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Prediction of Fluid Responsiveness in Atrial Fibrillation Patients Who Underwent Valvular Heart Surgery: Peep-induced Increase in Central Venous Pressure vs. Passive Leg Raising

Not Applicable
Completed
Conditions
Valvular Heart Surgery
Interventions
Procedure: passive leg raising(PLR)
Procedure: peep induced CVP
Registration Number
NCT02224378
Lead Sponsor
Yonsei University
Brief Summary

Dynamic indices of preload depending on the heart-lung interaction require sinus rhythm and cannot be applied to patients with atrial fibrillation. PEEP-induced increase in central venous pressure (CVP) was shown to be a valid predictor of fluid responsiveness after cardiac surgery in patients with sinus rhythm, and was speculated to be of value in patients with rhythm other than sinus. The aim of this study is to assess the predictability of PEEP-induced increase in CVP and passive leg raising (PLR)-induced changes in stroke volume index (SVI) on fluid responsiveness in patients with atrial fibrillation following valvular heart surgery.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
44
Inclusion Criteria
  1. age ≥20
  2. atrial fibrillation patients who underwent elective valvular heart surgery
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Exclusion Criteria
  1. age < 20
  2. LV ejection fraction < 40%
  3. any pulmonary disease
  4. end stage renal disease
  5. high intrabdominal pressure patient
  6. contraindication of passive leg raising
  7. deep vein thrombosis
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
passive leg raising(PLR)passive leg raising(PLR)-
peep induced CVPpeep induced CVP-
Primary Outcome Measures
NameTimeMethod
fluid responsiveness1hr after arriving at ICU

1. ventilator peep setting was adjusted to 0cmH2O as baseline

2. Then peep was increased to 10cmH2O for 5 min.

3. We set peep to baseline 0cmH2O again, making patients to semirecumbent position following passive leg raising at 30 degree for 5 min.

4. After that, 300 ml of hydroxyethyl starch 130/0.4 was infused in the supine position for 10-20 min and haemodynamic variables including SVI were assessed 5 min after completion of fluid challenge.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Department of Anesthesiology & Pain Medicine, Yonsei university college of medicine

🇰🇷

Seoul, Korea, Republic of

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