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Clinical Trials/NCT06354569
NCT06354569
Recruiting
Not Applicable

Risk Factors and Risk Grading Prediction of Perioperative Respiratory Adverse Events in Children

Sichuan Provincial People's Hospital1 site in 1 country600 target enrollmentDecember 31, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Perioperative Respiratory Adverse Events
Sponsor
Sichuan Provincial People's Hospital
Enrollment
600
Locations
1
Primary Endpoint
The occurrence of perioperative respiratory adverse events
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

to explore the risk factors of perioperative respiratory adverse events in children, and to establish a risk prediction model of perioperative respiratory adverse events in children

Detailed Description

600 children undergoing elective surgery under general anesthesia were selected. Age, sex, weight, height, allergy history, past history, snoring, passive smoking, abnormal laboratory examination and chest X-ray before operation, upper respiratory tract infection 14 days before operation, Operation Site, working years of anesthesiologist, anesthesia method, Operation Duration, anesthesia duration, perioperative vital signs and respiratory adverse events were collected. The risk prediction model of perioperative respiratory adverse events in children was established by using LASSO (least absolute shrinkage and selection operator) algorithm and gradient boosting machine (GBM) algorithm to screen the relevant data collected during routine diagnosis and treatment, such as demographic characteristics, physical conditions, airway sensitivity, environmental sensitivity and anesthesia management

Registry
clinicaltrials.gov
Start Date
December 31, 2024
End Date
December 31, 2024
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Sichuan Provincial People's Hospital
Responsible Party
Principal Investigator
Principal Investigator

Yanyu Liu

Principal Investigator

Sichuan Provincial People's Hospital

Eligibility Criteria

Inclusion Criteria

  • (1)Children aged 1 month to 12 years, (2) ASA Class I or II, (3)scheduled for surgery under general anesthesia

Exclusion Criteria

  • (1)Children and guardians declined to participate in the study (2) children with severe chronic respiratory, cardiovascular, central nervous system, liver and kidney diseases; (3) on the day of operation, the patients had active URTI and pulmonary infection, such as severe nasal obstruction, large amount of airway secretion, severe cough, fever (body temperature \> 37.5 ° C) , in addition to the above symptoms, signs of pulmonary consolidation and/or wet Rales, or peripheral white blood cells \> 10 × 109/L or \< 4 × 109/L with or without left shift of the nucleus, and chest X-ray showed new patchy, patchy infiltrative shadows or interstitial changes.
  • (4) the child had severe anaphylaxis to narcotic drugs

Outcomes

Primary Outcomes

The occurrence of perioperative respiratory adverse events

Time Frame: perioperative

Collection of respiratory adverse events including laryngeal spasm, Bronchospasm, decreased oxygen saturation, and increased secretions

Study Sites (1)

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