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Patient Specific Mitral Valve Modeling for Surgical Planning and Training

Conditions
Mitral Valve Disease
Mitral Regurgitation
Mitral Valve Prolapse
Interventions
Procedure: Mitral Valve Model
Registration Number
NCT03609931
Lead Sponsor
Lawson Health Research Institute
Brief Summary

Mitral valve disease is a common pathologic problem occurring in approximately 2% of the general population but climbing to 10% in those over the age of 75 in Canada\[1\]. This project has three primary goals all of which will positively affect cardiac patient care.

1) Create patient specific MV models for complex repairs that will allow surgeons the opportunity to practice the repair. 2) Potentially predict the outcomes following minimally invasive repair techniques such as transcatheter treatments (e.g., MitraClip). 3) Provide a model to train individuals on mitral valve repair techniques.

Detailed Description

BACKGROUND Mitral valve disease is a common pathologic problem occurring in approximately 2% of the general population, but climbing to 10% in those over the age of 75 in Canada. Of this group, approximately 20% have a sufficiently severe form of the disease that may require surgical intervention to restore normal valve function and prevent early mortality \[4\]. Evidence indicates that the surgeon's individual volume of mitral valve repair cases performed is a determinant of not only successful mitral repair rates, but also freedom from reoperation, and patient survival. For patients previously deemed inoperable due to co-morbidities, new techniques to treat mitral valve disease are being developed. However, assessing the optimal approach and the point at which clinical benefit is exceeded by the poor value or futility of the procedure is one of the biggest clinical challenges for physicians.

In the past decade, 3D echocardiography has emerged as a standard of care in diagnostic and interventional imaging for cardiac surgery and cardiology. This, coupled with the emergence of inexpensive 3D printing technology has led researchers and clinicians to explore how improved imaging and additive manufacturing can be used to improve patient outcomes.

In this context, the investigators have completed a proof-of-concept workflow for creating dynamic, patient specific mitral valve models. In concert with a left ventricle simulator 8\], these valve models can mimic patient valve pathologies both anatomically and dynamically, as shown in Doppler ultrasound. In a 10 patient retrospective study, the investigators have demonstrated the ability to accurately re-create patient pathology, perform realistic surgical repairs, and assess realistic valve function post repair. The study team's vision is to create a simulator that can be used to assess patient candidacy for percutaneous interventions, assess different repair options for both percutaneous and surgical interventions, and finally use the model as a simulator for competency-based MV interventions.

RATIONALE Based on our successful proof of concept, the goal is to translate this technology to clinical use by validating our valve models. There are two primary long term goals. First, to validate a system for using patient specific MV models to: 1- assess intervention options, and 2: plan repair strategies for improved patient outcomes. Second, by building a database of MV pathologies, create a competency based simulator/trainer to provide surgeons with increased experience in MV repair techniques.

OBJECTIVES

1. Validate the accuracy of patient specific MV pathologies and repairs in a prospective 65 patient study;

2. Optimize our work-flow for creating valve models, in terms of accuracy, manufacture time required, and expense;

3. Validate the accuracy of our patient models for both surgical cases and transcatheter MitraClip interventions;

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
65
Inclusion Criteria
  • Patients undergo mitral valve repair with either surgery of MitraClip techniques
  • Over 18 years old
Exclusion Criteria
  • Unable to place TEE probe
  • Refuse consent

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Mitral Valve repairMitral Valve ModelPatients undergoing mitral valve repair
Primary Outcome Measures
NameTimeMethod
MR following patient/model repairCreation and assessment of the model within 1 week before or after surgery/intervention on the patient.

The degree and location of residual MR following mitral repair surgery

Secondary Outcome Measures
NameTimeMethod
2D measurements of the mitral valve:Annular HeightAssessment of model within 1 week of surgical or interventional repair on the patient

A 2D measurements taken from the echocardiography images of the mitral valve and model

2D measurements of the mitral valve: Annular 3D CircumferenceAssessment of model within 1 week of surgical or interventional repair on the patient

A 2D measurements taken from the echocardiography images of the mitral valve and model

2D measurements of the mitral valve: Anterolateral-Posteromedial DiameterAssessment of model within 1 week of surgical or interventional repair on the patient

A 2D measurements taken from the echocardiography images of the mitral valve and model

2D measurements of the mitral valve: tenting Height.Assessment of model within 1 week of surgical or interventional repair on the patient

A 2D measurements taken from the echocardiography images of the mitral valve and model

ICU LOSPostoperative period until ICU discharge (expected mean of 1 days)]

length of stay in the ICU

DeliriumPostoperative period until hospital discharge (expected mean of 5 days)

Delirium in hospital

2D measurements of the mitral valve:Annular 2D AreaAssessment of model within 1 week of surgical or interventional repair on the patient

A 2D measurements taken from the echocardiography images of the mitral valve and model

2D measurements of the mitral valve: Annular EllipticityAssessment of model within 1 week of surgical or interventional repair on the patient

A 2D measurements taken from the echocardiography images of the mitral valve and model

2D measurements of the mitral valve: Anterior Leaflet 3D AreaAssessment of model within 1 week of surgical or interventional repair on the patient

A 2D measurements taken from the echocardiography images of the mitral valve and model

2D measurements of the mitral valve: Posterior Leaflet 3D AreaAssessment of model within 1 week of surgical or interventional repair on the patient

A 2D measurements taken from the echocardiography images of the mitral valve and model

2D measurements of the mitral valve: Leaflet 3D AreaAssessment of model within 1 week of surgical or interventional repair on the patient

A 2D measurements taken from the echocardiography images of the mitral valve and model

2D measurements of the mitral valve: Mitral Regurgitation Orifice AreaAssessment of model within 1 week of surgical or interventional repair on the patient

A 2D measurements taken from the echocardiography images of the mitral valve and model

2D measurements of the mitral valve: Tenting VolumeAssessment of model within 1 week of surgical or interventional repair on the patient

A 2D measurements taken from the echocardiography images of the mitral valve and model

2D measurements of the mitral valve: Nonplanar AngleAssessment of model within 1 week of surgical or interventional repair on the patient

A 2D measurements taken from the echocardiography images of the mitral valve and model

Hospital LOSPostoperative period until hospital discharge (expected mean of 5 days)

Length of stay in hospital

Renal failure requiring dialysisPostoperative period until hospital discharge (expected mean of 5 days)

Dialysis

Stroke,TIAPostoperative period until hospital discharge (expected mean of 5 days)

Diagnosis of stroke

Death in HospitalPostoperative period until hospital discharge (expected mean of 5 days)

Death

Reoperation for BleedingPostoperative period until hospital discharge (expected mean of 5 days)

Return to the operating room for re-exploration of the surgical procedure due to excess blood loss in the ICU

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