Superior Vena Cava Occlusion for Heart Failure Unloading
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Solution Overview
Problem
Current treatments for heart failure, including pharmacologic approaches, are limited in effectively arresting or reversing cardiac remodeling, exacerbate co-morbidities, and increase healthcare burden, with few options for ambulatory or chronic use.
Innovation Solution
A method involving the continuous occlusion of the Superior Vena Cava (SVC) using a balloon catheter for 6 hours to reduce venous return, thereby unloading the heart and promoting myocardial recovery, combined with a trans-valvular heart pump for assistance.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Reliability
If pharmacologic treatments are used to treat heart failure, then symptoms and survival may be improved, but costs and side effects increase
Solution Approach 1:
The patent replaces pharmacologic treatments with a mechanical intervention - a removable occlusion device that physically blocks the superior vena cava to reduce venous return. This mechanical approach directly addresses the hemodynamic problem of volume overload without the side effects and costs associated with multiple medications, while still achieving improved survival and reduced hospitalizations.
Solution Approach 2:
The occlusion device acts as an intermediary mechanism between the patient's heart failure condition and the desired therapeutic effect. By introducing this intermediate device that temporarily restricts blood flow, the system achieves cardiac unloading and promotes myocardial recovery without directly modifying the patient's physiology through drugs.
2Stress or pressure
If continuous occlusion of SVC is performed, then cardiac pressures are reduced and myocardial recovery is promoted, but device complexity and treatment duration increase
Solution Approach 1:
The occlusion device is designed to be dynamic rather than static - it can be inserted and removed based on patient needs. The device transitions between an occluding state (when inserted) and a non-occluding state (when removed), allowing flexibility in treatment duration and adaptation to patient response without requiring complex permanent modifications.
Solution Approach 2:
The treatment approach is segmented into discrete phases: device insertion, occlusion period (6 hours), device removal, and recovery period. This segmentation allows for controlled, temporary intervention rather than continuous permanent occlusion, reducing overall device complexity while achieving the desired pressure reduction and myocardial recovery effects.
3Duration of action of moving object
If occlusion device is removed after 6 hours, then treatment duration is limited, but reliability of sustained effect is reduced
Solution Approach 1:
The patent achieves continuity of useful action through repeated cycles of device insertion and removal. Rather than relying on a single prolonged occlusion event, the treatment can be administered multiple times, ensuring sustained therapeutic effect. Each 6-hour occlusion period provides immediate benefit, and repeated administrations maintain long-term improvement in cardiac function and reduction in hospitalizations.
Applied Scientific Principles
This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.
Function Achieved in This Case
This approach reduces cardiac pressures, improves renal function, decreases hospital stays, and reverses myocardial remodeling, enhancing quality of life and reducing the risk of co-morbidities associated with heart failure.
Implementation Method 1
delivering an occlusion device through the vasculature into the Superior Vena Cava ('SVC') of the patient. The occlusion device is activated within the SVC such that blood flow from the SVC is effectively continuously occluded
Data Source
AI summary
A method of treating heart failure in a patient includes delivering an occlusion device through the vasculature into the Superior Vena Cava (“SVC”) of the patient. The occlusion device is activated within the SVC such that blood flow from the SVC is effectively continuously occluded for a period of about 6 hours. After the 6-hour period of time, the occlusion device within the SVC is deactivated. The occlusion device is removed from the vasculature of the patient.


