MDT board diagnosis

MDT board diagnosis
Descripción

MDT board diagnosis

MDT board diagnosis available?
Descripción

mdt_available

Tipo de datos

integer

MDT diagnosis
Descripción

MDT diagnosis

Date of MDT-diagnosis
Descripción

mdt_dxdate

Tipo de datos

date

mdt_board_diagnosis.mdt_basedon___clinical
Descripción

mdt_board_diagnosis.mdt_basedon___clinical

MDT diagnosis based on: Clinical data
Descripción

mdt_basedon_Clinical data

Tipo de datos

integer

Radiological data
Descripción

mdt_basedon_Radiological data

Tipo de datos

integer

Pathological data
Descripción

mdt_basedon_Pathological data

Tipo de datos

integer

Interstitial Lung Abnormalities (ILA)
Descripción

mdt_ila

Tipo de datos

integer

Idiopathic Interstitial Pneumonia (IIP)
Descripción

mdt_iip

Tipo de datos

integer

Idiopathic Pulmonary Fibrosis (IPF)
Descripción

mdt_ipf

Tipo de datos

integer

Likelihood of diagnosis
Descripción

mdt_sub_ipf

Tipo de datos

text

Non-Specific Interstitial Pneumonia (NSIP)
Descripción

mdt_nsip

Tipo de datos

integer

Descripción

mdt_sub_nsip

Tipo de datos

text

Respiratory-Bronchiolitis-ILD
Descripción

mdt_rbild

Tipo de datos

integer

Desquamative Interstitial Pneumonia (DIP)
Descripción

mdt_dip

Tipo de datos

integer

Cryptogenic Organizing Pneumonia (COP)
Descripción

mdt_cop

Tipo de datos

integer

Acute Interstitial Pneumonia (AIP)
Descripción

mdt_aip

Tipo de datos

integer

Lymphoid Interstitial Pneumonia (LIP)
Descripción

mdt_lip

Tipo de datos

integer

Idiopathic Pleuroparenchymal Fibroelastosis (PPFE)
Descripción

mdt_ipleurofib

Tipo de datos

integer

Bronchiolocentric form of IIP
Descripción

mdt_bronchoiip

Tipo de datos

integer

Acute Fibrinous and Organizing Pneumonia (AFOP)
Descripción

mdt_afop

Tipo de datos

integer

Unclassifiable IIP
Descripción

mdt_unclassediip

Tipo de datos

integer

Meets IPAF criteria?
Descripción

mdt_ipaf

Tipo de datos

integer

Granulomatous lung diseases of non-infectious origin
Descripción

mdt_granudisease

Tipo de datos

integer

Type of granulomatous lung disease
Descripción

mdt_subgroup_gld_ni

Tipo de datos

text

Sarcoidosis stage according to chest X-ray
Descripción

mdt_subsarco_stage

Tipo de datos

text

Extrapulmonary organ manifestation of sarcoidosis null
Descripción

mdt_subsarco_manifest_null

Tipo de datos

integer

Skin
Descripción

mdt_subsarco_manifest_Skin

Tipo de datos

integer

Heart
Descripción

mdt_subsarco_manifest_Heart

Tipo de datos

integer

Liver
Descripción

mdt_subsarco_manifest_Liver

Tipo de datos

integer

Spleen
Descripción

mdt_subsarco_manifest_Spleen

Tipo de datos

integer

Kidney
Descripción

mdt_subsarco_manifest_Kidney

Tipo de datos

integer

Eye
Descripción

mdt_subsarco_manifest_Eye

Tipo de datos

integer

Bone
Descripción

mdt_subsarco_manifest_Bone

Tipo de datos

integer

Other
Descripción

mdt_subsarco_manifest_Other

Tipo de datos

integer

Type of Hypersensitivity pneumonitis
Descripción

mdt_hyperpneumo

Tipo de datos

text

ILD due to inhaled inorganic agents Please specify the causing agent in the section environmental exposure
Descripción

mdt_ildanorgdusts

Tipo de datos

integer

Silicates
Descripción

mdt_silicates

Tipo de datos

integer

Carbon compounds
Descripción

mdt_carboncompound

Tipo de datos

integer

Metals
Descripción

mdt_metals

Tipo de datos

integer

Chemicals
Descripción

mdt_chemical

Tipo de datos

integer

Gases
Descripción

mdt_gases

Tipo de datos

integer

ILD due to inhaled organic agents (non-allergic, no HP)  - inhaled or aspired- Please specify the causing agent in the section environmental exposure
Descripción

mdt_ildorgansub

Tipo de datos

integer

ILD in the context of rheumatoid arthritis or collagen/vascular disease
Descripción

mdt_ild_ra

Tipo de datos

integer

null
Descripción

mdt_subgroup_rheum_null

Tipo de datos

integer

Anti-synthetase syndrome (Jo-1-Syndrome)
Descripción

mdt_subgroup_rheum_Anti-synthetase syndrome (Jo-1-Syndrome)

Tipo de datos

integer

Descripción

mdt_subgroup_rheum_null

Tipo de datos

integer

Polymyositis/Dermatomyositis
Descripción

mdt_subgroup_rheum_Polymyositis/Dermatomyositis

Tipo de datos

integer

Descripción

mdt_subgroup_rheum_null

Tipo de datos

integer

Sjögren's Disease
Descripción

mdt_subgroup_rheum_Sjögren's Disease

Tipo de datos

integer

Descripción

mdt_subgroup_rheum_null

Tipo de datos

integer

Descripción

mdt_subgroup_rheum_null

Tipo de datos

integer

Descripción

mdt_subgroup_rheum_null

Tipo de datos

integer

Unclassifiable CVD-ILD
Descripción

mdt_subgroup_rheum_Unclassifiable CVD-ILD

Tipo de datos

integer

ILD in the context of a dysbalanced immune system
Descripción

mdt_ild_immunesys

Tipo de datos

integer

Descripción

mdt_subgroup_immunesys

Tipo de datos

text

Descripción

mdt_sub_bowel

Tipo de datos

text

Eosinophilic ILDs
Descripción

mdt_ild_eos

Tipo de datos

integer

Descripción

mdt_subgroup_eos

Tipo de datos

text

ILD in the context of semi-malignant or malignant diseases
Descripción

mdt_ild_maligndis

Tipo de datos

integer

Descripción

mdt_subgroup_malidis

Tipo de datos

text

ILD in the context of a "storage" / "deposition" diseases
Descripción

mdt_ild_storagedis

Tipo de datos

integer

Descripción

mdt_subgroup_storagedis

Tipo de datos

text

ILD due to medical measures Please specify in ILD-related drugs and medical measures
Descripción

mdt_ild_medical

Tipo de datos

integer

Descripción

mdt_medical_category

Tipo de datos

text

ILD due to drugs (acc. to pneumotox) Please specify in ILD-related drugs and medical measures
Descripción

mdt_ild_drugs

Tipo de datos

integer

Unclassifiable ILD
Descripción

mdt_ild_unclassed

Tipo de datos

integer

Any rare ILD not listed above
Descripción

mdt_ild_rare

Tipo de datos

text

Familial form of ILD Please specify in Family history
Descripción

mdt_ildfamilial

Tipo de datos

integer

Descripción

mdt_subfamilial

Tipo de datos

text

Descripción

mdt_subfamilialother

Tipo de datos

text

CPFE criteria fulfilled
Descripción

mdt_cpfecriteria

Tipo de datos

integer

Similar models

MDT board diagnosis

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item
MDT board diagnosis available?
integer
Code List
MDT board diagnosis available?
CL Item
Yes (1)
CL Item
No (0)
Item Group
mdt_dxdate
Item
Date of MDT-diagnosis
date
Item
MDT diagnosis based on: Clinical data
integer
Code List
MDT diagnosis based on: Clinical data
CL Item
Yes (1)
CL Item
No (0)
Item
Radiological data
integer
Code List
Radiological data
CL Item
Yes (1)
CL Item
No (0)
Item
Pathological data
integer
Code List
Pathological data
CL Item
Yes (1)
CL Item
No (0)
Item
Interstitial Lung Abnormalities (ILA)
integer
Code List
Interstitial Lung Abnormalities (ILA)
CL Item
Yes (1)
CL Item
No (0)
Item
Idiopathic Interstitial Pneumonia (IIP)
integer
Code List
Idiopathic Interstitial Pneumonia (IIP)
CL Item
Yes (1)
CL Item
No (0)
Item
Idiopathic Pulmonary Fibrosis (IPF)
integer
Code List
Idiopathic Pulmonary Fibrosis (IPF)
CL Item
Yes (1)
CL Item
No (0)
Item
Likelihood of diagnosis
text
Code List
Likelihood of diagnosis
CL Item
Definite IPF diagnosis (definite)
CL Item
Provisional high-confidence IPF diagnosis (highconf)
CL Item
Provisional low-confidence IPF diagnosis (lowconf)
Item
Non-Specific Interstitial Pneumonia (NSIP)
integer
Code List
Non-Specific Interstitial Pneumonia (NSIP)
CL Item
Yes (1)
CL Item
No (0)
Item
text
Code List
CL Item
Cellular (cellular)
CL Item
Fibrotic (fibrotic)
Item
Respiratory-Bronchiolitis-ILD
integer
Code List
Respiratory-Bronchiolitis-ILD
CL Item
Yes (1)
CL Item
No (0)
Item
Desquamative Interstitial Pneumonia (DIP)
integer
Code List
Desquamative Interstitial Pneumonia (DIP)
CL Item
Yes (1)
CL Item
No (0)
Item
Cryptogenic Organizing Pneumonia (COP)
integer
Code List
Cryptogenic Organizing Pneumonia (COP)
CL Item
Yes (1)
CL Item
No (0)
Item
Acute Interstitial Pneumonia (AIP)
integer
Code List
Acute Interstitial Pneumonia (AIP)
CL Item
Yes (1)
CL Item
No (0)
Item
Lymphoid Interstitial Pneumonia (LIP)
integer
Code List
Lymphoid Interstitial Pneumonia (LIP)
CL Item
Yes (1)
CL Item
No (0)
Item
Idiopathic Pleuroparenchymal Fibroelastosis (PPFE)
integer
Code List
Idiopathic Pleuroparenchymal Fibroelastosis (PPFE)
CL Item
Yes (1)
CL Item
No (0)
Item
Bronchiolocentric form of IIP
integer
Code List
Bronchiolocentric form of IIP
CL Item
Yes (1)
CL Item
No (0)
Item
Acute Fibrinous and Organizing Pneumonia (AFOP)
integer
Code List
Acute Fibrinous and Organizing Pneumonia (AFOP)
CL Item
Yes (1)
CL Item
No (0)
Item
Unclassifiable IIP
integer
Code List
Unclassifiable IIP
CL Item
Yes (1)
CL Item
No (0)
Item
Meets IPAF criteria?
integer
Code List
Meets IPAF criteria?
CL Item
Yes (1)
CL Item
No (0)
Item
Granulomatous lung diseases of non-infectious origin
integer
Code List
Granulomatous lung diseases of non-infectious origin
CL Item
Yes (1)
CL Item
No (0)
Item
Type of granulomatous lung disease
text
Code List
Type of granulomatous lung disease
CL Item
Sarcoidosis (sarc)
CL Item
Granulomatosis with polyangiitis (GPA) (gpa)
CL Item
Bronchiolocentric granulomatosis (brongra)
CL Item
Aspiration pneumonia (asppneu)
CL Item
Hypersensitivity pneumonitis (hp)
Item
Sarcoidosis stage according to chest X-ray
text
Code List
Sarcoidosis stage according to chest X-ray
CL Item
0 - no visible lung or mediastinal involvement (0)
CL Item
I - bihilar lymphadenopathia w/o lung involvement (I)
CL Item
II - bihilar lymphadenopathia and lung involvement (II)
CL Item
III - lung involvement in absence of bihilar lymphadenopathia (III)
CL Item
IV - lung fibrosis (IV)
Item
Extrapulmonary organ manifestation of sarcoidosis null
integer
Code List
Extrapulmonary organ manifestation of sarcoidosis null
CL Item
Yes (1)
CL Item
No (0)
CL Item
Yes (1)
CL Item
No (0)
CL Item
Yes (1)
CL Item
No (0)
CL Item
Yes (1)
CL Item
No (0)
Item
Spleen
integer
CL Item
Yes (1)
CL Item
No (0)
Item
Kidney
integer
CL Item
Yes (1)
CL Item
No (0)
CL Item
Yes (1)
CL Item
No (0)
CL Item
Yes (1)
CL Item
No (0)
CL Item
Yes (1)
CL Item
No (0)
Item
Type of Hypersensitivity pneumonitis
text
Code List
Type of Hypersensitivity pneumonitis
CL Item
Fibrotic (fibrotic)
CL Item
Non-fibrotic (nonfib)
Item
ILD due to inhaled inorganic agents Please specify the causing agent in the section environmental exposure
integer
Code List
ILD due to inhaled inorganic agents Please specify the causing agent in the section environmental exposure
CL Item
Yes (1)
CL Item
No (0)
Item
Silicates
integer
Code List
Silicates
CL Item
Yes (1)
CL Item
No (0)
Item
Carbon compounds
integer
Code List
Carbon compounds
CL Item
Yes (1)
CL Item
No (0)
Item
Metals
integer
Code List
Metals
CL Item
Yes (1)
CL Item
No (0)
Item
Chemicals
integer
Code List
Chemicals
CL Item
Yes (1)
CL Item
No (0)
Item
Gases
integer
Code List
Gases
CL Item
Yes (1)
CL Item
No (0)
Item
ILD due to inhaled organic agents (non-allergic, no HP)  - inhaled or aspired- Please specify the causing agent in the section environmental exposure
integer
Code List
ILD due to inhaled organic agents (non-allergic, no HP)  - inhaled or aspired- Please specify the causing agent in the section environmental exposure
CL Item
Yes (1)
CL Item
No (0)
Item
ILD in the context of rheumatoid arthritis or collagen/vascular disease
integer
Code List
ILD in the context of rheumatoid arthritis or collagen/vascular disease
CL Item
Yes (1)
CL Item
No (0)
Item
null
integer
CL Item
Yes (1)
CL Item
No (0)
Item
Anti-synthetase syndrome (Jo-1-Syndrome)
integer
Code List
Anti-synthetase syndrome (Jo-1-Syndrome)
CL Item
Yes (1)
CL Item
No (0)
CL Item
Yes (1)
CL Item
No (0)
Item
Polymyositis/Dermatomyositis
integer
Code List
Polymyositis/Dermatomyositis
CL Item
Yes (1)
CL Item
No (0)
CL Item
Yes (1)
CL Item
No (0)
Item
Sjögren's Disease
integer
Code List
Sjögren's Disease
CL Item
Yes (1)
CL Item
No (0)
CL Item
Yes (1)
CL Item
No (0)
CL Item
Yes (1)
CL Item
No (0)
CL Item
Yes (1)
CL Item
No (0)
Item
Unclassifiable CVD-ILD
integer
Code List
Unclassifiable CVD-ILD
CL Item
Yes (1)
CL Item
No (0)
Item
ILD in the context of a dysbalanced immune system
integer
Code List
ILD in the context of a dysbalanced immune system
CL Item
Yes (1)
CL Item
No (0)
CL Item
Common variable immunodeficiency syndrome (CVID) - ILD (cvid)
CL Item
IgG4-related disease (igg4)
CL Item
ILD in the context of inflammatory bowel disease (infbowel)
Item
text
Code List
CL Item
Crohn's disease (crohn)
CL Item
Ulcerative colitis (colitis)
Item
Eosinophilic ILDs
integer
Code List
Eosinophilic ILDs
CL Item
Yes (1)
CL Item
No (0)
CL Item
Acute eosinophilic pneumonia (AEP) (aep)
CL Item
Chronic eosinophilic pneumonia (CEP) (chroniceospneu)
CL Item
Eosinophilic granulomatosis with polyangiitis (EGPA) (agpa)
Item
ILD in the context of semi-malignant or malignant diseases
integer
Code List
ILD in the context of semi-malignant or malignant diseases
CL Item
Yes (1)
CL Item
No (0)
CL Item
Lymphangioleiomyomatosis (LAM) (lam)
CL Item
Pulmonary Langerhans Cell Histioystosis (LCH) (lch)
CL Item
Neurofibromatosis ILD (neurofibro)
CL Item
Birt-Hogg-Dubé-Syndrome (Cystic lung disease) (bhds)
Item
ILD in the context of a "storage" / "deposition" diseases
integer
Code List
ILD in the context of a "storage" / "deposition" diseases
CL Item
Yes (1)
CL Item
No (0)
CL Item
Hermansky-Pudlack syndrome (hpsip)
CL Item
Nieman Pick Disease (npd)
CL Item
Gauchers's Disease (gauchers)
CL Item
Pulmonary alveolar proteinosis (PAP) (pap)
CL Item
Amyloidosis (amyloidosis)
CL Item
Alveolar microlithiasis (Alveolarmicro)
Item
ILD due to medical measures Please specify in ILD-related drugs and medical measures
integer
Code List
ILD due to medical measures Please specify in ILD-related drugs and medical measures
CL Item
Yes (1)
CL Item
No (0)
CL Item
Post-ventilation ILD (postvent)
CL Item
Radiation induced ILD (radioild)
Item
ILD due to drugs (acc. to pneumotox) Please specify in ILD-related drugs and medical measures
integer
Code List
ILD due to drugs (acc. to pneumotox) Please specify in ILD-related drugs and medical measures
CL Item
Yes (1)
CL Item
No (0)
Item
Unclassifiable ILD
integer
Code List
Unclassifiable ILD
CL Item
Yes (1)
CL Item
No (0)
mdt_ild_rare
Item
Any rare ILD not listed above
text
Item
Familial form of ILD Please specify in Family history
integer
Code List
Familial form of ILD Please specify in Family history
CL Item
Yes (1)
CL Item
No (0)
CL Item
Familial IIP (familial)
CL Item
Hermansky-Pudlack Syndrom (hps)
CL Item
Telomeropathia (Telomeropathia)
CL Item
Alveolar microlithiasis (Alveolarmicro)
CL Item
Other (other)
mdt_subfamilialother
Item
text
Item
CPFE criteria fulfilled
integer
Code List
CPFE criteria fulfilled
CL Item
Yes (1)
CL Item
No (0)