ID

31453

Beskrivning

LOW BACK PAIN DATA COLLECTION Version 2.0.3 Revised August 24th, 2017 www.ichom.org ICHOM received an endorsement of Arthritis Research UK for the development of this standard set. 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. Use of the following Scores: 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/

Länk

www.ichom.org

Nyckelord

Versioner (4)
  1. 2018-07-20 2018-07-20 - Sarah Riepenhausen
  2. 2018-08-23 2018-08-23 - Sarah Riepenhausen
  3. 2018-08-31 2018-08-31 - Sarah Riepenhausen
  4. 2020-04-30 2020-04-30 - Sarah Riepenhausen
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23 augusti 2018

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Creative Commons BY-NC 3.0
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ICHOM Low Back Pain

Engelsk

Baseline Clinical Variables

1 Formulär  
Patient ID
Beskrivning

Patient ID

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

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

Datatyp

integer

Alias
UMLS CUI [1]
C1269815
Baseline Clinical Factors
Beskrivning

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
Beskrivning

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

Datatyp

integer

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

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

Datatyp

integer

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

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

Datatyp

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
Beskrivning

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

Datatyp

integer

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

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

Datatyp

integer

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

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

Datatyp

integer

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

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

Datatyp

integer

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

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

Datatyp

integer

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

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

Datatyp

integer

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

Prior Treatment

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

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

Datatyp

integer

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

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.

Datatyp

partialDate

Måttenheter
  • 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
Beskrivning

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

Datatyp

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
Beskrivning

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

Datatyp

integer

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

Procedure

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

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

Datatyp

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
Beskrivning

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

Datatyp

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
Beskrivning

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

Datatyp

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
Beskrivning

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

Datatyp

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
Beskrivning

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

Datatyp

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
Beskrivning

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

Datatyp

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
Beskrivning

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

Datatyp

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
Beskrivning

Acute Complications of Treatment

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

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

Datatyp

integer

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

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

Datatyp

date

Måttenheter
  • 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
Beskrivning

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

Datatyp

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
Beskrivning

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

Datatyp

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
Beskrivning

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

Datatyp

integer

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

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

Datatyp

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)
Beskrivning

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

Datatyp

integer

Alias
UMLS CUI [1,1]
C0741419
UMLS CUI [1,2]
C0009566
UMLS CUI [1,3]
C0205394
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Similar models

Baseline Clinical Variables

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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