In certain types of medical emergencies a patient's heart stops working, which stops the blood from flowing. Without the blood flowing, organs like the brain will start becoming damaged, and the patient will soon die. Cardiopulmonary resuscitation (CPR) can forestall these risks. CPR includes performing repeated chest compressions to the chest of the patient, so as to cause the patient's blood to circulate some. CPR also includes delivering rescue breaths to the patient, so as to create air circulation in the lungs. CPR is intended to merely forestall organ damage and death, until a more definitive treatment is made available. Defibrillation is such a definitive treatment: it is an electric shock delivered deliberately to the patient's heart, in the hope of restoring their heart rhythm.
Guidelines by medical experts such as the American Heart Association provide parameters for CPR to cause the blood to circulate effectively. The parameters are for aspects such as the frequency of the compressions, the depth that they should reach, and the full release that is to follow each of them. The depth is sometimes required to reach 5 cm (2 in.). The parameters for CPR also include instructions for the rescue breaths.
Traditionally, CPR has been performed manually. A number of people have been trained in CPR, including some who are not in the medical professions, just in case they are bystanders in an emergency event.
Manual CPR may be ineffective, however. Indeed, the rescuer might not be able to recall their training, especially under the stress of the moment. And even the best trained rescuer can become fatigued from performing the chest compressions for a long time, at which point their performance may become degraded. In the end, chest compressions that are not frequent enough, not deep enough, or not followed by a full release may fail to maintain the blood circulation required to forestall organ damage and death.
The risk of ineffective chest compressions has been addressed with CPR chest compression machines. Such machines have been known by a number of names, for example CPR chest compression machines, CPR machines, mechanical CPR devices, cardiac compressors, CPR systems, and so on.
CPR chest compression machines typically hold the patient supine, which means lying on his or her back. Such machines then repeatedly compress and release the chest of the patient. In fact, they can be programmed to automatically follow the guidelines, by compressing and releasing at the recommended rate or frequency, while reaching a specific depth.
The present description gives instances of Cardio-Pulmonary Resuscitation (CPR) systems, CPR machines, and methods for rescuers, the use of which may help overcome problems and limitations of the prior art.
In embodiments, a Cardio-Pulmonary Resuscitation (CPR) system includes a retention structure, a compression mechanism coupled to the retention structure and a backboard. The retention structure and the backboard can be assembled together so as to form a closed loop that surrounds the patient's torso, and a piston of the compression mechanism is movable towards and away from a chest of a patient. In addition, the CPR system has a stabilizing member, and a coupler configured to couple the stabilizing member to the backboard.
An advantage over the prior art is that the stabilizing member can prevent the retention structure from tilting while the CPR system delivers chest compressions to the patient. Tilting, if permitted for some time, may result in subsequent compressions being delivered by the piston to a point on the chest that migrates away from a point where the effect of the compressions is optimized.
In additional embodiments, a stretcher is modular, in that it has a back segment and a head segment that can be coupled to the back segment. It optionally has a legs segment that can be coupled to the back segment. The stretcher can be assembled around a backboard of a CPR machine that is on the ground. This permits rescuers to first attach the CPR machine to a patient and turn it on, so as to forestall the patient's death, and then to assemble the stretcher while the CPR machine is working. The stretcher can be used for transporting the patient to a care center. The modular stretcher may be later disassembled for easier storing, even fitting in a backpack.
These and other features and advantages of this description will become more readily apparent from the Detailed Description, which proceeds with reference to the associated drawings in which:
As has been mentioned, the present description is about Cardio-Pulmonary Resuscitation (CPR) systems, CPR machines, and methods. Embodiments are now described in more detail.
Components 101 are now described in more detail. Components 101 include a retention structure. In this example, the retention structure includes a box 120 and two legs 121, 122 coupled to box 120. In examples such as the one shown, legs 121, 122 are optionally rotatable with respect to box 120, so as to present a more compact object for storage.
Components 101 also include a compression mechanism 140 coupled to the retention structure. In this example, compression mechanism 140 is so coupled by being located within box 120. Compression mechanism 140 has a movable piston 141. Compression mechanism 140 can be configured to perform the CPR compressions to the patient's chest, and then releases after the compressions, by moving piston 141. Motion would be along arrow 142, with the compressions in the downward direction and the releases in the upward direction.
Components 101 additionally include a backboard 130. Backboard 130 could have the shape of a board. The intent is to place the patient's back on backboard 130. While backboard 130 is shown as flat in
Components 101 moreover include a stabilizing member 150, which is distinct, different from backboard 130. Embodiments of stabilizing member 150 are described in more detail later in this document.
Components 101 furthermore include a coupler 160, which is shown only generically in
Components 101 are shown in an unassembled state. In particular, edges 131, 132 of backboard 130 are not coupled respectively to legs 121, 122 of the retention structure. In some embodiments, components 101 may be disassembled by the user even further.
In embodiments, the retention structure (i.e. box 120 and legs 121, 122), and backboard 130 can be assembled together so as to form a closed loop that surrounds a torso of a patient completely. A closed loop is sometimes defined as a loop that can be drawn by a pencil on paper without lifting the pencil from the paper. Examples are now described.
Further, the assembling of the retention structure and the backboard may result in the piston of the compression mechanism being movable towards and away from a chest of a patient, which is part of their torso. For example, in
It will be observed that stabilizing member 150 cannot be assembled so as to become part of closed loop 177. In fact, stabilizing member 150 is movable at least some times with respect to backboard 130, as will be seen in more detail later in this document.
The retention structure (120, 122) has a risk of tilting. This risk is shown by a semi-axis 225 of the retention structure possibly tilting towards the head of the patient (arrow 226), or towards the feet of the patient (arrow 227). The risk of tilting may arise from how the chest of the patient is sloped at the point where the piston contacts the chest, given the force of the piston. If not addressed, this tilting may result, after some compressions and releases, in the piston migrating up or down along the chest of the patient, and thus continuing to compress at an unintended location on the chest. The retention structure (120, 122) also has a risk of tilting and falling when being displayed.
It will be appreciated that stabilizing member 150 can prevent this tilting along axis 225. In particular, it will be observed that stabilizing member 150 rests on ground 109 with its longer dimension parallel to the ground in the side view of
Stabilizing member 150 can be made from any number of suitable materials. Such materials can be hard plastics, metals, or even x-ray transparent materials, for example materials similar to those used for making backboard 130.
In some instances it is desired to extend stabilizing member 150. Such may be implemented by extensions, which can be adjustable, that can be selectively added to the ends of stabilizing member 150, so as to increase its length. Such extensions can be coupled to stabilizing member 150 by locking mechanisms, etc.
Embodiments for couplers are described later in this document. In
Backboard 430 has a long dimension shown by a straight axis 431, which is superimposed on backboard 430. Backboard 430 is shown as being flat in this example, but it will be understood that axis 431 could represent its long dimension even if backboard 430 were curved, as it was in the example of
In
Stabilizing member 450 has a long dimension shown by a straight axis 451, which is superimposed on stabilizing member 450. Moreover, axis 431 can be transferred so that it intersects axis 451 at a point 452. Around this point 452, an angle 461 is subtended by axes 451 with respect to axis 431. When angle 461 is zero, stabilizing member 450 is aligned with backboard 430, presenting the least volume for storage. Angle 461 is shown as 90° in
In
The patient can be further tethered or secured to the stabilizing member, preferably near the distal end. For example, returning to
The stabilizing strap can be implemented in a number of ways. For example, it can be implemented by a flexible strap, a belt, an elastic band, a cord, etc. It can be secured around the patient by a buckle, Velcro, hooks, etc.
Stabilizing strap 470 can be coupled to stabilizing member 150 in a number of ways. As one example,
As another example,
In some embodiments, the coupler is configured to be used in such a way that the stabilizing member can become fixedly attached to the backboard, and then the stabilizing member can become completely separated from the backboard. Examples are now described.
In some embodiments, the coupler can include a bracket that is coupled to either the stabilizing member or the backboard. For example,
Moreover, the coupler can permit the stabilizing member to become fixedly attached to the backboard by the bracket becoming engaged with the backboard or the stabilizing member, depending on which of these two does not include the bracket. For example,
The arrangement of
In some embodiments, the bracket is coupled to the stabilizing member or to the backboard by being attached fixedly to it, as is bracket 762. In some embodiments, the bracket is coupled to the stabilizing member or to the backboard while being rotatable with respect to it. For example, contrasting how bracket 764 in
Stabilizing member 750 has a top surface 752, and a bottom surface 758 opposite top surface 752. Bracket 764 is on the top surface. In embodiments such as that of
Methods are now described.
According to another operation 920, a coupler is used so as to cause the procured stabilizing member to become attached fixedly to the procured backboard. As also seen above, in some embodiments the coupler includes a bracket that is coupled to one of the stabilizing member and the backboard, and the procured stabilizing member becomes thus attached to the procured backboard by engaging the bracket with the other one of the stabilizing member and the backboard. Further, in some of those embodiments, the bracket is thus engaged by being rotated.
According to another operation 930, a retention structure and the backboard are assembled together so as to form a closed loop that surrounds a torso of a patient completely, the assembly such that the piston can be moved towards and away from a chest of the patient.
According to another, optional operation 940, a stabilizing strap is used to secure a body of the patient directly to the stabilizing member. As also seen above, the stabilizing member could include an opening near a distal end, and the stabilizing strap can thus be used by being passed through the opening.
According to another, optional operation 950, the coupler can be used afterwards so as to cause the stabilizing member to become completely separated from the backboard. This could be performed for purposes of storage, after CPR chest compressions have been administered to the patient by the piston.
In some embodiments, the coupler is configured to couple the stabilizing member to the backboard in such a way that the stabilizing member can be rotated with respect to the backboard by at least 30° within a plane. Referring back to
In the example of
In some embodiments, the backboard and/or stabilizing member includes one or more locking mechanisms to help lock the stabilizing member selectively in either the stabilization deployed mode, or the storage mode. For example, in one embodiment the locking mechanism may be implemented by using spring loaded balls that are fitted in the backboard, with corresponding holes or indentations in the stabilizing member for the 90° alignment of the stabilizing member and/or the storage mode alignment of the stabilizing member. Of course, other types of locking and/or snap fitting mechanisms can be used in other embodiments.
It is not necessary that the stabilizing member have a shape identical to the shape of the backboard. For example, as seen in
In some embodiments, there are additional stabilizers for the backboard. For example, some of the embodiments described above could further have an additional stabilizing member that is distinct from the retention structure, the backboard and the stabilizing member. Such an additional stabilizing member could be coupled to the backboard by an additional coupler, such that the additional stabilizing member can be rotated with respect to the backboard within another plane. The other plane could be the same or different than the plane of rotation of the original stabilizing member. The rotation of the additional stabilizing member can be by at least 30°, and possibly also larger angles as described above. Examples of embodiments with more than one stabilizer are now described.
What is different in
According to another, optional operation 1425, if an additional stabilizing member is provided with an additional coupler, the additional stabilizing member can be rotated with respect to the backboard by at least 30° within another plane, as permitted by the additional coupler. This rotation amounts to also deploying the additional stabilizing member.
According to another operation 1430, a retention structure and the backboard are assembled together so as to form a closed loop that surrounds a torso of a patient completely. The assembly can be such that a piston of the compression mechanism can be moved towards and away from a chest of the patient.
According to another, optional operation 1440, a stabilizing strap is used to secure a body of the patient directly to the stabilizing member. As also seen above, the stabilizing member could include an opening near a distal end, and the stabilizing strap can thus be used by being passed through the opening.
In the methods described above, each operation can be performed as an affirmative step of doing, or causing to happen, what is written that can take place. Such doing or causing to happen can be by the whole system or device, or just one or more components of it. It will be recognized that the methods and the operations may be implemented in a number of ways, including using systems, devices and implementations described above. In addition, the order of operations is not constrained to what is shown, and different orders may be possible according to different embodiments. Examples of such alternate orderings may include overlapping, interleaved, interrupted, reordered, incremental, preparatory, supplemental, simultaneous, reverse, or other variant orderings, unless context dictates otherwise. Moreover, in certain embodiments, new operations may be added, or individual operations may be modified or deleted. The added operations can be, for example, from what is mentioned while primarily describing a different system, apparatus, device or method.
In additional embodiments, a stretcher is modular so that it can be assembled around a backboard of a CPR machine. This permits rescuers to first attach the CPR machine so as to preserve the life of the patient, and then to assemble the stretcher for transporting to a care center. Such a stretcher can also be called a scoop board. The modular stretcher may be later disassembled for easier storing. Such a stretcher can be made, except where specified otherwise, by rigid materials such as hard plastic, metal, and so on.
In some embodiments, a modular stretcher is provided in combination with a CPR system that can be made as described above, and even such CPR systems that further lack a stabilizer. For example, returning to
In some embodiments, such a stretcher can be assembled around a backboard of such a CPR machine, when that backboard is on the ground and even when the CPR machine has been applied to a patient and is delivering chest compressions. This way, the patient can be transported without interrupting the on-going CPR chest compressions. The parts can be detachable for easy storing.
In some embodiments, such a stretcher includes a back segment, and a head segment that can be coupled to the back segment. Together they may define a blank space between them, in which the backboard can be received. In some embodiments, the back segment or the head segment or both engage the backboard, in whole or in part. Examples are now described.
In the embodiment of
In some embodiments, the head segment includes a rigid portion and a soft portion. The head segment can be coupled, by its rigid portion, to the back segment. The soft portion can be made from canvas, sheet, or other materials that can be bent. An example is now described.
Optionally, a modular stretcher according to embodiments further includes a legs segment that can be coupled to the back segment. The legs segment can be made from flexible materials such as canvas, in whole or in part. An example is in
A person skilled in the art will be able to practice the present invention in view of this description, which is to be taken as a whole. Details have been included to provide a thorough understanding. In other instances, well-known aspects have not been described, in order to not obscure unnecessarily this description. Plus, any reference to any prior art in this description is not, and should not be taken as, an acknowledgement or any form of suggestion that such prior art forms parts of the common general knowledge in any country or any art.
This description includes one or more examples, but this fact does not limit how the invention may be practiced. Indeed, examples, instances, versions or embodiments of the invention may be practiced according to what is described, or yet differently, and also in conjunction with other present or future technologies. Other such embodiments include combinations and sub-combinations of features described herein, including for example, embodiments that are equivalent to the following: providing or applying a feature in a different order than in a described embodiment; 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 features incorporated in such combinations and sub-combinations.
In this document, the phrases “constructed to” and/or “configured to” denote one or more actual states of construction and/or configuration that is fundamentally tied to physical characteristics of the element or feature preceding these phrases and, as such, reach well beyond merely describing an intended use. Any such elements or features can be implemented in a number of ways, as will be apparent to a person skilled in the art after reviewing the present disclosure, beyond any examples shown in this document.
Any and all parent, grandparent, great-grandparent, etc. patent applications, whether mentioned in this document or in an Application Data Sheet (“ADS”) of this patent application, are hereby incorporated by reference herein as originally disclosed, including any priority claims made in those applications and any material incorporated by reference, to the extent such subject matter is not inconsistent herewith.
In this description a single reference numeral may be used consistently to denote a single item, aspect, component, or process. Moreover, a further effort may have been made in the drafting of this description to use similar though not identical reference numerals to denote other versions or embodiments of an item, aspect, component or process that are identical or at least similar or related. Where made, such a further effort was not required, but was nevertheless made gratuitously so as to accelerate comprehension by the reader. Even where made in this document, such a further effort might not have been made completely consistently for all of the versions or embodiments that are made possible by this description. Accordingly, the description controls in defining an item, aspect, component or process, rather than its reference numeral. Any similarity in reference numerals may be used to infer a similarity in the text, but not to confuse aspects where the text or other context indicates otherwise.
The claims of this document define certain combinations and subcombinations of elements, features and steps or operations, which are regarded as novel and non-obvious. Additional claims for other such combinations and subcombinations may be presented in this or a related document. These claims are intended to encompass within their scope all changes and modifications that are within the true spirit and scope of the subject matter described herein. The terms used herein, including in the claims, are generally intended as “open” terms. For example, the term “including” should be interpreted as “including but not limited to,” the term “having” should be interpreted as “having at least,” etc. If a specific number is ascribed to a claim recitation, this number is a minimum but not a maximum unless stated otherwise. For example, where a claim recites “a” component or “an” item, it means that it can have one or more of this component or item.
This patent application is a continuation of U.S. patent application Ser. No. 15/047,514, filed on Feb. 18, 2016, which claims priority from U.S. Provisional Patent Application Ser. No. 62/120,324, filed on Feb. 24, 2015, the disclosures of which, as initially made, are hereby incorporated by reference.
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Parent | 15047514 | Feb 2016 | US |
Child | 16858132 | US |