QUALITY OF RECOVERY AFTER INTRAOPERATIVE MORPHINE OR METHADONE

QUALITY OF RECOVERY AFTER INTRAOPERATIVE MORPHINE OR METHADONE IN PATIENTS UNDERGOING LAPAROSCOPIC CHOLECYSTECTOMY

Introduction. Despite the advantages associated with the use of remifentanil during total intravenous anesthesia (TIVA), it has been observed a frequent difficulty in the control of postoperative pain due to the risk of developing hyperalgesia and acute tolerance associated with the administration of this opioid. There is evidence that NMDA receptors are involved in the development of these changes. Methadone is an opioid that exhibits analgesic potency similar to that of morphine but has NMDA antagonist activity and longer duration of action as additional features. The objective of the study was to evaluate the quality of recovery (QoR40) of patients undergoing TIVA for laparoscopic cholecystectomy and who received morphine or methadone to control postoperative pain. Methods. Patients aged 18 to 65 years, physical status ASA I and II, submitted to total venous anesthesia (propofol and remifentanil) for laparoscopic cholecystectomy and eligible to participate in this prospective and randomized clinical study will be evaluated. After induction of anesthesia, patients will receive a solution containing 0.1 mg.kg-1 morphine (MF group) or 0.1 mg.kg-1 methadone (MT group). Data on the presence of pain, nausea, vomiting, tremor, drowsiness, presence of SpO2 <92%, even with O2 face mask (5 L.min-1) and length of stay will be recorded at PACU. The pain will be evaluated every 15 minutes on a verbal numerical scale (ENV) from 0 to 10. E.v. morphine 0.1 mg.kg-1 (MF group) or methadone 0.1 mg.kg-1 (MT group) will be administered every 15 minutes to obtain the score below 3. After discharge from the PACU, all patients will receive intravenous ketoprofen every 12 hours and dipyrone every 6 hours. For cases where the patient considers the analgesic regimen insufficient, tramadol (100 mg) will be administered intravenously at 8-hour intervals. The consumption of analgesics, the intensity of pain, the occurrence of nausea, vomiting and other complications in the ward will be recorded. The application of the questionnaire (QoR40) will be performed in the ward the morning after the surgery by a medical student.

Study Overview

• Status: Completed
• Conditions: Pain, Postoperative; Nausea and Vomiting, Postoperative
• Intervention / Treatment: Drug: Methadone; Drug: Morphine

Detailed Description

We hypothesized that methadone treatment would beneficially affect patient-perceived quality of recovery after laparoscopic cholecystectomy under total intravenous anesthesia. The primary outcome was assessed using the Quality of Recovery Questionnaire (QoR-40), a 40-item quality of recovery scoring system, on postoperative day (POD) 1. In addition, the effects of both opioids on early clinical recovery variables, such as the time to eye opening, the occurrence of nausea and vomiting, pain score, use of analgesics, and length of PACU stay, were determined.

Methods. This randomised trial was approved by the Research Ethics Committee of the School of Medical and Health Sciences, Pontifical Catholic University of São Paulo.

Study sequence No premedication will be applied to the patients. Patients´ preoperative data including age, gender, physical status and, BMI will be collected. Subjects will be randomized using a computer-generated (www.random.org) table of random numbers into 2 groups: MT (methadone 0.1 mg.kg-1) or MF (morphine 0.1 mg.kg-1). Group assignments were sealed in sequentially numbered opaque envelopes that were opened after patient inclusion in the study. All care providers, researchers, and patients were blinded to group assignments. Two study 10-mL syringes will be prepared by an anesthesiologist independent of the study. Syringe 1 to be used during intraoperative phase and syringe 2 as a rescue for postoperative pain. Methadone 0.1 mg.kg-1 (made up to 10 mL with normal saline) or morphine 0.1 mg.kg-1 (made up to 10 mL with normal saline) will be drawn into each syringe which will be offered to the anesthesia provider after the opaque envelope is opened.

Anesthetic and Surgical Management After arrival in the operating room, standard ASA monitors will be applied. Lidocaine (30 mg) will be administered intravenously immediately after venoclysis. After anesthesia induction, capnographic monitoring will be added. Anesthesia will be induced with remifentanil 0.5 µg.kg-1.min-1 over three minutes followed by propofol 2.0 mg. kg-1. Rocuronium 0.6 mg.kg-1 will be administered to facilitate tracheal intubation. Anesthetic maintenance will be achieved with a continuous infusion of remifentanil 0.3 µg.kg-1.min-1 and propofol 4 to 6 mg. kg-1. h-1. Ventilation will be controlled mechanically to maintain an end-tidal carbon dioxide concentration of 30-40 mmHg using a 50% oxygen-air gas mixture. Immediately after the induction of anesthesia, patients will receive intravenously: MT group - Methadone 0.1 mg/kg or MF group - morphine 0.1 mg/kg. Patients who exhibit reductions in systolic arterial pressure (SAP) greater than 30% or heart rate (HR) reductions to less than 50 bpm will be given ephedrine (10 mg) and atropine (0.5 mg), respectively. Normal saline will be used for fluid replacement therapy at a rate of 500 ml throughout the first 30 minutes, and, then, 2 ml/kg/h until the end of the surgical procedure. All of the participants will receive dexamethasone (8 mg) and ketoprofen (100 mg) at the onset of surgery and ondansetron (4 mg) and dipyrone (1 g). Residual neuromuscular blockade will be antagonized by atropine (0.01 mg/ kg) and neostigmine (0.015 mg/kg). Extubation will be performed after awakening. The time elapsed from discontinuation of the anesthetics until the eye opening will be registered.

When stable vital signs and respiration are confirmed, all patients will be transferred to the post-anesthesia care unit (PACU). Early recovery times includes time to eye opening (time from the discontinuation of anaesthetics to eye opening) and time to Aldrete score ≥ 9. Data related to the occurrence of pain, nausea and vomiting at the PACU will be recorded. Pain will be assessed while at rest and after asking the subjects to cough, every 15 minutes using a 0-10 numeric pain rating scale (NRS), where zero meant no pain and 10 the worst imaginable pain. When stable vital signs and respiration are confirmed, all patients will be transferred to the post-anesthesia care unit (PACU). Early recovery times includes time to eye opening (time from the discontinuation of anaesthetics to eye opening) and time to Aldrete score ≥ 9. Data related to the occurrence of pain, nausea and vomiting at the PACU will be recorded. Pain will be assessed while at rest and after asking the subjects to cough, every 15 minutes using a 0-10 numeric pain rating scale (NRS), where zero meant no pain and 10 the worst imaginable pain. One or two mL from the solution previously prepared (Syringe 2) will be administered intravenously every 15 minutes to maintain the pain score below 3 (1 mg when the pain score is <7 and 2 mg when it is ≥7). Following discharge from the PACU (minimum stay 60 minutes and Aldrete score ≥ 9), all of the participants will receive ketoprofen (100 mg) every 12 hours and dipyrone (30 mg.kg-1, maximum 1 g) every six hours intravenously. Whenever patients judge that their analgesia is insufficient, tramadol (100 mg) will be administered intravenously at eight-hour minimum intervals. Postoperative nausea and vomiting (PONV) will be treated with ondansetron (4 mg) intravenously. An investigator who will be blinded to group assignment will collect all postoperative outcome data 24 hours after surgical procedure. Subjects will rate the higher score of pain (NRS) during the hospital ward stay. Tramadol consumption and the number of nausea and vomiting episodes will also be recorded. These findings will be confirmed with the ward nursing staff. All subjects will stay at hospital for at least 24 hours.

Data Collection The baseline QoR-40 questionnaire will be provided to subjects after informed consent is obtained in the preoperative holding area and 24 hours after surgery by a blinded investigator. The QoR-40 questionnaire assesses five dimensions of recovery (physical comfort - 12 items; emotional state - 7 items; physical independence - 5 items; physiological support - 7 items; and pain - 7 items). Each item is rated on a five-point Likert scale: none of the time, some of the time, usually, most of the time, and all the time. The total score on the QoR-40 ranges from 40 (poorest quality of recovery) to 200 (best quality of recovery). The primary outcome of interest will be the QoR-40 score, however the following data will also be recorded: age, gender, physical status, BMI, and length of PACU stay.

Statistical Analysis The sample size was calculated considering 90% power to detect a 10-point difference in QoR-40, which indicated the need to include 31 participants in each group. Taking possible losses into consideration, the final sample included 70 patients.

• Study Type: Interventional
• Enrollment (Actual): 70
• Phase: Phase 4

Contacts and Locations

Study Locations

• Brazil
  • SP
    • Sorocaba, SP, Brazil, 18030-230
      • Santa Lucinda Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 65 years (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• ASA physical status I or II, who will be scheduled to undergo laparoscopic cholecystectomy at Santa Lucinda Hospital

Exclusion Criteria:

• Patients who (i) refuse to participate in the study; (ii) are not able to communicate due to alterations in the level of consciousness, or neurologic, or psychiatric disease; - present with contraindication to any of the drugs used in the present study
• have history of alcohol or drug abuse
• present a body mass index (BMI) ≥ 40 will be excluded.
• Reasons for exclusion after randomization will be protocol violations or if the surgical procedure changes from a laparoscopic to an open approach.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: PREVENTION
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: QUADRUPLE

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
ACTIVE_COMPARATOR: MT group; Immediately after the induction of anesthesia, patients will receive intravenously methadone 0.1 mg/kg	Drug: Methadone; Immediately after the induction of anesthesia, patients will receive intravenously methadone 0.1 mg/kg
ACTIVE_COMPARATOR: MF group; Immediately after the induction of anesthesia, patients will receive intravenously morphine 0.1 mg/kg	Drug: Morphine; Immediately after the induction of anesthesia, patients will receive intravenously morphine 0.1 mg/kg

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Quality of recovery (QoR-40)	The baseline QoR-40 questionnaire will be provided to subjects after informed consent is obtained in the preoperative holding area and 24 hours after surgery by a blinded investigator. The QoR-40 questionnaire assesses five dimensions of recovery (physical comfort - 12 items; emotional state - 7 items; physical independence - 5 items; physiological support - 7 items; and pain - 7 items). Each item is rated on a five-point Likert scale: none of the time, some of the time, usually, most of the time, and all the time. The total score on the QoR-40 ranges from 40 (poorest quality of recovery) to 200 (best quality of recovery).	24 hours

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Time to eye opening	The time elapsed from discontinuation of the anesthetics until the eye opening	30 minutes
Postoperative pain (PACU)	Pain will be assessed while at rest and after asking the subjects to cough, every 15 minutes using a 0-10 numeric pain rating scale (NRS), where zero meant no pain and 10 the worst imaginable pain.	2 hours
Postoperative pain (Ward)	Subjects will rate the higher score of pain (NRS) during the hospital ward stay	24 hours
Tramadol consumption	Consumption, or not, of tramadol during the hospital ward stay	24 hours
Postoperative nausea and vomiting	Number of episodes of vomiting or the occurrence of nausea	24 hours
Time of PACU staying	Time required to meet and achieve PACU discharge criteria (Aldrete 9)	3 hours

Collaborators and Investigators

• Sponsor: Pontificia Universidade Catolica de Sao Paulo

Study record dates

Study Major Dates

• Study Start (ACTUAL): June 20, 2016
• Primary Completion (ACTUAL): July 20, 2016
• Study Completion (ACTUAL): April 20, 2017

Study Registration Dates

• First Submitted: February 3, 2017
• First Submitted That Met QC Criteria: February 6, 2017
• First Posted (ESTIMATE): February 7, 2017

Study Record Updates

• Last Update Posted (ACTUAL): May 8, 2017
• Last Update Submitted That Met QC Criteria: May 3, 2017
• Last Verified: May 1, 2017

More Information

Terms related to this study

• Keywords: Postoperative nausea and vomiting; Postoperative pain; Quality of recovery; Total intravenous anesthesia; QoR-40
• Additional Relevant MeSH Terms: Pathologic Processes; Postoperative Complications; Pain; Neurologic Manifestations; Signs and Symptoms, Digestive; Pain, Postoperative; Nausea; Vomiting; Postoperative Nausea and Vomiting; Physiological Effects of Drugs; Central Nervous System Depressants; Peripheral Nervous System Agents; Analgesics; Sensory System Agents; Analgesics, Opioid; Narcotics; Respiratory System Agents; Antitussive Agents; Morphine; Methadone
• Other Study ID Numbers: PUCSP 050539/2016

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No