Table III- Core Asthma Outcomes NIH AHRQ for children (511 years of age)

ID

13650

Descrição

Documentation part: Table III [Recommendations for core asthma outcomes for NIH- initiated clinical research for children (5-11 years of age)]. ODM derived from: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4259286/ Background: Asthma clinical research will highly benefit from standardization of major outcomes in terms of definition and assessment methodology. This will permit useful comparisons across interventional or observational studies and will allow more effective data sharing. Objective: National Institutes of Health (NIH) institutes and the Agency for Healthcare Research and Quality (AHRQ) convened a workshop involving 7 expert subcommittees to propose which asthma outcomes should be assessed with standardized methodology in future asthma clinical research studies. Permission granted by: Michelle Freemer.

Link

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4259286/

Palavras-chave

Acute Asthma Exacerbations

Atmungsphysiologie

D001249

D015415

05/01/2016 05/01/2016 -
23/02/2016 23/02/2016 -

Transferido a

23 de fevereiro de 2016

DOI

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Licença

Creative Commons BY-NC 3.0

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1 Formulários

StudyEvent: ODM
1. Table III- Core Asthma Outcomes NIH AHRQ for children (511 years of age)

Name

Tipo

Description | Question | Decode (Coded Value)

Tipo de dados

Alias

Characterization of study population for prospective clinical trials

Item Group

Characterization of study population for prospective clinical trials

C2348561 (UMLS CUI-1)
C1880022 (UMLS CUI-2)
C0008976 (UMLS CUI-4)

Biomarkers Serologic

Item

Serologic multiallergen screen (IgE) to define atopic status (also for observational studies)

text

C0005516 (UMLS CUI [1,1])
C0205473 (UMLS CUI [1,2])

childhood asthma control test

Item

Composite Scores: cACT (childhood Asthma Control Test)

text

C4027871 (UMLS CUI [1])

Exacerbation of asthma

Item

Events in the 12 months prior to study entry:

text

C0349790 (UMLS CUI [1])

Exacerbation of asthma

Code List

Events in the 12 months prior to study entry:

CL Item

Systemic corticosteroids for asthma (1)

CL Item

Asthma-specific hospital admissions (2)

CL Item

Asthma-specific ED visits (separate UC visits when these can be differentiated) (3)

Utilization healthcare; Costs healthcare

Item

History of:

text

C0042153 (UMLS CUI [1,1])
C0086388 (UMLS CUI [1,2])
C0010186 (UMLS CUI [2,1])
C0086388 (UMLS CUI [2,2])

Utilization healthcare; Costs healthcare

Code List

History of:

CL Item

Asthma-specific hospital admissions (1)

CL Item

Asthma-specific ED visits (2)

CL Item

Asthma-specific outpatient visits (3)

CL Item

Asthma-specific medication use (4)

Spirometry

Item

Physiology Pulmonary: Spirometry (pre and post bronchodilator)

text

C0037981 (UMLS CUI [1])

Prospective clinical trial efficacy/ effectiveness outcomes

Item Group

Prospective clinical trial efficacy/ effectiveness outcomes

C0008976 (UMLS CUI-1)
C1280519 (UMLS CUI-2)

Exacerbation of asthma

Item

Events in the 12 months prior to study entry:

text

C0349790 (UMLS CUI [1])

Exacerbation of asthma

Code List

Events in the 12 months prior to study entry:

CL Item

Systemic corticosteroids for asthma (1)

CL Item

Asthma-specific hospital admissions (2)

CL Item

Asthma-specific ED visits (separate UC visits when these can be differentiated) (3)

CL Item

Asthma-specific ICU admissions/intubations (4)

CL Item

Death (all cause and asthma related) (5)

Utilization healthcare; Costs healthcare

Item

History of:

text

C0042153 (UMLS CUI [1,1])
C0086388 (UMLS CUI [1,2])
C0010186 (UMLS CUI [2,1])
C0086388 (UMLS CUI [2,2])

Utilization healthcare; Costs healthcare

Code List

History of:

CL Item

Asthma-specific hospital admissions (1)

CL Item

Asthma-specific ED visits (2)

CL Item

Asthma-specific outpatient visits (3)

CL Item

Asthma-specific detailed medication use (name, dose, duration) (4)

CL Item

Resource use related to the intervention (eg, personnel time, mite eradication, equipment) (5)

medication asthma

Item

If option 4 chosen above, please mention the name, dose and duration of the asthma medication used

text

C0013227 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])

Spirometry

Item

Physiology Pulmonary: Spirometry (without bronchodilator)

text

C0037981 (UMLS CUI [1])

Observational study outcomes

Item Group

Observational study outcomes

C1518527 (UMLS CUI-1)
C0086749 (UMLS CUI-2)

childhood Asthma Control Test

Item

Composite Scores: cACT (childhood Asthma Control Test)

text

C4027871 (UMLS CUI [1])

Exacerbation of asthma

Item

Events in the 12 months prior to study entry:

text

C0349790 (UMLS CUI [1])

Exacerbation of asthma

Code List

Events in the 12 months prior to study entry:

CL Item

Systemic corticosteroids for asthma (1)

CL Item

Asthma-specific hospital admissions (2)

CL Item

Asthma-specific ED visits (separate UC visits when these can be differentiated) (3)

Utilization healthcare; Costs healthcare

Item

History of:

text

C0042153 (UMLS CUI [1,1])
C0086388 (UMLS CUI [1,2])
C0010186 (UMLS CUI [2,1])
C0086388 (UMLS CUI [2,2])

Utilization healthcare; Costs healthcare

Code List

History of:

CL Item

Asthma-specific hospital admissions (1)

CL Item

Asthma-specific ED visits (2)

CL Item

Asthma-specific outpatient visits (3)

CL Item

Asthma-specific detailed medication use (name, dose, duration) (4)

CL Item

Resource use related to the intervention (eg, personnel time, mite eradication, equipment) (5)

medication asthma

Item

If option 4 chosen above, please mention the name, dose and duration of the asthma medication used

text

C0013227 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])

Spirometry

Item

Physiology Pulmonary: Spirometry (pre and post bronchodilator)

text

C0037981 (UMLS CUI [1])

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Table III- Core Asthma Outcomes NIH AHRQ for children (5­11 years of age)