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PubMed · 41940446

Low-Dose Perineural Dexamethasone Enhances Analgesia After Pediatric Hand Surgery Without Elevating Systemic Stress Markers: A Randomized Controlled Trial.

Tomasz Reysner·Bahadir Ciftci·Szymon Bialka·Wojciech Gola·Piotr Czarecki·Pawel Pietraszek·Grzegorz Kowalski·Przemyslaw Daroszewski·Malgorzata Reysner
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Abstract

BACKGROUND: Supraclavicular brachial plexus block is a widely used technique for upper limb surgery in children. Although perineural dexamethasone has demonstrated efficacy in prolonging analgesia in adults, data on its optimal dosing and systemic safety in pediatric patients are limited. This study aimed to evaluate whether low-dose perineural dexamethasone can prolong postoperative analgesia without increasing systemic stress markers in young children undergoing hand or wrist surgery. METHODS: In this triple-blinded, randomized controlled trial (ClinicalTrials.gov Identifier: NCT06086392), 90 children aged 3 months to 6 years undergoing elective upper extremity surgery were assigned to receive supraclavicular brachial plexus block with 0.2% ropivacaine combined with either normal saline (control), dexamethasone 0.05&#xa0;mg/kg, or dexamethasone 0.1&#xa0;mg/kg. The primary outcome was time from arrival in the postanesthesia care unit to first administration of rescue opioid analgesia. Secondary outcomes included total opioid consumption, postoperative pain intensity using the FLACC scale, blood glucose levels, neutrophil-to-lymphocyte ratio, platelet-to-lymphocyte ratio, and time to motor recovery. RESULTS: Both dexamethasone groups demonstrated significantly prolonged time to first opioid use compared with the control group (mean&#xb1;SD: 19.4&#xb1;2.2&#xa0;h in the 0.1&#xa0;mg/kg group, 16.0&#xb1;1.9&#xa0;h in the 0.05&#xa0;mg/kg group, and 8.5&#xb1;1.3&#xa0;h in controls; P <0.0001). Total opioid consumption was significantly reduced in the dexamethasone groups. Postoperative pain scores were lower in both intervention groups, especially during the first 12 hours. No significant differences were found among groups in blood glucose, inflammatory markers, or incidence of nerve deficits. Motor recovery was delayed in the dexamethasone groups but did not interfere with early mobilization. CONCLUSIONS: Low-dose perineural dexamethasone (0.05 to 0.1&#xa0;mg/kg) safely and effectively prolongs postoperative analgesia and reduces opioid needs in children undergoing upper limb surgery, without causing systemic metabolic or inflammatory disturbances. The 0.05&#xa0;mg/kg dose may offer a more favorable balance between analgesic efficacy and motor recovery time. LEVEL OF EVIDENCE: Level I-randomized controlled trial.

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HumansDexamethasonePostoperative PainFemaleChild, PreschoolMaleInfantChildHandBrachial Plexus BlockRopivacaineAnalgesics, OpioidAnesthetics, LocalPain MeasurementBiomarkersTreatment OutcomePediatric AnesthesiaAnti-Inflammatory AgentsGlucocorticoidsFLACC scoreopioid-sparingpediatric analgesiaperineural dexamethasonepostoperative painregional anesthesiasupraclavicular brachial plexus blockJournal ArticleRandomized Controlled Trial

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Tomasz Reysner, Bahadir Ciftci, Szymon Bialka, Wojciech Gola, Piotr Czarecki, Pawel Pietraszek, Grzegorz Kowalski, Przemyslaw Daroszewski, Malgorzata Reysner. 2026-04-06. Low-Dose Perineural Dexamethasone Enhances Analgesia After Pediatric Hand Surgery Without Elevating Systemic Stress Markers: A Randomized Controlled Trial.. https://doi.org/10.1097/bpo.0000000000003287

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Journal Article; Randomized Controlled Trial resourceAnalgesics, Opioid subjectAnesthetics, Local subjectAnti-Inflammatory Agents subjectBiomarkers subjectChild subjectChild, Preschool subjectDexamethasone subjectFemale subjectHand subjectHumans subjectInfant subjectJournal Article subjectMale subjectPain Measurement subjectPostoperative Pain subject

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