4. Sensitivity analysis for easy participants.
Outcomes | Original results | RCTs only | Low ROB studies only | |
First‐pass success of cannulation | ES | 0.89 (0.85, 0.94) | 0.89 (0.85, 0.94) | 0.89 (0.85, 0.94) |
I2 | NA *1 | NA*1 | NA*1 | |
Overall success of cannulation | ES | NA *2 | NA *2 | NA *2 |
I2 | NA *2 | NA *2 | NA *2 | |
Pain | ES | 0.60 (0.17, 1.03) | 0.60 (0.17, 1.03) | 0.60 (0.17, 1.03) |
I2 | NA *1 | NA *1 | NA *1 | |
Procedure time for first‐pass cannulation | ES | 94.8 (81.2, 108.5) | 94.8 (81.2, 108.5) | 94.8 (81.2, 108.5) |
I2 | NA *1 | NA *1 | NA *1 | |
Procedure time for overall cannulation | ES | NA *2 | NA *2 | NA *2 |
I2 | NA *2 | NA *2 | NA *2 | |
Number of cannulation attempts | ES | NA *2 | NA *2 | NA *2 |
I2 | NA *2 | NA *2 | NA *2 | |
Patient satisfaction | ES | NA *2 | NA *2 | NA *2 |
I2 | NA *2 | NA *2 | NA *2 | |
Overall complications | ES | 2.48 (0.90, 6.87) | 2.48 (0.90, 6.87) | 2.48 (0.90, 6.87) |
I2 | NA *1 | NA *1 | NA *1 |
Dichotomous outcomes shown as RR (95% CI), continuous outcomes as MD or SMD (95% CI) ES: effect size; MD: mean difference; NA: not applicable; RCT: randomised controlled trial; ROB: risk of bias; RR: risk ratio; SMD: standardised mean difference *1: only one study; *2: no study