ID
40654
Descripción
ICHOM Atrial Fibrillation data collection Version 1.0.0 Published: 3rd April 2019 International Consortium for Health Outcomes Measurement (ICHOM), Source: http://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. The following conditions and treatment approaches (or interventions) are covered by our Standard Set. Conditions: Atrial Fibrillation Population: An adult (≥ 18 years) diagnosed with atrial fibrillation (including symptomatic patients) Treatment approaches: Management of cardiovascular risk factors and institution of preventive therapy | Pharmacological management| Non-Pharmacological management Excluded populations: Children and Young persons below 18 years Excluded conditions: Patients diagnosed with cardiotoxic acute atrial fibrillation This document contains the Ongoing – Clinical Form. It has to be filled in ongoing after 6 months and annually. Collecting Patient-Reported Outcome Measure: PROMIS Global Health. As there is an official distribution site, the questions of this questionnaire will not be included in this version of the standard set. For more information see: https://bit.ly/29aOZu9 Alternatively Optum SF-12, AFEQT, AFSS or WPAI:GH may be used. Montreal Cognitive Assessment Test. For more information see: https://www.mocatest.org/ The Standard set of ICHOM was supported by the BigData@Heart organization. Publication: Seligman WH, Das-Gupta Z, Jobi-Odeneye AO, Arbelo E, Banerjee A, Bollmann A, et al. Development of an international standard set of outcome measures for patients with atrial fibrillation: a report of the International Consortium for Health Outcomes Measurement (ICHOM) atrial fibrillation working group. Eur Heart J. 2020 Jan 29; 10.1093/eurheartj/ehz871 For this version of the standard set, semantic annotation with UMLS CUIs has been added.
Link
Palabras clave
Versiones (3)
- 22/8/19 22/8/19 -
- 26/8/19 26/8/19 - Sarah Riepenhausen
- 30/4/20 30/4/20 - Sarah Riepenhausen
Titular de derechos de autor
ICHOM
Subido en
30 de abril de 2020
DOI
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Licencia
Creative Commons BY-NC 4.0
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ICHOM Atrial Fibrillation
Ongoing - Clinical Form
- StudyEvent: ODM
Descripción
Long-term consequences of disease
Alias
- UMLS CUI-1
- C0443252
- UMLS CUI-2
- C0686907
- UMLS CUI-3
- C0012634
Descripción
Inclusion Criteria: All patients Timing: Ongoing Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0011065
Descripción
Inclusion Criteria: If ‘1 = Yes’ to DEATH Timing: Ongoing Data Source: Administrative date Type: Date by DD/MM/YYYY Response Options: DD/MM/YYYY
Tipo de datos
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C1148348
Descripción
Note: This item does not exist in the original version of the standard set. Please tick if you do not know the date of death. Inclusion Criteria: If ‘1 = Yes’ to DEATH Timing: Ongoing Data Source: Administrative date
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1148348
- UMLS CUI [1,2]
- C0439673
Descripción
Inclusion Criteria: If ‘1 = Yes’ to DEATH Timing: Ongoing Data Source: Administrative data Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0007465
Descripción
Inclusion Criteria: All patients Timing: Ongoing Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1320716
Descripción
Inclusion Criteria: If ‘1 = Yes’ to CARDIOVASCULAREVENT Timing: Ongoing Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0038454
- UMLS CUI [1,2]
- C0332307
Descripción
Inclusion Criteria: If ‘1, 2, or 3’ to EVENTTYPE Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Tipo de datos
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C1320716
- UMLS CUI [1,2]
- C0011008
Descripción
Inclusion Criteria: All patients Timing: Ongoing Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0205314
- UMLS CUI [1,3]
- C0332140
Descripción
Inclusion Criteria: If ‘1 = Yes’ to HF Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Tipo de datos
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0018801
- UMLS CUI [1,3]
- C0205314
- UMLS CUI [1,4]
- C0332140
Descripción
Inclusion Criteria: If ‘1 = Yes’ to HF Timing: Ongoing Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0428772
Descripción
Inclusion Criteria: If ‘1 = Yes’ to LVEF Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Tipo de datos
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0428772
Descripción
Inclusion Criteria: If ‘1 = Yes’ to LVEF Timing: Ongoing Data Source: Clinical Type: Numerical value Response Options: LVEF measurement value
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0428772
- UMLS CUI [1,2]
- C0242485
Descripción
Supporting Definition: * admission = at least one overnight stay at a hospital or acute care facility from first atrial fibrillation diagnosis **Cardiovascular causes for admission are ones in which the principal admitting diagnosis relates to the cardiovascular system: myocardial infarction / ischaemic heart disease, heart failure, stroke/TIA, peripheral arterial disease, AF, venous thromboembolism/PE, etc. Inclusion Criteria: All patients Timing: Ongoing Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0184666
- UMLS CUI [1,2]
- C0038454
Descripción
Inclusion Criteria: If ‘1 = Yes’ to CVHOSPADM Timing: Ongoing Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0184666
- UMLS CUI [1,3]
- C0038454
- UMLS CUI [1,4]
- C0085978
Descripción
Inclusion Criteria: All patients Timing: Ongoing Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0085611
- UMLS CUI [1,2]
- C0456962
Descripción
Inclusion Criteria: If ‘1 = Yes’ to FAA Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Tipo de datos
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0085611
- UMLS CUI [1,2]
- C0456962
- UMLS CUI [1,3]
- C0011008
Descripción
Inclusion Criteria: If ‘1 = Yes’ to FAA Timing: Ongoing Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0085611
- UMLS CUI [1,2]
- C0456962
- UMLS CUI [1,3]
- C0087111
Descripción
Inclusion Criteria: If ‘1 = Yes’ to FAA Timing: Ongoing Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0456962
- UMLS CUI [1,2]
- C0085611
- UMLS CUI [1,3]
- C0150496
- UMLS CUI [1,4]
- C2709088
Descripción
Inclusion Criteria: If ‘1 = Yes’ to FAA Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Tipo de datos
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C2709088
- UMLS CUI [1,3]
- C0030695
- UMLS CUI [1,4]
- C0456962
- UMLS CUI [1,5]
- C0004238
Descripción
Inclusion Criteria: If ‘1 = Yes’ to FAA Timing: Ongoing Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1298908
- UMLS CUI [1,2]
- C0456962
- UMLS CUI [1,3]
- C0085611
- UMLS CUI [1,4]
- C2709088
- UMLS CUI [1,5]
- C0030695
Descripción
Complications of treatment
Alias
- UMLS CUI-1
- C0087111
- UMLS CUI-2
- C0009566
Descripción
Inclusion Criteria: If ‘1 = Yes’ to CVEVENT Timing: Ongoing Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0038454
- UMLS CUI [1,2]
- C0333275
Descripción
Inclusion Criteria: If ‘1 = Yes’ to HSTROKE Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Tipo de datos
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0038454
- UMLS CUI [1,3]
- C0333275
Descripción
Inclusion Criteria: All patients Timing: Ongoing Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1302234
- UMLS CUI [1,2]
- C0019080
Descripción
Inclusion Criteria: If ‘1 = Yes’ to FBLEED Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Tipo de datos
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C1302234
- UMLS CUI [1,3]
- C0019080
Descripción
Inclusion Criteria: All patients Timing: Ongoing Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0231220
- UMLS CUI [1,2]
- C0019080
- UMLS CUI [1,3]
- C1511545
- UMLS CUI [1,4]
- C0205146
- UMLS CUI [2,1]
- C0231220
- UMLS CUI [2,2]
- C0019080
- UMLS CUI [2,3]
- C0178784
Descripción
Inclusion Criteria: If ‘1 = Yes’ to CRITICALBLEED Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Tipo de datos
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0231220
- UMLS CUI [1,3]
- C0019080
- UMLS CUI [1,4]
- C1511545
- UMLS CUI [1,5]
- C0205146
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C0231220
- UMLS CUI [2,3]
- C0019080
- UMLS CUI [2,4]
- C0178784
Descripción
Inclusion Criteria: All patients Timing: Ongoing Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0019080
- UMLS CUI [1,2]
- C0678227
- UMLS CUI [1,3]
- C0547047
- UMLS CUI [1,4]
- C0019046
- UMLS CUI [2,1]
- C0019080
- UMLS CUI [2,2]
- C0678227
- UMLS CUI [2,3]
- C0686904
- UMLS CUI [2,4]
- C1879316
Descripción
Inclusion Criteria: If ‘1 = Yes’ to BLEEDOUTCOME Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Tipo de datos
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0019080
- UMLS CUI [1,3]
- C0678227
- UMLS CUI [1,4]
- C0547047
- UMLS CUI [1,5]
- C0019046
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C0019080
- UMLS CUI [2,3]
- C0678227
- UMLS CUI [2,4]
- C0686904
- UMLS CUI [2,5]
- C1879316
Descripción
Procedure
Alias
- UMLS CUI-1
- C0087111
Descripción
Additional comment (not in the original standard set): Please fill in this item repeatedly if more than one procedure and provide a date for each of these procedures in a new PROCEDUREDATE item. Inclusion Criteria: All patients Timing: Ongoing Data Source: Clinical Type: Single or multiple answers
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0455713
Descripción
Inclusion Criteria: If ‘1-8’ to PROCEDURE Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Tipo de datos
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C2584899
Descripción
SAE
Alias
- UMLS CUI-1
- C1519255
Descripción
Inclusion Criteria: If ‘1-8’ to PROCEDURE Timing: Ongoing Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0332282
- UMLS CUI [1,3]
- C0184661
Descripción
Additional comment (not in the original standard set): Please fill in this item repeatedly if more than one serious adverse event due to procedure and provide a date for each event in a new SAEDATE item. Inclusion Criteria: If ‘1 = Yes’ to PROCEDURESAE Timing: Ongoing Data Source: Clinical Type: Single/multiple answers
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0332282
- UMLS CUI [1,3]
- C0087111
Descripción
Note: This item does not exist in the original standard set. It can be filled in for specification if you ticked the item "SAE_10". Inclusion Criteria: If ‘1 = Yes’ to PROCEDURESAE Timing: Ongoing Data Source: Clinical Type: Free text
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C1519255
- UMLS CUI [1,3]
- C0332282
- UMLS CUI [1,4]
- C0184661
- UMLS CUI [1,5]
- C2348235
Descripción
Inclusion Criteria: If ‘1 = Yes’ to PROCEDURESAE Timing: Ongoing Data Source: Clinical Type: Date(s) Response Options: DD/MM/YYYY(s)
Tipo de datos
date
Unidades de medida
- DD/MM/YYYY(s)
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C1519255
- UMLS CUI [1,3]
- C0332282
- UMLS CUI [1,4]
- C0184661
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Ongoing - Clinical Form
- StudyEvent: ODM
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C0456962 (UMLS CUI [1,2])
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C0030695 (UMLS CUI [1,3])
C0456962 (UMLS CUI [1,4])
C0004238 (UMLS CUI [1,5])
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C0085611 (UMLS CUI [1,3])
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C0333275 (UMLS CUI [1,2])
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C0038454 (UMLS CUI [1,2])
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C1302234 (UMLS CUI [1,2])
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C0231220 (UMLS CUI [1,2])
C0019080 (UMLS CUI [1,3])
C1511545 (UMLS CUI [1,4])
C0205146 (UMLS CUI [1,5])
C0011008 (UMLS CUI [2,1])
C0231220 (UMLS CUI [2,2])
C0019080 (UMLS CUI [2,3])
C0178784 (UMLS CUI [2,4])
C0678227 (UMLS CUI [1,2])
C0547047 (UMLS CUI [1,3])
C0019046 (UMLS CUI [1,4])
C0019080 (UMLS CUI [2,1])
C0678227 (UMLS CUI [2,2])
C0686904 (UMLS CUI [2,3])
C1879316 (UMLS CUI [2,4])
(Comment:en)
(Comment:en)
C0019080 (UMLS CUI [1,2])
C0678227 (UMLS CUI [1,3])
C0547047 (UMLS CUI [1,4])
C0019046 (UMLS CUI [1,5])
C0011008 (UMLS CUI [2,1])
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C0686904 (UMLS CUI [2,4])
C1879316 (UMLS CUI [2,5])
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C0543467 (UMLS CUI-2)
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C0009429 (UMLS CUI-2)
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C0543467 (UMLS CUI-4)
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(Comment:en)
C0205091 (UMLS CUI-2)
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C0441597 (UMLS CUI-7)
(Comment:en)
C0225860 (UMLS CUI-2)
C0598782 (UMLS CUI-3)
C0023690 (UMLS CUI-4)
C0004238 (UMLS CUI-5)
C0225860 (UMLS CUI-6)
C0598782 (UMLS CUI-7)
C0543467 (UMLS CUI-8)
C0728940 (UMLS CUI-9)
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C0013778 (UMLS CUI-2)
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C1963873 (UMLS CUI-2)
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C4489286 (UMLS CUI-2)
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C0332282 (UMLS CUI [1,2])
C0184661 (UMLS CUI [1,3])
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C0332282 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
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C1514873 (UMLS CUI-2)
C1879316 (UMLS CUI-3)
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C0189745 (UMLS CUI-2)
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C0205341 (UMLS CUI-2)
C0162563 (UMLS CUI-3)
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C0009566 (UMLS CUI-2)
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C0439669 (UMLS CUI-2)
C0035237 (UMLS CUI-3)
C0009566 (UMLS CUI-4)
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C0013922 (UMLS CUI-2)
C0009566 (UMLS CUI-3)
C0038454 (UMLS CUI-5)
C0007787 (UMLS CUI-7)
C0205373 (UMLS CUI-9)
C0013922 (UMLS CUI-10)
C0034065 (UMLS CUI-12)
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C1519255 (UMLS CUI [1,2])
C0332282 (UMLS CUI [1,3])
C0184661 (UMLS CUI [1,4])
C2348235 (UMLS CUI [1,5])
C1519255 (UMLS CUI [1,2])
C0332282 (UMLS CUI [1,3])
C0184661 (UMLS CUI [1,4])