ID
40539
Description
LOW BACK PAIN DATA COLLECTION Version 2.0.3 Revised August 24th, 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: Lumbar Disc Herniation | Lumbar Stenosis | Lumbar Spondylolisthesis | Degenerative Scoliosis | Adult Idiopathic Scoliosis | Degenerative Disc Disorder | Other Degenerative Lumbar Disorders | Mechanical, Acute, and Chronic Lumbar Back Pain and Back-Related Leg Pain Conditions Not Covered: Individuals < 18 Years of Age | Spinal Infection | Spinal Tumor | Spinal Fractures | Traumatic Dislocation | Congenital Scoliosis Documented as >20 Degrees, Moderate, Large, or Severe Treatment Approaches: Conservative Therapy (e.g. physical therapy, chiropractic, drug therapy, injections, etc.) | Surgical Therapy (e.g. spinal fusion, decompression, or discectomy) This ODM-file contains Patient reported Outcome Variables to be assessed at different timepoints: 3*, 6 months, 1, 2, 5* year after index event or when occurs (*recommended, but not essential). With use of the following Scores: Surveys used: ODI - Oswestry Disability Index Version 2.1a: The ODI is free for all health care organizations, but a license is needed for use (therefore not included verbatimly in this version of the standard set). Please visit eprovide: https://eprovide.mapi-trust.org/ NPRS - Numerical Pain Rating Scale: The NPRS is free for all health care organizations, and a license is not needed. EQ-5D-3L - EuroQol‐5D descriptive system (EQ-5D‐3L) and visual analogue scale (EQ-VAS): The EQ-5D-3L is free for non-profits and academic research, but a license is needed for use (therefore not included verbatimly in this version of the standard set). https://euroqol.org/support/how-to-obtain-eq-5d/ Publication: R Carter Clement, Adina Welander, Caleb Stowell, Thomas D Cha, John L Chen, Michelle Davies, Jeremy C Fairbank, Kevin T Foley, Martin Gehrchen, Olle Hagg, Wilco C Jacobs, Richard Kahler, Safdar N Khan, Isador H Lieberman, Beth Morisson, Donna D Ohnmeiss, Wilco C Peul, Neal H Shonnard, Matthew W Smuck, Tore K Solberg, Bjorn H Stromqvist, Miranda L Van Hooff, Ajay D Wasan, Paul C Willems, William Yeo & Peter FRitzell (2015) A proposed set of metrics for standardized outcome reporting in the management of low back pain, Acta Orthopaedica, 86:5, 523-533 ICHOM was supported for the Low Back Pain Standard Set by Arthritis Research UK. For this version of the standard set, semantic annotation with UMLS CUIs has been added.
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Keywords
Versions (5)
- 7/20/18 7/20/18 - Sarah Riepenhausen
- 8/23/18 8/23/18 - Sarah Riepenhausen
- 8/30/18 8/30/18 - Sarah Riepenhausen
- 8/31/18 8/31/18 - Sarah Riepenhausen
- 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 Low Back Pain
Patient-reported Outcome Variables
- StudyEvent: ODM
Description
Acute Complications of Treatment
Alias
- UMLS CUI-1
- C0087111
- UMLS CUI-2
- C0009566
Description
INCLUSION CRITERIA: Surgically treated patients TIMING: 6 months after index hospitalization REPORTING SOURCE: Patient-reported TYPE: Single Answer
Data type
integer
Alias
- UMLS CUI [1,1]
- C0406103
- UMLS CUI [1,2]
- C1442461
- UMLS CUI [1,3]
- C0241311
Description
INCLUSION CRITERIA: Surgically treated patients TIMING: 6 months after index hospitalization REPORTING SOURCE: Patient-reported TYPE: Single Answer
Data type
integer
Alias
- UMLS CUI [1,1]
- C0034065
- UMLS CUI [1,2]
- C1442461
- UMLS CUI [1,3]
- C0241311
Description
INCLUSION CRITERIA: Surgically treated patients TIMING: 6 months after index hospitalization REPORTING SOURCE: Patient-reported TYPE: Single Answer
Data type
integer
Alias
- UMLS CUI [1,1]
- C0600290
- UMLS CUI [1,2]
- C3887296
Description
Disease Recurrence
Alias
- UMLS CUI-1
- C0679254
Description
INCLUSION CRITERIA: Surgically treated patients TIMING: 3*, 6 months, 1, 2, 5* year after index event REPORTING SOURCE: Patient-reported TYPE: Single Answer
Data type
integer
Alias
- UMLS CUI [1,1]
- C0558347
- UMLS CUI [1,2]
- C0741423
Description
INCLUSION CRITERIA: Surgically treated patients TIMING: 3*, 6 months, 1, 2, 5* year after index event REPORTING SOURCE: Patient-reported
Data type
date
Measurement units
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0558347
- UMLS CUI [1,2]
- C0741423
- UMLS CUI [1,3]
- C0011008
Description
Patient-Reported Health Status
Alias
- UMLS CUI-1
- C0018759
- UMLS CUI-2
- C2987124
Description
INCLUSION CRITERIA: All patients TIMING: 3*, 6 months, 1, 2, 5* year after index event REPORTING SOURCE: Patient-reported TYPE: Single Answer
Data type
integer
Alias
- UMLS CUI [1,1]
- C0014003
- UMLS CUI [1,2]
- C0449438
Description
Time to return to work
Data type
integer
Alias
- UMLS CUI [1,1]
- C0425105
- UMLS CUI [1,2]
- C0449238
Description
INCLUSION CRITERIA: All patients TIMING: 3*, 6 months, 1, 2, 5* year after index event REPORTING SOURCE: Patient-reported TYPE: Single Answer
Data type
integer
Alias
- UMLS CUI [1,1]
- C4540969
- UMLS CUI [1,2]
- C0392756
Description
INCLUSION CRITERIA: All patients TIMING: 3*, 6 months, 1, 2, 5* year after index event REPORTING SOURCE: Patient-reported TYPE: Single Answer
Data type
integer
Alias
- UMLS CUI [1,1]
- C0242937
- UMLS CUI [1,2]
- C0549178
Description
INCLUSION CRITERIA: All patients TIMING: 3*, 6 months, 1, 2, 5* year after index event REPORTING SOURCE: Patient-reported TYPE: Single Answer
Data type
integer
Alias
- UMLS CUI [1,1]
- C0027409
- UMLS CUI [1,2]
- C0549178
Description
For use of ODI a licence is needed. Therefore no questions or answers are given in this version of the ICHOM Low Back Pain Standard Set. In the original standard set the 10 items of ODI have an ID from ODI_Q01 to ODI_Q10. INCLUSION CRITERIA: All patients TIMING: 3*, 6 months, 1, 2, 5* year after index event REPORTING SOURCE: Patient-reported
Data type
integer
Alias
- UMLS CUI [1]
- C4288568
Description
INCLUSION CRITERIA: All patients TIMING: 3*, 6 months, 1, 2, 5* year after index event REPORTING SOURCE: Patient-reported RESPONSE OPTIONS: Ordinal values from 0 to 10, with 'No pain' marked at '0' and 'Worst pain imaginable' marked at '10'
Data type
integer
Alias
- UMLS CUI [1,1]
- C1518471
- UMLS CUI [1,2]
- C0004604
Description
INCLUSION CRITERIA: All patients TIMING: 3*, 6 months, 1, 2, 5* year after index event REPORTING SOURCE: Patient-reported RESPONSE OPTIONS: Ordinal values from 0 to 10, with 'No pain' marked at '0' and 'Worst pain imaginable' marked at '10'
Data type
integer
Alias
- UMLS CUI [1,1]
- C1518471
- UMLS CUI [1,2]
- C0023222
Description
For use of EQ-5D-3L a licence is needed. Therefore it is not part of this version of the standard set. The items of EQ5D have the following IDs in the original standard set: EQ5D_Q01 to EQ5D_Q05 INCLUSION CRITERIA: All patients TIMING: 3*, 6 months, 1, 2, 5* year after index event REPORTING SOURCE: Patient-reported
Data type
integer
Alias
- UMLS CUI [1]
- C1880594
Description
For use of EQ-5D VAS a licence is needed. Therefore the verbatim formulations of the used questions and answers will not be integrated here. INCLUSION CRITERIA: All patients TIMING: 3*, 6 months, 1, 2, 5* year after index event REPORTING SOURCE: Patient-reported TYPE: VAS
Data type
float
Alias
- UMLS CUI [1]
- C3639380
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Patient-reported Outcome Variables
- StudyEvent: ODM
C1442488 (UMLS CUI [1,2])
C0009566 (UMLS CUI-2)
C1442461 (UMLS CUI [1,2])
C0241311 (UMLS CUI [1,3])
C1442461 (UMLS CUI [1,2])
C0241311 (UMLS CUI [1,3])
C3887296 (UMLS CUI [1,2])
C0741423 (UMLS CUI [1,2])
C0741423 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C2987124 (UMLS CUI-2)
C0449438 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
C0392756 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C0004604 (UMLS CUI [1,2])
C0023222 (UMLS CUI [1,2])