ID
32848
Beschreibung
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.
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Stichworte
Versionen (2)
- 16.11.18 16.11.18 - Sarah Riepenhausen
- 30.04.20 30.04.20 - Sarah Riepenhausen
Rechteinhaber
ICHOM
Hochgeladen am
16. November 2018
DOI
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ICHOM Heart Failure
Baseline Characteristics, at time of index event
- StudyEvent: ODM
Beschreibung
Demographic Factors
Alias
- UMLS CUI-1
- C1704791
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Administrative data TYPE: Date by DD/MM/YYYY
Datentyp
date
Maßeinheiten
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C0001779
- UMLS CUI [2]
- C0421451
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Administrative data TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C0079399
Beschreibung
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
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C1515945
Beschreibung
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
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C0078988
Beschreibung
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
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C0005680
- UMLS CUI [2,1]
- C0015031
- UMLS CUI [2,2]
- C0085756
Beschreibung
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
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C0086409
- UMLS CUI [2,1]
- C0015031
- UMLS CUI [2,2]
- C0086528
Beschreibung
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
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C1513907
Beschreibung
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
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C0007457
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0015031
- UMLS CUI [1,2]
- C0439673
- UMLS CUI [2,1]
- C0015031
- UMLS CUI [2,2]
- C0205394
Beschreibung
Baseline health status
Alias
- UMLS CUI-1
- C1442488
- UMLS CUI-2
- C0449440
Beschreibung
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
Datentyp
float
Alias
- UMLS CUI [1]
- C0005890
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported or administrative TYPE: Single answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0005890
- UMLS CUI [1,2]
- C1519795
Beschreibung
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
Datentyp
float
Alias
- UMLS CUI [1]
- C0005910
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported or administrative TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0005910
- UMLS CUI [1,2]
- C1519795
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1]
- C0004238
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1]
- C1275835
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1]
- C1519386
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1]
- C0001948
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C0020538
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1]
- C0011849
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1]
- C1533075
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1]
- C3279454
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C0013516
Beschreibung
INCLUSION CRITERIA: If "1 = Yes" to ECHOPERF TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C0232174
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0475224
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0020538
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0018824
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0277558
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C2053583
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0027059
- UMLS CUI [2,1]
- C0018801
- UMLS CUI [2,2]
- C0333348
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0332448
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0038435
- UMLS CUI [2,1]
- C0018801
- UMLS CUI [2,2]
- C1739395
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0041234
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0332240
- UMLS CUI [2,1]
- C0018801
- UMLS CUI [2,2]
- C0205394
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF REPORTING SOURCE: Clinician-reported TYPE: Multiple Answer
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0439673
- UMLS CUI [1,3]
- C0683312
Beschreibung
Treatment variables
Alias
- UMLS CUI-1
- C0087111
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0018801
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1]
- C0003015
Beschreibung
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C0521942
Beschreibung
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0521942
- UMLS CUI [1,2]
- C4051513
- UMLS CUI [1,3]
- C0205195
Beschreibung
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C0001645
Beschreibung
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C0006684
Beschreibung
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C0012265
Beschreibung
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C0012798
Beschreibung
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C0020223
- UMLS CUI [2]
- C0022252
Beschreibung
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C0257190
Beschreibung
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C1579268
Beschreibung
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0205394
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C2735362
- UMLS CUI [1,2]
- C0018787
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1]
- C3177146
Beschreibung
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
Datentyp
date
Maßeinheiten
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C2584899
- UMLS CUI [1,2]
- C2828363
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C0018821
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0018821
- UMLS CUI [1,2]
- C0332307
Beschreibung
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
Datentyp
date
Maßeinheiten
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0018821
- UMLS CUI [1,2]
- C0011008
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1]
- C0700431
Beschreibung
Burden of Care
Alias
- UMLS CUI-1
- C0087111
- UMLS CUI-2
- C2828008
Beschreibung
INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C2828363
Beschreibung
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
Datentyp
date
Maßeinheiten
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C2828363
Beschreibung
INCLUSION CRITERIA: All patients TIMING: Tracked at index event & acute admissions due to heart failure REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C0205721
Beschreibung
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
Datentyp
date
Maßeinheiten
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0205721
- UMLS CUI [1,2]
- C0011008
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C0013227
Beschreibung
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
Datentyp
date
Maßeinheiten
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0011008
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0184666
- UMLS CUI [1,2]
- C4086728
- UMLS CUI [1,3]
- C0018801
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0030675
- UMLS CUI [1,2]
- C4086728
- UMLS CUI [1,3]
- C0018801
Ähnliche Modelle
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)
(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])