CN112839576A - Cardiopulmonary resuscitation guidance method, guidance device and computer-readable storage medium - Google Patents

Cardiopulmonary resuscitation guidance method, guidance device and computer-readable storage medium Download PDF

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CN112839576A
CN112839576A CN201980066452.0A CN201980066452A CN112839576A CN 112839576 A CN112839576 A CN 112839576A CN 201980066452 A CN201980066452 A CN 201980066452A CN 112839576 A CN112839576 A CN 112839576A
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oscillogram
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CN112839576B (en
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王启
丁燕琼
左鹏飞
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Shenzhen Mindray Bio Medical Electronics Co Ltd
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • AHUMAN NECESSITIES
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    • A61B5/053Measuring electrical impedance or conductance of a portion of the body
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61HPHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
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Abstract

The invention provides a cardiopulmonary resuscitation guidance method, a cardiopulmonary resuscitation guidance device and a computer readable storage medium, the cardiopulmonary resuscitation guidance method comprises the following steps: acquiring a thoracic impedance oscillogram of a patient during rescue; comparing the thoracic impedance oscillogram with a preset oscillogram, wherein the preset oscillogram is the thoracic impedance oscillogram when the patient is rescued under an ideal condition; and sending out prompt information according to the comparison result, wherein the prompt information is used for guiding a rescuer to rescue the patient. The cardiopulmonary resuscitation guidance method provided by the embodiment of the invention is used for guiding the actual rescue process of cardiopulmonary resuscitation and is beneficial to ensuring the quality of chest compression.

Description

Cardiopulmonary resuscitation guidance method, guidance device and computer-readable storage medium Technical Field
The invention relates to the field of medical instruments, in particular to a cardiopulmonary resuscitation guidance method, a cardiopulmonary resuscitation guidance device and a computer readable storage medium.
Background
Currently, Cardiopulmonary resuscitation (CPR) is the only effective way to rescue patients with cardiac arrest. The defibrillator is mainly used for defibrillation treatment of dangerous diseases such as ventricular fibrillation and atrial fibrillation. An automatic defibrillator (AED) is one type of defibrillator intended for public use (airports, stations, etc. where there is a dense stream of people). Unlike in-hospital conventional defibrillators, AEDs are typically used by first-aid personnel who have undergone basic first-aid training. For emergency personnel in public places, most emergency training periods are 1-2 years or longer, the situations of manual and foot disorder or unfamiliarity with operation generally occur during actual emergency treatment, the situations directly influence the emergency treatment effect, and even cause emergency treatment failure. The cardio-pulmonary resuscitation operation is the basic skill of first aid in public places, and how to ensure the actual rescue effect which is directly determined by high-quality chest compression.
Disclosure of Invention
The embodiment of the invention provides a cardio-pulmonary resuscitation guidance method, which comprises the following steps:
acquiring a thoracic impedance oscillogram of a patient during rescue;
comparing the thoracic impedance oscillogram with a preset oscillogram;
and sending out prompt information according to the comparison result, wherein the prompt information is used for guiding a rescuer to rescue the patient.
According to the cardiopulmonary resuscitation guidance method, firstly, a thoracic impedance oscillogram of a patient during rescue is obtained, then the obtained thoracic impedance oscillogram is compared with a preset oscillogram, and finally prompt information is sent according to a comparison result to guide a rescuer to rescue the patient. The cardiopulmonary resuscitation guidance method provided by the embodiment of the invention is used for guiding the actual rescue process of cardiopulmonary resuscitation and is beneficial to ensuring the quality of chest compression.
The embodiment of the present invention further provides a cardiopulmonary resuscitation guidance device, including:
the first acquisition module is used for acquiring a thoracic impedance oscillogram of a patient during rescue;
the comparison module is used for comparing the thoracic impedance oscillogram with a preset oscillogram;
and the guiding module is used for sending out prompt information according to the comparison result, and the prompt information is used for guiding a rescuer to rescue the patient.
Embodiments of the present invention also provide a computer-readable storage medium storing a computer program for cpr guidance, wherein the computer program for cpr guidance when executed performs: the cardiopulmonary resuscitation guidance method described above.
Drawings
In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings needed in the embodiments will be briefly described below, and it is obvious that the drawings in the following description are only some embodiments of the present invention, and it is obvious for those skilled in the art to obtain other drawings without creative efforts.
Fig. 1 is a flowchart of a first method for cardiopulmonary resuscitation guidance according to an embodiment of the present invention.
Fig. 2 is a flowchart of a second method for cardiopulmonary resuscitation guidance according to an embodiment of the present invention.
Fig. 3 is a flowchart of a third method for cardiopulmonary resuscitation guidance according to an embodiment of the present invention.
Fig. 4 is a flowchart of a fourth method for cardiopulmonary resuscitation guidance according to an embodiment of the present invention.
Fig. 5 is a flowchart of a fifth method for cardiopulmonary resuscitation guidance according to an embodiment of the present invention.
Fig. 6 is a schematic circuit diagram of a circuit for measuring a body impedance value of a patient in a cardiopulmonary resuscitation guidance method according to an embodiment of the present invention.
Fig. 7 is a flowchart of a sixth method for cardiopulmonary resuscitation guidance according to an embodiment of the present invention.
Fig. 8 is a flowchart of a seventh cpr guidance method according to an embodiment of the present invention.
Fig. 9 is a flowchart of an eighth method for cardiopulmonary resuscitation guidance according to an embodiment of the present invention.
Fig. 10 is a flowchart of a ninth method for cardiopulmonary resuscitation guidance according to an embodiment of the present invention.
Fig. 11 is a schematic structural diagram of a first cardiopulmonary resuscitation guidance device according to an embodiment of the present invention.
Fig. 12 is a schematic structural diagram of a second cpr guidance device according to an embodiment of the present invention.
Fig. 13 is a schematic structural diagram of a third cardiopulmonary resuscitation guidance device according to an embodiment of the present invention.
Fig. 14 is a schematic structural diagram of a fourth cardiopulmonary resuscitation guidance device according to an embodiment of the present invention.
Fig. 15 is a schematic structural diagram of a fifth cpr guidance device according to an embodiment of the present invention.
Fig. 16 is a schematic structural diagram of a sixth cardiopulmonary resuscitation guidance device according to an embodiment of the present invention.
Fig. 17 is a schematic structural diagram of a seventh cpr guidance device according to an embodiment of the present invention.
Fig. 18 is a schematic structural diagram of an eighth cpr guidance device according to an embodiment of the present invention.
Fig. 19 is a schematic structural diagram of a ninth cpr guidance device according to an embodiment of the present invention.
Detailed Description
The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the drawings in the embodiments of the present invention, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
Referring to fig. 1, fig. 1 is a flowchart illustrating a first method for guiding cpr according to an embodiment of the present invention. In the present embodiment, the cardiopulmonary resuscitation guidance method includes, but is not limited to, steps S100, S200, and S300, and the detailed description of steps S100, S200, and S300 is as follows.
S100: obtaining a thoracic impedance oscillogram of the patient during rescue.
Impedance refers to the resistance of a circuit having a resistor, an inductor, and a capacitor to a current in the circuit.
The method for acquiring the thoracic impedance oscillogram of the patient during rescue can be one-time acquisition or multiple-time acquisition. The process of obtaining the chest impedance oscillogram of the patient during rescue can be synchronously carried out with the process of comparing the chest impedance oscillogram with the preset oscillogram, namely, the chest impedance oscillogram of the patient during rescue is obtained, and part of the obtained chest impedance oscillogram is compared with the preset oscillogram, so that the rescuer is guided in real time, the rescuer can quickly respond according to the guidance, the timeliness of rescuing the patient is improved, and the quality of chest compression is ensured.
S200: and comparing the thoracic impedance oscillogram with a preset oscillogram.
The preset oscillogram can be a thoracic impedance oscillogram when a patient is rescued under an ideal condition.
In an embodiment, the preset waveform diagram may be an ideal waveform diagram obtained through multiple tests, where the preset waveform diagram refers to a waveform diagram obtained when the rescuer has sufficient physical strength and focuses attention.
In another embodiment, the preset waveform may also be a waveform downloaded from a database of the authorities, thereby ensuring that the obtained preset waveform is in compliance with the standard specification.
In yet another embodiment, the preset waveform may be a preset waveform obtained after training through a neural network model. The method comprises the steps of obtaining a large number of thoracic impedance oscillograms when a patient is rescued, inputting the obtained thoracic impedance oscillograms into a neural network model, carrying out algorithm processing on the input thoracic impedance oscillograms through data in a database, outputting results, and enabling the output results to be considered as ideal preset oscillograms and to accord with relevant standards.
Further, the preset waveform map may be obtained by downloading in real time, or may be obtained by storing in advance. When the preset oscillogram is acquired in a real-time downloading mode, the acquired preset oscillogram can be the latest released oscillogram, namely the acquired preset oscillogram is the oscillogram which meets the latest specification, so that the cardio-pulmonary resuscitation guidance of a patient can be ensured to meet the latest standard. When the preset oscillogram is obtained by pre-storing, the time consumed in the downloading process can be avoided, and the process of comparing the preset oscillogram with the obtained oscillogram can be quickly completed by adopting the preset oscillogram, so that the timeliness of guiding the rescuer is ensured, and the chest compression quality is further ensured.
The step of "S200: comparing the thoracic impedance profile to a predetermined profile includes, but is not limited to, the following steps.
And comparing the waveform parameters of the thoracic impedance oscillogram with the waveform parameters of a preset oscillogram, wherein the waveform parameters comprise at least one of frequency, amplitude and period.
S300: and sending out prompt information according to the comparison result, wherein the prompt information is used for guiding a rescuer to rescue the patient.
The oscillogram obtained when the patient is rescued is compared with a preset oscillogram, and the comparison indexes can be the conditions of comparing the frequency, the amplitude, the complete period and the like of the two oscillograms. And then feeding back to the rescuer in real time according to the comparison result, and rescuing the patient by the rescuer according to the comparison result. For specific guidance, reference is made to the following description, which is not to be construed as being overly limiting.
The cardiopulmonary resuscitation guidance method comprises the steps of firstly obtaining a thoracic impedance oscillogram of a patient during rescue, then comparing the obtained thoracic impedance oscillogram with a preset oscillogram, wherein the preset oscillogram is the thoracic impedance oscillogram of the patient during rescue under an ideal condition, and finally guiding a rescuer to rescue the patient according to a comparison result. The cardiopulmonary resuscitation guidance method provided by the embodiment of the invention is used for guiding the actual rescue process of cardiopulmonary resuscitation and is beneficial to ensuring the quality of chest compression.
Referring to fig. 2, fig. 2 is a flowchart illustrating a second method for guiding cpr according to an embodiment of the present invention. The second cpr coaching method is substantially the same as the first cpr coaching method except that the step "S200: comparing the frequency corresponding to the thoracic impedance oscillogram with the frequency corresponding to the preset oscillogram and the step S300: sending out prompt information according to the comparison result, wherein the prompt information is used for guiding the rescuer to rescue the patient, and the steps include, but are not limited to, steps S210 and S220, and the detailed description about the steps S210 and S220 is as follows.
S210: and comparing the frequency corresponding to the thoracic impedance oscillogram with the frequency corresponding to the preset oscillogram.
Where frequency is the number of times a periodic change is made per unit time and is a quantity describing how frequently the periodic movement is. Generally, for unskilled rescuers, the frequency of chest compression performed on a patient is usually less than the frequency corresponding to the preset waveform diagram, which is usually 100ppm, probably due to fear.
S220: when the frequency corresponding to the thoracic impedance oscillogram is less than the frequency corresponding to the preset oscillogram, prompt information is sent to a rescuer, and the prompt information prompts the rescuer to improve the compression speed when the rescuer performs chest compression on the patient.
The chest impedance oscillogram acquired when the patient is rescued is compared with the preset oscillogram in real time, and when the fact that the frequency corresponding to the acquired chest impedance oscillogram is smaller than the frequency corresponding to the preset oscillogram is detected, the rescuer is prompted to accelerate the pressing speed when chest pressing is carried out on the patient, so that the chest pressing quality of the patient is guaranteed.
It can be understood that, in other embodiments, the thoracic impedance oscillogram acquired when the patient is rescued is compared with the preset oscillogram in real time, and when it is detected that the frequency corresponding to the acquired thoracic impedance oscillogram is greater than the frequency corresponding to the preset oscillogram, the rescuer is prompted to slow down the pressing speed when the chest pressing is performed on the patient, so as to ensure the quality of the chest pressing performed on the patient. When the frequency corresponding to the acquired thoracic impedance oscillogram is detected to be consistent with the frequency corresponding to the preset oscillogram, no prompt message is sent out, or normal pressing is prompted, and the current pressing frequency is continued to be maintained.
Referring to fig. 3, fig. 3 is a flowchart illustrating a third method for guiding cardiopulmonary resuscitation according to an embodiment of the present invention. The third cpr coaching method is substantially the same as the first cpr coaching method except that the step "S200: comparing the frequency corresponding to the thoracic impedance oscillogram with the frequency corresponding to the preset oscillogram and the step S300: sending out prompt information according to the comparison result, wherein the prompt information is used for guiding the rescuer to rescue the patient, including but not limited to steps S230 and S240, and the detailed description about steps S230 and S240 is as follows.
S230: and comparing the amplitude corresponding to the thoracic impedance oscillogram with the amplitude corresponding to the preset oscillogram.
Wherein the amplitude is half the peak to trough distance over a period. Generally, for unskilled rescuers, the amplitude of chest compression is usually less than the frequency corresponding to the preset waveform pattern, which may be a fear of mind when performing chest compression on a patient.
The amplitude of the acquired chest impedance oscillogram is compared with the amplitude of the preset oscillogram, and only the difference value operation needs to be carried out on the amplitude of the preset oscillogram and the amplitude of the acquired chest impedance oscillogram, so that the difference value between the amplitude of the acquired chest impedance oscillogram and the amplitude of the preset oscillogram can be acquired very intuitively, and the chest compression process of a rescuer can be guided in real time according to the difference value, and the chest compression quality is improved.
S240: when the amplitude corresponding to the thoracic impedance oscillogram is smaller than the amplitude corresponding to the preset oscillogram, prompt information is sent to the rescuer, and the prompt information prompts the rescuer to increase the compression depth when the chest compression is carried out on the patient.
The chest impedance oscillogram acquired when the patient is rescued is compared with the preset oscillogram in real time, and when the fact that the amplitude corresponding to the acquired chest impedance oscillogram is smaller than the amplitude corresponding to the preset oscillogram is detected, the rescuer is prompted to increase the pressing depth when chest pressing is carried out on the patient, so that the chest pressing quality of the patient is guaranteed.
Here, the compression depth is related to the degree of compression to some extent, and therefore, the compression depth at the time of chest compression on the patient can be increased by increasing the degree of compression.
It can be understood that, in other embodiments, the chest impedance oscillogram acquired when the patient is rescued is compared with the preset oscillogram in real time, and when the amplitude corresponding to the acquired chest impedance oscillogram is detected to be smaller than the amplitude corresponding to the preset oscillogram, the rescuer is prompted to reduce the compression depth when the chest compression is performed on the patient, so as to ensure the quality of the chest compression performed on the patient. When the amplitude corresponding to the acquired thoracic impedance oscillogram is detected to be consistent with the amplitude corresponding to the preset oscillogram, no prompt information is sent out, or normal pressing is prompted, and the current pressing depth is continued to be maintained.
Referring to fig. 4, fig. 4 is a flowchart illustrating a fourth method for guiding cardiopulmonary resuscitation according to an embodiment of the present invention. The fourth cpr coaching method is substantially the same as the first cpr coaching method except that the step "S200: comparing the frequency corresponding to the thoracic impedance oscillogram with the frequency corresponding to the preset oscillogram and the step S300: sending out prompt information according to the comparison result, wherein the prompt information is used for guiding the rescuer to rescue the patient, and the steps include, but are not limited to, steps S250 and S260, and the detailed description about the steps S250 and S260 is as follows.
S250: and comparing the thoracic impedance oscillogram with a preset oscillogram to judge whether the period of the thoracic impedance oscillogram is complete.
Where the period is the time required to complete one complete waveform change. Since there is a correspondence between the period of chest compressions and the frequency of the heart beat, whether the chest compression period is complete will directly affect the beat frequency of the heart. The standard preset oscillogram generally shows obvious periodic variation, and for unskilled rescuers, the acquired thoracic impedance oscillogram for rescuing patients generally has no obvious period, so that whether chest compression meets the standard or not during rescuing patients can be judged according to whether the period of the acquired thoracic impedance oscillogram is complete, and the rescuers are informed to rescue the patients by adopting a corresponding guidance strategy.
S260: when the period of the thoracic impedance oscillogram is incomplete, prompt information is sent to the rescuer, and the prompt information prompts the rescuer to improve the speed of the rescuer that the hands leave the body of the patient when the rescuer performs chest compression on the patient.
The chest impedance oscillogram obtained when the patient is rescued is compared with the preset oscillogram in real time, when the fact that the corresponding period of the obtained chest impedance oscillogram is incomplete is detected, pressing resilience of the patient during chest pressing is insufficient, and when the rescuer is prompted to perform chest pressing on the patient, the speed of the rescuer that the hands leave the body of the patient is improved. In addition, the degree of compression also affects the period corresponding to the acquired thoracic impedance oscillogram, so in some embodiments, the degree of compression during chest compression needs to be synchronously adjusted, and the completeness of the period during chest compression on a patient can be ensured by increasing the degree of compression.
It can be understood that, in other embodiments, the thoracic impedance oscillogram acquired when the patient is rescued is compared with the preset oscillogram in real time, and when the incomplete period corresponding to the acquired thoracic impedance oscillogram is detected, the rescuer is prompted to reduce the speed of the hand leaving the body of the patient, so as to ensure the quality of the chest compression on the patient. When the waveform integrity degree corresponding to the acquired thoracic impedance oscillogram is detected to be consistent with the waveform integrity degree corresponding to the preset oscillogram, no prompt message is sent, or normal pressing is prompted, and a current pressing state is continued to be maintained.
Referring to fig. 5, fig. 5 is a flowchart illustrating a fifth method for guiding cpr according to an embodiment of the present invention. The fifth cpr coaching method is substantially the same as the first cpr coaching method except that, at step "S100: before acquiring the thoracic impedance oscillogram of the patient during rescue, "the cpr guidance method further includes, but is not limited to, steps S80 and S90, and the details of steps S80 and S90 are as follows.
S80: and adhering the electrode slice to a preset part of the body of the patient, and acquiring an initial impedance value of the patient when the patient is not rescued.
Whether the electrode plates are normally attached to preset parts of the body of a patient directly influences the compression quality during chest compression, and therefore the attachment of the electrode plates is equivalent to the pretreatment process of chest compression.
The initial impedance corresponds to the impedance value of the patient's body at rest. Whether the electrode plate is attached or not is judged by measuring an initial impedance value when chest compression is not performed on a patient. If the electrode slice is normally attached to the preset part of the body of the patient, the subsequent external chest compression process can be started for the patient, and on the contrary, if the electrode slice is not normally attached to the preset part of the body of the patient, the position of the electrode slice on the body of the patient needs to be adjusted, so that the electrode slice is in a normally attached state.
S90: and judging whether the electrode plate is in a normal attaching state or not according to the initial impedance value.
Specifically, the resistance value corresponding to the electrode sheet in the normal attaching state should be in a range of 100 ohms to 600 ohms. When the resistance measured according to the electrode sheet is greater than 600 ohms, it may be because the electrode sheet is not completely attached to the body of the patient, so that the circuit of the detection resistor on the electrode sheet has an open circuit effect. When the resistance measured according to the electrode sheets is less than 100 ohms, it may be because the distance between the two electrode sheets is too close, and thus, the distance between the two electrode sheets needs to be adaptively adjusted so that the resistance measured according to the electrode sheets is within a preset range. The resistance value and the impedance have a corresponding relation, and when the resistance value is within a preset range, the impedance also accords with a normal value.
Further, with continued reference to FIG. 6, for the measurement of the patient's body impedance values, a circuit schematic as in FIG. 6 may be employed. When the electrode pad is attached to a human body, the equivalent impedance is as shown in fig. 6. Wherein Z1 and Z2 are equivalent impedance models of the electrode sheet contacting with the human body. When an alternating current carrier signal with a certain frequency is driven to a human body, a certain signal amplitude can be obtained on a chest resistance Z3 of the human body, and a corresponding impedance value can be obtained by sampling the signal amplitudes at two ends of Z3 and calculating through a certain algorithm. When the electrode plate is well connected with a human body, a stable impedance value can be measured by an alternating current small signal method.
Referring to fig. 7, fig. 7 is a flowchart illustrating a sixth method for guiding cpr according to an embodiment of the present invention. The sixth cpr coaching method is substantially the same as the fifth cpr coaching method except that the step "S90: the "determination of whether or not the electrode sheet is in the normal attached state based on the initial resistance value" includes, but is not limited to, steps S91, S92, and S93, and the following is introduced with respect to steps S91, S92, and S93.
S91: and judging whether the initial impedance value is between a first threshold value and a second threshold value, wherein the first threshold value is smaller than the second threshold value.
The first threshold may be an impedance value corresponding to a resistance of 100 ohms, and the second threshold may be an impedance value corresponding to a resistance of 600 ohms.
S92: and when the initial impedance value is between the first threshold value and the second threshold value, judging that the electrode plate is in a normal attaching state.
When the electrode slice is in a normal attaching state, the external chest compression operation can be performed on the patient.
S93: when the initial impedance value is smaller than the first threshold value or the initial impedance value is larger than the second threshold value, the electrode plate is judged to be in an abnormal attaching state, and prompt information is sent to a rescuer to guide the rescuer to attach the electrode plate again.
When the electrode slice is in the abnormal attaching state, the rescuers need to be reminded to attach the electrode slice again, and when the electrode slice is in the normal attaching state, the external chest pressing operation is carried out on the patient again.
Referring to fig. 8, fig. 8 is a flowchart illustrating a seventh cpr guidance method according to an embodiment of the present invention. The seventh cpr coaching method is substantially the same as the first cpr coaching method except that, at step "S92: after determining that the electrode pads are in the normal fit state "when the initial impedance value is between the first threshold and the second threshold, the cpr guidance method further includes, but is not limited to, steps S921, S922, S923, and S924, which are described below with respect to steps S921, S922, S923, and S924.
S921: an electrocardiogram signal of the patient is acquired.
Among them, Electrocardiogram (ECG) is a technique of recording a pattern of change in electrical activity generated every cardiac cycle of a heart from a body surface using an electrocardiograph.
S922: whether the patient is in a shockable rhythm is determined from the electrocardiogram signal.
A shockable rhythm refers to a state that satisfies electrical defibrillation, among other things. Electrical defibrillation, which is a method of stopping ventricular fibrillation by striking the heart with a certain amount of current, is an effective method of treating ventricular fibrillation. At present, except that the in vivo defibrillation (ventricular fibrillation) is carried out by using alternating current in the heart operation process, the defibrillation is generally carried out by using direct current.
S923: when the patient is in a shockable rhythm, the charging circuit is turned on.
S924: after the charging circuit finishes charging, the rescuer is prompted to start the discharging circuit to perform discharging treatment on the patient.
The discharge therapy is electrical defibrillation therapy. In an embodiment, precharge charging circuit in advance to make energy storage unit store sufficient electric quantity, when detecting that the patient is in the rhythm state of can shocking by electricity, direct suggestion rescuer carries out the treatment of discharging to the patient, thereby can save the time of charging storage, the timeliness when helping improving the patient to salvage, and then ensure to carry out the quality of pressing outside the chest to the patient, this kind of rescue mode is the rescue mode of a semi-automatic formula, needs the rescuer to participate in the discharge treatment of defibrillating.
Referring to fig. 9, fig. 9 is a flowchart illustrating an eighth method for guiding cardiopulmonary resuscitation according to an embodiment of the present invention. The eighth cpr coaching method is substantially the same as the first cpr coaching method except that, at step "S92: after determining that the electrode pad is in the normal fit state "when the initial impedance value is between the first threshold and the second threshold, the cpr guidance method further includes, but is not limited to, steps S925, S926, and S927, which are described below with respect to steps S925, S926, and S927.
S925: an electrocardiogram signal of the patient is acquired.
Among them, Electrocardiogram (ECG) is a technique of recording a pattern of change in electrical activity generated every cardiac cycle of a heart from a body surface using an electrocardiograph.
S926: whether the patient is in a shockable rhythm is determined from the electrocardiogram signal.
A shockable rhythm refers to a state that satisfies electrical defibrillation, among other things. Electrical defibrillation, which is a method of stopping ventricular fibrillation by striking the heart with a certain amount of current, is an effective method of treating ventricular fibrillation. At present, except that the in vivo defibrillation (ventricular fibrillation) is carried out by using alternating current in the heart operation process, the defibrillation is generally carried out by using direct current.
S927: when the patient is in the shockable rhythm state, after a preset time period, the patient is automatically subjected to discharge treatment.
Specifically, automatic external defibrillation equipment has timing circuit, and when the patient satisfied the condition of shock defibrillation, timing circuit opened immediately, and timing circuit has the countdown function, and after the length of time of predetermineeing, the automatic treatment of defibrillating of shocking to the patient to the time of control rescue that can be more accurate. The rescue mode is a full-automatic rescue mode, and is automatically completed by automatic external defibrillation equipment without a rescuer participating in defibrillation discharge treatment.
Referring to fig. 10, fig. 10 is a flowchart illustrating a ninth method for guiding cardiopulmonary resuscitation according to an embodiment of the present invention. The ninth cpr coaching method is substantially the same as the first cpr coaching method except that the "S925: acquiring an electrocardiogram signal of the patient "includes, but is not limited to, steps S9251, S9252 and S9253, and detailed descriptions about steps S9251, S9252 and S9253 are as follows.
S9251: a first signal is detected when the electrode patch is attached to the patient's body.
S9252: it is determined whether a second signal characteristic of the pacemaker is present in the first signal.
Among them, pacemakers are important components of pacing systems. The pacing system consists of a pacemaker, a pacing electrode lead and a program controller. Wherein the pacemaker and the pacing electrode lead are implanted in a human body. The pacemaker consists of a circuit and a battery mounted in a metal case.
The pacemaker sends tiny electric pulses to the heart when needed, and the pacing electrode lead consists of insulated leads and is responsible for transmitting the tiny electric pulses to the heart to stimulate the heart to beat.
S9253: when the second signal which is characterized by the pacemaker exists in the first signal, the electrocardiogram signal is obtained by subtracting the second signal from the first signal, and when the second signal which is characterized by the pacemaker does not exist in the first signal, the first signal is set as the electrocardiogram signal.
When the patient wears the pacemaker, the pacemaker can interfere with the judgment of whether the patient meets the electric shock condition, so that the interference of the pacemaker can be removed in the embodiment to avoid misjudgment.
Referring to fig. 11, fig. 11 is a schematic structural diagram of a first cpr guidance device according to an embodiment of the present invention. In the present embodiment, the cpr guidance device 10 includes, but is not limited to, the first acquisition module 100, the alignment module 200 and the guidance module 300, which are described below with respect to the first acquisition module 100, the alignment module 200 and the guidance module 300.
The first acquiring module 100 is used for acquiring a thoracic impedance oscillogram of a patient during rescue.
A comparison module 200 for comparing the thoracic impedance oscillogram with a preset oscillogram.
The preset oscillogram can be a thoracic impedance oscillogram when a patient is rescued under an ideal condition.
The comparison module 200 comprises a sub-comparison module 201, wherein the sub-comparison module 201 is configured to compare waveform parameters of the thoracic impedance oscillogram with waveform parameters of a preset oscillogram, wherein the waveform parameters include at least one of frequency, amplitude and period.
And the guiding module 300 is configured to send out prompt information according to the comparison result, where the prompt information is used to guide a rescuer to rescue the patient.
Referring to fig. 12, fig. 12 is a schematic structural diagram of a second cpr guidance device according to an embodiment of the present invention. The structure of the second cpr coaching device 10 is substantially the same as the structure of the first cpr coaching device 10 except that the comparison module 200 includes, but is not limited to, a first comparison module 210 and a first sending module 220, which are described below with respect to the first comparison module 210 and the first sending module 220.
The first comparing module 210 is configured to compare a frequency corresponding to the thoracic impedance oscillogram with a frequency corresponding to a preset oscillogram.
The first sending module 220 is configured to send a prompt message to the rescuer when the frequency corresponding to the thoracic impedance oscillogram is smaller than the frequency corresponding to the preset oscillogram, where the prompt message prompts the rescuer to increase the compression speed when performing chest compression on the patient.
Referring to fig. 13, fig. 13 is a schematic structural diagram of a third cpr guidance device according to an embodiment of the present invention. The third cpr guidance device 10 has substantially the same structure as the first cpr guidance device 10, except that the comparison module 200 includes, but is not limited to, a second comparison module 230 and a second sending module 240, which are described below with respect to the second comparison module 230 and the second sending module 240.
And a second comparing module 230 for comparing the amplitude corresponding to the thoracic impedance oscillogram with the amplitude corresponding to the preset oscillogram.
And a second sending module 240, configured to send a prompt message to the rescuer when the amplitude corresponding to the thoracic impedance oscillogram is smaller than the amplitude corresponding to the preset oscillogram, where the prompt message prompts the rescuer to increase the compression depth when performing chest compression on the patient.
Referring to fig. 14, fig. 15 is a schematic structural diagram of a fourth cpr guidance device according to an embodiment of the present invention. The fourth cpr guidance device 10 has substantially the same structure as the first cpr guidance device 10, except that the comparison module 200 includes, but is not limited to, a third comparison module 250 and a third sending module 260, which are described below with respect to the third comparison module 250 and the third sending module 260.
A third comparing module 250, configured to compare the thoracic impedance oscillogram with the preset oscillogram to determine whether the period of the thoracic impedance oscillogram is complete.
And the third sending module 260 is used for sending prompt information to the rescuer when the period of the thoracic impedance oscillogram is incomplete, and the prompt information prompts the rescuer to improve the speed of the rescuer that the hand leaves the body of the patient when the rescuer performs chest compression on the patient.
Referring to fig. 15, fig. 15 is a schematic structural diagram of a fifth cpr guidance device according to an embodiment of the present invention. The structure of the fifth cpr coaching device 10 is substantially the same as the structure of the first cpr coaching device 10, except that the cpr coaching device 10 further includes, but is not limited to, the second acquiring module 110 and the determining module 500, and the description about the second acquiring module 110 and the determining module 500 is as follows.
The second obtaining module 110 is configured to attach the electrode sheet to a preset portion of the body of the patient, and obtain an initial impedance value of the patient when the patient is not rescued.
And the judging module 500 is used for judging whether the electrode plate is in a normal attaching state according to the initial impedance value.
Referring to fig. 16, fig. 16 is a schematic structural diagram of a sixth cpr guidance device according to an embodiment of the present invention. The structure of the sixth cpr guidance device 10 is substantially the same as the structure of the fifth cpr guidance device 10, except that the judgment module 500 includes, but is not limited to, a first sub-judgment module 510, a first judgment module 520 and a second judgment module 530, and the description about the first sub-judgment module 510, the first judgment module 520 and the second judgment module 530 is as follows.
The first sub-determination module 510 is configured to determine whether the initial impedance value is between a first threshold and a second threshold, where the first threshold is smaller than the second threshold.
The first determination module 520 is configured to determine that the electrode sheet is in a normal attachment state when the initial impedance value is between a first threshold and a second threshold.
And the second determination module 530 is configured to determine that the electrode sheet is in an abnormal attachment state when the initial impedance value is smaller than the first threshold value or the initial impedance value is larger than the second threshold value, and send a prompt message to a rescuer to guide the rescuer to attach the electrode sheet again.
Referring to fig. 17, fig. 17 is a schematic structural diagram of a seventh cpr guidance device according to an embodiment of the present invention. The structure of the seventh cpr guidance device 10 is substantially the same as the structure of the first cpr guidance device 10, except that the cpr guidance device 10 further includes, but is not limited to, a third acquiring module 120, a second sub-determining module 540, an enabling module 410 and a prompting module 600, and the third acquiring module 120, the second sub-determining module 540, the enabling module 410 and the prompting module 600 are described as follows.
A third obtaining module 120 is configured to obtain an electrocardiogram signal of the patient.
And a second sub-determining module 540 for determining whether the patient is in a shockable rhythm state according to the electrocardiogram signal.
A power-on module 410 for powering on the charging circuit when the patient is in a shockable rhythm.
And the prompt module 600 is used for prompting the rescuer to start the discharging circuit to perform discharging treatment on the patient after the charging circuit finishes charging.
Referring to fig. 18, fig. 18 is a schematic structural diagram of an eighth cpr guidance device according to an embodiment of the present invention. The eighth cpr coaching device 10 has substantially the same structure as the first cpr coaching device 10 except for the first acquisition module 100 for acquiring an electrocardiogram signal of the patient. The cardiopulmonary resuscitation guidance device 10 further includes, but is not limited to, a third sub-judgment module 500 and a discharge module 700, which are described below with respect to the third sub-judgment module 550 and the discharge module 700.
And a third sub-determination module 550 for determining whether the patient is in a shockable rhythm state based on the electrocardiogram signal.
And the discharging module 700 is used for automatically performing discharging treatment on the patient after a preset time period when the patient is in the shockable rhythm state.
Referring to fig. 19, fig. 19 is a schematic structural diagram of a ninth cpr guidance device according to an embodiment of the present invention. The structure of the ninth cpr guidance device 10 is substantially the same as the structure of the first cpr guidance device 10, except that the first acquiring module 100 includes, but is not limited to, a detecting module 800, a fourth sub-determining module 560 and a setting module 900, and the following description is provided for the detecting module 800, the fourth sub-determining module 560 and the setting module 900.
The detecting module 800 is configured to detect a first signal when the electrode sheet is attached to the body of the patient.
And a fourth sub-determination module 560 for determining whether the second signal indicative of the pacemaker is present in the first signal.
The setting module 900 is configured to subtract the second signal from the first signal to obtain an electrocardiogram signal when the second signal characterizing the pacemaker exists in the first signal, and set the first signal as the electrocardiogram signal when the second signal characterizing the pacemaker does not exist in the first signal.
The present invention also provides a computer-readable storage medium storing a computer program for cardiopulmonary resuscitation guidance, wherein the computer program for cardiopulmonary resuscitation guidance, when executed, performs: the method of cardiopulmonary resuscitation guidance as provided in any one of the preceding embodiments.
Embodiments of the present application also provide a computer program product comprising a non-transitory computer readable storage medium storing a computer program operable to cause a computer to perform some or all of the steps of any of the methods as set forth in the above-described cardiopulmonary resuscitation guidance method embodiments. The computer program product may be a software installation package and the computer comprises the cardiopulmonary resuscitation guidance device.
It should be noted that, for simplicity of description, the above-mentioned method embodiments are described as a series of acts or combination of acts, but those skilled in the art will recognize that the present application is not limited by the order of acts described, as some steps may occur in other orders or concurrently depending on the application. Further, those skilled in the art should also appreciate that the embodiments described in the specification are preferred embodiments and that the acts and modules referred to are not necessarily required in this application.
In the foregoing embodiments, the descriptions of the respective embodiments have respective emphasis, and for parts that are not described in detail in a certain embodiment, reference may be made to related descriptions of other embodiments.
In the embodiments provided in the present application, it should be understood that the disclosed apparatus may be implemented in other manners. For example, the above-described embodiments of the apparatus are merely illustrative, and for example, a division of a unit is merely a logical division, and an actual implementation may have another division, for example, a plurality of units or components may be combined or integrated into another system, or some features may be omitted, or not executed. In addition, the shown or discussed mutual coupling or direct coupling or communication connection may be an indirect coupling or communication connection of some interfaces, devices or units, and may be an electric or other form.
Units described as separate parts may or may not be physically separate, and parts displayed as units may or may not be physical units, may be located in one place, or may be distributed on a plurality of network units. Some or all of the units can be selected according to actual needs to achieve the purpose of the solution of the embodiment.
In addition, functional units in the embodiments of the present application may be integrated into one processing unit, or each unit may exist alone physically, or two or more units are integrated into one unit. The integrated unit can be realized in a form of hardware, and can also be realized in a form of a software functional unit.
The integrated unit, if implemented in the form of a software functional unit and sold or used as a stand-alone product, may be stored in a computer readable memory. Based on such understanding, the technical solution of the present application may be substantially implemented or a part of or all or part of the technical solution contributing to the prior art may be embodied in the form of a software product stored in a memory, and including several instructions for causing a computer device (which may be a personal computer, a server, or a network device) to execute all or part of the steps of the method of the embodiments of the present application. And the aforementioned memory comprises: various media capable of storing program codes, such as a usb disk, a Read-Only Memory (ROM), a Random Access Memory (RAM), a removable hard disk, a magnetic disk, or an optical disk.
Those skilled in the art will appreciate that all or part of the steps in the methods of the above embodiments may be implemented by associated hardware instructed by a program, which may be stored in a computer-readable memory, which may include: flash disks, Read-Only memories (ROMs), Random Access Memories (RAMs), magnetic or optical disks, and the like.
Finally, it should be noted that: the above examples are only intended to illustrate the technical solution of the present invention, but not to limit it; although the present invention has been described in detail with reference to the foregoing embodiments, it will be understood by those of ordinary skill in the art that: the scope of the present invention is not limited thereto, and any changes or substitutions that can be easily made by those skilled in the art within the technical scope of the present invention will be covered by the scope of the present invention. Therefore, the protection scope of the present invention shall be subject to the protection scope of the claims.

Claims (21)

  1. A method for cardiopulmonary resuscitation guidance, comprising:
    acquiring a thoracic impedance oscillogram of a patient during rescue;
    comparing the thoracic impedance oscillogram with a preset oscillogram;
    and sending out prompt information according to the comparison result, wherein the prompt information is used for guiding a rescuer to rescue the patient.
  2. The cardiopulmonary resuscitation guidance method of claim 1 wherein said comparing said thoracic impedance profile to a predetermined profile comprises:
    and comparing the waveform parameters of the thoracic impedance oscillogram with the waveform parameters of a preset oscillogram, wherein the waveform parameters comprise at least one of frequency, amplitude and period.
  3. The cardiopulmonary resuscitation guidance method of claim 1, wherein the comparing the thoracic impedance oscillogram with a preset oscillogram and sending a prompt message for instructing a rescuer to rescue the patient according to the comparison comprises:
    comparing the frequency corresponding to the thoracic impedance oscillogram with the frequency corresponding to the preset oscillogram;
    and when the frequency corresponding to the thoracic impedance oscillogram is less than the frequency corresponding to the preset oscillogram, sending prompt information to the rescuer, wherein the prompt information prompts the rescuer to improve the compression speed of the patient during chest compression.
  4. The cardiopulmonary resuscitation guidance method of claim 1, wherein the comparing the thoracic impedance oscillogram with a preset oscillogram and sending a prompt message for instructing a rescuer to rescue the patient according to the comparison comprises:
    comparing the amplitude corresponding to the thoracic impedance oscillogram with the amplitude corresponding to the preset oscillogram;
    and when the amplitude corresponding to the thoracic impedance oscillogram is smaller than the amplitude corresponding to the preset oscillogram, sending prompt information to the rescuer, wherein the prompt information prompts the rescuer to increase the compression depth when the chest compression is performed on the patient.
  5. The cardiopulmonary resuscitation guidance method of claim 1, wherein the comparing the thoracic impedance oscillogram with a preset oscillogram and sending a prompt message for instructing a rescuer to rescue the patient according to the comparison comprises:
    comparing the thoracic impedance oscillogram with the preset oscillogram to judge whether the period of the thoracic impedance oscillogram is complete or not;
    when the period of the thoracic impedance oscillogram is incomplete, prompt information is sent to the rescuer, and the prompt information prompts the rescuer to improve the speed of the rescuer that the hands leave the body of the patient when the rescuer performs chest compression on the patient.
  6. The cardiopulmonary resuscitation guidance method of claim 1 further comprising, prior to said obtaining a rescue time patient thoracic impedance waveform map:
    adhering the electrode slice to a preset part of the body of a patient, and acquiring an initial impedance value of the patient when the patient is not rescued;
    and judging whether the electrode plate is in a normal attaching state or not according to the initial impedance value.
  7. The cardiopulmonary resuscitation guidance method of claim 6, wherein the determining whether the electrode pad is in a normal fit state according to the initial impedance value comprises:
    judging whether the initial impedance value is between a first threshold value and a second threshold value, wherein the first threshold value is smaller than the second threshold value;
    when the initial impedance value is between the first threshold value and the second threshold value, determining that the electrode sheet is in a normal fit state;
    when the initial impedance value is smaller than the first threshold value or the initial impedance value is larger than the second threshold value, the electrode plate is judged to be in an abnormal attaching state, and prompt information is sent to the rescuer to guide the rescuer to attach the electrode plate again.
  8. The cardiopulmonary resuscitation guidance method of claim 1, further comprising:
    acquiring an electrocardiogram signal of a patient;
    determining whether the patient is in a shockable rhythm state based on the electrocardiogram signal;
    turning on a charging circuit when the patient is in a shockable rhythm state;
    and after the charging circuit finishes charging, prompting a rescuer to start the discharging circuit so as to carry out discharging treatment on the patient.
  9. The cardiopulmonary resuscitation guidance method of claim 1, further comprising:
    acquiring an electrocardiogram signal of a patient;
    determining whether the patient is in a shockable rhythm state based on the electrocardiogram signal;
    when the patient is in a shockable rhythm state, automatically carrying out discharge treatment on the patient after a preset time period.
  10. The cardiopulmonary resuscitation guidance method of claim 1 wherein said obtaining an electrocardiogram signal of a patient comprises:
    detecting a first signal when the electrode sheet is attached to the body of the patient;
    judging whether a second signal which is characterized by a pacemaker exists in the first signal;
    and when the second signal which is characterized by the pacemaker exists in the first signal, subtracting the second signal from the first signal to obtain the electrocardiogram signal, and when the second signal which is characterized by the pacemaker does not exist in the first signal, setting the first signal as the electrocardiogram signal.
  11. A cardiopulmonary resuscitation guidance device, comprising:
    the first acquisition module is used for acquiring a thoracic impedance oscillogram of a patient during rescue;
    the comparison module is used for comparing the thoracic impedance oscillogram with a preset oscillogram;
    and the guiding module is used for sending out prompt information according to the comparison result, and the prompt information is used for guiding a rescuer to rescue the patient.
  12. The cardiopulmonary resuscitation guidance device of claim 11, wherein said alignment module comprises:
    and the sub-comparison module is used for comparing the waveform parameters of the thoracic impedance oscillogram with the waveform parameters of a preset oscillogram, wherein the waveform parameters comprise at least one of frequency, amplitude and period.
  13. The cardiopulmonary resuscitation guidance device of claim 11 wherein said alignment module comprises:
    the first comparison module is used for comparing the frequency corresponding to the thoracic impedance oscillogram with the frequency corresponding to the preset oscillogram;
    the guidance module comprises:
    and the first sending module is used for sending prompt information to the rescuer when the frequency corresponding to the thoracic impedance oscillogram is smaller than the frequency corresponding to the preset oscillogram, wherein the prompt information prompts the rescuer to improve the compression speed of the patient during chest compression.
  14. The cardiopulmonary resuscitation guidance device of claim 11, wherein said alignment module comprises:
    the second comparison module is used for comparing the amplitude corresponding to the thoracic impedance oscillogram with the amplitude corresponding to the preset oscillogram;
    the guidance module comprises:
    and the second sending module is used for sending prompt information to the rescuer when the amplitude corresponding to the thoracic impedance oscillogram is smaller than the amplitude corresponding to the preset oscillogram, wherein the prompt information prompts the rescuer to increase the compression depth of the patient during chest compression.
  15. The cardiopulmonary resuscitation guidance device of claim 11, wherein said alignment module comprises:
    a third comparing module, configured to compare the thoracic impedance oscillogram with the preset oscillogram to determine whether a cycle of the thoracic impedance oscillogram is complete;
    the guidance module comprises:
    and the third sending module is used for sending prompt information to the rescuer when the period of the thoracic impedance oscillogram is incomplete, wherein the prompt information prompts the rescuer to improve the speed of the rescuer that the hand leaves the body of the patient when the rescuer performs chest compression on the patient.
  16. The cardiopulmonary resuscitation guidance device of claim 11 further comprising:
    the second acquisition module is used for adhering the electrode slice to a preset part of the body of the patient and acquiring an initial impedance value of the patient when the patient is not rescued;
    and the judging module is used for judging whether the electrode plate is in a normal attaching state or not according to the initial impedance value.
  17. The cardiopulmonary resuscitation guidance device of claim 16 wherein said means for determining comprises:
    the first sub-judgment module is used for judging whether the initial impedance value is between a first threshold value and a second threshold value, wherein the first threshold value is smaller than the second threshold value;
    the first judging module is used for judging that the electrode plate is in a normal attaching state when the initial impedance value is between the first threshold value and the second threshold value;
    and the second judging module is used for judging that the electrode plate is in an abnormal attaching state when the initial impedance value is smaller than the first threshold value or the initial impedance value is larger than the second threshold value, and sending prompt information to the rescuer to guide the rescuer to attach the electrode plate again.
  18. The cardiopulmonary resuscitation guidance device of claim 11 further comprising:
    a third acquisition module for acquiring an electrocardiogram signal of the patient;
    the second sub-judgment module is used for judging whether the patient is in a shockable rhythm state or not according to the electrocardiogram signal;
    a starting module for starting a charging circuit when the patient is in a shockable rhythm state;
    and the prompting module is used for prompting a rescuer to start the discharging circuit to perform discharging treatment on the patient after the charging circuit finishes charging.
  19. The cardiopulmonary resuscitation guidance device of claim 11, wherein the first acquisition module is configured to acquire an electrocardiogram signal of the patient;
    the cardiopulmonary resuscitation guidance device further comprises:
    a third sub-judgment module for judging whether the patient is in a shockable rhythm state according to the electrocardiogram signal;
    and the discharging module is used for automatically carrying out discharging treatment on the patient after a preset time when the patient is in a shockable rhythm state.
  20. The cardiopulmonary resuscitation guidance device of claim 11, wherein said first acquisition module comprises:
    the detection module is used for detecting a first signal when the electrode slice is pasted on the body of a patient;
    the fourth sub-judgment module is used for judging whether a second signal representing a pacemaker exists in the first signal;
    the setting module is used for subtracting the second signal from the first signal to obtain an electrocardiogram signal when the second signal which is used for representing the pacemaker exists in the first signal, and setting the first signal as the electrocardiogram signal when the second signal which is used for representing the pacemaker does not exist in the first signal.
  21. A computer-readable storage medium storing a computer program for cardiopulmonary resuscitation guidance, wherein the cardiopulmonary resuscitation guidance computer program when executed performs: the cardiopulmonary resuscitation guidance method of any one of claims 1-10.
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