Atrial Fibrillation Risk After Miniinvasive Mitral Valve Repair
NCT ID: NCT06707506
Last Updated: 2024-11-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
114 participants
OBSERVATIONAL
2014-01-01
2024-08-01
Brief Summary
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Detailed Description
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Primary Objective To determine whether CT-derived tissue quality parameters (adipose tissue density, muscle density) independently predict post-operative atrial fibrillation risk following minimally invasive mitral valve surgery.
Study Design
Observational Model: Retrospective Cohort Setting: Single-center study at Complex Cardiovascular Center, Hospital AGEL Trinec-Podlesi Time Frame: January 2014 - November 2023 Follow-up: Through August 1, 2024
Primary Outcome Measure Post-operative Atrial Fibrillation \[Time Frame: Up to 30 days post-surgery\]
Defined as new-onset AF lasting more than 48 hours or requiring intervention Measured through continuous cardiac monitoring Analyzed separately for patients with and without preoperative AF history
Secondary Outcome Measures
Overall Survival \[Through August 1, 2024\]
Perioperative Complications:
Blood product utilization Duration of mechanical ventilation ICU length of stay Total hospital length of stay
Key Study Groups
AF-Naïve Group (n=56):
No previous AF history Primary prevention cohort
AF-History Group (n=48):
Preexisting AF with concurrent Maze procedure Secondary prevention cohort
CT Analysis Methods
Automated segmentation at L3 vertebral level
Parameters measured:
Muscle density (HU) Intramuscular adipose tissue density (IMAT HU) Visceral adipose tissue density (VAT HU) Subcutaneous adipose tissue density (SAT HU) Skeletal muscle index (SMI)
Statistical Analysis Plan
Primary analysis: Logistic regression for POAF prediction Interaction analysis between tissue parameters and AF history Adjustment for age, gender, and traditional risk factors Separate models for AF-naïve and AF-history groups
Eligibility Criteria
Inclusion Criteria:
Age ≥ 18 years Undergoing minimally invasive mitral valve surgery Preoperative CT scan available Surgery between January 2014 and November 2023
Exclusion Criteria:
Incomplete clinical data Poor quality CT images Previous cardiac surgery
Sample Size 114 total participants (104 included in primary analysis) Study Status
Completed enrollment Final follow-up: August 1, 2024 Ethics Committee Approval: EK 65/24
Principal Investigators
Matej Pekar, MD David Vician, MD Complex Cardiovascular Center, Hospital AGEL Trinec-Podlesi
Funding Sources
MUNI/A/1547/2023 MUNI/A/1555/2023 Ministry of Education, Youth, and Sports of the Czech Republic
Conditions
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Study Design
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COHORT
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Undergoing minimally invasive mitral valve surgery
* Preoperative CT scan available
* Surgery between January 2014 and November 2023
Exclusion Criteria
* Poor quality CT images
* Previous cardiac surgery
19 Years
110 Years
ALL
No
Sponsors
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Nemocnice AGEL Trinec-Podlesi a.s.
OTHER
Responsible Party
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Matej Pekar, MD, PhD
Matej Pekar, MD, PhD
Other Identifiers
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EK 65/24
Identifier Type: -
Identifier Source: org_study_id