Effect of Modified Endotracheal Intubation Protocol Combined With Early Oral Intake on Postoperative Recovery Quality in Thyroid and Parathyroid Surgery
- Conditions
- Thyroid Tumor
- Interventions
- Behavioral: Modified intubation protocolBehavioral: Conventional intubation protocolBehavioral: Delayed resumption of oral intakeBehavioral: Early resumption of oral intake
- Registration Number
- NCT05624463
- Lead Sponsor
- Peking Union Medical College Hospital
- Brief Summary
The purpose of this study is to assess the effect of modified endotracheal intubation procedure combined with early oral intake on postoperative recovery quality of patients, so as to further optimize the ERAS(enhanced recovery after surgery) program for thyroid or parathyroid surgery.
- Detailed Description
After being informed about the study and potential risk, all patients giving written informed consent will undergo a screening-period to determine eligibility for study entry. Before operation, patients will be randomly assigned to conventional intubation process group or modified intubation process group before the operation. After the operation, patients will enter the PACU(post-anaesthesia care unit) for further observation. When the anesthesiologists and surgeons agree that patients have no early oral drinking high-risk factors, patients will be randomly assigned to early resumption of oral intake group or late resumption of oral intake group for further observation and evaluation.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 200
- Age ≥ 18
- American Society of Anesthesiologists (ASA) physical status classification I-II
- Body mass index 18.5-29.9kg/m2
- First operation on operation day
- Patients or family members cannot understand the conditions and objectives of this study
- Preoperative patients with acute pharyngitis, hoarseness, cough, dysphagia, and high risk of aspiration
- The surgeons or anesthesiologists point out that the patient is not suitable for early postoperative drinking (such as considering the injury of recurrent laryngeal nerve or lymphatic vessels during the operation)
- Patients who cannot be intubated under visual laryngoscope(such as difficult airway, loose incisors and so on)
- Exclusion criteria of Quality of Recovery-15* (*Quality of Recovery-15 exclusion criteria: 1. Unable to understand words and language; 2. Difficult to cooperate due to mental disorders; 3. History of alcohol or drug abuse; 4. Any serious pre-existing medical condition that can limit the objective evaluation after surgery; 5. Any life-threatening complications; 6. Emergency surgery)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Modified intubation protocol+delayed resumption of oral intake Delayed resumption of oral intake Participants receive modified intubation protocol and delayed resumption of oral intake. Conventional intubation protocol+delayed resumption of oral intake Delayed resumption of oral intake Participants receive conventional intubation protocol and delayed resumption of oral intake. Modified intubation protocol+early resumption of oral intake Modified intubation protocol Participants receive modified intubation protocol and early resumption of oral intake. Modified intubation protocol+delayed resumption of oral intake Modified intubation protocol Participants receive modified intubation protocol and delayed resumption of oral intake. Modified intubation protocol+early resumption of oral intake Early resumption of oral intake Participants receive modified intubation protocol and early resumption of oral intake. Conventional intubation protocol+early resumption of oral intake Conventional intubation protocol Participants receive conventional intubation protocol and early resumption of oral intake. Conventional intubation protocol+early resumption of oral intake Early resumption of oral intake Participants receive conventional intubation protocol and early resumption of oral intake. Conventional intubation protocol+delayed resumption of oral intake Conventional intubation protocol Participants receive conventional intubation protocol and delayed resumption of oral intake.
- Primary Outcome Measures
Name Time Method Quality of Recovery-15 score on the first day after surgery one day Using Quality of Recovery-15 questionnaire to evaluate the quality of perioperative recovery. Quality of Recovery-15 consists of 15 comprehensive questions, including physical comfort (5 items), psychological support (2 items), physical independence (2 items), emotional state (4 items), and pain (2 items), each item is scored with 0-10 points, 0 represents poor state, 10 represents good state, and the total score is the Quality of Recovery-15 score of the patient.
- Secondary Outcome Measures
Name Time Method Patient satisfaction through patient discharge, an average of 2-3 days after surgery Patient satisfaction was assessed based on the postoperative numeric rating scale (NRS) scores, with 0 indicating extreme dissatisfaction and 10 indicating very satisfaction.
Quality of Recovery-15 score on the day of discharge one day Using Quality of Recovery-15 questionnaire to evaluate the quality of perioperative recovery. Quality of Recovery-15 consists of 15 comprehensive questions, including physical comfort (5 items), psychological support (2 items), physical independence (2 items), emotional state (4 items), and pain (2 items), each item is scored with 0-10 points, 0 represents poor state, 10 represents good state, and the total score is the Quality of Recovery-15 score of the patient.
Postoperative hospital stay length through patient discharge, an average of 2-3 days after surgery Postoperative hospital stay length
Drainage volume through removal of drainage tube, an average of 2 days after surgery Total drainage volume after operation.
Adverse event through patient discharge, an average of 2-3 days after surgery The occurrence of adverse events such as severe choking, reintubation, postoperative bleeding.
Postoperative pain one day The patients were given self-evaluation before resuming oral intake and one day after the surgery. Pharyngeal pain and surgical incision pain were assesed by a visual analogue scale (VAS), with 0 indicating no pain and 10 indicating the worst pain.
Postoperative patient discomfort one day The postoperative patient discomfort included the feeling of thirst and hunger. The patients were given self-evaluation before surgery and before resuming oral intake after surgery. The discomfort feelings were assesed by a visual analogue scale (VAS), with 0 indicating no discomfort and 10 indicating the worst discomfort.
Intubation time one day Time from the end of pre-oxygenation to the completion of intubation and position setted.
Endotracheal tube readjustment rate one day Rate of endotracheal tube readjustment caused by the lose or weakness of monitor signal during the surgery.
Postoperative nausea and vomiting through patient discharge, an average of 2-3 days after surgery Researchers recorded the occurences and treatments of postoperative nausea and vomiting.
Gastrointestinal recovery time through exhaustion after surgery, an average of 1-2 days after surgery The first postoperative exhaustion time recorded was considered as gastrointestinal recovery time.
Trial Locations
- Locations (1)
Peking Union Medical College Hospital
🇨🇳Beijing, Beijing, China