Bis Monitoring Effect on Delirium Occurrence and Nursing Quality Improvement Recovering From General Anesthesia

Bispectral Index Monitoring Effect on Delirium Occurrence and Nursing Quality Improvement in Post-anesthesia Care Unit Patients Recovering From General Anesthesia

①Effects of BIS Index (BIS) monitoring on delirium incidence in Post-anesthesia care unit (PACU) in patients undergoing general anesthesia

②Effects of BIS BIS Index (BIS) monitoring on the quality of nursing care in the Post-anesthesia care unit (PACU)

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

The effect of intraoperative anesthesia depth monitoring on delirium occurrence and improvement of nursing quality in the post-anesthesia care unit (PACU) remains unclear. We aimed to explore the effect of intraoperative anesthesia bispectral index (BIS) monitoring on delirium occurrence and improvement of nursing quality in the PACU for patients recovering from general anesthesia.

This randomized controlled trial included 120 patients, aged 20-80 years and classified as grades I-III according to the American Society of Anesthesiologists. The BIS-guided group (group B) underwent intraoperative monitoring of BIS anesthesia depth (maintained within the anesthetic range [40-60]). The depth of anesthesia was not monitored in the non-BIS-guided group (group C). The patients' vital signs were recorded at the beginning of the operation (T0), upon entering the PACU (T1), 15 min after extubation (T2), and after leaving the PACU (T3). Delirium score, emergence period (extubation and PACU observation times), and adverse events in the PACU were monitored. The nursing activity score (NAS) was used to evaluate the quality of care.

Study Type

Interventional

Enrollment (Actual)

134

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Zhejiang
      • Jinhua, Zhejiang, China, 322000
        • The Fourth Affiliated Hospital, School of Medicine, Zhejiang University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  1. age ranging from 20 to 80 years
  2. estimated operation time of 2 to 3 h
  3. body mass index ≤30 kg/m2
  4. normal preoperative heart, liver, lung, and renal function.

Exclusion Criteria:

  1. Past cognitive impairment (dementia, cognitive impairment, mental illness or mental disorder)
  2. Complex injuries: multiple fractures, chest and abdomen, pelvic and sacral trauma, head trauma, etc
  3. Contraindications to intraspinal puncture (coagulation dysfunction, thrombocytopenia, intraspinal space occupation, puncture site infection, etc.)
  4. Have a history of acute myocardial infarction or stroke within 3 months
  5. Patients with severe liver dysfunction (Child-Pugh C) or renal failure
  6. Contraindications to ketamine, such as malignant hypertension

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: non-BIS-guided group (group C)
The depth of anesthesia was not monitored in the non-BIS-guided group (group C).
Experimental: BIS-guided group (group B)
The BIS-guided group (group B) underwent intraoperative monitoring of BIS anesthesia depth
underwent intraoperative monitoring of BIS anesthesia depth

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Ricker sedation-agitation scale
Time Frame: ■evaluate immediately after recovery and tracheal intubation removal ■every five minutes after that ■take the highest value until the patient leave PACU
Delirium was assessed using the Ricker sedation-agitation scale (SAS; unable to awaken = 1, very calm = 2, calm = 3, quiet cooperation = 4, agitated = 5, very agitated = 6, and dangerously agitated = 7)
■evaluate immediately after recovery and tracheal intubation removal ■every five minutes after that ■take the highest value until the patient leave PACU
The nursing activity score (NAS)
Time Frame: ■at the begin of the patient enter PACU ■end with the transfer out of the PACU ■any nursing activitise will be scored

The nursing activity score (NAS), consists of 23 nursing items in five aspects, including monitoring health care, supporting patients and their families, and managing nursing administration. Each item was assigned a score of 1.2-32.0 according to the percentage of time spent on the task during a nurse's working day. The higher the score, the greater the workload. The NAS score of each patient ranged from 0-177, and the assessment was conducted at the beginning of resuscitation in the PACU by a trained investigator according to the nursing work items on the NAS scale.

According to the nursing records of patients, the nursing workload of PACU was evaluated and by the contents of NAS scale.

■at the begin of the patient enter PACU ■end with the transfer out of the PACU ■any nursing activitise will be scored
vital signs (Mean arterial pressure, heart rate, pulse oxygen saturation )
Time Frame: ■ at the beginning of surgery (T0), ■at the time of extubation (T1), ■10 minutes after extubation (T2), ■at the time of leaving the PACU (T3: when patients were transferred from the PACU to the ward).
collected from monitors (Mean arterial pressure, heart rate, pulse oxygen saturation)
■ at the beginning of surgery (T0), ■at the time of extubation (T1), ■10 minutes after extubation (T2), ■at the time of leaving the PACU (T3: when patients were transferred from the PACU to the ward).
Comparison of complications during the PACU period
Time Frame: The patients were transferred to PACU after surgery, the period during the PACU
including postoperative delirium, nausea, vomiting, respiratory complications (e.g., SPO2 < 90%, arterial oxygen partial pressure < 60 mmHg, or interventions requiring mask compression, oxygen supply, manual mandibular ventilation, and intubation), cardiovascular-related complications (e.g., blood pressure exceeding 20% of preoperative value, HR < 120 beats /min or < 50 beats /min, emerging arrhythmia, and ischemia), severe pain, chills/hypothermia (skin temperature < 35 °C), and unplanned transfer to ICU.
The patients were transferred to PACU after surgery, the period during the PACU
The comprehensive satisfaction score
Time Frame: The patients were followed up 24 hours after surgery
The comprehensive satisfaction score for anesthesia and nursing. The satisfaction score was categorized as excellent or generally poor based on criteria such as postoperative pain, influence on daily activities, and emotional stability. Excellent satisfaction indicated no or mild pain after surgery, no interference with daily activities, and emotional stability. General satisfaction indicated moderate pain that was tolerable, daily activities that were not affected or slightly reduced, and emotional stability. Poor satisfaction indicated moderate pain, significantly limited patient activities, low mood, or irritability.
The patients were followed up 24 hours after surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2020

Primary Completion (Actual)

May 31, 2022

Study Completion (Actual)

August 29, 2022

Study Registration Dates

First Submitted

February 20, 2024

First Submitted That Met QC Criteria

March 6, 2024

First Posted (Actual)

March 8, 2024

Study Record Updates

Last Update Posted (Actual)

March 8, 2024

Last Update Submitted That Met QC Criteria

March 6, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

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

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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