ID
37457
Beschrijving
ICHOM Breast Cancer data collection Version 1.0.1 Revised: March 30, 2017 International Consortium for Health Outcomes Measurement (ICHOM), Source: http://www.ichom.org/ For Breast Cancer, the following treatment approaches (or interventions) are covered by our Standard Set. Conditions*: All patients (men and women) with newly pathologically diagnosed invasive breast cancer (stage I-IV) and ductal carcinoma in situ (DCIS). *Excluded Conditions: Rare tumors (e.g. phyllodes tumor), lobular carcinoma in situ (LCIS) and patients with recurrent disease at baseline will be excluded. Treatment approaches: (Reconstructive) Surgery | Radiotherapy | Chemotherapy | Hormonal Therapy | Targeted Therapy | This document contains the Follow-up, 6 month, 3-10 years post treatment - Patient-reported form. It has to be filled in 6 month an 3-10 years after the begin of a new therapy. Annual follow-up reassessed from date of surgery so that it will run parallel with annual outpatient visit. At least 10 years post surgery. Distinction for long-term follow-up: Local disease: Up to 10 years follow-up; Metastatic disease: Annually for life Collecting Patient-Reported Outcome Measures: European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30, EORTC QLQ-BR23, EORTC QLQ-LMC21). As a permission is needed for use of these questionnaires, only the total score of each will be included in this version of the standard set. More information can be found at http://groups.eortc.be/qol/eortc-qlq-c30 BREAST-Q Patient Reported Outcomes Instrument (BREAST-Q). As a license is needed for use of this questionnaire, only the total score will be included in this version of the standard set. For more information, please visit: https:// eprovide.mapi-trust.org/instruments/ breast-q#contact_and_conditions_of_ use Functional Assessment of Cancer Therapy Endocrine Subscale (FACT-ES). As a permission is needed for use of this questionnaire, only the total score of each will be included in this version of the standard set. For more information see http://www.facit.org/facitorg/ questionnaires. Reference: Ong WL, Schouwenburg MG, van Bommel AC, et al. A Standard Set of Value-Based Patient-Centered Outcomes for Breast Cancer: The International Consortium for Health Outcomes Measurement (ICHOM) Initiative. JAMA Oncol. 2017;3(5):677–685. doi:10.1001/jamaoncol.2016.4851 The Standard set of ICHOM was supported by the Dutch Dnstitute for Clinical Auditing, Onderlinge Waarborgmaatschappij Centrale Zorgverzekeraars group, Ramsay Health Care and Karolinska Institute.
Link
Trefwoorden
Versies (4)
- 25-07-19 25-07-19 -
- 30-07-19 30-07-19 -
- 02-08-19 02-08-19 - Sarah Riepenhausen
- 30-04-20 30-04-20 - Sarah Riepenhausen
Houder van rechten
ICHOM
Geüploaded op
30 juli 2019
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY-NC 3.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
ICHOM Breast Cancer
Follow-up, 6 month, 3-10 years post treatment - Patient-reported
- StudyEvent: ODM
Beschrijving
Baseline clinical factors
Beschrijving
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C1298908
Beschrijving
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0018799
- UMLS CUI [3]
- C0002962
- UMLS CUI [4]
- C0027051
- UMLS CUI [5]
- C0018801
Beschrijving
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0020538
Beschrijving
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C1306889
Beschrijving
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0024115
- UMLS CUI [3]
- C0004096
- UMLS CUI [4]
- C0008677
- UMLS CUI [5]
- C0034067
Beschrijving
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0011849
Beschrijving
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0022658
Beschrijving
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0023895
Beschrijving
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2,1]
- C0038454
- UMLS CUI [2,2]
- C0678227
- UMLS CUI [2,3]
- C0033213
Beschrijving
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0027765
- UMLS CUI [3]
- C0030567
- UMLS CUI [4]
- C0026769
Beschrijving
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C1707251
Beschrijving
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0011581
Beschrijving
SUPPROTING DEFINITION: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline and after 5 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer, Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0003864
Beschrijving
Treatment variables
Beschrijving
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1298908
- UMLS CUI [1,2]
- C0543467
Beschrijving
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0543467
- UMLS CUI [1,2]
- C0085076
Beschrijving
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0543467
- UMLS CUI [1,2]
- C0024881
Beschrijving
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0543467
- UMLS CUI [1,2]
- C0193867
Beschrijving
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0543467
- UMLS CUI [1,2]
- C0439673
Beschrijving
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Date by DD/MM/YYYY; Please enter "999" if date is unknown
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C1624150
Beschrijving
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1515119
- UMLS CUI [1,2]
- C2003901
Beschrijving
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C1515119
- UMLS CUI [2,1]
- C0013227
- UMLS CUI [2,2]
- C2746065
Beschrijving
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C1515119
- UMLS CUI [2]
- C0392920
Beschrijving
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C1515119
- UMLS CUI [2]
- C2985566
Beschrijving
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C1515119
- UMLS CUI [2]
- C0279025
Beschrijving
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Datatype
boolean
Alias
- UMLS CUI [1]
- C1515119
- UMLS CUI [2]
- C0439673
Beschrijving
INCLUSION CRITERIA: All patients TIMING: 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Date by DD/MM/YYYY; Please enter "999" if date is unknown
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C1515119
- UMLS CUI [1,2]
- C3173309
Beschrijving
Degree of health
Beschrijving
As a permission is needed for use of this questionnaire, the actual 30 questions are not part of this version of the standard set. Instead you can note the total score. The ICHOM OID's are: EORTC QLQ-C30_Q01 to EORTC QLQ-C30_Q30. INCLUSION CRITERIA: All patients TIMING: Baseline, 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C4055104
- UMLS CUI [1,2]
- C2964552
Beschrijving
As a permission is needed for use of this questionnaire, the actual 23 questions are not part of this version of the standard set. Instead you can note the total score. The ICHOM OID's are: EORTCQLQBR23_Q31 to EORTCQLQBR23_Q53. INCLUSION CRITERIA: All patients TIMING: Baseline, 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C4724921
- UMLS CUI [1,2]
- C0451149
- UMLS CUI [1,3]
- C2964552
Beschrijving
European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-LMC21): A license is needed for use of this questionnaire as well, however only one question is used. The ICHOM OID's is: EORTC QLQ-LMC21 INCLUSION CRITERIA: All patients TIMING: Baseline, 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0451149
- UMLS CUI [1,2]
- C2116350
- UMLS CUI [1,3]
- C0347984
- UMLS CUI [1,4]
- C2987125
- UMLS CUI [2,1]
- C0451149
- UMLS CUI [2,2]
- C2116331
- UMLS CUI [2,3]
- C0347984
- UMLS CUI [2,4]
- C2987125
Beschrijving
As a permission is needed for use of this questionnaire, the actual 6 questions are not part of this version of the standard set. Instead you can note the total score. The ICHOM OID's are: FACTES_Q01 (BRM1), FACTES_Q02 to FACTES_Q06 (ES4-ES8) INCLUSION CRITERIA: All patients TIMING: Baseline, 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C3889662
- UMLS CUI [1,2]
- C0449820
Similar models
Follow-up, 6 month, 3-10 years post treatment - Patient-reported
- StudyEvent: ODM
C1442488 (UMLS CUI [1,2])
C1298908 (UMLS CUI [2])
C0018799 (UMLS CUI [2])
C0002962 (UMLS CUI [3])
C0027051 (UMLS CUI [4])
C0018801 (UMLS CUI [5])
C0020538 (UMLS CUI [2])
C1306889 (UMLS CUI [2])
C0024115 (UMLS CUI [2])
C0004096 (UMLS CUI [3])
C0008677 (UMLS CUI [4])
C0034067 (UMLS CUI [5])
C0011849 (UMLS CUI [2])
C0022658 (UMLS CUI [2])
C0023895 (UMLS CUI [2])
C0038454 (UMLS CUI [2,1])
C0678227 (UMLS CUI [2,2])
C0033213 (UMLS CUI [2,3])
C0027765 (UMLS CUI [2])
C0030567 (UMLS CUI [3])
C0026769 (UMLS CUI [4])
C1707251 (UMLS CUI [2])
C0011581 (UMLS CUI [2])
C0003864 (UMLS CUI [2])
C0543467 (UMLS CUI [1,2])
C0085076 (UMLS CUI [1,2])
C0024881 (UMLS CUI [1,2])
C0193867 (UMLS CUI [1,2])
C0439673 (UMLS CUI [1,2])
C2003901 (UMLS CUI [1,2])
C0013227 (UMLS CUI [2,1])
C2746065 (UMLS CUI [2,2])
C0392920 (UMLS CUI [2])
C2985566 (UMLS CUI [2])
C0279025 (UMLS CUI [2])
C0439673 (UMLS CUI [2])
C3173309 (UMLS CUI [1,2])
C2964552 (UMLS CUI [1,2])
C0451149 (UMLS CUI [1,2])
C2964552 (UMLS CUI [1,3])
C2116350 (UMLS CUI [1,2])
C0347984 (UMLS CUI [1,3])
C2987125 (UMLS CUI [1,4])
C0451149 (UMLS CUI [2,1])
C2116331 (UMLS CUI [2,2])
C0347984 (UMLS CUI [2,3])
C2987125 (UMLS CUI [2,4])
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C0449820 (UMLS CUI [1,2])