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The effect of emergence FIO2 on postoperative lung volume

Not Applicable
Recruiting
Conditions
Not Applicable
Registration Number
KCT0002642
Lead Sponsor
Samsung Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
81
Inclusion Criteria

18-80 aged, ASA I-III patients undergoing elective laparascopic abdominal surgery

Exclusion Criteria

1) patients who can not be applied the sensors of EIT device
2) any abnomality in diaphragmatic function
3) patients with any pace maker
4) hemodynamic instability during the perioperative period, who transferred to postoperative ICU
5) A woman in pregnancy
6) Obese patient with BMI over 30-
7) any neuromuscular disease patient
8) preoperative active or chronic lung disease (chronic obstructive pulmonary disease, pneumonia, asthma)
9) predicted airway difficulty
10) patient who refuse to enroll to the study
11) emergency operation

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
perioperative lung volume change according to the applied FIO2 at anesthesa emergence
Secondary Outcome Measures
NameTimeMethod
postoperative atelectasis
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