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ID

12565

Beskrivning

Emergency Department (ED)-Directed Interventions to Improve Asthma Outcomes; ODM derived from: https://clinicaltrials.gov/show/NCT01079000

Länk

https://clinicaltrials.gov/show/NCT01079000

Nyckelord

  1. 2015-11-30 2015-11-30 -
Uppladdad den

30 november 2015

DOI

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Licens

Creative Commons BY 4.0

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    Eligibility Acute Asthma NCT01079000

    Eligibility Acute Asthma NCT01079000

    Inclusion Criteria
    Beskrivning

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693 (Inclusion)
    age 17-55 years old;
    Beskrivning

    Age

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0001779 (Age)
    SNOMED
    424144002
    LOINC
    LP28815-6
    patients treated and discharged from one of the four study sites with acute asthma during the study period;
    Beskrivning

    (not simply for a prescription refill)

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0349790 (Exacerbation of asthma)
    SNOMED
    281239006
    UMLS CUI [1,2]
    C0019993 (Hospitalization)
    SNOMED
    394656005
    LOINC
    LA15417-1
    patients must have had a previous physician-diagnosis of asthma and an exacerbation diagnosed by the ed physician (e.g., past asthma history, recorded response to β-agonists in the ed, and increased asthma symptoms). in the event of a new diagnosis, the patient is still eligible for the study if the treating physician feels that the history is compatible with a diagnosis of asthma;
    Beskrivning

    patients must have had a previous physician-diagnosis of asthma and an exacerbation diagnosed by the ed physician

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0262926 (Medical History)
    SNOMED
    392521001
    LOINC
    LP6817-3
    UMLS CUI [2]
    C0004096 (Asthma)
    SNOMED
    195967001
    LOINC
    MTHU020815
    UMLS CUI [3]
    C0349790 (Exacerbation of asthma)
    SNOMED
    281239006
    patients must have evidence of airflow obstruction on presentation at the ed, defined as an fev1 or pef <80 percent of predicted;
    Beskrivning

    evidence of airflow obstruction on presentation at the ed

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C1527303 (Chronic Airflow Obstruction)
    SNOMED
    13645005
    patients must not have a history of more than 20 pack-years of smoking;
    Beskrivning

    patients must not have a history of more than 20 pack-years of smoking

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0038586 (Substance Use Disorders)
    all patients should have a pcp with whom to follow-up or attempts will be made to find one for them.
    Beskrivning

    (fp, nurse practitioner or internist)

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0033131 (Primary Care Physicians)
    SNOMED
    446050000
    LOINC
    LP57613-9
    Exclusion Criteria
    Beskrivning

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251 (Exclusion Criteria)
    these criteria ensure the exclusion of suspected copd patients and patients who require different treatments:
    Beskrivning

    suspected copd patients and patients who require different treatments

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0024117 (Chronic Obstructive Airway Disease)
    SNOMED
    13645005
    LOINC
    LP57616-2
    patients with asthma who are primarily cared for by a respirologist/pulmonologist;
    Beskrivning

    patients with asthma who are primarily cared for by a respirologist/pulmonologist

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0421318 (Full care by specialist)
    SNOMED
    268528005
    patients not seen by an emergency physician in the ed
    Beskrivning

    (e.g., direct referrals)

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C2065341 (emergency room physician services)
    physician diagnosis of acute copd
    Beskrivning

    (e.g., failure of fev1 or pef to respond to ed treatment and a fev1/fvc ratio ≤ 70%);

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0340044 (Acute exacerbation of chronic obstructive airways disease)
    SNOMED
    195951007
    radiologically confirmed pneumonia during the 10 days preceding trial entry;
    Beskrivning

    radiologically confirmed pneumonia

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C3843750 (Pneumonia, x-ray confirmed)
    LOINC
    LA14301-8
    patients with an active history of bronchiectasis, cystic fibrosis, or lung cancer;
    Beskrivning

    active history of bronchiectasis, cystic fibrosis, or lung cancer

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0006267 (Bronchiectasis)
    SNOMED
    12295008
    UMLS CUI [2]
    C0010674 (Cystic Fibrosis)
    SNOMED
    190905008
    UMLS CUI [3]
    C0242379 (Malignant neoplasm of lung)
    SNOMED
    363358000
    clinically confirmed congestive heart failure at ed presentation;
    Beskrivning

    congestive heart failure

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0018802 (Congestive heart failure)
    SNOMED
    42343007
    LOINC
    MTHU020787
    patients not able/unwilling to perform spirometry assessment
    Beskrivning

    patients not able/unwilling to perform spirometry assessment

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C1321605 (Compliance behavior)
    SNOMED
    405078008
    UMLS CUI [2]
    C0037981 (Spirometry)
    SNOMED
    127783003
    LOINC
    LP6527-8
    inability to provide informed consent or comply with the study protocol due to cognitive impairment, language barrier, or no contact details;
    Beskrivning

    inability to provide informed consent or comply with the study protocol due to cognitive impairment, language barrier, or no contact details;

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0021430 (Informed Consent)
    UMLS CUI [2]
    C0439801 (Limited (extensiveness))
    SNOMED
    255469002
    LOINC
    LP34047-8
    UMLS CUI [3]
    C0009488 (Comorbidity)
    patient has previously participated in the study;
    Beskrivning

    patient has previously participated in the study;

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C2348568 (Study Subject Participation Status)
    patients who in the opinion of the investigator are unsuitable for enrolment.
    Beskrivning

    patients who in the opinion of the investigator are unsuitable for enrolment.

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C1321605 (Compliance behavior)
    SNOMED
    405078008

    Similar models

    Eligibility Acute Asthma NCT01079000

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Age
    Item
    age 17-55 years old;
    boolean
    C0001779 (UMLS CUI [1])
    patients treated and discharged from one of the four study sites with acute asthma during the study period;
    Item
    patients treated and discharged from one of the four study sites with acute asthma during the study period;
    boolean
    C0349790 (UMLS CUI [1,1])
    C0019993 (UMLS CUI [1,2])
    patients must have had a previous physician-diagnosis of asthma and an exacerbation diagnosed by the ed physician
    Item
    patients must have had a previous physician-diagnosis of asthma and an exacerbation diagnosed by the ed physician (e.g., past asthma history, recorded response to β-agonists in the ed, and increased asthma symptoms). in the event of a new diagnosis, the patient is still eligible for the study if the treating physician feels that the history is compatible with a diagnosis of asthma;
    boolean
    C0262926 (UMLS CUI [1])
    C0004096 (UMLS CUI [2])
    C0349790 (UMLS CUI [3])
    evidence of airflow obstruction on presentation at the ed
    Item
    patients must have evidence of airflow obstruction on presentation at the ed, defined as an fev1 or pef <80 percent of predicted;
    boolean
    C1527303 (UMLS CUI [1])
    patients must not have a history of more than 20 pack-years of smoking
    Item
    patients must not have a history of more than 20 pack-years of smoking;
    boolean
    C0038586 (UMLS CUI [1])
    all patients should have a Primary care physician
    Item
    all patients should have a pcp with whom to follow-up or attempts will be made to find one for them.
    boolean
    C0033131 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    suspected copd patients and patients who require different treatments
    Item
    these criteria ensure the exclusion of suspected copd patients and patients who require different treatments:
    boolean
    C0024117 (UMLS CUI [1])
    patients with asthma who are primarily cared for by a respirologist/pulmonologist
    Item
    patients with asthma who are primarily cared for by a respirologist/pulmonologist;
    boolean
    C0421318 (UMLS CUI [1])
    patients not seen by an emergency physician
    Item
    patients not seen by an emergency physician in the ed
    boolean
    C2065341 (UMLS CUI [1])
    physician diagnosis of acute copd
    Item
    physician diagnosis of acute copd
    boolean
    C0340044 (UMLS CUI [1])
    radiologically confirmed pneumonia
    Item
    radiologically confirmed pneumonia during the 10 days preceding trial entry;
    boolean
    C3843750 (UMLS CUI [1])
    active history of bronchiectasis, cystic fibrosis, or lung cancer
    Item
    patients with an active history of bronchiectasis, cystic fibrosis, or lung cancer;
    boolean
    C0006267 (UMLS CUI [1])
    C0010674 (UMLS CUI [2])
    C0242379 (UMLS CUI [3])
    congestive heart failure
    Item
    clinically confirmed congestive heart failure at ed presentation;
    boolean
    C0018802 (UMLS CUI [1])
    patients not able/unwilling to perform spirometry assessment
    Item
    patients not able/unwilling to perform spirometry assessment
    boolean
    C1321605 (UMLS CUI [1])
    C0037981 (UMLS CUI [2])
    inability to provide informed consent or comply with the study protocol due to cognitive impairment, language barrier, or no contact details;
    Item
    inability to provide informed consent or comply with the study protocol due to cognitive impairment, language barrier, or no contact details;
    boolean
    C0021430 (UMLS CUI [1])
    C0439801 (UMLS CUI [2])
    C0009488 (UMLS CUI [3])
    patient has previously participated in the study;
    Item
    patient has previously participated in the study;
    boolean
    C2348568 (UMLS CUI [1])
    patients who in the opinion of the investigator are unsuitable for enrolment.
    Item
    patients who in the opinion of the investigator are unsuitable for enrolment.
    boolean
    C1321605 (UMLS CUI [1])

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