Patent Application
20100113990
1. Field of Invention
The present invention relates to a pneumatic device, and more particularly to a pneumatic device for cardiopulmonary resuscitation assist and that is easy to carry and provides a better cardiopulmonary resuscitation effect than a manual cardiopulmonary resuscitation procedure does.
2. Description of the Related Art
Accidents like traffic accident and drowning or illnesses like heart attack and hypertension may cause shock and result in cardiac and respiratory arrests. When a patient suffers cardiac and respiratory arrests, the patient's brain cells, tissues and organs cannot acquire enough oxygen supply and lack of oxygen. In order to prevent lack of oxygen, a cardiopulmonary resuscitation (CPR) procedure must be performed continuously on the patient to maintain oxygenated blood flowing to the brain and the heart.
A conventional CPR procedure relies on manual cardiac massage and mouth-to-mouth insufflation performed by first-aid personnel to maintain the flow of oxygenated blood. However, because compressing depth and frequency of a manual cardiac massage may not be stable, the cardiopulmonary resuscitation effect on the patient is not good enough. Thus, some conventional first-aid devices are developed for cardiopulmonary resuscitation assist.
With reference to
With reference to
To overcome the shortcomings, the present invention provides a pneumatic device for cardiopulmonary resuscitation assist to mitigate or obviate the aforementioned problems.
The primary objective of the present invention is to provide a pneumatic device for cardiopulmonary resuscitation assist that is easy to carry and provides a better cardiopulmonary resuscitation effect than a manual cardiopulmonary resuscitation procedure does.
A pneumatic device for cardiopulmonary resuscitation assist in accordance with the present invention comprises a back plate and a compressing member. The back plate has two sides and two securing members mounted respectively on the sides of the back plate. The compressing member comprises a mounting plate and a bladder. The mounting plate is detachably connected to the back plate and has two sides, an upper surface, a lower surface, a gas passage and two securing straps. The gas passage is formed on the upper surface of the mounting plate. The securing straps are respectively mounted on the sides of the mounting plate and respectively connected selectively to the securing members of the back plate. The bladder is mounted on the lower surface of the mounting plate and communicates with the gas passage of the mounting plate.
When a patient's upper body is secured on the back plate with the compressing member, the bladder is repeatedly inflated through the gas passage to compresses the patient's chest continuously and stably. Because the compressing member is connected to the back plate rather than wrapping directly around the patient upper body, a pressure resulting from the inflation of the bladder is applied only on the patient's chest rather than other parts of the patient's upper body, and this provides a good cardiac massage and CPR assist effect and prevents hurting the patient's ribs. Additionally, the pneumatic device is small and easy to carry.
Other objectives, advantages and novel features of the invention will become more apparent from the following detailed description when taken in conjunction with the accompanying drawings.
With reference to
The back plate (10) is substantially quadrangular and has two sides, a top surface, a receiving recess (13), two handles (14) and two securing members. The top surface is used for accommodating and securing a patient's upper body and has a body securing face (11) and a head placing face (12). The head placing face (12) is connected to and is inclined relative to the body securing face (11). The receiving recess (13) is defined in the head placing face (12) for holding the patient's head inside and can be formed at different positions to fit adults or children. When the patient's upper body is secured on the body securing face (11) and the patient's head is placed in the receiving recess (13), the patient's head is tilted and the patient's chin is lifted to facilitate airway management. The handles (14) are formed respectively on the sides of the back plate (10).
With further reference to
With reference to
The female buckle (15,18) is attached/connected to one side of the back plate (10) and comprises a housing (151) and an engaging member (152). The housing (151) is attached/connected to the back plate (10), is hollow and has a top and a mouth and a window (1511). The mouth is defined through the top of the housing (151). The window (1511) is defined in the housing (151) through one side opposite to the back plate (10). The engaging member (152) is held in the housing (151) and comprises a pressed segment (1521) and an engaging tab (1522). The pressed segment (1521) is formed on one side of the engaging member (152) and is held in the window (1511) in the housing (151). The engaging tab (1522) is formed on the other side of the engaging member (152) and extends toward the pressed segment (1521).
The slot (16) is defined through one of the sides of the back plate (10). The securing button is mounted beside the slot (16) and comprises a slide block (151), a spring (172) and a tongue (173). The slide block (171) is mounted slidably in the back plate (10). The spring (172) is mounted between the slide block (171) and the back plate (10) to provide a resilient force to the slide block (171). The tongue (173) is mounted on the slide block (171) and extends selectively into the slot (16).
Each securing strap (24) may have a male buckle (27) as shown in
When the pressed segment (1521) of the engaging member (152) is pressed through the window (1511), the engaging member (152) will be moved relative to the housing (151) to disengage the engaging tab (1522) from the corresponding male buckle (27) or teeth portion of the corresponding strap (24). Consequently, the male buckles (27) or straps (24) can be separated from the female buckles (15).
When the securing buttons are slid to bring the tongues (173) away respectively from the teeth portions of the straps (24), the straps (24) can be separated from the slots (16) of the back plate (10) and the compressing member (20) can be detached from the back plate (10) to release the patient's upper body.
The handles (25) are formed respectively on the sides of the mounting plate (21).
The bladder (22) is mounted on the lower surface of the mounting plate (21) to abut the patient's chest, communicates with the gas passage (23) of the mounting plate (21) and may comprise a lining plate (221) and a resilient bladder sheet (222). The lining plate (221) is attached to the middle frame (212) of the mounting plate (21) and has a through hole communicating with the gas passage (23) on the mounting plate (21). The bladder sheet (222) is attached securely to the lining plate (221) by ultrasonic or high frequency combining process to prevent gas from leaking out of the bladder (22) and form a space for holding gas and protrudes selectively from the opening of the lower frame (213). When the bladder (22) is inflated repeatedly with gas through the gas passage (23), the bladder (22) extends outwards and repeatedly compresses the patient's chest to provide a cardiac massage effect.
With reference to
The oxygen bottle (40) is connected to the gas inlet (31) of the control member (30) to supply the gas pipe with oxygen. Then oxygen flows through the inflation controller (36), the inflation pipe and gas passage (23) and into the bladder (22).
The mask (50) is connected to the gas outlet (35) of the control member (30) and is used to cover a patient's mouth and nose to perform an artificial respiration with oxygen supply. Therefore, the pneumatic device is driven by the oxygen bottle (40) to perform the cardiac massage and the artificial respiration at the same time. Accordingly, carrying and operating the pneumatic device are easy and convenient with the oxygen bottle (40).
With reference to
With reference to
Even though numerous characteristics and advantages of the present invention have been set forth in the foregoing description, together with details of the structure and function of the invention, the disclosure is illustrative only. Changes may be made in detail, especially in matters of shape, size and arrangement of parts within the principles of the invention to the full extent indicated by the broad general meaning of the terms in which the appended claims are expressed.
