Early Ultrasound-guided Nerve Block for Painful Hand Injuries in the Emergency Department
Hand Injuries, Hand Injuries and Disorders
About this trial
This is an interventional treatment trial for Hand Injuries focused on measuring Hand blast injury, Nerve block, Hand injury, Forearm nerve block, Ultrasound guided nerve block, Ultrasound nerve block, Emergency department, Emergency physician, Emergency room
Eligibility Criteria
Inclusion Criteria:
- Patient with moderate to severe hand blast injury or other significantly painful hand or distal forearm injury Also, patients who...
- Are awake and alert
- Are able to endorse or rate their pain
- Require intravenous pain medication for their hand injury
- Are determined to be clinically sober for consent. They will need to be fluent of speech and able to articulate understanding of the procedure they will undergo and the study they will enter.
Exclusion Criteria:
Patient's who...
- Require surgical management, within one half hour, for any injury
- Require any emergent care, including resuscitation, the should preclude their regional pain management
- Are hemodynamically unstable
- Have signs of coagulopathy
Have clinical features suggestive of compartment syndrome of the forearm, including:
- Tense or firm forearm compartment
- Expanding hematoma
- Regional neurologic deficit (weakness or numbness)
- Have weakness or a sensory deficit in an intact part of their hand or forearm
- Have a vascular injury proximal to the hand
- Are unconscious or otherwise unable to endorse or rate their pain
- Are not deemed clinically sober enough to articulate an understanding of the procedure they will undergo and the study they will enter.
- Are prisoners
- Are <18 years old
Sites / Locations
- Harborview Medical Center / University of Washington
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Nerve Block Arm
Control Arm
This group of patients will receive an ultrasound-guided forearm block intervention by the study team. The nerve block will be achieved with a solution of 1% lidocaine without epinephrine and 0.5% bupivacaine without epinephrine (mixed in a 1:1 volume ratio) dosed once. A second dose will be given only in the case of complete block failure.
This group will receive the standard of care in our emergency department, as determined by their primary team. If a patient here receives a nerve block from the primary team, they will be handled with intention-to-treat analysis.