Increased tracheal cuff pressure during insertion of a transoesophageal echocardiography probe: A prospective, observational study

Eur J Anaesthesiol. 2015 Aug;32(8):549-54. doi: 10.1097/EJA.0000000000000204.

Abstract

Background: Excessive tracheal cuff pressure reduces tracheal mucosal blood flow and increases tracheal morbidity. Inserting a transoesophageal echocardiography (TOE) probe has been shown to increase tracheal cuff pressure.

Objective: To evaluate the effect of inserting a TOE probe on tracheal cuff pressure and compare the effect in patients who received a single-lumen endotracheal tube (SLT) with those who received a double-lumen endotracheal tube (DLT).

Design: A prospective, observational study.

Setting: Single-centre trial, study period from October 2013 to January 2014.

Patients: Forty-four adult patients scheduled for elective cardiothoracic surgery requiring intraoperative TOE monitoring.

Interventions: After tracheal intubation with a SLT (n = 22) or DLT (n = 22), the tracheal cuff was inflated to 18 mmHg (25 cmH2O) with air. Tracheal cuff pressure was monitored continuously for 5 min after inserting the TOE probe.

Main outcome measures: The primary endpoint was steady-state tracheal cuff pressure after insertion of the TOE probe.

Results: Median (interquartile range, IQR) tracheal cuff pressure stabilised at 3 (2 to 3) min in the SLT group and at 2 (1 to 3) min in the DLT group. Steady-state cuff pressure was significantly higher in the DLT group than that in the SLT group [36.7 (31.3 to 44.1) vs. 31.3 (29.6 to 35.7) cmH2O; (P = 0.03)]. Steady-state cuff pressure more than 40 cmH2O was observed in two patients (18.2%) in the SLT group and nine patients (40.9%) in the DLT group (P = 0.02).

Conclusion: Insertion of a TOE probe increased tracheal cuff pressure in both the SLT and DLT groups. The increase in cuff pressure was greater in patients who received a DLT. Frequent measurement and adjustment of cuff pressure should be emphasised particularly when TOE is used in patients receiving a DLT.

Trial registration: Clinicaltrials.gov identifier: NCT02034643.

Publication types

  • Clinical Trial
  • Observational Study

MeSH terms

  • Aged
  • Echocardiography, Transesophageal / adverse effects
  • Echocardiography, Transesophageal / instrumentation*
  • Echocardiography, Transesophageal / methods
  • Female
  • Humans
  • Intubation, Intratracheal / adverse effects
  • Intubation, Intratracheal / instrumentation*
  • Intubation, Intratracheal / methods
  • Male
  • Middle Aged
  • Monitoring, Intraoperative / instrumentation*
  • Monitoring, Intraoperative / methods
  • Pressure* / adverse effects
  • Prospective Studies
  • Trachea / physiology*

Associated data

  • ClinicalTrials.gov/NCT02034643