MXPA02012176A - Un metodo para detectar un complejo de liproproteina -proteina de fase aguda y predecir un riesgo mayor de falla de sistema o mortalidad. - Google Patents

Un metodo para detectar un complejo de liproproteina -proteina de fase aguda y predecir un riesgo mayor de falla de sistema o mortalidad.

Info

Publication number
MXPA02012176A
MXPA02012176A MXPA02012176A MXPA02012176A MXPA02012176A MX PA02012176 A MXPA02012176 A MX PA02012176A MX PA02012176 A MXPA02012176 A MX PA02012176A MX PA02012176 A MXPA02012176 A MX PA02012176A MX PA02012176 A MXPA02012176 A MX PA02012176A
Authority
MX
Mexico
Prior art keywords
patient
acute phase
lipoprotein
phase protein
mortality
Prior art date
Application number
MXPA02012176A
Other languages
English (en)
Inventor
Timothy J Fischer
Original Assignee
Bio Merieux Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bio Merieux Inc filed Critical Bio Merieux Inc
Publication of MXPA02012176A publication Critical patent/MXPA02012176A/es

Links

Classifications

    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/557—Immunoassay; Biospecific binding assay; Materials therefor using kinetic measurement, i.e. time rate of progress of an antigen-antibody interaction
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/86—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving blood coagulating time or factors, or their receptors
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/92—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving lipids, e.g. cholesterol, lipoproteins, or their receptors
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2800/00—Detection or diagnosis of diseases
    • G01N2800/52—Predicting or monitoring the response to treatment, e.g. for selection of therapy based on assay results in personalised medicine; Prognosis
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00—Chemistry: analytical and immunological testing
    • Y10T436/25—Chemistry: analytical and immunological testing including sample preparation

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Molecular Biology (AREA)
  • Hematology (AREA)
  • Chemical & Material Sciences (AREA)
  • Biomedical Technology (AREA)
  • Urology & Nephrology (AREA)
  • Food Science & Technology (AREA)
  • General Physics & Mathematics (AREA)
  • Cell Biology (AREA)
  • Biotechnology (AREA)
  • Medicinal Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Microbiology (AREA)
  • Pathology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biophysics (AREA)
  • Endocrinology (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Peptides Or Proteins (AREA)

Abstract

Un metodo para diagnosticar una condicion de un paciente incluye los pasos de (a) agregar uno o mas reactivos a una muestra de prueba de un paciente, las muestras de prueba comprendiendo por lo menos parte de una muestra de sangre del paciente, para ocasionar la formacion de un complejo que comprende por lo menos una proteina de fase aguda y por lo menos una lipoproteina humana, sin causar sustancialmente polimerizacion de fibrina; (b) medir la formacion del complejo con respecto al tiempo, a fin de derivar un perfil de medicion dependiente del tiempo; y (c) determinar una pendiente y/o cambio total en el perfil de medicion dependiente del tiempo, a fin de diagnosticar una condicion del paciente; una mayor formacion del complejo se correlaciona con mayor probabilidad de muerte del paciente.
MXPA02012176A 2000-06-09 2001-06-08 Un metodo para detectar un complejo de liproproteina -proteina de fase aguda y predecir un riesgo mayor de falla de sistema o mortalidad. MXPA02012176A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US59164200A 2000-06-09 2000-06-09
PCT/US2001/018611 WO2001096864A2 (en) 2000-06-09 2001-06-08 A method for detecting a lipoprotein-acute phase protein complex

Publications (1)

Publication Number Publication Date
MXPA02012176A true MXPA02012176A (es) 2004-08-19

Family

ID=26680497

Family Applications (1)

Application Number Title Priority Date Filing Date
MXPA02012176A MXPA02012176A (es) 2000-06-09 2001-06-08 Un metodo para detectar un complejo de liproproteina -proteina de fase aguda y predecir un riesgo mayor de falla de sistema o mortalidad.

Country Status (10)

Country Link
US (1) US20070155018A1 (es)
EP (1) EP1309857B1 (es)
JP (1) JP5051960B2 (es)
AT (1) ATE302947T1 (es)
AU (2) AU6679501A (es)
BR (1) BR0111987A (es)
CA (1) CA2412317C (es)
DE (1) DE60112949T2 (es)
MX (1) MXPA02012176A (es)
WO (1) WO2001096864A2 (es)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1476752A4 (en) 2002-02-27 2008-02-13 Bio Merieux Inc METHOD FOR DIAGNOSING AND MONITORING HEMOSTATIC DYSFUNCTION, SEVERE INFECTION AND SYSTEMATIC INFLAMMATORY RESPONSE SYNDROME
CA2505921A1 (en) 2002-11-12 2004-05-27 Becton, Dickinson And Company Diagnosis of sepsis or sirs using biomarker profiles
MXPA05005072A (es) 2002-11-12 2005-07-22 Becton Dickinson Co Diagnostico de la sepsis o sirs usando perfiles de biomarcadores.
WO2006060386A1 (en) * 2004-12-01 2006-06-08 Biomerieux, Inc. Method for diagnosing critically ill patients
BRPI0609302A2 (pt) 2005-04-15 2011-10-11 Becton Dickinson Co métodos para prever o desenvolvimento de sepse e para diagnosticar sepse em um indivìduo a ser testado, microarranjo, kit para prever o desenvolvimento de sepse em um indivìduo a ser testado, produto de programa de computador, computador, sistema de computador para determinar se um indivìduo é susceptìvel de desenvolver sepse, sinal digital embutido em uma onda portadora, e, interface gráfica de usuário para determinar se um indivìduo é susceptìvel de desenvolver sepse
JP5125608B2 (ja) * 2008-02-28 2013-01-23 東ソー株式会社 イオン交換クロマトグラフィーによる血液中のＬｐ（ａ）の分離方法
WO2009123737A2 (en) 2008-04-03 2009-10-08 Becton, Dickinson And Company Advanced detection of sepsis
GB201223079D0 (en) 2012-12-20 2013-02-06 Sepsis Ltd Point of care sepsis assay device and method
GB201301611D0 (en) 2013-01-30 2013-03-13 Shaw Andrew M Systems and methods for medical data processing and analysis
GB202004047D0 (en) 2020-03-20 2020-05-06 Ainger Phill Point of care sepsis assay device and method
CN113252852B (zh) * 2021-06-04 2021-10-22 金科环境股份有限公司 絮凝剂性能评价与检验设备及方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5708591A (en) * 1995-02-14 1998-01-13 Akzo Nobel N.V. Method and apparatus for predicting the presence of congenital and acquired imbalances and therapeutic conditions
US6429017B1 (en) * 1999-02-04 2002-08-06 Biomerieux Method for predicting the presence of haemostatic dysfunction in a patient sample

Also Published As

Publication number Publication date
US20070155018A1 (en) 2007-07-05
BR0111987A (pt) 2003-10-28
EP1309857B1 (en) 2005-08-24
EP1309857A2 (en) 2003-05-14
JP5051960B2 (ja) 2012-10-17
AU6679501A (en) 2001-12-24
ATE302947T1 (de) 2005-09-15
WO2001096864A2 (en) 2001-12-20
DE60112949D1 (de) 2005-09-29
JP2004503254A (ja) 2004-02-05
AU2001266795B2 (en) 2006-07-13
WO2001096864A3 (en) 2003-02-06
CA2412317A1 (en) 2001-12-20
CA2412317C (en) 2016-03-22
DE60112949T2 (de) 2006-05-18

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