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The Analgesic Effects of Ultrasound-guided Recto-intercostal Fascial Plane Block in Laparoscopic Hiatus Hernia Repair: A Randomized Double-Blind Controlled Study

Revista

anaesthesia critical care pain medicine

Fecha de publicación

5 de diciembre de 2025

Anaesth Crit Care Pain Med. 2025 Dec 3:101724. Revista: 10.1016/j.accpm.2025.101724. Online ahead of print.

BACKGROUND: Pain after laparoscopic hiatus hernia repair (LHHR) is multifactorial, with parietal pain representing up to 70% of its origin. Opioid induced postoperative nausea and vomiting (PONV) is of great concern, as it may predispose to anatomical failure and the need for revision. This study evaluated the opioid sparing value of the recto-intercostal fascial plane block (RIFPB) in this manner.

METHODS: A randomized, double-blind, controlled trial was conducted on 44 patients who were assigned equally into a RIFPB group [20 mL of bupivacaine (0.25%) for each side] and a control group [(C), without block]. The primary aim was the total 24 h opioid consumption post-surgery, and secondary outcomes included intraoperative fentanyl consumption, postoperative pain scores, PONV incidence, and patient satisfaction scores.

RESULTS: The RIFPB group had significantly lower 24-h postoperative morphine consumption than the control group (9 ± 3 mg vs. 20.8 ± 6.9 mg); P < 0.001. The median (IQR) fentanyl dose was significantly lower in the RIFPB group than in group C, 0.5 (0 -1) vs. 2 (1-2) µg/kg; P < 0.001. The RIFPB group had a significantly prolonged time to first morphine request (P < 0.001), lower postoperative pain scores at all assessment time points (P < 0.05) except at 8 h after surgery, a higher median value of patient satisfaction scores (4 vs. 3; P < 0.001), and a lower incidence of PONV, P = 0.034.

CONCLUSION: The RIFPB reduced the intraoperative nociception and the 24-h postoperative opioid consumption after LHHR. Also, it delayed the need for rescue morphine; reduced pain scores, PONV incidence, and increased patient satisfaction after surgery.

REGISTRATION: ClinicalTrials.gov (NCT06820216).

PubMed:41349840 | Revista:10.1016/j.accpm.2025.101724

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El idioma original es este artículo es el inglés. Mediante el sistema de traducción automático de la IA de emergencing, el contenido se ha traducido al español. Esta es una traducción no supervisada por lo que puede que alguna parte del contenido no refleje con exactitud la publicación original del autor/autores.