Hip fractures are among the most common orthopedic traumas, particularly in elderly patients, and are usually associated with significant pain during positioning for spinal anesthesia. Adequate pain control during positioning can improve patient comfort and facilitate successful administration of anesthesia. The pericapsular nerve group (PENG) block has recently been introduced as a regional anesthesia technique that targets articular branches of the femoral, obturator, and accessory obturator nerves, and has been proposed as a method to reduce pain related to hip fracture positioning. This study is designed to compare the efficacy of preoperative PENG block versus no block in patients undergoing proximal femoral nailing surgery under spinal anesthesia. The primary objective is to assess its effect on positioning pain using visual analog scale (VAS) scores. Secondary objectives include evaluating its impact on postoperative analgesic consumption, time to first rescue analgesic, and potential side effects.
This is a prospective, single-center, randomized controlled trial conducted at the University of Health Sciences, Kartal Dr. Lütfi Kırdar City Hospital. A total of 60 patients, aged 18-90 years, with ASA I-III status, scheduled for proximal femoral nailing (PFN) surgery due to hip fracture, were enrolled. Patients were randomized into two groups using a sealed-envelope method: PENG Block Group: Received a preoperative ultrasound-guided pericapsular nerve group (PENG) block 30 minutes before spinal anesthesia. Control Group: Received no block prior to spinal anesthesia. Standard spinal anesthesia was performed in both groups. All patients received intravenous paracetamol for postoperative analgesia at regular intervals. Additional analgesia with intravenous tramadol was administered if VAS ≥ 4. The following parameters were collected: Demographics (age, sex, BMI, ASA status, comorbidities) Hemodynamic variables (SBP, DBP, HR, SpO₂) at baseline and during perioperative period VAS scores at baseline, during positioning, and at postoperative time intervals (0, 15, 30 minutes, and 1, 2, 6, 12, and 24 hours) Time to first rescue analgesic Total opioid consumption in the first 24 hours postoperatively Side effects such as nausea, vomiting, or other complications The study aims to test the hypothesis that PENG block can reduce pain during positioning for spinal anesthesia and may improve postoperative analgesia in patients undergoing hip fracture surgery.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
60
A single-shot PENG block was administered preoperatively using ultrasound guidance. The block was performed with the patient in the supine position, and 20 mL of local anesthetic (0.25% bupivacaine) was injected between the psoas tendon and the superior pubic ramus to achieve analgesia of the anterior hip capsule.
Patients in this arm were managed according to standard care protocols for spinal anesthesia in hip fracture surgery. No preoperative regional block was performed. Pain scores and postoperative tramadol use were measured for comparison with the experimental arm.
Facility Name: Kartal Dr. Lütfi Kırdar City Hospital, University of Health Sciences
Istanbul, Turkey (Türkiye)
Pain intensity during positioning for spinal anesthesia
Pain scores were recorded using the Visual Analog Scale (VAS; 0-10 cm, where 0 = no pain and 10 = worst pain imaginable) during positioning for spinal anesthesia prior to hip fracture surgery.
Time frame: During spinal anesthesia positioning (within 15 minutes preoperatively)
Postoperative VAS scores
Pain scores were assessed using the Visual Analog Scale (VAS) at 2, 6, 12, and 24 hours postoperatively.
Time frame: 0-24 hours after surgery
Cumulative tramadol requirement in the first 24 hours
The total dose of intravenous tramadol administered for breakthrough pain was recorded for each patient.
Time frame: 0-24 hours after surgery
Time to first request for rescue analgesia
The duration (in hours) between the end of surgery and the first administration of rescue tramadol was recorded.
Time frame: 0-24 hours after surgery
Incidence of adverse events related to anesthesia
Frequency of side effects such as nausea, vomiting, hypotension, and local anesthetic systemic toxicity were documented.
Time frame: Intraoperative to 24 hours postoperatively
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.