ID

37747

Description

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/ 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 Baseline – Clinical Form. It has to be filled in at index event. 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 Montreal Cognitive Assessment Test. For more information see: https://www.mocatest.org/ The Standard set of ICHOM was supported by the BigData@Heart organization.

Link

http://www.ichom.org/

Keywords

  1. 8/21/19 8/21/19 -
  2. 8/22/19 8/22/19 -
  3. 8/26/19 8/26/19 - Sarah Riepenhausen
  4. 4/30/20 4/30/20 - Sarah Riepenhausen
  5. 3/15/21 3/15/21 - Dr. rer. medic Philipp Neuhaus
Copyright Holder

ICHOM

Uploaded on

August 21, 2019

DOI

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License

Creative Commons BY-NC 3.0

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ICHOM Atrial Fibrillation

Baseline - Clinical Form

Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
Indicate the patient's medical record number
Description

This number will not be shared with ICHOM. In the case patient-level data is submitted to ICHOM for benchmarking or research purposes, a separate ICHOM Patient Identifier will be created and cross-linking between the ICHOM Patient Identifier and the medical record number will only be known at the treating institution INCLUSION CRITERIA: All patients TIMING: On all forms REPORTING SOURCE: Administrative or clinical RESPONSE OPTIONS: According to institution

Data type

integer

Alias
UMLS CUI [1]
C1269815
Lifestyle interventions measured
Description

Lifestyle interventions measured

Alias
UMLS CUI-1
C0023676
UMLS CUI-2
C0184661
Indicate patient’s weight
Description

Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinical/Admin Type: Numerical value Response Options: Numerical value of weight in kilograms or pounds

Data type

float

Alias
UMLS CUI [1]
C0005910
Indicate units of weight
Description

Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinical/Admin Type: Numerical value

Data type

integer

Alias
UMLS CUI [1,1]
C0005910
UMLS CUI [1,2]
C0439148
Please indicate the height of the patient
Description

Supporting Definition: Height and weight are used to calculate BMI Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinical/Admin Type: Numerical value Response Options: Numerical value of height in metric or imperial system

Data type

float

Alias
UMLS CUI [1]
C0005890
Indicate units of height
Description

Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinical/Admin Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0005890
UMLS CUI [1,2]
C1519795
Body mass index ranges
Description

Supporting Definition: BMI = kg/m2 or BMI = 0.45x weight in pounds / (0.025x height in inches)2 Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinical/Admin Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C1305855
UMLS CUI [1,2]
C0683312
Total minutes per week of physical activity (multiply PAVSDAY by PAVSTIME)
Description

Supporting Definition: Average minutes per week of moderate intensity physical activity performed by patient Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0026606
UMLS CUI [1,2]
C0556975
Baseline health status
Description

Baseline health status

Alias
UMLS CUI-1
C1442488
UMLS CUI-2
C0018759
Indicate whether the patient has a documented history or is currently diagnosed with Gastrointestinal haemorrhage/other major haemorrhage
Description

Inclusion Criteria: All patients Timing: Baseline at time of atrial fibrillation diagnosis Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0017181
UMLS CUI [2,1]
C0521116
UMLS CUI [2,2]
C0017181
UMLS CUI [3,1]
C0262926
UMLS CUI [3,2]
C0205394
UMLS CUI [3,3]
C0205164
UMLS CUI [3,4]
C0019080
UMLS CUI [4,1]
C0521116
UMLS CUI [4,2]
C0205394
UMLS CUI [4,3]
C0205164
UMLS CUI [4,4]
C0019080
Indicate whether the patient has a documented history or is currently diagnosed with Intracranial haemorrhage
Description

Inclusion Criteria: All patients Timing: Baseline at time of atrial fibrillation diagnosis Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0151699
UMLS CUI [2,1]
C0521116
UMLS CUI [2,2]
C0151699
Indicate whether the patient has a documented history or is currently diagnosed with Hypertension
Description

Inclusion Criteria: All patients Timing: Baseline at time of atrial fibrillation diagnosis Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0020538
UMLS CUI [2,1]
C0521116
UMLS CUI [2,2]
C0020538
Indicate whether the patient has a documented history or is currently diagnosed with Diabetes mellitus
Description

Inclusion Criteria: All patients Timing: Baseline at time of atrial fibrillation diagnosis Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0011849
UMLS CUI [2,1]
C0521116
UMLS CUI [2,2]
C0011849
Indicate whether the patient has a documented history or is currently diagnosed with Heart failure
Description

Inclusion Criteria: All patients Timing: Baseline at time of atrial fibrillation diagnosis Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0018801
UMLS CUI [2,1]
C0521116
UMLS CUI [2,2]
C0018801
Indicate whether the patient has a documented history or is currently diagnosed with Ischemic heart disease or has suffered Myocardial infarction
Description

Inclusion Criteria: All patients Timing: Baseline at time of atrial fibrillation diagnosis Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0151744
UMLS CUI [2,1]
C0521116
UMLS CUI [2,2]
C0151744
UMLS CUI [3]
C0027051
Indicate whether the patient has a documented history or is currently diagnosed with Vascular diseases
Description

Inclusion Criteria: All patients Timing: Baseline at time of atrial fibrillation diagnosis Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0042373
UMLS CUI [2,1]
C0521116
UMLS CUI [2,2]
C0042373
Indicate whether the patient has a documented history or is currently diagnosed with Chronic obstructive pulmonary disease
Description

Inclusion Criteria: All patients Timing: Baseline at time of atrial fibrillation diagnosis Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0024117
UMLS CUI [2,1]
C0521116
UMLS CUI [2,2]
C0024117
Indicate whether the patient has a documented history or is currently diagnosed with Chronic kidney disease
Description

Inclusion Criteria: All patients Timing: Baseline at time of atrial fibrillation diagnosis Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C1561643
UMLS CUI [2,1]
C0521116
UMLS CUI [2,2]
C1561643
Indicate whether the patient has a documented history or is currently diagnosed with Hyperthyroidism
Description

Inclusion Criteria: All patients Timing: Baseline at time of atrial fibrillation diagnosis Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0020550
UMLS CUI [2,1]
C0521116
UMLS CUI [2,2]
C0020550
Indicate whether the patient has a documented history or is currently diagnosed with sleep apnea (obstructive sleep apnea, central sleep apnea and mixed/complex sleep apnea).
Description

Inclusion Criteria: All patients Timing: Baseline at time of atrial fibrillation diagnosis Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0037315
UMLS CUI [2,1]
C0521116
UMLS CUI [2,2]
C0037315
Indicate whether the patient has a documented history or is currently diagnosed with Stroke / Transient ischaemic attack
Description

Inclusion Criteria: All patients Timing: Baseline at time of atrial fibrillation diagnosis Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0038454
UMLS CUI [2,1]
C0521116
UMLS CUI [2,2]
C0038454
UMLS CUI [3,1]
C0262926
UMLS CUI [3,2]
C0007787
UMLS CUI [4,1]
C0521116
UMLS CUI [4,2]
C0007787
Indicate whether the patient has a documented history or is currently diagnosed with Cancer (excluding non-melanoma skin cancer)
Description

Inclusion Criteria: All patients Timing: Baseline at time of atrial fibrillation diagnosis Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0006826
UMLS CUI [1,3]
C0332300
UMLS CUI [1,4]
C1518408
UMLS CUI [1,5]
C0007114
UMLS CUI [2,1]
C0521116
UMLS CUI [2,2]
C0006826
UMLS CUI [2,3]
C0332300
UMLS CUI [2,4]
C1518408
UMLS CUI [2,5]
C0007114
Montreal Cognitive Assessment for cognitive function
Description

Supporting Definition: The MoCA assesses several cognitive domains. The test is a one-page 30-point test administered in approximately 10 minutes. The test and administration instructions are available for clinicians online. Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinician Type: Single answer Response Options: Value out of 30

Data type

integer

Alias
UMLS CUI [1]
C3496286
Health status measured at baseline
Description

Health status measured at baseline

Alias
UMLS CUI-1
C0018759
UMLS CUI-2
C1442488
UMLS CUI-3
C0449440
Type of atrial fibrillation diagnosed
Description

Supporting Definition: - Paroxysmal (episode of AF that terminates spontaneously or with intervention in less than seven days) - Persistent (AF that lasts for more than seven days and requires intervention in order for cardioversion to occur) - Long-standing persistent (episodes of AF extending greater than 12 months) - Permanent (AF that will not be cardioverted or has failed cardioversion) Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0332307
Indicate the year of atrial fibrillation diagnosis
Description

Supporting Definition: - Recent (less than a year) date unknown - Diagnosed at DD/MM/ YYYY - Unknown Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinician Type: Single answer Response Options: 0 = Recent, data unknown 999 = Unknown Date of diagnosis (DD/MM/YYYY)

Data type

integer

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0872146
Indicate the Date of of atrial fibrillation diagnosis
Description

Note: This item does not exist in the original standard set. Please fill in if you know when atrial fibrillation was diagnosed. Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinician Type: Single answer Response Options: Date by DD/MM/YYYY

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C2316983
DD/MM/YYYY
Indicate whether the patient is currently being prescribed medication for atrial fibrillation
Description

Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0521116
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0004238
Indicate whether Antiplatelet agents are currently prescribed for atrial fibrillation
Description

Inclusion Criteria: If “1 = Yes” to PHARMACOTHERAPY Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0521116
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0004238
UMLS CUI [2]
C0085826
Indicate whether Anticoagulants are currently prescribed for atrial fibrillation
Description

Inclusion Criteria: If “1 = Yes” to PHARMACOTHERAPY Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0521116
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0004238
UMLS CUI [2]
C0003280
Indicate whether Vitamin K antagonists e.g. warfarin are currently prescribed for atrial fibrillation
Description

Inclusion Criteria: If “1 = Yes” to PHARMATYPE2 Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0521116
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0004238
UMLS CUI [2]
C3653316
UMLS CUI [3]
C0043031
Indicate whether Non-VKA (direct) oral anticoagulants (N/DOACs) e.g. dabigatran, rivaroxaban, apixaban or edoxaban are currently prescribed for atrial fibrillation
Description

Inclusion Criteria: If “1 = Yes” to PHARMATYPE2 Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0521116
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0004238
UMLS CUI [2,1]
C1947931
UMLS CUI [2,2]
C0354604
UMLS CUI [3]
C2348066
UMLS CUI [4]
C1739768
UMLS CUI [5]
C1831808
UMLS CUI [6]
C2975435
Indicate whether beta blockers e.g. bisoprolol are currently prescribed for atrial fibrillation
Description

Inclusion Criteria: If “1 = Yes” to PHARMACOTHERAPY Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0521116
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0004238
UMLS CUI [2]
C0304516
UMLS CUI [3]
C0053799
Indicate whether NDHP calcium channel blocker e.g. diltiazem is currently prescribed for atrial fibrillation
Description

Inclusion Criteria: If “1 = Yes” to PHARMACOTHERAPY Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0521116
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0004238
UMLS CUI [2]
C0006684
UMLS CUI [3]
C0012373
Indicate whether Cardiac glycosides e.g. digoxin are currently prescribed for atrial fibrillation
Description

Inclusion Criteria: If “1 = Yes” to PHARMACOTHERAPY Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0521116
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0004238
UMLS CUI [2]
C0007158
UMLS CUI [3]
C0012265
Indicate whether Sodium channel blockers e.g. flecainide, quinidine, disopryamide are currently prescribed for atrial fibrillation
Description

Inclusion Criteria: If “1 = Yes” to PHARMACOTHERAPY Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0521116
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0004238
UMLS CUI [2]
C0872271
UMLS CUI [3]
C0016229
UMLS CUI [4]
C0034414
Indicate whether Potassium channel blockers e.g. sotalol, dofetilide are currently prescribed for atrial fibrillation
Description

Inclusion Criteria: If “1 = Yes” to PHARMACOTHERAPY Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0521116
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0004238
UMLS CUI [2]
C0872245
UMLS CUI [3]
C0037707
UMLS CUI [4]
C0114771
Indicate whether Multichannel blockers e.g. amiodarone or dronedarone are currently prescribed for atrial fibrillation
Description

Inclusion Criteria: If “1 = Yes” to PHARMACOTHERAPY Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0521116
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0004238
UMLS CUI [2,1]
C0439064
UMLS CUI [2,2]
C0872051
UMLS CUI [3]
C0002598
UMLS CUI [4]
C0766326
Indicate whether other medications are currently prescribed for atrial fibrillation
Description

Inclusion Criteria: If “1 = Yes” to PHARMACOTHERAPY Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0521116
UMLS CUI [1,2]
C0205394
UMLS CUI [1,3]
C0013227
UMLS CUI [1,4]
C0004238
Indicate whether the patient has undergone a Catheter-based ablation
Description

Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1]
C2702800
Indicate whether the patient has undergone a Pulmonary vein isolation
Description

Inclusion Criteria: If “1 = Yes” to PROCEDURETYPE1 Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1]
C2702800
UMLS CUI [2]
C3544330
Indicate whether the patient has undergone a Complex left atrial catheter ablation
Description

Inclusion Criteria: If “1 = Yes” to PROCEDURETYPE1 Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C2702800
UMLS CUI [1,2]
C0443246
Indicate whether the patient has undergone an AV node ablation
Description

Inclusion Criteria: If “1 = Yes” to PROCEDURETYPE1 Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1]
C2702800
UMLS CUI [2]
C3275044
Indicate whether the patient has undergone an Atrial flutter ablation (simple)
Description

Inclusion Criteria: If “1 = Yes” to PROCEDURETYPE1 Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1]
C2702800
UMLS CUI [2]
C2702801
Indicate whether the patient has undergone a surgical ablation procedure (openheart maze procedure, minimally invasive maze surgery, robotically assisted maze surgery)
Description

Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2,1]
C0547070
UMLS CUI [2,2]
C0543467
UMLS CUI [2,3]
C0397414
Indicate whether the patient has undergone hybrid surgical-catheter ablation
Description

Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2,1]
C0009429
UMLS CUI [2,2]
C0547070
UMLS CUI [2,3]
C0543467
UMLS CUI [2,4]
C0397414
UMLS CUI [2,5]
C2702800
Indicate whether the patient has undergone left atrial appendage closure/occlusion procedure with device e.g. Watchman device or Amplatzer plug device
Description

Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2,1]
C4523927
UMLS CUI [2,2]
C0205091
Indicate whether the patient has undergone Left atrial appendage ligation/excision (surgical)
Description

Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2,1]
C0225860
UMLS CUI [2,2]
C0598782
UMLS CUI [2,3]
C0023690
UMLS CUI [2,4]
C0543467
UMLS CUI [3,1]
C0225860
UMLS CUI [3,2]
C0598782
UMLS CUI [3,3]
C0728940
UMLS CUI [3,4]
C0543467
Indicate whether the patient has undergone Electrocardioversion
Description

Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2]
C0013778
Indicate whether the patient has undergone Pharmacological cardioversion
Description

Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2]
C1963873
Indicate whether the patient has undergone a Pacemaker implantation
Description

Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinician Type: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2]
C0189842
Long-term consequences of disease
Description

Long-term consequences of disease

Alias
UMLS CUI-1
C0443252
UMLS CUI-2
C0686907
UMLS CUI-3
C0012634
Was the patient prescribed anticoagulation therapy?
Description

Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical Type: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0003281
Provide date when the treatment began
Description

Inclusion Criteria: If ‘1 = Yes’ to ANTICOAG Timing: Baseline Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0003281
UMLS CUI [1,2]
C1531783
DD/MM/YYYY
If the patient was not prescribed anticoagulation therapy, please provide reason
Description

Inclusion Criteria: If ‘0 = No’ to ANTICOAG Timing: Baseline Data Source: Clinical Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C1298908
UMLS CUI [1,2]
C0003281
UMLS CUI [1,3]
C0566251
Did the patient receive a left atrial appendage occlusion device, closure , ligation or excision of the left atrial appendage?
Description

Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C4523927
UMLS CUI [1,2]
C0205091
UMLS CUI [2]
C0441597
UMLS CUI [3]
C1521802
UMLS CUI [4,1]
C0023690
UMLS CUI [4,2]
C0728940
Please provide the date when the patient received a left atrial appendage occlusion device, closure or excision of the left atrial appendage?
Description

Inclusion Criteria: If ‘1 = Yes’ to LAAOD Timing: Baseline Data Source: Clinical Type: Single answer Response Options: DD/MM/YYYY

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C2584899
UMLS CUI [1,2]
C4523927
UMLS CUI [1,3]
C0205091
UMLS CUI [2]
C0441597
UMLS CUI [3]
C1521802
UMLS CUI [4,1]
C0023690
UMLS CUI [4,2]
C0728940
DD/MM/YYYY
Complications of treatment
Description

Complications of treatment

Alias
UMLS CUI-1
C0087111
UMLS CUI-2
C0009566
Indicate whether there was a cardiovascular event?
Description

Inclusion Criteria: All patients Timing: Baseline, Annually Data Source: Clinical Type: Single answer

Data type

integer

Alias
UMLS CUI [1]
C1320716
Which class of medication was discontinued by the patient 1 = Antithrombotic
Description

Inclusion Criteria: If ‘1 = Yes’ to MEDSEDISCONT Timing: Baseline, 6 monthly Data Source: Clinical Type: Multiple answer

Data type

boolean

Alias
UMLS CUI [1,1]
C0558681
UMLS CUI [1,2]
C1704311
Which class of medication was discontinued by the patient 2 = Anticoagulation
Description

Inclusion Criteria: If ‘1 = Yes’ to MEDSEDISCONT Timing: Baseline, 6 monthly Data Source: Clinical Type: Multiple answer

Data type

boolean

Alias
UMLS CUI [1,1]
C0558681
UMLS CUI [1,2]
C0003281
Which class of medication was discontinued by the patient 3 = Antiplatelet
Description

Inclusion Criteria: If ‘1 = Yes’ to MEDSEDISCONT Timing: Baseline, 6 monthly Data Source: Clinical Type: Multiple answer

Data type

boolean

Alias
UMLS CUI [1,1]
C0558681
UMLS CUI [1,2]
C1096021
Which class of medication was discontinued by the patient 4 = Rhythm control
Description

Inclusion Criteria: If ‘1 = Yes’ to MEDSEDISCONT Timing: Baseline, 6 monthly Data Source: Clinical Type: Multiple answer

Data type

boolean

Alias
UMLS CUI [1,1]
C0558681
UMLS CUI [1,2]
C0871269
UMLS CUI [1,3]
C2587213
Which class of medication was discontinued by the patient 5 = Rate control
Description

Inclusion Criteria: If ‘1 = Yes’ to MEDSEDISCONT Timing: Baseline, 6 monthly Data Source: Clinical Type: Multiple answer

Data type

boolean

Alias
UMLS CUI [1,1]
C0558681
UMLS CUI [1,2]
C0018810
UMLS CUI [1,3]
C2587213
Which class of medication was discontinued by the patient 6 = Other (specify)
Description

Inclusion Criteria: If ‘1 = Yes’ to MEDSEDISCONT Timing: Baseline, 6 monthly Data Source: Clinical Type: Multiple answer

Data type

boolean

Alias
UMLS CUI [1,1]
C0558681
UMLS CUI [1,2]
C0205394
Which class of medication was discontinued by the patient 999 = Unknown
Description

Inclusion Criteria: If ‘1 = Yes’ to MEDSEDISCONT Timing: Baseline, 6 monthly Data Source: Clinical Type: Multiple answer

Data type

boolean

Alias
UMLS CUI [1,1]
C0558681
UMLS CUI [1,2]
C0439673
Other class of medication discontinuation, specification
Description

Note: This item does not exist in the original standard set. It can be filled in if you tick "MEDCLASS_6". Inclusion Criteria: If you tick "MEDCLASS_6" Timing: Baseline, 6 monthly Data Source: Clinical Type: Free text

Data type

text

Alias
UMLS CUI [1,1]
C0558681
UMLS CUI [1,2]
C0205394
UMLS CUI [1,3]
C2348235

Similar models

Baseline - Clinical Form

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Patient ID
Item
Indicate the patient's medical record number
integer
C1269815 (UMLS CUI [1])
Item Group
Lifestyle interventions measured
C0023676 (UMLS CUI-1)
C0184661 (UMLS CUI-2)
Weight
Item
Indicate patient’s weight
float
C0005910 (UMLS CUI [1])
Item
Indicate units of weight
integer
C0005910 (UMLS CUI [1,1])
C0439148 (UMLS CUI [1,2])
Code List
Indicate units of weight
CL Item
kilograms  (1)
C0439209 (UMLS CUI-1)
(Comment:en)
CL Item
pounds (2)
C0439219 (UMLS CUI-1)
(Comment:en)
Height
Item
Please indicate the height of the patient
float
C0005890 (UMLS CUI [1])
Item
Indicate units of height
integer
C0005890 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Code List
Indicate units of height
CL Item
centimeters (1)
C0475210 (UMLS CUI-1)
(Comment:en)
CL Item
inches (2)
C0439204 (UMLS CUI-1)
(Comment:en)
Item
Body mass index ranges
integer
C1305855 (UMLS CUI [1,1])
C0683312 (UMLS CUI [1,2])
Code List
Body mass index ranges
CL Item
<18.5 Underweight (1)
C0041667 (UMLS CUI-1)
(Comment:en)
CL Item
18.5 – 24.9 Normal weight (2)
C2712185 (UMLS CUI-1)
(Comment:en)
CL Item
25-29.9 Pre-obesity (3)
C0497406 (UMLS CUI-1)
(Comment:en)
CL Item
>30.0 Obesity (4)
C0028754 (UMLS CUI-1)
(Comment:en)
Item
Total minutes per week of physical activity (multiply PAVSDAY by PAVSTIME)
integer
C0026606 (UMLS CUI [1,1])
C0556975 (UMLS CUI [1,2])
Code List
Total minutes per week of physical activity (multiply PAVSDAY by PAVSTIME)
CL Item
0 minutes (0)
C0919414 (UMLS CUI-1)
C0439232 (UMLS CUI-2)
(Comment:en)
CL Item
1-150 minutes (1)
C0205447 (UMLS CUI-1)
C4321486 (UMLS CUI-2)
C0439232 (UMLS CUI-3)
(Comment:en)
CL Item
>150 minutes (2)
C0205172 (UMLS CUI-1)
C4321486 (UMLS CUI-2)
C0439232 (UMLS CUI-3)
(Comment:en)
Item Group
Baseline health status
C1442488 (UMLS CUI-1)
C0018759 (UMLS CUI-2)
Item
Indicate whether the patient has a documented history or is currently diagnosed with Gastrointestinal haemorrhage/other major haemorrhage
integer
C0262926 (UMLS CUI [1,1])
C0017181 (UMLS CUI [1,2])
C0521116 (UMLS CUI [2,1])
C0017181 (UMLS CUI [2,2])
C0262926 (UMLS CUI [3,1])
C0205394 (UMLS CUI [3,2])
C0205164 (UMLS CUI [3,3])
C0019080 (UMLS CUI [3,4])
C0521116 (UMLS CUI [4,1])
C0205394 (UMLS CUI [4,2])
C0205164 (UMLS CUI [4,3])
C0019080 (UMLS CUI [4,4])
Code List
Indicate whether the patient has a documented history or is currently diagnosed with Gastrointestinal haemorrhage/other major haemorrhage
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has a documented history or is currently diagnosed with Intracranial haemorrhage
integer
C0262926 (UMLS CUI [1,1])
C0151699 (UMLS CUI [1,2])
C0521116 (UMLS CUI [2,1])
C0151699 (UMLS CUI [2,2])
Code List
Indicate whether the patient has a documented history or is currently diagnosed with Intracranial haemorrhage
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has a documented history or is currently diagnosed with Hypertension
integer
C0262926 (UMLS CUI [1,1])
C0020538 (UMLS CUI [1,2])
C0521116 (UMLS CUI [2,1])
C0020538 (UMLS CUI [2,2])
Code List
Indicate whether the patient has a documented history or is currently diagnosed with Hypertension
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has a documented history or is currently diagnosed with Diabetes mellitus
integer
C0262926 (UMLS CUI [1,1])
C0011849 (UMLS CUI [1,2])
C0521116 (UMLS CUI [2,1])
C0011849 (UMLS CUI [2,2])
Code List
Indicate whether the patient has a documented history or is currently diagnosed with Diabetes mellitus
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has a documented history or is currently diagnosed with Heart failure
integer
C0262926 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
C0521116 (UMLS CUI [2,1])
C0018801 (UMLS CUI [2,2])
Code List
Indicate whether the patient has a documented history or is currently diagnosed with Heart failure
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has a documented history or is currently diagnosed with Ischemic heart disease or has suffered Myocardial infarction
integer
C0262926 (UMLS CUI [1,1])
C0151744 (UMLS CUI [1,2])
C0521116 (UMLS CUI [2,1])
C0151744 (UMLS CUI [2,2])
C0027051 (UMLS CUI [3])
Code List
Indicate whether the patient has a documented history or is currently diagnosed with Ischemic heart disease or has suffered Myocardial infarction
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has a documented history or is currently diagnosed with Vascular diseases
integer
C0262926 (UMLS CUI [1,1])
C0042373 (UMLS CUI [1,2])
C0521116 (UMLS CUI [2,1])
C0042373 (UMLS CUI [2,2])
Code List
Indicate whether the patient has a documented history or is currently diagnosed with Vascular diseases
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has a documented history or is currently diagnosed with Chronic obstructive pulmonary disease
integer
C0262926 (UMLS CUI [1,1])
C0024117 (UMLS CUI [1,2])
C0521116 (UMLS CUI [2,1])
C0024117 (UMLS CUI [2,2])
Code List
Indicate whether the patient has a documented history or is currently diagnosed with Chronic obstructive pulmonary disease
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has a documented history or is currently diagnosed with Chronic kidney disease
integer
C0262926 (UMLS CUI [1,1])
C1561643 (UMLS CUI [1,2])
C0521116 (UMLS CUI [2,1])
C1561643 (UMLS CUI [2,2])
Code List
Indicate whether the patient has a documented history or is currently diagnosed with Chronic kidney disease
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has a documented history or is currently diagnosed with Hyperthyroidism
integer
C0262926 (UMLS CUI [1,1])
C0020550 (UMLS CUI [1,2])
C0521116 (UMLS CUI [2,1])
C0020550 (UMLS CUI [2,2])
Code List
Indicate whether the patient has a documented history or is currently diagnosed with Hyperthyroidism
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has a documented history or is currently diagnosed with sleep apnea (obstructive sleep apnea, central sleep apnea and mixed/complex sleep apnea).
integer
C0262926 (UMLS CUI [1,1])
C0037315 (UMLS CUI [1,2])
C0521116 (UMLS CUI [2,1])
C0037315 (UMLS CUI [2,2])
Code List
Indicate whether the patient has a documented history or is currently diagnosed with sleep apnea (obstructive sleep apnea, central sleep apnea and mixed/complex sleep apnea).
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has a documented history or is currently diagnosed with Stroke / Transient ischaemic attack
integer
C0262926 (UMLS CUI [1,1])
C0038454 (UMLS CUI [1,2])
C0521116 (UMLS CUI [2,1])
C0038454 (UMLS CUI [2,2])
C0262926 (UMLS CUI [3,1])
C0007787 (UMLS CUI [3,2])
C0521116 (UMLS CUI [4,1])
C0007787 (UMLS CUI [4,2])
Code List
Indicate whether the patient has a documented history or is currently diagnosed with Stroke / Transient ischaemic attack
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has a documented history or is currently diagnosed with Cancer (excluding non-melanoma skin cancer)
integer
C0262926 (UMLS CUI [1,1])
C0006826 (UMLS CUI [1,2])
C0332300 (UMLS CUI [1,3])
C1518408 (UMLS CUI [1,4])
C0007114 (UMLS CUI [1,5])
C0521116 (UMLS CUI [2,1])
C0006826 (UMLS CUI [2,2])
C0332300 (UMLS CUI [2,3])
C1518408 (UMLS CUI [2,4])
C0007114 (UMLS CUI [2,5])
Code List
Indicate whether the patient has a documented history or is currently diagnosed with Cancer (excluding non-melanoma skin cancer)
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Montreal Cognitive Assessment
Item
Montreal Cognitive Assessment for cognitive function
integer
C3496286 (UMLS CUI [1])
Item Group
Health status measured at baseline
C0018759 (UMLS CUI-1)
C1442488 (UMLS CUI-2)
C0449440 (UMLS CUI-3)
Item
Type of atrial fibrillation diagnosed
integer
C0004238 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Code List
Type of atrial fibrillation diagnosed
CL Item
Paroxysmal (1)
C0235480 (UMLS CUI-1)
(Comment:en)
CL Item
Persistent (2)
C2585653 (UMLS CUI-1)
(Comment:en)
CL Item
Long-standing persistent (3)
C3873617 (UMLS CUI-1)
(Comment:en)
CL Item
Permanent (4)
C2586056 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate the year of atrial fibrillation diagnosis
integer
C0004238 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
Code List
Indicate the year of atrial fibrillation diagnosis
CL Item
Recent, data unknown (0)
C0332185 (UMLS CUI-1)
C1511726 (UMLS CUI-2)
C0439673 (UMLS CUI-3)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Date of atrial fibrillation diagnosis
Item
Indicate the Date of of atrial fibrillation diagnosis
date
C0004238 (UMLS CUI [1,1])
C2316983 (UMLS CUI [1,2])
Item
Indicate whether the patient is currently being prescribed medication for atrial fibrillation
integer
C0521116 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
Code List
Indicate whether the patient is currently being prescribed medication for atrial fibrillation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether Antiplatelet agents are currently prescribed for atrial fibrillation
integer
C0521116 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
C0085826 (UMLS CUI [2])
Code List
Indicate whether Antiplatelet agents are currently prescribed for atrial fibrillation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether Anticoagulants are currently prescribed for atrial fibrillation
integer
C0521116 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
C0003280 (UMLS CUI [2])
Code List
Indicate whether Anticoagulants are currently prescribed for atrial fibrillation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether Vitamin K antagonists e.g. warfarin are currently prescribed for atrial fibrillation
integer
C0521116 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
C3653316 (UMLS CUI [2])
C0043031 (UMLS CUI [3])
Code List
Indicate whether Vitamin K antagonists e.g. warfarin are currently prescribed for atrial fibrillation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether Non-VKA (direct) oral anticoagulants (N/DOACs) e.g. dabigatran, rivaroxaban, apixaban or edoxaban are currently prescribed for atrial fibrillation
integer
C0521116 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
C1947931 (UMLS CUI [2,1])
C0354604 (UMLS CUI [2,2])
C2348066 (UMLS CUI [3])
C1739768 (UMLS CUI [4])
C1831808 (UMLS CUI [5])
C2975435 (UMLS CUI [6])
Code List
Indicate whether Non-VKA (direct) oral anticoagulants (N/DOACs) e.g. dabigatran, rivaroxaban, apixaban or edoxaban are currently prescribed for atrial fibrillation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether beta blockers e.g. bisoprolol are currently prescribed for atrial fibrillation
integer
C0521116 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
C0304516 (UMLS CUI [2])
C0053799 (UMLS CUI [3])
Code List
Indicate whether beta blockers e.g. bisoprolol are currently prescribed for atrial fibrillation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether NDHP calcium channel blocker e.g. diltiazem is currently prescribed for atrial fibrillation
integer
C0521116 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
C0006684 (UMLS CUI [2])
C0012373 (UMLS CUI [3])
Code List
Indicate whether NDHP calcium channel blocker e.g. diltiazem is currently prescribed for atrial fibrillation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether Cardiac glycosides e.g. digoxin are currently prescribed for atrial fibrillation
integer
C0521116 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
C0007158 (UMLS CUI [2])
C0012265 (UMLS CUI [3])
Code List
Indicate whether Cardiac glycosides e.g. digoxin are currently prescribed for atrial fibrillation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether Sodium channel blockers e.g. flecainide, quinidine, disopryamide are currently prescribed for atrial fibrillation
integer
C0521116 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
C0872271 (UMLS CUI [2])
C0016229 (UMLS CUI [3])
C0034414 (UMLS CUI [4])
Code List
Indicate whether Sodium channel blockers e.g. flecainide, quinidine, disopryamide are currently prescribed for atrial fibrillation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether Potassium channel blockers e.g. sotalol, dofetilide are currently prescribed for atrial fibrillation
integer
C0521116 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
C0872245 (UMLS CUI [2])
C0037707 (UMLS CUI [3])
C0114771 (UMLS CUI [4])
Code List
Indicate whether Potassium channel blockers e.g. sotalol, dofetilide are currently prescribed for atrial fibrillation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether Multichannel blockers e.g. amiodarone or dronedarone are currently prescribed for atrial fibrillation
integer
C0521116 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
C0439064 (UMLS CUI [2,1])
C0872051 (UMLS CUI [2,2])
C0002598 (UMLS CUI [3])
C0766326 (UMLS CUI [4])
Code List
Indicate whether Multichannel blockers e.g. amiodarone or dronedarone are currently prescribed for atrial fibrillation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether other medications are currently prescribed for atrial fibrillation
integer
C0521116 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
C0004238 (UMLS CUI [1,4])
Code List
Indicate whether other medications are currently prescribed for atrial fibrillation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has undergone a Catheter-based ablation
integer
C2702800 (UMLS CUI [1])
Code List
Indicate whether the patient has undergone a Catheter-based ablation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has undergone a Pulmonary vein isolation
integer
C2702800 (UMLS CUI [1])
C3544330 (UMLS CUI [2])
Code List
Indicate whether the patient has undergone a Pulmonary vein isolation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has undergone a Complex left atrial catheter ablation
integer
C2702800 (UMLS CUI [1,1])
C0443246 (UMLS CUI [1,2])
Code List
Indicate whether the patient has undergone a Complex left atrial catheter ablation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has undergone an AV node ablation
integer
C2702800 (UMLS CUI [1])
C3275044 (UMLS CUI [2])
Code List
Indicate whether the patient has undergone an AV node ablation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has undergone an Atrial flutter ablation (simple)
integer
C2702800 (UMLS CUI [1])
C2702801 (UMLS CUI [2])
Code List
Indicate whether the patient has undergone an Atrial flutter ablation (simple)
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has undergone a surgical ablation procedure (openheart maze procedure, minimally invasive maze surgery, robotically assisted maze surgery)
integer
C0004238 (UMLS CUI [1])
C0547070 (UMLS CUI [2,1])
C0543467 (UMLS CUI [2,2])
C0397414 (UMLS CUI [2,3])
Code List
Indicate whether the patient has undergone a surgical ablation procedure (openheart maze procedure, minimally invasive maze surgery, robotically assisted maze surgery)
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has undergone hybrid surgical-catheter ablation
integer
C0004238 (UMLS CUI [1])
C0009429 (UMLS CUI [2,1])
C0547070 (UMLS CUI [2,2])
C0543467 (UMLS CUI [2,3])
C0397414 (UMLS CUI [2,4])
C2702800 (UMLS CUI [2,5])
Code List
Indicate whether the patient has undergone hybrid surgical-catheter ablation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has undergone left atrial appendage closure/occlusion procedure with device e.g. Watchman device or Amplatzer plug device
integer
C0004238 (UMLS CUI [1])
C4523927 (UMLS CUI [2,1])
C0205091 (UMLS CUI [2,2])
Code List
Indicate whether the patient has undergone left atrial appendage closure/occlusion procedure with device e.g. Watchman device or Amplatzer plug device
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has undergone Left atrial appendage ligation/excision (surgical)
integer
C0004238 (UMLS CUI [1])
C0225860 (UMLS CUI [2,1])
C0598782 (UMLS CUI [2,2])
C0023690 (UMLS CUI [2,3])
C0543467 (UMLS CUI [2,4])
C0225860 (UMLS CUI [3,1])
C0598782 (UMLS CUI [3,2])
C0728940 (UMLS CUI [3,3])
C0543467 (UMLS CUI [3,4])
Code List
Indicate whether the patient has undergone Left atrial appendage ligation/excision (surgical)
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has undergone Electrocardioversion
integer
C0004238 (UMLS CUI [1])
C0013778 (UMLS CUI [2])
Code List
Indicate whether the patient has undergone Electrocardioversion
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has undergone Pharmacological cardioversion
integer
C0004238 (UMLS CUI [1])
C1963873 (UMLS CUI [2])
Code List
Indicate whether the patient has undergone Pharmacological cardioversion
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has undergone a Pacemaker implantation
integer
C0004238 (UMLS CUI [1])
C0189842 (UMLS CUI [2])
Code List
Indicate whether the patient has undergone a Pacemaker implantation
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item Group
Long-term consequences of disease
C0443252 (UMLS CUI-1)
C0686907 (UMLS CUI-2)
C0012634 (UMLS CUI-3)
Item
Was the patient prescribed anticoagulation therapy?
integer
C0003281 (UMLS CUI [1])
Code List
Was the patient prescribed anticoagulation therapy?
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
Date when anticoagulation therapy started
Item
Provide date when the treatment began
date
C0003281 (UMLS CUI [1,1])
C1531783 (UMLS CUI [1,2])
Item
If the patient was not prescribed anticoagulation therapy, please provide reason
integer
C1298908 (UMLS CUI [1,1])
C0003281 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
Code List
If the patient was not prescribed anticoagulation therapy, please provide reason
CL Item
Not recommended by current guidelines. Anticoagulants are not appropriate for beneficial reasons e.g. young patient with no underlying heart conditions (1)
C3846195 (UMLS CUI-1)
C1548788 (UMLS CUI-2)
C0003280 (UMLS CUI-3)
C0086387 (UMLS CUI-4)
(Comment:en)
CL Item
Not recommended by current guidelines. Anticoagulants inappropriate for harmful reason or due to harm reasons e.g. patients with serious bleeding events (2)
C3846195 (UMLS CUI-1)
C1548788 (UMLS CUI-2)
C0003280 (UMLS CUI-3)
C0035647 (UMLS CUI-4)
(Comment:en)
CL Item
Patient decline (3)
C0040809 (UMLS CUI-1)
(Comment:en)
CL Item
Medication and / or monitoring / follow-up unavailable (4)
C0013227 (UMLS CUI-1)
C1522577 (UMLS CUI-2)
C0686905 (UMLS CUI-3)
C0030695 (UMLS CUI-4)
C1522577 (UMLS CUI-5)
C0686905 (UMLS CUI-6)
(Comment:en)
CL Item
Cognitive dysfunction (5)
C0338656 (UMLS CUI-1)
(Comment:en)
CL Item
Short life expectancy (6)
C0023671 (UMLS CUI-1)
C1806781 (UMLS CUI-2)
(Comment:en)
CL Item
High costs (including health insurance issue) (7)
C0085552 (UMLS CUI-1)
C0021682 (UMLS CUI-2)
(Comment:en)
CL Item
Other (specify) (8)
C3840932 (UMLS CUI-1)
(Comment:en)
Item
Did the patient receive a left atrial appendage occlusion device, closure , ligation or excision of the left atrial appendage?
integer
C4523927 (UMLS CUI [1,1])
C0205091 (UMLS CUI [1,2])
C0441597 (UMLS CUI [2])
C1521802 (UMLS CUI [3])
C0023690 (UMLS CUI [4,1])
C0728940 (UMLS CUI [4,2])
Code List
Did the patient receive a left atrial appendage occlusion device, closure , ligation or excision of the left atrial appendage?
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
Date of Left atrial appendage occlusion device, closure or excision of the left atrial appendage
Item
Please provide the date when the patient received a left atrial appendage occlusion device, closure or excision of the left atrial appendage?
date
C2584899 (UMLS CUI [1,1])
C4523927 (UMLS CUI [1,2])
C0205091 (UMLS CUI [1,3])
C0441597 (UMLS CUI [2])
C1521802 (UMLS CUI [3])
C0023690 (UMLS CUI [4,1])
C0728940 (UMLS CUI [4,2])
Item Group
Complications of treatment
C0087111 (UMLS CUI-1)
C0009566 (UMLS CUI-2)
Item
Indicate whether there was a cardiovascular event?
integer
C1320716 (UMLS CUI [1])
Code List
Indicate whether there was a cardiovascular event?
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
Class of medication discontinued by patient: Antithrombotic
Item
Which class of medication was discontinued by the patient 1 = Antithrombotic
boolean
C0558681 (UMLS CUI [1,1])
C1704311 (UMLS CUI [1,2])
Class of medication discontinued by patient: Anticoagulation
Item
Which class of medication was discontinued by the patient 2 = Anticoagulation
boolean
C0558681 (UMLS CUI [1,1])
C0003281 (UMLS CUI [1,2])
Class of medication discontinued by patient: Antiplatelet
Item
Which class of medication was discontinued by the patient 3 = Antiplatelet
boolean
C0558681 (UMLS CUI [1,1])
C1096021 (UMLS CUI [1,2])
Class of medication discontinued by patient: Rhythm control
Item
Which class of medication was discontinued by the patient 4 = Rhythm control
boolean
C0558681 (UMLS CUI [1,1])
C0871269 (UMLS CUI [1,2])
C2587213 (UMLS CUI [1,3])
Class of medication discontinued by patient: Rate control
Item
Which class of medication was discontinued by the patient 5 = Rate control
boolean
C0558681 (UMLS CUI [1,1])
C0018810 (UMLS CUI [1,2])
C2587213 (UMLS CUI [1,3])
Class of medication discontinued by patient: Other
Item
Which class of medication was discontinued by the patient 6 = Other (specify)
boolean
C0558681 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Class of medication discontinued by patient: Unknown
Item
Which class of medication was discontinued by the patient 999 = Unknown
boolean
C0558681 (UMLS CUI [1,1])
C0439673 (UMLS CUI [1,2])
Other class of medication discontinuation, specification
Item
Other class of medication discontinuation, specification
text
C0558681 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])

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