This study is evaluating whether the timing of an interscalene nerve block affects pain control and recovery after arthroscopic rotator cuff repair surgery. An interscalene block is commonly used to reduce pain after shoulder surgery. However, it is not known whether administering the block before surgery or after surgery provides better outcomes. Participants undergoing arthroscopic rotator cuff repair are assigned to receive the interscalene block either before the surgical incision or after completion of the procedure. The study compares postoperative pain levels, opioid medication use, length of hospital stay, and ultrasound imaging quality during block administration between the two groups. Functional recovery is also assessed using patient-reported outcome measures during follow-up. The investigators hypothesize that administration of the interscalene block before surgery may provide superior early pain control and reduce postoperative opioid requirements while maintaining similar functional outcomes compared with administration after surgery.
Postoperative pain remains a major challenge following arthroscopic rotator cuff repair despite advances in multimodal analgesia protocols. Inadequate pain control may delay rehabilitation, increase opioid consumption, prolong hospitalization, and negatively affect patient satisfaction. Ultrasound-guided interscalene block has become a cornerstone of perioperative pain management for shoulder surgery because of its proven analgesic efficacy and favorable safety profile. Although interscalene block is routinely used in clinical practice, the optimal timing of administration remains controversial. Administration before surgical incision may provide preemptive analgesic effects by attenuating central sensitization and reducing nociceptive input during surgery. In contrast, administration after completion of surgery has been proposed as a strategy to extend the duration of postoperative analgesia. Existing literature provides limited and inconsistent evidence regarding the comparative clinical benefits of these approaches in patients undergoing arthroscopic rotator cuff repair. This study was designed to evaluate the impact of interscalene block timing within a contemporary shoulder surgery pathway. In addition to its potential influence on perioperative analgesia, the timing of block administration may affect procedural workflow and ultrasound visualization of relevant anatomical structures. Improved understanding of these factors may contribute to optimization of perioperative management strategies and support evidence-based recommendations for regional anesthesia practices in arthroscopic shoulder surgery.
Study Type
OBSERVATIONAL
Enrollment
42
Istinye University Bahcesehir Liv Research and Training Hospital
Istanbul, Turkey (Türkiye)
Early Postoperative Pain Intensity
Patients' postoperative pain intensity measured using the Visual Analog Scale (VAS) following arthroscopic rotator cuff repair. Pain scores will be compared between pre-procedure and post-procedure interscalene block groups. The scale ranges from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate worse pain intensity.
Time frame: Pre-procedure, postoperative 6th, 12th, 24th hours
Postoperative Opioid Consumption
Total opioid consumption recorded during the first postoperative 24 hours.
Time frame: 24 hours after surgery
Patient-Controlled Analgesia Usage
Number of patient-controlled analgesia (PCA) bolus demands during the postoperative period.
Time frame: 24 hours after surgery
Duration of hospitalization following arthroscopic rotator cuff repair.
Duration of hospitalization following arthroscopic rotator cuff repair.
Time frame: From surgery until hospital discharge
Ultrasound Image Quality During Interscalene Block Administration
Quality of ultrasound visualization of the interscalene region assessed by the performing anesthesiologist using a 5-point Likert scale.
Time frame: At the time of interscalene block administration
Oxford Shoulder Score
Functional shoulder outcome assessed using the Oxford Shoulder Score questionnaire. The Oxford Shoulder Score ranges from 0 to 48, with higher scores indicating better shoulder function.
Time frame: Baseline, 3 months, and 6 months after surgery
Disabilities of the Arm, Shoulder and Hand (DASH) Score
Upper extremity functional outcome assessed using the DASH questionnaire. The score ranges from 0 to 100, with higher scores indicating greater disability and worse upper extremity function.
Time frame: Baseline, 3 months, and 6 months after surgery
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