Literature DB >> 25985845

Replacing a double-lumen tube with a single-lumen tube or a laryngeal mask airway device to reduce coughing at emergence after thoracic surgery: a randomized controlled single-blind trial.

Issam Tanoubi1, Joanna Ng Man Sun, Pierre Drolet, Louis-Philippe Fortier, François Donati.   

Abstract

BACKGROUND: Coughing episodes occur frequently at extubation after thoracic surgery, and this may be due in part to the double-lumen tube (DLT). In this study, the DLT was replaced with either a single-lumen endotracheal tube (ETT) or a laryngeal mask airway (LMA) device or left in place, and the incidence of coughing at emergence was compared between the three groups.
METHODS: Fifty-eight adults scheduled for thoracic surgery with a DLT were included. Exclusion criteria were an anticipated difficult airway, obesity, and contraindication to the use of an LMA ProSeal™ (LMA-P). After surgery but before emergence, patients were randomized to having the DLT (1) removed and replaced by an LMA-P (LMA-P Group), (2) removed and replaced by an ETT (ETT Group), or (3) left in place (DLT Group). The primary outcome was the number of coughing episodes at extubation.
RESULTS: Among 184 patients screened, 124 did not meet inclusion criteria, and two patients, both in the ETT Group, were excluded after randomization, leaving 20, 18, and 20 patients in the LMA-P, ETT, and DLT Groups, respectively. There were fewer coughing episodes (median [quartiles]) in the LMA-P Group than in the DLT Group (0[0-1] vs 2[1-3], respectively; P = 0.01). In the DLT Group, 90% of patients coughed at least once. This incidence was not significantly different in the ETT Group (83%; P = 0.222) but was significantly reduced in the LMA-P Group (35%; P < 0.001). No patient had oxygen desaturation during airway exchange or at extubation. The incidence and severity of hoarseness and sore throat were similar in all groups.
CONCLUSION: Coughing at extubation after thoracic surgery can be reduced if the DLT is replaced by an LMA-P before emergence. The number of patients in this trial was too small to evaluate the risks associated with exchanging the airway device. This trial was registered at ClinicalTrials.gov: NCT00925613.

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Year:  2015        PMID: 25985845     DOI: 10.1007/s12630-015-0403-2

Source DB:  PubMed          Journal:  Can J Anaesth        ISSN: 0832-610X            Impact factor:   5.063


  5 in total

1.  Antitussive effect of a magnesium infusion during anesthetic emergence in patients with double-lumen endotracheal tube: a randomized controlled trial.

Authors:  Min Hur; Jong Yeop Kim; Dae Hee Kim; Ji Young Yoo; Han-Bit Shin; Bumhee Park; Myungseob Kim; Eunjeong Park; Sung Yong Park
Journal:  J Thorac Dis       Date:  2020-10       Impact factor: 2.895

2.  Comparison of dexmedetomidine and remifentanil on reducing coughing during emergence from anesthesia with tracheal intubation: A meta-analysis.

Authors:  Xing Fan; Hai Cai; Bingbing Pan; Yubo Xie
Journal:  Front Pharmacol       Date:  2022-09-30       Impact factor: 5.988

3.  Laryngeal mask airway without muscle relaxant in femoral head replacement in elderly patients.

Authors:  Ming Kong; Beiping Li; Yunping Tian
Journal:  Exp Ther Med       Date:  2015-11-09       Impact factor: 2.447

Review 4.  Anesthesia for Patients Undergoing Anesthesia for Elective Thoracic Surgery During the COVID-19 Pandemic: A Consensus Statement From the Israeli Society of Anesthesiologists.

Authors:  Ruth Shaylor; Vladimir Verenkin; Idit Matot
Journal:  J Cardiothorac Vasc Anesth       Date:  2020-07-21       Impact factor: 2.628

5.  The case for a 3rd generation supraglottic airway device facilitating direct vision placement.

Authors:  André A J Van Zundert; Chandra M Kumar; Tom C R V Van Zundert; Stephen P Gatt; Jaideep J Pandit
Journal:  J Clin Monit Comput       Date:  2020-06-15       Impact factor: 2.502

  5 in total

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