Illustrative embodiments of the present application include, without limitation, methods, structures, and systems. In one embodiment, a mechanical CPR device includes a back plate, a first tower removably attached to the back plate, a second tower removably attached to the back plate, and a beam releasably connected to each of the first tower and the second tower. The first tower can include a first linear motion device. The second tower can include a second linear motion device. Each of the first and second linear motion devices can be configured to move one end of the beam toward and away from the back plate. The first and second linear motion devices can be configured to operate in concert such that, when the back plate is resting on a surface, the beam remains substantially parallel to the surface during movement of the beam toward and away from the back plate.
In some examples, the first linear motion device can include a first shuttle and the second linear motion device can include a second shuttle. The first shuttle can be configured to releaseably connect with a first end of the beam and the second shuttle can be configured to releaseably connect with a second end of the beam. The first shuttle can include one or more engagement points configured to engage the first end of the beam and the second shuttle can include one or more engagement points configured to engage the second end of the beam. The first end of the beam can include a first rotatable end and the second end of the beam can include a second rotatable end. The beam can include a first locking mechanism and a second locking mechanism, where the first locking mechanism is configured to lock the first rotatable end in a first position and to permit the first rotatable end to rotate in a second position, and where the second locking mechanism is configured to lock the second rotatable end in a first position and to permit the second rotatable end to rotate in a second position. The first linear motion device can include a first motor and a first threaded shaft connected to the first shuttle, and the second linear motion device can include a second motor and a second threaded shaft connected to the second shuttle. The first tower further can include a first control unit configured to control movement of the first shuttle by controlling the first motor, and the second tower can include a second control unit configured to control movement of the second shuttle by controlling the second motor.
In other examples, the first tower can include a first control unit and the second tower can include a second control unit. The first control unit and the second control unit can be configured to communicate wirelessly. The first control unit and the second control unit can also be configured to communicate via a wired connection. The wired connection can include a first electrical connection in the first tower, a second electrical connection in the back plate, and a third electrical connection in the second tower. The first and second control units can be configured to verify that the back plate is properly aligned with the first and second towers based on an ability to communicate via the first, second, and third electrical connections. The wired connection can also include a fourth electrical connection in the first tower, a fifth electrical connection in the beam, and a sixth electrical connection in the second tower. The first and second control units can be configured to verify that the beam is properly aligned with the first and second towers based on an ability to communicate via the fourth, fifth, and sixth electrical connections. At least one of the first and second control units is configured to receive one or more user inputs. The first control unit can be configured to control the first linear motion device based on the received one or more user inputs, and the second control unit can be configured to control the second linear motion device based on the received one or more user inputs.
In another embodiment, a method can include placing a patient on a back plate; removably attaching a first tower to the back plate; removably attaching a second tower to the back plate; engaging a first rotatable end of a beam to a first linear motion device of the first tower; engaging a second rotatable end of the beam to a second linear motion device of the second tower; and locking the first and second rotatable ends of the beam such that the beam is located over the patient. The first and second linear motion devices can be configured to move the beam to compress a chest of the patient between the beam and the back plate.
In some examples, placing the patient on the back plate can include placing the back plate on a surface. The method can also include causing the first and second linear motion devices move the beam toward and away from the back plate to compress the chest of the patient, where the first and second linear motion devices are configured to maintain the beam in a position substantially parallel to the surface during motion of the beam. The beam can include a compression point configured to engage the chest of the patient during motion of the beam.
Throughout the drawings, reference numbers may be re-used to indicate correspondence between referenced elements. The drawings are provided to illustrate example embodiments described herein and are not intended to limit the scope of the disclosure.
Mechanical CPR compression devices can provide many advantages over manual CPR compressions. Mechanical CPR compression devices can include a back plate that is placed behind the back of the patient and a compression device located above the patient's sternum area. The compression device can be connected to the back plate on both sides of the patient. When the compression device pushes against the area around the patient's sternum, the back plate provides resistance that allows the compression device to compress the patient's chest.
Traditional mechanical compression devices can have a portion with significant weight located above a user's sternum. For example, a mechanical CPR device can have a back plate behind the patient's back, a compression device above the patient's sternum, and legs along both sides of the user's chest. The compression device above the patient's sternum can include components such as a piston to perform the compressions, a motor to drive the piston, a battery to provide power to the motor, a control system to control the motor and piston, and the like. All of the components in the compression device can have significant weight. When a patient is laying back-down on a surface, the compression device of the mechanical CPR device will be above the patient making the device somewhat top heavy. While this top-heavy configuration may be an inconvenience, the mechanical CPR device can effectively operate in this manner. However, if the patient is in any other position, the weight of the compression device of the mechanical CPR device may be burdensome. For example, a patient may need to be moved to an inclined or upright position, such as to be placed onto a stretcher, to enter an elevator, to be placed in an ambulance, and the like. In these circumstances, if the mechanical CPR device is around the patient when the patient is moved to an inclined or upright position, the weight of the compression device may cause the patient to fall forward and may cause the mechanical CPR device to be moved out of proper position.
The first tower 230 can also include a motor 232 and a threaded shaft 233. The threaded shaft 233 can engage a shuttle 234. The shuttle 234 can be releasably connected to one end of the beam 220. When the motor 232 turns the threaded shaft 233, the shuttle 234 moves linearly up or down; the end of the beam 220 attached to the shuttle 234 moves with the movement of the shuttle. While a threaded shaft and shuttle configuration have been depicted in
Similar to the first tower 230, the second tower 240 can include a motor 242 and a threaded shaft 243. The threaded shaft 243 can engage a shuttle 244. The shuttle 244 can be releasably connected to another end of the beam 220. When the motor 242 turns the threaded shaft 243, the shuttle 244 moves linearly up or down; the end of the beam 220 attached to the shuttle 244 moves with the movement of the shuttle. While a threaded shaft and shuttle configuration have been depicted in
Control units 235 and 245 can communicate to coordinate movements of shuttles 234 and 244 such that beam 220 remains substantially horizontal during compressions (i.e., substantially parallel to a surface upon which the back plate 210 rests). Control units 235 and 245 can communicate via a wired connection. As discussed in greater detail below with respect to
The beam 320 can include a compression point 321, rotatable ends 322 and 323, and locking mechanisms 324 and 325. Locking mechanism 324 is configured to releasably lock rotatable end 322 in place in the configuration shown in
First tower 330 can include a shuttle 331 that is configured to engage rotatable end 322 of beam 320. In the embodiment depicted in
In the configuration shown in
When compressions of the patient's chest are no longer desired, the beam 320 can be removed from the first tower 330 and the second tower 340. From the configuration shown in
The back plate 410 can be moved from the configuration shown in
An electrical connection can be made between the control unit 611 of the first tower 610 and the control unit 621 of the second tower 620 via the back plate 630. The first electrical connection point 612 of the first tower 610 can be configured to make an electrical connection with the first electrical connection point 631 of the back plate 630. In one embodiment, the first electrical connection point 612 of the first tower 610 can make an electrical connection with the first electrical connection point 631 of the back plate 630 when the back plate 630 is properly aligned with respect to the first tower 610, such as when ribs on a lower side of the back plate 630 are properly aligned with protrusions of a foot of first tower 610. The second electrical connection point 632 of the back plate 630 can be configured to make an electrical connection with the first electrical connection point 622 of the second tower 620. In one embodiment, the second electrical connection point 632 of the back plate 630 can make an electrical connection with the first electrical connection point 622 of the second tower 620 when the back plate 630 is properly aligned with respect to the second tower 620, such as when ribs on a lower side of the back plate 630 are properly aligned with protrusions of a foot of second tower 620. In this way, a wired electrical connection can be made between control unit 611 of the first tower 610 and the control unit 621 of the second tower 620 via the back plate 630. The electrical connection between control unit 611 of the first tower 610 and the control unit 621 of the second tower 620 via the back plate 630 can be used for the control unit 611 and the control unit 621 to communicate with each other and/or for the control unit 611 and the control unit 621 to ensure that the back plate 630 is properly aligned with respect to each of the first tower 610 and the second tower 620.
An electrical connection can be made between the control unit 611 of the first tower 610 and the control unit 621 of the second tower 620 via the beam 640. The second electrical connection point 614 of the first tower 610 can be configured to make an electrical connection with the first electrical connection point 641 of the beam 640. In one embodiment, the second electrical connection point 614 of the first tower 610 can make an electrical connection with the first electrical connection point 641 of the beam 640 when the beam 640 is securely attached to the first tower 610, such as when a rotatable end of the beam 640 is securely held by a shuttle of the first tower 610. The second electrical connection point 642 of the beam 640 can be configured to make an electrical connection with the second electrical connection point 624 of the second tower 620. In one embodiment, the second electrical connection point 642 of the beam 640 can make an electrical connection with the second electrical connection point 624 of the second tower 620 when the beam 640 is securely attached to the second tower 620, such as when a rotatable end of the beam 640 is securely held by a shuttle of the second tower 620. In this way, a wired electrical connection can be made between control unit 611 of the first tower 610 and the control unit 621 of the second tower 620 via the beam 640. The electrical connection between control unit 611 of the first tower 610 and the control unit 621 of the second tower 620 via the beam 640 can be used for the control unit 611 and the control unit 621 to communicate with each other and/or for the control unit 611 and the control unit 621 to ensure that the beam 640 is securely attached to each of the first tower 610 and the second tower 620.
The embodiment of the mechanical CPR device 600 in
Conditional language used herein, such as, among others, “can,” “could,” “might,” “may,” “e.g.,” and the like, unless specifically stated otherwise, or otherwise understood within the context as used, is generally intended to convey that certain examples include, while other examples do not include, certain features, elements, and/or steps. Thus, such conditional language is not generally intended to imply that features, elements and/or steps are in any way required for one or more examples or that one or more examples necessarily include logic for deciding, with or without author input or prompting, whether these features, elements and/or steps are included or are to be performed in any particular example. The terms “comprising,” “including,” “having,” and the like are synonymous and are used inclusively, in an open-ended fashion, and do not exclude additional elements, features, acts, operations, and so forth. Also, the term “or” is used in its inclusive sense (and not in its exclusive sense) so that when used, for example, to connect a list of elements, the term “or” means one, some, or all of the elements in the list.
In general, the various features and processes described above may be used independently of one another, or may be combined in different ways. For example, this disclosure includes other combinations and sub-combinations equivalent to: extracting an individual feature from one embodiment and inserting such feature into another embodiment; removing one or more features from an embodiment; or both removing a feature from an embodiment and adding a feature extracted from another embodiment, while providing the advantages of the features incorporated in such combinations and sub-combinations irrespective of other features in relation to which it is described. All possible combinations and subcombinations are intended to fall within the scope of this disclosure. In addition, certain method or process blocks may be omitted in some implementations. The methods and processes described herein are also not limited to any particular sequence, and the blocks or states relating thereto can be performed in other sequences that are appropriate. For example, described blocks or states may be performed in an order other than that specifically disclosed, or multiple blocks or states may be combined in a single block or state. The example blocks or states may be performed in serial, in parallel, or in some other manner. Blocks or states may be added to or removed from the disclosed example examples. The example systems and components described herein may be configured differently than described. For example, elements may be added to, removed from, or rearranged compared to the disclosed example examples.
While certain example or illustrative examples have been described, these examples have been presented by way of example only, and are not intended to limit the scope of the inventions disclosed herein. Indeed, the novel methods and systems described herein may be embodied in a variety of other forms. The accompanying claims and their equivalents are intended to cover such forms or modifications as would fall within the scope and spirit of certain of the inventions disclosed herein.
The present application claims to the benefit of U.S. Provisional Patent Application 61/761,128, filed Feb. 5, 2013, the contents of which are hereby incorporated by reference in their entirety. The present application is also related to U.S. patent application Ser. No. 14/019,016 filed Sep. 5, 2013, the contents of which are hereby incorporated by reference in their entirety. Cardiopulmonary resuscitation (CPR) is a medical procedure performed on patients to maintain some level of circulatory and respiratory functions when patients otherwise have limited or no circulatory and respiratory functions. CPR is generally not a procedure that restarts circulatory and respiratory functions, but can be effective to preserve enough circulatory and respiratory functions for a patient to survive until the patient's own circulatory and respiratory functions are restored. CPR typically includes frequent chest compressions that usually are performed by pushing on or around the patient's sternum while the patient is laying on the patient's back. For example, chest compressions can be performed at a rate of about 100 compressions per minute and at a depth of about 5 cm per compression for an adult patient. The frequency and depth of compressions can vary based on the age and size of a particular patient. Manual CPR has several disadvantages. A person performing CPR, such as a medical first-responder, must exert considerable physical effort to maintain proper compression timing and depth. Over time, fatigue can set in and compressions can become less regular and less effective. The person performing CPR must also divert mental attention to performing manual CPR properly and may not be able to focus on other tasks that could help the patient. For example, a person performing CPR at a rate of 100 compressions per minute would likely not be able to simultaneously prepare a defibrillator for use to attempt to restart the patient's heart. Mechanical compression devices can be used with CPR to perform compressions that would otherwise be done manually. Mechanical compression devices can provide advantages such as providing constant, proper compressions for sustained lengths of time without fatiguing, freeing medical personal to perform other tasks besides CPR compressions, and being usable in smaller spaces than would be required by a person performing CPR compressions.
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