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Comparison of Postoperative Outcomes Between Surgeries Anaesthetized With Propofol and Inhalational Anaesthetics

Comparison of Postoperative Outcomes Between Surgeries Anaesthetized With Propofol and Inhalational Anaesthetics With Regression Controls for Confounders

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03875872
Enrollment
3922
Registered
2019-03-15
Start date
2019-02-11
Completion date
2019-08-12
Last updated
2023-05-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Pain

Keywords

propofol, inhalation anaesthetics, postoperative outcomes, regression control

Brief summary

Propofol used as anaesthesia in surgery had shown small postoperative analgesic benefits over inhalational anaesthetics in some meta-analyses. It was also associated with reduced risk of postoperative nausea and vomiting. Small sample of studies together with high heterogeneity prevented some meta-analyses to confirm propofol's effect for postoperative morphine consumption and other outcomes. Acute Pain Service data bank can provide an alternative way of evaluating postoperative outcomes of propofol anaesthetics through supplying a very large sample size in a more homogeneous setting. Retrospective study comparing propofol and inhalational anaesthetics on postoperative pain matched on patients' demographic and clinical data had been done for liver surgery. Propofol's benefits for postoperative pain and morphine consumption was confirmed but not for adverse effects. This study plans to analyze the postoperative outcome data from an Acute Pain Service data bank in years 2015-17 to compare the anaesthetics of propofol and inhalational anaesthetics. Comprehensive regression adjustment for confounders are performed using all available patients' demographic, clinical and anaesthetic data. All major surgery types are included. Results will provide postoperative outcome differences between propofol and inhalational anaesthetics for all surgeries and for specific type of surgeries. The large sample bank will provide higher probability for detecting outcome difference between the anaesthetics for all the major surgical types.

Detailed description

Objective: To compare the postoperative outcomes between surgeries anaesthetized with propofol and inhalational anaesthetics in the Acute Pain Service records of Queen Mary Hospital for years 2015-17 Methods: Retrospective Data collection 1. Demographic data; 2. Type of surgery; 3. Type of anaesthetic techniques; 4. Postoperative NRS pain scores (Rest and Moving) for Postop Days 1, 2 & 3; 5. Accumulated amount of patient controlled analgesia (PCA) used in Postop Days 1, 2 & 3; 6. Postoperative incidence of nausea, vomitting, dizziness and pruritus.

Interventions

DRUGPropofol

Patients who had surgeries and were anaesthetized with propofol at Queen Mary Hospital, Hong Kong from Jan 2015 to Dec 2017

DRUGinhalation anaesthetics

Patients who had surgeries and were anaesthetized via inhalation at Queen Mary Hospital, Hong Kong from Jan 2015 to Dec 2017

Sponsors

The University of Hong Kong
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

1. Postoperative outcomes from Acute Pain Service data bank between Jan 2015 and Dec 2017 in Queen Mary Hospital would be retrieved; 2. Surgeries with general anaesthesia by either propofol or inhalational anaesthetics.

Exclusion criteria

1. Essential data missed; 2. Surgical types with small sample size below 30 for the data collection period.

Design outcomes

Primary

MeasureTime frameDescription
pain scoreup to postoperative day 3NRS (0-10) for both rest and moving

Secondary

MeasureTime frameDescription
analgesic consumptionup to postoperative day 3amount of accumulated patient controlled analgesia (PCA) of morphine use
Amount of patients with adverse events in post-operationup to postoperative day 3nausea and vomit, dizziness and pruritus

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026