ID

28423

Description

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

Lien

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

Mots-clés

Versions (1)
  1. 12/1/18 12/1/18 -
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12 de enero de 2018

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Breast Cancer Swedish National Quality Registry

Anglais ( localization.languageCode.US ) Suédois

Pre- or post operative adjuvant oncological treatment

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

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
Description

Hospital, clinic

Type de données

text

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

Correspondent

Type de données

text

Alias
UMLS CUI [1]
C0337611
Reporting Date
Description

Reporting Date

Type de données

date

Alias
UMLS CUI [1]
C0011008
Personal ID
Description

Personal ID

Type de données

text

Alias
UMLS CUI [1]
C2348585
Patient name
Description

Patient name

Type de données

text

Alias
UMLS CUI [1]
C1299487
Notifying doctor
Description

Notifying doctor

Type de données

text

Alias
UMLS CUI [1]
C1710470
breast cancer side
Description

breast cancer side

Type de données

integer

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

postoperative adjuvant oncological treatment

Type de données

boolean

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

Adjuvant oncological treatment

Type de données

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
Description

Remote Metastasis / Discovery within three months of sampling date

Type de données

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?
Description

contact nurse

Type de données

integer

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

included in the study

Type de données

integer

Alias
UMLS CUI [1]
C2348568
Chemotherapy
Description

Chemotherapy

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

Chemotherapy

Type de données

boolean

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

Start date, first course of chemotherapy

Type de données

date

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

Chemotherapy medication name

Type de données

integer

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

Treatment completed

Type de données

integer

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

Cause of interruption Chemotherapy

Type de données

integer

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

Cytokines primary prophylaxis

Type de données

integer

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

Inpatient care because treatment complications

Type de données

integer

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

Radiotherapy

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

Start date, first dose radiotherapy

Type de données

date

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

Target

Type de données

integer

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

Total dose excl. Boost

Type de données

float

Unités de mesure
  • Gy
Alias
UMLS CUI [1,1]
C2986497
UMLS CUI [1,2]
C1522449
Gy
Boost
Description

Boost

Type de données

boolean

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

Boost dose

Type de données

float

Unités de mesure
  • Gy
Alias
UMLS CUI [1,1]
C1511253
UMLS CUI [1,2]
C2986497
UMLS CUI [1,3]
C1522449
Gy
Endocrine treatment
Description

Endocrine treatment

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

Endocrine treatment

Type de données

boolean

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

Start date endocrine treatment

Type de données

date

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

Endocrine treatment medication name

Type de données

integer

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

Other endocrine treatment specification

Type de données

text

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

Antibody therapy

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

Antibody therapy

Type de données

boolean

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

Antibody therapy start date

Type de données

date

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

Antibody therapy medication name

Type de données

integer

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

Other Antibody therapy specification

Type de données

text

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

Bisphosphonates therapy

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

Bisphosphonates therapy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0012544
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C0678222
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Similar models

Pre- or post operative adjuvant oncological treatment

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])
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