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Departments of *Anesthesiology and
Critical Care Medicine, Institute of Clinical Medicine, University of Tsukuba, Tsukuba, Japan
Address correspondence and reprint requests to Shinji Takahashi, MD, Department of Anesthesiology, Institute of Clinical Medicine, University of Tsukuba, Tenodai 1-1-1, Tsukuba-city 305-8575, Japan. Address email to shinjitk{at}md.tsukuba.ac.jp
| Abstract |
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IMPLICATIONS: The magnitude of hemodynamic changes associated with tracheal intubation with the Trachlight® is almost the same as that which occurs with the direct laryngoscope. Hemodynamic changes are likely to occur because of direct tracheal irritation rather than direct stimulation of the larynx.
| Introduction |
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| Methods |
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After fasting for 810 h, all patients received ranitidine 150 mg orally 90 min before the induction of general anesthesia. Patients were randomly assigned according to computer-generated random numbers into one of the following three groups: lightwand (Trachlight®; Laerdal Medical, Armonk, NY) (8) intubation group (LWI group; n = 20), direct laryngoscope (Macintosh blade) intubation group (LSI group; n = 20), and direct laryngoscopy (Macintosh blade)-alone group (LSA group; n = 20). The anesthetic technique was standardized as follows: on arrival in the operating room, patients received standard anesthetic monitors, including electrocardiogram (lead II), noninvasive BP cuff, and pulse oximeter (AS3; Datex Instrumentarium, Helsinki, Finland). Then an arterial cannula was placed into a radial artery under adequate local anesthesia for subsequent BP measurement. Lactated Ringers solution was administered and maintained at a constant rate of approximately 15 mL · kg-1 · h-1 throughout the study period. General anesthesia was induced with thiopental 5 mg/kg IV, followed by vecuronium 0.2 mg/kg IV. The patients lungs were ventilated for approximately 5 min via face mask with 5% sevoflurane and 67% nitrous oxide in oxygen.
After the optimal end-tidal sevoflurane concentration (approximately 3.5%) was obtained, the trachea was intubated orally with either the Trachlight (LWI group) or the Macintosh laryngoscope (LSI group). The patients in the LSA group underwent direct laryngoscopy for a period adequate to intubate, without intubation, under direct visualization of the vocal cords. The laryngoscopes used were the No. 3 or 4 Macintosh blade (Igarashi, Tokyo, Japan) for female patients and the No. 4 or 5 Macintosh blade for male patients. Tracheal tubes (SIMS Portex, Inc., Keene, NH) with an internal diameter of 7 mm were used for female patients and 8 mm for male patients. The cuff of the tracheal tube was inflated immediately with air after intubation so it would not leak at a peak airway pressure of 20 cm H2O. The duration of each attempt was recorded as the interval from the time the device was inserted (Trachlight or laryngoscope) into the oropharynx to the time when the device was removed from the oral cavity. Failure to intubate was defined as the inability to place the tracheal tube into the trachea or to visualize the vocal cords in the LSA group on the first attempt. Patients in whom there was failure to intubate and those requiring more than 30 s to achieve tracheal intubation were excluded from this study. Anesthesia was maintained with 3% sevoflurane and 66% nitrous oxide in oxygen for 5 min. The patients lungs were ventilated with a tidal volume of 10 mL/kg and a respiratory rate of 1012 breaths/min to maintain end-tidal carbon dioxide tension (PETCO2) at 3540 mm Hg in all the groups. Systolic BP (SBP) and HR were recorded at the time immediately before either device insertion, at the time when the trachea was just intubated, and every 20 s after intubation or laryngoscopy in the LSA group for 5 min. Maximum SBP and HR values and the times when these values were obtained were determined. All intubating procedures were performed by a single investigator (ST) experienced in using the Trachlight and laryngoscope.
As a power analysis based on a previous article (6) revealed, a sample size of 20 patients per group was required to achieve a power of 80% and an
of 0.05 for detection of 20-bpm or 20 mm Hg differences in paired hemodynamic data. All data are expressed as mean ± SD. Statistical analysis consisted of analysis of variance with Bonferronis correction to detect differences in patients demographic data and hemodynamic data among the three groups. Pairwise hemodynamic data in each group were analyzed by using repeated-measures analysis of variance, followed by paired Students t-tests with Bonferronis correction. A P value of <0.05 was considered the minimal level of statistical significance.
| Results |
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98% in all patients during the entire course of the study. PETCO2 values immediately before the insertion of a device were 31 ± 3 mm Hg, 32 ± 3 mm Hg, and 33 ± 3 mm Hg in the LWI, LSI, and LSA groups, respectively. End-tidal sevoflurane concentrations immediately before the insertion of a device were 3.3% ± 0.3%, 3.3% ± 0.3%, and 3.4% ± 0.2% in the LWI, LSI, and LSA groups, respectively. The numbers of the patients who developed decreases in HR from the baseline values in response to insertion of the devices were 0, 1, and 2 in the LWI, LSI, and LSA groups, respectively. None of the patients developed severe bradycardia (HR
45 bpm) or severe hypotension (SBP
60 mm Hg) during the observation period. | Discussion |
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The use of a lightwand, in comparison with the use of a rigid laryngoscope, has resulted in a less frequent incidence and severity of sore throat, hoarseness, and dysphasia after surgery (1,2,5). Therefore, we assumed that use of the Trachlight, which does not require a laryngoscope to elevate the epiglottis, would attenuate the cardiovascular responses to tracheal intubation. Hirabayashi et al. (6) studied the effects of the lightwand technique on circulatory responses to tracheal intubation in adult patients. Preanesthetic medication consisted of atropine (0.5 mg) and hydroxyzine (50 mg) IM. Forty patients (2277 yr old, ASA status III) received propofol, lidocaine, and vecuronium, and their lungs were ventilated for three minutes via a face mask with 5% sevoflurane in oxygen. BPs were continuously measured by a catheter in a radial artery. Neither maximum mean arterial BP changes nor HR changes after tracheal intubation differed between the Trachlight group and the laryngoscope group (46 mm Hg and 18 bpm vs 44 mm Hg and 23 bpm, respectively). These results are in accordance with our study. However, their study did not demonstrate the difference in the duration of significant increases in HR in response to tracheal intubation between the Trachlight and laryngoscope. Also, the hemodynamic response to bronchoscopy alone was not examined.
However, Nishikawa et al. (4) showed that the lightwand technique attenuated hemodynamic changes after intubation in comparison with the laryngoscopic technique. The authors studied 40 normotensive patients (52.3 yr old in mean age, ASA status I) premedicated with atropine (0.01 mg/kg) and midazolam (0.05 mg/kg). Anesthesia was induced with 2 µg/kg of fentanyl, followed by 2 mg/kg of propofol three minutes later. The lungs were ventilated via face mask with 100% oxygen until the insertion of the devices two minutes after the administration of 0.15 mg/kg of vecuronium. The HR and BP were measured at one-minute intervals. Although the lightwand technique needed significantly more frequent attempts and a longer duration for intubation than the laryngoscopic technique, the lightwand technique was accompanied by smaller increases in SBP after tracheal intubation than the laryngoscopic technique. In their study, 2 µg/kg of fentanyl was administered before tracheal intubation. Previous studies (911) showed that fentanyl could attenuate the hemodynamic responses associated with tracheal intubation. Accordingly, the differences in anesthetic technique might affect the hemodynamic responses to tracheal intubation. In addition, the method of recording hemodynamic variables, i.e., intermittent measurement, in the study by Nishikawa et al. (4) could miss the maximum changes.
In this study, there were significant differences between cardiovascular responses to laryngoscopy with intubation and those without intubation. In contrast, Shribman et al. (12) reported that in 24 adult patients anesthetized with fentanyl 0.1 mg, thiopental 34 mg/kg, and 67% nitrous oxide, there were significant and similar increases in arterial BP and circulating catecholamine concentrations after laryngoscopy with and without intubation. However, intubation was associated with significant increases in HR; this did not occur in the laryngoscopy-alone group in their study. Also, SBP and diastolic BP were increased in the intubation groups at one and two minutes after laryngoscopy, although the increases were statistically insignificant. Possibly, therefore, a relatively small number in sample size might cause a ß error statistically. In addition, intermittent BP measurement might miss the maximum changes.
Maximum increases in the SBP values and the duration of significant increases from the baseline value after insertion of the devices did not differ between the LWI and LSI groups, although there were significant differences in maximum increases in SBP values compared with the LSA group. However, although the maximum HR increases after the insertion of the devices did not differ between the LWI and LSI groups, the duration of significant increases in HR from baseline values in the LSI group was longer than that in the LWI group. This result indicates that combined stimulation of the larynx and the trachea in the LSI group was more intense than stimulation of the trachea alone in the LWI group, although there was no difference in the maximum HR increase between the groups in this study.
The anesthetic methods using thiopental and sevoflurane in this study were selected according to our usual procedure. Approximately five minutes after inhalation of sevoflurane, the concentration of end-tidal sevoflurane was 3.5%, which is the sevoflurane requirement for achieving a 50% probability of no movement in response to laryngoscopy and tracheal intubation (13). Prolonged intubation time induces hypercarbia and decreasing anesthetic gas concentration, resulting in hypertension and tachycardia (14). There were no significant differences in the time necessary to intubate or to perform laryngoscopy among the groups in this study. Therefore, we believe that the data regarding hemodynamic variables were comparable.
Possible limitations of this study deserve mention. First, we conducted our study on patients with normal airways and no cardiac disease. A longer duration of intubation in difficult airways may produce different responses between the Trachlight and direct laryngoscope. Perhaps hemodynamic responses to intubation with these devices may be different in hypertensive patients. Second, we used the patients who were successfully intubated on the first attempt to clarify the effects of devices. Therefore, we could not observe the differences in hemodynamic changes in case of repeated trials. Third, although patients were randomly assigned into the groups, double-blinding to observe hemodynamic changes could not be used in this study. Fourth, we did not assess the postanesthetic complications associated with the lightwand and laryngoscope. Therefore, the severity of stimulation of the laryngeal tissue was not correctly compared with that of other studies.
We conclude that hemodynamic responses to tracheal intubation with the Trachlight do not differ from those with a direct laryngoscope under sevoflurane anesthesia. It is likely that direct stimulation of the trachea by a tracheal tube has a major role in causing the cardiovascular responses to tracheal intubation in sevoflurane-anesthetized patients.
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