Pressure monitoring type heart pacemaker sac compression haemostat

Abstract

The invention discloses a pressure-monitoring cardiac pacemaker pocket compression hemostat, which comprises: a bracket, a compression device, and a connecting rod; the bracket includes a bottom surface, a side arm and an upper arm connected in sequence; The bracket is a semi-enclosed structure; the front end of the upper arm is a retractable structure; the compression device is used for compression to stop bleeding; the compression device is connected to the front end of the upper arm through the connecting rod; the compression device includes a pressure sensor. The compression hemostat provided by the present invention can provide quantified and personalized compression hemostasis, has good hemostasis effect, low infection rate, and good patient experience.

Description

technical field [0001] The invention belongs to the technical field of cardiology, and in particular relates to a pressure-monitoring cardiac pacemaker pocket compression hemostat. Background technique [0002] A cardiac pacemaker is an electronic therapeutic device implanted in the body. It sends out electrical pulses through a pulse generator, and the electrical pulses stimulate the myocardium contacted by the electrodes through the conduction of the wire electrodes, so that the heart is excited and contracted, thereby achieving treatment due to certain heart rhythms. The purpose of cardiac dysfunction caused by abnormalities. [0003] Cardiac pacemaker implantation is a device implantation operation, which is usually completed in the catheterization laboratory. The operation process of pacemaker implantation is roughly as follows: anesthesia, subclavian puncture (insertion of guide wire), and intravenous pacing Electrodes and tests, pocket made and pacemaker inserted, st...

AI Technical Summary

Problems solved by technology

However, there are great technical defects in such methods: firstly, the sterility of the outer weight is difficult to guarantee, which may easily cause wound infection; secondly, although the outer weight can generate a certain pressure, the stability of the pressure is difficult to guarantee; thirdly, The true strength of the capsular bag cannot be quantified, and individualized hemostasis solutions cannot be formulated for different patients

[0006] In summary, the existing compression hemostasis methods cannot quantify the patient's body size, bleeding risk and other characteristics, and then develop a personalized compression hemostasis plan

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