Factors Analysis Related to Prolonged Stay in the Pediatric Post-Anesthesia Care Unit(PACU) (PACU)

May 1, 2024 updated by: Saiqiang Guo

Prolonged Stay in the Pediatric PACU

The purpose of this study is to determine which factors contribute to prolonged stay of children in the PACU.

Study Overview

Status

Not yet recruiting

Detailed Description

Studying the factors associated with prolonged stay of children in the PACU is of great significance to the medical team, as it can improve the quality and speed of anesthesia recovery, not only in line with the concept of accelerated rehabilitation surgery, but also through intervention and optimization of specific factors to improve the efficiency of children's postoperative discharge from the PACU, reduce the incidence of complications, lower medical costs, and increase patient and family satisfaction. Therefore, this study aims to explore the factors associated with prolonged stay of children in the PACU through retrospective analysis.

Study Type

Observational

Enrollment (Estimated)

10000

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

  • Child
  • Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

Pediatric patient entering the Pediatric Post-Anesthesia Care.

Description

Inclusion Criteria:

  • Children aged 0-18 years old; Child entering the Pediatric Post-Anesthesia Care.
  • Emergency surgery; Pediatric patients with incomplete medical history; Pediatric patients requiring postoperative ICU care; Pediatric patients with preoperative altered consciousness; Neurological disorders; Severe liver, kidney, lung, and heart diseases.

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Anesthesia Plan Selection
Time Frame: Day 1
Anesthesia options include general anesthesia, combined anesthesia, pure intravenous anesthesia, and nerve block anesthesia.
Day 1
Pain Score
Time Frame: Day 1
Evaluate pain using the Visual Analog Scale (VAS): 0 points: no pain; 1-3 points: mild pain; 4-6 points: moderate pain; 7-10 points: severe pain.
Day 1
Complications in PACU
Time Frame: Day 1
Nausea, vomiting, chills, pain, agitation
Day 1
American Society of Anesthesiologists(ASA)
Time Frame: Day 1

ASA I: Patients in good health, without systemic disease. ASA II: Patients with mild systemic disease, not significantly limiting daily activity.

ASA III: Patients with severe systemic disease, with definite functional limitation.

ASA IV: Patients with severe systemic disease that is a constant threat to life.

ASA V: Moribund patients who are not expected to survive without the operation. ASA VI: Brain-dead patients whose organs are being removed for donation.

Day 1
The medication usage in PACU
Time Frame: Day 1
Morphine, Propofol, Ketorolac, Fentanyl
Day 1

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The use of PCA(Patient-Controlled Analgesia)in PACU
Time Frame: Day 1
PCA usage statistics,yes or no
Day 1

Collaborators and Investigators

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

Sponsor

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 (Estimated)

May 31, 2024

Primary Completion (Estimated)

December 31, 2024

Study Completion (Estimated)

March 31, 2025

Study Registration Dates

First Submitted

April 23, 2024

First Submitted That Met QC Criteria

April 29, 2024

First Posted (Actual)

May 2, 2024

Study Record Updates

Last Update Posted (Actual)

May 3, 2024

Last Update Submitted That Met QC Criteria

May 1, 2024

Last Verified

May 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • FARPSPP

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.

Clinical Trials on Anesthesia; Adverse Effect

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