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Effects of nefopam with fentanyl in intravenous patient-controlled analgesia after arthroscopic orthopedic surgery: a prospective double-blind randomized trial

Authors
Oh, You NaKim, Kyu NamJeong, Mi AeKim, Dong WonKim, Ji YoonKi, Hyun Seo
Issue Date
2018
Publisher
TUBITAK SCIENTIFIC & TECHNICAL RESEARCH COUNCIL TURKEY
Keywords
Analgesia; balanced; analgesia; patient-controlled; nefopam; randomized controlled trial
Citation
TURKISH JOURNAL OF MEDICAL SCIENCES, v.48, no.1, pp.142 - 149
Indexed
SCIE
SCOPUS
Journal Title
TURKISH JOURNAL OF MEDICAL SCIENCES
Volume
48
Number
1
Start Page
142
End Page
149
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/150866
DOI
10.3906/sag-1707-113
ISSN
1300-0144
Abstract
Background/aim: We performed this prospective randomized double-blind study to compare the effects of nefopam versus ketorolac in intravenous fentanyl-based patient-controlled analgesia (PCA) after shoulder arthroscopic orthopedic surgery. Materials and methods: Ninety-two patients were randomly divided into two groups to receive intravenous PCA. Patients were assigned to either the nefopam group (nefopam 120 mg and fentanyl 20 mu g/kg) or the ketorolac group (ketorolac 2 mg/kg and fentanyl 20 mu g/kg). Pain was assessed on a visual analogue scale (VAS) and a numeric rating scale (NRS). Additionally, patient satisfaction, adverse events, and vital signs were monitored. Results: There were no significant differences in VAS score (P = 0.48) or NRS score (P = 0.15) between the two groups. Similarly, patient satisfaction did not differ between the two groups [8.5(0.8) vs. 8.2(1.0), P = 0.14]. There were no statistically significant differences in the incidence of nausea (P = 0.72), vomiting (P = 0.46), urinary retention (P = 0.82), sweating (P = 0.49), or dizziness (P = 0.45) between the two groups. Likewise, there were no differences in heart rate [78.2(7.7) vs. 75.2(6.5), P = 0.18] or SpO2 [98.4(1.8) vs. 98.5(1.9), P = 0.83]. Conclusion: Nefopam is an appropriate alternative for co-administration with fentanyl-based PCA in patients who have difficulty using nonsteroidal antiinflammatory drugs.
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