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Published on: October 23, 2018
Comparison of two sevoflurane formulations in low-flow anesthesia: a retrospective observational study
Ahmet Rıdvan Doğan1, Ali Fuat Erdem2, Ayça Taş Tuna2
1Department of Anesthesiology and Reanimation, Sakarya Training and Research Hospital, Adnan Menderes, Sakarya, 54100, Türkiye. a.ridvandogan@gmail.com.
Background:
This study aimed to compare two different sevoflurane formulations (Sevones® and Sevorane®) under low-flow anesthesia in terms of time to 1 Minimum Alveolar Concentration (MAC), agent consumption and uptake, emergence profile, and anesthesia-related complications.
Methods:
This retrospective observational study was conducted at Sakarya University Training and Research Hospital, Türkiye. A total of 89 female patients undergoing elective gynecologic surgery under general anesthesia with low-flow sevoflurane (≤ 1 L/min) were included. Patients received either Sevones® (n = 46) or Sevorane® (n = 43). Standardized anesthetic induction with propofol and rocuronium was followed by low-flow sevoflurane maintenance. The primary outcome was time to reach 1 MAC. Secondary outcomes included agent consumption and uptake during induction and maintenance, emergence characteristics, intraoperative hemodynamic and PSI trends, and anesthesia-related complications. Statistical comparisons were performed using t-test, Mann-Whitney U, and chi-square tests as appropriate.
Results:
Time to reach 1 MAC was similar between Sevones® and Sevorane® groups (198.26 ± 41.1 s vs. 205.63 ± 51.2 s; p = 0.455). Agent consumption and uptake during induction were comparable. Total agent uptake was significantly higher in the Sevones® group (16.63 ± 5.32 mL vs. 13.49 ± 7.45 mL; p = 0.024), while total agent consumption showed no significant difference. Emergence times, PSI trends, and complication rates were similar between groups.
Conclusions:
Both Sevones® and Sevorane® demonstrated comparable pharmacokinetic and pharmacodynamic profiles under low-flow anesthesia. The findings support their safe and effective use during elective gynecologic surgery.
Clinical Trial Number:
Not applicable.
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