Method for predicting whole blood platelet count

US2025161542A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2025161542-A1
Application numberUS-202418955258-A
CountryUS
Kind codeA1
Filing dateNov 21, 2024
Priority dateNov 22, 2023
Publication dateMay 22, 2025
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

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Blood processing systems, devices, and methods including a durable hardware component, a single use fluid flow circuit, and a controller configured to estimate the concentration of platelets in a donor's circulating blood.

First claim

Opening claim text (preview).

1 . A system for collecting platelets comprising: a reusable hardware unit, wherein the reusable hardware unit comprises a separator; a disposable fluid circuit configured to be associated with the reusable hardware unit; and a controller configured to estimate a platelet concentration of a donor's circulating blood (C donor ). 2 . The system of claim 1 , wherein C donor is based on a concentration of platelets in collected whole blood entering the separator (C wbcent ) and a percentage of collected whole blood in a separator inlet line (WB %). 3 . The system of claim 2 , wherein C donor is obtained by determining a product of the concentration of platelets in collected whole blood entering the separator (C wbcent ) and the percentage of collected whole blood in a separator inlet line (WB %), such that: C d ⁢ o ⁢ n ⁢ o ⁢ r = C wbcent ⁢ W ⁢ B ⁢ % . 4 . The system of claim 2 , wherein the WB % is obtained by dividing an amount of collected whole blood in the separator inlet line with a total amount of collected whole blood and other fluid in the separator inlet line. 5 . (canceled) 6 . The system of claim 4 , wherein the WB % is obtained by dividing parts of collected whole blood with a sum of the parts of collected whole blood (Parts WB) and parts of anticoagulant, such that: W ⁢ B ⁢ % = Parts ⁢ W ⁢ B / ( Parts ⁢ W ⁢ B + Parts ⁢ Anticoagulant ) . 7 . The system of claim 2 , wherein C wbcent is based on a platelet concentration of separated platelet rich plasma (C prp ) and a hematocrit of collected whole blood entering the separator (H wbcent ). 8 . (canceled) 9 . The system of claim 7 , wherein C wbcent is determined by an equation: C wbcent = C prp * ( 1 - H w ⁢ b ⁢ c ⁢ e ⁢ n ⁢ t ) . 10 . The system of claim 7 , wherein H wbcent is based on a flow rate of separated packed red blood cells exiting the separator (Q rbc ), a flow rate of collected whole blood flowing into the separator (Q wbcent ), and a hematocrit of the separated packed red blood cells exiting the separator (H rbc ). 11 . The system of claim 10 , wherein H wbcent is determined by dividing a product of H rbc and Q rbc with Q wbcent , such that: H wbcent = ( H rbc * Q rbc ) / Q wbcent . 12 . The system of claim 10 , wherein Q rbc is based on the flow rate of collected whole blood flowing into the separator (Q wbcent ) and a flow rate of separated platelet rich plasma flowing out of the separator (Q prp ), wherein Q rbc is determined by subtracting Q prp from Q wbcent such that: Q rbc =Q wbcent −Q prp . 13 . The system of claim 12 , wherein Q wbcent is based on a pump rate of a separator pump and Q prp is based on a pump rate of a platelet rich plasma pump. 14 . (canceled) 15 . (canceled) 16 . The system of claim 10 , wherein H rbc is a predetermined value. 17 . The system of claim 10 , wherein H rbc is determined by an optical sensor or based on separator flow rates and separator q-force. 18 . (canceled) 19 . The system of claim 11 , wherein the controller is configured to determine C wbcent , WB %, C prp , H wbcent , H rbc , and Q rbc . 20 . The system of claim 2 , wherein the controller is configured to estimate the platelet concentration of a donor's circulating blood (C donor ) with an equation: C donor = ( C prp * W ⁢ B ⁢ % ) * ( 1 - ( H

Assignees

Inventors

Classifications

  • by weighing the reservoir · CPC title

  • Controlling downstream pump pressure · CPC title

  • Controlling upstream pump pressure · CPC title

  • Measuring or controlling pressure at the body treatment site · CPC title

  • used as turbidity change detectors, e.g. for priming-blood or plasma-hemoglubine-interface detection · CPC title

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Frequently asked questions

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What does patent US2025161542A1 cover?
Blood processing systems, devices, and methods including a durable hardware component, a single use fluid flow circuit, and a controller configured to estimate the concentration of platelets in a donor's circulating blood.
Who is the assignee on this patent?
Fenwal Inc
What technology area does this patent fall under?
Primary CPC classification A61M1/0218. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu May 22 2025 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).