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40542

Beschreibung

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.

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www.ichom.org

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Versionen (4)
  1. 20.07.18 20.07.18 - Sarah Riepenhausen
  2. 23.08.18 23.08.18 - Sarah Riepenhausen
  3. 31.08.18 31.08.18 - Sarah Riepenhausen
  4. 30.04.20 30.04.20 - Sarah Riepenhausen
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ICHOM

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30. April 2020

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    ICHOM Low Back Pain

    Englisch

    Baseline Clinical Variables

    1 Formulare  
    Patient ID
    Beschreibung

    Patient ID

    Alias
    UMLS CUI-1
    C1269815
    Indicate the patient's medical record number.
    Beschreibung

    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

    Datentyp

    integer

    Alias
    UMLS CUI [1]
    C1269815
    Baseline Clinical Factors
    Beschreibung

    Baseline Clinical Factors

    Alias
    UMLS CUI-1
    C1442488
    UMLS CUI-2
    C0449440
    UMLS CUI-3
    C0035648
    Diagnostic classification (according to Glassman criteria): Symptoms - Select one
    Beschreibung

    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

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0683327
    UMLS CUI [1,2]
    C1457887
    Diagnostic classification (according to Glassman criteria): Structural pathology - Select one
    Beschreibung

    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

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0683327
    UMLS CUI [1,2]
    C0037933
    Diagnostic classification (according to Glassman criteria): Compressive pathology - Select one
    Beschreibung

    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

    Datentyp

    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
    Answer the following questions only if the patient is receiving spinal procedures (surgery or injections) Indicate the morbidity state of the patient
    Beschreibung

    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

    Datentyp

    integer

    Alias
    UMLS CUI [1]
    C1531480
    Indicate the reason for surgery
    Beschreibung

    INCLUSION CRITERIA: Surgically treated patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single Answer

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C3146298
    UMLS CUI [1,2]
    C0543467
    Indicate the patient's height
    Beschreibung

    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

    Datentyp

    integer

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

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

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0005890
    UMLS CUI [1,2]
    C1519795
    Indicate the patient's weight
    Beschreibung

    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

    Datentyp

    integer

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

    INCLUSION CRITERIA: All patients TIMING: Index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0005910
    UMLS CUI [1,2]
    C1519795
    Prior Treatment
    Beschreibung

    Prior Treatment

    Alias
    UMLS CUI-1
    C1514463
    Indicate if the patient has had previous procedural back interventions
    Beschreibung

    INCLUSION CRITERIA: Surgically treated patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single Answer

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0744961
    UMLS CUI [1,2]
    C0741419
    Indicate when the patient had previous procedural back interventions
    Beschreibung

    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.

    Datentyp

    partialDate

    Maßeinheiten
    • MM/YYYY
    Alias
    UMLS CUI [1,1]
    C0744961
    UMLS CUI [1,2]
    C0741419
    UMLS CUI [1,3]
    C0011008
    MM/YYYY
    Indicate the type of the previous procedural back interventions
    Beschreibung

    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

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0744961
    UMLS CUI [1,2]
    C0741419
    UMLS CUI [1,3]
    C0184661
    Indicate the levels of the previous procedural back interventions
    Beschreibung

    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

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0744961
    UMLS CUI [1,2]
    C0741419
    UMLS CUI [1,3]
    C0037949
    UMLS CUI [1,4]
    C2946261
    Procedure
    Beschreibung

    Procedure

    Alias
    UMLS CUI-1
    C0741419
    UMLS CUI-2
    C0184661
    Indicate type of current procedural intervention
    Beschreibung

    Decompression: e.g. laminectomy INCLUSION CRITERIA: All patients TIMING: During index visit or hospitalization for procedure REPORTING SOURCE: Clinical TYPE: Single Answer

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0741419
    UMLS CUI [1,2]
    C0184661
    UMLS CUI [1,3]
    C0332307
    Indicate the level of the current procedural intervention 1 = T12-L1
    Beschreibung

    INCLUSION CRITERIA: If answered 1-5 for PROCEDURETYPE TIMING: During index visit or hospitalization for procedure REPORTING SOURCE: Clinical TYPE: Multiple Answer

    Datentyp

    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
    Indicate the level of the current procedural intervention 2 = L1-L2
    Beschreibung

    INCLUSION CRITERIA: If answered 1-5 for PROCEDURETYPE TIMING: During index visit or hospitalization for procedure REPORTING SOURCE: Clinical TYPE: Multiple Answer

    Datentyp

    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
    Indicate the level of the current procedural intervention 3 = L2-L3
    Beschreibung

    INCLUSION CRITERIA: If answered 1-5 for PROCEDURETYPE TIMING: During index visit or hospitalization for procedure REPORTING SOURCE: Clinical TYPE: Multiple Answer

    Datentyp

    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
    Indicate the level of the current procedural intervention 4 = L3-L4
    Beschreibung

    INCLUSION CRITERIA: If answered 1-5 for PROCEDURETYPE TIMING: During index visit or hospitalization for procedure REPORTING SOURCE: Clinical TYPE: Multiple Answer

    Datentyp

    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
    Indicate the level of the current procedural intervention 5 = L4-L5
    Beschreibung

    INCLUSION CRITERIA: If answered 1-5 for PROCEDURETYPE TIMING: During index visit or hospitalization for procedure REPORTING SOURCE: Clinical TYPE: Multiple Answer

    Datentyp

    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
    Indicate the level of the current procedural intervention 6 = L5-S1
    Beschreibung

    INCLUSION CRITERIA: If answered 1-5 for PROCEDURETYPE TIMING: During index visit or hospitalization for procedure REPORTING SOURCE: Clinical TYPE: Multiple Answer

    Datentyp

    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
    Acute Complications of Treatment
    Beschreibung

    Acute Complications of Treatment

    Alias
    UMLS CUI-1
    C0087111
    UMLS CUI-2
    C0009566
    Indicate if patient died in-hospital following procedure (all-cause mortality)
    Beschreibung

    INCLUSION CRITERIA: Surgically treated patients TIMING: During the index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer

    Datentyp

    integer

    Alias
    UMLS CUI [1]
    C0277608
    Indicate date of death
    Beschreibung

    INCLUSION CRITERIA: Surgically treated patients TIMING: During the index hospitalization REPORTING SOURCE: Clinical TYPE: Date by DD/MM/YYYY

    Datentyp

    date

    Maßeinheiten
    • DD/MM/YYYY
    Alias
    UMLS CUI [1]
    C1148348
    DD/MM/YYYY
    Indicate if there was iatrogenic nerve root damage (including cauda equina) due to the intervention
    Beschreibung

    INCLUSION CRITERIA: Surgically treated patients TIMING: During the index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0007458
    UMLS CUI [1,2]
    C1708460
    UMLS CUI [2,1]
    C0037940
    UMLS CUI [2,2]
    C1708460
    Indicate if there was unintentional surgery on the wrong level/site, not on level of main pathology
    Beschreibung

    INCLUSION CRITERIA: Surgically treated patients TIMING: During the index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0741419
    UMLS CUI [1,2]
    C0037949
    UMLS CUI [1,3]
    C3845811
    Indicate if there was relevant iatrogenous damage to a vessel
    Beschreibung

    INCLUSION CRITERIA: Surgically treated patients TIMING: During the index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0005847
    UMLS CUI [1,2]
    C1708460
    Indicate if there was iatrogenous damage of a dura with liquor emission
    Beschreibung

    INCLUSION CRITERIA: Surgically treated patients TIMING: During the index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C1707833
    UMLS CUI [1,2]
    C0439669
    UMLS CUI [1,3]
    C0023182
    Indicate if there were other complications (e.g. superficial hematoma, malpositioned implant, donor-site pain, DVT without PE, and/or device failure)
    Beschreibung

    INCLUSION CRITERIA: Surgically treated patients TIMING: During the index hospitalization REPORTING SOURCE: Clinical TYPE: Single Answer

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0741419
    UMLS CUI [1,2]
    C0009566
    UMLS CUI [1,3]
    C0205394
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    Ähnliche Modelle

    Baseline Clinical Variables

    1 Formulare
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    Patient ID
    C1269815 (UMLS CUI-1)
    Patient ID
    Item
    Indicate the patient's medical record number.
    integer
    C1269815 (UMLS CUI [1])
    Item Group
    Baseline Clinical Factors
    C1442488 (UMLS CUI-1)
    C0449440 (UMLS CUI-2)
    C0035648 (UMLS CUI-3)
    Item
    Diagnostic classification (according to Glassman criteria): Symptoms - Select one
    integer
    C0683327 (UMLS CUI [1,1])
    C1457887 (UMLS CUI [1,2])
    Diagnostic classification (according to Glassman criteria): Symptoms
    Code List
    Diagnostic classification (according to Glassman criteria): Symptoms - Select one
    CL Item
    Back pain dominant, acute (1)
    CL Item
    Leg pain dominant, acute (2)
    CL Item
    Back pain = Leg pain, acute (3)
    CL Item
    Back pain dominant, chronic (4)
    CL Item
    Leg pain dominant, chronic (5)
    CL Item
    Back pain = leg pain, chronic (6)
    CL Item
    Neurogenic claudication (7)
    CL Item
    Cauda equina syndrome (8)
    Item
    Diagnostic classification (according to Glassman criteria): Structural pathology - Select one
    integer
    C0683327 (UMLS CUI [1,1])
    C0037933 (UMLS CUI [1,2])
    Diagnostic classification (according to Glassman criteria): Structural pathology
    Code List
    Diagnostic classification (according to Glassman criteria): Structural pathology - Select one
    CL Item
    Not defined (1)
    CL Item
    Age appropriate (2)
    CL Item
    Disc pathology with normal disc height (3)
    CL Item
    Disc space collapse (4)
    CL Item
    Spondylolisthesis/ Spondylolysis (5)
    CL Item
    Scoliosis/Kyphosis (6)
    CL Item
    Facet pathology (7)
    Item
    Diagnostic classification (according to Glassman criteria): Compressive pathology - Select one
    integer
    C0683327 (UMLS CUI [1,1])
    C0037926 (UMLS CUI [1,2])
    C0683327 (UMLS CUI [2,1])
    C0037941 (UMLS CUI [2,2])
    C0332459 (UMLS CUI [2,3])
    Diagnostic classification (according to Glassman criteria): Compressive pathology
    Code List
    Diagnostic classification (according to Glassman criteria): Compressive pathology - Select one
    CL Item
    Not defined (1)
    CL Item
    None (2)
    CL Item
    Central (3)
    CL Item
    Lateral (4)
    CL Item
    Combined (5)
    CL Item
    Recurrent (6)
    Item
    Answer the following questions only if the patient is receiving spinal procedures (surgery or injections) Indicate the morbidity state of the patient
    integer
    C1531480 (UMLS CUI [1])
    ASA rating
    Code List
    Answer the following questions only if the patient is receiving spinal procedures (surgery or injections) Indicate the morbidity state of the patient
    CL Item
    1 (1)
    CL Item
    2 (2)
    CL Item
    3 (3)
    CL Item
    4 (4)
    CL Item
    5 (5)
    CL Item
    Unknown (999)
    Item
    Indicate the reason for surgery
    integer
    C3146298 (UMLS CUI [1,1])
    C0543467 (UMLS CUI [1,2])
    Surgical indication
    Code List
    Indicate the reason for surgery
    CL Item
    Paramedian disc herniation (1)
    CL Item
    Central disc herniation (2)
    CL Item
    Central spinal stenosis with degen. listhesis (3)
    CL Item
    Central spinal stenosis without degen. listhesis (4)
    CL Item
    Lateral spinal stenosis (5)
    CL Item
    Spondylolysis/Spondylolisthesis, isthmic (6)
    CL Item
    Segmental pain (with or without degen. listhesis) (7)
    CL Item
    Postoperative instability (8)
    CL Item
    Degen. scoliosis (9)
    CL Item
    Other (999)
    Height
    Item
    Indicate the patient's height
    integer
    C0005890 (UMLS CUI [1])
    Item
    Indicate units of height
    integer
    C0005890 (UMLS CUI [1,1])
    C1519795 (UMLS CUI [1,2])
    Past medical history: Previous AMI
    Code List
    Indicate units of height
    CL Item
    centimeters (1)
    CL Item
    inches (2)
    Weight
    Item
    Indicate the patient's weight
    integer
    C0005910 (UMLS CUI [1])
    Item
    Indicate units of weight
    integer
    C0005910 (UMLS CUI [1,1])
    C1519795 (UMLS CUI [1,2])
    Weight units
    Code List
    Indicate units of weight
    CL Item
    kilograms (1)
    CL Item
    pounds (2)
    Item Group
    Prior Treatment
    C1514463 (UMLS CUI-1)
    Item
    Indicate if the patient has had previous procedural back interventions
    integer
    C0744961 (UMLS CUI [1,1])
    C0741419 (UMLS CUI [1,2])
    Prior back surgery
    Code List
    Indicate if the patient has had previous procedural back interventions
    CL Item
    No (0)
    CL Item
    Yes (1)
    Prior interventions dates
    Item
    Indicate when the patient had previous procedural back interventions
    partialDate
    C0744961 (UMLS CUI [1,1])
    C0741419 (UMLS CUI [1,2])
    C0011008 (UMLS CUI [1,3])
    Item
    Indicate the type of the previous procedural back interventions
    integer
    C0744961 (UMLS CUI [1,1])
    C0741419 (UMLS CUI [1,2])
    C0184661 (UMLS CUI [1,3])
    Prior interventions types*
    Code List
    Indicate the type of the previous procedural back interventions
    CL Item
    Discectomy (1)
    CL Item
    Decompression (2)
    CL Item
    Fusion (3)
    Item
    Indicate the levels of the previous procedural back interventions
    integer
    C0744961 (UMLS CUI [1,1])
    C0741419 (UMLS CUI [1,2])
    C0037949 (UMLS CUI [1,3])
    C2946261 (UMLS CUI [1,4])
    Prior interventions levels*
    Code List
    Indicate the levels of the previous procedural back interventions
    CL Item
    T12-L1 (1)
    CL Item
    L1-L2 (2)
    CL Item
    L2-L3 (3)
    CL Item
    L3-L4 (4)
    CL Item
    L4-L5 (5)
    CL Item
    L5-S1 (6)
    Item Group
    Procedure
    C0741419 (UMLS CUI-1)
    C0184661 (UMLS CUI-2)
    Item
    Indicate type of current procedural intervention
    integer
    C0741419 (UMLS CUI [1,1])
    C0184661 (UMLS CUI [1,2])
    C0332307 (UMLS CUI [1,3])
    Current procedural intervention: Type
    Code List
    Indicate type of current procedural intervention
    CL Item
    Discectomy (1)
    CL Item
    Decompression (laminectomy) (2)
    CL Item
    Fusion (3)
    CL Item
    Other back surgery (4)
    CL Item
    Injection therapy (5)
    CL Item
    other non-surgical therapy (6)
    Current procedural intervention: Level
    Item
    Indicate the level of the current procedural intervention 1 = T12-L1
    boolean
    C0741419 (UMLS CUI [1,1])
    C0184661 (UMLS CUI [1,2])
    C0037949 (UMLS CUI [1,3])
    C0446430 (UMLS CUI [1,4])
    C0446432 (UMLS CUI [1,5])
    Current procedural intervention: Level
    Item
    Indicate the level of the current procedural intervention 2 = L1-L2
    boolean
    C0741419 (UMLS CUI [1,1])
    C0184661 (UMLS CUI [1,2])
    C0037949 (UMLS CUI [1,3])
    C0446432 (UMLS CUI [1,4])
    C0446433 (UMLS CUI [1,5])
    Current procedural intervention: Level
    Item
    Indicate the level of the current procedural intervention 3 = L2-L3
    boolean
    C0741419 (UMLS CUI [1,1])
    C0184661 (UMLS CUI [1,2])
    C0037949 (UMLS CUI [1,3])
    C0446433 (UMLS CUI [1,4])
    C0446434 (UMLS CUI [1,5])
    Current procedural intervention: Level
    Item
    Indicate the level of the current procedural intervention 4 = L3-L4
    boolean
    C0741419 (UMLS CUI [1,1])
    C0184661 (UMLS CUI [1,2])
    C0037949 (UMLS CUI [1,3])
    C0446434 (UMLS CUI [1,4])
    C0446436 (UMLS CUI [1,5])
    Current procedural intervention: Level
    Item
    Indicate the level of the current procedural intervention 5 = L4-L5
    boolean
    C0741419 (UMLS CUI [1,1])
    C0184661 (UMLS CUI [1,2])
    C0037949 (UMLS CUI [1,3])
    C0446436 (UMLS CUI [1,4])
    C0446435 (UMLS CUI [1,5])
    Current procedural intervention: Level
    Item
    Indicate the level of the current procedural intervention 6 = L5-S1
    boolean
    C0741419 (UMLS CUI [1,1])
    C0184661 (UMLS CUI [1,2])
    C0037949 (UMLS CUI [1,3])
    C0446435 (UMLS CUI [1,4])
    C0446438 (UMLS CUI [1,5])
    Item Group
    Acute Complications of Treatment
    C0087111 (UMLS CUI-1)
    C0009566 (UMLS CUI-2)
    Item
    Indicate if patient died in-hospital following procedure (all-cause mortality)
    integer
    C0277608 (UMLS CUI [1])
    Death in hospital (all cause)
    Code List
    Indicate if patient died in-hospital following procedure (all-cause mortality)
    CL Item
    No (0)
    CL Item
    Yes (1)
    Date of death
    Item
    Indicate date of death
    date
    C1148348 (UMLS CUI [1])
    Item
    Indicate if there was iatrogenic nerve root damage (including cauda equina) due to the intervention
    integer
    C0007458 (UMLS CUI [1,1])
    C1708460 (UMLS CUI [1,2])
    C0037940 (UMLS CUI [2,1])
    C1708460 (UMLS CUI [2,2])
    Iatrogenic nerve root damage (incl. cauda equina)
    Code List
    Indicate if there was iatrogenic nerve root damage (including cauda equina) due to the intervention
    CL Item
    No (0)
    CL Item
    Yes (1)
    Item
    Indicate if there was unintentional surgery on the wrong level/site, not on level of main pathology
    integer
    C0741419 (UMLS CUI [1,1])
    C0037949 (UMLS CUI [1,2])
    C3845811 (UMLS CUI [1,3])
    Unintentional surgery on wrong site/level
    Code List
    Indicate if there was unintentional surgery on the wrong level/site, not on level of main pathology
    CL Item
    No (0)
    CL Item
    Yes (1)
    Item
    Indicate if there was relevant iatrogenous damage to a vessel
    integer
    C0005847 (UMLS CUI [1,1])
    C1708460 (UMLS CUI [1,2])
    Iatrogenous damage to a vessel
    Code List
    Indicate if there was relevant iatrogenous damage to a vessel
    CL Item
    No (0)
    CL Item
    Yes (1)
    Item
    Indicate if there was iatrogenous damage of a dura with liquor emission
    integer
    C1707833 (UMLS CUI [1,1])
    C0439669 (UMLS CUI [1,2])
    C0023182 (UMLS CUI [1,3])
    Iatrogenous damage of dura with liquor emission
    Code List
    Indicate if there was iatrogenous damage of a dura with liquor emission
    CL Item
    No (0)
    CL Item
    Yes (1)
    Item
    Indicate if there were other complications (e.g. superficial hematoma, malpositioned implant, donor-site pain, DVT without PE, and/or device failure)
    integer
    C0741419 (UMLS CUI [1,1])
    C0009566 (UMLS CUI [1,2])
    C0205394 (UMLS CUI [1,3])
    Other complications
    Code List
    Indicate if there were other complications (e.g. superficial hematoma, malpositioned implant, donor-site pain, DVT without PE, and/or device failure)
    CL Item
    No (0)
    CL Item
    Yes (1)
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