• BMC anesthesiology · Jan 2018

    Randomized Controlled Trial

    Perioperative incidence of airway obstructive and hypoxemic events in patients with confirmed or suspected sleep apnea - a prospective, randomized pilot study comparing propofol/remifentanil and sevoflurane/remifentanil anesthesia.

    • Philipp Fassbender, Silja Bürgener, Ali Haddad, Marie-Therese Silvanus, and Jürgen Peters.
    • Klinik für Anästhesiologie und Intensivmedizin, Universität Duisburg-Essen and Universitätsklinikum Essen, Hufelandstr 55, D-45147, Essen, Germany. philipp.fassbender@elisabethgruppe.de.
    • BMC Anesthesiol. 2018 Jan 27; 18 (1): 14.

    BackgroundObstructive sleep apnea (OSA) is a risk factor for perioperative complications but data on anesthesia regimen are scarce.MethodsIn patients with established or strongly suspected OSA, we assessed in a prospective, randomized design the effects on nocturnal apnea-hypopnea-index (AHI) and oxygen saturation (SpO2) of propofol/remifentanil or sevoflurane/remifentanil based anesthesia. Patients were selected by a history for OSA and / or a positive STOP - questionnaire and received general anesthesia using remifentanil (12 μg/kg/h) combined either with propofol (4-6 mg/kg/h, n = 27) or sevoflurane (approx. 2.2 vol% endtidal, n = 27). AHI and SpO2 were measured during the nights before and after anesthesia.ResultsThere were no differences in AHI between anesthetic regimens nor between the pre- and postoperative nights (propofol: 8.6 h- 1 (median, CI: 3.6-21.9) vs. 7.9 h- 1 (1.8-28.8); p = 0.97; sevoflurane: 3.8 h- 1 (1.8-7.3) vs. 2.9 h- 1 (1.2-9.5); p = 0.85). Postoperative minimum SpO2 (propofol: 80.7% ± 4.6, sevoflurane: 81.6 ± 4.6) did not differ from their respective preoperative baselines (propofol: 79.6% ± 6.5; p = 0.26, sevoflurane: 80.8% ± 5.2; p = 0.39). Even in patients with a preanesthetic AHI > 15, nocturnal AHI remained unchanged postoperatively.ConclusionThus, in a cohort of patients with suspected or confirmed OSA undergoing surgery of moderate duration and severity neither the volatile agent sevoflurane nor the intravenous anesthetic propofol altered nocturnal AHI or oxygen saturation, when combined with the short acting opioid remifentanil.Trial RegistrationGerman Clinical Trials Register, DRKS00005824 retrospectively registered on 03/12/2014.

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