ID
40542
Beschrijving
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 Baseline Clinical Variables to be assessed at baseline and/or during index visit or hospitalization for procedure. 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 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 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.
Link
Trefwoorden
Versies (4)
- 20-07-18 20-07-18 - Sarah Riepenhausen
- 23-08-18 23-08-18 - Sarah Riepenhausen
- 31-08-18 31-08-18 - Sarah Riepenhausen
- 30-04-20 30-04-20 - Sarah Riepenhausen
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ICHOM
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30 april 2020
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Creative Commons BY-NC 4.0
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ICHOM Low Back Pain
Baseline Clinical Variables
- StudyEvent: ODM
Beschrijving
Baseline Clinical Factors
Alias
- UMLS CUI-1
- C1442488
- UMLS CUI-2
- C0449440
- UMLS CUI-3
- C0035648
Beschrijving
Back pain dominant, acute: Primary complaint is LBP. Symptoms ≤3 months Leg pain dominant, acute: Primary complaint is leg pain. Symptoms ≤3 months Back pain = Leg pain, acute: Patient reports 50 +/- 10% of each. Symptoms ≤3 months Back pain dominant, chronic: Primary complaint is LBP. Symptoms >3 months Leg pain dominant, chronic: Primary complaint is leg pain. Symptoms >3 months Back pain = leg pain, chronic: Patient reports 50 +/- 10% of each. Symptoms >3 months Neurogenic claudication: Numbness, weakness, or pain to the buttocks or legs, exacerbated by walking or standing, relieved by sitting Cauda equina syndrome: Dominant complaint is motor weakness, incontinence or Cauda equina syndrome, with or without associated complaints of pain INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single Answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0683327
- UMLS CUI [1,2]
- C1457887
Beschrijving
Not defined: No study ordered, or no study interpretation available for determination of structural pathology Age appropriate: Structural changes are consistent with normal aging and not a clinically relevant source of symptoms Disc pathology with normal disc height: Disc pathology without significant loss of disc height, includes disc herniation, internal disc desiccation and annual tear Disc space collapse: Disc pathology with mechanical disc space collapse with or without associated disc space pathology Spondylolisthesis/Spondylolysis: Any listhesis, including degenerative and isthmic spondylolisthesis Scoliosis/Kyphosis: Lumbar spine deformity including localized scoliosis or kyphosis Facet pathology: Significant face arthrosis or degeneration, including synovial cysts INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single Answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0683327
- UMLS CUI [1,2]
- C0037933
Beschrijving
Not defined: No study ordered, or no study interpretation available for determination of compressive pathology None: No clinically relevant compressive pathology Central: Compression in the central canala region (between the lateral margins of the dura) from any etiology Lateral: Compression in the lateral recess or foraminal regions (lateral to the lateral margins of the dura) from any etiology Combined: Compression in the central canal and latera recess/foraminal regions from any etiology Recurrent: Recurrent compression following previous surgical treatment at the same level, either in a central canala and/or recess/foraminal regions INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single Answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0683327
- UMLS CUI [1,2]
- C0037926
- UMLS CUI [2,1]
- C0683327
- UMLS CUI [2,2]
- C0037941
- UMLS CUI [2,3]
- C0332459
Beschrijving
ASA1: no disturbance ASA2:mild/moderate ASA3: severe ASA4: life-threatening ASA5: moribund INCLUSION CRITERIA: Surgically treated patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single Answer
Datatype
integer
Alias
- UMLS CUI [1]
- C1531480
Beschrijving
INCLUSION CRITERIA: Surgically treated patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single Answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C3146298
- UMLS CUI [1,2]
- C0543467
Beschrijving
Height and weight are used to calculate BMI INCLUSION CRITERIA: All patients TIMING: Index hospitalization REPORTING SOURCE: Clinical RESPONSE OPTIONS: Numerical value of height in centimeters or inches
Datatype
integer
Alias
- UMLS CUI [1]
- C0005890
Beschrijving
INCLUSION CRITERIA: All patients TIMING: Index hospitalization REPORTING SOURCE: Clinical TYPE: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0005890
- UMLS CUI [1,2]
- C1519795
Beschrijving
Height and weight are used to calculate BMI INCLUSION CRITERIA: All patients TIMING: Index hospitalization REPORTING SOURCE: Clinical RESPONSE OPTIONS: Numerical value of weight in kilograms or pounds
Datatype
integer
Alias
- UMLS CUI [1]
- C0005910
Beschrijving
INCLUSION CRITERIA: All patients TIMING: Index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0005910
- UMLS CUI [1,2]
- C1519795
Beschrijving
Prior Treatment
Alias
- UMLS CUI-1
- C1514463
Beschrijving
INCLUSION CRITERIA: Surgically treated patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single Answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0744961
- UMLS CUI [1,2]
- C0741419
Beschrijving
INCLUSION CRITERIA: Surgically treated patients; If patient has had previous procedural back interventions (INTERVENT) TIMING: Baseline REPORTING SOURCE: Clinical Variable ID: In the Variable ID the numeral will have to be modified, up to 10 possible entries.
Datatype
partialDate
Maateenheden
- MM/YYYY
Alias
- UMLS CUI [1,1]
- C0744961
- UMLS CUI [1,2]
- C0741419
- UMLS CUI [1,3]
- C0011008
Beschrijving
INCLUSION CRITERIA: Surgically treated patients; If patient has had previous procedural back interventions (INTERVENT) TIMING: Baseline REPORTING SOURCE: Clinical Variable ID: In the Variable ID the numeral will have to be modified, up to 10 possible entries. TYPE: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0744961
- UMLS CUI [1,2]
- C0741419
- UMLS CUI [1,3]
- C0184661
Beschrijving
INCLUSION CRITERIA: Surgically treated patients; If patient has had previous procedural back interventions (INTERVENT) TIMING: Baseline REPORTING SOURCE: Clinical Variable ID: In the Variable ID the numeral will have to be modified, up to 10 possible entries. TYPE: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0744961
- UMLS CUI [1,2]
- C0741419
- UMLS CUI [1,3]
- C0037949
- UMLS CUI [1,4]
- C2946261
Beschrijving
Procedure
Alias
- UMLS CUI-1
- C0741419
- UMLS CUI-2
- C0184661
Beschrijving
Decompression: e.g. laminectomy INCLUSION CRITERIA: All patients TIMING: During index visit or hospitalization for procedure REPORTING SOURCE: Clinical TYPE: Single Answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0741419
- UMLS CUI [1,2]
- C0184661
- UMLS CUI [1,3]
- C0332307
Beschrijving
INCLUSION CRITERIA: If answered 1-5 for PROCEDURETYPE TIMING: During index visit or hospitalization for procedure REPORTING SOURCE: Clinical TYPE: Multiple Answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0741419
- UMLS CUI [1,2]
- C0184661
- UMLS CUI [1,3]
- C0037949
- UMLS CUI [1,4]
- C0446430
- UMLS CUI [1,5]
- C0446432
Beschrijving
INCLUSION CRITERIA: If answered 1-5 for PROCEDURETYPE TIMING: During index visit or hospitalization for procedure REPORTING SOURCE: Clinical TYPE: Multiple Answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0741419
- UMLS CUI [1,2]
- C0184661
- UMLS CUI [1,3]
- C0037949
- UMLS CUI [1,4]
- C0446432
- UMLS CUI [1,5]
- C0446433
Beschrijving
INCLUSION CRITERIA: If answered 1-5 for PROCEDURETYPE TIMING: During index visit or hospitalization for procedure REPORTING SOURCE: Clinical TYPE: Multiple Answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0741419
- UMLS CUI [1,2]
- C0184661
- UMLS CUI [1,3]
- C0037949
- UMLS CUI [1,4]
- C0446433
- UMLS CUI [1,5]
- C0446434
Beschrijving
INCLUSION CRITERIA: If answered 1-5 for PROCEDURETYPE TIMING: During index visit or hospitalization for procedure REPORTING SOURCE: Clinical TYPE: Multiple Answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0741419
- UMLS CUI [1,2]
- C0184661
- UMLS CUI [1,3]
- C0037949
- UMLS CUI [1,4]
- C0446434
- UMLS CUI [1,5]
- C0446436
Beschrijving
INCLUSION CRITERIA: If answered 1-5 for PROCEDURETYPE TIMING: During index visit or hospitalization for procedure REPORTING SOURCE: Clinical TYPE: Multiple Answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0741419
- UMLS CUI [1,2]
- C0184661
- UMLS CUI [1,3]
- C0037949
- UMLS CUI [1,4]
- C0446436
- UMLS CUI [1,5]
- C0446435
Beschrijving
INCLUSION CRITERIA: If answered 1-5 for PROCEDURETYPE TIMING: During index visit or hospitalization for procedure REPORTING SOURCE: Clinical TYPE: Multiple Answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0741419
- UMLS CUI [1,2]
- C0184661
- UMLS CUI [1,3]
- C0037949
- UMLS CUI [1,4]
- C0446435
- UMLS CUI [1,5]
- C0446438
Beschrijving
Acute Complications of Treatment
Alias
- UMLS CUI-1
- C0087111
- UMLS CUI-2
- C0009566
Beschrijving
INCLUSION CRITERIA: Surgically treated patients TIMING: During the index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0277608
Beschrijving
INCLUSION CRITERIA: Surgically treated patients TIMING: During the index hospitalization REPORTING SOURCE: Clinical TYPE: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C1148348
Beschrijving
INCLUSION CRITERIA: Surgically treated patients TIMING: During the index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0007458
- UMLS CUI [1,2]
- C1708460
- UMLS CUI [2,1]
- C0037940
- UMLS CUI [2,2]
- C1708460
Beschrijving
INCLUSION CRITERIA: Surgically treated patients TIMING: During the index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0741419
- UMLS CUI [1,2]
- C0037949
- UMLS CUI [1,3]
- C3845811
Beschrijving
INCLUSION CRITERIA: Surgically treated patients TIMING: During the index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0005847
- UMLS CUI [1,2]
- C1708460
Beschrijving
INCLUSION CRITERIA: Surgically treated patients TIMING: During the index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1707833
- UMLS CUI [1,2]
- C0439669
- UMLS CUI [1,3]
- C0023182
Beschrijving
INCLUSION CRITERIA: Surgically treated patients TIMING: During the index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0741419
- UMLS CUI [1,2]
- C0009566
- UMLS CUI [1,3]
- C0205394
Similar models
Baseline Clinical Variables
- StudyEvent: ODM
C0449440 (UMLS CUI-2)
C0035648 (UMLS CUI-3)
C1457887 (UMLS CUI [1,2])
C0037933 (UMLS CUI [1,2])
C0037926 (UMLS CUI [1,2])
C0683327 (UMLS CUI [2,1])
C0037941 (UMLS CUI [2,2])
C0332459 (UMLS CUI [2,3])
C0543467 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,2])
C0741419 (UMLS CUI [1,2])
C0741419 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0741419 (UMLS CUI [1,2])
C0184661 (UMLS CUI [1,3])
C0741419 (UMLS CUI [1,2])
C0037949 (UMLS CUI [1,3])
C2946261 (UMLS CUI [1,4])
C0184661 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,3])
C0184661 (UMLS CUI [1,2])
C0037949 (UMLS CUI [1,3])
C0446430 (UMLS CUI [1,4])
C0446432 (UMLS CUI [1,5])
C0184661 (UMLS CUI [1,2])
C0037949 (UMLS CUI [1,3])
C0446432 (UMLS CUI [1,4])
C0446433 (UMLS CUI [1,5])
C0184661 (UMLS CUI [1,2])
C0037949 (UMLS CUI [1,3])
C0446433 (UMLS CUI [1,4])
C0446434 (UMLS CUI [1,5])
C0184661 (UMLS CUI [1,2])
C0037949 (UMLS CUI [1,3])
C0446434 (UMLS CUI [1,4])
C0446436 (UMLS CUI [1,5])
C0184661 (UMLS CUI [1,2])
C0037949 (UMLS CUI [1,3])
C0446436 (UMLS CUI [1,4])
C0446435 (UMLS CUI [1,5])
C0184661 (UMLS CUI [1,2])
C0037949 (UMLS CUI [1,3])
C0446435 (UMLS CUI [1,4])
C0446438 (UMLS CUI [1,5])
C0009566 (UMLS CUI-2)
C1708460 (UMLS CUI [1,2])
C0037940 (UMLS CUI [2,1])
C1708460 (UMLS CUI [2,2])
C0037949 (UMLS CUI [1,2])
C3845811 (UMLS CUI [1,3])
C1708460 (UMLS CUI [1,2])
C0439669 (UMLS CUI [1,2])
C0023182 (UMLS CUI [1,3])
C0009566 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])