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Evaluation of whether 100 ml of fluid infusion can predict fluid responsiveness in patients with atrial fibrillatio

Not Applicable
Recruiting
Conditions
Diseases of the circulatory system
Registration Number
KCT0006540
Lead Sponsor
Samsung Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
63
Inclusion Criteria

(1) Adult patients aged 18 to 80 years with atrial fibrillation scheduled for elective surgery that takes more than 1 hour from induction of anesthesia to start of surgery
(2) Patients without moderate or more acute/chronic respiratory problems in the pre-operative questionnaire, physical examination, and respiratory examination findings

Exclusion Criteria

(1) Patients with moderate or more severe heart valve disease
(2) In case of moderate or more obstructive pulmonary disease (COPD grade 2 or higher)
(3) Left ventricle ejection fraction < 40% of patients
(4) Heart failure patients requiring preoperative inotropics
(5) Patients with preoperative blood creatinine levels of 1.3 mg/dL or higher
(6) Patients with moderate to severe kidney disease or liver disease
(7) Patients with acute lung disease, such as acute lung injury, acute pneumonia, or ARDS
(8) Patients who need to maintain spontaneous breathing

Study & Design

Study Type
Observational Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
AUC values for fluid responder prediction of change rate in cardiac output index after 100ml fluid Infusion
Secondary Outcome Measures
NameTimeMethod
Gray zone for change rate in cardiac output index after 100ml fluid Infusion
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