522.85) 1254.50 (997.67, 1900.62)

CKD, chronic kidney disease; E max, maximum heart rate variation. *One‐way analysis of variance and Tukey's post‐test, P < 0.05 (control vs. CKD) and (control vs. haemodialysis).