公开(公告)号：US20180353716A1

公开(公告)日：2018-12-13

申请号：US16103258

申请日：2018-08-14

申请人： ResMed Limited

发明人： John David OATES ,  Mark David BUCKLEY ,  Philip Rodney KWOK ,  Mark Alexander ABOURIZK ,  Thomas Evan MILLER ,  Simone Marie JEHA ,  Mark John PAYNE ,  Muditha Pradeep DANTANARAYANA

IPC分类号： A61M16/00 ,  A61M16/06 ,  A61M16/08 ,  H04L29/08

CPC分类号： A61M16/0057 ,  A61M16/00 ,  A61M16/0003 ,  A61M16/0051 ,  A61M16/0066 ,  A61M16/024 ,  A61M16/0616 ,  A61M16/0666 ,  A61M16/0875 ,  A61M2205/18 ,  A61M2205/3334 ,  A61M2205/3546 ,  A61M2205/3561 ,  A61M2205/3584 ,  A61M2205/502 ,  A61M2205/52 ,  H04L67/125

摘要： A flow generator for delivering breathable gas to a patient includes a processor coupled with operation sensors and a user interface. The processor is programmed to generate at least one of time-based or event-based messages relating to at least one of flow generator operation, flow generator service, flow generator use, patient health, peripheral devices and services, patient treatment, and reminders. Time-based messages are generated at predetermined time intervals based on either time of use or elapsed time. The event-based messages are generated based on signals from the operation sensors. The user interface is configured to deliver the messages to at least one of a display, a flow generator service provider, the patient and a physician. By this system, operation of the flow generator is facilitated and enhanced.

公开(公告)号：US20170246408A1

公开(公告)日：2017-08-31

申请号：US15593563

申请日：2017-05-12

申请人： ResMed Limited

发明人： Philip Rodney KWOK ,  Ron RICHARD ,  Rohan MULLINS ,  Chee Keong PHUAH ,  Karthikeyan SELVARAJAN ,  Adrian BARNES ,  Thomas Evan MILLER ,  David Richard VORREITER

IPC分类号： A61M16/00

CPC分类号： A61M16/0051 ,  A61M16/0069 ,  A61M16/024 ,  A61M16/06 ,  A61M2016/0021 ,  A61M2016/0027 ,  A61M2016/0036 ,  A61M2205/15 ,  A61M2205/502 ,  A61M2205/52 ,  A61M2205/80

摘要： A method of acclimatizing a user to provide continuous positive airway pressure (CPAP) therapy, including operating a device for treating sleep disordered breathing (SDB) during successive treatment sessions, wherein the device provides continuous positive airway pressure during sleep, includes determining a clinically-derived full therapeutic pressure, applying a sub-therapeutic treatment pressure for the duration of a first session, obtaining responses to a series of pre-programmed patient and/or bed partner feedback questions before the start of a second session, and, based on the responses, either incrementally increasing the treatment pressure for the second session if the responses indicate that the patient is adjusting to therapy, or maintaining the treatment pressure for the second session if the responses do not indicate that the patient is adjusting to therapy.