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Patient identification for pacing therapy using normalized lv-rv pressure loop

机译:使用归一化lv-rv压力环路确定起搏治疗的患者身份

摘要

A method and apparatus for determining whether a patient with congestive heart failure (CHF) will benefit from pacing therapy through the use of an implantable cardiac rhythm management device. A patient's right ventricular and left ventricular pressures are measured, and the patient's PP_Area is calculated for each normal heartbeat that occurs during the testing period. Depending upon the value of the patient's mean PP_Area, it can be determined whether the patient will or will not respond well acutely to pacing therapy. A mean PP_Area value of greater than or equal to a predetermined threshold, which is about 0.3, indicates that the patient is a responder to pacing therapy, while a value of less than the predetermined threshold of about 0.3 indicates that the patient is a non-responder.
机译:一种用于确定充血性心力衰竭(CHF)患者是否将通过使用植入式心律管理设备而受益于起搏治疗的方法和装置。测量患者的右心室和左心室压力,并针对测试期间发生的每个正常心跳计算患者的PP_Area。根据患者平均PP_Area的值,可以确定患者是否会对起搏治疗产生强烈的急性反应。 PP_Area平均值大于或等于预定阈值(约为0.3),表明该患者对起搏治疗有反应,而小于预定阈值(约为0.3)则表明该患者非起搏治疗。响应者。

著录项

  • 公开/公告号AU5741500A

    专利类型

  • 公开/公告日2001-05-30

    原文格式PDF

  • 申请/专利权人 CARDIAC PACEMAKERS INC.;

    申请/专利号AU20000057415

  • 发明设计人 JULIO SPINELLI;JIANG DING;YINGHONG YU;

    申请日2000-06-15

  • 分类号A61N1/365;G06F19/00;

  • 国家 AU

  • 入库时间 2022-08-22 01:20:13

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