Methods |
Randomized controlled trial |
Participants |
N = 104; adult; 58 male, 46 female; ASA 1‐3; trauma
surgery on inferior third of humerus to hand; French
study |
Interventions |
Infraclavicular block (Minville 2005).
Localization method: surface landmarks ‐ 1cm
medial to the coracoid process and 1cm below the
clavicle. Endpoint for injection: motor response
in the distribution of MCN and 1 of 3 other nerve
distributions (MN/UN/RN) to neurostimulation at
0.3‐0.5mA. Dual‐injection through needle (10ml at
MCN, 30ml at other site).
Humeral block. Localization method: surface
landmarks ‐ axillary arterial pulsation at the
junction of proximal and middle third of arm.
Endpoint for injection: motor response in all 4
nerve distributions (MCN/MN/UN/RN) to
neurostimulation at 0.3‐0.5mA. Quadruple‐injection
through needle, equally divided.
Injectate in both blocks: lidocaine 1.5% +
epinephrine 1:200,000 in volume of 40mls Sedation for block: IV sufentanil 0.1 μg/kg Intraoperative sedation: none |
Outcomes |
Block success, defined as absent sensation of
cold and pinprick in 4 nerve distributions (RN,
MN, UN, MCN) at 30 min
Sensory block to cold and pinprick, scored as
scored as 0 (none), 1 (analgesia), 2 (anaesthesia)
in each nerve distribution
(RN/UN/MN/MCN/AN/MBCN/MABCN). Assessed every 5 min
up to 30 min post‐block
Block performance time, defined as needle
insertion to withdrawal
Onset time of sensory block, defined as end of
procedure to analgesia in 4 nerve distributions
(RN, MN, UN, MCN)
Duration of block (not defined)
Pain associated with block, and further
subdivided according to components (skin
transfixion, needle redirection, local anaesthetic
injection causing paraesthesia or dysaesthesia,
electrolocation causing movement‐associated pain),
and assessed by visual analogue score (VAS)
Patient satisfaction post‐surgery, scored on
scale of 0‐5
Preference for similar block in future
Complications (vascular puncture, systemic
local anaesthetic toxicity, recurrent laryngeal
nerve palsy, phrenic nerve palsy, paraesthesia,
Horner's syndrome, pneumothorax)
|
Notes |
Patient satisfaction was converted to a dichotomous
outcome as follows: satisfied = score of 4 or 5,
dissatisfied = score of 3 or less. It is not clear how they surveyed for complications.
The list mentioned above was stated in the Results
section and not in the Methods. Authors did not report the incidences of sensory
block in the individual nerve distributions at the
various time intervals. This data was not available
on request. Abbreviations: AN = axillary nerve, MABCN = medial
antebrachial cutaneous nerve, MBCN = medial brachial
cutaneous nerve, MCN = musculocutaneous nerve, MN =
medial nerve, RN = radial nerve, UN = ulnar
nerve |
Risk of bias |
Bias |
Authors' judgement |
Support for judgement |
Random sequence generation (selection bias) |
Unclear risk |
No mention of randomization method in text |
Allocation concealment (selection bias) |
Unclear risk |
No mention of randomization method in text |
Blinding (performance bias and detection bias)
All outcomes |
Unclear risk |
No mention of blinding of the patient or outcome
assessor in text |
Incomplete outcome data (attrition bias)
All
outcomes |
Low risk |
Complete follow‐up for all patients |
Selective reporting (reporting bias) |
Low risk |
All pre‐specified outcomes reported |
Other bias |
Low risk |
None identified |