ID

37759

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 Annual – Clinical Form. It has to be filled in annually after 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

Versions (2)
  1. 8/22/19 8/22/19 -
  2. 4/30/20 4/30/20 - Sarah Riepenhausen
Copyright Holder

ICHOM

Uploaded on

August 22, 2019

DOI

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License

Creative Commons BY-NC 3.0
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ICHOM Atrial Fibrillation

English

Annual – Clinical Form

1 forms  
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
Time Relative to Baseline
Description

This Item does not exist in the original standard set, instead it is asked to do the following: Please timestamp all variables. Some Standard Set variables are collected at multiple timepoints, and we will ask you to submit these variables in a concatenated VARIABLEID_TIMESTAMP form for future analyses. For example, VARIABLEID_AT (After treatment); VARIABLEID_AS (After surgery); VARIABLEID_UPDATE (Update at least annually), etc.

Data type

text

Alias
UMLS CUI [1,1]
C0439564
UMLS CUI [1,2]
C1442488
Lifestyle interventions measured at annually
Description

Lifestyle interventions measured at annually

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]
C1519795
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]
C1513375
UMLS CUI [1,2]
C0556975
Health status measured at annually
Description

Health status measured at annually

Alias
UMLS CUI-1
C0018759
UMLS CUI-2
C0449440
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
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
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
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Similar models

Annual – Clinical Form

1 forms
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])
Time Relative to Baseline
Item
Time Relative to Baseline
text
C0439564 (UMLS CUI [1,1])
C1442488 (UMLS CUI [1,2])
Item Group
Lifestyle interventions measured at annually
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])
C1519795 (UMLS CUI [1,2])
Unit of Weight
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])
Height units
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])
BMI
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
C1513375 (UMLS CUI [1,1])
C0556975 (UMLS CUI [1,2])
The Physical Activity Q3
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)
C0439232 (UMLS CUI-2)
C0547043 (UMLS CUI-3)
C4321486 (UMLS CUI-4)
C0439232 (UMLS CUI-5)
(Comment:en)
CL Item
>150 minutes (2)
C0205172 (UMLS CUI-1)
C4321486 (UMLS CUI-2)
C0439232 (UMLS CUI-3)
(Comment:en)
Item Group
Health status measured at annually
C0018759 (UMLS CUI-1)
C0449440 (UMLS CUI-2)
Montreal Cognitive Assessment
Item
Montreal Cognitive Assessment for cognitive function
integer
C3496286 (UMLS CUI [1])
Item
Type of atrial fibrillation diagnosed
integer
C0004238 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Type of atrial fibrillation
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])
Disease duration
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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])
Gastrointestinal/other major haemorrhage
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
Complications of treatment
C0087111 (UMLS CUI-1)
C0009566 (UMLS CUI-2)
Item
Indicate whether there was a cardiovascular event?
integer
C1320716 (UMLS CUI [1])
Anticoagulation therapy
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)
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