ID
40546
Beschreibung
HEART FAILURE DATA COLLECTION Version 1.1.4 Revised October 31st, 2017 www.ichom.org Notice: This work was conducted using resources from ICHOM, the International Consortium for Health Outcomes Measurement (www.ICHOM.org). The content is solely the responsibility of the authors and does not necessarily represent the official views of ICHOM. Conditions: Heart Failure Treatment Approaches: Pharmacotherapy | Invasive Therapy | Rehabilitation This ODM-file contains clinician-reported outcome variables. It should be tracked 6-monthly for life, starting 30 days and 6 months post-index event. The collection rhythm has to be reset in case of an acute admission (including complications): It should be collected during the acute admission, 30 days post-discharge, 6 months following last admission and 6 monthly from then on. 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 for the Heart Failure Standard Set by GIG Cymru NHS Wales, American Heart Association, British Heart Foundation, Heart Failure Association of the ESC and European Society of Cardiology. Publication: Burns DJP, Arora J, Okunade O, Beltrame JF, Bernardez-Pereira S, Crespo-Leiro MG, et al. International Consortium for Health Outcomes Measurement (ICHOM): Standardized Patient-Centered Outcomes Measurement Set for Heart Failure Patients. JACC: Heart Failure. 2020 Mar 1;8(3):212–22. For this version of the standard set, semantic annotation with UMLS CUIs has been added.
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Stichworte
Versionen (2)
- 16.11.18 16.11.18 - Sarah Riepenhausen
- 30.04.20 30.04.20 - Sarah Riepenhausen
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ICHOM
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30. April 2020
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ICHOM Heart Failure
Clinician-reported Outcome
- StudyEvent: ODM
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 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
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
Degree of Health
Alias
- UMLS CUI-1
- C0018759
Beschreibung
NYHA - New York Heart Association classification of heart failure (Functional Capacity) INCLUSION CRITERIA: All patients TIMING: Tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1275491
- UMLS CUI [1,2]
- C1457887
Beschreibung
NYHA - New York Heart Association classification of heart failure (Objective assessment by clinician) INCLUSION CRITERIA: All patients TIMING: Tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1275491
- UMLS CUI [1,2]
- C1571702
Beschreibung
Burden of Care
Alias
- UMLS CUI-1
- C0087111
- UMLS CUI-2
- C2828008
Beschreibung
Date used to calculate total length of stay and post-procedure length of stay INCLUSION CRITERIA: All patients TIMING: Tracked ongoing REPORTING SOURCE: Administrative data TYPE: Date by DD/MM/YYYY
Datentyp
date
Maßeinheiten
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C3263562
- UMLS CUI [1,2]
- C0011008
Beschreibung
Date used to calculate total length of stay INCLUSION CRITERIA: All patients TIMING: Tracked ongoing REPORTING SOURCE: Administrative data TYPE: Date by DD/MM/YYYY
Datentyp
date
Maßeinheiten
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0030685
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
Beschreibung
Mortality
Alias
- UMLS CUI-1
- C0026566
Beschreibung
INCLUSION CRITERIA: All patients TIMING: Tracked ongoing REPORTING SOURCE: Administrative data TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C0011065
Beschreibung
Patients who die before during a hospital admission before baseline baseline data have been collected should also be included INCLUSION CRITERIA: If "1 = Yes” to DEATH TIMING: Tracked ongoing REPORTING SOURCE: Administrative data TYPE: Date by DD/MM/YYYY RESPONSE OPTIONS: DD/MM/YYYY or 999 = Unknown
Datentyp
date
Maßeinheiten
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C1148348
Beschreibung
INCLUSION CRITERIA: If "1 = Yes” to DEATH TIMING: Tracked ongoing REPORTING SOURCE: Administrative data TYPE: Single Answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C2924451
Ähnliche Modelle
Clinician-reported Outcome
- StudyEvent: ODM
C1442488 (UMLS CUI [1,2])
C0449440 (UMLS CUI-2)
C1519795 (UMLS CUI [1,2])
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C0020538 (UMLS CUI [1,2])
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C0018801 (UMLS CUI [1,2])
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C4051513 (UMLS CUI [1,2])
C0205195 (UMLS CUI [1,3])
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C0022252 (UMLS CUI [2])
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C0205394 (UMLS CUI [1,2])
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C0018787 (UMLS CUI [1,2])
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C2936377 (UMLS CUI-2)
C0205195 (UMLS CUI-3)
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C0018787 (UMLS CUI-2)
C0205394 (UMLS CUI-3)
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C0018787 (UMLS CUI-2)
C0439673 (UMLS CUI-3)
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C2828363 (UMLS CUI [1,2])
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C0332307 (UMLS CUI [1,2])
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C1292963 (UMLS CUI-2)
C0205195 (UMLS CUI-3)
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C0018821 (UMLS CUI-2)
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C0439673 (UMLS CUI-2)
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C0011008 (UMLS CUI [1,2])
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C1457887 (UMLS CUI [1,2])
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C1571702 (UMLS CUI [1,2])
C3662279 (UMLS CUI-2)
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C3536548 (UMLS CUI-2)
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C3532937 (UMLS CUI-2)
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C3532936 (UMLS CUI-2)
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C0011008 (UMLS CUI [1,2])
C0030685 (UMLS CUI [1,2])
C2828363 (UMLS CUI [1,2])
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C2828363 (UMLS CUI [1,2])
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C0011008 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])
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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])
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