ID
40654
Beschreibung
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
Stichworte
Versionen (3)
- 22.08.19 22.08.19 -
- 26.08.19 26.08.19 - Sarah Riepenhausen
- 30.04.20 30.04.20 - Sarah Riepenhausen
Rechteinhaber
ICHOM
Hochgeladen am
30. April 2020
DOI
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Lizenz
Creative Commons BY-NC 4.0
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ICHOM Atrial Fibrillation
Ongoing - Clinical Form
- StudyEvent: ODM
Beschreibung
Long-term consequences of disease
Alias
- UMLS CUI-1
- C0443252
- UMLS CUI-2
- C0686907
- UMLS CUI-3
- C0012634
Beschreibung
Inclusion Criteria: All patients Timing: Ongoing Data Source: Clinical Type: Single answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C0011065
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to DEATH Timing: Ongoing Data Source: Administrative date Type: Date by DD/MM/YYYY Response Options: DD/MM/YYYY
Datentyp
date
Maßeinheiten
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C1148348
Beschreibung
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
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1148348
- UMLS CUI [1,2]
- C0439673
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to DEATH Timing: Ongoing Data Source: Administrative data Type: Single answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C0007465
Beschreibung
Inclusion Criteria: All patients Timing: Ongoing Data Source: Clinical Type: Single answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C1320716
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to CARDIOVASCULAREVENT Timing: Ongoing Data Source: Clinical Type: Single answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0038454
- UMLS CUI [1,2]
- C0332307
Beschreibung
Inclusion Criteria: If ‘1, 2, or 3’ to EVENTTYPE Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Datentyp
date
Maßeinheiten
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C1320716
- UMLS CUI [1,2]
- C0011008
Beschreibung
Inclusion Criteria: All patients Timing: Ongoing Data Source: Clinical Type: Single answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0205314
- UMLS CUI [1,3]
- C0332140
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to HF Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Datentyp
date
Maßeinheiten
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0018801
- UMLS CUI [1,3]
- C0205314
- UMLS CUI [1,4]
- C0332140
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to HF Timing: Ongoing Data Source: Clinical Type: Single answer
Datentyp
integer
Alias
- UMLS CUI [1]
- C0428772
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to LVEF Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Datentyp
date
Maßeinheiten
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0428772
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to LVEF Timing: Ongoing Data Source: Clinical Type: Numerical value Response Options: LVEF measurement value
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0428772
- UMLS CUI [1,2]
- C0242485
Beschreibung
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
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0184666
- UMLS CUI [1,2]
- C0038454
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to CVHOSPADM Timing: Ongoing Data Source: Clinical Type: Single answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0184666
- UMLS CUI [1,3]
- C0038454
- UMLS CUI [1,4]
- C0085978
Beschreibung
Inclusion Criteria: All patients Timing: Ongoing Data Source: Clinical Type: Single answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0085611
- UMLS CUI [1,2]
- C0456962
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to FAA Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Datentyp
date
Maßeinheiten
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0085611
- UMLS CUI [1,2]
- C0456962
- UMLS CUI [1,3]
- C0011008
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to FAA Timing: Ongoing Data Source: Clinical Type: Single answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0085611
- UMLS CUI [1,2]
- C0456962
- UMLS CUI [1,3]
- C0087111
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to FAA Timing: Ongoing Data Source: Clinical Type: Single answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0456962
- UMLS CUI [1,2]
- C0085611
- UMLS CUI [1,3]
- C0150496
- UMLS CUI [1,4]
- C2709088
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to FAA Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Datentyp
date
Maßeinheiten
- 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
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to FAA Timing: Ongoing Data Source: Clinical Type: Single answer
Datentyp
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
Beschreibung
Complications of treatment
Alias
- UMLS CUI-1
- C0087111
- UMLS CUI-2
- C0009566
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to CVEVENT Timing: Ongoing Data Source: Clinical Type: Single answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0038454
- UMLS CUI [1,2]
- C0333275
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to HSTROKE Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Datentyp
date
Maßeinheiten
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0038454
- UMLS CUI [1,3]
- C0333275
Beschreibung
Inclusion Criteria: All patients Timing: Ongoing Data Source: Clinical Type: Single answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1302234
- UMLS CUI [1,2]
- C0019080
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to FBLEED Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Datentyp
date
Maßeinheiten
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C1302234
- UMLS CUI [1,3]
- C0019080
Beschreibung
Inclusion Criteria: All patients Timing: Ongoing Data Source: Clinical Type: Single answer
Datentyp
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
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to CRITICALBLEED Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Datentyp
date
Maßeinheiten
- 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
Beschreibung
Inclusion Criteria: All patients Timing: Ongoing Data Source: Clinical Type: Single answer
Datentyp
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
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to BLEEDOUTCOME Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Datentyp
date
Maßeinheiten
- 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
Beschreibung
Procedure
Alias
- UMLS CUI-1
- C0087111
Beschreibung
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
Datentyp
text
Alias
- UMLS CUI [1]
- C0455713
Beschreibung
Inclusion Criteria: If ‘1-8’ to PROCEDURE Timing: Ongoing Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY
Datentyp
date
Maßeinheiten
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C2584899
Beschreibung
SAE
Alias
- UMLS CUI-1
- C1519255
Beschreibung
Inclusion Criteria: If ‘1-8’ to PROCEDURE Timing: Ongoing Data Source: Clinical Type: Single answer
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0332282
- UMLS CUI [1,3]
- C0184661
Beschreibung
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
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0332282
- UMLS CUI [1,3]
- C0087111
Beschreibung
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
Datentyp
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
Beschreibung
Inclusion Criteria: If ‘1 = Yes’ to PROCEDURESAE Timing: Ongoing Data Source: Clinical Type: Date(s) Response Options: DD/MM/YYYY(s)
Datentyp
date
Maßeinheiten
- 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
Ähnliche Modelle
Ongoing - Clinical Form
- StudyEvent: ODM
C1442488 (UMLS CUI [1,2])
C0686907 (UMLS CUI-2)
C0012634 (UMLS CUI-3)
(Comment:en)
(Comment:en)
C0439673 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C0019080 (UMLS CUI-2)
(Comment:en)
C0205394 (UMLS CUI-2)
C0007222 (UMLS CUI-3)
C1704436 (UMLS CUI-4)
(Comment:en)
C1298908 (UMLS CUI-2)
C0007222 (UMLS CUI-3)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C0332307 (UMLS CUI [1,2])
(Comment:en)
C0205373 (UMLS CUI-2)
(Comment:en)
C1298908 (UMLS CUI-2)
C0008902 (UMLS CUI-3)
(Comment:en)
(Comment:en)
C0011008 (UMLS CUI [1,2])
C0205314 (UMLS CUI [1,2])
C0332140 (UMLS CUI [1,3])
(Comment:en)
(Comment:en)
C0018801 (UMLS CUI [1,2])
C0205314 (UMLS CUI [1,3])
C0332140 (UMLS CUI [1,4])
(Comment:en)
(Comment:en)
C0428772 (UMLS CUI [1,2])
C0242485 (UMLS CUI [1,2])
C0038454 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
C0184666 (UMLS CUI [1,2])
C0038454 (UMLS CUI [1,3])
C0085978 (UMLS CUI [1,4])
C1869045 (UMLS CUI-2)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C0007226 (UMLS CUI-2)
C0085978 (UMLS CUI-3)
(Comment:en)
C0456962 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
C0456962 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0456962 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
C0013227 (UMLS CUI-2)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C2007105 (UMLS CUI-2)
(Comment:en)
C0543467 (UMLS CUI-2)
(Comment:en)
(Comment:en)
(Comment:en)
C0085611 (UMLS CUI [1,2])
C0150496 (UMLS CUI [1,3])
C2709088 (UMLS CUI [1,4])
(Comment:en)
C0030695 (UMLS CUI-2)
(Comment:en)
(Comment:en)
(Comment:en)
C2709088 (UMLS CUI [1,2])
C0030695 (UMLS CUI [1,3])
C0456962 (UMLS CUI [1,4])
C0004238 (UMLS CUI [1,5])
C0456962 (UMLS CUI [1,2])
C0085611 (UMLS CUI [1,3])
C2709088 (UMLS CUI [1,4])
C0030695 (UMLS CUI [1,5])
(Comment:en)
(Comment:en)
C0009566 (UMLS CUI-2)
C0333275 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
C0038454 (UMLS CUI [1,2])
C0333275 (UMLS CUI [1,3])
C0019080 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
C1302234 (UMLS CUI [1,2])
C0019080 (UMLS CUI [1,3])
C0019080 (UMLS CUI [1,2])
C1511545 (UMLS CUI [1,3])
C0205146 (UMLS CUI [1,4])
C0231220 (UMLS CUI [2,1])
C0019080 (UMLS CUI [2,2])
C0178784 (UMLS CUI [2,3])
(Comment:en)
(Comment:en)
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])
C0019080 (UMLS CUI [2,2])
C0678227 (UMLS CUI [2,3])
C0686904 (UMLS CUI [2,4])
C1879316 (UMLS CUI [2,5])
(Comment:en)
(Comment:en)
C0443246 (UMLS CUI-2)
(Comment:en)
(Comment:en)
(Comment:en)
C0543467 (UMLS CUI-2)
C0397414 (UMLS CUI-3)
(Comment:en)
C0009429 (UMLS CUI-2)
C0547070 (UMLS CUI-3)
C0543467 (UMLS CUI-4)
C0397414 (UMLS CUI-5)
C2702800 (UMLS CUI-6)
(Comment:en)
C0205091 (UMLS CUI-2)
C4523927 (UMLS CUI-3)
C0004238 (UMLS CUI-5)
C0205091 (UMLS CUI-6)
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)
(Comment:en)
C0013778 (UMLS CUI-2)
(Comment:en)
(Comment:en)
C1963873 (UMLS CUI-2)
(Comment:en)
C4489286 (UMLS CUI-2)
(Comment:en)
C0332282 (UMLS CUI [1,2])
C0184661 (UMLS CUI [1,3])
(Comment:en)
(Comment:en)
C0332282 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
(Comment:en)
(Comment:en)
(Comment:en)
C1514873 (UMLS CUI-2)
C1879316 (UMLS CUI-3)
(Comment:en)
(Comment:en)
(Comment:en)
C0189745 (UMLS CUI-2)
(Comment:en)
C0205341 (UMLS CUI-2)
C0162563 (UMLS CUI-3)
(Comment:en)
(Comment:en)
C0009566 (UMLS CUI-2)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C0439669 (UMLS CUI-2)
C0035237 (UMLS CUI-3)
C0009566 (UMLS CUI-4)
(Comment:en)
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)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
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])