Modified clavipectoral block reduces pain and hemidiaphragmatic paralysis in clavicular surgery
This randomized controlled trial compared two regional anesthesia approaches in 56 patients scheduled for midshaft clavicular surgery. The experimental group received ultrasound-guided modified clavipectoral fascial plane block plus superficial cervical plexus block, while the control group received ultrasound-guided interscalene brachial plexus block plus superficial cervical plexus block. Both groups achieved 100% block success with no differences in performance or onset times.
The primary outcome was Numerical Rating Scale score at 12 hours postoperatively, which was significantly lower in the experimental group (estimated mean difference -1.29, P<0.001). At 24 hours, pain scores remained significantly lower in the experimental group (estimated mean difference -2.36, P<0.001). Rescue analgesic requirements within 24 hours were also significantly reduced in the experimental group (P=0.002). Most notably, hemidiaphragmatic paralysis incidence was 71.4% in the control group versus 0% in the experimental group (P<0.001).
Safety and tolerability data were not reported. The study's key limitation is its small sample size, and the authors note that these findings require validation in larger multicenter trials. While the modified clavipectoral approach appears promising for reducing both pain and respiratory complications in clavicular surgery, clinicians should await further evidence before changing practice.