An Open-label Comparison of a New Generic Sevoflurane Formulation with Original Sevoflurane in Patients Scheduled for Elective Surgery under General Anesthesia

  • Hyo Jin Byon
  • , Byung Moon Choi
  • , Ji Yeon Bang
  • , Eun Kyung Lee
  • , Sang Seok Lee
  • , Gyu Jeong Noh

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Purpose To compare the stability, effectiveness, and safety profiles of a new generic sevoflurane with those of the original sevoflurane formulation in patients undergoing elective surgery. Methods An accelerated 3-month storage test was performed to evaluate the compositional changes in generic sevoflurane stored in glass bottles. In addition, 182 patients were randomly allocated to receive generic (n = 89 [54 men and 35 women]; mean [SD] age, 49.9 [11.6] years) or original (n = 93 [61 men and 32 women]; mean [SD] age, 49.6 [11.1] years) sevoflurane at a gas flow of 3 L/min for approximately 3 hours. The mean minimum alveolar concentration (MAC) during sevoflurane anesthesia was evaluated, and gas samples for measuring compound A were collected from the inspiratory limb of the circuit at preset intervals. Blood samples for measuring serum inorganic fluoride were obtained at preset intervals (pharmacokinetic group: generic/original sevoflurane = 45/46). Renal biomarkers, such as N-acetyl-β-glucosaminidase, α- and π-glutathione-S-transferase, albumin, urine protein and osmolality, serum creatinine and osmolality, creatinine clearance, and blood urea nitrogen, were measured at preset intervals (renal biomarker group: generic/original sevoflurane = 44/47). Adverse reactions were monitored for 72 hours after discontinuation of sevoflurane use. Findings Generic sevoflurane contained in glass bottles was stable for 3 months. The mean MAC was similar for generic and original sevoflurane (median [range], 0.93 [0.67-1.29] vs 0.94 [0.63-1.5] vol%). Adverse event rates were similar (90.3% vs 84.3%), as were the AUClast of inorganic fluoride (333.7 [112.7-1264.7] vs 311.9 [81.5-1266.5] hours·μmol/L) and compound A (51.8 [6.3-204.5] vs 55.3 [10.8-270.6] hours·ppm). Biomarkers associated with renal injury were not significantly different between the 2 formulations. Implications No significant difference was found in the mean MAC between generic and original sevoflurane. ClinicalTrials.gov identifier: NCT01096212.

Original languageEnglish
Pages (from-to)887-901
Number of pages15
JournalClinical Therapeutics
Volume37
Issue number4
DOIs
StatePublished - 1 Apr 2015

Bibliographical note

Funding Information:
This study was supported by Hana Pharmaceutical, Co., Ltd., Seoul, Korea.

Publisher Copyright:
© 2015 Elsevier HS Journals, Inc. All rights reserved.

Keywords

  • compound A
  • effectiveness
  • generic sevoflurane
  • inorganic fluoride

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