JPWO2021044656A5 - - Google Patents

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JPWO2021044656A5
JPWO2021044656A5 JP2021543942A JP2021543942A JPWO2021044656A5 JP WO2021044656 A5 JPWO2021044656 A5 JP WO2021044656A5 JP 2021543942 A JP2021543942 A JP 2021543942A JP 2021543942 A JP2021543942 A JP 2021543942A JP WO2021044656 A5 JPWO2021044656 A5 JP WO2021044656A5
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analysis unit
analysis
unit
detector
automatic analyzer
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JPWO2021044656A1 (en
JP7246498B2 (en
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Priority claimed from PCT/JP2020/012171 external-priority patent/WO2021044656A1/en
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Claims (15)

第1の分析を実施する第1の分析部と、
前記第1の分析とは異なる種類の第2の分析を実施する第2の分析部と、
前記第1の分析部に対応する第1の検出器と、
前記第2の分析部に対応する第2の検出器と、
前記第1の分析部、前記第2の分析部に共通に用いられる機構部と、制御部と、を備え、
前記制御部は、
前記第1の分析部または前記第2の分析部のうち、一の分析部の異常要因の特定を、予め記憶された、前記第1の分析部または前記第2の分析部のうち、他の分析部の測定データに基づき実行し、
前記測定データとして、前記第1の検出器または前記第2の検出器によって取得された時系列データを含むことを特徴とする複合型自動分析装置。
The first analysis department that carries out the first analysis,
A second analysis unit that performs a second analysis of a different type from the first analysis,
The first detector corresponding to the first analysis unit and
The second detector corresponding to the second analysis unit and
A mechanism unit and a control unit commonly used for the first analysis unit and the second analysis unit are provided.
The control unit
Of the first analysis unit or the second analysis unit, the identification of the abnormal factor of one analysis unit is stored in advance in the first analysis unit or the second analysis unit of the other analysis unit. Execute based on the measurement data of the analysis department,
A composite automatic analyzer characterized in that the measurement data includes time-series data acquired by the first detector or the second detector.
請求項1に記載の複合型自動分析装置であって、
前記制御部で特定した異常要因に対して、必要とされる対策の情報を提供する表示部を更に備える、
ことを特徴とする複合型自動分析装置。
The combined automated analyzer according to claim 1.
Further provided with a display unit that provides information on necessary countermeasures against the abnormal factor identified by the control unit.
A complex automatic analyzer characterized by this.
請求項1に記載の複合型自動分析装置であって、
前記第1の分析部が生化学分析部であり、前記第2の分析部が血液凝固分析部であり、前記測定データは、前記血液凝固分析部で測定した時系列データである、
ことを特徴とする複合型自動分析装置。
The combined automated analyzer according to claim 1.
The first analysis unit is a biochemical analysis unit, the second analysis unit is a blood coagulation analysis unit, and the measurement data is time-series data measured by the blood coagulation analysis unit.
A complex automatic analyzer characterized by this.
請求項3に記載の複合型自動分析装置であって、
前記第1の検出器または前記第2の検出器は光度計を含み、
前記制御部は、前記光度計から取得した光強度を時系列に並べた反応過程曲線を作成し、前記反応過程曲線に基づいて前記生化学分析部が異常と判定する、
ことを特徴とする複合型自動分析装置。
The combined automatic analyzer according to claim 3.
The first detector or the second detector includes a photometer and
The control unit creates a reaction process curve in which the light intensities acquired from the photometer are arranged in chronological order, and the biochemical analysis unit determines that the abnormality is based on the reaction process curve.
A complex automatic analyzer characterized by this.
請求項4に記載の複合型自動分析装置であって、
前記制御部は、前記生化学分析部が異常と判定した場合に、前記測定データを参照し、異常の発生頻度を考慮することで前記異常要因を特定する、
ことを特徴とする複合型自動分析装置。
The combined automatic analyzer according to claim 4.
When the biochemical analysis unit determines that an abnormality occurs, the control unit refers to the measurement data and identifies the cause of the abnormality by considering the frequency of occurrence of the abnormality.
A complex automatic analyzer characterized by this.
請求項1に記載の複合型自動分析装置であって、
前記第1の分析部が血液凝固分析部であり、前記第2の分析部が生化学分析部であり、前記測定データは、前記生化学分析部のキャリブレーションデータである、
ことを特徴とする複合型自動分析装置。
The combined automated analyzer according to claim 1.
The first analysis unit is a blood coagulation analysis unit, the second analysis unit is a biochemical analysis unit, and the measurement data is calibration data of the biochemical analysis unit.
A complex automatic analyzer characterized by this.
請求項1に記載の複合型自動分析装置であって、
前記第1の分析部が免疫分析部であり、前記第2の分析部が生化学分析部又は血液凝固分析部である、
ことを特徴とする複合型自動分析装置。
The combined automated analyzer according to claim 1.
The first analysis unit is an immunoanalysis unit, and the second analysis unit is a biochemical analysis unit or a blood coagulation analysis unit.
A complex automatic analyzer characterized by this.
請求項1に記載の複合型自動分析装置であって、
前記第1の分析部が生化学分析部であり、前記第2の分析部が免疫分析部、及び血液凝固分析部である、
ことを特徴とする複合型自動分析装置。
The combined automated analyzer according to claim 1.
The first analysis unit is a biochemical analysis unit, and the second analysis unit is an immunoanalysis unit and a blood coagulation analysis unit.
A complex automatic analyzer characterized by this.
第1の分析を実施する第1の分析部と、前記第1の分析とは異なる種類の第2の分析を実施する第2の分析部と、前記第1の分析部に対応する第1の検出器と、前記第2の分析部に対応する第2の検出器と、前記第1の分析部、前記第2の分析部に共通に用いられる機構部と、を有する複合型自動分析装置と、制御部と、を備え、
前記制御部は、
前記第1の分析部または前記第2の分析部のうち、一の分析部の異常要因の特定を、予め記憶された、前記第1の分析部または前記第2の分析部のうち、他の分析部の測定データに基づき実行し、
前記測定データとして、前記第1の検出器または前記第2の検出器によって取得された時系列データを含むことを特徴とする複合型自動分析システム。
A first analysis unit that carries out the first analysis, a second analysis unit that carries out a second analysis of a type different from the first analysis, and a first analysis unit corresponding to the first analysis unit. A composite automatic analyzer having a detector, a second detector corresponding to the second analysis unit, and a mechanism unit commonly used for the first analysis unit and the second analysis unit. , With control unit,
The control unit
Of the first analysis unit or the second analysis unit, the identification of the abnormal factor of one analysis unit is stored in advance in the first analysis unit or the second analysis unit of the other analysis unit. Execute based on the measurement data of the analysis department,
A complex automatic analysis system characterized in that the measurement data includes time-series data acquired by the first detector or the second detector.
請求項9に記載の複合型自動分析システムであって、
前記制御部で特定した前記異常要因に対して、必要とされる対策の情報を提供する表示部を更に備える、ことを特徴とする複合型自動分析システム。
The combined automated analysis system according to claim 9.
A complex automatic analysis system further comprising a display unit that provides information on necessary countermeasures against the abnormal factor identified by the control unit.
請求項9に記載の複合型自動分析システムであって、
前記第1の分析部が生化学分析部であり、前記第2の分析部が血液凝固分析部であり、前記測定データは、前記血液凝固分析部で測定した時系列データである、
ことを特徴とする複合型自動分析システム。
The combined automated analysis system according to claim 9.
The first analysis unit is a biochemical analysis unit, the second analysis unit is a blood coagulation analysis unit, and the measurement data is time-series data measured by the blood coagulation analysis unit.
A complex automated analysis system characterized by this.
請求項11に記載の複合型自動分析システムであって、
前記第1の検出器または前記第2の検出器は光度計を含み、前記制御部は、前記第1の検出器または前記第2の検出器から取得した光強度を時系列に並べた反応過程曲線を作成し、前記反応過程曲線に基づいて前記生化学分析部が異常と判定する、
ことを特徴とする複合型自動分析システム。
The combined automated analysis system according to claim 11.
The first detector or the second detector includes a photometer, and the control unit is a reaction process in which the light intensities obtained from the first detector or the second detector are arranged in chronological order. A curve is created, and the biochemical analysis unit determines that it is abnormal based on the reaction process curve.
A complex automated analysis system characterized by this.
異常判定方法であって、
複合型自動分析装置が、第1の分析を実施する第1の分析部と、前記第1の分析とは異なる種類の第2の分析を実施する第2の分析部と、前記第1の分析部に対応する第1の検出器と、前記第2の分析部に対応する第2の検出器と、前記第1の分析部、前記第2の分析部に共通に用いられる機構部と、制御部と、を備え、
前記制御部は、前記第1の分析部または前記第2の分析部のうち、一の分析部の異常要因の特定を、予め記憶された、前記第1の分析部または前記第2の分析部のうち、他の分析部の測定データに基づき実行する、ことを特徴とする異常判定方法。
It is an abnormality judgment method,
The combined automatic analyzer has a first analysis unit that performs the first analysis, a second analysis unit that performs a second analysis of a type different from the first analysis, and the first analysis. A first detector corresponding to the unit, a second detector corresponding to the second analysis unit, a mechanism unit commonly used for the first analysis unit and the second analysis unit, and a control unit. With a department,
The control unit stores in advance the identification of the abnormal factor of one analysis unit among the first analysis unit or the second analysis unit, and the first analysis unit or the second analysis unit stores the identification in advance. Among them, an abnormality determination method characterized in that it is executed based on the measurement data of another analysis unit.
請求項13に記載の異常判定方法であって、
前記第1の分析部が生化学分析部であり、前記第2の分析部が血液凝固分析部であり、前記測定データは、前記血液凝固分析部で測定した時系列データである、ことを特徴とする異常判定方法。
The abnormality determination method according to claim 13, wherein the abnormality is determined.
The first analysis unit is a biochemical analysis unit, the second analysis unit is a blood coagulation analysis unit, and the measurement data is time-series data measured by the blood coagulation analysis unit. Abnormality judgment method.
請求項14に記載の異常判定方法であって、
前記第1の検出器または前記第2の検出器は光度計を含み、
前記制御部は、前記第1の検出器または前記第2の検出器から取得した光強度を時系列に並べた反応過程曲線を作成し、前記反応過程曲線に基づいて前記生化学分析部が異常と判定する、
ことを特徴とする異常判定方法。
The abnormality determination method according to claim 14, wherein the abnormality is determined.
The first detector or the second detector includes a photometer and
The control unit creates a reaction process curve in which the light intensities acquired from the first detector or the second detector are arranged in chronological order, and the biochemical analysis unit is abnormal based on the reaction process curve. Judging,
An abnormality determination method characterized by this.
JP2021543942A 2019-09-04 2020-03-19 COMBINED AUTOMATIC ANALYZER, SYSTEM, AND ABNORMALITY DETERMINATION METHOD Active JP7246498B2 (en)

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JP2019160913 2019-09-04
JP2019160913 2019-09-04
PCT/JP2020/012171 WO2021044656A1 (en) 2019-09-04 2020-03-19 Complex-type auto analysis device, system, and abnormality determination method

Publications (3)

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JPWO2021044656A1 JPWO2021044656A1 (en) 2021-03-11
JPWO2021044656A5 true JPWO2021044656A5 (en) 2022-06-23
JP7246498B2 JP7246498B2 (en) 2023-03-27

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