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Effects of esketamine on postoperative pain and inflammatory factors in children undergoing tonsillectomy and adenoidectomy.

Yuchang Zhu, Xujian Wang, Lifeng Wang, Yi Zhang

Minerva anestesiologica 2025 DOI: 10.23736/S0375-9393.24.18277-6 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Randomized controlled trial Peer reviewed
Sample size 80
Population Children undergoing tonsillectomy and adenoidectomy
Intervention Esketamine
Topics Esketamine Ketamine
Keywords Pediatric_medicine Pain_management Anesthesiology Surgical_recovery Esketamine_therapy
Citations 3
Key findings Esketamine reduced postoperative pain scores, emergence agitation, and inflammatory markers compared to control without increasing adverse reactions.

Abstract

This study aimed to observe the effect of esketamine on postoperative pain and inflammatory factors in children undergoing tonsillectomy and adenoidectomy. Eighty children scheduled for tonsillectomy and adenoidectomy were randomly divided into two groups using a random number table: an esketamine group (S-ketamine group, N.=40) and a control group (control group, N.=40). The primary outcome was the postoperative pain score, measured using the Face, Legs, Activity, Cry, and Consolability (FLACC) pain scale score. Secondary outcomes include the emergence agitation score (Pediatric Anesthesia Emergence Delirium [PAED]), the operation time, recovery time, postanesthesia care unit (PACU) stay time, adverse reactions within 48 h after operation, and the plasma C-reactive protein (CRP) and interleukin-6 (IL-6) concentrations. At T1, T2, T3, T4, and T5, the FLACC pain scores of the S-ketamine group were significantly lower than those of the control group (15 min: 2.4±0.7 vs. 3.4±0.8, P<0.01; 1 h: 1.7±0.6 vs. 2.2±0.7, P<0.01; 6 h: 1.5±0.6 vs. 2.0±0.5, P<0.01; 12 h: 1.5±0.6 vs. 1.8±0.7, P<0.05; 24 h: 1.4±0.6 vs. 1.7±0.6, P<0.05). The PAED scores at T1 and T2 in the S-ketamine group were significantly lower than those in the control group (15 min: 4.0±0.9 vs. 6.4±1.3, P<0.01; 1 h: 1.7±0.6 vs. 2.1±0.5, P<0.01). Compared with T0, the plasma CRP and IL-6 concentrations at T3 in the two groups were significantly increased (P<0.01), but the increase in the S-ketamine group was significantly smaller than that in the control group at T3 (IL-6: 111.8±19.2 vs. 145.8±22.5, P<0.01; CRP: 1.2±0.5 vs. 1.5±0.5, P<0.01). The other outcomes were similar between the two groups. Esketamine used in pediatric tonsillectomy and adenoidectomy can effectively reduce postoperative FLACC, PAED score, and levels of inflammatory factors without increasing adverse reactions.

Comparable studies

Other randomized controlled trials on esketamine, most cited first.

Study Year Design Participants
Efficacy and Safety of Flexibly Dosed Esketamine Nasal Spray Combined With a Newly Initiated Oral Antidepressant in Treatment-Resistant Depression: A Randomized Double-Blind Active-Controlled Study Adults with moderate to severe nonpsychotic depression and a history of nonresponse to... 2019 Phase 3, double-blind, active-controlled, multicenter randomized controlled trial n = 227
Efficacy of Esketamine Nasal Spray Plus Oral Antidepressant Treatment for Relapse Prevention in Patients With Treatment-Resistant Depression Adults with treatment-resistant depression who achieved stable remission or stable... 2019 Phase 3, multicenter, double-blind, randomized withdrawal study n = 297
Efficacy and Safety of Intranasal Esketamine Adjunctive to Oral Antidepressant Therapy in Treatment-Resistant Depression Adults with DSM-IV-TR diagnosis of major depressive disorder and history of inadequate... 2017 Phase 2, double-blind, doubly randomized, delayed-start, placebo-controlled study n = 67
Efficacy and Safety of Intranasal Esketamine for the Rapid Reduction of Symptoms of Depression and Suicidality in Patients at Imminent Risk for Suicide: Results of a Double-Blind, Randomized, Placebo-Controlled Study Depressed patients at imminent risk for suicide 2018 Randomized controlled trial n = 68
Efficacy and Safety of Fixed-Dose Esketamine Nasal Spray Combined With a New Oral Antidepressant in Treatment-Resistant Depression: Results of a Randomized, Double-Blind, Active-Controlled Study (TRANSFORM-1) Adults with moderate-to-severe depression and nonresponse to at least two... 2019 Randomized controlled trial n = 346

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