TOTAL HEART ASSISTANCE DEVICE
20200069854 ยท 2020-03-05
Inventors
Cpc classification
A61M60/113
HUMAN NECESSITIES
A61M60/468
HUMAN NECESSITIES
A61M60/892
HUMAN NECESSITIES
A61M60/289
HUMAN NECESSITIES
A61M60/191
HUMAN NECESSITIES
A61M60/894
HUMAN NECESSITIES
A61M60/274
HUMAN NECESSITIES
International classification
Abstract
The present invention relates generally to the field of cardiac, vascular system, and heart assistance devices. It provides the energy required to keep the blood flowing in the pulmonary and systemic circuits to a desired level, acting on one or more chambers. Actual problems of Total Artificial Heart pumping blood are design limitations, infection, hemorrhage, end organ failure, thromboembolism, device dysfunction, life span of diaphragms, and impossibility to restore the heart but with a transplant. The device is external and has four units replicating the natural heart and its dynamics, driving by a pneumatic transcutaneous system to provide the energy needed up to the desired working level of a healthy organ. Applications are on those types of surgical or clinical treatment of patients with Diastolic Heart Failure or used to treat Heart Failure with Reduced Ejection Fraction (Systolic Heart Failure), the device can be left connected permanently or for healing.
Claims
1) An assembly as attachments to assist a cardiovascular biological system comprising: Four inflatable flexible patches located on the external surface of the heart chambers with an external control panel.
2) The inflatable flexible patches of claim 1, which are inflated with pressurized air conveyed from patient transcutaneous piping from a pneumatic unit on two ways: one for the pulmonary circuit and another for the systemic circuit, or four units: one for each heart's chamber independent managed.
3) The assembly attachments of claim 1, wherein the piping air flows is controlled by means of valves and servomechanisms where these activate an alternating passage of compressed air from the exhaust of compressed returning it to the pneumatic unit inlet, closing a variable-alternate cycle.
4) The assembly attachments of claim 1 where automation is managed by connecting the SA (sinoatrial node), or another point in the circuit brain-heart, to the external control panel.
5) A pneumatic unit where the functioning and piping system adapts to mimic properly the dynamic of the functioning of one or more chambers of the healthy patient's heart.
6) The piping from a pneumatic unit including alternative means, like electronic hardware including the use of proportional valves in the circuit, to provide internally compressed air from a pneumatic unit powered by transcutaneous transfer of energy.
7) Application of this assembly attachments, or parts of, to other human or animal organs to provide blood pressure, dosing drugs, lubricants, organ or tissues. healing or other needs of clinical interest.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION OF THE DRAWING
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DETAILED DESCRIPTION OF THE INVENTION
[0046] These heart attachments are activated by compressed air outlet of a pneumatic source, where the potential energy applied produce expansive work against the heart walls, and the consequent kinetic energy returns working as the suction force before re-entering at the inlet of the pneumatic source completing a cycle. The air flow is different for each patch to mimic or follow the total or remaining dynamic of the natural heart with which they interact fully. The compressed air fills a pocket, pouch, as a patch to add partial, or total, force such that the atria or ventricle complete its work efficiently providing blood flow, pressure and pulsation across the vascular system to reach those points in the body that require them. In doing so, strict maximum and minimum limits must be followed not to damage the heart itself or any part of the systemic or pulmonary system or irrigated tissues or organs.
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[0048] Regime is obtained by the servomotors at a 180 steps (
[0049] The Control Panel can be replaced easily by a new one at any time in seconds if there is remaining activity in the patient heart. The Control Panel can operate under water as if in an accident or sport, in these cases the Panel must be waterproofed, and with a pouch of air instead of the air circuit connected to the atmosphere in the pneumatic unit.
[0050] In and out of the assistance to a beaten natural heart: The in-operation is done by looking at the pressure gages of the patient and the output from the pneumatic unit in the control external box, the reading at the patient most probably is lower than normal, then a single valve must be activated in the control box to start from zero to add pressure to the wall of the failing chamber, atria or ventricle, slowly. Continuing sequentially with the other three (if needed) chambers. The opposite will be done if the intention is an out-operation, receding to zero the reading in the control box. Once completed the failing heart will work as a failing organ, until reconnecting the control box. DANGER: If pressure is applied and the patient pressure didn't rise, is negative or is zero, means that such applied pressure work against the heart and must be stopped immediately thou slowly. When all chambers are set to work conveniently they are put fix to provide the delivered assistance. Only a trained professional is responsible to made changes thereof, by operating the governing valves, for a new assessment and set up the operation properly or disconnect the control box, if applicable.
[0051] Security and alarms for emergencies has been taken in consideration, in particular stop by run out of range of pre-stablished rates and loss of air into the thorax cavity.
[0052] While the invention has been described in conjunction with specific embodiments thereof, it is evident that many alterations, modifications, and variations will be apparent to those skilled in the art in light of the foregoing description. Accordingly, it is intended to embrace all such alterations, modifications and variations in the appended Claims, which doesn't include the patches for two reasons: [0053] (i) This device though for final use in humans, begin as a tool to medical researchers to test parches and setting them up in place, which may deserve an additional patent. [0054] (ii) This device works independent of a complete Total Heart Assistance Device but could be used as an implantable/external, any suggestion of a patch system cannot be used in the US or other countries that are not permitted under local regulations. [0055] (iii) If the law permit can be used for studies in open chest animal under anesthesia and closing chest without sacrificing the animal.