Gabapentin Pretreatment for Propofol and Rocuronium Injection Pain: A Randomized, Double-Blind, Placebo-Controlled Study

dc.contributor.authorCakirgoz, M. Y.
dc.contributor.authorDemirel, I.
dc.contributor.authorDuran, E.
dc.contributor.authorOzer, A. B.
dc.contributor.authorTurkmen, U. A.
dc.contributor.authorErsoy, A.
dc.contributor.authorHanci, V.
dc.date.accessioned2026-08-12T17:17:29Z
dc.date.issued2018
dc.departmentFırat Üniversitesi
dc.description.abstractAim: This prospectively-planned, randomized, double-blind and placebo-controlled study aims to evaluate the effect of 1200 mg gabapentin premedication on the incidence and severity of propofol and rocuronium injection pain. Method: One hundred patients, between 18-60 years of age and ASA I-II for elective surgery planned under general anaesthetic, were randomized and divided into two groups. Two hours before the operation, the patients were given either a placebo tablet (Group P, n = 50) or 1200 mg gabapentin tablet (Group G, n = 50). On the back of the non-dominant hand, a vein was opened using a 20 G cannula , 0.9% NaCl was begun and preoxygenation was provided. For anaesthesia induction, 1% propofol at 800 ml/hr infusion rate was administered for 20 s. Propofol injection pain was evaluated up to the 20th second and recorded using a scale between 0 and 3 developed by McCrirrick and HunteR The remaining propofol dose (2.5 mg/kg), 5 ml saline and 0.6 mg/kg rocuronium were injected in that order over 10 seconds and rocuronium injection pain response was evaluated with a four point scale. Results: Pain after propofol infusion average score (degree >= 1) (Group G = 0.5; Group P = 1.0) and incidence (Group G = 46%; Group P = 68%); and average withdrawal movements response score linked to rocuronium injection pain (>= 1 response) (Group G = 0.3; Group P = 1.2) and incidence (Group G = 20%; Group P = 80%) were detected to be significantly lower in the gabapentin group compared to the placebo group (p < 0.001). Conclusion: Premedication with 1200 mg gabapentin 2 hours before propofol and rocuronium injection reduced the incidence and severity of injection pain.
dc.identifier.doi10.4103/1119-3077.224791
dc.identifier.endpage48
dc.identifier.issn1119-3077
dc.identifier.issue1
dc.identifier.orcid0000-0002-2227-194X
dc.identifier.orcid0000-0001-7687-0924
dc.identifier.pmid29411722
dc.identifier.scopus2-s2.0-85041721414
dc.identifier.scopusqualityQ2
dc.identifier.startpage43
dc.identifier.urihttps://doi.org/10.4103/1119-3077.224791
dc.identifier.urihttps://hdl.handle.net/11508/52677
dc.identifier.volume21
dc.identifier.wosWOS:000424796100008
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWolters Kluwer Medknow Publications
dc.relation.ispartofNigerian Journal of Clinical Practice
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectGabapentin
dc.subjectinjection pain
dc.subjectpropofol
dc.subjectrocuronium
dc.titleGabapentin Pretreatment for Propofol and Rocuronium Injection Pain: A Randomized, Double-Blind, Placebo-Controlled Study
dc.typeArticle

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