The National Institutes of Health reports that each year 2,000,000 Americans develop deep venous thrombosis (DVT). Of these, about 600,000 are hospitalized for pulmonary embolism (PE) and 60,000 are fatal. Degenerative muscle fiber condition and diminishing muscle contraction performance are factors associated with aging, diabetes, obesity, inactivity, and life style factors including unhealthy nutrition. Left untreated, these factors could result in peripheral blood pooling and the development of PE or DVT. Peripheral blood pooling and associated diminished blood circulation has other consequences such as inadequate delivery of nutrition and oxygen to parts of the body including the brain, and that could result in mild cognitive impairment with progression to Alzheimer's disease. A method to counter these negative factors to human health irrespective of individual mobility status and without side effects is not available.
Medication to prevent blood clot include blood thinners (anticoagulants) such as heparin and warfarin (Coumadin); aspirin as oral and liquid antiplatelet agents; low-molecular-weight heparin Dalteparin (FRAGMIN®), Enoxaparin (LOVENOX®) and Tinzaparin (INNOHEP®) heparin sodium unfractionated heparin; Factor Xa inhibitors Fondaparinux (Arixtra®) Rivaroxaban (XARELTO®); and Vitamin K antagonists. While the thinning action prevents coagulation and thereby prevents blood clots, there is great potential that increased bleeding following surgery, excessive bleeding from injuries, and internal bleeding could occur.
Devices to prevent blood clots include compression stockings to reduce swelling by compressing the leg and keeping blood flowing; intermittent pneumatic compression device to inflate and deflate with air pump to squeeze the leg; and venous foot pump to inflate and deflate with air pump to increase blood flow in the leg. However, mechanical compression therapy exemplified by U.S. Pat. No. 6,123,681 does not improve the decline in the physiologic system such as fading motor unit activation and muscle fiber excitability. Effectiveness may depend on the level and state of individual adipose tissue even when transportability of the device is guaranteed. None of these mechanical devices are as effective as the pharmaceutical drugs in [0002], and the devices may be noisy and patients are prevented from ambulation during use. These contradictions draw consistent complaints from patients leading to lack of compliance and inability to overcome the intended problem in [0001]. Electrical stimulation devices have found use in prevention of DVT. The device disclosed in U.S. Pat. No. 6,226,552 “Neuromuscular electrical stimulation (NES) in prevention of deep vein thrombosis,” is intended to conduct electrical current to a patient's limb, contracting the superficial muscles. In U.S. Pat. Nos. 6,181,965; 6,175,764; and 6,051,017, implantable micro-stimulators are disclosed. While NES systems use less electrical current intensity and are thus more tolerable than painful functional electrical stimulation (FES) models, the NES method is invasive and requires surgery for implanting NES thin-film electrodes. Prolonged use of implanted thin film electrodes could suffer fatigue problems from mechanical stress as surrounding muscles strengthen, and thermal stress could occur when electric charges are not fully conducted away before the next inflow of current thereby creating local heating that may continue to build up along the electrode thin films. When the combined mechanical and thermal stress overcome the thin-film strength of materials, the thin films will breakdown and enter the individual's blood stream.
Physical exercise by the actions of contracting muscles during therapy has been proven to prevent blood clots. However, bed-ridden patients recovering from major surgery and others unable to exercise such as older adults do not take advantage of exercise to prevent blood clots. Therapy such as raising the leg while immobilized have been used, but this will not improve decline in muscle fiber excitability and motor activation due to age and immobility. People unable to exercise due to age or immobilization will be susceptible to blood clots and diminished health [0001].
A whole body vibration (WBV) device was developed to provide exercise to the muscular and skeletal system. Current WBV device philosophy is to cause the displacement of the platform for human support to execute oscillatory vertical movements, or center pivoted platform triangular movements, or triplanar sonic movements. Some have been implemented for use while standing, seated or in bed, and the user has the option to select preferred platform motion frequency and displacement amplitude before use. U.S. Pat. No. 5,070,555 discloses a bed with footboard oscillation, with the footboard adaptable to be attached to either or both sides of a bed; U.S. Pat. No. 7,530,960 discloses a vibration platform having an upper surface and a bottom surface where a reversible motor is mounted and connected to a mounted drive shaft on the bottom surface. Platform motion occurs from unbalanced weight of a rotatable weight eccentrically mounted to the drive shaft in relation to another fixed weight also mounted to the drive shaft. In U.S. Patent No. 2004/0210173 by Swidle, a synchronous impact table with a support system has a control system, a power system coupled to the control system; a lift system coupled to the power system and the support system; and a patient support system coupled to the lift system. However, major drawbacks with applying current WBV devices to overcome problems in [0001] are multi-faceted. There could be bone fracture by increasing the displacement level in order to obtain better outcome, and current WBV devices presents options to users to vary this operating parameter. Muscle fibers have different frequencies. Selected operating frequency may favor the muscle fiber type with twitch frequency close to the selection against other muscle fiber types which is unlike scenario during exercise and may cause tingling sensation. Selection of key therapy parameters at different locations renders standardization impossible.
The problem addressed by the embodiments of the present invention is to provide solution to the problems in [0001] without contraindications in existing solution methods shown in [0002], [0003], [0004] and [0005]. The focus is to provide the physiologic system the ability to overcome problems in [0001] safely. Individuals suffering from decline of muscle fiber excitation and motor unit activation due to age, prolonged immobilization following orthopedic and vascular surgery, disease and obesity face the problem of blood pooling that could progress to life threatening deep venous thrombosis, lack of adequate blood circulation, insufficient nutrient and oxygen to vital parts of the body including the brain. Given that no previously known device and method is effective without contraindications, or applicable irrespective of individual mobility status and ability to engage in physical therapy, there is a need for effective therapy device and method in preventing decline in muscle fiber excitation and motor unit activation, to deliver improved muscle contraction, blood flow and bone mineral density.
The inventive muscle fiber excitation system (MFES) provides a device to externally energize muscle fibers at muscle fiber twitch frequencies to improve motor unit activation and muscle contraction, to improve blood flow thereby prevent blood pooling/clot and deep venous thrombosis, and to improve bone mineral density. MFES externally provides muscle fibers optimal excitation stimuli encompassing muscle fiber twitch frequencies. The stimuli set off a sequence of actions of improved motor unit activation leading to improved muscle contraction sufficient to improve blood flow thereby prevent blood pooling and blood clots without side effect therefore differs remarkably from medication. Wearable MFES device is usable and concealable under clothes while mobile and in immobility state, thereby differs from physical exercise [0004] and patented mechanical devices [0002], [0003] and [0005].
The inventive MFES device and performance include multiple micro displacements 1 mm (minimum) to 4 mm (maximum) of a telescoping platform in vertical (Z), medial-lateral (X), and anterior-posterior (Y) directions per cyclic revolution using 4 donut-like cams, with a cam defined as a rotating or sliding piece in a mechanical linkage used to transform rotary motion into linear motion or vice versa, characterized by surround peaks and troughs with different ascend gradients to the tops and different descend gradients troughs. During assembly, each cam's surround peak and trough of a dimension is aligned out of phase with peak and trough of similar dimension with other cams' peaks and troughs. The outcome result during use is asynchronous contacts of all four cams surround profile on a device telescoping platform thereby delivering non-deterministic quantum displacement stress on the platform that is delivered to the human contact surface. Contrary to user selected displacement height in WBV devices that could predispose brittle bones to potential fractures, MFES fixed 1 mm to 4 mm displacements provides stress on the bone equivalent to walking. Contrary to user selected single operating frequency in WBV devices which is sub-optimal because intact muscle system is composed of muscle fibers with different twitch frequencies, MFES delivers non-deterministic quantum displacement stress in [0008] within 2 Hz and 130 Hz frequency band, thus providing muscle fibers the twitch frequencies for equal opportunity optimal excitation. User option to select displacement level, or device operating frequency or both with WBV devices creates safety concerns for brittle bones and makes study outcomes at different study stations incomparable. Without the options of selecting the operational displacement levels and frequencies MFES system devices deliver more unit activation, muscle contraction, blood flow improvement and stress on the bone for improved bone mineral density. The forgoing short falls of WBV systems, the associated pain and potential electrode failure in implantable neuromuscular stimulation, the side effects of medication and the inefficiency and patient complaints of compression devices leaves physical exercise as the current viable method to deal with human health improvement including blood pooling prevention [0001], but this will be possible if only the individual is able to and willing to exercise. What is needed is a device that does not provide options to vary the displacement and operating frequency parameters, but operates at safe displacement levels and efficiently energizes all muscle fiber types, each at corresponding twitch frequency to activate motor unites for muscle recruitment and contraction. The current MFES invention differentiates the device from alternatives to fill the need for a safe and effective therapy device and method for preventing decline in muscle fiber excitation, motor unit activation and muscle contraction to safely deliver improved muscular skeletal system and blood flow as summarized in MFES.
Various embodiments of the invention are specific for attaining system performance effectively and the desired results. Thus, the invention provides CAMs means by which displacement levels of the platform are limited to 1 mm to 4 mm by special design of each ascend to peak and descend to trough around each CAM extremities illustrated in
MFES CAMs performance provide pseudo random low displacement levels with brief quantum contacts with the platform causes the platform to telescope, generating low-level displacement (1 mm to 4 mm) platform stress signals at frequency encompassing 2 Hz to 130 Hz transferable to human point of contact. Continuous cyclic CAMs' operation and platform human contacts over time causes continuous low-level displacement signal generation at muscle twitch frequency 2 Hz to 130 Hz to spread from point of platform human contact to distal anatomic locations.
MFES invention externally delivers multiple displacement nodes 1 mm to 4 mm maximum per cycle within pre-determined and fixed frequency bandwidth such as 2 Hz to 250 Hz (or 20 Hz to 250 Hz when ripples are included) implemented in the standing model and 2 Hz to 130 Hz (or 2 Hz to 250 Hz when ripples are included) in the wearable model as excitation stimuli to improve muscular and skeletal system declines and to prevent blood clots. The ripple effect of the frequency bandwidth is similar to the ripples from a stone thrown in water. MFES device comprises an enclosure with 2 bar-like pillar blocks from the base. Each pillar block has 2 strategically implemented bearings and 2 channel openings from the top. MFES device also comprises of 2 shafts each affixed with pulley arrangements and matching timing belts at one end, and 2 CAMs (rotating donut-like shaped mechanical construction towards the other end) each with unique surround peaks of varying heights and ascend gradients, and troughs of varying depths with varying descend gradients. MFES also comprises of a platform with combination of slippery stiffener and foam material on one side, compliant material on the other side, and a plunger at each of the four corners. A top with opening to transmit therapeutic stimuli and counter sink holes and screw arrangements is used as cover.
To assemble, the two shafts are attached to the four bearings in the bar-like pillar blocks and tied with timing belt over pulleys attached the shafts with adequate tension. After electrical connection between the input electric jack and DC motor terminals, the DC motor is tied to one of the shafts with another timing belt over a second pulley set. The platform's four plungers are inserted into the four channels on the bar-like pillar blocks making sure that the stiffener side faces the CAMs. The device cover is engaged with screws. Two models of MFES device, the wearable model and the standing model are identical in innovation philosophy. They differ in size, wearable model is 6 cm by 6 cm by 2.5 cm and weighs 118 grams but can range from 100 g to 130 g depending on the material used to construct. Preferably it should weigh 118 g or less. In one embodiment, the standing model is 40.64 cm by 40.64 cm by 13.97 cm, and weighs 46 pounds.
In the large form factor standing model, beneath the top enclosure are fast-acting recovery composite material combination with stiffener materials strategically positioned for the revolving CAMs to make contact during cyclic rotation. Standing surface is prepped with non-skid material. This constitute the telescoping platform and it covers all the top surface. In the wearable model, the top enclosure sandwiches a platform comprising of a side with fast-acting recovery composite material combination with stiffener material strategically positioned for the revolving CAMs to make contact during cyclic rotation, and a compliant opposite side for human contact which flushes with the enclosure. The contact side is made from materials with properties to prevent local skin shear. For example, such materials may be foam materials with elastomers and a leather cover. The body contact stress is less than 0.002 g. A belt and Velcro arrangements are used to wear one or more wearable units as desired.
The nodal displacement are pre-determined and fixed by design and the frequency bandwidth is fixed to encompass muscle fiber twitch frequencies. By delivering low-intensity stress as stimuli at the desired muscle fiber excitation twitch frequencies to a user continuously over a period of time, muscle fibers are energized to activate more motor units to recruit more muscle contraction, thereby improving muscle contraction, bone mineral density, and blood flow. Fixing nodal displacement to safe level and frequency that encompass muscle fiber frequencies is intended to deliver gradual recovery and to be safe to fragile bone and cartilage. The following examples will further the understanding of the exemplary nature of MFES in any of its models.
Exemplary Nature of the Embodiment. Because in the art of quantum mechanics stress transfer is recognized, one may recognize from the embodiment substantially equivalent structures or substantially equivalent acts may be used to achieve the same results in exactly the same way, or to achieve the same results in a not dissimilar way, the embodiment should not be interpreted as limiting the invention to one embodiment.
Likewise, individual aspects of the invention (such as media-lateral, anterior-posterior and vertical platform excursions) are provided as examples, and, accordingly, one of ordinary skill in the art may recognize from exemplary performance that an equivalent performance may be used to either achieve the same results in substantially the same way, or to achieve the same results in a not dissimilar way.
Accordingly, it is recognized that as technology develops, a number of additional alternatives to achieve an aspect of the invention may arise. Such advances are hereby incorporated within their respective aspects of the invention, and should be recognized as being functionally equivalent or structurally equivalent to the aspect shown or described.
Second, the only essential aspects of the invention are identified by the claims. Thus, aspects of the invention, including elements, acts, functions, and relationships (shown or described) should not be interpreted as being essential unless they are explicitly described and identified as essential.
Third, a function or an act should be interpreted as incorporating all modes of doing that function or act, unless otherwise explicitly stated.
Fourth, unless explicitly stated otherwise, conjunctive words such as “or”, “and”, “including”, or “comprising” should be interpreted in the inclusive, not the exclusive, sense explicitly described and identified as essential.
Fifth, muscle fiber function or an act or characteristics in the forgoing should be interpreted as common to all mammals' humans and animals alike or act, unless otherwise explicitly stated. Unless explicitly stated otherwise, conjunctive words such as “or”, “and”, “including”, or “comprising” should be interpreted in the inclusive, not the exclusive, sense are covered my MFES technology.
This invention in any of the embodiment mode delivers displacement nodes and excitation stimuli to a user in the same specific pattern always. Accordingly, the embodiment application method is specific and independent of the mode implemented. The stimuli frequency span is fixed to specifically energize all muscle fibers, and there is no option to vary the frequency span.
In any of the invention embodiment mode each muscle fiber type is energized at corresponding twitch (resonance) frequency. Muscle fiber excitation at twitch frequency result in increased motor unit activation. Accordingly, muscle contraction is increased.
In the invention embodiment increased muscle contraction apply pressure on blood vessels and momentarily vary blood volume flow, velocity and circulation. Accordingly, increased muscle contraction improves blood circulation.
In the invention embodiment the stress from platform displacement and the stress from muscle contraction apply more stress on the bone matrix. Accordingly, increased stress on bone matrix enable influx of bone nutrients for improved bone mineral density and strength.
Wearable MFES final assembly
The stress on the platform from the pseudo non-deterministic quantum 4-CAM contact on the platform CAM-contact side is transmitted to the CAM body contact side. The CAM surround geometry iteratively optimized to deliver a frequency band that encompass muscle fiber twitch frequencies 2 Hz to 130 Hz per cyclic revolution in the wearable model and 2 Hz to 250 Hz in the standing model is delivered to the body for use in therapy. A continuously adjustable belt provides wearable model a means for the device to be engaged with the comfortable top of the platform (17) in contact with the human body, when an individual just stands on top of the standing model. The displacement nodes and each frequency band parameters are fixed upon assembly and cannot be varied after. Compressive force triggers system short down because the MFES was not designed for load bearing. The embodiments of the present MFES invention and methods accomplishes blood clot prevention by preventing blood pooling; muscular system decline by improving motor unit activation and muscle contraction; skeletal system decline by improving bone mineral density, and muscular system decline by improving muscle fiber excitability for more motor unit activation and muscle contraction recruitment.
The bone mineral density improvement demonstrates the outcomes targeted in the design: to apply sufficient vertical stress to the skeletal system to support influx of bone minerals into bone matrix for bone strength remodeling and strengthening. To prevent telescoping shaft binding along the vertical telescoping channels, the diameter of the channel was set slightly larger than the telescoping shaft diameter, and therefore the preponderance of force applied to the telescoping platform was used for vertical displacement magnitude.
In contrast, the wearable MFES is designed to attain the concept of equality in orthogonal stimuli stress delivery intended for blood flow improvement without adversely affecting the skin surface. CAM peaks and troughs gradients were designed to reduce vertical displacement, and the peaks were widened to achieve micro time delay. Further, the telescoping platform vertical displacement range was restricted to control impact on skin surface, and the telescoping platform shafts (plungers) were provided succinct channel diameter to enable equal execution of 3-D telescoping actions in response to CAM contacts below. This is crucial in the design because equal magnitude orthogonal displacement, i.e. x, y, z, displacements, is suitable for MFES stimuli to penetrate deep, for example to the superficial lower back and between vertebrae muscles. It achieves the intent of assisting a physiological system perform the process of blood flow improvement by energizing the muscle fibers. The MFES test was conducted in the frequency domain, if the x-, y-, z-components were different in magnitude, the magnitudes will be different in magnitude in the frequency domain.
The embodiments shown and described in the specification are only specific embodiments of inventors who are skilled in the art and are not limiting in any way. Therefore, various changes, modifications, or alterations to those embodiments may be made without departing from the spirit of the invention in the scope of the following claims. The references cited are expressly incorporated by reference herein in their entirety.
This application is a continuation-in-part of U.S. Ser. No. 14/277,028 filed May 13, 2014, which is expressly incorporated by reference herein in its entirety.
This invention was made possible in part with government support under 1R43HL115916-01A1 grant awarded by National Institutes of Health.
Number | Date | Country | |
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Parent | 14277028 | May 2014 | US |
Child | 15251753 | US |