Ventricular assist devices
US-2015290375-A1 · Oct 15, 2015 · US
US10111996B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10111996-B2 |
| Application number | US-201715819725-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 21, 2017 |
| Priority date | Apr 15, 2014 |
| Publication date | Oct 30, 2018 |
| Grant date | Oct 30, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
An implantable blood pump includes a control unit storing patient specific settings. The control unit is configured to store patient specific settings. The patient specific settings can be used to determine a target operating speed for the blood pump and/or a target operating mode for the blood pump. The patient specific settings can include at least one of an operating mode for the pump, a set speed for the pump, a lower speed limit for the pump, a patient hematocrit value, a patient hematocrit date, a patient blood density, and a periodic log rate for event and periodic data.
Opening claim text (preview).
What is claimed is: 1. A method of controlling an implantable blood pump, the method comprising: storing preprogrammed patient specific settings within an implantable control unit; communicating at least one of the preprogrammed patient specific settings from the implantable control unit to a non-implanted external control unit; and controlling, by the non-implanted external control unit, operation of the implantable blood pump in accordance with the at least one of the preprogrammed patient specific settings communicated to the external control unit from the implantable control unit. 2. The method of claim 1 , wherein the implantable control unit is integrally housed with the implantable blood pump or in a separate implantable housing. 3. The method of claim 1 , wherein: the preprogrammed patient specific settings include at least one of a patient specific set speed and a patient specific low speed limit; and the non-implanted external control unit controls the implantable pump to operate at a target speed that is based on at least one of the patient specific set speed, the patient specific low speed limit, and a set of event based rules for the target speed. 4. The method of claim 3 , wherein the set of event based rules for the target speed is based on at least one of the following events: a target running mode for the implantable blood pump is set as stopped; the implantable blood pump has just started up; a suction event is occurring; instability of a rotor of the implantable blood pump is occurring; a critical power hazard has been active for more than a predetermined period of time; the implantable blood pump is running on an emergency backup battery; and voltage of a backup battery is less than a predetermined value. 5. The method of claim 1 , wherein: the preprogrammed patient specific settings include at a patient specific operating mode of the implantable blood pump; and the non-implanted external control unit controls the implantable pump to operate in a target operating mode that is based on at least one of the patient specific operating mode of the implantable blood pump and a set of event based rules for the target operating mode. 6. The method of claim 5 , wherein the set of event based rules for the target operating mode is based on at least one of the following events: a target running mode for the implantable blood pump is set as stopped; a current set speed for the implantable blood pump is set to be an auto-start threshold speed; the non-implanted external control unit is running on an emergency backup battery; and a critical power hazard is active. 7. The method of claim 1 , further comprising changing at least one of the preprogrammed patient specific settings stored within the implantable control unit while the implantable control unit remains implanted. 8. The method of claim 1 , further comprising: replacing the non-implanted external controller with a second non-implanted external controller, the second non-implanted external controller being different from the non-implanted external controller; and communicating at least one of the preprogrammed patient specific settings from the implantable control unit to the second non-implanted external controller for use in processing performed by the second non-implanted external controller. 9. The method of claim 1 , wherein the preprogrammed patient specific settings include a patient specific operating mode of the implantable blood pump. 10. The method of claim 9 , wherein the preprogrammed patient specific operating mode for the implantable blood pump can be selected to be continuous or pulsatile. 11. The method of claim 10 , wherein the non-implanted external control unit controls the implantable blood pump to run in a target operating mode selected as either the patient specific operating mode or continuous. 12. The method of claim 1 , wherein the preprogrammed patient specific settings include a patient specific set speed of the implantable blood pump. 13. The method of claim 1 , wherein the preprogrammed patient specific settings include a patient specific low speed limit for the implantable blood pump. 14. The method of claim 1 , wherein the preprogrammed patient specific settings include at least one of: a patient specific hemacrit; a patient specific hematocrit and a patient specific hematocrit date; and a patient specific blood density. 15. The method of claim 1 , wherein the preprogrammed patient specific settings include a patient specific periodic log rate for event and periodic data. 16. The method of claim 1 , wherein the preprogrammed patient specific settings include a patient specific spoken language. 17. The method of claim 1 , further comprising selectively changing one or more of the preprogrammed patient specific settings stored within the implantable control unit while the implantable control unit remains implanted. 18. The method of claim 17 , wherein the one or more preprogrammed patient specific settings stored within the implantable control unit are changed via wireless communication. 19. The method of claim 18 , wherein the non-implanted external control unit controls the implantable blood pump to run at a target speed based at least in part on at least one of a patient specific low speed limit of the implantable blood pump and a patient specific set speed limit of the implantable blood pump. 20. The method of claim 1 , wherein the implantable control unit is configured to transmit one or more of the preprogrammed patient specific settings stored on the implantable control unit to the non-implanted external control unit in response to a data request transmitted by the non-implanted external control unit to the implantable control unit.
hematocrit · CPC title
Measuring or controlling the flow rate · CPC title
with memories providing a history of measured variating parameters of apparatus or patient · CPC title
using telemetric means · CPC title
by induction · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.