ID
40634
Descrizione
ICHOM Macular Degeneration data collection Version 3.0.1 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 Macular Degeneration, the following conditions and treatment approaches (or interventions) are covered by our Standard Set. Conditions: Neovascular Macular Degeneration Neovascular Age Related Macular Degeneration | Polypoidal Choroidal Vasculopathy | Myopic Neovascular Macular Degeneration | Other Forms of Neovascular Macular Degeneration (includes Post-Traumatic, Inflammatory, Idiopathic, Macular Telangiectasia Type 2) Non-Neovascular Age Related Macular Degeneration Treatment approaches: Intravitreal anti-VEGF treatment | Other intravitreal treatment | Photodynamic therapy | Thermal laser photocoagulation | Retinal radiation therapy | Transpupillary thermotherapy | Retinal surgical treatment This document contains the Each Clinical Visit - Clinical Form. Collecting Patient-Reported Outcome Measure: Brief Impact of Vision Impairment Questionnaire (Brief IVI): The Brief IVI includes costs for commercial use, and requires an agreement license. Therefore this questionnaire is not included in this Version of the standard set. Reference: Rodrigues IA, Sprinkhuizen SM, Barthelmes D, et al. Defining a Minimum Set of Standardized Patient-centered Outcome Measures for Macular Degeneration. American Journal of Opthalmology. 2016;168:1–12. doi: 10.1016/j.ajo.2016.04.012 The Standard set of ICHOM was supported by the WillsEye Hospital (America’s First World’s Best), Retina Suisse, St. Erik Eye Hospital, Macular Society, The Retina Society, Save sight Institute and The Macula Foundation (Preserving and Restoring Vision). For this version of the standard set, semantic annotation with UMLS CUIs has been added.
collegamento
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versioni (6)
- 25/07/19 25/07/19 -
- 30/07/19 30/07/19 -
- 30/07/19 30/07/19 -
- 02/08/19 02/08/19 - Sarah Riepenhausen
- 30/04/20 30/04/20 - Sarah Riepenhausen
- 30/04/20 30/04/20 - Sarah Riepenhausen
Titolare del copyright
ICHOM
Caricato su
30 aprile 2020
DOI
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Licenza
Creative Commons BY-NC 4.0
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ICHOM Macular Degeneration
Follow-up, 1+2 years post treatment - Patient-reported
- StudyEvent: ODM
Descrizione
Treatment variables
Descrizione
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 "";""
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C1298908
- UMLS CUI [1,2]
- C0543467
Descrizione
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 "";""
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0543467
- UMLS CUI [1,2]
- C0085076
Descrizione
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 "";""
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0543467
- UMLS CUI [1,2]
- C0024881
Descrizione
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 "";""
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0543467
- UMLS CUI [1,2]
- C0193867
Descrizione
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 "";""
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0543467
- UMLS CUI [1,2]
- C0439673
Descrizione
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
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C1624150
Descrizione
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 "";""
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C1515119
- UMLS CUI [1,2]
- C2003901
Descrizione
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 "";""
Tipo di dati
boolean
Alias
- UMLS CUI [1]
- C1515119
- UMLS CUI [2,1]
- C0013227
- UMLS CUI [2,2]
- C2746065
Descrizione
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 "";""
Tipo di dati
boolean
Alias
- UMLS CUI [1]
- C1515119
- UMLS CUI [2]
- C0392920
Descrizione
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 "";""
Tipo di dati
boolean
Alias
- UMLS CUI [1]
- C1515119
- UMLS CUI [2]
- C2985566
Descrizione
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 "";""
Tipo di dati
boolean
Alias
- UMLS CUI [1]
- C1515119
- UMLS CUI [2]
- C0279025
Descrizione
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 "";""
Tipo di dati
boolean
Alias
- UMLS CUI [1]
- C1515119
- UMLS CUI [2]
- C0439673
Descrizione
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
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C1515119
- UMLS CUI [1,2]
- C3173309
Descrizione
Degree of health
Descrizione
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
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C4055104
- UMLS CUI [1,2]
- C2964552
Descrizione
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
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C4724921
- UMLS CUI [1,2]
- C0451149
- UMLS CUI [1,3]
- C2964552
Descrizione
As a license is needed for use of this questionnaire, the actual 4 questions of BREAST-Q (to Mastectomy) are not part of this version of the standard set. Instead you can note the total score. The ICHOM OID's are: BREASTQMASTP_Q01 to BREASTQMASTP_Q04 INCLUSION CRITERIA: Patients with mastectomy TIMING: 1 and 2 year post treatment REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C4683551
- UMLS CUI [1,2]
- C0024881
- UMLS CUI [1,3]
- C2964552
Descrizione
As a license is needed for use of this questionnaire, the actual 11 questions of BREAST-Q (to Breast conserving therapy) are not part of this version of the standard set. Instead you can note the total score. The ICHOM OID's are: BREASTQBCTP_Q01 to BREASTQBCTP_Q11 INCLUSION CRITERIA: Patients with breast conserving therapy TIMING: 1 and 2 year post treatment REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C4683551
- UMLS CUI [1,2]
- C0917927
- UMLS CUI [1,3]
- C2964552
Descrizione
As a license is needed for use of this questionnaire, the actual 16 questions of BREAST-Q (to Reconstruction) are not part of this version of the standard set. Instead you can note the total score. The ICHOM OID's are: BREASTQRECP_Q01 to BREASTQRECP_Q16 INCLUSION CRITERIA:Patients with reconstruction TIMING: 1 and 2 year post treatment REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C4683551
- UMLS CUI [1,2]
- C0524865
- UMLS CUI [1,3]
- C2964552
Descrizione
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
Tipo di dati
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
Descrizione
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
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C3889662
- UMLS CUI [1,2]
- C0449820
Similar models
Follow-up, 1+2 years post treatment - Patient-reported
- StudyEvent: ODM
C1442488 (UMLS CUI [1,2])
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])
C0024881 (UMLS CUI [1,2])
C2964552 (UMLS CUI [1,3])
C0917927 (UMLS CUI [1,2])
C2964552 (UMLS CUI [1,3])
C0524865 (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])
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C0449820 (UMLS CUI [1,2])