ID

15742

Descrizione

The CoDe (”Coding of Death in HIV”) Project A significant proportion of deaths in HIV-1 infected persons are now caused by non-AIDS events. It is important to closely monitor the causes of death in this population in order to target interventions appropriately, should specific causes of death emerge or become predominant. It is possible that deaths from diseases related to an accelerated aging process will become more frequent. The same applies for causes of death related to co-infections (e.g. hepatitis) or other co-morbidities (e.g. sequelae of intravenous drug use). Furthermore, it is important to be able to evaluate the risk factors for such emerging diseases, including their possible relationship with immunodeficiency. Until now there has not been a uniform classification system for causes of death in HIV patients. Studies have either created their own coding systems based o­n frequent and/or ‘important’ causes (e.g. rare but important adverse events such as lactic acidosis and pancreatitis), or have used ICD9 or ICD10 codes from death certificates. In many cases, the ICD system cannot be directly adapted to HIV infected persons. Many AIDS defining illnesses are poorly identified in the ICD system, and some diseases (e.g. CNS diseases) have a different aetiology in HIV patients and are therefore not covered by the ICD system, or at great risk of mis-classification. In July 2004, a meeting was held in Copenhagen with the participation from executive committees of a large number of pivotal observational studies and clinical trials that routinely collect data o­n causes of death. At this meeting, it became clear that there was a need for a harmonization and standardization of the approach taken when collecting data o­n cause of death and when reviewing these deaths. As a result, the CoDe Project was initiated. The CoDe Project is a uniform coding system that can be applied to studies of individuals with HIV infection, including a detailed data collection o­n the causes of death and contributing factors, as well as a centralised review process of the data collected. http://www.cphiv.dk/Tools-Standards/CoDe/About Contains: ART and laboratory values prior to death and adverse effects to medical treatment

collegamento

http://www.cphiv.dk/Tools-Standards/CoDe/About

Keywords

  1. 20/05/16 20/05/16 -
  2. 07/06/16 07/06/16 -
  3. 10/06/16 10/06/16 - Julian Varghese
Caricato su

10 giugno 2016

DOI

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Licenza

Creative Commons BY-NC 3.0

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    ART and laboratory values The CoDe (”Coding of Death in HIV”) Project

    ART and laboratory values The CoDe (”Coding of Death in HIV”) Project

    Section 7 ART
    Descrizione

    Section 7 ART

    A. Has the patient EVER received ART:
    Descrizione

    ART (antiretroviral therapy)

    Tipo di dati

    text

    Alias
    UMLS CUI [1]
    C1963724
    If YES, when was ART started (in months before death):
    Descrizione

    Months of ART

    Tipo di dati

    integer

    Alias
    UMLS CUI [1,1]
    C0439231
    UMLS CUI [1,2]
    C0332152
    UMLS CUI [1,3]
    C1306577
    B. Did the patient receive ART at the time of death?
    Descrizione

    ART at time of death

    Tipo di dati

    text

    Alias
    UMLS CUI [1,1]
    C1963724
    UMLS CUI [1,2]
    C1301931
    If No, Date of stopping
    Descrizione

    If ART at time of death no

    Tipo di dati

    date

    Alias
    UMLS CUI [1]
    C0806020
    C. Laboratory values
    Descrizione

    C. Laboratory values

    Laboratory values
    Descrizione

    Laboratory values

    Tipo di dati

    text

    Alias
    UMLS CUI [1]
    C1254595
    1. Most recent prior to last stopping ART
    Descrizione

    Time 1.

    Tipo di dati

    time

    Alias
    UMLS CUI [1,1]
    C0040223
    UMLS CUI [1,2]
    C0806020
    2. Most recent prior to death
    Descrizione

    Time 2.

    Tipo di dati

    time

    Alias
    UMLS CUI [1,1]
    C0040223
    UMLS CUI [1,2]
    C0332152
    UMLS CUI [1,3]
    C1301931
    Value
    Descrizione

    Value

    Tipo di dati

    float

    Alias
    UMLS CUI [1]
    C0519835
    Unit
    Descrizione

    Unit

    Tipo di dati

    text

    Alias
    UMLS CUI [1]
    C1519795
    Date
    Descrizione

    Date dd/mmm/yy

    Tipo di dati

    date

    Alias
    UMLS CUI [1]
    C0011008
    Section 8 Adverse effects to medical treatment
    Descrizione

    Section 8 Adverse effects to medical treatment

    A. Was the death considered to be related to a medical treatment?
    Descrizione

    Death As Adverse Effect

    Tipo di dati

    text

    Alias
    UMLS CUI [1,1]
    C0007465
    UMLS CUI [1,2]
    C0237726
    B. The suspected relation was to:
    Descrizione

    Medical Treatment as Cause of Death

    Tipo di dati

    text

    Alias
    UMLS CUI [1,1]
    C0007465
    UMLS CUI [1,2]
    C0332281
    Please provide a brief narrative of the suspected association including the name of the medication and the date of starting:
    Descrizione

    Brief summary regarding Cause of Death

    Tipo di dati

    text

    Alias
    UMLS CUI [1,1]
    C0007465
    UMLS CUI [1,2]
    C0242482

    Similar models

    ART and laboratory values The CoDe (”Coding of Death in HIV”) Project

    Name
    genere
    Description | Question | Decode (Coded Value)
    Tipo di dati
    Alias
    Item Group
    Section 7 ART
    Item
    A. Has the patient EVER received ART:
    text
    C1963724 (UMLS CUI [1])
    Code List
    A. Has the patient EVER received ART:
    CL Item
    Yes (Yes)
    CL Item
    No (No)
    CL Item
    Unknown (Unknown)
    Months of ART
    Item
    If YES, when was ART started (in months before death):
    integer
    C0439231 (UMLS CUI [1,1])
    C0332152 (UMLS CUI [1,2])
    C1306577 (UMLS CUI [1,3])
    Item
    B. Did the patient receive ART at the time of death?
    text
    C1963724 (UMLS CUI [1,1])
    C1301931 (UMLS CUI [1,2])
    Code List
    B. Did the patient receive ART at the time of death?
    CL Item
    Yes (Yes)
    CL Item
    No (No)
    CL Item
    Unknown (Unknown)
    Ending Date ART
    Item
    If No, Date of stopping
    date
    C0806020 (UMLS CUI [1])
    Item Group
    C. Laboratory values
    Item
    Laboratory values
    text
    C1254595 (UMLS CUI [1])
    Code List
    Laboratory values
    CL Item
    CD4+ cell count (CD4+ cell count)
    CL Item
    HIV RNA (HIV RNA)
    CL Item
    Haemoglobin (Haemoglobin)
    Time 1.
    Item
    1. Most recent prior to last stopping ART
    time
    C0040223 (UMLS CUI [1,1])
    C0806020 (UMLS CUI [1,2])
    Time 2.
    Item
    2. Most recent prior to death
    time
    C0040223 (UMLS CUI [1,1])
    C0332152 (UMLS CUI [1,2])
    C1301931 (UMLS CUI [1,3])
    Value
    Item
    Value
    float
    C0519835 (UMLS CUI [1])
    Item
    Unit
    text
    C1519795 (UMLS CUI [1])
    Code List
    Unit
    CL Item
    Cells/mm³ (Cells/mm³)
    CL Item
    Copies/mL (Copies/mL)
    CL Item
    / (/)
    Date
    Item
    Date
    date
    C0011008 (UMLS CUI [1])
    Item Group
    Section 8 Adverse effects to medical treatment
    Item
    A. Was the death considered to be related to a medical treatment?
    text
    C0007465 (UMLS CUI [1,1])
    C0237726 (UMLS CUI [1,2])
    Code List
    A. Was the death considered to be related to a medical treatment?
    CL Item
    Yes (Yes)
    CL Item
    No  (No )
    CL Item
    Possibly (Possibly)
    Item
    B. The suspected relation was to:
    text
    C0007465 (UMLS CUI [1,1])
    C0332281 (UMLS CUI [1,2])
    Code List
    B. The suspected relation was to:
    CL Item
    Antiretroviral treatment  (Antiretroviral treatment )
    CL Item
    Other medical treatment (Other medical treatment)
    Brief summary regarding Cause of Death
    Item
    Please provide a brief narrative of the suspected association including the name of the medication and the date of starting:
    text
    C0007465 (UMLS CUI [1,1])
    C0242482 (UMLS CUI [1,2])

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