Anesthesia, Anesthesia Management, Regional Anesthesia
Conditions
Keywords
Regional Anesthesia, Anesthesia Management
Brief summary
The Ultrasound-guided Supra-inguinal Fascia Iliaca Block (SIFIB) is an advanced regional anesthesia technique strategically directed at the three primary nerves of the lumbar plexus. As the scope of regional anesthesia methods continues to grow in clinical application, this approach emerges as a versatile method. It can be used independently for pain management or as the primary anesthetic method, particularly in well-selected patients undergoing isolated limb surgeries or in combination with other regional anesthesia approaches.
Detailed description
The study follows a retrospective cohort feasibility design, conducted within the confines of a tertiary hospital. The requisite data for analysis was acquired by accessing patient records and electronic data systems. A cohort of 16 patients was carefully chosen for inclusion in the study, and the administration of blocks was carried out before the surgical procedures.
Interventions
The design of this study involved the retrospective analysis of data. Data was gathered from adult patients falling into the American Society of Anesthesiology (ASA) categories I to III, who were scheduled for elective lower limb surgical procedures. More specifically, patients who had undergone SIFIB either as the primary anesthesia approach or as part of their anesthesia regimen were included. Those who had received general anesthesia, neuraxial anesthesia, or infiltration anesthesia were excluded from the study. Importantly, all patients who participated in the study provided written informed consent for both their involvement in the study and the publication of their data.
Sponsors
Samsun University
Study design
Observational model
COHORT
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No
Inclusion criteria
* ASA I-III patients who underwent elective lower limb surgical procedures.
Exclusion criteria
* Patients who received general anesthesia, neuraxial anesthesia, or infiltration anesthesia were excluded.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Block Success which provided surgical anesthesia, intraoperatively | Intraoperatively and PACU unit (up to 2 hours) | After performing the blocks, the sensory block was examined with a pinprick test using a 27-gauge hypodermic needle, (0 = no sensory block; 1 = tactile sense present, no pain; 2 = no tactile sense and no pain). Cases with a score of 1 or 2 after 30 min were considered successful. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Additional analgesic requirement | Intraoperatively and PACU unit (up to 2 hours) | The number of patient who required intravenous ketamine or propofol infusion were recorded. |
Countries
Turkey (Türkiye)
Outcome results
None listed