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Randomized Controlled Trial
. 2022 Dec 15:2022:6022380.
doi: 10.1155/2022/6022380. eCollection 2022.

Reduced Opioid Consumption with Pericapsular Nerve Group Block for Hip Surgery: A Randomized, Double-Blind, Placebo-Controlled Trial

Affiliations
Randomized Controlled Trial

Reduced Opioid Consumption with Pericapsular Nerve Group Block for Hip Surgery: A Randomized, Double-Blind, Placebo-Controlled Trial

Chan Jong Chung et al. Pain Res Manag. .

Abstract

The pericapsular nerve group (PENG) block targets the nerves innervating the anterior hip surface; however, few studies on this technique are currently available. We investigated the effects of the PENG block on postoperative opioid consumption after a hip surgery. This was a randomized, double-blind, placebo-controlled study conducted at a single institution. Fifty patients undergoing hip surgery were randomly allocated, 25 in each group, to receive a PENG block either using 25 mL of 0.5% ropivacaine (PENG group) or 25 mL of saline (control group). The primary outcome was the total opioid consumption 24 h postoperatively. The secondary outcomes were postoperative pain scores, time to first opioid demand, sensory block efficiency, quadriceps muscle strength, complications, and patient satisfaction. Compared with those in the control group, patients in the PENG group had a significantly lower total opioid consumption 24 h postoperatively (440.72 ± 242.20 μg vs. 611.07 ± 313.89 μg, P = 0.037) and significantly lower pain scores at 30 min postblock and 6 postoperatively (P < 0.001 and P < 0.001, respectively). The time to first opioid demand was significantly shorter in the control group than in the PENG group (P < 0.001). Sensory block effectiveness was better in the PENG group 30 min postblock and 6 and 12 h postoperatively than in the control group. Patient satisfaction was also better in the PENG group than in the control group. There were no differences in the other outcomes. The PENG block reduced the total opioid consumption in the first 24 h after hip surgery with no significant effects on quadriceps muscle strength and complication rate. This study was registered at the Korea Clinical Research Information Service (cris.nih.go.kr; Reg. No. KCT0006348) on July 16, 2021.

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Conflict of interest statement

The authors declare that they have no conflicts of interest regarding the publication of this paper.

Figures

Figure 1
Figure 1
Ultrasound images of pericapsular nerve group block performed via a lateromedial approach. (a) Shows the needle position. The needle is outlined by yellow arrows. (b) Shows the local anesthetic spread following injection. FA, femoral artery; LA, local anesthetic; IPE, iliopubic eminence; AIIS, anterior inferior iliac spine; PT, psoas tendon.
Figure 2
Figure 2
CONSORT flow diagram. CONSORT, consolidated standards of reporting trials; PENG, pericapsular nerve group; control, control group.
Figure 3
Figure 3
Comparison in intravenous fentanyl equivalent consumption (μg) during the first postoperative 24 hrs, presented as mean ± standard deviation (SD). IV, intravenous; PENG, pericapsular nerve group; control, control group. A statistically significant difference. P values were derived by the independent t-test. The Shapiro–Wilk test was employed to test the normality assumption.
Figure 4
Figure 4
Mean ± standard deviation (SD) plot of pain scores during the first postoperative 24 hrs. NRS, numerical rating scale; PENG, pericapsular nerve group; control, control group; preop, preoperatively; postop, postoperatively. A statistically significant difference. P values were derived from Mann–Whitney's U test and adjusted by the Bonferroni correction method. Shapiro–Wilk's test was employed to test the normality assumption.
Figure 5
Figure 5
Comparison of sensory block effectiveness between the groups 30 min postblock and 6, 12, and 24 h postoperatively. PENG, pericapsular nerve group; control, control group; postop, postoperatively. A statistically significant difference. P values were derived by the chi-square test.

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