Informationen:
Fehler:
ID
14683
Beschreibung
This measure assesses if an individual has had a myocardial infarction (MI) through collection of personal history of disease, treatment and procedure histories, and medical record abstraction. ODM derived from: https://cde.nlm.nih.gov Primary source: https://www.phenxtoolkit.org/ Recent publication: Hendershot, T., Pan, H., Haines, J., Harlan, W.R., Marazita, M.L., McCarty, C.A., Ramos, E.M., and Hamilton, C.M. (2015) Using the PhenX toolkit to add standard measures to a study. Curr. Protoc. Hum. Genet. 86:1.21.1-1.21.17. doi: 10.1002/0471142905.hg0121s86 Permission to publish granted by Carol M. Hamilton.
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- 26.04.16 26.04.16 -
Hochgeladen am
26. April 2016
DOI
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Creative Commons BY-NC 3.0
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Myocardial Infarction Protocol PhenX Toolkit
Myocardial Infarction Protocol PhenX Toolkit
- StudyEvent: SE
Ähnliche Modelle
Myocardial Infarction Protocol PhenX Toolkit
- StudyEvent: SE
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
PhenX - myocardial infarct protocol
C3169387 (UMLS CUI-1)
Item
Has a doctor ever told you that you had a myocardial infarction or heart attack?
integer
C0027051 (UMLS CUI [1])
Code List
Has a doctor ever told you that you had a myocardial infarction or heart attack?
CL Item
No (1)
C1298908 (UMLS CUI-1)
CL Item
Yes (2)
C1705108 (UMLS CUI-1)
CL Item
Don't know (3)
C3843613 (UMLS CUI-1)
OP procedure to unblock heart vessels
Item
Have you had an outpatient or day surgery procedure to unblock blocked or narrowed blood vessels of the heart?
boolean
C0190211 (UMLS CUI [1])
Item
Was there an acute episode of pain, discomfort or tightness in the chest, left arm or jaw within 72 hours of the hospitalization or within 72 hours of the hospitalization or in-hospital event
integer
C0232292 (UMLS CUI [1])
C0008031 (UMLS CUI [2])
C0564820 (UMLS CUI [3])
C2032377 (UMLS CUI [4])
C0019993 (UMLS CUI [5])
C0008031 (UMLS CUI [2])
C0564820 (UMLS CUI [3])
C2032377 (UMLS CUI [4])
C0019993 (UMLS CUI [5])
Code List
Was there an acute episode of pain, discomfort or tightness in the chest, left arm or jaw within 72 hours of the hospitalization or within 72 hours of the hospitalization or in-hospital event
CL Item
No (1)
C1298908 (UMLS CUI-1)
CL Item
Yes (2)
C1705108 (UMLS CUI-1)
CL Item
Don't know (3)
C3843613 (UMLS CUI-1)
Item
Was the discomfort or pain diagnosed as having a non-cardiac origin?
integer
C0476281 (UMLS CUI [1])
Code List
Was the discomfort or pain diagnosed as having a non-cardiac origin?
CL Item
No (1)
C1298908 (UMLS CUI-1)
CL Item
Yes (2)
C1705108 (UMLS CUI-1)
CL Item
Don't know (3)
C3843613 (UMLS CUI-1)
Item
Were electrocardiograms (ECGs or EKGs) recorded?
integer
C0013798 (UMLS CUI [1])
CL Item
No (1)
C1298908 (UMLS CUI-1)
CL Item
Yes (2)
C1705108 (UMLS CUI-1)
CL Item
Don't know (3)
C3843613 (UMLS CUI-1)
EKG study
Item
EKG study
text
C0551716 (UMLS CUI [1])
cardiac enzyme tests done during admission
Item
Were any cardiac enzyme measurements performed during this admission?
boolean
C0201934 (UMLS CUI [1,1])
C0184666 (UMLS CUI [1,2])
C0184666 (UMLS CUI [1,2])
participant had active liver disease
Item
Did the participant have any active liver disease (cirrhosis, hepatitis, liver cancer, etc.)?
boolean
C0023895 (UMLS CUI [1])
hemolytic disease
Item
Is there any evidence of hemolytic disease during this hospitalization?
boolean
C1263988 (UMLS CUI [1,1])
C0019993 (UMLS CUI [1,2])
C0019993 (UMLS CUI [1,2])
Item
Is there any mention of the participant having either trauma, a surgical procedure, or rhabdomyolysis within one week prior to the measurement of the
integer
C3263723 (UMLS CUI [1])
C0543467 (UMLS CUI [2])
C0035410 (UMLS CUI [3])
C0543467 (UMLS CUI [2])
C0035410 (UMLS CUI [3])
Code List
Is there any mention of the participant having either trauma, a surgical procedure, or rhabdomyolysis within one week prior to the measurement of the
CL Item
No (1)
C1298908 (UMLS CUI-1)
CL Item
Yes (2)
C1705108 (UMLS CUI-1)
CL Item
Don't know (3)
C3843613 (UMLS CUI-1)
Date of trauma or procedure
Item
Date of trauma or procedure
date
C2584899 (UMLS CUI [1])
C3263723 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
C3263723 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
type of trauma or procedure
Item
Type of trauma or procedure
text
C3263723 (UMLS CUI [1])
C0543467 (UMLS CUI [2])
C0543467 (UMLS CUI [2])
CL Item
Definite (Definite)
CL Item
Probable (Probable)
CL Item
No MI (skip to end) (No MI (skip to end))
date of myocardial infarction
Item
Date of myocardial infarction
date
C2924287 (UMLS CUI [1])
CL Item
Absent (Absent)
CL Item
Present (Present)
CL Item
Abnormal (Abnormal )
CL Item
Equivocal (Equivocal )
CL Item
Incomplete (Incomplete )
CL Item
Normal (Normal)
CL Item
Evolution of Major Q-Wave (Evolution of Major Q-Wave )
CL Item
Evolution of ST-T Elevation with or without Q-Wave (Evolution of ST-T Elevation with or without Q-Wave )
CL Item
New LBBB (New LBBB )
CL Item
Evolution of ST-Depression/Inversion alone (Evolution of ST-Depression/Inversion alone )
CL Item
Evolution of Minor Q-Wave alone (Evolution of Minor Q-Wave alone)
CL Item
Single ECG with Major Q-Wave (Single ECG with Major Q-Wave)
CL Item
Single ECG with LBBB, described as new (Single ECG with LBBB, described as new )
CL Item
Absent, Uncodable or Other ECG (Absent, Uncodable or Other ECG)
CL Item
Hospital inpatient (Hospital inpatient )
CL Item
Hospital outpatient facility or clinic (Hospital outpatient facility or clinic )
CL Item
Radiology or imaging facility (Radiology or imaging facility)
CL Item
Physician's office/private medical practitioner (Physician's office/private medical practitioner)
CL Item
Nursing/convalescent home/hospice (Nursing/convalescent home/hospice)
CL Item
Autopsy Only (Autopsy Only)
CL Item
Death Certificate Only (Death Certificate Only )
CL Item
Other (Other)