ID

40546

Description

HEART FAILURE DATA COLLECTION Version 1.1.4 Revised October 31st, 2017 www.ichom.org Notice: This work was conducted using resources from ICHOM, the International Consortium for Health Outcomes Measurement (www.ICHOM.org). The content is solely the responsibility of the authors and does not necessarily represent the official views of ICHOM. Conditions: Heart Failure Treatment Approaches: Pharmacotherapy | Invasive Therapy | Rehabilitation This ODM-file contains clinician-reported outcome variables. It should be tracked 6-monthly for life, starting 30 days and 6 months post-index event. The collection rhythm has to be reset in case of an acute admission (including complications): It should be collected during the acute admission, 30 days post-discharge, 6 months following last admission and 6 monthly from then on. Use of the following Scores for this standard set: KCCQ-12: Kansas City Cardiomyopathy Questionnaire-Short Version: You can obtain a license to use this instrument at your institution by visiting http://cvoutcomes.org/licenses NYHA – New York Heart Association Functional Classification: The NYHA is free for all health care organizations, and a license is not needed. PROMIS Physical Function Short Form 4a – Patient-Reported Outcome Measurement Information System: PROMIS Physical Function is free for all health care organizations, and a license is not needed. For more information, please visit http://www.healthmeasures.net/explore-measurement-systems/promis/obtain-administer-measures . As http://www.nihpromis.org/ is the official distribution site for PROMIS questionnaires and translations, only the total score will be included in this version of the standard set. Patient Health Questionnaire (PHQ-2): Copyright by Pfizer: "content found on the PHQ Screeners site is free for download and use as stated within the PHQ Screeners site, please visit http://www.phqscreeners.com/ for more information. ICHOM was supported for the Heart Failure Standard Set by GIG Cymru NHS Wales, American Heart Association, British Heart Foundation, Heart Failure Association of the ESC and European Society of Cardiology. Publication: Burns DJP, Arora J, Okunade O, Beltrame JF, Bernardez-Pereira S, Crespo-Leiro MG, et al. International Consortium for Health Outcomes Measurement (ICHOM): Standardized Patient-Centered Outcomes Measurement Set for Heart Failure Patients. JACC: Heart Failure. 2020 Mar 1;8(3):212–22. For this version of the standard set, semantic annotation with UMLS CUIs has been added.

Link

www.ichom.org

Keywords

  1. 11/16/18 11/16/18 - Sarah Riepenhausen
  2. 4/30/20 4/30/20 - Sarah Riepenhausen
Copyright Holder

ICHOM

Uploaded on

April 30, 2020

DOI

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License

Creative Commons BY-NC 4.0

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ICHOM Heart Failure

Clinician-reported Outcome

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 (e.g. 30 days after index event, 6 months follow-up, 1 year follow-up, ...)
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_BASE (baseline); VARIABLEID_6MO (6 month follow-up); VARIABLEID_1YR (1 year follow-up), etc.

Data type

text

Alias
UMLS CUI [1,1]
C0439564
UMLS CUI [1,2]
C1442488
Baseline health status
Description

Baseline health status

Alias
UMLS CUI-1
C1442488
UMLS CUI-2
C0449440
Please indicate the weight of the patient
Description

Height and weight are used to calculate BMI INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported or administrative RESPONSE OPTIONS: Numeric value of weight in metric or imperial system

Data type

float

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

INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported or administrative TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1,1]
C0005910
UMLS CUI [1,2]
C1519795
Have you ever been told by your doctor that you have atrial fibrillation?
Description

Item is phrased as a patient reported measure. However, if the patient is unable to answer, this information can be abstracted from the medical records. INCLUSION CRITERIA: All patients TIMING: At index event for HF and if "0 = No" or "999 = Unknown" to AFIB, tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0004238
Have you ever been told by your doctor that you've had a heart attack (this is sometimes called a myocardial infarction, or MI)?
Description

Item is phrased as a patient reported measure. However, if the patient is unable to answer, this information can be abstracted from the medical records. INCLUSION CRITERIA: All patients TIMING: At index event for HF and if "0 = No" or "999 = Unknown" to PRIORMI, tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C1275835
Do you currently smoke, or have you smoked cigarettes or tobacco over the past year?
Description

Smoking status (of cigarettes or tobacco). Item is phrased as a patient reported measure. However, if the patient is unable to answer, this information can be abstracted from the medical records. INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C1519386
Do you drink more than one alcoholic drink a day?
Description

One standard alcoholic drink is: 12 ounces of regular beer (about 5 percent alcohol) 5 ounces of wine (about 12 percent alcohol) 1.5 ounces of distilled spirits (about 40 percent alcohol) Item is phrased as a patient reported measure. However, if the patient is unable to answer, this information can be abstracted from the medical records. INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0001948
Indicate whether the patient has a documented history of hypertension, diagnosed and treated with medication and/or diet and/or exercise
Description

INCLUSION CRITERIA: All patients TIMING: At index event for HF and if "0 = No" or "999 = Unknown" to HYPERTEN, tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0020538
Have you ever been told by your doctor that you have diabetes?
Description

Item is phrased as a patient reported measure. However, if the patient is unable to answer, this information can be abstracted from the medical records. INCLUSION CRITERIA: All patients TIMING: At index event for HF and if "0 = No" or "999 = Unknown" to DIAB, tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0011849
Indicate whether the patient has a chronic lung disease
Description

Including but not limited to COPD and asthma INCLUSION CRITERIA: All patients TIMING: At index event for HF and if "0 = No" or "999 = Unknown" to CHRONLD, tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C1533075
Indicate whether the patient has a diagnosis of renal dysfunction
Description

Renal dysfunction is the documented history of AKI or Increase in serum creatinine by ≥ 0.3 mg/dl (≥ 26.5 l mol/l) within 48 hours; or increase in serum creatinine to ≥ 1.5 times baseline, which is known or presumed to have occurred within the prior 7 days; or urine volume < 0.5 ml/kg/h for 6 hours; or new requirement for dialysis INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C3279454
Treatment variables
Description

Treatment variables

Alias
UMLS CUI-1
C0087111
Indicate whether the patient is currently being prescribed medication for heart failure
Description

INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0018801
Indicate whether ACE inhibitors are currently prescribed for heart failure
Description

INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and if "0 = No" or "999 = Unknown" to AFIB, tracked ongoing REPORTING SOURCE: Clinician-reported, patient-reported, or administrative TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0003015
Indicate whether Angiotensin Receptor II Blockers are currently prescribed for heart failure
Description

INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0521942
Indicate whether an Angiotensin Receptor Blocker/Neprilysin Inhibitor combination is currently prescribed for heart failure
Description

INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1,1]
C0521942
UMLS CUI [1,2]
C4051513
UMLS CUI [1,3]
C0205195
Indicate whether Beta Blockers are currently prescribed for heart failure
Description

INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0001645
Indicate whether Calcium Channel Blockers are currently prescribed for heart failure
Description

INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0006684
Indicate whether Digoxin is currently prescribed for heart failure
Description

INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0012265
Indicate whether Diuretics are currently prescribed for heart failure
Description

INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0012798
Indicate whether Hydralazine and Isosorbide Dinitrate are currently prescribed for heart failure
Description

INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0020223
UMLS CUI [2]
C0022252
Indicate whether Ivabradine is currently prescribed for heart failure
Description

INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0257190
Indicate whether Mineralocorticoid Receptor Antagonists are currently prescribed for heart failure
Description

INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C1579268
Indicate whether other medications are currently prescribed for heart failure
Description

INCLUSION CRITERIA: If "1 = Yes" to PHARMACOTHERAPY TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0205394
Did the patient receive a cardiac device to treat heart failure?
Description

INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1,1]
C2735362
UMLS CUI [1,2]
C0018787
Indicate the device type
Description

ICD = Implantable Cardioverter Defibrillator CRT = Cardiac Resynchronisation Therapy INCLUSION CRITERIA: If "1 = Yes" to DEVPROCEDURE TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C3177146
Indicate the date of DEVPROCEDURE
Description

INCLUSION CRITERIA: If "1 = Yes" to DEVPROCEDURE TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Date by DD/MM/YYYY

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C2584899
UMLS CUI [1,2]
C2828363
DD/MM/YYYY
Did the patient undergo cardiac surgery?
Description

INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0018821
Indicate the cardiac surgery type
Description

CABG = Cardiac surgery for heart failure INCLUSION CRITERIA: if "1 = Yes" to CARDSURG TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1,1]
C0018821
UMLS CUI [1,2]
C0332307
Indicate the date of CARDSURG
Description

INCLUSION CRITERIA: If "1 = Yes" to CARDSURG TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Date by DD/MM/YYYY

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0018821
UMLS CUI [1,2]
C0011008
DD/MM/YYYY
Has cardiac rehabilitation been initiated?
Description

Cardiac rehabilitation is a medically-supervised programme that involves adopting heart-healthy lifestyle changes to address risk factors for cardiovascular disease. This programme includes exercise training, education on heart-healthy living, and counseling to reduce stress and helps patients return to an active life. INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0700431
Degree of Health
Description

Degree of Health

Alias
UMLS CUI-1
C0018759
Patient symptoms
Description

NYHA - New York Heart Association classification of heart failure (Functional Capacity) INCLUSION CRITERIA: All patients TIMING: Tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1,1]
C1275491
UMLS CUI [1,2]
C1457887
Objective assessment of patient
Description

NYHA - New York Heart Association classification of heart failure (Objective assessment by clinician) INCLUSION CRITERIA: All patients TIMING: Tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1,1]
C1275491
UMLS CUI [1,2]
C1571702
Burden of Care
Description

Burden of Care

Alias
UMLS CUI-1
C0087111
UMLS CUI-2
C2828008
Indicate the date the patient was admitted
Description

Date used to calculate total length of stay and post-procedure length of stay INCLUSION CRITERIA: All patients TIMING: Tracked ongoing REPORTING SOURCE: Administrative data TYPE: Date by DD/MM/YYYY

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C3263562
UMLS CUI [1,2]
C0011008
DD/MM/YYYY
Indicate the date the patient was discharged
Description

Date used to calculate total length of stay INCLUSION CRITERIA: All patients TIMING: Tracked ongoing REPORTING SOURCE: Administrative data TYPE: Date by DD/MM/YYYY

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0030685
DD/MM/YYYY
Did the patient’s appointment or admission have any complications which were related to a device for Heart Failure including, but not exclusively: active bleeding requiring exploration and/or transfusion, abscess related to the device, minor infection (localized, treated with antibiotics and surgical drainage) related to the device, major infection (systemic, requiring device explant) related to the device, minor malfunction (requiring follow-up appointment/reprogramming), and/or major malfunction (requiring explant or revision)?
Description

INCLUSION CRITERIA: All patients TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C2828363
Indicate the date of COMPLDEVICE
Description

INCLUSION CRITERIA: if "1 = Yes" to COMPLDEVICE TIMING: At index event for HF and tracked ongoing REPORTING SOURCE: Clinician-reported TYPE: Date by DD/MM/YYYY RESPONSE OPTIONS: DD/MM/YYYY or 999 = Unknown

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C2828363
DD/MM/YYYY
Did the patient have a major healthcare-associated infection (requiring IV antibiotics and/or prolonged hospital stay – 14 days or more) during this admission?
Description

INCLUSION CRITERIA: All patients TIMING: Tracked at index event & acute admissions due to heart failure REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0205721
Indicate the date of COMPLHOSP
Description

INCLUSION CRITERIA: If "1 = Yes" to COMPLHOSP TIMING: Tracked at index event & acute admissions due to heart failure REPORTING SOURCE: Clinician-reported TYPE: Date by DD/MM/YYYY RESPONSE OPTIONS: DD/MM/YYYY or 999 = Unknown

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0205721
UMLS CUI [1,2]
C0011008
DD/MM/YYYY
Did the patient have a major adverse event related to Heart Failure medication during this admission, and/or as a cause of this admission?
Description

A major adverse event is a response to a drug which is noxious and unintended, and which occurs at doses normally used in a person for the prophylaxis, diagnosis, or therapy of disease, or for the modifications of physiological function. INCLUSION CRITERIA: All patients TIMING: Tracked at index event & acute admissions due to heart failure REPORTING SOURCE: Clinician-reported TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C0013227
Indicate the date of COMPLMED
Description

INCLUSION CRITERIA: If "1 = Yes" to COMPLMED TIMING: Tracked at index event & acute admissions due to heart failure REPORTING SOURCE: Clinician-reported TYPE: Date by DD/MM/YYYY RESPONSE OPTIONS: DD/MM/YYYY or 999 = Unknown

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0011008
DD/MM/YYYY
How many times has the patient been hospitalised in the last 12 months due to heart failure?
Description

This variable is acollected every 12 months from date of entry into the set. INCLUSION CRITERIA: All patients TIMING: Baseline and 12-monthly REPORTING SOURCE: Adminstrative or patient/caregiver reported TYPE: Numerical RESPONSE OPTIONS: Numerical value or 999 = Unknown

Data type

integer

Alias
UMLS CUI [1,1]
C0184666
UMLS CUI [1,2]
C4086728
UMLS CUI [1,3]
C0018801
How many hospital appointments has the patient had in the last 12 months due to heart failure?
Description

This variable is acollected every 12 months from date of entry into the set. INCLUSION CRITERIA: All patients TIMING: Baseline and 12-monthly REPORTING SOURCE: Adminstrative or patient/caregiver reported TYPE: Numerical RESPONSE OPTIONS: Numerical value or 999 = Unknown

Data type

integer

Alias
UMLS CUI [1,1]
C0030675
UMLS CUI [1,2]
C4086728
UMLS CUI [1,3]
C0018801
Mortality
Description

Mortality

Alias
UMLS CUI-1
C0026566
Indicate if the patient has died
Description

INCLUSION CRITERIA: All patients TIMING: Tracked ongoing REPORTING SOURCE: Administrative data TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C0011065
Indicate the date the patient was declared dead
Description

Patients who die before during a hospital admission before baseline baseline data have been collected should also be included INCLUSION CRITERIA: If "1 = Yes” to DEATH TIMING: Tracked ongoing REPORTING SOURCE: Administrative data TYPE: Date by DD/MM/YYYY RESPONSE OPTIONS: DD/MM/YYYY or 999 = Unknown

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1]
C1148348
DD/MM/YYYY
Indicate where patient died
Description

INCLUSION CRITERIA: If "1 = Yes” to DEATH TIMING: Tracked ongoing REPORTING SOURCE: Administrative data TYPE: Single Answer

Data type

integer

Alias
UMLS CUI [1]
C2924451

Similar models

Clinician-reported Outcome

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 (e.g. 30 days after index event, 6 months follow-up, 1 year follow-up, ...)
text
C0439564 (UMLS CUI [1,1])
C1442488 (UMLS CUI [1,2])
Item Group
Baseline health status
C1442488 (UMLS CUI-1)
C0449440 (UMLS CUI-2)
Weight
Item
Please indicate the weight of the patient
float
C0005910 (UMLS CUI [1])
Item
Indicate units of weight
integer
C0005910 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Code List
Indicate units of weight
CL Item
kg (1)
C0439209 (UMLS CUI-1)
(Comment:en)
CL Item
lbs (2)
C0439219 (UMLS CUI-1)
(Comment:en)
Item
Have you ever been told by your doctor that you have atrial fibrillation?
integer
C0004238 (UMLS CUI [1])
Code List
Have you ever been told by your doctor that you have 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
Have you ever been told by your doctor that you've had a heart attack (this is sometimes called a myocardial infarction, or MI)?
integer
C1275835 (UMLS CUI [1])
Code List
Have you ever been told by your doctor that you've had a heart attack (this is sometimes called a myocardial infarction, or MI)?
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
Do you currently smoke, or have you smoked cigarettes or tobacco over the past year?
integer
C1519386 (UMLS CUI [1])
Code List
Do you currently smoke, or have you smoked cigarettes or tobacco over the past year?
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
Do you drink more than one alcoholic drink a day?
integer
C0001948 (UMLS CUI [1])
Code List
Do you drink more than one alcoholic drink a day?
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 of hypertension, diagnosed and treated with medication and/or diet and/or exercise
integer
C0262926 (UMLS CUI [1,1])
C0020538 (UMLS CUI [1,2])
Code List
Indicate whether the patient has a documented history of hypertension, diagnosed and treated with medication and/or diet and/or exercise
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
Have you ever been told by your doctor that you have diabetes?
integer
C0011849 (UMLS CUI [1])
Code List
Have you ever been told by your doctor that you have diabetes?
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 chronic lung disease
integer
C1533075 (UMLS CUI [1])
Code List
Indicate whether the patient has a chronic lung 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 diagnosis of renal dysfunction
integer
C3279454 (UMLS CUI [1])
Code List
Indicate whether the patient has a diagnosis of renal dysfunction
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
Treatment variables
C0087111 (UMLS CUI-1)
Item
Indicate whether the patient is currently being prescribed medication for heart failure
integer
C0013227 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
Code List
Indicate whether the patient is currently being prescribed medication for 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 ACE inhibitors are currently prescribed for heart failure
integer
C0003015 (UMLS CUI [1])
Code List
Indicate whether ACE inhibitors are currently prescribed for 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 Angiotensin Receptor II Blockers are currently prescribed for heart failure
integer
C0521942 (UMLS CUI [1])
Code List
Indicate whether Angiotensin Receptor II Blockers are currently prescribed for 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 an Angiotensin Receptor Blocker/Neprilysin Inhibitor combination is currently prescribed for heart failure
integer
C0521942 (UMLS CUI [1,1])
C4051513 (UMLS CUI [1,2])
C0205195 (UMLS CUI [1,3])
Code List
Indicate whether an Angiotensin Receptor Blocker/Neprilysin Inhibitor combination is currently prescribed for 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 Beta Blockers are currently prescribed for heart failure
integer
C0001645 (UMLS CUI [1])
Code List
Indicate whether Beta Blockers are currently prescribed for 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 Calcium Channel Blockers are currently prescribed for heart failure
integer
C0006684 (UMLS CUI [1])
Code List
Indicate whether Calcium Channel Blockers are currently prescribed for 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 Digoxin is currently prescribed for heart failure
integer
C0012265 (UMLS CUI [1])
Code List
Indicate whether Digoxin is currently prescribed for 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 Diuretics are currently prescribed for heart failure
integer
C0012798 (UMLS CUI [1])
Code List
Indicate whether Diuretics are currently prescribed for 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 Hydralazine and Isosorbide Dinitrate are currently prescribed for heart failure
integer
C0020223 (UMLS CUI [1])
C0022252 (UMLS CUI [2])
Code List
Indicate whether Hydralazine and Isosorbide Dinitrate are currently prescribed for 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 Ivabradine is currently prescribed for heart failure
integer
C0257190 (UMLS CUI [1])
Code List
Indicate whether Ivabradine is currently prescribed for 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 Mineralocorticoid Receptor Antagonists are currently prescribed for heart failure
integer
C1579268 (UMLS CUI [1])
Code List
Indicate whether Mineralocorticoid Receptor Antagonists are currently prescribed for 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 other medications are currently prescribed for heart failure
integer
C0013227 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Code List
Indicate whether other medications are currently prescribed for 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
Did the patient receive a cardiac device to treat heart failure?
integer
C2735362 (UMLS CUI [1,1])
C0018787 (UMLS CUI [1,2])
Code List
Did the patient receive a cardiac device to treat 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 the device type
integer
C3177146 (UMLS CUI [1])
Code List
Indicate the device type
CL Item
ICD (1)
C0162589 (UMLS CUI-1)
(Comment:en)
CL Item
CRT (2)
C2936377 (UMLS CUI-1)
(Comment:en)
CL Item
ICD + CRT (3)
C0162589 (UMLS CUI-1)
C2936377 (UMLS CUI-2)
C0205195 (UMLS CUI-3)
(Comment:en)
CL Item
Other (4)
C2735362 (UMLS CUI-1)
C0018787 (UMLS CUI-2)
C0205394 (UMLS CUI-3)
(Comment:en)
CL Item
Unknown (999)
C2735362 (UMLS CUI-1)
C0018787 (UMLS CUI-2)
C0439673 (UMLS CUI-3)
(Comment:en)
Date of device procedure
Item
Indicate the date of DEVPROCEDURE
date
C2584899 (UMLS CUI [1,1])
C2828363 (UMLS CUI [1,2])
Item
Did the patient undergo cardiac surgery?
integer
C0018821 (UMLS CUI [1])
Code List
Did the patient undergo cardiac 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 the cardiac surgery type
integer
C0018821 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Code List
Indicate the cardiac surgery type
CL Item
CABG only (1)
C0010055 (UMLS CUI-1)
(Comment:en)
CL Item
Valve (2)
C1292963 (UMLS CUI-1)
(Comment:en)
CL Item
CABG + valve (3)
C0010055 (UMLS CUI-1)
C1292963 (UMLS CUI-2)
C0205195 (UMLS CUI-3)
(Comment:en)
CL Item
Other (4)
C0205394 (UMLS CUI-1)
C0018821 (UMLS CUI-2)
(Comment:en)
CL Item
Unknown (999)
C0018821 (UMLS CUI-1)
C0439673 (UMLS CUI-2)
(Comment:en)
Date of cardiac surgery
Item
Indicate the date of CARDSURG
date
C0018821 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Has cardiac rehabilitation been initiated?
integer
C0700431 (UMLS CUI [1])
Code List
Has cardiac rehabilitation been initiated?
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
Degree of Health
C0018759 (UMLS CUI-1)
Item
Patient symptoms
integer
C1275491 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
Code List
Patient symptoms
CL Item
Class I: No limitation of physical activity. Ordinary physical activity does not cause undue fatigue, palpitation, dyspnea (shortness of breath). (0)
C1319793 (UMLS CUI-1)
(Comment:en)
CL Item
Class II: Slight limitation of physical activity. Comfortable at rest. Ordinary physical activity results in fatigue, palpitation, dyspnea (shortness of breath). (1)
C1319794 (UMLS CUI-1)
(Comment:en)
CL Item
Class III: Marked limitation of physical activity. Comfortable at rest. Less than ordinary activity causes fatigue, palpitation, or dyspnea. (2)
C1319795 (UMLS CUI-1)
(Comment:en)
CL Item
Class IV: Unable to carry on any physical activity without discomfort. Symptoms of heart failure at rest. If any physical activity is undertaken, discomfort increases. (3)
C1319796 (UMLS CUI-1)
(Comment:en)
Item
Objective assessment of patient
integer
C1275491 (UMLS CUI [1,1])
C1571702 (UMLS CUI [1,2])
Code List
Objective assessment of patient
CL Item
Class A: No objective evidence of cardiovascular disease. No symptoms and no limitation in ordinary physical activity. (0)
C1275491 (UMLS CUI-1)
C3662279 (UMLS CUI-2)
(Comment:en)
CL Item
Class B: Objective evidence of minimal cardiovascular disease. Mild symptoms and slight limitation during ordinary activity. Comfortable at rest. (1)
C1275491 (UMLS CUI-1)
C3536548 (UMLS CUI-2)
(Comment:en)
CL Item
Class C: Objective evidence of moderately severe cardiovascular disease. Marked limitation in activity due to symptoms, even during less-than-ordinary activity. Comfortable only at rest. (2)
C1275491 (UMLS CUI-1)
C3532937 (UMLS CUI-2)
(Comment:en)
CL Item
Class D: Objective evidence of severe cardiovascular disease. Severe limitation. Experiences symptoms even while at rest. (3)
C1275491 (UMLS CUI-1)
C3532936 (UMLS CUI-2)
(Comment:en)
Item Group
Burden of Care
C0087111 (UMLS CUI-1)
C2828008 (UMLS CUI-2)
Date of arrival
Item
Indicate the date the patient was admitted
date
C3263562 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Date of discharge
Item
Indicate the date the patient was discharged
date
C0011008 (UMLS CUI [1,1])
C0030685 (UMLS CUI [1,2])
Item
Did the patient’s appointment or admission have any complications which were related to a device for Heart Failure including, but not exclusively: active bleeding requiring exploration and/or transfusion, abscess related to the device, minor infection (localized, treated with antibiotics and surgical drainage) related to the device, major infection (systemic, requiring device explant) related to the device, minor malfunction (requiring follow-up appointment/reprogramming), and/or major malfunction (requiring explant or revision)?
integer
C0009566 (UMLS CUI [1,1])
C2828363 (UMLS CUI [1,2])
Code List
Did the patient’s appointment or admission have any complications which were related to a device for Heart Failure including, but not exclusively: active bleeding requiring exploration and/or transfusion, abscess related to the device, minor infection (localized, treated with antibiotics and surgical drainage) related to the device, major infection (systemic, requiring device explant) related to the device, minor malfunction (requiring follow-up appointment/reprogramming), and/or major malfunction (requiring explant or revision)?
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)
Date of complication due to device
Item
Indicate the date of COMPLDEVICE
date
C0009566 (UMLS CUI [1,1])
C2828363 (UMLS CUI [1,2])
Item
Did the patient have a major healthcare-associated infection (requiring IV antibiotics and/or prolonged hospital stay – 14 days or more) during this admission?
integer
C0205721 (UMLS CUI [1])
Code List
Did the patient have a major healthcare-associated infection (requiring IV antibiotics and/or prolonged hospital stay – 14 days or more) during this admission?
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)
Date of diagnosis of healthcare-associated infection
Item
Indicate the date of COMPLHOSP
date
C0205721 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Did the patient have a major adverse event related to Heart Failure medication during this admission, and/or as a cause of this admission?
integer
C0009566 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Code List
Did the patient have a major adverse event related to Heart Failure medication during this admission, and/or as a cause of this admission?
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)
Date of diagnosis of complication due to medication
Item
Indicate the date of COMPLMED
date
C0009566 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Hospital admissions
Item
How many times has the patient been hospitalised in the last 12 months due to heart failure?
integer
C0184666 (UMLS CUI [1,1])
C4086728 (UMLS CUI [1,2])
C0018801 (UMLS CUI [1,3])
Hospital appointments
Item
How many hospital appointments has the patient had in the last 12 months due to heart failure?
integer
C0030675 (UMLS CUI [1,1])
C4086728 (UMLS CUI [1,2])
C0018801 (UMLS CUI [1,3])
Item Group
Mortality
C0026566 (UMLS CUI-1)
Item
Indicate if the patient has died
integer
C0011065 (UMLS CUI [1])
Code List
Indicate if the patient has died
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)
Date of death
Item
Indicate the date the patient was declared dead
date
C1148348 (UMLS CUI [1])
Item
Indicate where patient died
integer
C2924451 (UMLS CUI [1])
Code List
Indicate where patient died
CL Item
Hospital: acute or community hospitals/units but not psychiatric hospitals (1)
C0019994 (UMLS CUI-1)
(Comment:en)
CL Item
Own residence: the death occurred in the place of usual residence where this is not a communal establishment (2)
C0682130 (UMLS CUI-1)
(Comment:en)
CL Item
Care home: private home or residential home or specialist nursing homes (3)
C0028688 (UMLS CUI-1)
(Comment:en)
CL Item
Hospices: many hospices are 'freestanding' but some are found within hospitals. Also, hospices increasingly work in the community  (4)
C3826197 (UMLS CUI-1)
(Comment:en)
CL Item
Other (888)
C0205394 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)

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