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Effect of Pressure Support Ventilation During Anesthetic Emergence on Postoperative Atelectasis in Infant

Yonsei University logo

Yonsei University

Status

Unknown

Conditions

Infants Aged 0 Days to 13 Months Scheduled for Elective Surgery

Treatments

Other: pressure support, group PS
Other: conventional ventilation, group C

Study type

Interventional

Funder types

Other

Identifiers

NCT05373589
4-2022-0119

Details and patient eligibility

About

Atelectasis occurs in patients of all ages who receive mechanical ventilation under general anesthesia, and although fatal cases are rare, it is known as a cause of postoperative hypoxia or fever. In pediatric patients, it has a particularly high incidence of 68-100%, and the incidence is inversely proportional to age. Pediatric patients,compared to adults, have a small capacity for functional residual capacity while a high metabolic demand, making them fundamentally vulnerable to hypoxia. Increased atelectasis during anesthesia causes hypoxia not only during anesthesia but also during recovery after anesthesia. Therefore, it is important to establish and apply a strategy to minimize the occurrence of atelectasis during mechanical ventilation under general anesthesia in pediatric patients. The aim of this study is to investigate whether pressure support ventilation at emergence period could reduce the incidence of postoperative atelectasis in infants undergoing surgery under general anesthesia.

Enrollment

136 estimated patients

Sex

All

Ages

Under 1 year old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. infant patients aged 0 day to 13 month
  2. American Society of Anesthesiologists (ASA) classification 1~2 who are scheduled for elective surgery under general anesthesia

Exclusion criteria

  1. patients with symptomatic bronchopulmonary dysplasia
  2. patients with uncorrected congenital heart or pulmonary disease
  3. Hemodynamically unstable requiring preoperative vasopressor administration
  4. fever (>37.5°) or URI symptoms on the day of surgery

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

136 participants in 2 patient groups

group C
Experimental group
Treatment:
Other: conventional ventilation, group C
group PS
Experimental group
Treatment:
Other: pressure support, group PS

Trial contacts and locations

1

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Central trial contact

Jeong-Rim Lee

Data sourced from clinicaltrials.gov

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