Abstract
Objective
To investigate the incidence of postoperative sore throat (POST) in Korean patients undergoing general anaesthesia with endotracheal intubation and to assess potential risk factors.
Methods
This prospective study enrolled patients who underwent all types of elective surgical procedures with endotracheal intubation and general anaesthesia. The patients were categorized into group S (those with a POST) or group N (those without a POST). The demographic, clinical and anaesthetic characteristics of each group were compared.
Results
This study enrolled 207 patients and the overall incidence of POST was 57.5% (
Conclusions
An intracuff pressure ≥17 cmH2O and a cough at emergence were risk factors for POST in Korean patients. Intracuff monitoring during anaesthesia and a smooth emergence are needed to prevent POST.
Introduction
Despite rapid advancement in anaesthetic techniques, sore throat following endotracheal intubation still is a long-standing concern for anaesthesiologists. In a recent report, postoperative sore throat (POST) was ranked as the second most common minor adverse event during anaesthesia recovery. 1 The overall incidence of POST after general anaesthesia varies from 20% to 74%.1,2 The aetiology is multifactorial, including patient-related factors such as age, 3 sex,4–6 smoking; 7 and intubation factors including technique, 8 duration, 3 tube size, 4 intracuff pressure,9,10 cuff design, 3 intraoperative tube movement, 4 and suctioning. 8 Postoperative pain, including sore throat, increases analgesic use. 11 The aims of this study were to assess the incidence and possible risk factors of POST in Korean patients undergoing elective surgery with endotracheal intubation.
Patients and methods
Patient population
This prospective study enrolled consecutive patients who underwent elective surgery requiring endotracheal intubation under general anaesthesia in the Department of Anaesthesiology and Pain Medicine, Seoul St Mary’s Hospital, The Catholic University of Korea, Seoul, Korea between April 2011 and December 2011. Inclusion criteria included: (i) patients aged 18–80 years; (ii) American Society of Anesthesiologists (ASA) physical status I or II. 12 Exclusion criteria included: (i) emergency surgery, airway-related surgery, laparoscopic surgery; (ii) any history of difficult intubation; (iii) loose teeth; (iv) current upper respiratory tract infections, pre-existing sore throat and/or hoarseness, difficult intubation requiring more than two attempts; (v) nasogastric tube insertion; (vi) operation time longer than 2 h.
The following baseline demographic and clinical characteristics were recorded for all patients: age, sex, body mass index, ASA physical status, Charlson comorbidity index, presence of diabetes mellitus, and smoking status.
The study was approved by the Institutional Review Board of Seoul St Mary’s Hospital, The Catholic University of Korea, Seoul, Korea (Ref: KC11OISI0303) and registered with the Clinical Research Information Service (http://cris.cdc.go.kr; Ref: KCT0000405). All patients provided written informed consent prior to study enrolment.
Anaesthesia
Anaesthetic management was standardized. No patients were premedicated. Standard monitoring (IntelliVue MP70 patient monitor; Philips Healthcare, Best, the Netherlands), including electrocardiogram, end-tidal carbon dioxide, pulse oximeter, and non-invasive arterial blood pressure, was performed. Anaesthesia was induced with 2 mg/kg propofol intravenous (i.v.) and 1 µg/kg per min remifentanil i.v.; and muscle paralysis was obtained with 0.6 mg/kg rocuronium i.v. Endotracheal intubation was performed with a Macintosh laryngoscope by an experienced anaesthesiologist (J.Y.L. and H.J.P.) after approximately 5 min of mask ventilation and loss of all four twitches by train-of-four stimulation of the ulnar nerve. The laryngoscopic view was assessed according to the Cormack-Lehane grade. 13 Endotracheal tubes of 7.0 mm internal diameter for women and 8.0 mm internal diameter for men were used (Lo-Contour® Murphy; Mallinckrodt Medical, Athlone, Ireland). The cuff was inflated manually with air to a clinical endpoint of loss of an audible leak. Next, the intracuff pressure was measured using a hand-held manometer (Posey Cufflator™ Endotracheal Tube Inflator and Manometer; Posey Company, Arcadia, CA, USA). None of the patients received topical lidocaine or lidocaine jelly during the intubation procedure. The lungs were ventilated with 50% oxygen with air. This was adjusted to maintain an end-tidal carbon dioxide of 32–42 mmHg. Anaesthesia was maintained with 1.5–3.0 vol% sevoflurane and with a continuous infusion of 0.05–0.1 µg/kg per min remifentanil. At the end of surgery, patients were administered 0.03 mg/kg pyridostigmine i.v. and 0.002 mg/kg glycopyrrolate i.v. The intracuff pressure was measured, then the cuff was completely deflated, and the endotracheal tube was suctioned and extubation was performed. Two anaesthesiologists (J.Y.L. and H.J.P.) conducted all anaesthesia procedures to ensure consistency.
Study outcomes
The primary outcomes of this study were to evaluate the incidence and possible risk factors of POST. The secondary outcome was to identify other laryngeal complaints, such as cough and hoarseness. These symptoms were scored by an independent nurse and/or patient. It was recorded either ‘yes’ or ‘no’ during the 10 min after arrival to the postanaesthetic care unit (PACU). Sore throat was defined as pain at the larynx or pharynx. It was asked with a direct questionnaire survey, ‘Do you have a sore throat after operation?’. Cough was defined as a sudden, strong abdominal contraction. It was checked twice, at emergence and at the PACU. Even a single cough was recorded as ‘yes’. Hoarseness was defined as a harsh or stained voice assessed by patients. If a nurse observed the patient’s voice change, it was also scored as ‘yes’. After the survey, patients with a postoperative pain score over 6 on a visual analogue scale (VAS; 0 = no pain, 10 = the worst pain imaginable) received 0.5 µg/kg fentanyl i.v. and/or a patient-controlled analgesia (PCA) as a rescue analgesic. The PCA regimen comprised of 15 µg/ml fentanyl i.v. in normal saline 100 ml.
The following surgery-related characteristics were recorded for all patients: surgery type, patient’s position during surgery, duration of anaesthesia, intubation trial number, Cormack-Lehane grade, total rocuronium dose, total remifentanil dose, cuff pressures at intubation and emergence, cough at emergence, and hoarseness at PACU. 13
Statistical analyses
All statistical analyses were performed using the SAS® statistical package, version 9.4 (SAS Institute, Cary, NC, USA). Data are expressed as the mean ± SD or as frequencies and proportions, as appropriate. The intergroup differences were assessed using Fisher’s exact test and the Mann–Whitney
Results
Baseline demographic and clinical characteristics and potential predictive factors for postoperative sore throat in patients undergoing elective surgery requiring endotracheal intubation under general anaesthesia (
All data are presented as the mean ± SD or
Group S, patients with a postoperative sore throat; Group N, patients without a postoperative sore throat; CI, confidential interval; OR, odds ratio; ASA, American Society of Anesthesiologists; PACU, postanaesthetic care unit; NS, not statistically significant (
Of the 207 patients, 119 (57.5%) developed a POST. Group S was defined as those who had a POST ( Receiver operating characteristic curve of intracuff pressure for predicting postoperative sore throat in patients in group S (
Spearman’s correlation coefficient analysis of the associations between cough and hoarseness with having an intubation or emergence intracuff pressure ≥ 17 cmH2O.
Discussion
Sore throat, cough, and hoarseness are common complaints after tracheal intubation.1–11,14–16 In this present study, the incidence of POST was 57.5%. An intracuff pressure ≥17 cmH2O at emergence was a risk factor for POST in the present study. Intracuff pressure depends on both tracheal and cuff compliance.
17
Although evidence from
The incidence of cough at emergence ranges from 40% to 96%. 21 In the present study, the incidence of cough was 66.4% in group S and 38.6% in group N. Cough is essentially a reflex for airway protection. It can be evoked by mechanical and/or chemical stimuli, which activate sensory receptors distributed along the respiratory tract. 22 At light anaesthesia or during emergence, endotracheal tube movement may irritate the trachea and laryngeal mucosa, leading to cough. An appropriate cough can remove respiratory secretions and decrease the risk of aspiration, but it also activates the sympathetic nervous system, leading to tachycardia, hypertension, intraocular hypertension, intracranial hypertension, and surgical site bleeding. 23 Cough at emergence was a risk factor for POST in the present study. These findings suggest that at the time of extubation, patients who are almost awake may have more head and neck movement, leading to an irritated airway and intracuff pressure change associated with increased postoperative laryngotracheal morbidity. In addition, hoarseness is known to relate to increased cuff pressure.9,24 Hoarseness results from oedema of the vocal cords following endotracheal intubation, mechanical contact, and abrasion by the tube in the glottis area. 24 This present study showed that the incidence of hoarseness in group S was higher compared with group N, and it significantly increased with an intracuff pressure ≥17 cmH2O at emergence.
Numerous modalities for preventing or minimizing POST have been performed with uncertain efficacy.11,19,25–27 During anaesthesia, intracuff pressure can be influenced by anaesthetic depth, degree of muscle relaxation, patient temperature and position, ventilation mode, and additional drug administration.28,29 Although there is no standard for the frequency of monitoring cuff pressure during anaesthesia, routine cuff pressure measurements are important in reducing POST. 30
This study had several limitations. First, intracuff pressure was not monitored continuously during anaesthesia, but only twice, after intubation and at emergence. Intermittent monitoring may give a false interpretation that the pressure is within a therapeutic range. Secondly, POST and other laryngeal symptoms were evaluated using binary scale (yes or no),27,31 because incomplete data collection was experienced during our pilot study, when a four-point scale was used.15,32 Thirdly, various types of surgical procedures were included, which may have influenced airway reactivity. Fourthly, the present study only followed patients through the PACU recovery period without a longer follow-up because enrolled patients were composed of both inpatients and outpatients. There is no established guideline for POST evaluation time, but several publications have described that POST is measured from 15 minutes to 24 hours postextubation, because POST is worse in the early postoperative period up to 6 hours, then decreases over time.5,24,27 Despite these limitations, this present study attempted to quantify the proper airway pressure limit in Korean patients. The current findings also warrant future well-controlled, prospective randomized trials for reducing POST. Also, these current findings suggest that intracuff pressure should be adjusted based on each patient’s characteristics.
In conclusion, POST in Korean patients was significantly associated with a lower intracuff pressure threshold compared with previous reports. These current findings suggest that intracuff monitoring during anaesthesia and a smooth emergence are necessary to prevent POST.
Footnotes
Contribution of authors
Jin Young Lee: study design, data collection and analysis, writing and revising the manuscript; Woo Seog Sim, Eun Sung Kim, Sangmin M Lee: providing criticism of the manuscript; Hue Jung Park: study design, data collection and analysis, writing and revising the manuscript; Duk Kyung Kim, Yu Ri Na and Dahye Park: providing criticism of the manuscript.
Declaration of conflicting interests
The authors declare that there are no conflicts of interest.
Funding
This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.
