Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
  • A61M16/06—Respiratory or anaesthetic masks
  • A61M16/0666—Nasal cannulas or tubing
  • A61M16/0672—Nasal cannula assemblies for oxygen therapy
  • A61M16/0677—Gas-saving devices therefor
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
  • A61M16/0051—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes with alarm devices
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
  • A61M16/021—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes operated by electrical means
  • A61M16/022—Control means therefor
  • A61M16/024—Control means therefor including calculation means, e.g. using a processor
• • A—HUMAN NECESSITIES
  • A62—LIFE-SAVING; FIRE-FIGHTING
  • A62B—DEVICES, APPARATUS OR METHODS FOR LIFE-SAVING
  • A62B9/00—Component parts for respiratory or breathing apparatus
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
  • A61M16/10—Preparation of respiratory gases or vapours
  • A61M16/105—Filters
  • A61M16/106—Filters in a path
  • A61M16/107—Filters in a path in the inspiratory path
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
  • A61M16/0003—Accessories therefor, e.g. sensors, vibrators, negative pressure
  • A61M2016/0015—Accessories therefor, e.g. sensors, vibrators, negative pressure inhalation detectors
  • A61M2016/0018—Accessories therefor, e.g. sensors, vibrators, negative pressure inhalation detectors electrical
  • A61M2016/0021—Accessories therefor, e.g. sensors, vibrators, negative pressure inhalation detectors electrical with a proportional output signal, e.g. from a thermistor

Definitions

• the present invention is directed to a portable, battery powered device used to supply or deliver oxygen to a patient or user.
• Known devices and systems provide a continuous flow of oxygen from a regulated oxygen source.
• a pressurized container of oxygen includes an adjustable valve that provides a continuous flow of oxygen gas to the patient. The flow rate can be adjusted but, once set, the system is intended to provide a continuous flow.
• a patient of course, does not continuously inhale so that a portion of the oxygen provided under a continuous flow system is not actually used by the patient.
• Other manufacturers therefore, have developed oxygen conserving devices that provide a pulse or dose of oxygen. For example, the following U.S.
• patents are generally related to these types of structures: 3,923,056; 4,462,398; 4,570,631; 4,706,664; 4,823,788; 4,873,971; 4,932,402; 5,005,570; 5,038,770; and 5,315,990.
• Many of these alternative arrangements are simply too complex, expensive, or inadequate so that a need exists for a simple, economical, and effective device that controls oxygen supply to a user, and that allows the user to easily convert the device from a pulse mode operation to a continuous flow mode without difficulty or attendant complexity or cost associated with the device.
• an oxygen conserving device includes an inlet connected to an oxygen source, an outlet that communicates oxygen to a patient, a mass flow sensor connected to the outlet for detecting a patient's inhalation, and a valve disposed between the inlet and outlet for controlling oxygen to the patient in response to inhalation detection and thereby providing a pulse of oxygen.
• the valve can be manually switched from a pulse mode to a continuous flow mode.
• the valve remains open for a predetermined period of time, for example, approximately one second, and the valve will not operate for a lock-out period after a pulse of oxygen has been delivered to the patient.
• a principal advantage of the invention is a compact device that conserves oxygen by providing oxygen only after detecting inhalation.
• Another advantage of the invention is the ability to easily switch between a pulse mode and continuous flow mode.
• Yet another advantage of the invention resides in various visual and audible alarm features that apprise the user of the operation of the device.
• the invention may take physical form in certain parts and arrangements of parts, a preferred embodiment of which will be described in detail in this speci ication and illustrated in the accompanying drawings.
• FIGURE 1 is a perspective view of the demand oxygen conserving device.
• FIGURE 2 is a perspective view from the opposite side of the demand oxygen conserving device.
• FIGURE 3 is a perspective view of the demand oxygen conserving device with a top housing portion removed and illustrating various internal components.
• FIGURE 4 is a perspective view of the device with a bottom housing portion removed.
• FIGURE 5 is a perspective view of the internal components with both the upper and lower portions of the housing removed.
• FIGURE 6 is an exploded view of a manually actuated switch lever and a solenoid valve used in the demand oxygen conserving device.
• FIGURE 7 is a schematic representation of a movable pin assembly that cooperates with the lever to transfer actuating movement to a poppet in the valve.
• a portable, battery powered, electrically operated, demand oxygen conserving device 10 is shown assembled in FIGURES 1 and 2. It includes a housing comprised of a first or upper housing portion 12 and a second or lower housing portion 14. Preferably, the housing is made of a flame retardant thermoplastic that is sufficiently sturdy to withstand impact loads if the device is inadvertently dropped.
• a series of controls and indicating features are provided on the device. For example, individual controls are provided for "pulse on" 16 and a “pulse off” 18 operation of the device. As will become more evident below these controls are designed to turn the power on and off, i.e., connect a rechargeable battery pack to a printed circuit board and solenoid valve, again, particulars of which will be described in greater detail.
• LEDs 20 such as a series of light emitting diodes (LED) s 20 are also provided on the housing. As shown, four LEDs 20a, 20b, 20c, and 20d are spaced along a peripheral portion of the upper housing. Of course, one skilled in the art will recognize that a greater or lesser number of indicators may be used depending on what features and information are to be conveyed to the patient.
• LED light emitting diodes
• An inlet 26 extends through the housing, particularly shown as extending through an end wall of the lower housing portion 14.
• the inlet is adapted to receive a fluid line (not shown) that extends from an oxygen source such as a pressurized tank of oxygen.
• a regulator valve is typically located at the outlet of the pressurized oxygen supply to provide a preselected, continuous flow of oxygen to the inlet 26.
• An outlet 28 is shown with a tapered or barbed configuration so that it is capable of receiving a fluid line that extends to the patient.
• the outlet provides pulsed oxygen flow or continuous flow to the patient, depending on the mode of operation of the device.
• a lever 30 (FIGURE 1) extends outwardly from the housing and is adapted for movement between first and second positions. The lever is sized to be easily manipulated by a finger of a patient/user, and further details of the lever and switching arrangement will be described below.
• An additional opening 32 (FIGURE 2) is also provided in the housing and is capable of receiving an adaptor plug (not shown) .
• the adaptor plug when connected to an electrical outlet, provides for a rapid or quick charge of the rechargeable batteries, such as nickel cadmium batteries, that operate the device 10.
• a printed circuit board 40 (FIGURE 4) is enclosed within the housing and is electrically connected to the solenoid valve 42, rechargeable batteries 44, mass flow sensor 46, and mode switch 30.
• a clock circuit is provided on the circuit board to control the preselected pulse periods, preferably at one second, in response to detection of inhalation. Still other pulse periods than one second can be used without departing from the scope and intent of the subject invention.
• Each of the indicator LEDs is also connected to the printed circuit board to provide an appropriate signal, for example, when a pulse flow is delivered, a low battery condition is detected, the batteries are being recharged, or a default pulse is detected.
• Selected ones of these visual signals may be combined with an audible signal also controlled through appropriate connection to the printed circuit board.
• the solenoid valve interfaces with the printed circuit board to control oxygen flow from the inlet to the outlet.
• the outlet fitting is connected to the mass air flow sensor 46. Since the solenoid valve 42 is normally closed, no oxygen from the inlet fitting reaches the outlet fitting through oxygen conserving device. Instead the patient/user's breathing is detected by the mass flow sensor due to the interconnection established between these components in the de-energized position of the valve.
• the mass flow sensor that is operatively associated with the printed circuit board, and thus operatively associated with the solenoid valve.
• the solenoid is energized, the outlet fitting 28 is connected to the inlet fitting 26 and the mass air flow sensor is disconnected. This description is applicable when the lever 30 is positioned in the pulse mode. Continuous flow is provided from the source to the inlet, and when inhalation is detected by the sensor 46, the solenoid is energized and provides a pulse flow between the inlet and the outlet, i.e. from the device to the patient.
• pin 50 extends outwardly from one end of the solenoid valve.
• the pin is adapted to abuttingly engage a portion of the lever 30, shown in the drawings as a pair of ramped surfaces on the lever.
• the pin is actuated to change the solenoid valve from an energized to a non-energized state, or vice versa, and change the oxygen conserving device from a pulse mode to a continuous flow mode, or vice versa, as desired.
• a ball 52 is provided at one end of movable pin 54. The pin and ball are urged outwardly toward abutting engagement with the lever.
• the pin is preferably sealed about its periphery by, for example, a flexible diaphragm 56 which can also provide an outward biasing force to the assembly.
• a second ball 58 abuttingly engages the opposite end of the movable pin 54.
• the valve is quick-acting in response to patient inhalation and opens the passageway leading from the regulator associated with the source of oxygen. While the valve is open, the flow rate of oxygen is essentially constant.
• a prescription level or desired flow rate is set at the source tank. For example, a patient having a pulse prescription of two liters per minute (LPM) will be delivered a flow rate of two liters per minute for a period of one second. Thereafter, the valve closes until another inhalation is detected by the sensor.
• LPM pulse prescription of two liters per minute
• BPM forty breaths per minute
• the conservation of oxygen is also achieved even if the pulse duration is greater or les ⁇ than one second, or is variable. Since the pulse of oxygen is based on the breathing rate, a substantial conservation of oxygen is achieved when compared to continuous flow arrangements and the device comes closer to delivering oxygen only during inhalation.
• a pulse of oxygen is provided whenever the mass flow sensor detects patient inhalation.
• the valve may be closed, for example, for a period of 0.4 seconds if the high end of a predetermined frequency range is met.
• a separate LED is illuminated upon each pulse delivery.
• Another LED can be illuminated during recharge of the battery pack.
• Yet another LED can indicate battery status.
• a preferred arrangement uses two different modes of intermittent and continuous illumination combined with a pattern of audible beeps to represent the condition of the batteries.
• the manually operated switch to provide selective control of the oxygen flow and easily switch from a continuous flow to a pulsed flow mode, or vice versa.
• a pulse flow of oxygen is provided whenever inhalation is detected, and in a manner as described above.
• the switch is integral to the valve and of simplified, reliable structure. All of this is achieved with a single solenoid valve in which the oxygen inlet line is normally closed and the oxygen outlet line is normally open. This greatly simplifies the structure and allows the above-described operation to be achieved.

Landscapes

• Health & Medical Sciences (AREA)
• Pulmonology (AREA)
• Emergency Medicine (AREA)
• General Health & Medical Sciences (AREA)
• Hematology (AREA)
• Anesthesiology (AREA)
• Biomedical Technology (AREA)
• Heart & Thoracic Surgery (AREA)
• Engineering & Computer Science (AREA)
• Life Sciences & Earth Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Otolaryngology (AREA)
• Business, Economics & Management (AREA)
• Emergency Management (AREA)
• Respiratory Apparatuses And Protective Means (AREA)

Applications Claiming Priority (3)

Publications (2)

Family

ID=21716784

Family Applications (1)

Country Status (4)

Citations (2)

Family Cites Families (7)

• 1996
  • 1996-10-18 AU AU74490/96A patent/AU715963B2/en not_active Ceased
  • 1996-10-18 NZ NZ321230A patent/NZ321230A/xx not_active IP Right Cessation
  • 1996-10-18 WO PCT/US1996/016623 patent/WO1997014463A1/en not_active Application Discontinuation
  • 1996-10-18 EP EP96936610A patent/EP0858353A4/de not_active Withdrawn

Patent Citations (2)

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events