Aortic Coarctation, Aortic Stenosis, Atrial Septal Defect, Cardiomyopathy, Patent Ductus Arteriosus, Post Heart Transplant Catheter Procedure
Conditions
Keywords
radiation free cardiac catheterization
Brief summary
Currently catheters used in heart catheterization procedures are guided throughout the heart chambers and blood vessels by pictures taken by x-rays. This technology exposes patients to radiation. With this study protocol the investigators will use MRI technology to take real-time pictures to navigate catheters throughout heart chambers. MRI uses electromagnetic energy; therefore, it does not expose participants to radiation energy.
Detailed description
Participants undergo general anesthesia, and vascular access is obtained in the x-ray catheterization lab. Next the participant is transferred into the MRI scanner where a focused MRI examination is performed. Catheters are then guided into the heart chambers using real-time MRI guidance to perform conventional cardiac catheterization steps. If time allows, additional research MRI is performed before the participant is returned to the x-ray catheterization lab. If any MRI guided catheterization steps are unsuccessful, the clinically indicated step is performed after the participant returns to the x-ray catheterization lab using conventional x-ray guided pictures.
Interventions
PROCEDUREMRI guided cardiac catheterization
Magnetic resonance imaging will be used to guide cardiac catheterization procedures whenever possible to avoid or minimize x-ray radiation exposure.
DEVICEMagnetic resonance imaging
Sponsors
Joshua Kanter
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
* Undergoing a medically necessary cardiovascular catheterization
Exclusion criteria
* Cardiovascular instability including hemodynamic instability (such as requiring significant vasoactive infusion support) or mechanical hemodynamic support. * Women who are pregnant * Women who are nursing and who do not plan to discard breast milk for 24 hours * Patients with a contraindication to MRI scanning will be excluded. These contraindications include patients with the following devices: 1. Central nervous system aneurysm clips 2. Implanted neural stimulator 3. Implanted cardiac pacemaker or defibrillator which are not MR safe or MR conditional according to the manufacturer 4. Cochlear implant 5. Ocular foreign body (e.g. metal shavings) 6. Implanted Insulin pump 7. Metal shrapnel or bullet
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Test the feasibility of navigating catheters into right heart structures using real-time MRI | At the end of each catheterization procedure through study completion,up to 5 years. | Heart catheterization usually uses X-ray guidance. Using commercially available MRI-compatible catheters, the right heart catheterization procedure will be done using real-time magnetic resonance imaging (MRI). MRI guidance does not use X-ray radiation. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of participants whose MRI cardiac catheterization procedure was prematurely terminated | At the end of each catheterization procedure through study completion,up to 5 years | Premature termination will occur under the following circumstances: * Hemodynamic or other clinical instability * Technical failure of catheter procedure such as being unable to navigate the catheters to the heart chamber * Equipment malfunction * Any other circumstance that in the opinion of the Principal Investigator poses hazard to the research subject |
| Measurement of radiation exposure | End of study, 5 years. | Comparison of radiation exposure in this cohort of subjects to historical controls undergoing matched invasive cardiology procedure at CNMC. |
Countries
United States
Outcome results
None listed