ID
40572
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 Follow-up - Clinical Form. It includes different points in time: After treatment, After surgery, Update at least annually, 1 year post initiation of treatment and Tracked ongoing annually for life (when hospital is able to track this ongoing). 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
Trefwoorden
Versies (5)
- 15-05-19 15-05-19 -
- 20-05-19 20-05-19 -
- 30-04-20 30-04-20 - Sarah Riepenhausen
- 13-04-21 13-04-21 - Dr. rer. medic Philipp Neuhaus
- 20-09-21 20-09-21 -
Houder van rechten
ICHOM
Geüploaded op
30 april 2020
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY-NC 4.0
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 Lung Cancer
Follow-up - Clinical Form
- StudyEvent: ODM
Beschrijving
Degree of health
Alias
- UMLS CUI-1
- C0018759
Beschrijving
Supporting Definition: ECOG / WHO scale: -‐ PS = 0 normal activity level; -‐ PS = 1 restricted with strenuous activity, but can do light activity; -‐ PS = 2 active >/= 50% of day; -‐ PS = 3 spends >50% of day in chair or bed; -‐ PS = 4 totally confined to bed 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
Datatype
integer
Alias
- UMLS CUI [1]
- C1520224
Beschrijving
Baseline tumor factors
Alias
- UMLS CUI-1
- C0475752
- UMLS CUI-2
- C1442488
Beschrijving
Supporting Definition: Pathologic staging preferred, if available pT0: no primary tumor pT1: if not able to select T1a or T1b: Tumor ≤3 cm diameter, surrounded by lung or visceral pleura, without invasion more proximal than lobar bronchus pT1a: Tumor ≤2 cm in diameter pT1b: Tumor >2 cm but ≤3 cm in diameter pT2: if not able to select T2a or T2b: Tumor >3 cm but ≤7 cm, or tumor with any of the following features: Involves main bronchus, ≥2 cm distal to carina. Invades visceral pleura. Associated with atelectasis or obstructive pneumonitis that extends to the hilar region but does not involve the entire lung pT2a: Tumor >3 cm but ≤5 cm pT2b: Tumor >5 cm but ≤7 cm pT3: Tumor >7 cm or any of the following: Directly invades any of the following: chest wall, diaphragm, phrenic nerve, mediastinal pleura, parietal pericardium, main bronchus <2 cm from carina (without involvement of carina), Atelectasis or obstructive pneumonitis of the entire lung. Separate tumor nodules in the same lobe pT4: Tumor of any size that invades the mediastinum, heart, great vessels, trachea, recurrent laryngeal nerve, esophagus, vertebral body, carina, or with separate tumor nodules in a different ipsilateral lobe pTX: Primary tumor cannot be assessed Inclusion Criteria: All patients Timing: After surgery Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1300072
- UMLS CUI [1,2]
- C1521733
Beschrijving
Supporting Definition: Pathologic staging preferred, if available pN0: No regional lymph node metastases pN1: Metastasis in ipsilateral peribronchial and/or ipsilateral hilar lymph nodes and intrapulmonary nodes, including involvement by direct extension pN2: Metastasis in ipsilateral mediastinal and/or subcarinal lymph node(s) pN3: Metastasis in contralateral mediastinal, contralateral hilar, ipsilateral or contralateral scalene, or supraclavicular lymph node(s) pNX: Regional lymph nodes were not assessed Inclusion Criteria: All patients Timing: After surgery Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0456532
- UMLS CUI [1,2]
- C1300072
- UMLS CUI [1,3]
- C0205469
Beschrijving
Treatment Factors
Alias
- UMLS CUI-1
- C0679853
Beschrijving
Inclusion Criteria: All patients Timing: After treatment Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0580352
Beschrijving
Treatment Variables
Alias
- UMLS CUI-1
- C0087111
Beschrijving
Inclusion Criteria: All patients Timing: Update at least annually Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0543467
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on surgery (SURGERY) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C1624150
Beschrijving
Inclusion Criteria: All patients Timing: Update at least annually Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C2985566
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on targeted therapy (TARGETTX) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C2985566
- UMLS CUI [1,2]
- C3173309
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on targeted therapy (TARGETTX) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C2985566
- UMLS CUI [1,2]
- C1531784
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on targeted therapy (TARGETTX), and no end date is entered (TARGETTXSTOPDATE) Timing: Update at least annually Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C2985566
- UMLS CUI [1,2]
- C0549178
Beschrijving
Inclusion Criteria: All patients Timing: Update at least annually Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0392920
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on chemotherapy (CTX) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0392920
- UMLS CUI [1,2]
- C0808070
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on chemotherapy (CTX) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0392920
- UMLS CUI [1,2]
- C0806020
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on chemotherapy (CTX), and no end date is entered (CTXSTOPDATE) Timing: Update at least annually Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0549178
- UMLS CUI [1,2]
- C0392920
Beschrijving
Inclusion Criteria: All patients Timing: Update at least annually Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0021083
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on immunotherapy (ITX) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0021083
- UMLS CUI [1,2]
- C0808070
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on immunotherapy (ITX) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0021083
- UMLS CUI [1,2]
- C0806020
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on immunotherapy (ITX), and no end date is entered (ITXSTOPDATE) Timing: Update at least annually Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0021083
- UMLS CUI [1,2]
- C0549178
Beschrijving
Inclusion Criteria: All patients Timing: Update at least annually Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C1522449
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on radiotherapy (RTX) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C1522449
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on radiotherapy (RTX) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C1522449
- UMLS CUI [1,2]
- C0806020
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on radiotherapy (RTX), and no end date is entered (RTXSTOPDATE) Timing: Update at least annually Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1522449
- UMLS CUI [1,2]
- C0549178
Beschrijving
Acute complications of treatment
Alias
- UMLS CUI-1
- C0679861
Beschrijving
Supporting Definition: Grade III: Requiring surgical, endoscopic, or radiological intervention, with our without general anesthesia Grade IV: Life threatening complication (including CNS complications) requiring IC/ICU management; includes single organ dysfunction and multiorgan dysfunction Source: Annals of Surgery. 250(2):187-196, August 2009. Inclusion Criteria: All patients receiving resectional surgery If answered 'yes' on surgery (SURGERY) Timing: Update at least annually Data Source: Clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C4055231
- UMLS CUI [1,2]
- C0032787
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010-06-14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with radiotherapy If answered 'yes' on radiotherapy (RADIOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1522449
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C1298908
- UMLS CUI [2,3]
- C0013221
- UMLS CUI [2,4]
- C1522449
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010-06-14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with radiotherapy If answered 'yes' on radiotherapy (RADIOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1522449
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C0010828
- UMLS CUI [2,3]
- C1522449
- UMLS CUI [3,1]
- C0009566
- UMLS CUI [3,2]
- C0002871
- UMLS CUI [3,3]
- C1522449
- UMLS CUI [4,1]
- C0009566
- UMLS CUI [4,2]
- C0746883
- UMLS CUI [4,3]
- C1522449
- UMLS CUI [5,1]
- C0009566
- UMLS CUI [5,2]
- C0040034
- UMLS CUI [5,3]
- C1522449
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010-06-14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with radiotherapy If answered 'yes' on radiotherapy (RADIOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1522449
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C0009450
- UMLS CUI [2,3]
- C0205225
- UMLS CUI [2,4]
- C1515974
- UMLS CUI [2,5]
- C1522449
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010-06-14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with radiotherapy If answered 'yes' on radiotherapy (RADIOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1522449
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C0015230
- UMLS CUI [2,3]
- C1522449
- UMLS CUI [3,1]
- C0009566
- UMLS CUI [3,2]
- C0034561
- UMLS CUI [3,3]
- C1522449
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010-06-14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with radiotherapy If answered 'yes' on radiotherapy (RADIOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1522449
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C3714636
- UMLS CUI [2,3]
- C1522449
- UMLS CUI [3,1]
- C0009566
- UMLS CUI [3,2]
- C0010200
- UMLS CUI [3,3]
- C1522449
- UMLS CUI [4,1]
- C0009566
- UMLS CUI [4,2]
- C0013404
- UMLS CUI [4,3]
- C1522449
- UMLS CUI [5,1]
- C0009566
- UMLS CUI [5,2]
- C0205394
- UMLS CUI [5,3]
- C0024109
- UMLS CUI [5,4]
- C0040539
- UMLS CUI [5,5]
- C1522449
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010-06-14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with radiotherapy If answered 'yes' on radiotherapy (RADIOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1522449
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C0014868
- UMLS CUI [2,3]
- C1522449
- UMLS CUI [3,1]
- C0009566
- UMLS CUI [3,2]
- C1568868
- UMLS CUI [3,3]
- C1522449
- UMLS CUI [4,1]
- C0009566
- UMLS CUI [4,2]
- C0027497
- UMLS CUI [4,3]
- C1522449
- UMLS CUI [5,1]
- C0009566
- UMLS CUI [5,2]
- C0042963
- UMLS CUI [5,3]
- C1522449
- UMLS CUI [6,1]
- C0009566
- UMLS CUI [6,2]
- C0011991
- UMLS CUI [6,3]
- C1522449
- UMLS CUI [7,1]
- C0009566
- UMLS CUI [7,2]
- C0009806
- UMLS CUI [7,3]
- C1522449
- UMLS CUI [8,1]
- C0009566
- UMLS CUI [8,2]
- C0205394
- UMLS CUI [8,3]
- C0521362
- UMLS CUI [8,4]
- C0600688
- UMLS CUI [8,5]
- C1522449
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010-06-14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with radiotherapy If answered 'yes' on radiotherapy (RADIOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1522449
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C0442874
- UMLS CUI [2,3]
- C1522449
- UMLS CUI [3,1]
- C0009566
- UMLS CUI [3,2]
- C0040264
- UMLS CUI [3,3]
- C1522449
- UMLS CUI [4,1]
- C0009566
- UMLS CUI [4,2]
- C1384666
- UMLS CUI [4,3]
- C1522449
- UMLS CUI [5,1]
- C0009566
- UMLS CUI [5,2]
- C0205394
- UMLS CUI [5,3]
- C0205494
- UMLS CUI [5,4]
- C0600688
- UMLS CUI [5,5]
- C1522449
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010-06-14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with radiotherapy If answered 'yes' on radiotherapy (RADIOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1522449
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C2609414
- UMLS CUI [2,3]
- C1522449
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010-06-14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with radiotherapy If answered 'yes' on radiotherapy (RADIOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1522449
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C0205394
- UMLS CUI [2,3]
- C1522449
Beschrijving
Inclusion Criteria: Patients with radiotherapy If answered 'Other' on CTCAE III‐IV complications due to radiotherapy (COMPLRAD) Timing: Update at least annually Data Source: Clinical Type: Free text Response Options: CTCAE grade III-‐IV complication due to radiotherapy
Datatype
text
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C1516728
- UMLS CUI [1,3]
- C1522449
- UMLS CUI [1,4]
- C0205394
Beschrijving
Inclusion Criteria: Patients with radiotherapy If answered Cytopenias on CTCAE III-‐IV complications due to radiotherapy (COMPLRAD) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0010828
- UMLS CUI [1,2]
- C0011008
Beschrijving
Inclusion Criteria: Patients with radiotherapy If answered Infection on CTCAE III‐IV complications due to radiotherapy (COMPLRAD) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0009450
- UMLS CUI [1,2]
- C0011008
Beschrijving
Inclusion Criteria: Patients with radiotherapy If answered Skin reaction on CTCAE III‐IV complications due to radiotherapy (COMPLRAD) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0221743
- UMLS CUI [1,2]
- C0011008
Beschrijving
Inclusion Criteria: Patients with radiotherapy If answered Pneumonitis, cough, dyspnea, other lung toxicity on CTCAE III‐IV complications due to radiotherapy (COMPLRAD) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C3714636
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C0010200
- UMLS CUI [3,1]
- C0011008
- UMLS CUI [3,2]
- C0013404
- UMLS CUI [4,1]
- C0011008
- UMLS CUI [4,2]
- C0205394
- UMLS CUI [4,3]
- C0024109
- UMLS CUI [4,4]
- C0040539
Beschrijving
Inclusion Criteria: Patients with radiotherapy If answered Oesophagitis, mucositis oral, nausea, vomiting, diarrhea, constipation, other GI toxicity on CTCAE III‐IV complications due to radiotherapy (COMPLRAD) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0014868
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C1568868
- UMLS CUI [3,1]
- C0011008
- UMLS CUI [3,2]
- C0027497
- UMLS CUI [4,1]
- C0011008
- UMLS CUI [4,2]
- C0042963
- UMLS CUI [5,1]
- C0011008
- UMLS CUI [5,2]
- C0011991
- UMLS CUI [6,1]
- C0011008
- UMLS CUI [6,2]
- C0009806
- UMLS CUI [7,1]
- C0011008
- UMLS CUI [7,2]
- C0205394
- UMLS CUI [7,3]
- C0521362
- UMLS CUI [7,4]
- C0600688
Beschrijving
Inclusion Criteria: Patients with radiotherapy If answered Neuropathy, tinnitus, hearing impaired, other neurologic toxicity on CTCAE III-IV complications due to radiotherapy (COMPLRAD) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0442874
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C0040264
- UMLS CUI [3,1]
- C0011008
- UMLS CUI [3,2]
- C1384666
- UMLS CUI [4,1]
- C0011008
- UMLS CUI [4,2]
- C0205394
- UMLS CUI [4,3]
- C0205494
- UMLS CUI [4,4]
- C0600688
Beschrijving
Inclusion Criteria: Patients with radiotherapy If answered Acute kidney injury on CTCAE III‐IV complications due to radiotherapy (COMPLRAD) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C2609414
Beschrijving
Inclusion Criteria: Patients with radiotherapy If answered Other on CTCAE III‐IV complications due to radiotherapy (COMPLRAD) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0009566
- UMLS CUI [1,3]
- C0011008
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010‐06‐14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with systemic therapy If answered 'yes' on chemotherapy or immunotherapy (CHEMOTX or IMMUNOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1515119
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C1298908
- UMLS CUI [2,3]
- C0013221
- UMLS CUI [2,4]
- C1515119
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010‐06‐14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with systemic therapy If answered 'yes' on chemotherapy or immunotherapy (CHEMOTX or IMMUNOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1515119
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C0010828
- UMLS CUI [2,3]
- C1515119
- UMLS CUI [3,1]
- C0009566
- UMLS CUI [3,2]
- C0002871
- UMLS CUI [3,3]
- C1515119
- UMLS CUI [4,1]
- C0009566
- UMLS CUI [4,2]
- C0746883
- UMLS CUI [4,3]
- C1515119
- UMLS CUI [5,1]
- C0009566
- UMLS CUI [5,2]
- C0040034
- UMLS CUI [5,3]
- C1515119
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010‐06‐14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with systemic therapy If answered 'yes' on chemotherapy or immunotherapy (CHEMOTX or IMMUNOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1515119
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C0009450
- UMLS CUI [2,3]
- C0205225
- UMLS CUI [2,4]
- C1515974
- UMLS CUI [2,5]
- C1515119
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010‐06‐14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with systemic therapy If answered 'yes' on chemotherapy or immunotherapy (CHEMOTX or IMMUNOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1515119
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C0015230
- UMLS CUI [2,3]
- C1515119
- UMLS CUI [3,1]
- C0009566
- UMLS CUI [3,2]
- C0034561
- UMLS CUI [3,3]
- C1515119
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010‐06‐14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with systemic therapy If answered 'yes' on chemotherapy or immunotherapy (CHEMOTX or IMMUNOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1515119
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C3714636
- UMLS CUI [2,3]
- C1515119
- UMLS CUI [3,1]
- C0009566
- UMLS CUI [3,2]
- C0010200
- UMLS CUI [3,3]
- C1515119
- UMLS CUI [3,4]
- |C0009566
- UMLS CUI [3,5]
- C0013404
- UMLS CUI [3,6]
- C1515119
- UMLS CUI [4,1]
- C0009566
- UMLS CUI [4,2]
- C0205394
- UMLS CUI [4,3]
- C0024109
- UMLS CUI [4,4]
- C0040539
- UMLS CUI [4,5]
- C1515119
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010‐06‐14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with systemic therapy If answered 'yes' on chemotherapy or immunotherapy (CHEMOTX or IMMUNOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1515119
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C0014868
- UMLS CUI [2,3]
- C1515119
- UMLS CUI [3,1]
- C0009566
- UMLS CUI [3,2]
- C1568868
- UMLS CUI [3,3]
- C1515119
- UMLS CUI [4,1]
- C0009566
- UMLS CUI [4,2]
- C0027497
- UMLS CUI [4,3]
- C1515119
- UMLS CUI [5,1]
- C0009566
- UMLS CUI [5,2]
- C0042963
- UMLS CUI [5,3]
- C1515119
- UMLS CUI [6,1]
- C0009566
- UMLS CUI [6,2]
- C0011991
- UMLS CUI [6,3]
- C1515119
- UMLS CUI [7,1]
- C0009566
- UMLS CUI [7,2]
- C0009806
- UMLS CUI [7,3]
- C1515119
- UMLS CUI [8,1]
- C0009566
- UMLS CUI [8,2]
- C0205394
- UMLS CUI [8,3]
- C0521362
- UMLS CUI [8,4]
- C0600688
- UMLS CUI [8,5]
- C1515119
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010‐06‐14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with systemic therapy If answered 'yes' on chemotherapy or immunotherapy (CHEMOTX or IMMUNOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1515119
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C0442874
- UMLS CUI [2,3]
- C1515119
- UMLS CUI [3,1]
- C0009566
- UMLS CUI [3,2]
- C0040264
- UMLS CUI [3,3]
- C1515119
- UMLS CUI [4,1]
- C0009566
- UMLS CUI [4,2]
- C1384666
- UMLS CUI [4,3]
- C1515119
- UMLS CUI [5,1]
- C0009566
- UMLS CUI [5,2]
- C0205394
- UMLS CUI [5,3]
- C0205494
- UMLS CUI [5,4]
- C0600688
- UMLS CUI [5,5]
- C1515119
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010‐06‐14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with systemic therapy If answered 'yes' on chemotherapy or immunotherapy (CHEMOTX or IMMUNOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1515119
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C2609414
- UMLS CUI [2,3]
- C1515119
Beschrijving
Supporting Definition: A CTCAE v 4 grade III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010‐06‐14_QuickReference_5x7.pdf for a list of domains and grades of complications Inclusion Criteria: Patients with systemic therapy If answered 'yes' on chemotherapy or immunotherapy (CHEMOTX or IMMUNOTX) Timing: Update at least annually Data Source: Clinical Type: Multiple answer
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516728
- UMLS CUI [1,2]
- C1515119
- UMLS CUI [2,1]
- C0009566
- UMLS CUI [2,2]
- C0205394
- UMLS CUI [2,3]
- C1515119
Beschrijving
Inclusion Criteria: Patients with systemic therapy If answered 'Other' on CTCAE III‐IV complications due to systemic therapy (COMPLSYS) Timing: Update at least annually Data Source: Clinical Type: Free text Response Options: CTCAE grade III-IV complication due to systemic therapy
Datatype
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0009566
- UMLS CUI [1,3]
- C1515119
- UMLS CUI [1,4]
- C1516728
Beschrijving
Inclusion Criteria: Patients with systemic therapy If answered Cytopenias on CTCAE grade II-IV complications (COMPLSYS) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0010828
- UMLS CUI [1,2]
- C0011008
Beschrijving
Inclusion Criteria: Patients with systemic therapy If answered Infection on CTCAE grade II-IV complications (COMPLSYS) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0009450
- UMLS CUI [1,2]
- C0011008
Beschrijving
Inclusion Criteria: Patients with systemic therapy If answered Skin reaction on CTCAE grade II-IV complications (COMPLSYS) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0221743
- UMLS CUI [1,2]
- C0011008
Beschrijving
Inclusion Criteria: Patients with systemic therapy If answered Pneumonitis, cough, dyspnea, other lung toxicity on CTCAE grade II‐IV complications (COMPLSYS) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C3714636
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C0010200
- UMLS CUI [3,1]
- C0011008
- UMLS CUI [3,2]
- C0013404
- UMLS CUI [4,1]
- C0011008
- UMLS CUI [4,2]
- C0205394
- UMLS CUI [4,3]
- C0024109
- UMLS CUI [4,4]
- C0040539
Beschrijving
Inclusion Criteria: Patients with systemic therapy If answered Oesophagitis, mucositis oral, nausea, vomiting, diarrhea, constipation, other GI toxicity on CTCAE grade II‐IV complications (COMPLSYS) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0014868
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C1568868
- UMLS CUI [3,1]
- C0011008
- UMLS CUI [3,2]
- C0027497
- UMLS CUI [4,1]
- C0011008
- UMLS CUI [4,2]
- C0042963
- UMLS CUI [5,1]
- C0011008
- UMLS CUI [5,2]
- C0011991
- UMLS CUI [6,1]
- C0011008
- UMLS CUI [6,2]
- C0009806
- UMLS CUI [7,1]
- C0011008
- UMLS CUI [7,2]
- C0205394
- UMLS CUI [7,3]
- C0521362
- UMLS CUI [7,4]
- C0600688
Beschrijving
Inclusion Criteria: Patients with systemic therapy If answered Neuropathy, tinnitus, hearing impaired, other neurologic toxicity on CTCAE grade II-IV complications (COMPLSYS) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0442874
- UMLS CUI [2,1]
- C0011008
- UMLS CUI [2,2]
- C0040264
- UMLS CUI [3,1]
- C0011008
- UMLS CUI [3,2]
- C1384666
- UMLS CUI [4,1]
- C0011008
- UMLS CUI [4,2]
- C0205394
- UMLS CUI [4,3]
- C0205494
- UMLS CUI [4,4]
- C0600688
Beschrijving
Inclusion Criteria: Patients with systemic therapy If answered Acute kidney injury on CTCAE grade II‐IV complications (COMPLSYS) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C2609414
Beschrijving
Inclusion Criteria: Patients with systemic therapy If answered Other on CTCAE grade II-IV complications (COMPLSYS) Timing: Update at least annually Data Source: Clinical Type: Date by DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0009566
- UMLS CUI [1,3]
- C0011008
Beschrijving
Survival
Alias
- UMLS CUI-1
- C1148433
Beschrijving
Inclusion Criteria: All patients If answered "yes” on the question "indicate if the patient has died" (DEATH) Timing: 1 year post initiation of treatment Tracked ongoing annually for life (when hospital is able to track this ongoing) Data Source: Administrative data (Death registry) or clinical Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0007465
- UMLS CUI [2]
- C0242379
Beschrijving
Supporting Definition: This is needed to calculate the 30 and 90 day treatment related mortality Inclusion Criteria: All patients receiving treatment If answered "yes” on the question "indicate if the patient has died" (DEATH) Timing: 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
Datatype
integer
Alias
- UMLS CUI [1]
- C0007465
- UMLS CUI [2,1]
- C0242379
- UMLS CUI [2,2]
- C0920425
Beschrijving
Quality of death
Alias
- UMLS CUI-1
- C0011065
- UMLS CUI-2
- C0332306
Beschrijving
Inclusion Criteria: All patients with end-‐stage disease If answered 'yes' on overall survival (OVERALLSURV) Timing: 1 year post initiation of treatment Tracked ongoing annually for life (when hospital is able to track this ongoing) Data Source: Clinical Type: Numerical value Response Options: Numerical value of number of days
Datatype
integer
Alias
- UMLS CUI [1]
- C3694481
Similar models
Follow-up - Clinical Form
- StudyEvent: ODM
C1442488 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C1520224 (UMLS CUI-2)
(Comment:en)
C1442488 (UMLS CUI-2)
C1521733 (UMLS CUI [1,2])
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C0205469 (UMLS CUI-2)
(Comment:en)
C1521733 (UMLS CUI-2)
C1300072 (UMLS CUI-3)
(Comment:en)
C1300072 (UMLS CUI [1,2])
C0205469 (UMLS CUI [1,3])
(Comment:en)
(Comment:en)
(Comment:en)
(Comment:en)
C1521733 (UMLS CUI-2)
(Comment:en)
C0456532 (UMLS CUI-2)
C1300072 (UMLS CUI-3)
C0205469 (UMLS CUI-4)
(Comment:en)
(Comment:en)
C3665472 (UMLS CUI-2)
C1707814 (UMLS CUI-3)
(Comment:en)
C1522449 (UMLS CUI-2)
C1707814 (UMLS CUI-3)
(Comment:en)
C3841966 (UMLS CUI-2)
(Comment:en)
C0600688 (UMLS CUI-2)
(Comment:en)
C0011065 (UMLS CUI-2)
(Comment:en)
(Comment:en)
(Comment:en)
C0677930 (UMLS CUI-2)
(Comment:en)
C2939420 (UMLS CUI-2)
C0332300 (UMLS CUI-3)
C0220650 (UMLS CUI-4)
(Comment:en)
C0006104 (UMLS CUI-2)
C0027627 (UMLS CUI-3)
(Comment:en)
(Comment:en)
(Comment:en)
C3173309 (UMLS CUI [1,2])
C1531784 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C0549178 (UMLS CUI-2)
(Comment:en)
(Comment:en)
(Comment:en)
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,2])
C0392920 (UMLS CUI-2)
(Comment:en)
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C0549178 (UMLS CUI-2)
(Comment:en)
(Comment:en)
C0677930 (UMLS CUI-2)
(Comment:en)
C2939420 (UMLS CUI-2)
C0332300 (UMLS CUI-3)
C0220650 (UMLS CUI-4)
(Comment:en)
C0006104 (UMLS CUI-2)
C0027627 (UMLS CUI-3)
(Comment:en)
C1522449 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C0549178 (UMLS CUI-2)
(Comment:en)
C0032787 (UMLS CUI [1,2])
(Comment:en)
C4055231 (UMLS CUI-2)
C0450094 (UMLS CUI-3)
(Comment:en)
C4055231 (UMLS CUI-2)
C0547054 (UMLS CUI-3)
(Comment:en)
C1522449 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C1298908 (UMLS CUI [2,2])
C0013221 (UMLS CUI [2,3])
C1522449 (UMLS CUI [2,4])
C1522449 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C0010828 (UMLS CUI [2,2])
C1522449 (UMLS CUI [2,3])
C0009566 (UMLS CUI [3,1])
C0002871 (UMLS CUI [3,2])
C1522449 (UMLS CUI [3,3])
C0009566 (UMLS CUI [4,1])
C0746883 (UMLS CUI [4,2])
C1522449 (UMLS CUI [4,3])
C0009566 (UMLS CUI [5,1])
C0040034 (UMLS CUI [5,2])
C1522449 (UMLS CUI [5,3])
C1522449 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C0009450 (UMLS CUI [2,2])
C0205225 (UMLS CUI [2,3])
C1515974 (UMLS CUI [2,4])
C1522449 (UMLS CUI [2,5])
C1522449 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C0015230 (UMLS CUI [2,2])
C1522449 (UMLS CUI [2,3])
C0009566 (UMLS CUI [3,1])
C0034561 (UMLS CUI [3,2])
C1522449 (UMLS CUI [3,3])
C1522449 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C3714636 (UMLS CUI [2,2])
C1522449 (UMLS CUI [2,3])
C0009566 (UMLS CUI [3,1])
C0010200 (UMLS CUI [3,2])
C1522449 (UMLS CUI [3,3])
C0009566 (UMLS CUI [4,1])
C0013404 (UMLS CUI [4,2])
C1522449 (UMLS CUI [4,3])
C0009566 (UMLS CUI [5,1])
C0205394 (UMLS CUI [5,2])
C0024109 (UMLS CUI [5,3])
C0040539 (UMLS CUI [5,4])
C1522449 (UMLS CUI [5,5])
C1522449 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C0014868 (UMLS CUI [2,2])
C1522449 (UMLS CUI [2,3])
C0009566 (UMLS CUI [3,1])
C1568868 (UMLS CUI [3,2])
C1522449 (UMLS CUI [3,3])
C0009566 (UMLS CUI [4,1])
C0027497 (UMLS CUI [4,2])
C1522449 (UMLS CUI [4,3])
C0009566 (UMLS CUI [5,1])
C0042963 (UMLS CUI [5,2])
C1522449 (UMLS CUI [5,3])
C0009566 (UMLS CUI [6,1])
C0011991 (UMLS CUI [6,2])
C1522449 (UMLS CUI [6,3])
C0009566 (UMLS CUI [7,1])
C0009806 (UMLS CUI [7,2])
C1522449 (UMLS CUI [7,3])
C0009566 (UMLS CUI [8,1])
C0205394 (UMLS CUI [8,2])
C0521362 (UMLS CUI [8,3])
C0600688 (UMLS CUI [8,4])
C1522449 (UMLS CUI [8,5])
C1522449 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C0442874 (UMLS CUI [2,2])
C1522449 (UMLS CUI [2,3])
C0009566 (UMLS CUI [3,1])
C0040264 (UMLS CUI [3,2])
C1522449 (UMLS CUI [3,3])
C0009566 (UMLS CUI [4,1])
C1384666 (UMLS CUI [4,2])
C1522449 (UMLS CUI [4,3])
C0009566 (UMLS CUI [5,1])
C0205394 (UMLS CUI [5,2])
C0205494 (UMLS CUI [5,3])
C0600688 (UMLS CUI [5,4])
C1522449 (UMLS CUI [5,5])
C1522449 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C2609414 (UMLS CUI [2,2])
C1522449 (UMLS CUI [2,3])
C1522449 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
C1522449 (UMLS CUI [2,3])
C1516728 (UMLS CUI [1,2])
C1522449 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C3714636 (UMLS CUI [1,2])
C0011008 (UMLS CUI [2,1])
C0010200 (UMLS CUI [2,2])
C0011008 (UMLS CUI [3,1])
C0013404 (UMLS CUI [3,2])
C0011008 (UMLS CUI [4,1])
C0205394 (UMLS CUI [4,2])
C0024109 (UMLS CUI [4,3])
C0040539 (UMLS CUI [4,4])
C0014868 (UMLS CUI [1,2])
C0011008 (UMLS CUI [2,1])
C1568868 (UMLS CUI [2,2])
C0011008 (UMLS CUI [3,1])
C0027497 (UMLS CUI [3,2])
C0011008 (UMLS CUI [4,1])
C0042963 (UMLS CUI [4,2])
C0011008 (UMLS CUI [5,1])
C0011991 (UMLS CUI [5,2])
C0011008 (UMLS CUI [6,1])
C0009806 (UMLS CUI [6,2])
C0011008 (UMLS CUI [7,1])
C0205394 (UMLS CUI [7,2])
C0521362 (UMLS CUI [7,3])
C0600688 (UMLS CUI [7,4])
C0442874 (UMLS CUI [1,2])
C0011008 (UMLS CUI [2,1])
C0040264 (UMLS CUI [2,2])
C0011008 (UMLS CUI [3,1])
C1384666 (UMLS CUI [3,2])
C0011008 (UMLS CUI [4,1])
C0205394 (UMLS CUI [4,2])
C0205494 (UMLS CUI [4,3])
C0600688 (UMLS CUI [4,4])
C2609414 (UMLS CUI [1,2])
C0009566 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C1515119 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C1298908 (UMLS CUI [2,2])
C0013221 (UMLS CUI [2,3])
C1515119 (UMLS CUI [2,4])
C1515119 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C0010828 (UMLS CUI [2,2])
C1515119 (UMLS CUI [2,3])
C0009566 (UMLS CUI [3,1])
C0002871 (UMLS CUI [3,2])
C1515119 (UMLS CUI [3,3])
C0009566 (UMLS CUI [4,1])
C0746883 (UMLS CUI [4,2])
C1515119 (UMLS CUI [4,3])
C0009566 (UMLS CUI [5,1])
C0040034 (UMLS CUI [5,2])
C1515119 (UMLS CUI [5,3])
C1515119 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C0009450 (UMLS CUI [2,2])
C0205225 (UMLS CUI [2,3])
C1515974 (UMLS CUI [2,4])
C1515119 (UMLS CUI [2,5])
C1515119 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C0015230 (UMLS CUI [2,2])
C1515119 (UMLS CUI [2,3])
C0009566 (UMLS CUI [3,1])
C0034561 (UMLS CUI [3,2])
C1515119 (UMLS CUI [3,3])
C1515119 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C3714636 (UMLS CUI [2,2])
C1515119 (UMLS CUI [2,3])
C0009566 (UMLS CUI [3,1])
C0010200 (UMLS CUI [3,2])
C1515119 (UMLS CUI [3,3])
|C0009566 (UMLS CUI [3,4])
C0013404 (UMLS CUI [3,5])
C1515119 (UMLS CUI [3,6])
C0009566 (UMLS CUI [4,1])
C0205394 (UMLS CUI [4,2])
C0024109 (UMLS CUI [4,3])
C0040539 (UMLS CUI [4,4])
C1515119 (UMLS CUI [4,5])
C1515119 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C0014868 (UMLS CUI [2,2])
C1515119 (UMLS CUI [2,3])
C0009566 (UMLS CUI [3,1])
C1568868 (UMLS CUI [3,2])
C1515119 (UMLS CUI [3,3])
C0009566 (UMLS CUI [4,1])
C0027497 (UMLS CUI [4,2])
C1515119 (UMLS CUI [4,3])
C0009566 (UMLS CUI [5,1])
C0042963 (UMLS CUI [5,2])
C1515119 (UMLS CUI [5,3])
C0009566 (UMLS CUI [6,1])
C0011991 (UMLS CUI [6,2])
C1515119 (UMLS CUI [6,3])
C0009566 (UMLS CUI [7,1])
C0009806 (UMLS CUI [7,2])
C1515119 (UMLS CUI [7,3])
C0009566 (UMLS CUI [8,1])
C0205394 (UMLS CUI [8,2])
C0521362 (UMLS CUI [8,3])
C0600688 (UMLS CUI [8,4])
C1515119 (UMLS CUI [8,5])
C1515119 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C0442874 (UMLS CUI [2,2])
C1515119 (UMLS CUI [2,3])
C0009566 (UMLS CUI [3,1])
C0040264 (UMLS CUI [3,2])
C1515119 (UMLS CUI [3,3])
C0009566 (UMLS CUI [4,1])
C1384666 (UMLS CUI [4,2])
C1515119 (UMLS CUI [4,3])
C0009566 (UMLS CUI [5,1])
C0205394 (UMLS CUI [5,2])
C0205494 (UMLS CUI [5,3])
C0600688 (UMLS CUI [5,4])
C1515119 (UMLS CUI [5,5])
C1515119 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C2609414 (UMLS CUI [2,2])
C1515119 (UMLS CUI [2,3])
C1515119 (UMLS CUI [1,2])
C0009566 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
C1515119 (UMLS CUI [2,3])
C0009566 (UMLS CUI [1,2])
C1515119 (UMLS CUI [1,3])
C1516728 (UMLS CUI [1,4])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C3714636 (UMLS CUI [1,2])
C0011008 (UMLS CUI [2,1])
C0010200 (UMLS CUI [2,2])
C0011008 (UMLS CUI [3,1])
C0013404 (UMLS CUI [3,2])
C0011008 (UMLS CUI [4,1])
C0205394 (UMLS CUI [4,2])
C0024109 (UMLS CUI [4,3])
C0040539 (UMLS CUI [4,4])
C0014868 (UMLS CUI [1,2])
C0011008 (UMLS CUI [2,1])
C1568868 (UMLS CUI [2,2])
C0011008 (UMLS CUI [3,1])
C0027497 (UMLS CUI [3,2])
C0011008 (UMLS CUI [4,1])
C0042963 (UMLS CUI [4,2])
C0011008 (UMLS CUI [5,1])
C0011991 (UMLS CUI [5,2])
C0011008 (UMLS CUI [6,1])
C0009806 (UMLS CUI [6,2])
C0011008 (UMLS CUI [7,1])
C0205394 (UMLS CUI [7,2])
C0521362 (UMLS CUI [7,3])
C0600688 (UMLS CUI [7,4])
C0442874 (UMLS CUI [1,2])
C0011008 (UMLS CUI [2,1])
C0040264 (UMLS CUI [2,2])
C0011008 (UMLS CUI [3,1])
C1384666 (UMLS CUI [3,2])
C0011008 (UMLS CUI [4,1])
C0205394 (UMLS CUI [4,2])
C0205494 (UMLS CUI [4,3])
C0600688 (UMLS CUI [4,4])
C2609414 (UMLS CUI [1,2])
C0009566 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0242379 (UMLS CUI [2])
(Comment:en)
(Comment:en)
(Comment:en)
C0242379 (UMLS CUI [2,1])
C0920425 (UMLS CUI [2,2])
(Comment:en)
(Comment:en)
(Comment:en)