Portable emergency safety resuscitator

Gray, David Scott;

A resuscitator having a collapsible bag with an inlet for attachment to a source of oxygen. The collapsible bag has a major outlet and a minor outlet. The major outlet is connected to a first arm of a three-armed connector. The minor outlet is attached to a flexible tube which, in turn, may either be connected to an adapter that is connected to a second arm of the three-armed connector or to a nebulizer or aerosolizer that is attached to the second arm of the three-armed connector. The third arm of the three-armed connector is connected to a housing containing a one-way valve to permit the flow of oxygen away from the collapsible bag and to preclude the flow of liquids and gases toward the collapsible bag. Preferably, the housing also contains, between the one-way valve and the second end of the housing, an exhaust aperture; and the exhaust aperture is preferably covered by a filter. The second end of the housing is attached to the first aperture of a tube that has a self-sealing membrane removably covering a second aperture and a third aperture that may be connected either to a mask or an endotracheal tube.

BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates to a medical device and more particularly to a resuscitator, i.e., manually operated device utilized to provide emergency ventilatory assistance to facilitate the breathing of a sick or injured patient.

2. Description of the Related Art

The inventor is unaware of any prior art resuscitator which incorporates the ability to provide endotracheally administered medications, nebulized medications, and suction to a patient.

SUMMARY OF THE INVENTION

The present invention inserts, between a source of air or oxygen and a patient, a collapsible bag and a connecting complex. A nebulizer or aerosolizer for providing medication can be attached to the connecting complex. Additionally, the connecting complex includes an aperture with a removably attached self-sealing membrane through medications can be administered with a syringe. When the self-sealing membrane has been removed, a suction catheter may be placed through the aperture.

The connecting complex can communicate with the patient either through a mask or an endotracheal tube.

A one-way valve precludes liquids or gases expelled by the patient from reaching either the point of attachment for the nebulizer and aerosolizer or the collapsible bag.

And a filtered exhaust aperture permits the exhaled breath of the patient to reach the atmosphere.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates the Portable Emergency Safety Resuscitator.

DESCRIPTION OF THE PREFERRED EMBODIMENT

The present invention utilizes a collapsible bag 1 having an inlet 2, a major outlet 3, and a minor outlet 4. Attached to the major outlet 3 of the collapsible bag 1 and communicating with the interior 5 of the collapsible bag 1 is a first arm 6 of a hollow three-armed connector 7.

A second arm 8 of the hollow three-armed connector 7 is available for attachment to a nebulizer or aerosolizer 100. The open end 9 of the second arm 8 is preferably sized to accommodate commercially available nebulizers and aerosolizers 100.

A first end 10 of a flexible tube 11 is attached to the minor outlet 4 of the collapsible bag 1. A second end 12 of the flexible tube 11 may be attached to a nebulizer or aerosolizer 100. If no nebulizer or aerosolizer 100 is employed, the second end 12 of the flexible tube 11 is attached to the open end 9 of the second arm 8 of the hollow three-armed connector 7.

The inlet 2 of the collapsible bag 1 is available to be releasably connected to a source of air or, preferably, oxygen. When such connection has been made, oxygen can flow into the interior 5 of the collapsible bag 1, through the collapsible bag 1, through the major outlet 3 of the collapsible bag 1, and into the first arm 6 of the hollow three-armed connector 7.

Oxygen can also flow through the minor outlet 4 of the collapsible bag 1 and through the flexible tube 11. If the flexible tube 11 has been connected to a nebulizer or aerosolizer 100, the oxygen will then enter the nebulizer or aerosolizer 100 and carry medication from such nebulizer or aerosolizer 100 into the second arm 8 of the hollow three-armed connector 7. If no nebulizer or aerosolizer 100 has been attached to the open end 9 of the second arm 8 of the hollow three-armed connector 7, the flexible tube 11 is attached to a first end 13 of a hollow adapter 14; and a second end 15 of the hollow adapter 14 is connected to the second arm 8 of the hollow three-armed connector 7. Oxygen can then flow from the flexible tube 11, through the hollow adapter 14, and into the second arm 8 of the hollow three-armed connector 7.

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Preferably, the major outlet 3 and the minor outlet 4 are of such sizes that the flow of oxygen through the major outlet 3 is 17 liters per minute; and the flow of oxygen through the minor outlet 4 is 8 liters per minute when the collapsible bag 1 is receiving oxygen at a typical rate of flow from a source of oxygen. Also, the collapsible bag 1 may be squeezed by a care giver to vary the rate of flow of oxygen.

Attached to and communicating with a third arm 16 of the hollow three-armed connector 7 is a first end 17 of a housing 18 containing one-way valve 19 to permit air, oxygen, and medication to flow toward the patient but to preclude the transmission of liquids or gases flowing from the patient.

Preferably, the housing 18 also contains, between the one-way valve 19 and the second end 20 of the housing 18, an exhaust aperture 21 through which the exhaled breath of the patient can reach the atmosphere. Also preferably, a filter 22 covers the exhaust aperture 21 to minimize the possibility that contaminants from the patient will enter the atmosphere.

And the hollow three-armed connector 7 is preferably T-shaped.

Attached to and communicating with a second end 20 of the housing 18 is a first aperture 23 of a tube 24. The tube 24 is preferably L-shaped. And the hollow three-armed connector 7, the housing 18, and the tube 24 are preferably constructed of rigid clear plastic.

A second aperture 25 of the tube 24 is releasably covered by a self-sealing membrane 26. The self-sealing membrane is preferably siliconized.

To a third aperture 27 of the tube 24 may be connected either a mask or an endotracheal tube.

When the endotracheal tube is employed, the needle of a syringe can be inserted through the self-sealing membrane 26, through the second aperture 25, through the tube 24, through the third aperture 27, and into the endotracheal tube so that medications can be pushed from the syringe into the endotracheal tube for the patient.

Alternatively, when the self-sealing membrane 26 has been removed from the second aperture 25 of the tube 24, a suction catheter may be inserted through the second aperture 25, through the tube 24, through the third aperture 27, and through the endotracheal tube to remove fluids such as blood, emesis, and secretions from the patient's airway in order to permit the patient to breathe.

Preferably, first ends 28 of strips of flexible plastic 29 are attached to the inside 30 of the tube 24 between the first aperture 23 and the second aperture 25. The second ends 31 of the strips of flexible plastic 29 push against one another so that when a suction catheter is inserted, a seal is formed between the inside 30 of the tube 24 and the suction catheter to preclude contamination from the patient escaping into the atmosphere. The location of the strips of flexible plastic 29 prevents their interfering with the flow of oxygen from the first aperture 23 to the third aperture 27.