Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/17184
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dc.contributor.authorKusumaphanyo C.
dc.contributor.authorSuthachiva A.
dc.contributor.authorSriramatr D.
dc.contributor.authorPromma C.
dc.contributor.authorJulla N.
dc.date.accessioned2022-03-10T13:16:36Z-
dc.date.available2022-03-10T13:16:36Z-
dc.date.issued2021
dc.identifier.issn1252208
dc.identifier.other2-s2.0-85115994022
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/17184-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85115994022&doi=10.35755%2fjmedassocthai.2021.S03.00022&partnerID=40&md5=3f148c87806b9954320406db24021686
dc.description.abstractBackground: Postoperative sore throat (POST) is a common complication found in surgical patients undergoing general anesthesia with endotracheal tube (ETT). Its severity varies and may affect postoperative outcomes and patient satisfaction. Aescin is an extract from horse chestnut (Aesculus Hippocastanum) that possesses the anti-inflammatory, venous decongestion, and antiedema property with few side effects. Objective: To demonstrate the reduction of incidence and severity of POST in patients undergoing general anesthesia with ETT. Materials and Methods: One hundred and seventeen patients, ASA I and II undergoing general anesthesia with ETT with elective surgery (abdominal, breast, gynecological, orthopedics) in a university hospital were enrolled and allocated randomly to aescin (A) or placebo (P) group. Patients, investigators, and research assistants were blinded to the allocation. Patients in A group (n=58) received aescin (Reparil®) 40 mg orally 2 to 6 hours prior to surgery and P group (n=59) received placebo. Anesthesia care was identical and under blinded staff anesthesiologist's discretion. The presence/absence of POST, numerical pain score of POST, adverse events and cumulative analgesics consumption were recorded postoperatively at 30, 60 minutes, 2, 4, and 24 hours. Results: Thirty-seven and 34 patients in A and P group, respectively, developed POST which was not different significantly at all time points. Numerical pain score at all time points did not differ between groups statistically. However, log-rank test analysis revealed that A group had a slightly more rapid recovery from POST than P group (0.0013 vs. 0.0007 case/person-minute, p=0.03). Side effects and analgesics consumption did not differ between groups. Conclusion: Single 40 mg oral dose of aescin preoperatively, compare to placebo, did not reduce the incidence or severity of POST in the first 24 postoperative hours. Aescin, however, hastened the speed of recovery of POST compare to placebo with statistical significance. © JOURNAL OF THE MEDICAL ASSOCIATION OF THAILAND, 2021.
dc.languageen
dc.subjectanalgesic agent
dc.subjectatropine
dc.subjectescin
dc.subjectfentanyl
dc.subjectmidazolam
dc.subjectneostigmine
dc.subjectparecoxib
dc.subjectthiopental
dc.subjectabdominal cramp
dc.subjectadult
dc.subjectAldrete score
dc.subjectAmerican Society of Anaesthesiologists score
dc.subjectanesthesia
dc.subjectanesthesiologist
dc.subjectArticle
dc.subjectbody height
dc.subjectbody weight
dc.subjectclinical trial
dc.subjectcontrolled study
dc.subjectdizziness
dc.subjectdouble blind procedure
dc.subjectfemale
dc.subjectgeneral anesthesia
dc.subjectheadache
dc.subjecthuman
dc.subjectlaryngoscopy
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectoperation duration
dc.subjectorthopedic surgery
dc.subjectpain
dc.subjectpostoperative complication
dc.subjectpruritus
dc.subjectrandomized controlled trial
dc.subjectrash
dc.subjectside effect
dc.subjectsingle drug dose
dc.subjectsore throat
dc.titleThe efficacy of single-dose aescin in preventing postoperative sore throat compared to placebos: A double-blinded, randomized controlled trial
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationJournal of the Medical Association of Thailand. Vol 104, No.9 (2021), p.S65-S71
dc.identifier.doi10.35755/jmedassocthai.2021.S03.00022
Appears in Collections:Scopus 1983-2021

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