ID

40549

Description

INFLAMMATORY ARTHRITIS DATA COLLECTION Version 1.0.0 Revised: April 27 th, 2018 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: Rheumatoid Arthritis | Psoriatic Arthritis | Ankylosing Spondylitis | Juvenile Idiopathic Arthritis This ODM-file contains Clinical Variables to be administered at baseline visit and (a large number of the variables) annually. The following scores are the ones that are integrated into the standard set. There are alternatives for each category: see questionnaire or data collection guide. PAIN: - Numerical Rating Scale (Adult/Paediatric) FATIGUE - Numerical rating Scale (Adult/Paediatric) ACTIVITY LIMITATION: - HAQ-II* (Adult): copyright FORWARD-The National Data Bank for Rheumatic Diseases, arthritis-research.org ; http://bit.ly/HAQIIIA ; Wolfe F, Michaud K, Pincus T. Development and validation of the health assessment questionnaire II: a revised version of the health assessment questionnaire. Arthritis & Rheumatism. 2004;50(10):3296-305. OVERALL EMOTIONAL AND PHYSICAL HEALTH IMPACT - Numerical rating scale (Adult/Paediatric) WORK/SCHOOL/HOUSEWORK ABILITY AND PRODUCTIVITY: - WPAI (Adult): reillyassociates.net/WPAI_General.html, they ask to inform them about publication or presentation of WPAI-data ICHOM was supported for the Inflammatory Arthritis Standard Set by Santeon, Arthritis Research UK, TiH Transparency in Healthcare, Maasstad Ziekenhuis, Karolinska Universitetssjukhuset and Sheba Academic Medical Center Hospital. Publication: Oude Voshaar MAH, Das Gupta Z, Bijlsma JWJ, et al. International Consortium for Health Outcome Measurement Set of Outcomes That Matter to People Living With Inflammatory Arthritis: Consensus From an International Working Group. Arthritis Care Res (Hoboken). 2019;71(12):1556‐1565. doi:10.1002/acr.23799 For this version of the standard set, semantic annotation with UMLS CUIs has been added.

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www.ichom.org

Mots-clés

Versions (2)
  1. 21/09/2018 21/09/2018 - Sarah Riepenhausen
  2. 30/04/2020 30/04/2020 - Sarah Riepenhausen
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30 avril 2020

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Creative Commons BY-NC 4.0
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ICHOM Inflammatory Arthritis

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Baseline and Annual Clinical Form

1 Formulaires  
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 TYPE: Numerical RESPONSE OPTIONS: According to institution

Type de données

integer

Alias
UMLS CUI [1]
C1269815
Time Relative to Baseline (e.g. 3 months follow-up, 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. In this case 6 months, 1, and 2 years should be done, 3 months and 5 years follow-up are recommended, but not essential.

Type de données

text

Alias
UMLS CUI [1,1]
C0439564
UMLS CUI [1,2]
C1442488
Baseline Condition Factors
Description

Baseline Condition Factors

Alias
UMLS CUI-1
C0262926
UMLS CUI-2
C1442488
Indicate whether the patient has hypertension and/or uses antihypertensive medication
Description

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinician TYPE: Single answer

Type de données

integer

Alias
UMLS CUI [1]
C0020538
UMLS CUI [2]
C0003364
Indicate whether the patient has had a myocardial infarction
Description

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinician TYPE: Single answer

Type de données

integer

Alias
UMLS CUI [1]
C0027051
Indicate whether the patient has had a stroke (excluding transient ischemic attacks)
Description

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Type de données

integer

Alias
UMLS CUI [1,1]
C0038454
UMLS CUI [1,2]
C0332300
UMLS CUI [1,3]
C0007787
Indicate whether the patient has any other heart disease
Description

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Type de données

integer

Alias
UMLS CUI [1,1]
C0018799
UMLS CUI [1,2]
C0205394
Indicate whether the patient has chronic lung disease
Description

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Type de données

integer

Alias
UMLS CUI [1]
C0746102
Indicate whether the patient has diabetes mellitus
Description

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Type de données

integer

Alias
UMLS CUI [1]
C0011849
Indicate whether the patient has any malignancies
Description

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Type de données

integer

Alias
UMLS CUI [1]
C0006826
Indicate whether the patient has depression
Description

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Type de données

integer

Alias
UMLS CUI [1]
C0011581
Indicate whether the patient has a fracture
Description

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Type de données

integer

Alias
UMLS CUI [1]
C0016658
Indicate whether the patient has stomach ulcers
Description

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Type de données

integer

Alias
UMLS CUI [1]
C0038358
Indicate whether the patient has stomach problems
Description

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Type de données

integer

Alias
UMLS CUI [1]
C0577027
Indicate whether the patient is obese
Description

Obesity is defined as a BMI ≥30 INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Type de données

integer

Alias
UMLS CUI [1]
C1305855
UMLS CUI [2]
C0028754
Indicate the current diagnosis/diagnoses of inflammatory arthritis 1 = Rheumatoid arthritis
Description

INCLUSION CRITERIA: All patients TIMING: Baseline and annually REPORTING SOURCE: Clinical TYPE: Multiple answer

Type de données

boolean

Alias
UMLS CUI [1]
C0003873
Indicate the current diagnosis/diagnoses of inflammatory arthritis 2 = Spondyloarthritis
Description

INCLUSION CRITERIA: All patients TIMING: Baseline and annually REPORTING SOURCE: Clinical TYPE: Multiple answer

Type de données

boolean

Alias
UMLS CUI [1]
C0949690
Indicate the current diagnosis/diagnoses of inflammatory arthritis 3 = Psoriatic arthritis
Description

INCLUSION CRITERIA: All patients TIMING: Baseline and annually REPORTING SOURCE: Clinical TYPE: Multiple answer

Type de données

boolean

Alias
UMLS CUI [1]
C0003872
Indicate the current diagnosis/diagnoses of inflammatory arthritis 4 = Juvenile idiopathic arthritis
Description

INCLUSION CRITERIA: All patients TIMING: Baseline and annually REPORTING SOURCE: Clinical TYPE: Multiple answer

Type de données

boolean

Alias
UMLS CUI [1]
C3495559
Indicate the year of inflammatory arthritis diagnosis
Description

INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Date by YYYY

Type de données

partialDate

Unités de mesure
  • YYYY
Alias
UMLS CUI [1]
C0872146
UMLS CUI [2,1]
C0439234
UMLS CUI [2,2]
C0011900
YYYY
Indicate the presence of rheumatoid factor
Description

INCLUSION CRITERIA: If "1 = Rheumatoid arthritis" or "4 = Juvenile idiopathic arthritis" to IA_DIAG TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer RESPONSE OPTIONS:

Type de données

integer

Alias
UMLS CUI [1]
C0201660
Indicate the presence of anti-citrullinated protein antibodies (ACPA)
Description

INCLUSION CRITERIA: If "1 = Rheumatoid arthritis" or "4 = Juvenile idiopathic arthritis" to IA_DIAG TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer

Type de données

integer

Alias
UMLS CUI [1]
C4505301
Treatment-Specific
Description

Treatment-Specific

Alias
UMLS CUI-1
C0087111
Has the patient suffered from any serious adverse events in the past 12 months?
Description

According to the FDA, a serious adverse event is an undesirable experience associated with the use of a medical product in a patient. The event is serious when the patient outcome is: death; life-threatening; hospitalisation; disability or permanent damage; congenital anomaly/birth defect; required intervention to prevent permanent impairment or damage; other serious (important medical events). INCLUSION CRITERIA: All patients TIMING: Baseline and annually REPORTING SOURCE: Clinical TYPE: Single answer

Type de données

integer

Alias
UMLS CUI [1,1]
C1519255
UMLS CUI [1,2]
C4086728
Which serious adverse event(s) has the patient suffered from in the past 12 months? 1 = Death
Description

INCLUSION CRITERIA: If "1 = Yes" to SAE TIMING: Baseline and annually REPORTING SOURCE: Clinical TYPE: Multiple answer

Type de données

boolean

Alias
UMLS CUI [1,1]
C1705232
UMLS CUI [1,2]
C1519255
Which serious adverse event(s) has the patient suffered from in the past 12 months? 2 = Life-threatening
Description

INCLUSION CRITERIA: If "1 = Yes" to SAE TIMING: Baseline and annually REPORTING SOURCE: Clinical TYPE: Multiple answer

Type de données

boolean

Alias
UMLS CUI [1,1]
C1519255
UMLS CUI [1,2]
C1517874
Which serious adverse event(s) has the patient suffered from in the past 12 months? 3 = Hospitalization
Description

INCLUSION CRITERIA: If "1 = Yes" to SAE TIMING: Baseline and annually REPORTING SOURCE: Clinical TYPE: Multiple answer

Type de données

boolean

Alias
UMLS CUI [1,1]
C1519255
UMLS CUI [1,2]
C2826664
Which serious adverse event(s) has the patient suffered from in the past 12 months? 4 = Disability or permanent damage
Description

INCLUSION CRITERIA: If "1 = Yes" to SAE TIMING: Baseline and annually REPORTING SOURCE: Clinical TYPE: Multiple answer

Type de données

boolean

Alias
UMLS CUI [1,1]
C1519255
UMLS CUI [1,2]
C3640792
Which serious adverse event(s) has the patient suffered from in the past 12 months? 5 = Congenital anomaly/birth defect
Description

INCLUSION CRITERIA: If "1 = Yes" to SAE TIMING: Baseline and annually REPORTING SOURCE: Clinical TYPE: Multiple answer

Type de données

boolean

Alias
UMLS CUI [1,1]
C1519255
UMLS CUI [1,2]
C2826727
Which serious adverse event(s) has the patient suffered from in the past 12 months? 6 = Required intervention to prevent permanent impairment or damage
Description

INCLUSION CRITERIA: If "1 = Yes" to SAE TIMING: Baseline and annually REPORTING SOURCE: Clinical TYPE: Multiple answer

Type de données

boolean

Alias
UMLS CUI [1,1]
C1519255
UMLS CUI [1,2]
C1546955
Which serious adverse event(s) has the patient suffered from in the past 12 months? 7 = Other serious (important medical events)
Description

INCLUSION CRITERIA: If "1 = Yes" to SAE TIMING: Baseline and annually REPORTING SOURCE: Clinical TYPE: Multiple answer

Type de données

boolean

Alias
UMLS CUI [1,1]
C1519255
UMLS CUI [1,2]
C2826256
What was the disease activity target?
Description

INCLUSION CRITERIA: All patients TIMING: Baseline and annually REPORTING SOURCE: Clinical TYPE: Single answer

Type de données

integer

Alias
UMLS CUI [1,1]
C0544450
UMLS CUI [1,2]
C1521840
Was the disease activity target reached?
Description

INCLUSION CRITERIA: All patients TIMING: Baseline and annually REPORTING SOURCE: Clinical TYPE: Single answer

Type de données

integer

Alias
UMLS CUI [1,1]
C0544450
UMLS CUI [1,2]
C1521840
UMLS CUI [1,3]
C1550543
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Similar models

Baseline and Annual Clinical Form

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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. 3 months follow-up, 6 months follow-up, 1 year follow-up, ...)
text
C0439564 (UMLS CUI [1,1])
C1442488 (UMLS CUI [1,2])
Item Group
Baseline Condition Factors
C0262926 (UMLS CUI-1)
C1442488 (UMLS CUI-2)
Item
Indicate whether the patient has hypertension and/or uses antihypertensive medication
integer
C0020538 (UMLS CUI [1])
C0003364 (UMLS CUI [2])
High blood pressure
Code List
Indicate whether the patient has hypertension and/or uses antihypertensive medication
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 had a myocardial infarction
integer
C0027051 (UMLS CUI [1])
High blood pressure
Code List
Indicate whether the patient has had a myocardial infarction
CL Item
No  (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has had a stroke (excluding transient ischemic attacks)
integer
C0038454 (UMLS CUI [1,1])
C0332300 (UMLS CUI [1,2])
C0007787 (UMLS CUI [1,3])
High blood pressure
Code List
Indicate whether the patient has had a stroke (excluding transient ischemic attacks)
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 any other heart disease
integer
C0018799 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
High blood pressure
Code List
Indicate whether the patient has any other heart 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 chronic lung disease
integer
C0746102 (UMLS CUI [1])
High blood pressure
Code List
Indicate whether the patient has 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 diabetes mellitus
integer
C0011849 (UMLS CUI [1])
High blood pressure
Code List
Indicate whether the patient has diabetes mellitus
CL Item
No  (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether the patient has any malignancies
integer
C0006826 (UMLS CUI [1])
High blood pressure
Code List
Indicate whether the patient has any malignancies
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 depression
integer
C0011581 (UMLS CUI [1])
High blood pressure
Code List
Indicate whether the patient has depression
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 fracture
integer
C0016658 (UMLS CUI [1])
High blood pressure
Code List
Indicate whether the patient has a fracture
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 stomach ulcers
integer
C0038358 (UMLS CUI [1])
High blood pressure
Code List
Indicate whether the patient has stomach ulcers
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 stomach problems
integer
C0577027 (UMLS CUI [1])
High blood pressure
Code List
Indicate whether the patient has stomach problems
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 is obese
integer
C1305855 (UMLS CUI [1])
C0028754 (UMLS CUI [2])
High blood pressure
Code List
Indicate whether the patient is obese
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)
Inflammatory arthritis diagnosis: Rheumatoid arthritis
Item
Indicate the current diagnosis/diagnoses of inflammatory arthritis 1 = Rheumatoid arthritis
boolean
C0003873 (UMLS CUI [1])
Inflammatory arthritis diagnosis: Spondylarthritis
Item
Indicate the current diagnosis/diagnoses of inflammatory arthritis 2 = Spondyloarthritis
boolean
C0949690 (UMLS CUI [1])
Inflammatory arthritis diagnosis: Psoriatic Arthritis
Item
Indicate the current diagnosis/diagnoses of inflammatory arthritis 3 = Psoriatic arthritis
boolean
C0003872 (UMLS CUI [1])
Inflammatory arthritis diagnosis: Juvenile idiopathic arthritis
Item
Indicate the current diagnosis/diagnoses of inflammatory arthritis 4 = Juvenile idiopathic arthritis
boolean
C3495559 (UMLS CUI [1])
Disease duration
Item
Indicate the year of inflammatory arthritis diagnosis
partialDate
C0872146 (UMLS CUI [1])
C0439234 (UMLS CUI [2,1])
C0011900 (UMLS CUI [2,2])
Item
Indicate the presence of rheumatoid factor
integer
C0201660 (UMLS CUI [1])
Rheumatoid factor
Code List
Indicate the presence of rheumatoid factor
CL Item
Negative (0)
C0205160 (UMLS CUI-1)
(Comment:en)
CL Item
Positive (1)
C1446409 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate the presence of anti-citrullinated protein antibodies (ACPA)
integer
C4505301 (UMLS CUI [1])
Rheumatoid factor
Code List
Indicate the presence of anti-citrullinated protein antibodies (ACPA)
CL Item
Negative (0)
C0205160 (UMLS CUI-1)
(Comment:en)
CL Item
Positive (1)
C1446409 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item Group
Treatment-Specific
C0087111 (UMLS CUI-1)
Item
Has the patient suffered from any serious adverse events in the past 12 months?
integer
C1519255 (UMLS CUI [1,1])
C4086728 (UMLS CUI [1,2])
Serious Adverse Events
Code List
Has the patient suffered from any serious adverse events in the past 12 months?
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)
Serious Adverse Events - Classification: Death
Item
Which serious adverse event(s) has the patient suffered from in the past 12 months? 1 = Death
boolean
C1705232 (UMLS CUI [1,1])
C1519255 (UMLS CUI [1,2])
Serious Adverse Events - Classification: Life-threatening
Item
Which serious adverse event(s) has the patient suffered from in the past 12 months? 2 = Life-threatening
boolean
C1519255 (UMLS CUI [1,1])
C1517874 (UMLS CUI [1,2])
Serious Adverse Events - Classification: Hospitalization
Item
Which serious adverse event(s) has the patient suffered from in the past 12 months? 3 = Hospitalization
boolean
C1519255 (UMLS CUI [1,1])
C2826664 (UMLS CUI [1,2])
Serious Adverse Events - Classification: Disability or permanent damage
Item
Which serious adverse event(s) has the patient suffered from in the past 12 months? 4 = Disability or permanent damage
boolean
C1519255 (UMLS CUI [1,1])
C3640792 (UMLS CUI [1,2])
Serious Adverse Events - Classification: Congenital anomaly/birth defect
Item
Which serious adverse event(s) has the patient suffered from in the past 12 months? 5 = Congenital anomaly/birth defect
boolean
C1519255 (UMLS CUI [1,1])
C2826727 (UMLS CUI [1,2])
Serious Adverse Events - Classification: Required intervention to prevent permanent impairment or damage
Item
Which serious adverse event(s) has the patient suffered from in the past 12 months? 6 = Required intervention to prevent permanent impairment or damage
boolean
C1519255 (UMLS CUI [1,1])
C1546955 (UMLS CUI [1,2])
Serious Adverse Events - Classification: Other serious (important medical events)
Item
Which serious adverse event(s) has the patient suffered from in the past 12 months? 7 = Other serious (important medical events)
boolean
C1519255 (UMLS CUI [1,1])
C2826256 (UMLS CUI [1,2])
Item
What was the disease activity target?
integer
C0544450 (UMLS CUI [1,1])
C1521840 (UMLS CUI [1,2])
Disease activity target
Code List
What was the disease activity target?
CL Item
Clinical remission (1)
C0544452 (UMLS CUI-1)
C0205210 (UMLS CUI-2)
(Comment:en)
CL Item
Low disease activity (2)
C0544450 (UMLS CUI-1)
C0205251 (UMLS CUI-2)
(Comment:en)
CL Item
Both (3)
C0544450 (UMLS CUI-1)
C0205251 (UMLS CUI-2)
C0544452 (UMLS CUI-3)
C0205210 (UMLS CUI-4)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
C1521840 (UMLS CUI-2)
(Comment:en)
Item
Was the disease activity target reached?
integer
C0544450 (UMLS CUI [1,1])
C1521840 (UMLS CUI [1,2])
C1550543 (UMLS CUI [1,3])
High blood pressure
Code List
Was the disease activity target reached?
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)
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