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. 2022 Dec 12;2022(12):CD013434. doi: 10.1002/14651858.CD013434.pub2
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 evidenceHigh 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.