Outcome | Number of included trials | Early RRT patients | Control patients | OR or MD | 95% CI | P for effect | P for heterogeneity | I2 (%) |
---|---|---|---|---|---|---|---|---|
Overall trials | 10 | 1073 | 1141 | |||||
Primary outcomes | ||||||||
-Mortality | 10 | 1073 | 1141 | 0.99 | 0.66 to 1.50 | 0.97 | < 0.0001 | 74 |
General ICU patients | 7 | 926 | 992 | 1.15 | 0.79 to 1.68 | 0.47 | 0.005 | 68 |
Cardiac surgery patients | 3 | 147 | 149 | 0.19 | 0.01 to 2.66 | 0.22 | 0.003 | 88 |
SENSITIVITY ANALYSIS (including only low risk of bias studies) | 4 | 771 | 865 | 1.13 | 0.66 to 1.95 | 0.65 | 0.0005 | 83 |
-Survival with dependence on RRT | 6 | 931 | 939 | 0.86 | 0.54 to 1.37 | 0.51 | 0.54 | 0 |
General ICU patients | 5 | 819 | 827 | 0.86 | 0.54 to 1.37 | 0.51 | 0.54 | 0 |
Cardiac surgery patients | 1 | 112 | 112 | na | na | na | na | na |
SENSITIVITY ANALYSIS (including only low risk of bias studies) | 4 | 771 | 775 | 0.90 | 0.56 to 1.45 | 0.66 | 0.53 | 0 |
SENSITIVITY ANALYSIS (removing 1 study at time) | All 95% CIs of OR > 1 and p < 0.05 | |||||||
Secondary outcomes | ||||||||
-ICU stay (days) | 6 | 808 | 780 | −0.87 | −2.02 to 0.27 | 0.14 | 0.11 | 44 |
-HLOS (days) | 6 | 808 | 780 | −2.92 | −4.47 to − 1.38 | 0.0002 | 0.35 | 10 |
SENSITIVITY ANALYSIS (including only low risk of bias studies) | 3 | 669 | 669 | −3.03 | −5.36 to −0.71 | 0.10 | 0.11 | 58 |
Adverse events | ||||||||
-Bleeding Complications | 8 | 1038 | 1014 | 0.90 | 0.70 to 1.17 | 0.44 | 0.68 | 0 |
-Blood transfusions | 3 | 659 | 656 | 0.94 | 0.72 to 1.23 | 0.65 | 0.62 | 0 |
-Catheter-related bacteremia | 4 | 498 | 505 | 1.70 | 0.98 to 2.93 | 0.06 | 0.53 | 0 |
-Rhythm disturbances | 6 | 775 | 783 | 1.09 | 0.56 to 2.13 | 0.80 | 0.09 | 47 |
-Thrombocytopenia | 2 | 423 | 420 | 1.42 | 0.76 to 2.63 | 0.27 | 0.05 | 75 |