Abstract

Study objectivesTo verify the clinical feasibility of parasacral ischial plane (PIP) block in hip surgery, we conducted a randomized controlled trial comparing the effects of combined lumbar and PIP block and general anesthesia on patient pain and outcomes. DesignRandomized controlled trial. SettingOperating room. Patients60 participating patients scheduled for elective total hip arthroplasty. InterventionsAll patients were divided into two groups. The first group (n=30) received general anesthesia, and the second group, the LPIP group (n=30), received a combined lumbar and parasacral ischial plane block. MeasurementsPostoperative outcomes were investigated using Shapiro–Wilk test, X2 test and mixed model accounting. The primary outcome was total intravenous patient control analgesia (PCA) pump consumption of sufentanil in the first 24 h. Secondary outcomes included pain scores at 3, 6, 12, and 24 h after surgery; time to rehabilitation placement; hospital length of stay; and postoperative nausea and vomiting. Main resultsThere was significant difference in the postoperative 24-hour PCA pump consumption of sufentanil (general anesthesia group, median [interquartile range], 74 [66 to 87] μg versus LPIP group, 65 [57 to 72] μg; median difference, 12; 95% CI, 4 to 19; P =0.004). The pain scores (rest or movement) at 3h and 6h after surgery were significantly different between the two groups (p<0.001). There was no statistical difference between the two groups in time to rehabilitation placement (median difference, 1.3; 95% CI, 22.5 to 27.5; P = 0.155), hospital length of stay, and postoperative nausea and vomiting. ConclusionsThe LPIP block facilitates comfortable and uneventful hip surgery, reduces the PCA consumption of sufentanil, and does not affect the postoperative recovery time.

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