Methods and Systems for Parasitic Sensing
    1.
    发明申请
    Methods and Systems for Parasitic Sensing 有权
    寄生感测方法与系统

    公开(公告)号:US20080103767A1

    公开(公告)日:2008-05-01

    申请号:US11929068

    申请日:2007-10-30

    CPC classification number: G08B31/00 G08B13/1654 G10L15/26

    Abstract: Methods and systems of parasitic sensing are shown and described. The method includes, measuring, at a first time using one or more electrical elements native to a domain, a parameter of a circuit within the domain and measuring, at a second time using the one or more electrical elements native to the domain, the parameter. The method also includes, comparing the parameter measurement from the first time to the parameter measurement at the second time and determining, in response to the comparison, that an activity occurred within the domain.

    Abstract translation: 显示和描述了寄生感测的方法和系统。 该方法包括:使用一个或多个本机域的电元件在第一时间测量该域内的电路的参数,并且在第二时间使用所述域本征的一个或多个电元件来测量参数 。 该方法还包括:将第一次的参数测量与第二次的参数测量进行比较,并且响应于比较确定在域内发生活动。

    Endolumenal aortic isolation assembly and method
    3.
    发明授权
    Endolumenal aortic isolation assembly and method 失效
    腔内主动脉分离装置及方法

    公开(公告)号:US06695810B2

    公开(公告)日:2004-02-24

    申请号:US09859884

    申请日:2001-05-16

    Abstract: A medical device system and method allows an arterial bypass graft to be proximally anastomosed to an aorta during a beating heart procedure without substantial loss of blood by use of an endolumenal aorta isolation assembly provided along the distal end portion of an elongate catheter body. The aorta isolation assembly includes proximal and distal portions that are separated by an isolation region and that are adjustable to first and second extended positions, respectively, which are adapted to circumferentially engage the aortic wall and isolate upstream and downstream aspects of an exterior space between the elongate body and the aortic wall. The intermediate region is adapted to be positioned along the proximal anastomosis site such that the distal and proximal portions when adjusted to the first and second extended positions circumferentially engage the aortic wall on upstream and downstream sides of the proximal anastomosis site. Blood flowing within the aorta is thereby isolated from the proximal anastomosis site along the intermediate region and is shunted from an upstream region of the aorta, through the distal port into the flow lumen, proximally along the flow lumen, out from the flow lumen though the proximal port.

    Abstract translation: 医疗装置系统和方法允许动脉旁路移植物在搏动心脏手术期间向近端吻合到主动脉,而不会通过使用沿着细长导管体的远端部分设置的腔内主动脉隔离组件而不会显着损失血液。 主动脉分离组件包括近端部分和远端部分,其分隔开隔离区域并且可分别调整到第一和第二延伸位置,第一和第二延伸位置适于周向地接合主动脉壁并且隔离主动脉壁之间的外部空间的上游和下游方面 细长体和主动脉壁。 中间区域适于沿着近端吻合部位定位,使得当调节到第一和第二延伸位置时的远侧和近端部分周向接合近端吻合部位的上游侧和下游侧的主动脉壁。 在主动脉内流动的血液从而沿着中间区域从近端吻合部位分离,并且从主动脉的上游区域分流通过远端端口进入流腔,沿着流腔向近侧从流腔流出, 近端口。

    Cardiac bypass catheter system and method of use

    公开(公告)号:US5928181A

    公开(公告)日:1999-07-27

    申请号:US976250

    申请日:1997-11-21

    Abstract: A medical device assembly is adapted to isolate the heart from systemic circulation while perfusing oxygenated blood to the systemic arterial circulation during a minimally invasive bypass procedure. The assembly includes an arterial catheter with an external shunt valve which forms an anchor to secure the distal end portion within the aortic arch and which also forms a funnel which shunts antegrade aortic blood flow from the aortic root, into a distal flow port and through an internal flow lumen in the catheter, out an intermediate flow port along the catheter proximally of the anchor, and into the systemic arterial circulation. A distal internal valve is further provided within the internal flow lumen between the distal and intermediate flow ports. The distal internal valve selectively occludes the shunted antegrade aortic blood flow between the distal flow port and the intermediate flow port and isolates the left heart chambers from the systemic arterial circulation. Oxygenated blood may then flow from a cardiopulmonary bypass pump, distally through the internal flow lumen, out the intermediate port. The assembly also includes a venous catheter which aspirates venous blood from the vena cavae and into the cardiopulmonary bypass pump while substantially isolating the right heart chambers from the vena cavae and without circumferentially engaging the internal walls of the vena cavae. Distal and intermediate external valves are positioned along the venous catheter within the superior and inferior vena cava, respectively, and between the sinus venarum into the right atrium and either a distal or intermediate flow port, also respectively. The flow ports communicate with a cardiopulmonary bypass pump through at least one flow lumen through the catheter. Each external valve is adjustable to have an outer diameter which is slightly less than the inner diameter of the respective vena cava so that venous blood is substantially occluded from flowing into the sinus venarum and is instead aspirated into the adjacent flow port. A leakage port may also be provided between the distal and intermediate flow ports. The venous catheter may alternatively include an external valve with a valve member which is adjustable from a first radial position at a discrete location around the catheter's circumference to a radially displaced position within the right atrium.

    Catheter system and method for venting the left ventricle
    5.
    发明授权
    Catheter system and method for venting the left ventricle 失效
    导管系统和排泄左心室的方法

    公开(公告)号:US5765568A

    公开(公告)日:1998-06-16

    申请号:US566405

    申请日:1995-12-01

    Abstract: An extracorporeal support system including an extracorporeal support apparatus and an arterial circulation support catheter. The arterial circulation support catheter includes a blood lumen with a proximal end coupled to extracorporeal support apparatus and a distal end inserted into the blood circulation. A vent lumen has a distal end that crosses the aortic valve into the left ventricle and provides direct venting of the left ventricle through the vent lumen. An arterial circulation support catheter occluding member is positioned either in an interior or at an exterior of the arterial circulation support catheter. A venous circulation support catheter is provided and includes a blood lumen with a proximal end coupled to the extracorporeal support apparatus and a distal end inserted into the blood circulation. A venous circulation support catheter occluding member is included and positioned in an interior or at an exterior of the venous circulation support catheter. The venous circulation support catheter occluding member occludes the superior vena cava and the inferior vena cava.

    Abstract translation: 一种体外支持系统,包括体外支持装置和动脉循环支持导管。 动脉循环支撑导管包括血管腔,近端连接到体外支撑装置,并且远端插入血液循环中。 排气腔具有远侧主动脉瓣进入左心室,并通过排气腔直接排出左心室。 动脉循环支持导管闭塞构件位于动脉循环支撑导管的内部或外部。 提供了一种静脉循环支持导管,其包括血管腔,近端连接到体外支持装置,并且远端插入血液循环中。 包括静脉循环支撑导管闭塞构件并定位在静脉循环支撑导管的内部或外部。 静脉循环支持导管闭塞器阻塞上腔静脉和下腔静脉。

    METHOD AND SYSTEM FOR USING A BAYESIAN BELIEF NETWORK TO ENSURE DATA INTEGRITY
    7.
    发明申请
    METHOD AND SYSTEM FOR USING A BAYESIAN BELIEF NETWORK TO ENSURE DATA INTEGRITY 有权
    使用贝叶斯网络确保数据完整性的方法和系统

    公开(公告)号:US20120004949A1

    公开(公告)日:2012-01-05

    申请号:US13231240

    申请日:2011-09-13

    Applicant: Ronald COLEMAN

    Inventor: Ronald COLEMAN

    Abstract: The present invention relates to a method and system for assessing the risks and/or exposures associated with financial transactions using various statistical and probabilistic techniques. Specifically, the present invention relates to a method and system for identifying plausible sources of error in data used as input to financial risk assessment systems using Bayesian belief networks as a normative diagnostic tool to model relationships between and among inputs/outputs of the risk assessment system and other external factors.

    Abstract translation: 本发明涉及使用各种统计和概率技术来评估与金融交易相关的风险和/或风险的方法和系统。 具体地,本发明涉及一种用于识别用作金融风险评估系统的输入的可信的误差来源的方法和系统,其使用贝叶斯信念网络作为对风险评估系统的输入/输出之间的关系进行建模的规范性诊断工具 和其他外部因素。

    Method and system for using a Bayesian belief network to ensure data integrity
    8.
    发明授权
    Method and system for using a Bayesian belief network to ensure data integrity 有权
    使用贝叶斯信念网络确保数据完整性的方法和系统

    公开(公告)号:US08041632B1

    公开(公告)日:2011-10-18

    申请号:US09697497

    申请日:2000-10-27

    Applicant: Ronald Coleman

    Inventor: Ronald Coleman

    Abstract: The present invention relates to a method and system for assessing the risks and/or exposures associated with financial transactions using various statistical and probabilistic techniques. Specifically, the present invention relates to a method and system for identifying plausible sources of error in data used as input to financial risk assessment systems using Bayesian belief networks as a normative diagnostic tool to model relationships between and among inputs/outputs of the risk assessment system and other external factors.

    Abstract translation: 本发明涉及使用各种统计和概率技术来评估与金融交易相关的风险和/或风险的方法和系统。 具体地,本发明涉及一种用于识别用作金融风险评估系统的输入的可信的误差来源的方法和系统,其使用贝叶斯信念网络作为对风险评估系统的输入/输出之间的关系进行建模的规范性诊断工具 和其他外部因素。

    Trailer and method of transporting an engine
    9.
    发明授权
    Trailer and method of transporting an engine 失效
    拖车和运输发动机的方法

    公开(公告)号:US07841814B2

    公开(公告)日:2010-11-30

    申请号:US11823952

    申请日:2007-06-29

    CPC classification number: B62B3/10 B62B2202/60 B64F5/50

    Abstract: In a particular embodiment, a trailer is disclosed that includes a base, a frame extending from the base, and mounting structures coupled to the frame. The mounting structures are adapted to releasably secure an engine, such as an aircraft engine, to the frame such that the engine is secured to the frame and suspended above the base without contacting the base.

    Abstract translation: 在特定实施例中,公开了一种拖车,其包括底座,从底座延伸的框架以及联接到框架的安装结构。 安装结构适于将诸如飞机发动机的发动机可释放地固定到框架,使得发动机固定到框架并悬挂在基座上方而不接触基座。

    Small single-port arthroscopic lavage, directed tissue drying, biocompatible tissue scaffold and autologous regenerated cell placement delivery system

    公开(公告)号:US20150025311A1

    公开(公告)日:2015-01-22

    申请号:US13999743

    申请日:2014-03-19

    Abstract: A system for performing arthroscopic lavage, directed tissue drying, and the accurate placement of a biocompatible tissue scaffold for the adherence of autologous regenerated cells through a small single port of entry into a joint compartment. The system is comprised of a handpiece having valves for irrigation and suctioning and a dual valve swivel cannula attached to the handpiece. The system includes a mobile cart, high resolution camera, light source, optical coupler, high-resolution monitor, an air compressor to power individually controlled irrigation pumps to deliver irrigation fluid to a handpiece and a vacuum suction console to collect fluid. The system also includes an insufflator to maintain distension immediately following the lavage and to dry tissue in preparation for directed tissue scaffold and regenerative cell placement. The delivery system achieves accurate biocompatible tissue scaffold placement to a specific tissue site or sites within the joint utilizing a small diameter arthroscope for direct visualization while inserting and advancing a grasping instrument or device through one of two valves located on the cannula. While holding the tissue scaffold in the jaws of the grasping device, it is advanced through the cannula lumen and extended beyond the distal tip and placed on the dried tissue site. Removing the grasping device, a catheter is then inserted and advanced through a cannula valve into the lumen and extended beyond the distal tip to the scaffold placed and prepared tissue site. A means of applying torque to the catheter tip further enhances the ability for accurate, exact placement of cells to a specific scaffold receptive tissue site. The cells are then injected into and through the catheter and applied under direct visualization to the scaffold. As comprised, the small single-port system allows a physician to perform the diagnosis, clean the joint space of debris and degradative enzymes using pressurized irrigation and suction, followed by a rapid conversion from a sterile saline fluid distension media to a dry gas CO2 distension media and directed tissue drying, and the accurate placement of a biocompatible tissue scaffold for the adherence and accurate placement of regenerated cells through a catheter to a specific tissue site within a joint.

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