ID

40600

Description

ICHOM Hypertension in low- and middle-income countries data collection Version 1.0.0 Revised: November 3rd, 2017 International Consortium for Health Outcomes Measurement (ICHOM), Source: http://www.ichom.org/ Notice: This work was conducted using resources from ICHOM, the International Consortium for Health Outcomes Measurement (www.ICHOM.org). The content is solely the responsibility of the authors and does not necessarily represent the official views of ICHOM. The following condition and treatment approaches (or interventions) are covered by our Standard Set. Condition: Hypertension (ICD-10: I10) Treatment Approaches: Pharmacological and Non-Pharmacological Collecting Patient-Reported Outcome Measures: Survey Used: EuroQol-5D-3L (EQ-5D-3L). As a licence is needed for use of EQ-5D-3L questionnaires, the actual questions are not part of this version of the standard set. For licensing information see: https://euroqol.org/support/how-to-obtain-eq-5d/ This document contains the Baseline - Clinical Form. It has to be filled in for patient's entry into study. PROMIS Single Question on erectile Dysfunction. Free for use in clinical practice. 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. Beliefs about Medication Questionnaire (BMQ)-Specific: Copyrighted, permission to use the scale can be obtained from Professor Rob Horne’s research team. The scoring guide can be found in the original validation article: Horne et al. (1999) The beliefs about medicines questionnaire: The development and evaluation of a new method for assessing the cognitive representation of medication. Psychology & Health, 14:1. Hill-Bone Compliance to High Blood Pressure Therapy Scale - South Africa Version: Permission to use the scale can be obtained from Estelle V. Lambert’s research team, The scoring guide can be found in the original validation article: Lambert, E.V. et al. (2006) Cross-Cultural Validation of the Hill-Bone Compliance To High Blood Pressure Therapy Scale in a South African, Primary Healthcare Setting. Ethnicity and Disease, 16. WHO STEPS Instrument. Free for use in clinical practice and a license is not required. http://www.who.int/chp/steps/instrument/en/ International Physical Activity Questionnaire(IPAQ)-Short Form: Publically available, open access, and no permissions are required to use it. https://sites.google.com/site/theipaq/ Alternative Quality of Life Surveys: PROMIS Global-10 Free for use in clinical practice. 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. Veteran’s Rand 12-Item Health Survey (VR-12). Free for all health care organizations, license required and can be requested at: http://bit.ly/2ir84sG. As a license is needed, the actual questions are not part of this version of the standard set. 12-Item Short Form Survey (SF-12). As a license is needed for use of SF-12 questionaires, the actual questions are not part of this version of the standard set. For more information see: http://bit.ly/2AcNLrme This Standard set was supported by the Novartis Foundation. Publication: Zack R, Okunade O, Olson E, et al. Improving Hypertension Outcome Measurement in Low- and Middle-Income Countries. Hypertension. 2019;73:990–997. doi: 10.1161/HYPERTENSIONAHA.118.11916 For this version of the standard set, semantic annotation with UMLS CUIs has been added.

Link

http://www.ichom.org/

Keywords

  1. 6/4/19 6/4/19 -
  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 Hypertension in low- and middle-income countries

Baseline - Clinical Form

Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
Patient ID
Description

Supporting Definition: 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: Administratively-­‐reported or clinician-­‐reported Type: Numerical Response Options: According to institution

Data type

integer

Alias
UMLS CUI [1]
C2348585
Demographic factors
Description

Demographic factors

Indicate the patient's date of birth
Description

Inclusion Criteria: All patients Timing: Baseline Reporting Source: Administratively‐reported or clinician-­reported Type: Date by DD/MM/YYYY Response Options: DD/MM/YYYY

Data type

date

Measurement units
  • DD/MM/YYYY
Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C0421451
DD/MM/YYYY
Indicate the patient's sex at birth
Description

Inclusion Criteria: All patients Timing: Baseline Reporting Source: Administratively-­reported or clinician-­reported Type: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0079399
Clinical Factors
Description

Clinical Factors

Indicate if the patient has a documented history of diabetes mellitus (regardless of duration of disease or need for anti-diabetic agents). If newly diagnosed, the diagnosis should meet the following criteria: Fasting plasma glucose >= 7.0mmol/L (126 mg/dL) or 2-hour plasma glucose >= 11.1 mmol/L (200mg/dL) [2 hours post 75g glucose load]
Description

Inclusion Criteria: All patients Timing: Baseline and annually until positive diagnosis of diabetes Reporting Source: Clinician-­reported Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0011849
UMLS CUI [2,1]
C0011849
UMLS CUI [2,2]
C1518321
For newly diagnosed diabetics indicate fasting plasma glucose if available
Description

Supporting Definition: Fasting plasma glucose value in mg/dL or mmol/L Inclusion Criteria: Optional Timing: Baseline and annually Reporting Source: Clinician­‐reported Type: Numerical Response Options: N/A

Data type

float

Alias
UMLS CUI [1]
C0583513
Units of fasting plasma glucose
Description

Inclusion Criteria: If fasting plasma glucose value is provided Timing: Baseline and annually Reporting Source: Clinician-­reported Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0583513
UMLS CUI [1,2]
C1519795
Indicate the patient's height in centimeters or inches
Description

Supporting Definition: Height and weight are used to calculate BMI Inclusion Criteria: All patients Timing: Baseline Reporting Source: Clinician­‐reported Type: Numerical Response Options: Numerical value

Data type

float

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

Inclusion Criteria: All patients Timing: Baseline Reporting Source: Clinician­‐reported Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0005890
UMLS CUI [1,2]
C1519795
Indicate the patient's weight in kilograms or pounds
Description

Supporting Definition: Height and weight are used to calculate BMI Inclusion Criteria: All patients Timing: Baseline and annually Reporting Source: Clinician-­reported Type: Numerical Response Options: Numerical value

Data type

float

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

Inclusion Criteria: All patients Timing: Baseline and annually Reporting Source: Clinician-­reported Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0005910
UMLS CUI [1,2]
C1519795
Indicate if the patient is on lipid lowering therapy
Description

Inclusion Criteria: All patients Timing: Baseline and annually Reporting Source: Clinician-­reported Type: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0585943
Specify lipid lowering therapy
Description

Inclusion Criteria: If answered 1 to LIPIDLOW Timing: Baseline and annually Reporting Source: Clinician-­reported Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0585943
UMLS CUI [1,2]
C2348235
Has the patient had a creatinine test?
Description

Inclusion Criteria: Optional Timing: Baseline and annually Reporting Source: Clinician-­reported Type: Single answer

Data type

integer

Alias
UMLS CUI [1]
C0201976
Provide the patient's serum creatinine reading
Description

Supporting Definition: Please provide the most recent value Inclusion Criteria: If responded "yes" to CREADONE Timing: Baseline and annually Reporting Source: Clinician­‐reported Type: Numerical, enter "000" if unknown Response Options: Numerical value

Data type

float

Alias
UMLS CUI [1,1]
C0201976
UMLS CUI [1,2]
C1274040
What are the units of creatinine?
Description

Inclusion Criteria: If value for creatinine is provided Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0201976
UMLS CUI [1,2]
C1519795
Was the creatinine reader calibrated to IDMS (isotope dilution mass spectrometry)
Description

Inclusion Criteria: If value for creatinine is provided Timing: Baseline and annually Reporting Source: Clinician-­reported/administratively­‐reported Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0201976
UMLS CUI [1,2]
C0006751
UMLS CUI [1,3]
C3274766
Treatment variables
Description

Treatment variables

Alias
UMLS CUI-1
C0087111
What is the management approach?
Description

Supporting Definition: Non‐pharmacological management includes lifestyle interventions, exercise, diet and other non-­pharmacological approaches. Inclusion Criteria: All patients Timing: Baseline and annually Reporting Source: Clinician-­reported Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0449445
Is patient on any of the following drug classes? 1 = ACEi/ARB
Description

Supporting Definition: Please select all options that apply Inclusion Criteria: If answered '1' to treatment approach (TX) Timing: Baseline and annually Reporting Source: Clinician­‐reported Type: Multiple answer

Data type

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C0596463
UMLS CUI [2]
C0003015
UMLS CUI [3]
C0521942
Is patient on any of the following drug classes? 2 = Alpha‐blocker
Description

Supporting Definition: Please select all options that apply Inclusion Criteria: If answered '1' to treatment approach (TX) Timing: Baseline and annually Reporting Source: Clinician­‐reported Type: Multiple answer

Data type

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C0596463
UMLS CUI [2]
C0001641
Is patient on any of the following drug classes? 3 = Beta-blocker
Description

Supporting Definition: Please select all options that apply Inclusion Criteria: If answered '1' to treatment approach (TX) Timing: Baseline and annually Reporting Source: Clinician­‐reported Type: Multiple answer

Data type

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C0596463
UMLS CUI [2]
C0001645
Is patient on any of the following drug classes? 4 = Loop Diuretics
Description

Supporting Definition: Please select all options that apply Inclusion Criteria: If answered '1' to treatment approach (TX) Timing: Baseline and annually Reporting Source: Clinician­‐reported Type: Multiple answer

Data type

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C0596463
UMLS CUI [2]
C0354100
Is patient on any of the following drug classes? 5 = Thiazides
Description

Supporting Definition: Please select all options that apply Inclusion Criteria: If answered '1' to treatment approach (TX) Timing: Baseline and annually Reporting Source: Clinician­‐reported Type: Multiple answer

Data type

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C0596463
UMLS CUI [2]
C0012802
Is patient on any of the following drug classes? 6 = Calcium channel blocker
Description

Supporting Definition: Please select all options that apply Inclusion Criteria: If answered '1' to treatment approach (TX) Timing: Baseline and annually Reporting Source: Clinician­‐reported Type: Multiple answer

Data type

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C0596463
UMLS CUI [2]
C0006684
Is patient on any of the following drug classes? 7 = Other
Description

Supporting Definition: Please select all options that apply Inclusion Criteria: If answered '1' to treatment approach (TX) Timing: Baseline and annually Reporting Source: Clinician­‐reported Type: Multiple answer

Data type

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C0596463
UMLS CUI [2]
C0205394
Is patient on any of the following drug classes? 999 = Unknown
Description

Supporting Definition: Please select all options that apply Inclusion Criteria: If answered '1' to treatment approach (TX) Timing: Baseline and annually Reporting Source: Clinician­‐reported Type: Multiple answer

Data type

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C0596463
UMLS CUI [2]
C0439673
Survival, disease control and cardiovascular complications
Description

Survival, disease control and cardiovascular complications

Alias
UMLS CUI-1
C1148433
UMLS CUI-2
C0012634
UMLS CUI-3
C0243148
UMLS CUI-4
C0007226
UMLS CUI-5
C0009566
Patient systolic blood pressure reading in mmHg
Description

Inclusion Criteria: All patients Timing: Minimum annually (included here as it is a factor of disease control (due to the timeline information in the reference guide obtainable from ICHOM.org)) Reporting Source: Clinician‐reported Type: Numerical Response Options: Numerical value

Data type

integer

Measurement units
  • mmHg
Alias
UMLS CUI [1]
C0871470
mmHg
Patient diastolic blood pressure reading in mmHg
Description

Inclusion Criteria: All patients Timing: Minimum annually (included here as it is a factor of disease control (due to the timeline information in the reference guide obtainable from ICHOM.org)) Reporting Source: Clinician‐reported Type: Numerical Response Options: Numerical value

Data type

integer

Measurement units
  • mmHg
Alias
UMLS CUI [1]
C0428883
mmHg
Does the patient have chronic kidney disease as evidenced by proteinuria?
Description

Supporting Definition: Renal disease (ICD10: I12 Hypertensive renal disease incl. any condition in N00-­‐ N07, N18.-­‐, N19 or N26 due to hypertension) (Please ensure that other causes of proteinuria, such as urinary tract infection, have been ruled out) Inclusion Criteria: All patients Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Single answer

Data type

integer

Alias
UMLS CUI [1]
C1561643
UMLS CUI [2]
C0033687
How was proteinuria detected?
Description

Inclusion Criteria: If "yes" to CKD Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0033687
UMLS CUI [1,2]
C3887511
Proteinuria as provided by electronically read urine dipstick
Description

Inclusion Criteria: If responded "1" or "2" to PROTEINEVID Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Single response

Data type

integer

Alias
UMLS CUI [1,1]
C1274040
UMLS CUI [1,2]
C1160927
Evidence of proteinuria as evidenced by urinary ACR
Description

Inclusion Criteria: If responded "3" to PROTEINEVID Timing: Baseline and annually Reporting Source: Clinician-­reported Type: Numerical Response Options: Numerical value

Data type

float

Alias
UMLS CUI [1,1]
C0455271
UMLS CUI [1,2]
C2826772
Units of urinary ACR
Description

Inclusion Criteria: If ACR value provided Timing: Baseline and annually Reporting Source: Clinician‐reported Type: Single answer

Data type

integer

Alias
UMLS CUI [1,1]
C0455271
UMLS CUI [1,2]
C1519795

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
Patient ID
integer
C2348585 (UMLS CUI [1])
Item Group
Demographic factors
Age
Item
Indicate the patient's date of birth
date
C0001779 (UMLS CUI [1])
C0421451 (UMLS CUI [2])
Item
Indicate the patient's sex at birth
integer
C0079399 (UMLS CUI [1])
Code List
Indicate the patient's sex at birth
CL Item
Male (1)
C1706180 (UMLS CUI-1)
(Comment:en)
CL Item
Female (2)
C0086287 (UMLS CUI-1)
(Comment:en)
CL Item
Undisclosed (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item Group
Clinical Factors
Item
Indicate if the patient has a documented history of diabetes mellitus (regardless of duration of disease or need for anti-diabetic agents). If newly diagnosed, the diagnosis should meet the following criteria: Fasting plasma glucose >= 7.0mmol/L (126 mg/dL) or 2-hour plasma glucose >= 11.1 mmol/L (200mg/dL) [2 hours post 75g glucose load]
integer
C0262926 (UMLS CUI [1,1])
C0011849 (UMLS CUI [1,2])
C0011849 (UMLS CUI [2,1])
C1518321 (UMLS CUI [2,2])
Code List
Indicate if the patient has a documented history of diabetes mellitus (regardless of duration of disease or need for anti-diabetic agents). If newly diagnosed, the diagnosis should meet the following criteria: Fasting plasma glucose >= 7.0mmol/L (126 mg/dL) or 2-hour plasma glucose >= 11.1 mmol/L (200mg/dL) [2 hours post 75g glucose load]
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)
Fasting plasma glucose
Item
For newly diagnosed diabetics indicate fasting plasma glucose if available
float
C0583513 (UMLS CUI [1])
Item
Units of fasting plasma glucose
integer
C0583513 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Code List
Units of fasting plasma glucose
CL Item
mg/dL (1)
C0439269 (UMLS CUI-1)
(Comment:en)
CL Item
mmol/L (2)
C1532563 (UMLS CUI-1)
(Comment:en)
Height
Item
Indicate the patient's height in centimeters or inches
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)
Weight
Item
Indicate the patient's weight in kilograms or pounds
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
Kilograms (1)
C0439209 (UMLS CUI-1)
(Comment:en)
CL Item
Pounds (2)
C0439219 (UMLS CUI-1)
(Comment:en)
Item
Indicate if the patient is on lipid lowering therapy
integer
C0585943 (UMLS CUI [1])
Code List
Indicate if the patient is on lipid lowering therapy
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
Specify lipid lowering therapy
integer
C0585943 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Code List
Specify lipid lowering therapy
CL Item
Statin (1)
C0360714 (UMLS CUI-1)
(Comment:en)
CL Item
Ezetimibe (2)
C1142985 (UMLS CUI-1)
(Comment:en)
CL Item
Fibrates (3)
C1449704 (UMLS CUI-1)
(Comment:en)
CL Item
Other (4)
C0205394 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Has the patient had a creatinine test?
integer
C0201976 (UMLS CUI [1])
Code List
Has the patient had a creatinine test?
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)
Creatinine
Item
Provide the patient's serum creatinine reading
float
C0201976 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
Item
What are the units of creatinine?
integer
C0201976 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Code List
What are the units of creatinine?
CL Item
mg/dL (1)
C0439269 (UMLS CUI-1)
(Comment:en)
CL Item
mmol/L (2)
C1532563 (UMLS CUI-1)
(Comment:en)
Item
Was the creatinine reader calibrated to IDMS (isotope dilution mass spectrometry)
integer
C0201976 (UMLS CUI [1,1])
C0006751 (UMLS CUI [1,2])
C3274766 (UMLS CUI [1,3])
Code List
Was the creatinine reader calibrated to IDMS (isotope dilution mass spectrometry)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
No (2)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item Group
Treatment variables
C0087111 (UMLS CUI-1)
Item
What is the management approach?
integer
C0087111 (UMLS CUI [1,1])
C0449445 (UMLS CUI [1,2])
Code List
What is the management approach?
CL Item
Non­‐pharmacological management only (0)
C1518422 (UMLS CUI-1)
C0013216 (UMLS CUI-2)
(Comment:en)
CL Item
Pharmacological management (with or without non‐pharmacological treatment) (1)
C0013216 (UMLS CUI-1)
(Comment:en)
Antihypertensive drug class: ACEi/ARB
Item
Is patient on any of the following drug classes? 1 = ACEi/ARB
boolean
C0003364 (UMLS CUI [1,1])
C0596463 (UMLS CUI [1,2])
C0003015 (UMLS CUI [2])
C0521942 (UMLS CUI [3])
Antihypertensive drug class: Alpha‐blocker
Item
Is patient on any of the following drug classes? 2 = Alpha‐blocker
boolean
C0003364 (UMLS CUI [1,1])
C0596463 (UMLS CUI [1,2])
C0001641 (UMLS CUI [2])
Antihypertensive drug class: Beta-blocker
Item
Is patient on any of the following drug classes? 3 = Beta-blocker
boolean
C0003364 (UMLS CUI [1,1])
C0596463 (UMLS CUI [1,2])
C0001645 (UMLS CUI [2])
Antihypertensive drug class: Loop Diuretics
Item
Is patient on any of the following drug classes? 4 = Loop Diuretics
boolean
C0003364 (UMLS CUI [1,1])
C0596463 (UMLS CUI [1,2])
C0354100 (UMLS CUI [2])
Antihypertensive drug class: Thiazides
Item
Is patient on any of the following drug classes? 5 = Thiazides
boolean
C0003364 (UMLS CUI [1,1])
C0596463 (UMLS CUI [1,2])
C0012802 (UMLS CUI [2])
Antihypertensive drug class: Calcium channel blocker
Item
Is patient on any of the following drug classes? 6 = Calcium channel blocker
boolean
C0003364 (UMLS CUI [1,1])
C0596463 (UMLS CUI [1,2])
C0006684 (UMLS CUI [2])
Antihypertensive drug class: Other
Item
Is patient on any of the following drug classes? 7 = Other
boolean
C0003364 (UMLS CUI [1,1])
C0596463 (UMLS CUI [1,2])
C0205394 (UMLS CUI [2])
Antihypertensive drug class: Unknown
Item
Is patient on any of the following drug classes? 999 = Unknown
boolean
C0003364 (UMLS CUI [1,1])
C0596463 (UMLS CUI [1,2])
C0439673 (UMLS CUI [2])
Item Group
Survival, disease control and cardiovascular complications
C1148433 (UMLS CUI-1)
C0012634 (UMLS CUI-2)
C0243148 (UMLS CUI-3)
C0007226 (UMLS CUI-4)
C0009566 (UMLS CUI-5)
Systolic blood pressure
Item
Patient systolic blood pressure reading in mmHg
integer
C0871470 (UMLS CUI [1])
Diastolic blood pressure
Item
Patient diastolic blood pressure reading in mmHg
integer
C0428883 (UMLS CUI [1])
Item
Does the patient have chronic kidney disease as evidenced by proteinuria?
integer
C1561643 (UMLS CUI [1])
C0033687 (UMLS CUI [2])
Code List
Does the patient have chronic kidney disease as evidenced by proteinuria?
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
How was proteinuria detected?
integer
C0033687 (UMLS CUI [1,1])
C3887511 (UMLS CUI [1,2])
Code List
How was proteinuria detected?
CL Item
Manually read urine dipstick (1)
C0430370 (UMLS CUI-1)
C2911685 (UMLS CUI-2)
C0175674 (UMLS CUI-3)
(Comment:en)
CL Item
Electronically read urine dipstick (2)
C0430370 (UMLS CUI-1)
C2911685 (UMLS CUI-2)
C0022885 (UMLS CUI-3)
(Comment:en)
CL Item
Urinary albumin/creatinine ratio (3)
C0455271 (UMLS CUI-1)
(Comment:en)
Item
Proteinuria as provided by electronically read urine dipstick
integer
C1274040 (UMLS CUI [1,1])
C1160927 (UMLS CUI [1,2])
Code List
Proteinuria as provided by electronically read urine dipstick
CL Item
+ (1)
C3525587 (UMLS CUI-1)
C1446409 (UMLS CUI-2)
C0205447 (UMLS CUI-3)
(Comment:en)
CL Item
++ (2)
C3525587 (UMLS CUI-1)
C1446409 (UMLS CUI-2)
C0205448 (UMLS CUI-3)
(Comment:en)
CL Item
+++ (3)
C3525587 (UMLS CUI-1)
C1446409 (UMLS CUI-2)
C0205449 (UMLS CUI-3)
(Comment:en)
CL Item
Unknown/results unavailable (4)
C0439673 (UMLS CUI-1)
C1254595 (UMLS CUI-2)
(Comment:en)
Results of urine ACR if done in place of urine dip
Item
Evidence of proteinuria as evidenced by urinary ACR
float
C0455271 (UMLS CUI [1,1])
C2826772 (UMLS CUI [1,2])
Item
Units of urinary ACR
integer
C0455271 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Code List
Units of urinary ACR
CL Item
mg/g (1)
C1300563 (UMLS CUI-1)
(Comment:en)
CL Item
mg/mmol (2)
C0567349 (UMLS CUI-1)
(Comment:en)

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