• Br J Anaesth · Jun 2011

    Randomized Controlled Trial Comparative Study

    Randomized clinical trial comparing double-lumen tube and EZ-Blocker for single-lung ventilation.

    • K Ruetzler, G Grubhofer, W Schmid, D Papp, S Nabecker, D Hutschala, G Lang, and H Hager.
    • Department of Cardiothoracic and Vascular Anesthesia and Intensive Care Medicine, University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria. kurt.ruetzler@meduniwien.ac.at
    • Br J Anaesth. 2011 Jun 1;106(6):896-902.

    BackgroundIn several clinical situations, lung separation and single-lung ventilation (SLV) is essential. In these cases, the double-lumen tube (DLT) is the most widely used device. Bronchial blocker such as Univent or Arndt Blocker serves as an alternative. The EZ-Blocker(®) (EZ; AnaesthetIQ B.V., Rotterdam, The Netherlands) is a new device promising to exceed clinical performance of DLT. The aim of this study was to assess the clinical performance of EZ in comparison with conventional left-sided DLT.MethodsForty adult patients undergoing elective thoracic surgery requiring thoracotomy and SLV were included in this study. The patients were randomly assigned to one of two groups: EZ (combined with conventional 7.5 or 8.5 mm single-lumen tube) or DLT (37 or 39 Fr left-sided DLT). Time for intubation procedure and time to verification of the correct position of EZ or DLT using fibreoptic bronchoscopy (FOB) were recorded. After surgery, a thoracic surgeon rated the quality of collapse of the lung (1-3 on a three-level scale).ResultsTime for intubation using DLT 85.5 (54.8) s was significantly faster (P<0.001) than using EZ 192 (89.7) s, whereas time for bronchoscopy was not significantly different (P=0.556). Conditions of surgery were rated equally [DLT 1.3 (0.6) vs EZ 1.4 (0.6), P=0.681].ConclusionsAlthough time for intubation was longer with the EZ, the device proved to be an efficient and easy-to-use device. The EZ is a valuable alternative device to conventional DLT. Verification of the correct position of the EZ by FOB seems to be obligatory. This study was registered at http://www.clinicaltrials.gov (identifier: NCT01171560).

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