Skip to main content
. 2013 Sep 30;6(10):1170–1194. doi: 10.3390/ph6101170

Table 2.

Meta-analysis results of outcomes reported by studies comparing TAC vs. CsA a.

Outcome Study Design (N) Time in months Relative Risk b (95% CI) Statistics c
p I2
CMV RCT [23,24,29,61] (1519) 12 0.85 (0.64, 1.15) 0.30 0
Diabetes RCT [22,23,24,25,27,28,29,30,32,61] (2389) 12 1.72 (1.17, 2.52) 0.006 35
Cohort [62,66] (738) 36 2.71 (1.61, 4.57) 0.0002 0
Dyslipidemia RCT [29,30,61] (1435) 12 0.75 (0.60, 0.94) 0.01 0
Hypertension RCT [23,26,27,29,61] (1714) 12 0.97 (0.82, 1.16) 0.76 25
Total Infections RCT [23,24,25,61] (1376) 12 1.03 (0.93, 1.14) 0.55 12
Lymphoceles RCT [30,61] (1235) 12 0.61 (0.34, 1.07) 0.09 10
Malignancies RCT [23,29,61] (1459) 12 1.16 (0.40, 3.38) 0.79 0
Withdraw RCT [23,24,27,28,29,30,32,61] (2384) 12 0.98 (0.34, 2.81) 0.97 82 *

a Results reaching statistical significance are in bold font. b Relatives risk values of <1 favor treatment with TAC. c p: p-value for relative risk estimation; I2: test for heterogeneity. * The high heterogeneity (p < 0.00001) could be caused by the following trials: Mayer 1997 [23], Hardinger 2005 [29] and Vicenti 1996 [32]. Sensitivity analysis showed much reduced heterogeneity (p = 0.23, I2 = 29%) when these trials were removed from the analysis.