Skip to main content

Table 2 Study outcomes pre- and post-intervention

From: Using pharmacists to improve risk stratification and management of stage 3A chronic kidney disease: a feasibility study

 

Control (n = 23)

Pharmacist MTM (n = 24)

 
 

Baseline

End-of-trial

Baseline

End-of-trial

OR (95 % CI)

P value

Proteinuria screeninga

14 (60.9 %)

17 (73.9 %)

10 (41.7 %)

21 (87.5 %)

Entire population: 2.6 (0.5–14.0) Previously unscreened subgroup:7.3 (0.96–56.3)

Entire population: 0.3 Previously unscreened subgroup: 0.05

Lipid screening

23 (100 %)

23 (100 %)

21 (87.5 %)

24 (100 %)

N/A

N/A

Treatment with statin

16 (69.6 %)

17 (73.9 %)

13 (54.2 %)

12 (50.0 %)

0.4 (0.1–1.3)

0.1

Achieved BP goal

9 (39.1 %)

13 (56.5 %)

10 (41.7 %)

13 (54.2 %)

0.9 (0.3–3.0)

0.9

  1. aRandom effects logistic regression was used to determine the effects of pharmacist MTM on proteinuria screening in the entire population, and then just among patients who were unscreened at baseline, accounting for the clustered design