ID
40546
Descrição
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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Versões (2)
- 16/11/2018 16/11/2018 - Sarah Riepenhausen
- 30/04/2020 30/04/2020 - Sarah Riepenhausen
Titular dos direitos
ICHOM
Transferido a
30 de abril de 2020
DOI
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Licença
Creative Commons BY-NC 4.0
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ICHOM Heart Failure
Clinician-reported Outcome
- StudyEvent: ODM
Descrição
Baseline health status
Alias
- UMLS CUI-1
- C1442488
- UMLS CUI-2
- C0449440
Descrição
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 de dados
float
Alias
- UMLS CUI [1]
- C0005910
Descrição
INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported or administrative TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0005910
- UMLS CUI [1,2]
- C1519795
Descrição
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 de dados
integer
Alias
- UMLS CUI [1]
- C0004238
Descrição
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 de dados
integer
Alias
- UMLS CUI [1]
- C1275835
Descrição
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 de dados
integer
Alias
- UMLS CUI [1]
- C1519386
Descrição
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 de dados
integer
Alias
- UMLS CUI [1]
- C0001948
Descrição
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 de dados
integer
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C0020538
Descrição
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 de dados
integer
Alias
- UMLS CUI [1]
- C0011849
Descrição
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 de dados
integer
Alias
- UMLS CUI [1]
- C1533075
Descrição
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 de dados
integer
Alias
- UMLS CUI [1]
- C3279454
Descrição
Treatment variables
Alias
- UMLS CUI-1
- C0087111
Descrição
INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0018801
Descrição
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 de dados
integer
Alias
- UMLS CUI [1]
- C0003015
Descrição
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0521942
Descrição
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0521942
- UMLS CUI [1,2]
- C4051513
- UMLS CUI [1,3]
- C0205195
Descrição
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0001645
Descrição
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0006684
Descrição
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0012265
Descrição
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0012798
Descrição
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0020223
- UMLS CUI [2]
- C0022252
Descrição
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0257190
Descrição
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C1579268
Descrição
INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0205394
Descrição
INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C2735362
- UMLS CUI [1,2]
- C0018787
Descrição
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 de dados
integer
Alias
- UMLS CUI [1]
- C3177146
Descrição
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 de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C2584899
- UMLS CUI [1,2]
- C2828363
Descrição
INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0018821
Descrição
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 de dados
integer
Alias
- UMLS CUI [1,1]
- C0018821
- UMLS CUI [1,2]
- C0332307
Descrição
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 de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0018821
- UMLS CUI [1,2]
- C0011008
Descrição
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 de dados
integer
Alias
- UMLS CUI [1]
- C0700431
Descrição
Degree of Health
Alias
- UMLS CUI-1
- C0018759
Descrição
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
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C1275491
- UMLS CUI [1,2]
- C1457887
Descrição
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
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C1275491
- UMLS CUI [1,2]
- C1571702
Descrição
Burden of Care
Alias
- UMLS CUI-1
- C0087111
- UMLS CUI-2
- C2828008
Descrição
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
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C3263562
- UMLS CUI [1,2]
- C0011008
Descrição
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
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0030685
Descrição
INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C2828363
Descrição
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 de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C2828363
Descrição
INCLUSION CRITERIA: All patients TIMING: Tracked at index event & acute admissions due to heart failure REPORTING SOURCE: Clinician-reported TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0205721
Descrição
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 de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0205721
- UMLS CUI [1,2]
- C0011008
Descrição
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 de dados
integer
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C0013227
Descrição
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 de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0011008
Descrição
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 de dados
integer
Alias
- UMLS CUI [1,1]
- C0184666
- UMLS CUI [1,2]
- C4086728
- UMLS CUI [1,3]
- C0018801
Descrição
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 de dados
integer
Alias
- UMLS CUI [1,1]
- C0030675
- UMLS CUI [1,2]
- C4086728
- UMLS CUI [1,3]
- C0018801
Descrição
Mortality
Alias
- UMLS CUI-1
- C0026566
Descrição
INCLUSION CRITERIA: All patients TIMING: Tracked ongoing REPORTING SOURCE: Administrative data TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0011065
Descrição
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
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C1148348
Descrição
INCLUSION CRITERIA: If "1 = Yes” to DEATH TIMING: Tracked ongoing REPORTING SOURCE: Administrative data TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C2924451
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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])
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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)
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C0018787 (UMLS CUI-2)
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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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