Abstract: The present invention provides an information acquisition device, comprising: a cushion for supporting a subject to be tested; a neck pillow for the subject to be tested to place his neck thereon; a fiber-optic sensor group for obtaining physical signs of the subject to be tested; and a signal acquisition module connected to the fiber-optic sensor group; wherein the signal acquisition module is wrapped in the neck pillow, the fiber-optic sensor group is placed in the cushion, and the neck pillow is connected with the cushion. In the present invention, by setting a neck pillow connected with the cushion so that the subject can adjust the body position independently without assistance to a preferred measurement position, and can complete information acquisition by himself. In addition, the signal acquisition module is placed in the neck pillow, so that the structure of the information acquisition device is more concise.

Abstract: Disclosed is a cardiac diastolic function assessment method applicable to the field of cardiac monitoring. The method comprises: acquiring vibration information of the thoracic cavity body surface of an object in a noninvasive manner; preprocessing the vibration information to generate hemodynamic-related information; determining a target wave group on the basis of the hemodynamic-related information; determining the highest peak on the target wave group, determining a rising edge amplitude before the highest peak as a first characteristic value, and determining, as a second characteristic value, an amplitude between the highest peak and the subsequent lowest valley; and generating an indicating parameter on the basis of the first characteristic value and the second characteristic value, and assessing a cardiac diastolic function of the object on the basis of the indicating parameter.

Abstract: A cardiac diastolic function assessment method, for use in the field of cardiac monitoring. The method comprises: noninvasively acquiring vibration information of the thoracic body surface of a subject; preprocessing the vibration information to generate hemodynamics-related information; determining a first parameter and a second parameter on the basis of the hemodynamics-related information; generating an indicating parameter on the basis of the first parameter and of the second parameter, and assessing the cardiac diastolic function of the subject on the basis of the indicating parameter.

Abstract: A method for obtaining a vital signal, includes steps of: acquiring cardiac vibration signals of the subject through at least one vibration sensor placed under the back of the supine subject, and acquiring the ECG data of the subject synchronously; performing data validation testing on the ECG data and the cardiac vibration signals to generate a total validation duration of the ECG data and a total validation duration of the cardiac vibration signals; and determining an end of data acquisition based on the total validation duration of the ECG data and the total validation duration of the cardiac vibration signals.

Abstract: A method for evaluating cardiac diastolic function, which applies to the field of cardiac monitoring. The method comprises: obtaining vibration information of the surface of the thoracic cavity of a subject by means of one or more optical fiber sensors; preprocessing the vibration information to generate hemodynamic related information; performing high-frequency component extraction on the hemodynamic related information to generate high-frequency component information; determining a first feature value and a second feature value based on the hemodynamic related information and the high-frequency component information; generating indicating parameters based on the first feature value and the second feature value, and evaluating the cardiac diastolic function of the subject based on the indicating parameters.

Abstract: Provided are a heart physiological parameter measurement method, device and terminal, and a computer storage medium. The method comprises: respectively obtaining back vibration information and shoulder vibration information of an object to be measured in a supine state by means of one or more shoulder vibration sensitive sensors and back vibration sensitive sensors; respectively generating first hemodynamic related information and second hemodynamic related information on the basis of the back vibration information and the shoulder vibration information, the second hemodynamic related information comprising right shoulder second hemodynamic related information generated from right shoulder vibration information; determining a reference AVC time point of an AVC event on the basis of the first hemodynamic related information; and determining an AVC feature point of the AVC event on the basis of the reference AVC time point and the right shoulder second hemodynamic related information.

Abstract: The present invention belongs to the field of medicine and discloses a method for assessing volume responsiveness and a processing device for assessing volume responsiveness. The method comprises: acquiring, by using one or more vibration sensitive sensors, a first parameter associated with a change in preload in a first time interval before a subject performs a passive straight-leg lift in a passive leg raising (PLR) test; acquiring, by using the one or more vibration sensitive sensors, a second parameter associated with a change in preload in a second time interval after the subject performs a passive straight-leg lift in the PLR test; and determining the volume responsiveness of the subject according to the first parameter associated with a change in preload and the second parameter associated with a change in preload. The method provides a convenient and easy determination of volume responsiveness.

Abstract: A pulse wave conduction parameter measurement system and method comprises: acquiring, by one or more processors, first vibration information of a supine subject from a first fiber optic sensor, the first fiber optic sensor being configured to be placed under a back region corresponding to the fourth thoracic vertebral body of the supine subject (step 711); acquiring, by the one or more processors, second vibration information of the supine subject from a second fiber optic sensor, the second fiber optic sensor being configured to be placed under a lumbar region corresponding to the fourth lumbar body of the supine subject (step 713); and generating, by the one or more processors, first hemodynamic related information on the basis of the first vibration information, and generating second hemodynamic related information on the basis of the second vibration information (step 715), thereby determining an aortic Pulse Wave Transit Time of the supine subject (step 719).

Abstract: A cardiac physiological parameter measuring method, a device, a terminal and a computer storage medium, comprising: by means of one or more vibration sensors, acquiring vibration information of a subject to be tested that is in a supine state, the vibration sensors being configured to be disposed below the left shoulder of the subject to be tested; generating hemodynamic related information on the basis of the vibration information determining an MC feature point of an MC event on the basis the hemodynamic related information.

Abstract: An occluder includes a first occluder disc, a second occluder disc, a waist portion connecting the first occluder disc and the second occluder disc, and at least one soft and fibrous strand bundle structure. The strand bundle structure is disposed on at least one of a disc surface of the first occluder disc and a disc surface of the second occluder disc, the two disc surfaces faces each other, and the strand bundle structure is disposed near the waist portion. By disposing the strand bundle structure to be immediately adjacent to the waist portion, a defect opening can be occluded after implantation, thereby effectively blocking blood from flowing from one side of the defect to the other side thereof, and preventing a shunt from being formed.

Abstract: The present invention provides a pulse wave conduction parameter measuring method and a pulse wave conduction parameter processing device. The method comprises: acquiring vibration information of a subject from one or more vibration-sensitive sensors configured to be placed at a predetermined position; generating hemodynamic related information on the basis of the vibration information; determining a first feature point and a second feature point in the hemodynamic related information, wherein the first feature point is a point related to an aortic valve opening time of the subject, and the second feature point is related to a pulse wave arrival time of the subject; and determining a pulse wave conduction time of the subject on the basis of the first feature point and the second feature point.

Abstract: An intravascular stent (100, 200, 300) comprises a framework with openings and at least one radiopaque structure (103, 201, 301). Each radiopaque structure (103, 201, 301) comprises fixed bodies and radiopaque markers (105, 208, 307) filled in the fixed bodies. The fixed bodies are connected with the framework, and are at least partially disposed in the openings. The envelope enclosed area of all the radiopaque markers (105, 208, 307) in each radiopaque structure (103, 201, 301) is less than or equal to 2 mm2, and a sum of effective areas of all the radiopaque markers (105, 208, 307) in each radiopaque structure (103, 201, 301) is greater than or equal to 0.15 mm2, and a ratio of said sum of effective areas to said envelope enclosed area is greater than or equal to 1:5. The radiopaque structure (103, 201, 301) has a desirable visibility, and does not substantially affect the crimped diameter of the intravascular stent (100, 200, 300).

Abstract: An occluder includes a first occluder disc, a second occluder disc, a waist portion connecting the first occluder disc and the second occluder disc, and at least one soft and fibrous strand bundle structure. The strand bundle structure is disposed on at least one of a disc surface of the first occluder disc and a disc surface of the second occluder disc, the two disc surfaces faces each other, and the strand bundle structure is disposed near the waist portion. By disposing the strand bundle structure to be immediately adjacent to the waist portion, a defect opening can be occluded after implantation, thereby effectively blocking blood from flowing from one side of the defect to the other side thereof, and preventing a shunt from being formed.

Abstract: An intravascular stent (100, 200, 300) comprises a framework with openings and at least one radiopaque structure (103, 201, 301). Each radiopaque structure (103, 201, 301) comprises fixed bodies and radiopaque markers (105, 208, 307) filled in the fixed bodies. The fixed bodies are connected with the framework, and are at least partially disposed in the openings. The envelope enclosed area of all the radiopaque markers (105, 208, 307) in each radiopaque structure (103, 201, 301) is less than or equal to 2 mm2, and a sum of effective areas of all the radiopaque markers (105, 208, 307) in each radiopaque structure (103, 201, 301) is greater than or equal to 0.15 mm2, and a ratio of said sum of effective areas to said envelope enclosed area is greater than or equal to 1:5. The radiopaque structure (103, 201, 301) has a desirable visibility, and does not substantially affect the crimped diameter of the intravascular stent (100, 200, 300).

Abstract: Disclosed is an occlusion device having an angle variable flat disk, comprising a single-layer disk (4), a plug (6) and a waist (5) connecting the single-layer disk (4) and the plug (6). The single-layer disk (4) is braided from elastic strands and comprises a plurality of radially-arranged support rods (40). Grids braided from elastic strands are provided on the surface of the plug (6). The waist (5) comprises at least one connecting strand. An annular interlocking structure is provided in the center of the single-layer disk (4). The plurality of support rods (40) are connected into a flat integral body via the annular interlocking structure. The connecting strand of the waist (5) is connected to the annular interlocking structure and the grids of the plug (6).

Abstract: An ablation catheter device (100) comprises a hollow catheter main body (102), an ablation mechanism (103) and a control mechanism. The ablation mechanism (103) comprises a support assembly (110) capable of being expanded and compressed radially, an end (120) and a plurality of modulation units. The support assembly (110) is provided between the distal end of the catheter main body (102) and the end (120). The modulation units are provided on the support assembly (110), and an axial through hole (122) is formed in the end (120). The control mechanism comprises a drawing wire (104) and a limit unit (118) fixed on the drawing wire (104). The drawing wire (104) axially extends through the catheter main body (102) and the through hole (122). The end (120) is provided between the support assembly (110) and the limit unit (118), and the outer diameter of the limit unit (118) is larger than the inner diameter of the through hole (122).

Abstract: Disclosed is an occlusion device having an angle variable flat disk, comprising a single-layer disk (4), a plug (6) and a waist (5) connecting the single-layer disk (4) and the plug (6). The single-layer disk (4) is braided from elastic strands and comprises a plurality of radially-arranged support rods (40). Grids braided from elastic strands are provided on the surface of the plug (6). The waist (5) comprises at least one connecting strand. An annular interlocking structure is provided in the center of the single-layer disk (4). The plurality of support rods (40) are connected into a flat integral body via the annular interlocking structure. The connecting strand of the waist (5) is connected to the annular interlocking structure and the grids of the plug (6).