ID
40559
Descripción
ICHOM Lung cancer data collection Version 2.3.1 Revised: April 10th, 2017 International Consortium for Health Outcomes Measurement (ICHOM), Source: http://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. For Lung Cancer, the following conditions and treatment approaches (or interventions) are covered by our Standard Set. Conditions: Small Cell and Non-Small Cell Lung Cancer Treatment Approaches: Surgery | Radiotherapy | Chemotherapy | Targeted Therapy | Immunotherapy | Other This document contains the Baseline - Patient-Reported Form. It depicts first doctor's visit. Collecting Patient-Reported Outcome Measures: European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30). European Organization for Research and Treatment of Cancer Quality of Life Lung Cancer-Specific Questionnaire (EORTC QLQ-LC13). Both are free for all health care organizations, but a license is needed for use. http:// groups.eortc.be/qol/eortc-qlq-c30 is the official distribution site for EORTC QLQ-C30 and EORTC QLQ-LC13 questionnaires. Therefore only the total score will be included in this version of the standard set. Publication: Mak KS, van Bommel AC, Stowell C, et al. Defining a standard set of patient-centred outcomes for lung cancer. Eur Respir J. 2016;48(3):852–860. doi:10.1183/13993003.02049-2015 For this standard set ICHOM was supported by the Alliance of Dedicated Cancer Centers. For this version of the standard set, semantic annotation with UMLS CUIs has been added.
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Versiones (3)
- 14/5/19 14/5/19 -
- 16/5/19 16/5/19 -
- 30/4/20 30/4/20 - Sarah Riepenhausen
Titular de derechos de autor
ICHOM
Subido en
30 de abril de 2020
DOI
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Licencia
Creative Commons BY-NC 4.0
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ICHOM Lung Cancer
Baseline - Patient-Reported Form
- StudyEvent: ODM
Descripción
Demographic factors
Alias
- UMLS CUI-1
- C1704791
Descripción
Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical or patient‐reported Type: Date by DD/MM/YYYY
Tipo de datos
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C0421451
Descripción
Inclusion Criteria: All patients Timing: Baseline Data Source: Clinical or patient‐reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0079399
Descripción
In the original form response option is N/A. A codelist is not supplemented because it varies by country and should be determined by country (not for cross country comparison). Inclusion Criteria: All patients Timing: Baseline Data Source: Patient-reported Type: Single answer
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0015031
Descripción
Supporting Definition: The level of schooling is defined in each country as per ISCED [International Standard Classification] Inclusion Criteria: All patients Timing: Baseline Data Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0013658
Descripción
Baseline Clinical factors
Alias
- UMLS CUI-1
- C0449440
- UMLS CUI-2
- C1442488
Descripción
Inclusion Criteria: All patients Timing: Baseline Data Source: Patient‐reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1262477
Descripción
Supporting Definition: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline Data Source: Patient-reported Type: Multiple answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0549184
Descripción
Supporting Definition: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline Data Source: Patient-reported Type: Multiple answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0018799
Descripción
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline Data Source: Patient-reported Type: Multiple answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0020538
Descripción
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline Data Source: Patient-reported Type: Multiple answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C1306889
Descripción
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline Data Source: Patient-reported Type: Multiple answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0024115
Descripción
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline Data Source: Patient-reported Type: Multiple answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0011849
Descripción
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline Data Source: Patient-reported Type: Multiple answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0022658
Descripción
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline Data Source: Patient-reported Type: Multiple answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0023895
Descripción
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline Data Source: Patient-reported Type: Multiple answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0038454
Descripción
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline Data Source: Patient-reported Type: Multiple answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0027765
Descripción
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline Data Source: Patient-reported Type: Multiple answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C1707251
Descripción
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline Data Source: Patient-reported Type: Multiple answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0011581
Descripción
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline Data Source: Patient-reported Type: Multiple answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0003864
Descripción
Inclusion Criteria: All patients Timing: Baseline Data Source: Patient‐reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1519386
Descripción
Degree of health
Alias
- UMLS CUI-1
- C0018759
Descripción
As a license is needed for use of this questionnaire, the 30 actual questions are not included in this version of the standard set. ICHOM IDs are EORTCQLQC30_Q01 up to EORTCQLQC30_Q30. Inclusion Criteria: All patients Timing: Baseline 1 year post initiation of treatment Tracked ongoing annually for life (when hospital is able to track this ongoing) Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C4055104
- UMLS CUI [1,2]
- C2964552
Descripción
As a license is needed for use of this questionnaire, the 13 actual questions are not included in this version of the standard set. ICHOM IDs are EORTCQLQLC13_Q01 up to EORTCQLQLC30_Q13. EORTCQLQLC30_Q12 and EORTCQLQLC30_Q13 have each an additionally ID: EORTCQLQLC30_Q12SUB and EORTCQLQLC30_Q13SUB. Inclusion Criteria: All patients Inclusion Criteria: All patients Timing: Baseline 1 year post initiation of treatment Tracked ongoing annually for life (when hospital is able to track this ongoing) Data Source: Clinical Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0451149
- UMLS CUI [1,2]
- C0242379
- UMLS CUI [1,3]
- C2964552
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- StudyEvent: ODM
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