Informações:
Falhas:
ID
28423
Descrição
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/
Palavras-chave
Versões (1)
- 12/1/18 12/1/18 -
Titular dos direitos
cancercentrum.se (Bröst)
Transferido a
12 de enero de 2018
DOI
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Licença
Creative Commons BY-NC 3.0
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Breast Cancer Swedish National Quality Registry
Pre- or post operative adjuvant oncological treatment
- StudyEvent: ODM
Similar models
Pre- or post operative adjuvant oncological treatment
- StudyEvent: ODM
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
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)
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])
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])
C0441987 (UMLS CUI [1,2])
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])
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])
C0087111 (UMLS CUI [1,2])
C1522673 (UMLS CUI [1,3])
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])
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])
C0332158 (UMLS CUI [1,2])
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)
Code List
The patient is included in the study
CL Item
No (1)
CL Item
Yes (2)
CL Item
Missing data (3)
Chemotherapy
Item
Chemotherapy
boolean
C3665472 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
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])
C0808070 (UMLS CUI [1,2])
Item
Chemotherapy medication name (several can be specified)
integer
C3665472 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,2])
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])
C0580352 (UMLS CUI [1,2])
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])
C1512900 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
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])
C0199176 (UMLS CUI [1,2])
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])
C0679861 (UMLS CUI [1,2])
C3665472 (UMLS CUI [1,3])
Code List
Inpatient care because treatment complications
CL Item
No (1)
CL Item
Yes (2)
CL Item
Missing data (3)
Start date, first dose radiotherapy
Item
Start date, first dose radiotherapy
date
C1522449 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
Item
Target (several can be specified)
integer
C1515974 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
C1522449 (UMLS CUI [1,2])
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])
C1522449 (UMLS CUI [1,2])
Boost
Item
Boost
boolean
C1511253 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
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])
C2986497 (UMLS CUI [1,2])
C1522449 (UMLS CUI [1,3])
Endocrine treatment
Item
Endocrine treatment
boolean
C0279025 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
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])
C0808070 (UMLS CUI [1,2])
Item
Endocrine treatment (several can be specified)
integer
C0279025 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,2])
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])
C2360065 (UMLS CUI [1,2])
Antibody therapy
Item
Antibody therapy
boolean
C0279694 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
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])
C0808070 (UMLS CUI [1,2])
Item
Antibody therapy (several can be specified)
integer
C0279694 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,2])
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])
C2360065 (UMLS CUI [1,2])
Item Group
Bisphosphonates therapy
C0012544 (UMLS CUI-1)
C0087111 (UMLS CUI-2)
C0678222 (UMLS CUI-3)
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])
C0087111 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])