ID
32848
Descrizione
HEART FAILURE DATA COLLECTION Version 1.1.4 Revised October 31st, 2017 www.ichom.org Conditions: Heart Failure Treatment Approaches: Pharmacotherapy | Invasive Therapy | Rehabilitation This ODM-file contains baseline characteristics. It should be filled in at the time of the index event. The index event represents the entry into the set. This could either be after diagnosis/first encounter in an outpatient setting, or at discharge from hospital if the initial presentation was severe enough to require admission. Use of the following Scores for this standard set: KCCQ-12: Kansas City Cardiomyopathy Questionnaire-Short Version: You can obtain a license to use this instrument at your institution by visiting http://cvoutcomes.org/licenses NYHA – New York Heart Association Functional Classification: The NYHA is free for all health care organizations, and a license is not needed. PROMIS Physical Function Short Form 4a – Patient-Reported Outcome Measurement Information System: PROMIS Physical Function is free for all health care organizations, and a license is not needed. For more information, please visit http://www.healthmeasures.net/explore-measurement-systems/promis/obtain-administer-measures . As http://www.nihpromis.org/ is the official distribution site for PROMIS questionnaires and translations, only the total score will be included in this version of the standard set. Patient Health Questionnaire (PHQ-2): Copyright by Pfizer: "content found on the PHQ Screeners site is free for download and use as stated within the PHQ Screeners site, please visit http://www.phqscreeners.com/ for more information. ICHOM was supported by GIG Cymru NHS Wales, American Heart Association, British Heart Foundation, Heart Failure Association of the ESC and European Society of Cardiology.
collegamento
Keywords
versioni (2)
- 16/11/18 16/11/18 - Sarah Riepenhausen
- 30/04/20 30/04/20 - Sarah Riepenhausen
Titolare del copyright
ICHOM
Caricato su
16 novembre 2018
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY-NC 3.0
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ICHOM Heart Failure
Baseline Characteristics, at time of index event
- StudyEvent: ODM
Descrizione
Demographic Factors
Alias
- UMLS CUI-1
- C1704791
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Administrative data TYPE: Date by DD/MM/YYYY
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C0001779
- UMLS CUI [2]
- C0421451
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Administrative data TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0079399
Descrizione
This is based upon the U.S. Standards for the Classification of Federal Data on Race and Ethnicity, and reflects standards in the U.S. Please adapt questions according to your country’s guidelines. Varies by country and should be determined by country (not for cross country comparison) INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C1515945
Descrizione
This is based upon the U.S. Standards for the Classification of Federal Data on Race and Ethnicity, and reflects standards in the U.S. Please adapt questions according to your country’s guidelines. Varies by country and should be determined by country (not for cross country comparison) INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C0078988
Descrizione
This is based upon the U.S. Standards for the Classification of Federal Data on Race and Ethnicity, and reflects standards in the U.S. Please adapt questions according to your country’s guidelines. Varies by country and should be determined by country (not for cross country comparison) INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C0005680
- UMLS CUI [2,1]
- C0015031
- UMLS CUI [2,2]
- C0085756
Descrizione
This is based upon the U.S. Standards for the Classification of Federal Data on Race and Ethnicity, and reflects standards in the U.S. Please adapt questions according to your country’s guidelines. Varies by country and should be determined by country (not for cross country comparison) INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C0086409
- UMLS CUI [2,1]
- C0015031
- UMLS CUI [2,2]
- C0086528
Descrizione
This is based upon the U.S. Standards for the Classification of Federal Data on Race and Ethnicity, and reflects standards in the U.S. Please adapt questions according to your country’s guidelines. Varies by country and should be determined by country (not for cross country comparison) INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C1513907
Descrizione
This is based upon the U.S. Standards for the Classification of Federal Data on Race and Ethnicity, and reflects standards in the U.S. Please adapt questions according to your country’s guidelines. Varies by country and should be determined by country (not for cross country comparison) INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C0007457
Descrizione
This is based upon the U.S. Standards for the Classification of Federal Data on Race and Ethnicity, and reflects standards in the U.S. Please adapt questions according to your country’s guidelines. Varies by country and should be determined by country (not for cross country comparison) INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C0439673
- UMLS CUI [2,1]
- C0015031
- UMLS CUI [2,2]
- C0205394
Descrizione
Baseline health status
Alias
- UMLS CUI-1
- C1442488
- UMLS CUI-2
- C0449440
Descrizione
Height and weight are used to calculate BMI INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported or administrative RESPONSE OPTIONS: Numeric value of height in metric or imperial system
Tipo di dati
float
Alias
- UMLS CUI [1]
- C0005890
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported or administrative TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0005890
- UMLS CUI [1,2]
- C1519795
Descrizione
Height and weight are used to calculate BMI INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported or administrative RESPONSE OPTIONS: Numeric value of weight in metric or imperial system
Tipo di dati
float
Alias
- UMLS CUI [1]
- C0005910
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported or administrative TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0005910
- UMLS CUI [1,2]
- C1519795
Descrizione
Item is phrased as a patient reported measure. However, if the patient is unable to answer, this information can be abstracted from the medical records. INCLUSION CRITERIA: All patients TIMING: At index event for HF and if "0 = No" or "999 = Unknown" to AFIB, tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0004238
Descrizione
Item is phrased as a patient reported measure. However, if the patient is unable to answer, this information can be abstracted from the medical records. INCLUSION CRITERIA: All patients TIMING: At index event for HF and if "0 = No" or "999 = Unknown" to PRIORMI, tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C1275835
Descrizione
Smoking status (of cigarettes or tobacco). Item is phrased as a patient reported measure. However, if the patient is unable to answer, this information can be abstracted from the medical records. INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C1519386
Descrizione
One standard alcoholic drink is: 12 ounces of regular beer (about 5 percent alcohol) 5 ounces of wine (about 12 percent alcohol) 1.5 ounces of distilled spirits (about 40 percent alcohol) Item is phrased as a patient reported measure. However, if the patient is unable to answer, this information can be abstracted from the medical records. INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0001948
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF and if "0 = No" or "999 = Unknown" to HYPERTEN, tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C0020538
Descrizione
Item is phrased as a patient reported measure. However, if the patient is unable to answer, this information can be abstracted from the medical records. INCLUSION CRITERIA: All patients TIMING: At index event for HF and if "0 = No" or "999 = Unknown" to DIAB, tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0011849
Descrizione
Including but not limited to COPD and asthma INCLUSION CRITERIA: All patients TIMING: At index event for HF and if "0 = No" or "999 = Unknown" to CHRONLD, tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C1533075
Descrizione
Renal dysfunction is the documented history of AKI or Increase in serum creatinine by ≥ 0.3 mg/dl (≥ 26.5 l mol/l) within 48 hours; or increase in serum creatinine to ≥ 1.5 times baseline, which is known or presumed to have occurred within the prior 7 days; or urine volume < 0.5 ml/kg/h for 6 hours; or new requirement for dialysis INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3279454
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0013516
Descrizione
INCLUSION CRITERIA: If "1 = Yes" to ECHOPERF TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0232174
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0475224
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0020538
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0018824
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0277558
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C2053583
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0027059
- UMLS CUI [2,1]
- C0018801
- UMLS CUI [2,2]
- C0333348
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0332448
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0038435
- UMLS CUI [2,1]
- C0018801
- UMLS CUI [2,2]
- C1739395
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0041234
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0332240
- UMLS CUI [2,1]
- C0018801
- UMLS CUI [2,2]
- C0205394
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0439673
- UMLS CUI [1,3]
- C0683312
Descrizione
Treatment variables
Alias
- UMLS CUI-1
- C0087111
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0018801
Descrizione
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and if "0 = No" or "999 = Unknown" to AFIB, tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0003015
Descrizione
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0521942
Descrizione
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0521942
- UMLS CUI [1,2]
- C4051513
- UMLS CUI [1,3]
- C0205195
Descrizione
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0001645
Descrizione
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0006684
Descrizione
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0012265
Descrizione
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0012798
Descrizione
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0020223
- UMLS CUI [2]
- C0022252
Descrizione
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0257190
Descrizione
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C1579268
Descrizione
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0205394
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C2735362
- UMLS CUI [1,2]
- C0018787
Descrizione
ICD = Implantable Cardioverter Defibrillator CRT = Cardiac Resynchronisation Therapy INCLUSION CRITERIA: If "1 = Yes" to DEVPROCEDURE TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3177146
Descrizione
INCLUSION CRITERIA: If "1 = Yes" to DEVPROCEDURE TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Date by DD/MM/YYYY
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C2584899
- UMLS CUI [1,2]
- C2828363
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0018821
Descrizione
CABG = Cardiac surgery for heart failure INCLUSION CRITERIA: if "1 = Yes" to CARDSURG TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0018821
- UMLS CUI [1,2]
- C0332307
Descrizione
INCLUSION CRITERIA: If "1 = Yes" to CARDSURG TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Date by DD/MM/YYYY
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0018821
- UMLS CUI [1,2]
- C0011008
Descrizione
Cardiac rehabilitation is a medically-supervised programme that involves adopting heart-healthy lifestyle changes to address risk factors for cardiovascular disease. This programme includes exercise training, education on heart-healthy living, and counseling to reduce stress and helps patients return to an active life. INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0700431
Descrizione
Burden of Care
Alias
- UMLS CUI-1
- C0087111
- UMLS CUI-2
- C2828008
Descrizione
INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C2828363
Descrizione
INCLUSION CRITERIA: if "1 = Yes" to COMPLDEVICE TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Date by DD/MM/YYYY RESPONSE OPTIONS: DD/MM/YYYY or 999 = Unknown
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C2828363
Descrizione
INCLUSION CRITERIA: All patients TIMING: Tracked at index event & acute admissions due to heart failure REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0205721
Descrizione
INCLUSION CRITERIA: If "1 = Yes" to COMPLHOSP TIMING: Tracked at index event & acute admissions due to heart failure REPORTING SOURCE: Clinician-reported TYPE: Date by DD/MM/YYYY RESPONSE OPTIONS: DD/MM/YYYY or 999 = Unknown
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0205721
- UMLS CUI [1,2]
- C0011008
Descrizione
A major adverse event is a response to a drug which is noxious and unintended, and which occurs at doses normally used in a person for the prophylaxis, diagnosis, or therapy of disease, or for the modifications of physiological function. INCLUSION CRITERIA: All patients TIMING: Tracked at index event & acute admissions due to heart failure REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C0013227
Descrizione
INCLUSION CRITERIA: If "1 = Yes" to COMPLMED TIMING: Tracked at index event & acute admissions due to heart failure REPORTING SOURCE: Clinician-reported TYPE: Date by DD/MM/YYYY RESPONSE OPTIONS: DD/MM/YYYY or 999 = Unknown
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0011008
Descrizione
This variable is acollected every 12 months from date of entry into the set. INCLUSION CRITERIA: All patients TIMING: Baseline and 12-monthly REPORTING SOURCE: Adminstrative or patient/caregiver reported TYPE: Numerical RESPONSE OPTIONS: Numerical value or 999 = Unknown
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0184666
- UMLS CUI [1,2]
- C4086728
- UMLS CUI [1,3]
- C0018801
Descrizione
This variable is acollected every 12 months from date of entry into the set. INCLUSION CRITERIA: All patients TIMING: Baseline and 12-monthly REPORTING SOURCE: Adminstrative or patient/caregiver reported TYPE: Numerical RESPONSE OPTIONS: Numerical value or 999 = Unknown
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0030675
- UMLS CUI [1,2]
- C4086728
- UMLS CUI [1,3]
- C0018801
Similar models
Baseline Characteristics, at time of index event
- StudyEvent: ODM
C0421451 (UMLS CUI [2])
C1515945 (UMLS CUI [1,2])
C0078988 (UMLS CUI [1,2])
C0005680 (UMLS CUI [1,2])
C0015031 (UMLS CUI [2,1])
C0085756 (UMLS CUI [2,2])
C0086409 (UMLS CUI [1,2])
C0015031 (UMLS CUI [2,1])
C0086528 (UMLS CUI [2,2])
C1513907 (UMLS CUI [1,2])
C0007457 (UMLS CUI [1,2])
C0439673 (UMLS CUI [1,2])
C0015031 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
C0449440 (UMLS CUI-2)
C1519795 (UMLS CUI [1,2])
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C1519795 (UMLS CUI [1,2])
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C0020538 (UMLS CUI [1,2])
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(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C0475224 (UMLS CUI [1,2])
C0020538 (UMLS CUI [1,2])
C0018824 (UMLS CUI [1,2])
C0277558 (UMLS CUI [1,2])
C2053583 (UMLS CUI [1,2])
C0027059 (UMLS CUI [1,2])
C0018801 (UMLS CUI [2,1])
C0333348 (UMLS CUI [2,2])
C0332448 (UMLS CUI [1,2])
C0038435 (UMLS CUI [1,2])
C0018801 (UMLS CUI [2,1])
C1739395 (UMLS CUI [2,2])
C0041234 (UMLS CUI [1,2])
C0332240 (UMLS CUI [1,2])
C0018801 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
C0439673 (UMLS CUI [1,2])
C0683312 (UMLS CUI [1,3])
C0018801 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C4051513 (UMLS CUI [1,2])
C0205195 (UMLS CUI [1,3])
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C0022252 (UMLS CUI [2])
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C0205394 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
(Comment:en)
C0018787 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C2936377 (UMLS CUI-2)
C0205195 (UMLS CUI-3)
(Comment:en)
C0018787 (UMLS CUI-2)
C0205394 (UMLS CUI-3)
(Comment:en)
C0018787 (UMLS CUI-2)
C0439673 (UMLS CUI-3)
(Comment:en)
C2828363 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
(Comment:en)
C0332307 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
C1292963 (UMLS CUI-2)
C0205195 (UMLS CUI-3)
(Comment:en)
C0018821 (UMLS CUI-2)
(Comment:en)
C0439673 (UMLS CUI-2)
(Comment:en)
C0011008 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
(Comment:en)
C2828363 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
(Comment:en)
C2828363 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
(Comment:en)
C0011008 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
(Comment:en)
C0013227 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C4086728 (UMLS CUI [1,2])
C0018801 (UMLS CUI [1,3])
C4086728 (UMLS CUI [1,2])
C0018801 (UMLS CUI [1,3])