Brull 2009.
Methods | RCT, parallel design | |
Participants | 106 ASA I ‐ III participants scheduled for elbow, forearm, wrist or hand surgery Excluded: age < 18 or > 70 yr, language barrier, contraindication(s) to regional anaesthesia, weight > 100 kg, pre‐existing neurological deficit in the distribution to be anaesthetized, local infection, coagulopathy, chest or shoulder deformities, severe respiratory disease, or clavicle fracture. |
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Interventions | Ultrasound (n = 53) versus nerve stimulation (n = 53) Intraclavicular brachial plexus block of radial, ulnar, median and musculocutaneous nerves. Total volume 30 ml local anaesthetic (2% lidocaine 15 mL and 0.5% bupivacaine 15 mL with epinephrine 1:200,000) Ultrasound: either linear probe 7 – 13 MHz (Philips/ATL HDI 5000) a 5 – 12 MHz (Philips HD11); endpoint ‐ visualization of lateral and posterior cord, LA injected incrementally to total volume of 30 ml. Nerve stimulation (Stimuplex): motor endpoints sought (elbow/ finger flexion, thumb opposition, wrist extension) at stimulating current of 0.3 ‐ 0.5 mA. 15 mL of LA injected incrementally at each position for a total of 30 mL. All participants given midazolam 2 – 4 mg iv as premedication. For nerve stimulation group, If 2 motor responses were not elicited within 20 min of needle insertion, procedure abandoned in favour of a different approach to brachial plexus blockade, and participant excluded from analysis. |
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Outcomes |
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Notes | One of 4 experienced regional anaesthesiologists ‐ no further details of whether experience is balanced between techniques Supported by grant funding, equipment received from manufacturers for purpose of study ‐ no interests declared. Time to perform block reported as median (interquartile range) and therefore not possible to combine in this review |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Computer‐generated randomization table |
Allocation concealment (selection bias) | Unclear risk | No details given |
Blinding of participants and personnel (performance bias):Complications | High risk | Anaesthetist not blinded |
Blinding of participants and personnel (performance bias): time outcomes | High risk | Anaesthetist not blinded |
Blinding of participants and personnel (performance bias): Patient discomfort | High risk | Anaesthetist not blinded |
Blinding of outcome assessment (detection bias): adequacy of block, supplementation of block | Low risk | Evaluated by blinded observer |
Blinding of outcome assessment (detection bias): Complications | Low risk | Evaluated by blinded observer |
Blinding of outcome assessment (detection bias): time outcomes | Low risk | Evaluated by blinded observer |
Blinding of outcome assessment (detection bias): Patient discomfort | Low risk | Participants blinded with use of 'sham' equipment |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Small number of exclusions (5 participants) with clear reasons given. However, only 49% participants available for assessment of complications at postoperative day 7 |
Selective reporting (reporting bias) | Unclear risk | No data available for pain on injection. Also published protocol not sought |
Baseline characteristics | Low risk | Largely comparable, although some differences in types of surgery between groups |
Funding sources | High risk | Funding from grants, equipment supplied by named manufacturers. Unclear whether any bias has been introduced |
Operator expertise | Unclear risk | Anaesthetists described as experienced but no detail of whether experience is equivalent for both techniques |