Comparison of Pericapsular Nerve Group Block With Suprainguinal Fascia Compartment Block in Hip Fractures
- Conditions
- Hip Fractures
- Interventions
- Procedure: PENG block+ SIFCBProcedure: PENG block
- Registration Number
- NCT06169462
- Lead Sponsor
- Karaman Training and Research Hospital
- Brief Summary
Ultrasound-guided Supra-inguinal Fascia Iliaca compartment Block (SIFCB) and Pericapsular Nerve Group Block (PENG) are increasingly being used for postoperative analgesia for hip surgery. The postoperative analgesic efficacy of SIFCB added to PENG block in elderly hip fracture patients will be evaluated. Postoperative opioid consumption and quality of recovery will also be evaluated.
- Detailed Description
The study was conducted as a retrospective cohort feasibility design within a tertiary hospital. Patient records and electronic data systems were used to gather the required data for analysis. Before surgery, a carefully selected cohort of patients who underwent PENG block and PENG block added SIFCB were included in the study.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 38
- Physical status according to American Society of Anesthesiologists (ASA ) I-III
- Previous operation on the same hip
- Hepatic or renal insufficiency
- Patients undergoing general anesthesia
- Allergy or intolerance to one of the study medications
- BMI >40
- ASA IV
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Suprainguinal fascia compartment block (SIFCB) + PENG PENG block+ SIFCB Patients who underwent PENG+SIFCB in Hip surgery under spinal anesthesia will be evaluated retrospectively in terms of opioid consumption and NRS scores. Pericapsular nerve group (PENG) block PENG block Patients who underwent PENG in Hip surgery under spinal anesthesia will be evaluated retrospectively in terms of opioid consumption and NRS scores.
- Primary Outcome Measures
Name Time Method Opioid consumption Postoperative 48th hour If the patient's Numerical Rating Scale (NRS) score is equal to or above 4, tramadol 50 mg IV or oxycodone 5 mg orally every 4 hours will be administered as rescue analgesia.
- Secondary Outcome Measures
Name Time Method Postoperative complications 24 hours Presence of postoperative nausea, vomiting, pruritus, urinary retention, respiratory depression
Numerical Rating Scale (NRS) scores Postoperative 48th hour Range 0-10, 0=no pain, 10=the worse pain ever
Quality of Recovery 15 Score Postoperative day 1 and 1 month Quality of Recovery (QoR)-15 survey.Minimum value: 0, Maximum value: 150, higher scores mean better
Mobilization time 24 hours Mobilization time
Trial Locations
- Locations (1)
Karaman Training and Research Hospital
🇹🇷Karaman, Karaman/Merkez, Turkey