ultra-sound guided blockade of the brachial pluexus
Conditions
Interventions
Group 1: Observation group: Pat. that have received a ultrasound-guided blockade of the axillary brachial plexus. Retrospective examination of clinical routine data of all included patients to determi
Sponsors
BG Klinikum Hamburg
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: underwent surgery and received an ultrasound-guided ABPB between January 2021 - May 2024 in BG Klinikum Hamburg, planned to be the only means of anaesthesia, performed with 1.5% mepivacaine exclusively and an ASA-Classification of =3. Multiple participations are not permitted.
Exclusion criteria
Exclusion criteria: none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| failure of the nerve blockade, resulting in an intraoperative conversion to general anesthesia The primary endpoint is the failure of the brachial plexus nerve block. This is considered met if, in addition to the regional anesthesia, the patient requires general anesthesia with placement of an airway intraoperatively. This situation is documented in the anesthesia protocol, which is also analyzed as part of the study. | — |
Secondary
| Measure | Time frame |
|---|---|
| success rate of nerve blockade | — |
Countries
Germany
Contacts
Public ContactMathias Baustert
BG Klinikum Hamburg
Outcome results
None listed