Blood sample determination method and blood sample analyzer

US10215766B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10215766-B2
Application numberUS-201514969698-A
CountryUS
Kind codeB2
Filing dateDec 15, 2015
Priority dateDec 19, 2014
Publication dateFeb 26, 2019
Grant dateFeb 26, 2019

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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Abstract

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Disclosed is a blood sample determination method including: emitting light to a measurement specimen prepared by mixing a clotting time measuring reagent and a blood sample suspected to be derived from a subject having lupus anticoagulant or a coagulation factor inhibitor, to obtain optical information about an amount of light from the measurement specimen; obtaining at least one parameter regarding derivative of clot waveform, based on the obtained optical information; and determining, based on a value of the obtained parameter, whether the blood sample is suspected to be a sample derived from a subject having lupus anticoagulant or is suspected to be a sample derived from a subject having a coagulation factor inhibitor.

First claim

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What is claimed is: 1. A blood sample determination method comprising: emitting light to a measurement specimen prepared by mixing a clotting time measuring reagent and a blood sample suspected to be derived from a subject having lupus anticoagulant or a coagulation factor inhibitor, to obtain optical information about an amount of light from the measurement specimen; obtaining at least one parameter regarding derivative of clot waveform, based on the obtained optical information; and determining, based on a value of the obtained at least one parameter, that the blood sample is suspected to be a sample derived from a subject having lupus anticoagulant, and if not, then determining that the blood sample is suspected to be a sample derived from a subject having a coagulation factor inhibitor. 2. The blood sample determination method of claim 1 , wherein in the determining, the value of the obtained at least one parameter is compared with a predetermined threshold, and determination on the blood sample is made based on a result of the comparison. 3. The blood sample determination method of claim 1 , wherein the optical information is an amount of scattered light, transmittance, or absorbance which has been measured continuously or intermittently, and the clot waveform is a waveform representing temporal change in the amount of scattered light, the transmittance, or the absorbance. 4. The blood sample determination method of claim 1 , wherein the at least one parameter regarding derivative of clot waveform is at least one selected from the group consisting of maximum coagulation velocity (|min 1|), maximum coagulation acceleration (|min 2|) and maximum coagulation deceleration (max 2). 5. The blood sample determination method of claim 4 , wherein in the determining, the value of |min 1| is compared with a first threshold in a case where |min 1| has been obtained, the value of |min 2| is compared with a second threshold in a case where |min 2| has been obtained, and the value of max 2 is compared with a third threshold in a case where max 2 has been obtained, when at least one of the values that have been obtained among |min 1|, |min 2|, and max 2 is greater than or equal to a predetermined threshold corresponding to that value, it is determined that the blood sample is suspected to be a sample derived from a subject having lupus anticoagulant, and when all the values that have been obtained among |min 1|, |min 2|, and max 2 are smaller than predetermined thresholds corresponding to those values, it is determined that the blood sample is suspected to be a sample derived from a subject having a coagulation factor inhibitor. 6. The blood sample determination method of claim 4 , wherein |min 1| is obtained in the obtaining of the at least one parameter, and in the determining, the value of |min 1| is compared with a first threshold, and when the value of |min 1| is greater than or equal to the first threshold, it is determined that the blood sample is suspected to be a sample derived from a subject having a lupus anticoagulant, and when the value of |min 1| is smaller than the first threshold, it is determined that the blood sample is suspected to be a sample derived from a subject having a coagulation factor inhibitor. 7. The blood sample determination method of claim 4 , wherein |min 1|, |min 2<, and max 2 are obtained in the obtaining of the at least one parameter, in the determining, the value of |min 1| is compared with a first threshold, the value of |min 2| is compared with a second threshold, and the value of max 2 is compared with a third threshold, when at least one value of |min 1|, |min 2|, and max 2 is greater than or equal to the threshold corresponding to that value, it is determined that the blood sample is suspected to be a sample derived from a subject having lupus anticoagulant, and when the value of |min 1| is smaller than the first threshold, the value of |min 2| is smaller than the second threshold, and the value of max 2 is smaller than the third threshold, it is determined that the blood sample is suspected to be a sample derived from a subject having a coagulation factor inhibitor. 8. The blood sample determination method of claim 1 , wherein the clotting time measuring reagent is a reagent for measuring at least one selected from the group consisting of prothrombin time, activated partial thromboplastin time, dilute prothrombin time, dilute activated partial thromboplastin time, kaolin clotting time, dilute Russell's Viper Venom time, thrombin time, and dilute thrombin time. 9. The blood sample determination method of claim 1 , wherein the blood sample is whole blood or plasma. 10. A blood sample determination method comprising: emitting light to a measurement specimen prepared by mixing a blood sample and a clotting time measuring reagent, to obtain optical information about an amount of light from the measurement specimen; obtaining a clotting time and obtaining at least one parameter regarding derivative of clot waveform, based on the obtained optical information; and with respect to a blood sample for which prolongation of the clotting time is observed, determining, based on a value of the obtained at least one parameter, that the blood sample is suspected to be a sample derived from a subject having lupus anticoagulant, and if not, then determining that the blood sample is suspected to be a sample derived from a subject having a coagulation factor inhibitor.

Assignees

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Classifications

  • within a body or fluid · CPC title

  • Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated (systems in which material is burnt in a flame or plasma G01N21/72, G01N21/73) · CPC title

  • G01N33/86Primary

    involving blood coagulating time {or factors, or their receptors} · CPC title

  • producing a precipitate or turbidity · CPC title

  • Determining clotting time of blood (by chemical methods G01N33/86, C12Q1/56) · CPC title

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What does patent US10215766B2 cover?
Disclosed is a blood sample determination method including: emitting light to a measurement specimen prepared by mixing a clotting time measuring reagent and a blood sample suspected to be derived from a subject having lupus anticoagulant or a coagulation factor inhibitor, to obtain optical information about an amount of light from the measurement specimen; obtaining at least one parameter rega…
Who is the assignee on this patent?
Public Univ Corporation Nara Medical Univ, Sysmex Corp
What technology area does this patent fall under?
Primary CPC classification G01N33/86. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Feb 26 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).