PMID- 37145010 OWN - NLM STAT- MEDLINE DCOM- 20230508 LR - 20230916 IS - 1536-5964 (Electronic) IS - 0025-7974 (Print) IS - 0025-7974 (Linking) VI - 102 IP - 18 DP - 2023 May 5 TI - Popliteal sciatic nerve block for high-risk patients undergoing lower limb angioplasty: A prospective double-blinded randomized controlled trial. PG - e33690 LID - 10.1097/MD.0000000000033690 [doi] LID - e33690 AB - BACKGROUND: To assess the rate of conversion to general anesthesia, sedative and analgesic drug-sparing effects, and complications of popliteal sciatic nerve block (PSNB) compared with a sham block during lower limb angioplasty. METHODS: A randomized, controlled, double-blinded trial of patients with chronic limb-threatening ischemia (CLTI) who receive PSNB with 0.25% levobupivacaine 20 mL compared with a sham block (control) during lower limb angioplasty. Pain scores, conversion rate to general anesthesia, amount of sedoanalgesia drug usage, complications, and satisfaction with the anesthesia technique by surgeons and patients were assessed. RESULTS: Forty patients were enrolled in this study. Two of 20 (10%) control group patients were converted to general anesthesia, while none of the patients in the intervention group required general anesthesia (P = .487). Pain scores before PSNB did not differ between the groups (P = .771). After the block, pain scores in the block group were lower than those in the control group: 0 (0, 1.5) (median, interquartile range) and 2.5 (0.5, 3.5), respectively (P = .024). The analgesic effect persisted until immediately after the surgery (P = .035). There was no difference in pain scores at the 24-hours follow-up visit (P = .270). The total propofol and fentanyl dosage requirements, a number of patients who required propofol and fentanyl, side effects, and satisfaction were not different between the groups. No major complications were noted. CONCLUSIONS: PSNB provided effective pain relief during and immediately after lower limb angioplasty, but did not statistically affect the rate of conversion to general anesthesia, sedoanalgesia drug usage, or complications. CI - Copyright (c) 2023 the Author(s). Published by Wolters Kluwer Health, Inc. FAU - Noikham, Alif AU - Noikham A AUID- ORCID: 0000-0003-3644-4562 AD - Department of Anesthesiology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand. FAU - Tivirach, Wannapa AU - Tivirach W AD - Department of Anesthesiology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand. FAU - Pongraweewan, Orawan AU - Pongraweewan O AD - Department of Anesthesiology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand. FAU - Suphathamwit, Aphichat AU - Suphathamwit A AD - Department of Anesthesiology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand. FAU - Puangpunngam, Nattawut AU - Puangpunngam N AD - Division of Vascular Surgery, Department of Surgery, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand. FAU - Jirativanont, Tachawan AU - Jirativanont T AD - Department of Anesthesiology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand. LA - eng PT - Journal Article PT - Randomized Controlled Trial PL - United States TA - Medicine (Baltimore) JT - Medicine JID - 2985248R RN - YI7VU623SF (Propofol) RN - UF599785JZ (Fentanyl) RN - 0 (Analgesics) SB - IM MH - Humans MH - Pain, Postoperative/etiology/drug therapy MH - *Propofol/therapeutic use MH - Prospective Studies MH - *Nerve Block/methods MH - Sciatic Nerve MH - Fentanyl/therapeutic use MH - Lower Extremity/surgery MH - Analgesics/therapeutic use MH - Angioplasty PMC - PMC10158915 COIS- The authors have no conflicts of interest to disclose. EDAT- 2023/05/05 12:42 MHDA- 2023/05/08 06:42 PMCR- 2023/05/05 CRDT- 2023/05/05 10:13 PHST- 2023/05/08 06:42 [medline] PHST- 2023/05/05 12:42 [pubmed] PHST- 2023/05/05 10:13 [entrez] PHST- 2023/05/05 00:00 [pmc-release] AID - 00005792-202305050-00027 [pii] AID - 10.1097/MD.0000000000033690 [doi] PST - ppublish SO - Medicine (Baltimore). 2023 May 5;102(18):e33690. doi: 10.1097/MD.0000000000033690.