Patient or population: adults undergoing peripheral venous cannulation classed as difficulta Settings: emergency department, ICU, operating room Intervention: USG Comparison: LM | |||||||
Outcomes | Subgroups | Anticipated absolute effects* (95% CI) | Relative effect (95% CI) | No. of participants (studies) | Certainty of the evidence (GRADE) | Comments | |
Risk with LM | Risk with USG | ||||||
First‐pass success of cannulation Follow‐up: immediately after the procedure |
Operators had any clinical experience | 361 per 1000 | 519 per 1000 (328 to 819) | RR 1.44 (0.91 to 2.27) | 460 (5 RCTs) |
⊕⊝⊝⊝ Very lowb | |
Operators did not have any clinical experience | 446 per 1000 |
594 per 1000 (442 to 799) |
RR 1.33 (0.99 to 1.79) | 235 (3 RCTs) |
⊕⊕⊝⊝ Lowc | ||
Operators experience was not specified | 183 per 1000 |
403 per 1000 (224 to 726) |
RR 2.20 (1.22 to 3.96) | 120 (2 RCTs) |
⊕⊕⊝⊝ Lowd | ||
Overall success of cannulation Follow‐up: immediately after the procedure |
Operators had any clinical experience | 726 per 1000 | 835 per 1000 (661 to 1000) | RR 1.15 (0.91 to 1.44) | 315 (5 RCTs) |
⊕⊝⊝⊝ Very lowe | |
Operators did not have any clinical experience | 509 per 1000 | 743 per 1000 (601 to 911) | RR 1.46 (1.18 to 1.79) | 235 (3 RCTs) |
⊕⊝⊝⊝ Very lowf | ||
Operators experience was not specified | 333 per 1000 | 693 per 1000 (470 to 1000) | RR 2.08 (1.41 to 3.09) | 120 (2 RCTs) |
⊕⊝⊝⊝ Very lowg | ||
Pain NRS: from 0, no pain to 10, maximum pain Follow‐up: immediately after the procedure |
Operators had any clinical experience | Not performed due to insufficient number of studies | |||||
Operators did not have any clinical experience | Not performed due to insufficient number of studies | ||||||
Operators experience was not specified | Not performed due to insufficient number of studies | ||||||
*The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI). CI: confidence interval; ICU: intensive care unit; LM: landmark method; MD: mean difference; NRS: numerical rating scale; RCTs: randomised controlled trials; RR: risk ratio; USG: ultrasound guidance | |||||||
GRADE Working Group grades of evidence High certainty: we are very confident that the true effect lies close to that of the estimate of the effect. Moderate certainty: we are moderately confident in the effect estimate: the true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different. Low certainty: our confidence in the effect estimate is limited: the true effect may be substantially different from the estimate of the effect. Very low certainty: we have very little confidence in the effect estimate: the true effect is likely to be substantially different from the estimate of effect. |