ID

40571

Beschrijving

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 At time of treatment decision - Clinical Form. 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.

Link

http://www.ichom.org/

Trefwoorden

Versies (3)
  1. 14/05/2019 14/05/2019 -
  2. 20/05/2019 20/05/2019 -
  3. 30/04/2020 30/04/2020 - Sarah Riepenhausen
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30 de abril de 2020

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ICHOM Lung Cancer

Engels

At time of treatment decision - Clinical Form

1 Formulieren  
Administrative data
Beschrijving

Administrative data

Alias
UMLS CUI-1
C1320722
Indicate the patient's medical record number
Beschrijving

Supporting Definition: 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 Data Source: Administrative or clinical Type: Numerical Response Options: According to institution

Datatype

integer

Alias
UMLS CUI [1]
C2348585
Treatment Factors
Beschrijving

Treatment Factors

Alias
UMLS CUI-1
C0679853
Indicate intent of treatment
Beschrijving

Inclusion Criteria: All patients Timing: At time of treatment decision Data Source: Clinical Type: Single answer

Datatype

integer

Alias
UMLS CUI [1]
C1292734
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Similar models

At time of treatment decision - Clinical Form

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Administrative data
C1320722 (UMLS CUI-1)
Patient ID
Item
Indicate the patient's medical record number
integer
C2348585 (UMLS CUI [1])
Item Group
Treatment Factors
C0679853 (UMLS CUI-1)
Item
Indicate intent of treatment
integer
C1292734 (UMLS CUI [1])
Intent of treatment
Code List
Indicate intent of treatment
CL Item
Curative/Radical (1)
C1276305 (UMLS CUI-1)
(Comment:en)
CL Item
Palliative (includes ablative treatment for oligometastatic disease) (2)
C1285530 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
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