Abstract
Objective
We aimed to evaluate the efficacy of rhomboid intercostal block (RIB) for analgesia management in patients who underwent video-assisted thoracoscopic surgery.
Methods
Adult patients who underwent VATS under general anesthesia between July 2020 and June 2022 were included in the study. There was two groups in this study: RIB (n = 25) vs control (n = 25) group. RIB was performed with 30 ml 0.25% bupivacaine at the end of the surgery. Surgical intercostal blockade was performed with 30 ml 0.25% bupivacaine in the control group. The patients received intravenous fentanyl patient-controlled postoperative analgesia. The numerical rating score (NRS), opioid consumption, and adverse events were recorded.
Results
A total of 50 patients were randomized into 2 groups. There were no significant difference in terms of the demographic data between groups (P > 0.05). Postoperative opioid consumption at 0–8, 8–16, 16–24, and 24–48 h and rescue analgesic use were significantly lower in RIB group (P < 0.05). At all times, the static/dynamic NRS were significantly lower in RIB group. The rate of nausea and itching was higher in control group (P < 0.05).
Conclusion
US-guided RIB provides effective post-VATS analgesia.
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Data availability
The datasets generated and/or analyzed during the current study are available from the corresponding author on reasonable request
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This study has been approved by Istanbul Medipol University Ethics and Research Committee (16/06/2020, Decision No: E.17828). All methods were carried out in accordance with relevant guidelines and regulations.
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Ciftci, B., Alver, S., Güngör, H. et al. The efficacy of rhomboid intercostal block for pain management after video-assisted thoracoscopic surgery: a prospective, randomized-controlled trial. Gen Thorac Cardiovasc Surg (2024). https://doi.org/10.1007/s11748-024-02036-8
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DOI: https://doi.org/10.1007/s11748-024-02036-8