Eligibility Acute Asthma NCT01079000

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StudyEvent: Eligibility
1. Eligibility Acute Asthma NCT01079000

Name

Type

Description | Question | Decode (Coded Value)

Type de données

Alias

Inclusion Criteria

Item Group

C1512693 (UMLS CUI)

age

Item

1. age 17-55 years old;

boolean

C0001779 (UMLS CUI [1])

acute asthma

Item

2. patients treated and discharged from one of the four study sites with acute asthma (not simply for a prescription refill) during the study period;

boolean

C0582415 (UMLS CUI [1])

asthma exacerbation; β-agonists

Item

3. 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

C0349790 (UMLS CUI [1])
C0001644 (UMLS CUI [2])

fev1; Airflow Obstruction

Item

4. patients must have evidence of airflow obstruction on presentation at the ed, defined as an fev1 or pef <80% of predicted;

boolean

C0588029 (UMLS CUI [1])
C1527303 (UMLS CUI [2])

Smoking History

Item

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

boolean

C1519384 (UMLS CUI [1])

Primary Care Physicians

Item

6. all patients should have a pcp (fp, nurse practitioner or internist) with whom to follow-up or attempts will be made to find one for them.

boolean

C0033131 (UMLS CUI [1])

Exclusion Criteria

Item Group

C0680251 (UMLS CUI)

Chronic Obstructive Airway Disease

Item

these criteria ensure the exclusion of suspected copd patients and patients who require different treatments:

boolean

C0024117 (UMLS CUI [1])

pulmonologist

Item

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

boolean

C0586859 (UMLS CUI [1])

emergency physician

Item

2. patients not seen by an emergency physician in the ed (e.g., direct referrals);

boolean

C0420374 (UMLS CUI [1])

acute copd

Item

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

boolean

C0340044 (UMLS CUI [1])

pneumonia radiologically confirmed

Item

4. radiologically confirmed pneumonia during the 10 days preceding trial entry;

boolean

C0032285 (UMLS CUI [1,1])
C0043299 (UMLS CUI [1,2])

bronchiectasis; cystic fibrosis; lung cancer

Item

5. 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

6. clinically confirmed congestive heart failure at ed presentation;

boolean

C0018802 (UMLS CUI [1])

compliance behavior spirometry assessment

Item

7. patients not able/unwilling to perform spirometry assessment;

boolean

C1321605 (UMLS CUI [1,1])
C0037981 (UMLS CUI [1,2])
C0220825 (UMLS CUI [1,3])

informed consent Limited Comorbidity

Item

8. 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 [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])

Study Subject Participation Status

Item

9. patient has previously participated in the study;

boolean

C2348568 (UMLS CUI [1])

compliance behavior Limited Comorbidity

Item

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

boolean

C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])

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Eligibility Acute Asthma NCT01079000