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. 2023 Mar 3;2023(3):CD011364. doi: 10.1002/14651858.CD011364.pub3

Min 2019.

Study characteristics
Methods RCT
Participants Number: 74 radial arteries
Number per intervention
  1. Ultrasound: 37 radial arteries

  2. Palpation: 37 radial arteries


Inclusion criteria
  1. Age < 12 months

  2. Scheduled cardiac surgery


Exclusion criteria:
  1. Signs of skin infection or a recent wound at or near the puncture site

  2. Diagnosed abnormal peripheral circulation of the hand

  3. Diagnosed vascular abnormality or radial arterial variation

  4. Problem at the radial or ulnar artery sites

  5. Haemodynamic instability 


Surgery/setting: cardiac surgeries for congenital heart disease
Baseline characteristics
Ultrasound
  1. Mean age: 1.7 (SD 2.7) months

  2. Mean weight: 4.8 (SD 1.9) kg

  3. Sex ratio (male:female): 18:19


Palpation
  1. Mean age: 3.5 (SD 3.5) months

  2. Mean weight: 5.7 (SD 2.1) kg

  3. Sex ratio (male:female): 24:13

Interventions Randomisation: participants were assigned randomly to either a palpation‐guided group or an ultrasound‐guided group using computer‐generated numbers found in sealed envelopes.
Intervention: a linear ultrasound transducer in the short‐axis view was used in the US group. The least depth‐of‐field setting was 1.5 cm, and a 24‐gauge angiocatheter was inserted. The needle was advanced until a bright white dot of the needle tip was observed. The needle was then advanced, targeting the radial artery using an anterior or posterior puncture technique.
Control: palpation of the radial arterial pulse
Co‐intervention: general anaesthesia with inhaled sevoflurane, intravenous midazolam (0.15 to 0.3 mg/kg) and rocuronium (0.6 to 0.9 mg/kg)
Experience of operator: all ultrasound recordings and arterial catheterisations were performed by one of two anaesthesiologists (> 2 years of experience in paediatric cardiac anaesthesia and > 50 cases of ultrasound‐guided radial arterial catheterisation in paediatric patients).
Outcomes Primary endpoints
  1.  First‐pass success

  2.  Success within 10 minutes

  3. Total number of attempts

  4. Total procedural time for successful catheterisation 


Secondary endpoints
  1. Complications during the procedures (e.g. haematoma formation, arterial spasm or ischaemic signs) 

Notes Supported by institutional resources. Study authors disclosed no potential conflicts of interest.
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Low risk Quote: "Patients were assigned randomly to either a palpation‐guided group or an ultrasound‐guided group using computer‐generated numbers found in sealed envelopes."
Allocation concealment (selection bias) Low risk Quote: "The sealed envelope was opened by a physician just after induction of general anaesthesia."
Blinding of participants and personnel (performance bias)
All outcomes High risk All participants underwent induction of general anaesthesia prior to arterial catheterisation (low risk of bias). The anaesthesiologist was aware of the allocated intervention before performing arterial catheterisation (high risk of bias).
Blinding of outcome assessment (detection bias)
All outcomes Low risk Successful arterial cannulation is the endpoint of the procedure for both techniques (unequivocal endpoint).
Incomplete outcome data (attrition bias)
All outcomes Low risk No missing data.
Selective reporting (reporting bias) Low risk  An investigator recorded all procedures on video for analysis.
Other bias Unclear risk Participant age and height were significantly different between the 2 groups. The investigators set a time limit of 10 minutes.