Literature DB >> 8712397

Renal and hepatic function in surgical patients after low-flow sevoflurane or isoflurane anesthesia.

H Bito1, K Ikeda.   

Abstract

The safety of low-flow sevoflurane anesthesia, which produces higher concentrations of toxic compounds, has been questioned. One hundred surgical patients received sevoflurane or isoflurane anesthesia at a total flow rate of 1 L/min. End-tidal CO2 concentrations and inspired and end-tidal anesthetic concentrations were monitored during anesthesia. Pre- and postanesthetic clinical laboratory studies were performed in both groups, and no significant differences were found between groups. In the sevoflurane group, the concentrations of degradation products in the circuit were measured by gas chromatography and the temperature of the CO2 absorbent was also measured. Two degradation products were detected: CF2 = C(CF3-O-CH2F (Compound A) and CH3OCF2CH(CF3)OCH2F (Compound B). The highest measured mean concentration of Compound A was 24.6 +/- 7.2 (13.6-41.3) ppm, and that of Compound B (detected in 12 patients) was 1.5 ppm. In both groups, total bilirubin, direct bilirubin, aspartate aminotransferase, and alanine aminotransferase were increased postoperatively. There was no difference between groups. Low concentrations of Compound A were present in low-flow sevoflurane anesthesia, but no significant differences in clinical laboratory values were observed between low-flow sevoflurane and isoflurane anesthesia.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8712397     DOI: 10.1097/00000539-199601000-00032

Source DB:  PubMed          Journal:  Anesth Analg        ISSN: 0003-2999            Impact factor:   5.108


  10 in total

Review 1.  Sevoflurane in paediatric anaesthesia: a review.

Authors:  K L Goa; S Noble; C M Spencer
Journal:  Paediatr Drugs       Date:  1999 Apr-Jun       Impact factor: 3.022

2.  Comparison between low flow sevoflurane anesthesia and total intravenous anesthesia during intermediate-duration surgery: effects on renal and hepatic toxicity.

Authors:  S H Sahin; S O Cinar; I Paksoy; N Sut; S Oba
Journal:  Hippokratia       Date:  2011-01       Impact factor: 0.471

Review 3.  Comparative tolerability profiles of the inhaled anaesthetics.

Authors:  J P Fee; G H Thompson
Journal:  Drug Saf       Date:  1997-03       Impact factor: 5.606

Review 4.  Sevoflurane. A review of its pharmacodynamic and pharmacokinetic properties and its clinical use in general anaesthesia.

Authors:  S S Patel; K L Goa
Journal:  Drugs       Date:  1996-04       Impact factor: 9.546

Review 5.  Clinical pharmacokinetics of sevoflurane.

Authors:  M Behne; H J Wilke; S Harder
Journal:  Clin Pharmacokinet       Date:  1999-01       Impact factor: 6.447

6.  Perioperative management of a patient with hemophilia A and crigler-najjar syndrome.

Authors:  Debesh Bhoi; Lokesh Kashyap
Journal:  J Anaesthesiol Clin Pharmacol       Date:  2013-10

7.  Cost analysis of three techniques of administering sevoflurane.

Authors:  Asha Tyagi; Vineeta Venkateswaran; Ajai Kumar Jain; Uttam Chandra Verma
Journal:  Anesthesiol Res Pract       Date:  2014-10-29

Review 8.  Hepatotoxicity of halogenated inhalational anesthetics.

Authors:  Saeid Safari; Mahsa Motavaf; Seyed Alireza Seyed Siamdoust; Seyed Moayed Alavian
Journal:  Iran Red Crescent Med J       Date:  2014-09-05       Impact factor: 0.611

Review 9.  The impact of sevoflurane anesthesia on postoperative renal function: a systematic review and meta-analysis of randomized-controlled trials.

Authors:  Rakesh V Sondekoppam; Karim H Narsingani; Trent A Schimmel; Brie M McConnell; Karen Buro; Timur J-P Özelsel
Journal:  Can J Anaesth       Date:  2020-08-18       Impact factor: 6.713

10.  Case report: proximal tubule impairment following volatile anesthetic exposure.

Authors:  Evan C Ray; Khaled Abdel-Kader; Nicholas Bircher; Helbert Rondon-Berrios
Journal:  Physiol Rep       Date:  2015-09
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.