ID

17569

Description

ODM form derived from 100days past HSCT EBMT. please refer to: http://www.ebmt.org/Contents/Data-Management/Registrystructure/MED-ABdatacollectionforms/Pages/MED-AB-data-collection-forms.aspx HLA typing results of patient and donor should be attached and sent: - to your NATIONAL REGISTRY if - you normally report to your National Registry and - you are based in the Netherlands, Switzerland, Turkey or the UK - to the EBMT REGISTRY OFFICE in London for any other centre Contact: Shelley Hewerdine EBMT Registry Office 4th Floor, Tabard House Guy's Hospital Great Maze Pond London SE1 9RT United Kingdom Phone: 00 44-207-188-8409 Fax: 00 44-207-188-8411 Email: shelley.hewerdine@ebmt.org

Link

http://www.ebmt.org/Contents/Data-Management/Registrystructure/MED-ABdatacollectionforms/Pages/MED-AB-data-collection-forms.aspx

Keywords

  1. 8/9/16 8/9/16 -
  2. 9/23/16 9/23/16 -
  3. 9/24/16 9/24/16 -
  4. 9/20/21 9/20/21 -
Uploaded on

September 24, 2016

DOI

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License

Creative Commons BY-NC 3.0

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100 days past HSCT EBMT

100 days past HSCT EBMT

CENTRE IDENTIFICATION
Description

CENTRE IDENTIFICATION

EBMT Code (CIC)
Description

EBMT Code (CIC)

Data type

integer

Alias
UMLS CUI [1,1]
C3826859
UMLS CUI [1,2]
C0600091
Hospital
Description

Klinik

Data type

text

Alias
UMLS CUI [1]
C0019994
Unit
Description

Unit

Data type

integer

Alias
UMLS CUI [1]
C1519795
Contact person
Description

Contact person

Data type

integer

Alias
UMLS CUI [1]
C0337611
Phone
Description

Phone

Data type

integer

Alias
UMLS CUI [1]
C1550483
Fax
Description

Fax

Data type

integer

Alias
UMLS CUI [1]
C1549619
e-mail
Description

e-mail

Data type

integer

Alias
UMLS CUI [1]
C1705961
PATIENT DATA
Description

PATIENT DATA

Date of this report
Description

Date of this report

Data type

date

Alias
UMLS CUI [1]
C1302584
Patient following national / international study / trial
Description

Patient following national / international study / trial

Data type

integer

Alias
UMLS CUI [1]
C1997894
Name of study / trial
Description

Name of study / trial

Data type

integer

Alias
UMLS CUI [1]
C0008976
Hospital Unique Patient Number/Code
Description

Hospital Unique Patient Number

Data type

integer

Alias
UMLS CUI [1]
C2348585
Initials (first name(s) _family name(s))
Description

Initials

Data type

integer

Alias
UMLS CUI [1]
C2986440
Date of Birth
Description

Date of Birth

Data type

date

Alias
UMLS CUI [1]
C0421451
Sex
Description

Sex

Data type

text

Alias
UMLS CUI [1]
C0079399
DISEASE
Description

DISEASE

Date of initial diagnosis
Description

Date of initial diagnosis

Data type

date

Alias
UMLS CUI [1]
C2316983
PRIMARY DISEASE DIAGNOSIS
Description

PRIMARY DISEASE DIAGNOSIS

Data type

integer

Alias
UMLS CUI [1]
C0277554
HSCT
Description

HSCT

Performance score (if alive)
Description

Performance score

Data type

integer

Alias
UMLS CUI [1]
C1518965
Score achived
Description

Score

Data type

text

Alias
UMLS CUI [1]
C1518965
Type of HSCT
Description

Type of HSCT

Data type

integer

Alias
UMLS CUI [1]
C0472699
Patient CMV status (for allografts)
Description

Patient CMV status

Data type

integer

Alias
UMLS CUI [1]
C0582172
Multiple donors/products
Description

Multiple donors

Data type

boolean

Alias
UMLS CUI [1]
C0013018
Multiple donors: if yes:
Description

if yes, Number (including multiple CB units or different stem cell products from same donor)

Data type

integer

Alias
UMLS CUI [1]
C0013018
STEM CELLS (autograft or allograft)
Description

STEM CELLS (autograft or allograft)

Source of Stem Cells
Description

(check all that apply)

Data type

integer

Alias
UMLS CUI [1]
C0018956
Source of Stem Cells: if other, please specify
Description

Source of Stem Cells

Data type

integer

Alias
UMLS CUI [1]
C0018956
Donor ID
Description

Donor ID

Data type

text

Alias
UMLS CUI [1]
C1718162
Donor ID
Description

if autograft, go to Graft manipulation below

Data type

integer

Alias
UMLS CUI [1]
C1718162
HLA match type (for allografts)
Description

HLA match type

Data type

integer

Alias
UMLS CUI [1]
C0242318
Degree of mismatch
Description

Degree of mismatch

Data type

integer

Alias
UMLS CUI [1]
C1881865
Name of donor registry/CB Bank
Description

donor registry

Data type

integer

Alias
UMLS CUI [1]
C0034975
BMDW/WMDA code (up to 4 characters)
Description

BMDW/WMDA code

Data type

integer

Alias
UMLS CUI [1]
C2987198
Number of mismatches A
Description

Number of mismatches A

Data type

integer

Alias
UMLS CUI [1,1]
C1881865
UMLS CUI [1,2]
C0449788
Number of mismatches B
Description

Number of mismatches B

Data type

integer

Alias
UMLS CUI [1,1]
C1881865
UMLS CUI [1,2]
C0449788
Number of mismatches C
Description

Number of mismatches C

Data type

integer

Alias
UMLS CUI [1,1]
C1881865
UMLS CUI [1,2]
C0449788
Number of mismatches DRB1
Description

Number of mismatches DRB1

Data type

integer

Alias
UMLS CUI [1,1]
C1881865
UMLS CUI [1,2]
C0449788
Number of mismatches DQB1
Description

Number of mismatches DQB1

Data type

integer

Alias
UMLS CUI [1,1]
C1881865
UMLS CUI [1,2]
C0449788
Number of mismatches DPB1
Description

Number of mismatches DPB1

Data type

integer

Alias
UMLS CUI [1,1]
C1881865
UMLS CUI [1,2]
C0449788
Donor Sex
Description

Donor Sex

Data type

integer

Alias
UMLS CUI [1]
C0079399
Donor age
Description

Donor age

Data type

integer

Alias
UMLS CUI [1,1]
C0013018
UMLS CUI [1,2]
C0421451
Graft manipulation ex-vivo (including T-cell depletion) other than for RBC removal or volume reduction
Description

Graft manipulation ex-vivo (including T-cell depletion) other than for RBC removal or volume reduction

Data type

boolean

Alias
UMLS CUI [1]
C0677960
HSCT
Description

HSCT

Chronological number of HSCT for this patient?
Description

Chronological number of HSCT

Data type

integer

Alias
UMLS CUI [1,1]
C1318453
UMLS CUI [1,2]
C0449788
If >1, date of last HSCT before this one
Description

If >1, date of last HSCT before this one

Data type

date

Alias
UMLS CUI [1,1]
C0018956
UMLS CUI [1,2]
C0029216
UMLS CUI [1,3]
C2745955
UMLS CUI [1,4]
C0011008
HSCT part of a planned multiple graft protocol?
Description

HSCT part of a planned multiple graft protocol?

Data type

boolean

Alias
UMLS CUI [1]
C0548370
Preparative (conditioning) regimen given?
Description

Preparative (conditioning) regimen given?

Data type

boolean

Alias
UMLS CUI [1]
C1882454
Was this intended to be myeloablative?
Description

Was this intended to be myeloablative?

Data type

boolean

Alias
UMLS CUI [1]
C1831742
Reason
Description

Reason HSCT

Data type

integer

Alias
UMLS CUI [1]
C0392360
Ara-C (cytarabine)
Description

Ara-C

Data type

float

Measurement units
  • mg
Alias
UMLS CUI [1]
C0733521
mg
Ara-C (cytarabine): Unit of dosing
Description

Ara-C (cytarabine)

Data type

integer

Alias
UMLS CUI [1,1]
C0733521
UMLS CUI [1,2]
C1321095
ALG, ATG (ALS, ATS)
Description

ALS

Data type

float

Alias
UMLS CUI [1]
C0002736
AST: Unit of dosing
Description

AST: Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C1321095
UMLS CUI [1,2]
C0004002
Animal origin
Description

Animal origin

Data type

integer

Alias
UMLS CUI [1]
C3494749
Bleomycin
Description

Bleomycin

Data type

float

Alias
UMLS CUI [1]
C0005740
Unit of dosing
Description

Unit of doseing

Data type

integer

Alias
UMLS CUI [1]
C1321095
Busulfan
Description

Busulfan

Data type

float

Alias
UMLS CUI [1]
C0006463
Busulfan Unit of dosing:
Description

Busulfan Unit of dosing:

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0006463
Busulfan application
Description

Busulfan application

Data type

integer

Alias
UMLS CUI [1,1]
C0006463
UMLS CUI [1,2]
C1533134
BCNU
Description

BCNU

Data type

float

Alias
UMLS CUI [1]
C0007257
BCNU Unit of dosing
Description

BCNU Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0007257
Bexar (radiolabelled MoAB)
Description

Bexar (radiolabelled MoAB)

Data type

float

Alias
UMLS CUI [1]
C3831356
Bexar Unit of dosing
Description

Bexar Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C3831356
CCNU
Description

CCNU

Data type

float

Alias
UMLS CUI [1]
C0687700
CCNU Unit of dosing
Description

CCNU Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0687700
Campath (antiCD52)
Description

Campath

Data type

float

Alias
UMLS CUI [1]
C0939276
Campath Unit of dosing
Description

Campath Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0939276
Carboplatin
Description

Carboplatin

Data type

float

Alias
UMLS CUI [1]
C0079083
Carboplatin Unit of dosing
Description

Carboplatin Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0079083
Cisplatin
Description

Cisplatin

Data type

float

Alias
UMLS CUI [1]
C0008838
Cisplatin Unit of dosing
Description

Cisplatin Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0008838
Corticosteroids
Description

Corticosteroids

Data type

float

Alias
UMLS CUI [1]
C0001617
Corticosteroids Unit of dosing
Description

Corticosteroids Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0001617
Cyclophosphamide
Description

Cyclophosphamide

Data type

float

Alias
UMLS CUI [1]
C0010583
Cyclophosphamide Unit of dosing
Description

Cyclophosphamide Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0010583
Daunorubicin
Description

Daunorubicin

Data type

float

Alias
UMLS CUI [1]
C0011015
Unit of dosing Daunorubicin
Description

Unit of dosing Daunorubicin

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0011015
Doxorubicin (adriamycine)
Description

Doxorubicin

Data type

float

Alias
UMLS CUI [1]
C0013089
Doxorubicin Unit of dosing
Description

Doxorubicin Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0013089
Etoposide (VP16)
Description

Etoposide

Data type

float

Alias
UMLS CUI [1]
C0015133
Etoposide Unit of dosing
Description

Etoposide Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0015133
Fludarabine
Description

Fludarabine

Data type

float

Alias
UMLS CUI [1]
C0059985
Fludarabine Unit of dosing
Description

Fludarabine Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0059985
Gemtuzumab
Description

Gemtuzumab

Data type

float

Alias
UMLS CUI [1]
C0872968
Gemtuzumab Unit of dosing
Description

Gemtuzumab Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0872968
Idarubicin
Description

Idarubicin

Data type

float

Alias
UMLS CUI [1]
C0020789
Idarubicin Unit of dosing
Description

Idarubicin Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0020789
Ifosfamide
Description

Ifosfamide

Data type

float

Alias
UMLS CUI [1]
C0020823
Ifosfamide Unit of dosing
Description

Ifosfamide Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0020823
Imatinib mesylate
Description

Imatinib mesylate

Data type

float

Alias
UMLS CUI [1]
C0939537
Imatinib mesylate Unit of dosing
Description

Imatinib mesylate Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0939537
Melphalan
Description

Melphalan

Data type

float

Alias
UMLS CUI [1]
C0025241
Melphalan Unit of dosing
Description

Melphalan Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0025241
Mitoxantrone
Description

Mitoxantrone

Data type

float

Alias
UMLS CUI [1]
C0026259
Mitoxantrone Unit of dosing
Description

Mitoxantrone Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0026259
Paclitaxel
Description

Paclitaxel

Data type

float

Alias
UMLS CUI [1]
C0144576
Paclitaxel Unit of dosing
Description

Paclitaxel Unit of dosing

Data type

integer

Alias
UMLS CUI [1]
C0869039
Rituximab (mabthera, antiCD20)
Description

Rituximab

Data type

float

Alias
UMLS CUI [1]
C0393022
Rituximab Unit of dosing
Description

Rituximab Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0393022
Teniposide
Description

Teniposide

Data type

float

Alias
UMLS CUI [1]
C0039512
Teniposide Unit of dosing
Description

Teniposide Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0039512
Thiotepa
Description

Thiotepa

Data type

float

Alias
UMLS CUI [1]
C0039871
Thiotepa Unit of dosing
Description

Thiotepa Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0039871
Zevalin (radiolabelled MoAB)
Description

Zevalin

Data type

float

Alias
UMLS CUI [1]
C0919274
Zevalin Unit of dosing
Description

Zevalin Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0919274
Other radiolabelled MoAB
Description

other radiolabelled MoAB

Data type

float

Alias
UMLS CUI [1,1]
C0003250
UMLS CUI [1,2]
C0454110
other radiolabelled MoAB Unit of dosing
Description

other radiolabelled MoAB Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0003250
UMLS CUI [1,3]
C0454110
Other radiolabelled MoAB: if other, please specify
Description

Other radiolabelled MoAB: if other, please specify

Data type

integer

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C0003250
UMLS CUI [1,3]
C0454110
Other MoAB
Description

Other MoAB

Data type

float

Alias
UMLS CUI [1]
C0003250
MoAB Unit of dosing
Description

MoAB Unit of dosing

Data type

integer

Alias
UMLS CUI [1,1]
C0869039
UMLS CUI [1,2]
C0003250
Total body irradiation
Description

Total body irradiation

Data type

boolean

Alias
UMLS CUI [1]
C0043162
Total Body Irradiation: if yes, please specify value
Description

Total Body Irradiation: if yes, please specify value

Data type

integer

Alias
UMLS CUI [1,1]
C4035158
UMLS CUI [1,2]
C0043162
TLI, TNI, TAI
Description

TLI, TNI, TAI

Data type

boolean

Alias
UMLS CUI [1]
C4035158
UMLS CUI [2]
C0043162
AFTER HSCT
Description

AFTER HSCT

GvHD prophylaxis or preventive treatment (Allografts only)
Description

GvHD prophylaxis

Data type

boolean

Alias
UMLS CUI [1]
C0278845
GvHD prophylaxis or preventive treatment: if yes, please specify
Description

GvHD prophylaxis or preventive treatment: if yes, please specify

Data type

integer

Alias
UMLS CUI [1,1]
C0278845
UMLS CUI [1,2]
C4035158
GvHD prophylaxis or preventive treatment: if other, please specify
Description

GvHD prophylaxis or preventive treatment: if other, please specify

Data type

integer

Alias
UMLS CUI [1,1]
C4035158
UMLS CUI [1,2]
C4035158
GvHD prophylaxis or preventive treatment: if Other monoclonal antibody, please specify
Description

GvHD prophylaxis or preventive treatment: if Other monoclonal antibody, please specify

Data type

integer

Alias
UMLS CUI [1,1]
C4035158
UMLS CUI [1,2]
C4035158
UMLS CUI [1,3]
C0003250
Absolute neutrophil count (ANC) recovery (engraftment) (Neutrophils >0.5X109 /L)
Description

Absolute neutrophil count

Data type

integer

Alias
UMLS CUI [1]
C0948762
Date of last assessment
Description

Date of last assessment

Data type

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C1516048
Date of ANC recovery
Description

Date of ANC recovery

Data type

date

Alias
UMLS CUI [1,1]
C0948762
UMLS CUI [1,2]
C2004454
UMLS CUI [1,3]
C0011008
Date of last assessment
Description

Date of last assessment

Data type

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C1516048
Maximum Grade
Description

Maximum grade

Data type

integer

Alias
UMLS CUI [1,1]
C0856825
UMLS CUI [1,2]
C0441800
ADDITIONAL TREATMENT INCLUDING CELL THERAPY
Description

ADDITIONAL TREATMENT INCLUDING CELL THERAPY

Cell infusion (CI)
Description

Cell infusion

Data type

boolean

Alias
UMLS CUI [1]
C2145394
Date of first infusion
Description

(can be the same as HSCT date)

Data type

date

Alias
UMLS CUI [1,1]
C0574032
UMLS CUI [1,2]
C0011008
Type of cell(s): (check all that apply)
Description

Type of cell

Data type

integer

Alias
UMLS CUI [1]
C0449475
Type of cell(s): if other, please specify
Description

(check all that apply)

Data type

integer

Alias
UMLS CUI [1,1]
C0449475
UMLS CUI [1,2]
C4035158
Chronological no. of CI for this patient
Description

Chronological no. of CI for this patient

Data type

text

Indication (check all that apply)
Description

Indication

Data type

text

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0302189
Indication if other, please specify
Description

Indication if other, please specify

Data type

integer

Alias
UMLS CUI [1]
C3146298
Number of infusions within 10 weeks (count only infusions that are part of same regimen and given for the same indication)
Description

Infusion count

Data type

float

Alias
UMLS CUI [1,1]
C0574032
UMLS CUI [1,2]
C0750480
Disease treatment
Description

Disease treatment

Data type

integer

Alias
UMLS CUI [1]
C0087111
DISEASE STATUS
Description

DISEASE STATUS

Best disease status (response) after HSCT
Description

(prior to treatment modification in response to a post HSCT disease assessment)

Data type

integer

Alias
UMLS CUI [1]
C1704632
CR achieved: Date achieved
Description

CR achieved: Date achieved

Data type

date

Alias
UMLS CUI [1,1]
C0677874
UMLS CUI [1,2]
C0011008
Never in CR: Date assessed
Description

Never in CR: Date assessed

Data type

date

Alias
UMLS CUI [1]
C0544452
Date of last follow up or death
Description

Date of last follow up or death

Data type

date

Alias
UMLS CUI [1,1]
C3694716
UMLS CUI [1,2]
C0011065
Date of last follow up or death
Description

Date of last follow up or death

First Relapse or Progression after HSCT
Description

First Relapse

Data type

text

Alias
UMLS CUI [1]
C0035020
Date assessed
Description

Date assessed

Data type

date

Alias
UMLS CUI [1,1]
C2316983
UMLS CUI [1,2]
C2985720
Date first seen
Description

Date first seen

Data type

date

Alias
UMLS CUI [1]
C1830429
Relapse/progression detected by clinical/haematological method
Description

Relapse

Data type

integer

Alias
UMLS CUI [1]
C0277556
Relapse/progression detected by cytogenetic method
Description

Relapse detected by cytogenetic method

Data type

integer

Alias
UMLS CUI [1,1]
C0277556
UMLS CUI [1,2]
C0200896
Date first seen
Description

Date first seen

Data type

date

Alias
UMLS CUI [1]
C1830429
Relapse/progression detected by molecular method
Description

Relapse/progression detected by molecular method

Data type

integer

Date assessed
Description

Date assessed

Data type

date

Alias
UMLS CUI [1]
C2985720
DISEASE PRESENCE/DETECTION AT LAST CONTACT
Description

DISEASE PRESENCE/DETECTION AT LAST CONTACT

Was disease detected by clinical/haematological method?:
Description

haematological method

Data type

boolean

Alias
UMLS CUI [1]
C0279810
Last date assessed
Description

date assessed

Data type

date

Alias
UMLS CUI [1]
C2985720
Was disease detected by cytogenetic/FISH method?:
Description

Was disease detected by cytogenetic/FISH method?:

Data type

integer

Alias
UMLS CUI [1]
C0162789
Considered disease relapse/progression
Description

progression

Data type

boolean

Alias
UMLS CUI [1]
C0242656
Last date assessed
Description

date assessed

Data type

date

Alias
UMLS CUI [1]
C2985720
PATIENT STATUS AT LAST CONTACT
Description

PATIENT STATUS AT LAST CONTACT

Survival Status
Description

Survival Status

Data type

integer

Alias
UMLS CUI [1]
C1148433
Check here if patient lost to follow up
Description

lost to follow up

Data type

boolean

Alias
UMLS CUI [1]
C1302313
Main Cause of Death
Description

Cause of Death

Data type

integer

Alias
UMLS CUI [1]
C0007465
HSCT related cause
Description

HSCT related cause

Data type

integer

Alias
UMLS CUI [1,1]
C0007465
UMLS CUI [1,2]
C0472699
Date of this HSCT
Description

DATE OF HSCT

Data type

date

Alias
UMLS CUI [1]
C2584899
COVER PAGE FOR HISTOCOMPATIBILITY REPORTS
Description

COVER PAGE FOR HISTOCOMPATIBILITY REPORTS

EBMT Code (CIC):
Description

EBMT Code

Data type

text

Alias
UMLS CUI [1,1]
C3826859
UMLS CUI [1,2]
C0600091
Name of the hospital
Description

Hospital

Data type

text

Alias
UMLS CUI [1]
C0019994
Unit:
Description

Unit

Data type

text

Alias
UMLS CUI [1]
C1519795
Contact person
Description

Contact person

Data type

integer

Alias
UMLS CUI [1]
C0337611
e-mail
Description

e-mail

Data type

text

Alias
UMLS CUI [1]
C1705961
Has the HSCT been registered in the EBMT database ?
Description

Has the HSCT been registered in the EBMT database ?

Data type

boolean

Alias
UMLS CUI [1]
C0421512
Hospital Unique Patient Number/ Code
Description

Hospital Unique Patient Number

Data type

integer

Alias
UMLS CUI [1]
C1827636
Initials
Description

Initials

Data type

integer

Alias
UMLS CUI [1]
C2986440
Gender
Description

Gender

Data type

integer

Alias
UMLS CUI [1]
C0079399
Date of Birth
Description

Date of Birth

Data type

date

Alias
UMLS CUI [1]
C0421451
Date of HSCT
Description

Date of HSCT

Data type

date

Alias
UMLS CUI [1]
C2584899
Donor ID
Description

Donor ID

Data type

integer

Alias
UMLS CUI [1]
C1718162
PATIENT ETHNIC OR RACIAL ORIGIN
Description

PATIENT ETHNIC OR RACIAL ORIGIN

Ethnic Group
Description

Ethnic Group

Data type

integer

Alias
UMLS CUI [1]
C0015031
Race
Description

Race

Data type

integer

Alias
UMLS CUI [1]
C0034510
DISEASE OF SECONDARY ORIGIN
Description

DISEASE OF SECONDARY ORIGIN

Agents involved
Description

Tick all that apply:

Data type

integer

Alias
UMLS CUI [1]
C0392920
Janus kinase 2
Description

Compulsory for CIBMTR Research centres. Fill only for MPS. Janus kinase 2 (jak2)

Data type

integer

Alias
UMLS CUI [1]
C0169661
THERAPY GIVEN PRIOR TO THIS HSCT
Description

THERAPY GIVEN PRIOR TO THIS HSCT

THERAPY GIVEN PRIOR TO THIS HSCT
Description

THERAPY

Data type

boolean

Alias
UMLS CUI [1]
C0087111
Date started
Description

Date started

Data type

date

Alias
UMLS CUI [1]
C3173309
Tyrosine kinase receptor antagonist given
Description

Tyrosine kinase antagonist

Data type

boolean

Alias
UMLS CUI [1]
C0879484
Tyrosine kinase receptor antagonist given: if yes, please specify
Description

Tyrosine kinase receptor antagonist given: if yes, please specify

Data type

integer

Alias
UMLS CUI [1,1]
C0879484
UMLS CUI [1,2]
C4035158
Other agent, Fill only for CML
Description

Other agent

Data type

integer

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C1254351
Were there any clinically significant co-existing disease or organ impairment at time of patient assessment prior to preparative (conditioning) regimen?
Description

co-existing disease

Data type

boolean

Alias
UMLS CUI [1,1]
C0012634
Comorbidity
Description

Comorbidity

Solid tumour, previously present
Description

Treated at any time point in the patient's past history, excluding nonmelanoma skin cancer

Data type

integer

Alias
UMLS CUI [1]
C0006826
limited food choices due to celiac sprue or inflammatory bowel disease
Description

Crohn's disease or ulcerative colitis

Data type

integer

Alias
UMLS CUI [1]
C0021390
Rheumatologic
Description

SLE, RA, polymyositis, mixed CTD, or polymyalgia rheumatica

Data type

integer

Alias
UMLS CUI [1]
C1328842
Infection
Description

Requiring continuation of antimicrobial treatment after day 0

Data type

integer

Alias
UMLS CUI [1]
C0009450
Diabetes
Description

Requiring treatment with insulin or oral hypoglycaemics but not diet alone

Data type

integer

Alias
UMLS CUI [1]
C0011849
Renal: moderate/severe
Description

Serum creatinine > 2 mg/dL or >177 μmol/L, on dialysis, or prior renal transplantation

Data type

integer

Alias
UMLS CUI [1]
C0022658
Hepatic: mild
Description

Chronic hepatitis, bilirubin between Upper Limit Normal (ULN) and 1.5 x the ULN, or AST/ALT between ULN and 2.5 × ULN

Data type

integer

Alias
UMLS CUI [1]
C0023895
Hepatic: moderate/severe
Description

Liver cirrhosis, bilirubin greater than 1.5 × ULN, or AST/ALT greater than 2.5 × ULN

Data type

integer

Alias
UMLS CUI [1,1]
C0023895
UMLS CUI [1,2]
C0205082
Arrhythmia
Description

Atrial fibrillation or flutter, sick sinus syndrome, or ventricular arrhythmias

Data type

integer

Alias
UMLS CUI [1]
C0003811
Cardiac CARDIAC
Description

Coronary artery disease, congestive heart failure, myocardial infarction, or EF ≤ 50%

Data type

integer

Alias
UMLS CUI [1]
C1522601
Cerebrovascular disease
Description

Transient ischemic attack or cerebrovascular accident

Data type

integer

Alias
UMLS CUI [1]
C0007820
Heart valve disease
Description

Except mitral valve prolapse

Data type

integer

Alias
UMLS CUI [1]
C0018824
Pulmonary: moderate
Description

DLco and/or FEV1 66-80% or dyspnoea on slight activity

Data type

integer

Alias
UMLS CUI [1,1]
C0024115
UMLS CUI [1,2]
C0205081
Pulmonary severe
Description

DLco and/or FEV1 ≤ 65% or dyspnoea at rest or requiring oxygen

Data type

integer

Alias
UMLS CUI [1,1]
C0024115
UMLS CUI [1,2]
C0205082
Obesity
Description

Patients with a body mass index > 35 kg/m2

Data type

integer

Alias
UMLS CUI [1]
C0028754
Peptic ulcer
Description

Peptic ulcer

Data type

integer

Alias
UMLS CUI [1]
C0030920
Psychiatric disturbance
Description

Depression or anxiety requiring psychiatric consult or treatment

Data type

integer

Alias
UMLS CUI [1]
C0004936
if other Comorbidity, please specify
Description

if other Comorbidity, please specify

Data type

text

GRAFT PERFORMANCE Compulsory for CIBMTR Research centres
Description

GRAFT PERFORMANCE Compulsory for CIBMTR Research centres

Platelet reconstitution
Description

(Platelets >20X109 /L; first of 3 consecutive days)

Data type

integer

Alias
UMLS CUI [1,1]
C0005821
UMLS CUI [1,2]
C0301944
Date Platelets > 20 x 10 9 /l
Description

Platelets

Data type

date

Alias
UMLS CUI [1,1]
C0005821
UMLS CUI [1,2]
C0011008
GRAFT PERFORMANCE
Description

GRAFT PERFORMANCE

Platelet reconstitution
Description

(Platelets >20X109 /L; first of 3 consecutive days)

Data type

integer

Alias
UMLS CUI [1,1]
C0005821
UMLS CUI [1,2]
C0301944
Date Platelets > 20 x 10 9 /l
Description

Date Platelets > 20 x 10 9 /l

Data type

date

Alias
UMLS CUI [1,1]
C0005821
UMLS CUI [1,2]
C0011008
PLANNED THERAPY GIVEN AFTER THIS HSCT, Date started
Description

Compulsory for CIBMTR Research centres. Fill in only if you answered Yes: Planned to the question on Disease treatment under Additional treatment

Data type

date

Alias
UMLS CUI [1]
C0087111
Chemotherapy Regimen
Description

Chemotherapy Regimen

Data type

boolean

Alias
UMLS CUI [1]
C0392920
Chemotherapy Regimen: if yes, please specify
Description

Chemotherapy Regimen

Data type

integer

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C4035158
Radiotherapy
Description

Radiotherapy

Data type

boolean

Alias
UMLS CUI [1]
C1522449
HSCT - Minimum Essential Data - A First report - 100 days after HSCT DISEASE CLASSIFICATION SHEET 1
Description

HSCT - Minimum Essential Data - A First report - 100 days after HSCT DISEASE CLASSIFICATION SHEET 1

EBMT Centre Identification Code (CIC)
Description

EBMT Centre Identification Code (CIC)

Data type

text

Alias
UMLS CUI [1]
C2348585
Hospital Unique Patient Number/Code (UPN)
Description

Hospital Unique Patient Number

Data type

integer

Alias
UMLS CUI [1]
C2348585
Date of Initial Diagnosis
Description

Date of Initial Diagnosis

Data type

date

Alias
UMLS CUI [1]
C2316983

Similar models

100 days past HSCT EBMT

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
CENTRE IDENTIFICATION
EBMT Code (CIC)
Item
EBMT Code (CIC)
integer
C3826859 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Klinik
Item
Hospital
text
C0019994 (UMLS CUI [1])
Unit
Item
Unit
integer
C1519795 (UMLS CUI [1])
Contact person
Item
Contact person
integer
C0337611 (UMLS CUI [1])
Phone
Item
Phone
integer
C1550483 (UMLS CUI [1])
Fax
Item
Fax
integer
C1549619 (UMLS CUI [1])
e-mail
Item
e-mail
integer
C1705961 (UMLS CUI [1])
Item Group
PATIENT DATA
Date of this report
Item
Date of this report
date
C1302584 (UMLS CUI [1])
Item
Patient following national / international study / trial
integer
C1997894 (UMLS CUI [1])
Code List
Patient following national / international study / trial
CL Item
no (1)
C1298908 (UMLS CUI-1)
CL Item
yes (2)
C1705108 (UMLS CUI-1)
CL Item
unknown (3)
C0439673 (UMLS CUI-1)
Name of study / trial
Item
Name of study / trial
integer
C0008976 (UMLS CUI [1])
Hospital Unique Patient Number
Item
Hospital Unique Patient Number/Code
integer
C2348585 (UMLS CUI [1])
Initials
Item
Initials (first name(s) _family name(s))
integer
C2986440 (UMLS CUI [1])
Date of Birth
Item
Date of Birth
date
C0421451 (UMLS CUI [1])
Item
Sex
text
C0079399 (UMLS CUI [1])
Code List
Sex
CL Item
Male (1)
C1706180 (UMLS CUI-1)
CL Item
Female (2)
C0015780 (UMLS CUI-1)
Item Group
DISEASE
Date of initial diagnosis
Item
Date of initial diagnosis
date
C2316983 (UMLS CUI [1])
PRIMARY DISEASE DIAGNOSIS
Item
PRIMARY DISEASE DIAGNOSIS
integer
C0277554 (UMLS CUI [1])
Item Group
HSCT
Item
Performance score (if alive)
integer
C1518965 (UMLS CUI [1])
Code List
Performance score (if alive)
CL Item
Karnofsky (1)
C0206065 (UMLS CUI-1)
CL Item
Lansky (2)
C1522275 (UMLS CUI-1)
Item
Score achived
text
C1518965 (UMLS CUI [1])
Code List
Score achived
CL Item
10 (1)
CL Item
100 (10)
CL Item
20 (2)
CL Item
30 (3)
CL Item
40 (4)
CL Item
50 (5)
CL Item
60 (6)
CL Item
70 (7)
CL Item
80 (8)
CL Item
90 (9)
Item
Type of HSCT
integer
C0472699 (UMLS CUI [1])
Code List
Type of HSCT
CL Item
Autologous (1)
C0194037 (UMLS CUI-1)
CL Item
Allogeneic (2)
C2242529 (UMLS CUI-1)
Item
Patient CMV status (for allografts)
integer
C0582172 (UMLS CUI [1])
Code List
Patient CMV status (for allografts)
CL Item
Negative  (Negative )
C0205160 (UMLS CUI-1)
CL Item
Positive (Positive)
C1446409 (UMLS CUI-1)
CL Item
Not evaluated  (Not evaluated )
C3846720 (UMLS CUI-1)
CL Item
Unknown (Unknown)
C0439673 (UMLS CUI-1)
Multiple donors
Item
Multiple donors/products
boolean
C0013018 (UMLS CUI [1])
Multiple donors
Item
Multiple donors: if yes:
integer
C0013018 (UMLS CUI [1])
Item Group
STEM CELLS (autograft or allograft)
Item
Source of Stem Cells
integer
C0018956 (UMLS CUI [1])
Code List
Source of Stem Cells
CL Item
Bone Marrow  (Bone Marrow VBMSC )
C0005953 (UMLS CUI-1)
CL Item
Peripheral Blood  (Peripheral Blood VPBSC)
C0229664 (UMLS CUI-1)
CL Item
Cord Blood  (Cord Blood VCBSC )
C0162371 (UMLS CUI-1)
CL Item
Other (Other)
C0205394 (UMLS CUI-1)
Source of Stem Cells
Item
Source of Stem Cells: if other, please specify
integer
C0018956 (UMLS CUI [1])
Donor ID
Item
Donor ID
text
C1718162 (UMLS CUI [1])
Item
Donor ID
integer
C1718162 (UMLS CUI [1])
Code List
Donor ID
CL Item
N/A (1)
Item
HLA match type (for allografts)
integer
C0242318 (UMLS CUI [1])
Code List
HLA match type (for allografts)
CL Item
Syngeneic (monozygotic twin) (Syngeneic (monozygotic twin))
C0041432 (UMLS CUI-1)
CL Item
HLA-identical sibling (may include non-monozygotic twin)  (HLA-identical sibling (may include non-monozygotic twin) )
C0019633 (UMLS CUI-1)
C1960320 (UMLS CUI-2)
CL Item
HLA-matched other relative (HLA-matched other relative)
C1548978 (UMLS CUI-1)
CL Item
HLA-mismatched relative (HLA-mismatched relative)
C0854634 (UMLS CUI-1)
CL Item
Unrelated donor (Unrelated donor)
C3179133 (UMLS CUI-1)
Item
Degree of mismatch
integer
C1881865 (UMLS CUI [1])
Code List
Degree of mismatch
CL Item
HLA antigen mismatch (1)
C0456471 (UMLS CUI-1)
CL Item
HLA antigen mismatch (2)
donor registry
Item
Name of donor registry/CB Bank
integer
C0034975 (UMLS CUI [1])
BMDW/WMDA code
Item
BMDW/WMDA code (up to 4 characters)
integer
C2987198 (UMLS CUI [1])
Item
Number of mismatches A
integer
C1881865 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Code List
Number of mismatches A
CL Item
match (0)
C1708943 (UMLS CUI-1)
CL Item
one mismatch (1)
C1708943 (UMLS CUI-1)
CL Item
2 mismatches (2)
C1708943 (UMLS CUI-1)
CL Item
not done (ND)
C1272696 (UMLS CUI-1)
Item
Number of mismatches B
integer
C1881865 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Code List
Number of mismatches B
CL Item
match (0)
C1708943 (UMLS CUI-1)
CL Item
one mismatch (1)
C1708943 (UMLS CUI-1)
CL Item
2 mismatches (2)
C1708943 (UMLS CUI-1)
CL Item
not done (ND)
C1272696 (UMLS CUI-1)
Item
Number of mismatches C
integer
C1881865 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Code List
Number of mismatches C
CL Item
match (0)
C1708943 (UMLS CUI-1)
CL Item
one mismatch (1)
C1708943 (UMLS CUI-1)
CL Item
2 mismatches (2)
C1708943 (UMLS CUI-1)
CL Item
not done (ND)
C1272696 (UMLS CUI-1)
Item
Number of mismatches DRB1
integer
C1881865 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Code List
Number of mismatches DRB1
CL Item
match (0)
C1708943 (UMLS CUI-1)
CL Item
one mismatch (1)
C1708943 (UMLS CUI-1)
CL Item
2 mismatches (2)
C1708943 (UMLS CUI-1)
CL Item
not done (ND)
C1272696 (UMLS CUI-1)
Item
Number of mismatches DQB1
integer
C1881865 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Code List
Number of mismatches DQB1
CL Item
match (0)
C1708943 (UMLS CUI-1)
CL Item
one mismatch (1)
C1708943 (UMLS CUI-1)
CL Item
2 mismatches (2)
C1708943 (UMLS CUI-1)
CL Item
not done (ND)
C1272696 (UMLS CUI-1)
Item
Number of mismatches DPB1
integer
C1881865 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Code List
Number of mismatches DPB1
CL Item
match (0)
C1708943 (UMLS CUI-1)
CL Item
one mismatch (1)
C1708943 (UMLS CUI-1)
CL Item
2 mismatches (2)
C1708943 (UMLS CUI-1)
CL Item
not done (ND)
C1272696 (UMLS CUI-1)
Item
Donor Sex
integer
C0079399 (UMLS CUI [1])
Code List
Donor Sex
CL Item
Male  (Male )
C1706180 (UMLS CUI-1)
CL Item
Female (Female)
C0015780 (UMLS CUI-1)
Item
Donor age
integer
C0013018 (UMLS CUI [1,1])
C0421451 (UMLS CUI [1,2])
Code List
Donor age
CL Item
Negative (1)
CL Item
Positive (2)
CL Item
Not evaluated (3)
CL Item
Unknown (4)
Graft manipulation ex-vivo (including T-cell depletion) other than for RBC removal or volume reduction
Item
Graft manipulation ex-vivo (including T-cell depletion) other than for RBC removal or volume reduction
boolean
C0677960 (UMLS CUI [1])
Item Group
HSCT
Chronological number of HSCT
Item
Chronological number of HSCT for this patient?
integer
C1318453 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
If >1, date of last HSCT before this one
Item
If >1, date of last HSCT before this one
date
C0018956 (UMLS CUI [1,1])
C0029216 (UMLS CUI [1,2])
C2745955 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
HSCT part of a planned multiple graft protocol?
Item
HSCT part of a planned multiple graft protocol?
boolean
C0548370 (UMLS CUI [1])
Preparative (conditioning) regimen given?
Item
Preparative (conditioning) regimen given?
boolean
C1882454 (UMLS CUI [1])
Was this intended to be myeloablative?
Item
Was this intended to be myeloablative?
boolean
C1831742 (UMLS CUI [1])
Item
Reason
integer
C0392360 (UMLS CUI [1])
Code List
Reason
CL Item
Age of recipient (Age of recipient)
CL Item
Comorbid conditions (Comorbid conditions)
CL Item
Prior HSCT (Prior HSCT)
CL Item
Protocol driven REASRIOT (Protocol driven REASRIOT)
CL Item
Other (Other)
Ara-C
Item
Ara-C (cytarabine)
float
C0733521 (UMLS CUI [1])
Item
Ara-C (cytarabine): Unit of dosing
integer
C0733521 (UMLS CUI [1,1])
C1321095 (UMLS CUI [1,2])
Code List
Ara-C (cytarabine): Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
ALS
Item
ALG, ATG (ALS, ATS)
float
C0002736 (UMLS CUI [1])
Item
AST: Unit of dosing
integer
C1321095 (UMLS CUI [1,1])
C0004002 (UMLS CUI [1,2])
Code List
AST: Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Item
Animal origin
integer
C3494749 (UMLS CUI [1])
Code List
Animal origin
CL Item
Horse  (1)
CL Item
Rabbit  (2)
CL Item
Other (3)
Bleomycin
Item
Bleomycin
float
C0005740 (UMLS CUI [1])
Item
Unit of dosing
integer
C1321095 (UMLS CUI [1])
Code List
Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Busulfan
Item
Busulfan
float
C0006463 (UMLS CUI [1])
Item
Busulfan Unit of dosing:
integer
C0869039 (UMLS CUI [1,1])
C0006463 (UMLS CUI [1,2])
Code List
Busulfan Unit of dosing:
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Item
Busulfan application
integer
C0006463 (UMLS CUI [1,1])
C1533134 (UMLS CUI [1,2])
Code List
Busulfan application
CL Item
Oral  (1)
CL Item
IV  (2)
CL Item
Both (3)
BCNU
Item
BCNU
float
C0007257 (UMLS CUI [1])
Item
BCNU Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0007257 (UMLS CUI [1,2])
Code List
BCNU Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Bexar (radiolabelled MoAB)
Item
Bexar (radiolabelled MoAB)
float
C3831356 (UMLS CUI [1])
Item
Bexar Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C3831356 (UMLS CUI [1,2])
Code List
Bexar Unit of dosing
CL Item
mCi  (1)
CL Item
MBq (2)
CCNU
Item
CCNU
float
C0687700 (UMLS CUI [1])
Item
CCNU Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0687700 (UMLS CUI [1,2])
Code List
CCNU Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Campath
Item
Campath (antiCD52)
float
C0939276 (UMLS CUI [1])
Item
Campath Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0939276 (UMLS CUI [1,2])
Code List
Campath Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Carboplatin
Item
Carboplatin
float
C0079083 (UMLS CUI [1])
Item
Carboplatin Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0079083 (UMLS CUI [1,2])
Code List
Carboplatin Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Cisplatin
Item
Cisplatin
float
C0008838 (UMLS CUI [1])
Item
Cisplatin Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0008838 (UMLS CUI [1,2])
Code List
Cisplatin Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Corticosteroids
Item
Corticosteroids
float
C0001617 (UMLS CUI [1])
Item
Corticosteroids Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0001617 (UMLS CUI [1,2])
Code List
Corticosteroids Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Cyclophosphamide
Item
Cyclophosphamide
float
C0010583 (UMLS CUI [1])
Item
Cyclophosphamide Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0010583 (UMLS CUI [1,2])
Code List
Cyclophosphamide Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Daunorubicin
Item
Daunorubicin
float
C0011015 (UMLS CUI [1])
Item
Unit of dosing Daunorubicin
integer
C0869039 (UMLS CUI [1,1])
C0011015 (UMLS CUI [1,2])
Code List
Unit of dosing Daunorubicin
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Doxorubicin
Item
Doxorubicin (adriamycine)
float
C0013089 (UMLS CUI [1])
Item
Doxorubicin Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0013089 (UMLS CUI [1,2])
Code List
Doxorubicin Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Etoposide
Item
Etoposide (VP16)
float
C0015133 (UMLS CUI [1])
Item
Etoposide Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0015133 (UMLS CUI [1,2])
Code List
Etoposide Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Fludarabine
Item
Fludarabine
float
C0059985 (UMLS CUI [1])
Item
Fludarabine Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0059985 (UMLS CUI [1,2])
Code List
Fludarabine Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Gemtuzumab
Item
Gemtuzumab
float
C0872968 (UMLS CUI [1])
Item
Gemtuzumab Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0872968 (UMLS CUI [1,2])
Code List
Gemtuzumab Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Idarubicin
Item
Idarubicin
float
C0020789 (UMLS CUI [1])
Item
Idarubicin Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0020789 (UMLS CUI [1,2])
Code List
Idarubicin Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Ifosfamide
Item
Ifosfamide
float
C0020823 (UMLS CUI [1])
Item
Ifosfamide Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0020823 (UMLS CUI [1,2])
Code List
Ifosfamide Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Imatinib mesylate
Item
Imatinib mesylate
float
C0939537 (UMLS CUI [1])
Item
Imatinib mesylate Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0939537 (UMLS CUI [1,2])
Code List
Imatinib mesylate Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Melphalan
Item
Melphalan
float
C0025241 (UMLS CUI [1])
Item
Melphalan Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0025241 (UMLS CUI [1,2])
Code List
Melphalan Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Mitoxantrone
Item
Mitoxantrone
float
C0026259 (UMLS CUI [1])
Item
Mitoxantrone Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0026259 (UMLS CUI [1,2])
Code List
Mitoxantrone Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Paclitaxel
Item
Paclitaxel
float
C0144576 (UMLS CUI [1])
Item
Paclitaxel Unit of dosing
integer
C0869039 (UMLS CUI [1])
Code List
Paclitaxel Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Rituximab
Item
Rituximab (mabthera, antiCD20)
float
C0393022 (UMLS CUI [1])
Item
Rituximab Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0393022 (UMLS CUI [1,2])
Code List
Rituximab Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Teniposide
Item
Teniposide
float
C0039512 (UMLS CUI [1])
Item
Teniposide Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0039512 (UMLS CUI [1,2])
Code List
Teniposide Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Thiotepa
Item
Thiotepa
float
C0039871 (UMLS CUI [1])
Item
Thiotepa Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0039871 (UMLS CUI [1,2])
Code List
Thiotepa Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Zevalin
Item
Zevalin (radiolabelled MoAB)
float
C0919274 (UMLS CUI [1])
Item
Zevalin Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0919274 (UMLS CUI [1,2])
Code List
Zevalin Unit of dosing
CL Item
mCi  (1)
CL Item
MBq (2)
other radiolabelled MoAB
Item
Other radiolabelled MoAB
float
C0003250 (UMLS CUI [1,1])
C0454110 (UMLS CUI [1,2])
Item
other radiolabelled MoAB Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0003250 (UMLS CUI [1,2])
C0454110 (UMLS CUI [1,3])
Code List
other radiolabelled MoAB Unit of dosing
CL Item
mCi  (1)
CL Item
MBq (2)
Other radiolabelled MoAB: if other, please specify
Item
Other radiolabelled MoAB: if other, please specify
integer
C0205394 (UMLS CUI [1,1])
C0003250 (UMLS CUI [1,2])
C0454110 (UMLS CUI [1,3])
Other MoAB
Item
Other MoAB
float
C0003250 (UMLS CUI [1])
Item
MoAB Unit of dosing
integer
C0869039 (UMLS CUI [1,1])
C0003250 (UMLS CUI [1,2])
Code List
MoAB Unit of dosing
CL Item
mg/m2  (1)
C3898329 (UMLS CUI-1)
CL Item
mg/Kg (2)
C0560741 (UMLS CUI-1)
Total body irradiation
Item
Total body irradiation
boolean
C0043162 (UMLS CUI [1])
Total Body Irradiation: if yes, please specify value
Item
Total Body Irradiation: if yes, please specify value
integer
C4035158 (UMLS CUI [1,1])
C0043162 (UMLS CUI [1,2])
TLI, TNI, TAI
Item
TLI, TNI, TAI
boolean
C4035158 (UMLS CUI [1])
C0043162 (UMLS CUI [2])
Item Group
AFTER HSCT
GvHD prophylaxis
Item
GvHD prophylaxis or preventive treatment (Allografts only)
boolean
C0278845 (UMLS CUI [1])
Item
GvHD prophylaxis or preventive treatment: if yes, please specify
integer
C0278845 (UMLS CUI [1,1])
C4035158 (UMLS CUI [1,2])
Code List
GvHD prophylaxis or preventive treatment: if yes, please specify
CL Item
Drugs (Immunosuppressive chemo) VAGVHDP5 (1)
CL Item
ALG, ALS, ATG, ATS (given after day 0) (2)
CL Item
Anti CD25 (MoAB in vivo) (3)
CL Item
Campath (MoAB in vivo; can be "in the bag") (4)
CL Item
Corticosteroids (5)
CL Item
Cyclosporine (6)
CL Item
Cyclophosphamide (given after day 0) (7)
CL Item
Etanercept (MoAB in vivo) (8)
CL Item
FK 506 (Tacrolimus, Prograf) (9)
CL Item
Infliximab (MoAB in vivo) (10)
CL Item
Methotrexate (11)
CL Item
Mycophenolate (MMF) (12)
CL Item
Sirolimus (13)
CL Item
Other monoclonal antibody (in vivo), (14)
CL Item
specify (15)
CL Item
Other agent (in vivo), specify (16)
CL Item
Extracorporeal photopheresis (ECP) (17)
CL Item
Other, specify (18)
GvHD prophylaxis or preventive treatment: if other, please specify
Item
GvHD prophylaxis or preventive treatment: if other, please specify
integer
C4035158 (UMLS CUI [1,1])
C4035158 (UMLS CUI [1,2])
GvHD prophylaxis or preventive treatment: if Other monoclonal antibody, please specify
Item
GvHD prophylaxis or preventive treatment: if Other monoclonal antibody, please specify
integer
C4035158 (UMLS CUI [1,1])
C4035158 (UMLS CUI [1,2])
C0003250 (UMLS CUI [1,3])
Item
Absolute neutrophil count (ANC) recovery (engraftment) (Neutrophils >0.5X109 /L)
integer
C0948762 (UMLS CUI [1])
Code List
Absolute neutrophil count (ANC) recovery (engraftment) (Neutrophils >0.5X109 /L)
CL Item
No (1)
CL Item
Yes (2)
CL Item
Lost fraft (3)
CL Item
Never below (4)
CL Item
Unknown (5)
Date of last assessment
Item
Date of last assessment
date
C0011008 (UMLS CUI [1,1])
C1516048 (UMLS CUI [1,2])
Date of ANC recovery
Item
Date of ANC recovery
date
C0948762 (UMLS CUI [1,1])
C2004454 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Date of last assessment
Item
Date of last assessment
date
C0011008 (UMLS CUI [1,1])
C1516048 (UMLS CUI [1,2])
Item
Maximum Grade
integer
C0856825 (UMLS CUI [1,1])
C0441800 (UMLS CUI [1,2])
Code List
Maximum Grade
CL Item
0 (none) (1)
CL Item
I (2)
CL Item
II (3)
CL Item
III (4)
CL Item
IV (5)
CL Item
Present but grade unknown (6)
CL Item
Not evaluated (7)
Item Group
ADDITIONAL TREATMENT INCLUDING CELL THERAPY
Cell infusion
Item
Cell infusion (CI)
boolean
C2145394 (UMLS CUI [1])
Date of first infusion
Item
Date of first infusion
date
C0574032 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Type of cell(s): (check all that apply)
integer
C0449475 (UMLS CUI [1])
Code List
Type of cell(s): (check all that apply)
CL Item
Lymphocyte  (1)
C0024264 (UMLS CUI-1)
CL Item
Mesenchymal  (2)
C1513143 (UMLS CUI-1)
CL Item
Fibroblasts (3)
C0016030 (UMLS CUI-1)
CL Item
Dendritic cells  (4)
C0011306 (UMLS CUI-1)
CL Item
Other (5)
C0205394 (UMLS CUI-1)
Type of cell(s): if other, please specify
Item
Type of cell(s): if other, please specify
integer
C0449475 (UMLS CUI [1,1])
C4035158 (UMLS CUI [1,2])
Chronological no. of CI for this patient
Item
Chronological no. of CI for this patient
text
Item
Indication (check all that apply)
text
C3146298 (UMLS CUI [1,1])
C0302189 (UMLS CUI [1,2])
Code List
Indication (check all that apply)
CL Item
Loss/decreased chimaerism (Loss/decreased chimaerism)
CL Item
Mixed chimaerism (Mixed chimaerism)
CL Item
Other (Other)
CL Item
Planned/ protocol (Planned/ protocol)
CL Item
Prophylactic (Prophylactic)
CL Item
Treatment for disease (Treatment for disease)
CL Item
Treatment of GvHD (Treatment of GvHD)
CL Item
Treatment PTLD, EBV, lymphoma (Treatment PTLD, EBV, lymphoma)
CL Item
Treatment viral infection (Treatment viral infection)
Indication if other, please specify
Item
Indication if other, please specify
integer
C3146298 (UMLS CUI [1])
Infusion count
Item
Number of infusions within 10 weeks (count only infusions that are part of same regimen and given for the same indication)
float
C0574032 (UMLS CUI [1,1])
C0750480 (UMLS CUI [1,2])
Item
Disease treatment
integer
C0087111 (UMLS CUI [1])
Code List
Disease treatment
CL Item
No (1)
CL Item
Yes: Planned (planned before HSCT took place) (2)
CL Item
Yes: Not planned (for relapse/progression or persistent disease) (3)
CL Item
Unknown (4)
Item Group
DISEASE STATUS
Item
Best disease status (response) after HSCT
integer
C1704632 (UMLS CUI [1])
Code List
Best disease status (response) after HSCT
CL Item
Continued complete remission (CCR) (1)
C0677874 (UMLS CUI-1)
CL Item
CR achieved: Date achieved (2)
C0677874 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
CL Item
Never in CR: Date assessed (3)
C0544452 (UMLS CUI-1)
CL Item
Not evaluated (4)
C3846720 (UMLS CUI-1)
CR achieved: Date achieved
Item
CR achieved: Date achieved
date
C0677874 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Never in CR: Date assessed
Item
Never in CR: Date assessed
date
C0544452 (UMLS CUI [1])
Date of last follow up or death
Item
Date of last follow up or death
date
C3694716 (UMLS CUI [1,1])
C0011065 (UMLS CUI [1,2])
Item Group
Date of last follow up or death
Item
First Relapse or Progression after HSCT
text
C0035020 (UMLS CUI [1])
Code List
First Relapse or Progression after HSCT
CL Item
No (No)
CL Item
Yes (Yes)
CL Item
Continuous progression since HSCT (Continuous progression since HSCT)
Date assessed
Item
Date assessed
date
C2316983 (UMLS CUI [1,1])
C2985720 (UMLS CUI [1,2])
Date first seen
Item
Date first seen
date
C1830429 (UMLS CUI [1])
Item
Relapse/progression detected by clinical/haematological method
integer
C0277556 (UMLS CUI [1])
Code List
Relapse/progression detected by clinical/haematological method
CL Item
No (No)
CL Item
Yes (Yes)
CL Item
Mot evaluated (Mot evaluated)
Item
Relapse/progression detected by cytogenetic method
integer
C0277556 (UMLS CUI [1,1])
C0200896 (UMLS CUI [1,2])
Code List
Relapse/progression detected by cytogenetic method
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Date first seen
Item
Date first seen
date
C1830429 (UMLS CUI [1])
Item
Relapse/progression detected by molecular method
integer
Code List
Relapse/progression detected by molecular method
CL Item
No  (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Date assessed
Item
Date assessed
date
C2985720 (UMLS CUI [1])
Item Group
DISEASE PRESENCE/DETECTION AT LAST CONTACT
haematological method
Item
Was disease detected by clinical/haematological method?:
boolean
C0279810 (UMLS CUI [1])
date assessed
Item
Last date assessed
date
C2985720 (UMLS CUI [1])
Item
Was disease detected by cytogenetic/FISH method?:
integer
C0162789 (UMLS CUI [1])
Code List
Was disease detected by cytogenetic/FISH method?:
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
progression
Item
Considered disease relapse/progression
boolean
C0242656 (UMLS CUI [1])
date assessed
Item
Last date assessed
date
C2985720 (UMLS CUI [1])
Item Group
PATIENT STATUS AT LAST CONTACT
Item
Survival Status
integer
C1148433 (UMLS CUI [1])
Code List
Survival Status
CL Item
Alive  (Alive )
CL Item
Dead  (Dead )
CL Item
Died before HSCT (Died before HSCT)
lost to follow up
Item
Check here if patient lost to follow up
boolean
C1302313 (UMLS CUI [1])
Item
Main Cause of Death
integer
C0007465 (UMLS CUI [1])
Code List
Main Cause of Death
CL Item
Relapse or Progression (if indication: primary disease) (1)
CL Item
HSCT related (if applicable) (2)
CL Item
Cell Therapy  (3)
CL Item
Other (4)
CL Item
Unknown (5)
Item
HSCT related cause
integer
C0007465 (UMLS CUI [1,1])
C0472699 (UMLS CUI [1,2])
Code List
HSCT related cause
CL Item
GVHD GVH  (1)
CL Item
Cardiac Toxicity CTX (2)
CL Item
Rejection/Poor graft function REJ  (3)
CL Item
Infection INF (4)
CL Item
Pulmonary toxicity PTX  (5)
CL Item
Veno occlusive disorder (6)
CL Item
Other (7)
DATE OF HSCT
Item
Date of this HSCT
date
C2584899 (UMLS CUI [1])
Item Group
COVER PAGE FOR HISTOCOMPATIBILITY REPORTS
EBMT Code
Item
EBMT Code (CIC):
text
C3826859 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Hospital
Item
Name of the hospital
text
C0019994 (UMLS CUI [1])
Unit
Item
Unit:
text
C1519795 (UMLS CUI [1])
Contact person
Item
Contact person
integer
C0337611 (UMLS CUI [1])
e-mail
Item
e-mail
text
C1705961 (UMLS CUI [1])
Has the HSCT been registered in the EBMT database ?
Item
Has the HSCT been registered in the EBMT database ?
boolean
C0421512 (UMLS CUI [1])
Hospital Unique Patient Number
Item
Hospital Unique Patient Number/ Code
integer
C1827636 (UMLS CUI [1])
Initials
Item
Initials
integer
C2986440 (UMLS CUI [1])
Gender
Item
Gender
integer
C0079399 (UMLS CUI [1])
Date of Birth
Item
Date of Birth
date
C0421451 (UMLS CUI [1])
Date of HSCT
Item
Date of HSCT
date
C2584899 (UMLS CUI [1])
Donor ID
Item
Donor ID
integer
C1718162 (UMLS CUI [1])
Item
Ethnic Group
integer
C0015031 (UMLS CUI [1])
Code List
Ethnic Group
CL Item
Hispanic or Latino  (Hispanic or Latino )
CL Item
Not Hispanic or Latino (Not Hispanic or Latino)
Item
Race
integer
C0034510 (UMLS CUI [1])
Code List
Race
CL Item
White (White)
CL Item
Black (Black)
CL Item
Asian ETHNIC12  (Asian ETHNIC12 )
CL Item
American Indian/Alaska Native  (American Indian/Alaska Native )
CL Item
Native Hawaiian/Other Pacific Islander (Native Hawaiian/Other Pacific Islander)
Item Group
DISEASE OF SECONDARY ORIGIN
Item
Agents involved
integer
C0392920 (UMLS CUI [1])
Code List
Agents involved
CL Item
Alkylating agent/radiation-related (Alkylating agent/radiation-related)
C0002073 (UMLS CUI-1)
CL Item
Topoisomerase II inhibitor-related (Topoisomerase II inhibitor-related)
C1336769 (UMLS CUI-1)
CL Item
Unknown (Unknown)
C0439673 (UMLS CUI-1)
Item
Janus kinase 2
integer
C0169661 (UMLS CUI [1])
Code List
Janus kinase 2
CL Item
Absent  (1)
CL Item
Present  (2)
CL Item
Unknown (3)
Item Group
THERAPY GIVEN PRIOR TO THIS HSCT
THERAPY
Item
THERAPY GIVEN PRIOR TO THIS HSCT
boolean
C0087111 (UMLS CUI [1])
Date started
Item
Date started
date
C3173309 (UMLS CUI [1])
Tyrosine kinase antagonist
Item
Tyrosine kinase receptor antagonist given
boolean
C0879484 (UMLS CUI [1])
Item
Tyrosine kinase receptor antagonist given: if yes, please specify
integer
C0879484 (UMLS CUI [1,1])
C4035158 (UMLS CUI [1,2])
Code List
Tyrosine kinase receptor antagonist given: if yes, please specify
CL Item
Imatinib mesylate  (1)
C0939537 (UMLS CUI-1)
CL Item
Dasatinib (Sprycel) (2)
C1455147 (UMLS CUI-1)
CL Item
Nilotinib (Tasigna) (3)
C1721377 (UMLS CUI-1)
CL Item
Other (4)
C0205394 (UMLS CUI-1)
Item
Other agent, Fill only for CML
integer
C0205394 (UMLS CUI [1,1])
C1254351 (UMLS CUI [1,2])
Code List
Other agent, Fill only for CML
CL Item
Combination chemotherapy  (Combination chemotherapy )
C0013218 (UMLS CUI-1)
CL Item
Hydroxyurea (Hydroxyurea)
C0020402 (UMLS CUI-1)
CL Item
Interferon (Interferon)
C0733470 (UMLS CUI-1)
CL Item
Other (Other)
C0205394 (UMLS CUI-1)
co-existing disease
Item
Were there any clinically significant co-existing disease or organ impairment at time of patient assessment prior to preparative (conditioning) regimen?
boolean
C0012634 (UMLS CUI [1,1])
Item Group
Comorbidity
Item
Solid tumour, previously present
integer
C0006826 (UMLS CUI [1])
Code List
Solid tumour, previously present
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Item
limited food choices due to celiac sprue or inflammatory bowel disease
integer
C0021390 (UMLS CUI [1])
Code List
limited food choices due to celiac sprue or inflammatory bowel disease
CL Item
Combination chemotherapy  (Combination chemotherapy )
C0013218 (UMLS CUI-1)
CL Item
Hydroxyurea (Hydroxyurea)
C0020402 (UMLS CUI-1)
CL Item
Interferon (Interferon)
C0733470 (UMLS CUI-1)
CL Item
Other (Other)
C0205394 (UMLS CUI-1)
Item
Rheumatologic
integer
C1328842 (UMLS CUI [1])
Code List
Rheumatologic
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Item
Infection
integer
C0009450 (UMLS CUI [1])
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Item
Diabetes
integer
C0011849 (UMLS CUI [1])
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Item
Renal: moderate/severe
integer
C0022658 (UMLS CUI [1])
Code List
Renal: moderate/severe
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Item
Hepatic: mild
integer
C0023895 (UMLS CUI [1])
Code List
Hepatic: mild
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Item
Hepatic: moderate/severe
integer
C0023895 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Code List
Hepatic: moderate/severe
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Item
Arrhythmia
integer
C0003811 (UMLS CUI [1])
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Item
Cardiac CARDIAC
integer
C1522601 (UMLS CUI [1])
Code List
Cardiac CARDIAC
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Item
Cerebrovascular disease
integer
C0007820 (UMLS CUI [1])
Code List
Cerebrovascular disease
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Item
Heart valve disease
integer
C0018824 (UMLS CUI [1])
Code List
Heart valve disease
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Item
Pulmonary: moderate
integer
C0024115 (UMLS CUI [1,1])
C0205081 (UMLS CUI [1,2])
Code List
Pulmonary: moderate
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Item
Pulmonary severe
integer
C0024115 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Code List
Pulmonary severe
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Item
Obesity
integer
C0028754 (UMLS CUI [1])
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Item
Peptic ulcer
integer
C0030920 (UMLS CUI [1])
Code List
Peptic ulcer
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
Item
Psychiatric disturbance
integer
C0004936 (UMLS CUI [1])
Code List
Psychiatric disturbance
CL Item
No (1)
CL Item
Yes (2)
CL Item
Not evaluated (3)
if other Comorbidity, please specify
Item
if other Comorbidity, please specify
text
Item Group
GRAFT PERFORMANCE Compulsory for CIBMTR Research centres
Item
Platelet reconstitution
integer
C0005821 (UMLS CUI [1,1])
C0301944 (UMLS CUI [1,2])
Code List
Platelet reconstitution
CL Item
No (No)
CL Item
Yes (Yes)
CL Item
Never below this lever (Never below this lever)
CL Item
Unknown (Unknown)
Platelets
Item
Date Platelets > 20 x 10 9 /l
date
C0005821 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Platelet reconstitution
integer
C0005821 (UMLS CUI [1,1])
C0301944 (UMLS CUI [1,2])
Code List
Platelet reconstitution
CL Item
No (No)
C1298908 (UMLS CUI-1)
CL Item
Yes (Yes)
C1705108 (UMLS CUI-1)
CL Item
Never below this level (Never below this lever)
C0443151 (UMLS CUI-1)
CL Item
Unknown (Unknown)
C0439673 (UMLS CUI-1)
Date Platelets > 20 x 10 9 /l
Item
Date Platelets > 20 x 10 9 /l
date
C0005821 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
PLANNED THERAPY
Item
PLANNED THERAPY GIVEN AFTER THIS HSCT, Date started
date
C0087111 (UMLS CUI [1])
Chemotherapy Regimen
Item
Chemotherapy Regimen
boolean
C0392920 (UMLS CUI [1])
Item
Chemotherapy Regimen: if yes, please specify
integer
C0392920 (UMLS CUI [1,1])
C4035158 (UMLS CUI [1,2])
Code List
Chemotherapy Regimen: if yes, please specify
CL Item
Imatinib mesylate  (Imatinib mesylate (Gleevec, Glivec))
C0939537 (UMLS CUI-1)
CL Item
Dasatinib  (Dasatinib (Sprycel))
C1455147 (UMLS CUI-1)
CL Item
Nilotinib  (Nilotinib (Tasigna))
C1721377 (UMLS CUI-1)
CL Item
Bortezomib (Bortezomib (Velcade))
C1176309 (UMLS CUI-1)
CL Item
Intrathecal chemotherapy (Intrathecal chemotherapy)
C1517560 (UMLS CUI-1)
C1520143 (UMLS CUI-2)
CL Item
Lenalidomide  (Lenalidomide (Revlimid))
C1144149 (UMLS CUI-1)
CL Item
Rituximab  (Rituximab (Rituxan, mabthera))
C0393022 (UMLS CUI-1)
CL Item
Velafermin  (Velafermin (FGF))
C1710622 (UMLS CUI-1)
CL Item
Lepivance (KGF, palifermin) (Lepivance (KGF, palifermin))
C0064294 (UMLS CUI-1)
CL Item
Thalidomide (Thalidomide)
C0039736 (UMLS CUI-1)
CL Item
Other (Other)
C0205394 (UMLS CUI-1)
Radiotherapy
Item
Radiotherapy
boolean
C1522449 (UMLS CUI [1])
Item Group
HSCT - Minimum Essential Data - A First report - 100 days after HSCT DISEASE CLASSIFICATION SHEET 1
EBMT Centre Identification Code (CIC)
Item
EBMT Centre Identification Code (CIC)
text
C2348585 (UMLS CUI [1])
Hospital Unique Patient Number
Item
Hospital Unique Patient Number/Code (UPN)
integer
C2348585 (UMLS CUI [1])
Date of Initial Diagnosis
Item
Date of Initial Diagnosis
date
C2316983 (UMLS CUI [1])

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