ID

28423

Descripción

Description of registry: The aim of the National Quality Registry for Breast Cancer is to: -in an objective and standardised manner, monitor the continuum of care from diagnosis to any recurrence and death -enable the identification of regional differences -collectively relate to current guidelines and quality targets set by specialist associations and the National Board of Health and Welfare -facilitate research and developments in breast cancer. Pre- or post operative adjuvant oncological treatment Source: http://www.cancercentrum.se/samverkan/cancerdiagnoser/brost/kvalitetsregister/dokument/ Facts Owner: Kerstin Sandelin surgeon, Karolinska University Hospital, Solna kerstin.sandelin@sll.se

Link

http://www.cancercentrum.se/samverkan/cancerdiagnoser/brost/kvalitetsregister/dokument/

Palabras clave

Versiones (1)
  1. 12/01/18 12/01/18 -
Titular de derechos de autor

cancercentrum.se (Bröst)

Subido en

12 gennaio 2018

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Breast Cancer Swedish National Quality Registry

Inglés ( localization.languageCode.US ) Sueco

Pre- or post operative adjuvant oncological treatment

1 formularios  
National Quality Register for Breast Cancer, Pre- or post operative adjuvant oncological treatment
Descripción

National Quality Register for Breast Cancer, Pre- or post operative adjuvant oncological treatment

Alias
UMLS CUI-1
C0678222
UMLS CUI-2
C0034975
UMLS CUI-3
C0087111
UMLS CUI-4
C1522673
Hospital, clinic
Descripción

Hospital, clinic

Tipo de datos

text

Alias
UMLS CUI [1]
C0019994
UMLS CUI [2]
C0442592
Correspondent
Descripción

Correspondent

Tipo de datos

text

Alias
UMLS CUI [1]
C0337611
Reporting Date
Descripción

Reporting Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0011008
Personal ID
Descripción

Personal ID

Tipo de datos

text

Alias
UMLS CUI [1]
C2348585
Patient name
Descripción

Patient name

Tipo de datos

text

Alias
UMLS CUI [1]
C1299487
Notifying doctor
Descripción

Notifying doctor

Tipo de datos

text

Alias
UMLS CUI [1]
C1710470
breast cancer side
Descripción

breast cancer side

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0441987
postoperative adjuvant oncological treatment?
Descripción

postoperative adjuvant oncological treatment

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0032790
UMLS CUI [1,3]
C1522673
UMLS CUI [2]
C0678222
Adjuvant oncological treatment
Descripción

Adjuvant oncological treatment

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C1522673
Remote Metastasis / Discovery within three months of sampling date
Descripción

Remote Metastasis / Discovery within three months of sampling date

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0200345
UMLS CUI [1,3]
C2316983
Has the patient been offered, in the journal, documented contact nurse?
Descripción

contact nurse

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0028661
UMLS CUI [1,2]
C0332158
The patient is included in the study
Descripción

included in the study

Tipo de datos

integer

Alias
UMLS CUI [1]
C2348568
Chemotherapy
Descripción

Chemotherapy

Alias
UMLS CUI-1
C3665472
UMLS CUI-2
C0678222
Chemotherapy
Descripción

Chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3665472
UMLS CUI [1,2]
C0678222
Start date, first course of chemotherapy
Descripción

Start date, first course of chemotherapy

Tipo de datos

date

Alias
UMLS CUI [1,1]
C1302181
UMLS CUI [1,2]
C0808070
Chemotherapy medication name (several can be specified)
Descripción

Chemotherapy medication name

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C3665472
UMLS CUI [1,2]
C2360065
Treatment completed according to plan
Descripción

Treatment completed

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C3665472
UMLS CUI [1,2]
C0580352
If no, cause of interruption / change
Descripción

Cause of interruption Chemotherapy

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C3665472
UMLS CUI [1,2]
C1512900
UMLS CUI [1,3]
C0392360
Cytokines primary prophylaxis (eg G-CSF)
Descripción

Cytokines primary prophylaxis

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0079459
UMLS CUI [1,2]
C0199176
Inpatient care because treatment complications
Descripción

Inpatient care because treatment complications

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0679861
UMLS CUI [1,3]
C3665472
Radiotherapy
Descripción

Radiotherapy

Alias
UMLS CUI-1
C1522449
UMLS CUI-2
C0678222
Start date, first dose radiotherapy
Descripción

Start date, first dose radiotherapy

Tipo de datos

date

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0808070
Target (several can be specified)
Descripción

Target

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C1515974
UMLS CUI [1,2]
C1522449
Total dose excl. Boost
Descripción

Total dose excl. Boost

Tipo de datos

float

Unidades de medida
  • Gy
Alias
UMLS CUI [1,1]
C2986497
UMLS CUI [1,2]
C1522449
Gy
Boost
Descripción

Boost

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1511253
UMLS CUI [1,2]
C1522449
Boost dose
Descripción

Boost dose

Tipo de datos

float

Unidades de medida
  • Gy
Alias
UMLS CUI [1,1]
C1511253
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1522449
Gy
Endocrine treatment
Descripción

Endocrine treatment

Alias
UMLS CUI-1
C0279025
UMLS CUI-2
C0678222
Endocrine treatment
Descripción

Endocrine treatment

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0279025
UMLS CUI [1,2]
C0678222
Start date endocrine treatment
Descripción

Start date endocrine treatment

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0279025
UMLS CUI [1,2]
C0808070
Endocrine treatment (several can be specified)
Descripción

Endocrine treatment medication name

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0279025
UMLS CUI [1,2]
C2360065
Other endocrine treatment specification
Descripción

Other endocrine treatment specification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0279025
UMLS CUI [1,2]
C2360065
Antibody therapy
Descripción

Antibody therapy

Alias
UMLS CUI-1
C0279694
UMLS CUI-2
C0678222
Antibody therapy
Descripción

Antibody therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0279694
UMLS CUI [1,2]
C0678222
Antibody therapy start date
Descripción

Antibody therapy start date

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0279694
UMLS CUI [1,2]
C0808070
Antibody therapy (several can be specified)
Descripción

Antibody therapy medication name

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0279694
UMLS CUI [1,2]
C2360065
Other Antibody therapy specification
Descripción

Other Antibody therapy specification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0279694
UMLS CUI [1,2]
C2360065
Bisphosphonates therapy
Descripción

Bisphosphonates therapy

Alias
UMLS CUI-1
C0012544
UMLS CUI-2
C0087111
UMLS CUI-3
C0678222
Bisphosphonates therapy
Descripción

Bisphosphonates therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0012544
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C0678222
Volver a la parte superior de la página

Similar models

Pre- or post operative adjuvant oncological treatment

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
National Quality Register for Breast Cancer, Pre- or post operative adjuvant oncological treatment
C0678222 (UMLS CUI-1)
C0034975 (UMLS CUI-2)
C0087111 (UMLS CUI-3)
C1522673 (UMLS CUI-4)
Hospital, clinic
Item
Hospital, clinic
text
C0019994 (UMLS CUI [1])
C0442592 (UMLS CUI [2])
Correspondent
Item
Correspondent
text
C0337611 (UMLS CUI [1])
Reporting Date
Item
Reporting Date
date
C0011008 (UMLS CUI [1])
Personal ID
Item
Personal ID
text
C2348585 (UMLS CUI [1])
Patient name
Item
Patient name
text
C1299487 (UMLS CUI [1])
Notifying doctor
Item
Notifying doctor
text
C1710470 (UMLS CUI [1])
Item
breast cancer side
integer
C0678222 (UMLS CUI [1,1])
C0441987 (UMLS CUI [1,2])
breast cancer side
Code List
breast cancer side
CL Item
Right (1)
CL Item
Left (2)
postoperative adjuvant oncological treatment
Item
postoperative adjuvant oncological treatment?
boolean
C0087111 (UMLS CUI [1,1])
C0032790 (UMLS CUI [1,2])
C1522673 (UMLS CUI [1,3])
C0678222 (UMLS CUI [2])
Item
Adjuvant oncological treatment
integer
C0678222 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C1522673 (UMLS CUI [1,3])
Adjuvant oncological treatment
Code List
Adjuvant oncological treatment
CL Item
Applies to preoperative adjuvant oncological treatment (1)
CL Item
Applies to postoperative adjuvant oncological treatment (2)
Remote Metastasis / Discovery within three months of sampling date
Item
Remote Metastasis / Discovery within three months of sampling date
boolean
C0027627 (UMLS CUI [1,1])
C0200345 (UMLS CUI [1,2])
C2316983 (UMLS CUI [1,3])
Item
Has the patient been offered, in the journal, documented contact nurse?
integer
C0028661 (UMLS CUI [1,1])
C0332158 (UMLS CUI [1,2])
Has the patient been offered, in the journal, documented contact nurse?
Code List
Has the patient been offered, in the journal, documented contact nurse?
CL Item
No (1)
CL Item
Yes (2)
CL Item
Missing data (3)
Item
The patient is included in the study
integer
C2348568 (UMLS CUI [1])
Has the patient been offered, in the journal, documented contact nurse?
Code List
The patient is included in the study
CL Item
No (1)
CL Item
Yes (2)
CL Item
Missing data (3)
Item Group
Chemotherapy
C3665472 (UMLS CUI-1)
C0678222 (UMLS CUI-2)
Chemotherapy
Item
Chemotherapy
boolean
C3665472 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
Start date, first course of chemotherapy
Item
Start date, first course of chemotherapy
date
C1302181 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Item
Chemotherapy medication name (several can be specified)
integer
C3665472 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
Treatment (several can be specified)
Code List
Chemotherapy medication name (several can be specified)
CL Item
Anthracycline (1)
CL Item
Docetaxel (2)
CL Item
Paklitaxel (3)
CL Item
Other (4)
Item
Treatment completed according to plan
integer
C3665472 (UMLS CUI [1,1])
C0580352 (UMLS CUI [1,2])
Has the patient been offered, in the journal, documented contact nurse?
Code List
Treatment completed according to plan
CL Item
No (1)
CL Item
Yes (2)
CL Item
Missing data (3)
Item
If no, cause of interruption / change
integer
C3665472 (UMLS CUI [1,1])
C1512900 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
If no, cause of interruption / change
Code List
If no, cause of interruption / change
CL Item
Toxicity (1)
CL Item
Other (2)
CL Item
Missing data (3)
Item
Cytokines primary prophylaxis (eg G-CSF)
integer
C0079459 (UMLS CUI [1,1])
C0199176 (UMLS CUI [1,2])
Has the patient been offered, in the journal, documented contact nurse?
Code List
Cytokines primary prophylaxis (eg G-CSF)
CL Item
No (1)
CL Item
Yes (2)
CL Item
Missing data (3)
Item
Inpatient care because treatment complications
integer
C0019993 (UMLS CUI [1,1])
C0679861 (UMLS CUI [1,2])
C3665472 (UMLS CUI [1,3])
Has the patient been offered, in the journal, documented contact nurse?
Code List
Inpatient care because treatment complications
CL Item
No (1)
CL Item
Yes (2)
CL Item
Missing data (3)
Item Group
Radiotherapy
C1522449 (UMLS CUI-1)
C0678222 (UMLS CUI-2)
Start date, first dose radiotherapy
Item
Start date, first dose radiotherapy
date
C1522449 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Item
Target (several can be specified)
integer
C1515974 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
Target (several can be specified)
Code List
Target (several can be specified)
CL Item
Breast / chest wall (1)
CL Item
Axilla (2)
CL Item
Fossa supraclavicularis (3)
CL Item
Parasternal area (4)
Total dose excl. Boost
Item
Total dose excl. Boost
float
C2986497 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
Boost
Item
Boost
boolean
C1511253 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
Boost dose
Item
Boost dose
float
C1511253 (UMLS CUI [1,1])
C2986497 (UMLS CUI [1,2])
C1522449 (UMLS CUI [1,3])
Item Group
Endocrine treatment
C0279025 (UMLS CUI-1)
C0678222 (UMLS CUI-2)
Endocrine treatment
Item
Endocrine treatment
boolean
C0279025 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
Start date endocrine treatment
Item
Start date endocrine treatment
date
C0279025 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Item
Endocrine treatment (several can be specified)
integer
C0279025 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
Endocrine treatment (several can be specified)
Code List
Endocrine treatment (several can be specified)
CL Item
Tamoxifen (1)
CL Item
GnRH agonist (2)
CL Item
Aromatase inhibitors (3)
CL Item
Other, specify (4)
Other endocrine treatment specification
Item
Other endocrine treatment specification
text
C0279025 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
Item Group
Antibody therapy
C0279694 (UMLS CUI-1)
C0678222 (UMLS CUI-2)
Antibody therapy
Item
Antibody therapy
boolean
C0279694 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
Antibody therapy start date
Item
Antibody therapy start date
date
C0279694 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Item
Antibody therapy (several can be specified)
integer
C0279694 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
Antibody therapy (several can be specified)
Code List
Antibody therapy (several can be specified)
CL Item
Trastuzumab  (1)
CL Item
Pertuzumab (2)
Other Antibody therapy specification
Item
Other Antibody therapy specification
text
C0279694 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
Item Group
Bisphosphonates therapy
C0012544 (UMLS CUI-1)
C0087111 (UMLS CUI-2)
C0678222 (UMLS CUI-3)
Bisphosphonates therapy
Item
Bisphosphonates therapy
boolean
C0012544 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial