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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
Intervention: USG
Comparison: LM
Outcomes 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
339 per 1000 549 per 1000
(433 to 698) RR 1.62 
(1.28 to 2.06) 780
(9 RCTs) ⊕⊕⊕⊝
Moderateb
 
 
 
Overall success of cannulation
 
Follow‐up: immediately after the procedure
541 per 1000 828 per 1000
(606 to 1000) RR 1.53 
(1.12 to 2.08) 588
(8 RCTs) ⊕⊝⊝⊝
Very lowc
 
 
 
Pain
NRS: from 0, no pain to 10, maximum pain
 
Follow‐up: immediately after the procedure
The mean pain score was 4.07 MD 0.49 lower (1.48 lower to 0.49 higher) 305 (3 RCTs) ⊕⊝⊝⊝
Very lowd  
Procedure time for first‐pass cannulation (seconds)
 
Follow‐up: immediately after the procedure
The mean procedure time for first‐pass cannulation was 137.8 seconds MD 120.6 seconds longer (88.3 longer to 152.9 longer) 192 (1 RCT) ⊕⊕⊕⊝
Moderatee
 
 
Number of cannulation attempts
 
Follow‐up: immediately after the procedure
The mean number of cannulation attempts was 2.20 MD 0.36 lower (0.75 lower to 0.03 higher) 468 (6 RCTs) ⊕⊝⊝⊝
Very lowf  
Patient satisfaction
NRS from 0 to 10 or
4‐step Likert scale
The higher the score, the higher the level of satisfaction
Follow‐up: immediately after the procedure
The mean patient satisfaction score was 5.96 SMD 0.52 higher (0.01 lower to 1.05 higher) 286 (4 RCTs) ⊕⊝⊝⊝
Very lowg  
Overall complications
 
Follow‐up: immediately after the procedure
121 per 1000 78 per 1000
(45 to 133) RR 0.64
(0.37 to 1.10) 431
(5 RCTs) ⊕⊕⊝⊝
Lowh  
*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: numeric rating scale; RCTs: randomised controlled trials; RR: risk ratio; SMD: standardised mean difference; 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.