Classifications

• • G—PHYSICS
  • G06—COMPUTING; CALCULATING OR COUNTING
  • G06F—ELECTRIC DIGITAL DATA PROCESSING
  • G06F3/00—Input arrangements for transferring data to be processed into a form capable of being handled by the computer; Output arrangements for transferring data from processing unit to output unit, e.g. interface arrangements
  • G06F3/01—Input arrangements or combined input and output arrangements for interaction between user and computer
  • G06F3/016—Input arrangements with force or tactile feedback as computer generated output to the user
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/0002—Remote monitoring of patients using telemetry, e.g. transmission of vital signals via a communication network
  • A61B5/0015—Remote monitoring of patients using telemetry, e.g. transmission of vital signals via a communication network characterised by features of the telemetry system
  • A61B5/0022—Monitoring a patient using a global network, e.g. telephone networks, internet
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/103—Detecting, measuring or recording devices for testing the shape, pattern, colour, size or movement of the body or parts thereof, for diagnostic purposes
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
  • A61B5/6801—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be attached to or worn on the body surface
  • A61B5/6802—Sensor mounted on worn items
  • A61B5/6804—Garments; Clothes
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
  • A61B5/6801—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be attached to or worn on the body surface
  • A61B5/6802—Sensor mounted on worn items
  • A61B5/6804—Garments; Clothes
  • A61B5/6805—Vests
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/74—Details of notification to user or communication with user or patient ; user input means
  • A61B5/7475—User input or interface means, e.g. keyboard, pointing device, joystick
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B8/00—Diagnosis using ultrasonic, sonic or infrasonic waves
  • A61B8/08—Detecting organic movements or changes, e.g. tumours, cysts, swellings
• • G—PHYSICS
  • G06—COMPUTING; CALCULATING OR COUNTING
  • G06F—ELECTRIC DIGITAL DATA PROCESSING
  • G06F3/00—Input arrangements for transferring data to be processed into a form capable of being handled by the computer; Output arrangements for transferring data from processing unit to output unit, e.g. interface arrangements
  • G06F3/01—Input arrangements or combined input and output arrangements for interaction between user and computer
  • G06F3/011—Arrangements for interaction with the human body, e.g. for user immersion in virtual reality
• • G—PHYSICS
  • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
  • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
  • G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
  • G16H40/60—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices
  • G16H40/67—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for remote operation
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B2562/00—Details of sensors; Constructional details of sensor housings or probes; Accessories for sensors
  • A61B2562/02—Details of sensors specially adapted for in-vivo measurements
  • A61B2562/0247—Pressure sensors
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B2562/00—Details of sensors; Constructional details of sensor housings or probes; Accessories for sensors
  • A61B2562/04—Arrangements of multiple sensors of the same type
  • A61B2562/046—Arrangements of multiple sensors of the same type in a matrix array
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B2562/00—Details of sensors; Constructional details of sensor housings or probes; Accessories for sensors
  • A61B2562/16—Details of sensor housings or probes; Details of structural supports for sensors
  • A61B2562/168—Fluid filled sensor housings
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
  • A61B5/6801—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be attached to or worn on the body surface
  • A61B5/6802—Sensor mounted on worn items
  • A61B5/6804—Garments; Clothes
  • A61B5/6806—Gloves
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
  • A61B5/6801—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be attached to or worn on the body surface
  • A61B5/6813—Specially adapted to be attached to a specific body part
  • A61B5/6825—Hand
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
  • A61B5/6801—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be attached to or worn on the body surface
  • A61B5/683—Means for maintaining contact with the body
  • A61B5/6831—Straps, bands or harnesses

Definitions

• This invention relates to medical devices that transmit tactile information from a remote location to an individual and, in particular, to devices that assist in the examination of a patient at a location remote from the location of a medical examiner.
• Medical practice is also a very unique type of personal service.
• a sick patient interacts with a unique skilled professional with the expectation of improving his or her health condition or alleviating suffering.
• the underlying physician-patient encounter is in actuality a complex data gathering interaction which is processed by the physician, who then develops an optimal diagnosis and treatment plan.
• the input data from the physician-patient encounter comes from a variety of sources which include the physical examination of the patient, laboratory tests, and radiological imaging studies. The most important source of input information is often the actual physical examination of the patient.
• the physical examination consists of the transfer of personal historical information from the patient to the physician, a review of the patient's current medications, and a direct visual and manual examination of the patient's body by the physician.
• the manual examination of the patient's body includes applying gentle hand pressure along various parts of the abdomen, chest, and extremities in order to determine the body's response to direct manipulation.
• Inflammatory processes such as infections, abscesses, thromboses (clots), hollow or solid organ perforations, or fractures will yield a pain response with an increase in resistance in order to "guard” or protect against the noxious applied stimulus.
• Tumors or organ enlargement may be detected by resistance changes detected below an otherwise normal skin surface, analogous to perceiving a stone trapped in one's shoe.
• Fluid within the abdomen (ascites) can also be detected by applying hand pressure at one end of the abdomen and detecting the resultant fluid wave at an opposite location within the same cavity.
• the physician functions as a computer by collecting all of the available input data from the various sources, processing that information with respect to the physician's personal knowledge or reference base, and establishing a list of likely diagnostic possibilities based on the input information. The physician then recommends a plan of treatment which is expected to improve the patient's health condition.
• a portion of the data required to make an accurate medical diagnosis can be exchanged between the patient, laboratory, radiology, and physician using a variety of communications methods without the need for direct face to face contact between the communicating entities.
• the current communications revolution has allowed for the exchange of historical information, laboratory data, telemetry, and radiological studies via telephone, pager, fax, e-mail, and video. These advances have benefited all types of businesses, and medicine is no exception. There is, however, one unique piece of the data gathering process specific to medicine—the direct manual examination of the patient's body by the physician—which currently is not amenable to remote data acquisition.
• the present invention provides a system satisfying the needs identified above.
• the device includes a hand control unit, a remote examination module, and a computer system connecting the hand control unit to the remote examination module.
• the present invention relates generally to a system enabling a user to send tactile stimuli such as a pressure input to a remote body such that the stimuli is experienced by the remote body to produce a response, detect the tactile response of the remote body to generate feedback, and transmit that tactile feedback to the user.
• a preferred embodiment of the invention is directed to remote patient examinations, and includes a physician's hand control unit (HCU) that is used by a physician to generate tactile stimuli, and is coupled by a computer system to a patient examination module (PEM) that applies the tactile stimuli to a patient and detects and transmits feedback corresponding to the detected response back to the HCU.
• HCU physician's hand control unit
• PEM patient examination module
• the HCU has at least one and preferably a plurality of sensory modulation subunits, and is adapted to receive the physician's hand such that the physician has access to the sensory modulation subunits.
• the PEM is adapted to contact or receive a portion of a patient's anatomy, preferably by wrapping around a portion of the patient, and has at least one and preferably a plurality of sensory modulation subunits that are thereby placed adjacent to the patient.
• the sensory modulation subunits detect forces or pressures applied to the subunits to produce corresponding output signals, and exert forces and/or displacements in response to input signals. Preferably, detection and exertion of forces occur approximately simultaneously.
• the sensory modulation subunits in the HCU are coupled to the sensory modulation subunits on the PEM through the computer system.
• the computer system includes a first computer attached to the HCU and a second computer attached to the PEM, wherein the first and second computers have compatible communication systems to enable communications therebetween over a network.
• the sensory modulation subunits on the HCU are coupled to the sensory modulation subunits on the PEM through software that feeds back the pressures detected, which permits the physician to simulate actual physical contact with a remote patient.
• the PEM utilizes sensory modulation subunits with mechanical piston-type variable pressure-producing devices, such as linear actuators, to exert pressure in response to input signals.
• the PEM utilizes pneumatic or hydraulic systems and expandable cells to produce the exerted pressure in response to input signals.
• the HCU includes a tracking ball and a button accessible to the user's hand which allows the physician to use the HCU in a manner similar to a computer mouse to interact with the computer — for example, to select specific portions of the PEM with which to interface.
• FIGURE 1 illustrates a preferred embodiment of the system of the present invention in use, showing a physician examining a patient who is located remotely from the physician.
• FIGURE 2 is a plan view of a hand control unit in accordance with the present invention.
• FIGURE 3 is a schematic cross-sectional view of the hand control unit of FIGURE 2.
• FIGURE 4 is a cross-sectional sketch of a sensory modulation subunit for the hand control unit shown in FIGURE 3, in accordance with the present invention.
• FIGURE 5 is a front view of a preferred embodiment of a patient examination module for examination of a patient's torso, in accordance with the present invention.
• FIGURE 6 is a cross-sectional view of a cell from the patient examination module shown in FIGURE 5.
• FIGURE 7 is a front view of a second preferred embodiment of a patient examination module for examination of a patient's torso, in accordance with the present invention.
• FIGURE 8 is a cross-sectional view of a cell from the patient examination module shown in FIGURE 7.
• FIGURE 9 is a general process flow diagram of a preferred embodiment of the present invention.
• FIGURES 10 A- IOC present a flow diagram detailing the functions of the software controlling the preferred embodiment shown in FIGURE 1. Detailed Description of the Preferred Embodiment
• the device disclosed herein enables a physician to perform a direct physical examination of a patient's body without direct physical contact or proximity between the patient and the physician.
• This allows physical data of the type normally acquired from direct manual contact between the patient and the physician to be gathered and transmitted via conventional global communications systems.
• "telemedicine" or the exchange of medical information between a patient and physician for the purpose of rendering a diagnosis and treatment plan can only proceed to a point, and if the physical exam findings become critical in the decision making process, the patient is advised to actually see their personal physician or present to an emergency room where a physician can perform a physical examination.
• Sensory modulation subunit means any device capable of (1) detecting a force applied to the device and generating an output signal related to the detected force; and (2) receiving an input signal and generating a force and/or displacement related to the received input signal.
• Hand control unit means any device adapted to contact or receive a portion of a user's body — such as a user's hand — and having sensory modulation subunits that can be accessed by the received user's hand.
• Patient examination module, or PEM means any device adapted to receive a portion of a person's (or other biological organism's) anatomy, and having sensory modulation subunits that are adjacent to the received portion of anatomy. PEMs may be used in accordance with the present invention for patient examination, but the term PEM is to be understood to also encompass devices adapted for tactile sensing of anatomy for other purposes, or for tactile sensing of other objects or substances.
• the present invention for the remote acquisition and transmission of physically derived medical data, includes three general parts: the hand control unit 100 (HCU), the patient examination module 200 (PEM), and computer software to control the acquisition, calibration, transfer, and translation of the physical data between the physician (through the HCU) and the patient (through the PEM).
• the present invention allows a physician to apply hand pressures to the HCU 100 that are transmitted to a remotely situated patient and applied to selected portions of the patient's body through the PEM 200. The pressure response from the patient's body is transmitted back to the physician, thereby simulating direct contact between the physician and patient.
• Hand Control Unit HCU
• the HCU 100 shown in FIGURE 2, has a molded plastic shell 101 formed in the shape of an actual hand.
• the advantages of this type of construction are that it is lightweight, easy to manufacture, durable, and impact resistant. Other materials such as wood, paper, aluminum, stone, PlexiglasTM, or as of yet to be developed materials could also be used for device construction.
• the HCU 100 is shaped to accommodate a portion or preferably the entire inner surface of the human hand, having a palmar surface 102 including a proximal palm portion 108 and a distal palm portion 107, fingertips 106, and a thumb portion 105.
• An objective of any design configuration is to provide a comfortable contact surface between sensory and motor portions of the user's hand and the HCU 100.
• the HCU 100 has a slight central rise in the palmar surface 102.
• the periphery of the palmar surface 102 has a slight depression with respect to a border 104 of the HCU 100 to accommodate the user's hand resting comfortably on the palmar surface 102.
• the slight palmar rise with respect to the position of the fingertips 106 and proximal palm portion 108 (such that the level of the user's knuckles will be higher than the other parts of the fingers and hand) forms a broad based, pyramidal configuration. This design allows for maximum flexibility with respect to fingertips, distal palm, and proximal palm pressure application and reception, device control, and functionality.
• the HCU 100 allows for complete contact between all parts of the palmar surface of the user's palm and fingers with the palmar surface 102 of the HCU 100.
• the shell 101 of the HCU 100 is formed in two laterally disposed segments 101a, 101b, with a transverse break 110 located generally at the location of the user's mid-palmar crease.
• the two segments 101a, 101b are slidably connected to permit relative longitudinal motion to allow for adjustments with respect to hand length in order to accommodate various hand sizes.
• the HCU 100 could include a "glove" component (not shown) where the whole hand is inserted into a hand control unit. This would allow for contact with the top (dorsal) hand surface permitting functions related to examination motions and sensory inputs derived from the top surface of the operator's hand.
• Depressions or cavities 112, 114, 116 are provided in the fingertips 106, distal palm 107, and proximal palm portions 108, respectively.
• a pressure relay and reception sensory modulation subunit 140 is housed, as seen most clearly in FIGURE 3.
• the top of the sensory modulation subunit 140 consists of a slab 142 of a pliable material such as silicon rubber or a soft plastic matrix forming a simulated skin surface.
• suitable materials may include other natural or artificial biomaterials (artificial, simulated, cultured, or engineered skin cells or substitutes) for this "skin" contact surface.
• the size of each slab 142 will vary with the size of each depression 112, 114, 116 in the HCU 100.
• each module could be multiply subdivided and each depression could include a collection of smaller functional subunits based on the general subunit description below.
• the sensory modulation subunit 140 includes a one-way single channel pressure transducer 144 embedded within the slab 142 of simulated skin.
• the working surface or pressure receiving face 145 of the pressure transducer 144 is oriented upward, i.e., in the direction facing the palmar surface of the user's hand.
• the pressure transducer 144 is oriented such that pressure applied by the user is applied to the working surface 145 of the pressure transducer 144, while pressure or force applied from behind the transducer 144 is not sensed directly.
• a single pressure transducer 144 is located within each fingertip 106, while each palmar portion 107, 108, is subdivided into two pressure zones. Wires or other appropriate connecting mechanism (not shown) provide signal access to and from the pressure transducer 144.
• the simulated skin slab 142 with the embedded single channel pressure transducer 144 is mounted on a thin support platform 146, preferably made of metal or plastic. Attached to the undersurface of the support platform 146 is a linear actuator, a variable force-producing device such as a single channel piston-type variable resistor, or other variable pressure-producing device 148.
• the linear actuator, or variable pressure- producing device 148 may be embodied in a number of ways that are known in the art, including devices that produce a variable force by electrical, mechanical, pneumatic, or hydraulic processes. A representative sampling of such devices are described, for example, in U.S. Patent No.
• the piston resistor 148 provides counter pressure or a resistance force against the undersurface of the simulated skin slab 142 dependent upon the response signal derived from the patient examination module 200 (described below).
• the slab 142, transducer 144, support platform 146, and piston resistor 148 are disposed within the depressions 112, 114, 116, in the HCU 100.
• Holes 150 are provided within each depression 112, 114, 116, to accommodate insertion of the free end of the piston resistor 148.
• the hole 150 depth is selected such that the support platform 146 is slightly elevated from the depression lower surface and therefore the only resistance felt by the user is that of the simulated skin slab 142 itself.
• U.S. Patent No. 6,033,370 issued to Reinbold et al discloses a capacitative pressure force transducer having a polyurethane foam dielectric sandwiched between two conductor layers.
• a similar device is disclosed by Duncan et al. in U.S. Patent No. 4,852,443, wherein compressible projections on the capacitor electrodes are disposed on either side of a dielectric sheet.
• a pressure transducer based on variable resistance components is disclosed in U.S. Patent No. 5,060,527 by Burgess.
• the corresponding thumb portion 105 of the HCU 100 houses a button 152 for controlling and selecting functions and options related to the computer software (e.g., a mouse click control or other input device).
• the under surface of the HCU 100 supports a tracking ball 154 to allow for computer selection functions, and two-dimensional coordinate location of the HCU 100 in space as related to the patient through the PEM 200.
• the button 152 and tracking ball 154 provide the basic functionality of a computer mouse and can be used to selectively interact with the computer in a familiar and well-known manner. It will also be apparent that other types of selecting mechanisms could be utilized, including touch-sensitive pads and optical systems.
• the HCU 100 is also linked to a signal processor 130 and an analog-to-digital/digital-to-analog signal converter 132.
• the HCU 100 acts as the interface or contact point between the physician and the remote patient.
• the HCU 100 receives the mechanically applied pressure signal generated by the physician's hand and converts it to an electrical signal via the pressure transducer 144, while simultaneously converting the incoming electrical signal derived from the pressure response at the patient examination module 200 into a resistance signal that is applied to the piston resistor 148 mounted against the support platform.
• This ability of the sensory modulation subunit 140 to both "sense" the input pressure applied by the user and simultaneously provide a direct resistance feedback response to the user simulates the actual events that occur when one presses their hand against another object.
• the thumb portion 105 could alternatively house a sensory modulation subunit 140.
• the ability to integrate thumb motions into the examination process as well as having sensory input back to this part of the hand would allow for expanded functional capacity and sensitivity of the HCU 100.
• the most complex embodiment of an HCU would include full contact with every portion of the operator's hand, and a large number of sensory modulation subunits 140 applied throughout the HCU.
• the number of subunits 140 is limited only by the ability to miniaturize these bidirectional pressure transducing devices.
• a large number of sensory modulation subunits would allow the user to produce and receive mechanical and sensory inputs from every portion of the operator's hand.
• PEM 200 consists of a pad or pad-like structure 202 made of soft, semi-compliant material such as nylon, rubber, silicon, or a soft plastic substrate.
• the entire pad 202 is solid, preferably with viscoelastic properties similar to the simulated skin slab 142 of the HCU 100.
• the pad 202 is subdivided into a basic structural unit called a cell or cell zone 204.
• the overall size of the pad 202, as well as the number of cells 204 within the pad 202, will vary depending upon the particular application.
• Each cell zone 204 corresponds to an area within the pad 202, preferably similar in size to the corresponding sensory modulation subunit 140 of the HCU 100.
• a single channel pressure transducer 244 is mounted within each cell 204, oriented with the working/receiving surface 245 facing in the direction of the patient.
• the preferred pad 202 is a continuous gel-type structure 242 with a multitude of embedded pressure transducers 244.
• the back surface 206 of the pad 202 includes a flexible, semi-rigid sheeting.
• the currently preferred material for the back surface 206 is a plastic or polymer substance that will maintain a rigid backing to the cell zones 204, yet allow for some bending to accommodate applications to a variety of body sizes. More solid materials such as metal, wood, or composite materials could also be used as long as it provided a solid backing structure and allowed for articulation around various contoured surfaces of the body.
• a linear actuator comprising a single channel piston-type variable pressure producing sensory modulation subunit 240 is attached to the undersurface of a thin support platform 246, preferably made of metal or plastic.
• the support platform 246 is preferably similar to the size of the fingertips 106 in the HCU 100.
• a piston-type variable pressure producing device 248, or similar linear actuator is embedded within the backing 206, oriented beneath the center of the support platform 246 below the pressure transducer 244.
• the examination pad 202 is applied directly over the portion of the patient's body surface to be examined and held in place, for example, by a nylon loop-and-hook type of closure 250.
• the nylon loop-and-hook closure 250 would provide adjustability and allow for application to a wide variety of body shapes and sizes.
• the pad 202 could also be fashioned into vests for chest applications; binders for abdominal applications; sleeves, gauntlets, or gloves for upper extremity applications; pant legs or boots for lower extremity applications; or small strips for small applications such as fingers or toes.
• a PEM is constructed as a stationary positioned pad
• a mobile sensing unit that the patient, other personnel, or a robotic guide moves over a surface of the patient's epidermis or within a body cavity, is also within the- scope of the invention.
• the PEM 200 is attached to a command control box 300 via an electrical umbilical 302.
• the command control box 300 includes a power supply 304, a small central processing unit (CPU) 306, a signal processor 308, digital-to-analog converter 310, and a communications system 312,
• the command control box 300 receives and transmits data to and from the PEM 200, and links the PEM 200 to the physician's HCU 100.
• the power supply 304 preferably allows for both the ability to work from alternating current (household or industrial) or direct current (battery operations). While an umbilical 302 is illustrated, other data links such as a wireless data link are also within the scope of the invention.
• the communications system 312 of the preferred embodiment includes an internal modem (not shown) which would allow a physician's computer 160 located near the HCU 100 to connect to a remote computer 260 located near the PEM 200.
• Other communication systems are also possible, including systems based on: (1) light-based/optical based communications including fiber-optic cable channels and non-fiber, light based methods of data/voice/visual signal transmission; (2) wireless communications including but not limited to radio frequency, ultrahigh frequency, microwave, or satellite systems in which voice and/or data information can be transmitted or received; and (3) any future methods of voice or data transmission utilizing any currently unused mediums such as infrared light, magnetism, other wavelengths of visible and non-visible radiation, biomaterials (including biorobots or viral vectors), or atomic/subatomic particles.
• the command control box 300 is connected to the pad 202 through a flexible umbilical 302 for considerations of reduced weight being applied directly to the patient, size limitations, and possibly safety (i.e., reduced RF or microwave radiation exposure from communications/data transmissions).
• the umbilical 302 also connects the pressure transducers 244 and variable pressure producing devices 248 within the sensory modulation subunits 240 to the power supply 304.
• each cell zone 204 could be multiply subdivided and a large number of sensory modulation subunits applied throughout the PEM 200.
• the number of functional subunits would only be limited by the ability to miniaturize these bidirectional sensory modulation subunits.
• a large number of small sensory modulation subunits would provide the ability to produce and receive mechanical and sensory inputs from every portion of the PEM 200.
• a second embodiment of the PEM 400 utilizes a pneumatic pressurizing medium or hydraulic pressurizing medium as shown in FIGURE 7 and FIGURE 8, rather than the electromechanical structure described above.
• the PEM 400 consists of a pad 402 or pad-like structure made of soft, semicompliant material such as nylon, rubber, silicon, or a soft plastic substrate.
• the pad 402 is subdivided into a plurality of cells 404.
• the overall size of the pad 402, as well as the number of cells 404 within the pad 402, will vary by device model and application.
• Each cell 404 is designed as an air- and water-tight hollow chamber 416 with one dual function inlet/outlet line 410 and one valve 414 to allow inflow and outflow of a pressurizing medium, such as air, water, hydraulic fluid, or an electrochemical gel, and a single pressure transducer 444.
• the pressure transducer 444 is a single channel transducer similar to the transducer 144 described above for the HCU 100.
• the pressure transducer 444 is mounted within the material sheet applied directly to the patient's body surface. The open cell structure would therefore be behind the pressure transducer 444.
• the receiving surface 445 of the transducer would be oriented facing in the direction of the patient.
• the pad 402 is applied directly over the portion of the patient's body surface to be examined, and is held in place, for example, by a loop-and-hook type of closure 250.
• the loop-and-hook closure 250 provides adjustability and allow for application to a wide variety of body shapes and sizes.
• the pad 402 could also be fashioned into vests, binders, sleeves, gauntlets, gloves, pant legs, boots, or small strips for small applications such as fingers or toes, as previously described.
• the outer surface of the pad 402 could also include a heavy reinforcing layer (i.e., lead, metal, or plastic) to provide added stability or counter pressure if required.
• the inlet/outlet line 410 for each cell 404 is connected to a pumping mechanism which would include a pump (not shown) and a pressurizing reservoir 418 for housing the pressurizing medium.
• An intervening valve 414 is placed along the inlet/outlet line 410 between the pressure reservoir 418 and each cell 404.
• the PEM 400 is attached to a command control box 300 via an umbilical 302 as previously described.
• this control section of the PEM 400 is disposed away from the patient for considerations of reduced weight being applied directly on the patient, size limitations if the pack is placed on a small section of the body such as a limb or finger, or possibly safety (i.e., reduced RF or microwave radiation exposure from communications/data transmissions).
• the specifications and functions of the command control box 300 are described above.
• the umbilical 302 also connects the pressure transducers 444 and the power supply 304, as well as the inlet/outlet lines 410 and valve 414 for the pressurizing medium.
• the pump and pressurizing reservoir 418 could be contained both together in the command control box 300 section, together on the PEM 400 itself, or in either area independent of one another.
• a PEM 400 utilizing air as a pressurizing medium would utilize a semi-closed circuit design.
• the pumping mechanism draws air from outside the unit into a single pressurizing reservoir 418 applied to the back of the pad 402.
• the pressurizing reservoir 418 is generally the same size as the pad 402.
• Nalves 414 are located at multiple positions within the pressurizing reservoir 418 corresponding to underlying cells 404.
• the pressurizing reservoir 418 is therefore in direct communication with each pressure cell 404 via the intervening valve 414.
• a pressure regulating circuit (not shown) is integrated into the pressurizing reservoir 418 in order to sense internal chamber pressure, and relay that information back to the command control box 300 in order to ensure appropriate chamber pressure.
• the desired pump chamber pressure achieved (corresponding to the appropriate applied pressure signal from the HCU 100), and the resulting patient response signal is transmitted back to the HCU 100 via the command control box 300, the pump vents the contents of the pressure chamber 416 back into the atmosphere via the pump.
• a PEM 400 utilizing a hydraulic pressurizing medium consists of a self contained, closed fluid system circuit.
• the function of the PEM 400 is to "transmit" the pressure applied by the user at the HCU 1 0 directly to the patient and send the resultant resistance response signal from the patient back to the physician's HCU 100.
• various segments of the body within the confines of the PEM 400 can be examined by "selecting" the appropriate overlying cells 404 to be pressurized.
• the software sends the appropriate command to open the valves 414 corresponding to the selected cells 404.
• the number of selected cells 404 corresponds to the area of the patient's body the physician wishes to "press on” to elicit the patient's response to the applied "hand" pressure.
• the physician can independently select the cells or area of the body from which the return pressure data can be sent back to the user. While in many circumstances the cells which are being pressurized will also be sending the return pressure data signals back to the physician's HCU 100, for some examination functions, it is optimal to pressurize one cell set and receive from a different one.
• a second HCU could be incorporated, configured to accommodate the hand opposite the first HCU, wherein the physician could use one hand to apply pressure to one location on the patient (through the first HCU and the PEM) and receive a pressure response to the other hand from another location on the patient (through the second HCU).
• the computer software controls the commands for the various functions of the physician HCU 100, PEM 200 or 400, system dynamics, and the communications protocols.
• HCU 100 functions include cell selection functions to activate those specific cells or group of cells to be activated and the cells to transmit the resultant return signals.
• the software also allows for assignment of specific pressure response pads of the physician HCU 100 to be designated as send patches to transmit the physician's pressure signal as well as receive pads to transmit the patient data back to the physician.
• the spatial orientation of the physician's HCU 100 with respect to the patient's body is also tracked by the computer software. Movements of the HCU 100 can be translated and sent to the PEM 200 or 400 to simulate movement of the hand across the patient's body.
• an anatomy database can be incorporated to provide cross- sectional anatomy and three-dimensional renderings of the specific body area being examined.
• the software translates the physical pressure response applied by the physician to the HCU 100 into an electrical signal. Standardization, calibration, and real-time monitoring of the signal and signal strength are typical program functions.
• the software is also responsible for the transmission protocols for electrical signal conversion and transmission from the HCU 100 to the PEM 200 or 400, and vice versa. Transmission protocols include signal transmission over land-based and non-land-based communications platforms. All pump and valve commands, including pump chamber pressurization, calibration and conversion of the transmitted electrical signal back into the appropriate pressurization command correlating with a magnitude equivalent to the actual pressure applied at the hand control unit, and selected valve on/off status are also controlled by the device software.
• FIGURE 9 represents the general process flow diagram of device functions for both the electromechanical and pneumatic/hydraulic embodiments of the present invention.
• the physician selects the area of interest underlying the cells 204 or 404 to be activated corresponding to the area to be manually examined.
• Applying pressure to the HCU 100 via the sensory modulation subunits 140 generates signals that are sent through a signal processor 130 and analog-to-digital converter 132 to a physician's computer 160 that, in turn, sends a computer command to activate the PEM's 200 or 400 sensory modulation subunits 240 or 440 underlying the area of interest to which the HCU 100 pressure signals will be directed.
• the pressure transducers 244 or 444 corresponding to the area of the patient the user wishes to "feel" after the pressure stimulus is applied are then activated. This command activates the receiving cell's pressure transducers 244 or 444 so the output signal can be transmitted back to the physician's HCU 100.
• the physician then presses directly on the sensory modulation subunits 140 of the HCU 100 using any combination of fingertips, proximal palmar, and distal palmar hand surfaces (ranging from a single fingertip to the whole palmar hand surface) to generate the desired input pressure stimulus equal to the force he or she would normally apply during manual examination of a patient.
• the applied force will vary between individuals, circumstances, and the patient areas being examined.
• the pressure applied by the physician against the sensory modulation subunits 140 of the HCU 100 is sensed by the pressure transducer 144 and translated into an electrical output signal.
• the electrical output signal is sent to the signal processor 130 and the processed analog electrical signal is converted to a digital signal 132.
• the digital signal is then input to a physician's computer 160.
• the software program is responsible for software commands for linked system pathways between the various send and receive portions of the HCU 100 and the PEM 200 or 400; calibration of the signal processors 130, 308, pressure transducers 144, 244, 444, piston resistors 148, and variable pressure-producing devices 248 for both the user side and patient side equipment, and conversion of the HCU 100 electrical input signal into a corresponding PEM 200, 400 electrical output signal. If a pump system is used for the PEM 400, a pressure sensor (not shown) within the medium pressurizing reservoir 418 will be calibrated.
• the physician's computer 160 transmits the PEM 200, 400 electrical signal and associated software commands to the remote computer 260 via the communication systems 312.
• the patient side, or remote side may utilize a free standing command control box 300, located near the PEM 200 or 400.
• the digital pressure generating signal is then converted back to an analog electrical signal 310 by a digital to analog converter, post-processed 308, then relayed to the appropriate, preselected pressure generating device of the PEM 200 or 400.
• the PEM 200 or 400 then applies a directed force to the patient that is based on the force applied by the user or physician to the HCU 100.
• the software is responsible for receiving the incoming electrical signals from each active area of the HCU 100, assessing the corresponding magnitude of each of the input pressures applied to the various portions of the HCU 100 and converting this information into a specific pump command.
• the pressure commands are then transmitted to either a remote computer 260 at the patient's remote location, or directly to the command control box 300 portion of the PEM 400 previously described.
• the PEM 400 would then activate the pumping mechanism and pressurize the pressurizing chamber 418 in order to achieve an output pressure equal to the pressure directly applied by the physician to the HCU 100.
• the internal pressure of the chamber 418 is monitored by a pressure sensor that provides continuous feedback regarding the need to continue or discontinue pumping until the desired input pressure is achieved.
• the pressurized medium in the pressurizing chamber 418 is then transmitted to each of the selected cells 404 with open pressure valves 414 via the inlet/outlet line 410.
• the pressurized medium then flows into the selected cells 404 and increase the cell volume and internal cell pressure corresponding to the force applied by the physician at the HCU 100.
• the downward force applied to the patient by either PEM 200 or 400 will elicit a counter-response from the patient ranging from no resistance at all and further indentation of the area being examined to great resistance or "guarding.” This resistance from the patient in response to the applied force from the activated cells will be detected by the cell pressure transducer 244 or 444.
• the mechanical resistance response detected by the activated pressure transducer 244 or 444 of the PEM 200 or 400 is converted into an electrical signal which is transmitted back to the command control box 300 or the remote computer 260 at the patient's location. As previously described for the input command set, this analog electrical signal will be processed 308 and converted to a digital signal 31.0. This digital signal is then transmitted back to the physician's computer 160 via the communications systems 312. As previously described for the HCU 100 output signal, the software program is responsible for receiving the incoming digital electrical signal(s) from each active area of the PEM 200, 400, assessing the corresponding magnitude of each of the PEM 200, 400 output pressures, and converting them into equivalent digital HCU 100 resistance signals.
• the digital signals are then converted to an equivalent analog electrical signal 132, post-processed 130, then directed to the appropriate preselected piston resistors of the HCU 100.
• the output resistance produced by the piston resistors 148 at the HCU 100 is equal to response pressure produced by the patient in response to the HCU 100 input pressure stimulus.
• the counter-resistance provided by the piston resistor 148 will provide the physician with a tactile simulation of the patient's response to pressure applied over the selected area of the patient's anatomy.
• the system is real-time and dynamic such that the physician may simulate press-release or press-partial release maneuvers on a continuous basis within the region of preselected cells.
• the three key components of the device: the physician hand control unit, the computer software, and the patient examination module provide a system for a continuous, real-time, action-reaction feedback loop. It is the differential resistance between the physician's applied pressure and the patient's resistive response perceived by the physician's hand against the hand control unit that the physician can then interpret and use for medical decision-making.
• FIGURES lOA-lOC A flow chart showing the overall process that will be controlled by the software in the preferred embodiment is diagrammed in FIGURES lOA-lOC.
• the user generally the physician, first logs into the system 500.
• a mechanism for logging in is provided by any conventional means, including for example a biometric scanner in the HCU (i.e., a fingerprint reader, not shown) or a more conventional requester for a user identification and password may be provided at the physician's computer 160.
• the software queries for the system date and time 502, establishes a connection with the PEM and checks the status of the HCU and PEM 504, then establishes the necessary communications links 506 therebetween.
• a first database is accessed 508 by the physician's computer 160 to obtain the various calibration factors for the HCU and PEM components, such as the pressure transducers and pressure producing devices (linear actuators).
• Various other initiation functions are then performed by the software 510, which functions may include establishing the sampling rates for the pressure transducers and initiating and calibrating the components (for example, establish the "zero pressure" level for the pressure transducers).
• Patient identification and biometric information may then be input 512, both to verify the identity of the patent for the medical records and to establish baseline parameters that may be helpful to the examination, such as the general size and age of the patient.
• the physician selects the anatomical location to be examined 514.
• a database of anatomical data is accessed 516, which may include generic still or animated pictures of the portion of the anatomy that is to be examined. It is contemplated that embodiments of the present invention may use the patient medical and biometric information, in addition to generic information relating to the portion of the anatomy that is to be examined, to adjust various system parameters, such as the sensitivity of the pressure transducers and linear actuators.
• the physician selects the portions of the HCU that will provide output signals to the PEM 518, the portions of the HCU that will receive feedback pressures from the PEM 520, the cells of the PEM that will receive the pressure signals from the HCU 522, and the cells of the PEM that will send pressure signals back to the HCU 524. It is anticipated that in most applications there will be a one-to-one correspondence between the active HCU portions, and the activated PEM cells, for example, that the HCU sensory modulation subunits will send and receive pressure signals to and from the same PEM cells. However, the ability to disassociate the send and receive signals is believed to provide additional functionality to the system. The present invention contemplates systems wherein it is not possible to disassociate the HCU input and output pressure signals.
• the software can also coordinate the position of the activated segments of the HCU with the PEM 526, such that movement of the HCU, in a manner similar to moving a mouse, is tracked by the system to make a corresponding change in the PEM cells that are activated.
• predetermined force alteration functions can be applied 528, such as force amplification/magnification or reduction/minimization of the HCU and PEM output signals. Forces are applied to the HCU 530 by the user, and the pressure signals generate low-amperage signals 532 in the pressure transducers 144 (HCU-P1), that are sent to the signal processor to produce corresponding higher-amperage signals 534, and then converted to digital signals 536 (D-HCU-P1).
• the D-HCU-P1 are used to generate digital pressure signals for the PEM 538 (D-PEM-P1), and transmitted 540 from the physician's computer 160 to the remote computer 260.
• the D-PEM-P1 pressure signal is then converted to a low amperage analog signal (PEM-P1) 542, that is applied to the variable pressure producing device 248 of the PEM, and a corresponding force is applied to the patient 546.
• PEM-P1 digital pressure signals for the PEM 538
• PEM-P1 pressure signal is then converted to a low amperage analog signal (PEM-P1) 542, that is applied to the variable pressure producing device 248 of the PEM, and a corresponding force is applied to the patient 546.
• the patient resistance response is detected by the selected PEM cell 548, producing a pressure response signal (PEM-P2) 550, that is processed to produce a higher amperage signal 552 and digitized (D-PEM-P2) 554.
• the D-PEM-P2 pressure signal is used to generate a corresponding digital pressure signal for the HCU 556, transmitted from the remote computer to the physician's computer 558, and converted to an analog signal 560 that is provided 562 to the appropriate HCU piston-type variable resister 148 to produce a responsive force at the HCU. If the examination is complete 566, then the system will reset to allow the physician to begin another exam of a different part of the patient's anatomy. Otherwise the physician can apply additional forces and detect additional responses from the patient.
• While the original intent of the HCU 100 is to simulate a physical examination of a patient in a remote location, applications within the field of medicine would include the ability to examine a patient in hostile environments such as deep sea, space, battlefield conditions, remote locations, and/or mountain/jungle expeditions.
• the present invention may also be adapted for non-medical and/or recreational usages, where it is desirable for an individual to examine, feel, or otherwise elicit a tactile response from another individual, body or object in a remote location.
• Portable versions could also be applied in a medical station within the workplace, obviating the necessity of a patient having to actually leave work and traveling to a physicians office. This is very inefficient for both the patient and the physician. It is also contemplated that with the growing use of robotic tools for performing operations, that the above-described invention could be modified in a straightforward manner to provide a physician with tactile feedback while performing an operation using a robotic system. Portable versions could also be applied in the home where some evaluations could preclude the need for after-hours trips to the emergency room. This efficiency would have a significant effect on overall health care costs.
• the present invention could also be adapted to enhance the ability of the visually impaired to communicate or feel objects without actual direct physical contact between the object and the blind individual.

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