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Glossopharyngeal nerve block versus tonsillar fossa ropivacaine infiltration within multimodal analgesia for pediatric post-tonsillectomy pain: a randomized controlled clinical trial

In brief

Glossopharyngeal nerve block doubles time to first rescue analgesic after pediatric tonsillectomy

In a double-blind trial of 90 children, bilateral glossopharyngeal nerve block with 0.2% ropivacaine extended the median time to first pain medication to 4 hours versus 2 hours with standard care, while also lowering resting and swallowing pain, reducing nausea, and improving sleep and parental satisfaction. No increase in sedation or serious anesthetic complications was observed.

Journal
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery (Q1)
Published
5 August 2026
Study design
Randomized controlled trial
Evidence level
Level 1, High (CEBM 1b)
Authors
Mohammad Faramarzi, Maryam Nemati, Arash Farbood, Ali Faramarzi
PMID
42552476
DOI
10.1007/s00405-026-10522-3

Why clinicians should know about it

  • Picked for Otorhinolaryngology (top studies of the week, 9 August 2026): Glossopharyngeal nerve block reduces post‑tonsillectomy pain in children

Abstract

PURPOSE: Pediatric tonsillectomy is associated with substantial postoperative pain. We compared glossopharyngeal nerve block (GNB) with peritonsillar ropivacaine infiltration (RI) within multimodal analgesia. METHODS: In this double-blind randomized trial, 90 children (4-10 years) undergoing day-case tonsillectomy were randomly allocated in a 1:1:1 ratio (30 per group) to receive bilateral GNB with 0.2% ropivacaine, RI with 0.2% ropivacaine, or sham control. The primary outcome was post-anesthesia care unit (PACU) pain measured by the Face, Legs, Activity, Cry, Consolability (FLACC) scale; secondary outcomes included pain at rest and during swallowing measured by the Wong-Baker FACES Pain Rating Scale (FACES) at rest and during swallowing (2-24 h), time to first analgesic request, nausea, sleep quality, parental satisfaction, and adverse events. RESULTS: Time to first analgesic request was significantly longer in the GNB group than in the control group (median 240 vs. 120 min; P < 0.001). Pain at rest was lower with GNB than control from 2 to 12 h and lower than RI at 6 h, and swallowing pain was lower with GNB than both comparators from 2 to 24 h (all P ≤ 0.008) . Nausea was less frequent with GNB (6.7%) than RI (20%) or control (33.3%) (P = 0.036), and sleep quality and parental satisfaction were higher with GNB (P = 0.010 and P < 0.001). PACU FLACC and sedation scores were similar, and no serious anesthetic-related arrhythmias or bronchospasm were observed. CONCLUSIONS: Within the studied multimodal analgesic regimen, bilateral GNB with 0.2% ropivacaine was associated with lower postoperative pain scores, improved swallowing comfort, longer time to first rescue analgesia, and better caregiver-reported outcomes in this randomized cohort, without increased sedation or observed major anesthetic-related complications.

Abstract as published, via PubMed.

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For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.