COOLED MECHANICAL CIRCULATORY SUPPORT SYSTEM AND METHOD OF OPERATION

    公开(公告)号:US20200330665A1

    公开(公告)日:2020-10-22

    申请号:US16852433

    申请日:2020-04-18

    申请人: ABIOMED, Inc.

    IPC分类号: A61M1/10 A61M1/12

    摘要: A mechanical circulatory support system for a heart having a cooling element and a method for using the system to treat the effects of a cardiac episode. The support system has a pump having a distal end and a proximal end, the pump comprising a rotor, the rotor having at least one blade. The system also has a catheter having a distal end, a proximal end, and inner surface, and an outer surface, the catheter extending proximally of relative to the pump housing. The outer surface of the catheter is configured to contact blood when disposed within patient vasculature. The outer surface of the catheter comprises a heat transfer surface configured for cooling blood that comes in contact with the outer surface. The cooling element can be either a helix or double helix extending along a catheter surface or a Peltier element on the surface. The support system is operated to provide a temperature selected to cool the circulating blood in contact with the outer surface of the catheter to a temperature selected to reduce or prevent an effect of a cardiac episode

    METHODS AND APPARATUS FOR EXTRACTION OF CLINICAL TRIAL DATA FROM AN ELECTRONIC MEDICAL RECORD

    公开(公告)号:US20240127914A1

    公开(公告)日:2024-04-18

    申请号:US18488576

    申请日:2023-10-17

    申请人: Abiomed, Inc.

    IPC分类号: G16H10/60 G16H10/20

    CPC分类号: G16H10/60 G16H10/20

    摘要: Methods and systems for extracting patient information from an electronic medical record (EMR) for use in a clinical trial are described. The method includes receiving an indication that a new clinical trial subject has been identified from a subject identification source, retrieving, from an EMR associated with the new clinical trial subject, patient information, processing the retrieved patient information to de-identify the retrieved patient information thereby generating de-identified patient information, and providing a portion of the de-identified patient information as input to an electronic data capture (EDC) system for the clinical trial.