Ontario Health - Cancer Care Ontario's Data Book - 2022-2023 |
|
Updated December 2020
Entity |
Data Element |
Definition |
Format |
Valid Values |
Purpose and Use |
Completion Requirement |
Changes |
Systemic Drug Delivery Event |
Patient Chart Number |
Patient identifier code that is unique within the healthcare facility. |
CHAR 10 |
Consistent with CIHI NACRS definition and format. |
Uniquely identifies a patient within an RCC. Necessary to determine a case. Foundational to most measures and indicators. |
Mandatory |
|
Systemic Drug Delivery Event |
Visit Hospital Number |
MOHLTC Master Number for the healthcare facility where the cancer activity occurred (known by CIHI as Institution Numbers) |
CHAR
4 |
Same as CIHI’s Institution Number for NACRS or DAD submissions, but does not include CIHI’s provincial identifier digit. For current valid MOHLTC master numbers, see Appendix A. |
Uniquely identifies the hospital organization to which this visit belong. |
Mandatory |
|
Systemic Drug Delivery Event |
Submitting Hospital Number |
The MOHLTC healthcare facility that submits activity to OH-CCO. |
CHAR 4 |
Valid MOHLTC facility numbers only. Same 3-digit number that is used for MIS submissions. An additional leading zero is acceptable. For current valid MOHLTC facility numbers, see Appendix A. |
Allows the hospital organization submitting the data to be distinguished from the hospital site where the service was delivered. |
Mandatory |
|
Systemic Drug Delivery Event |
MIS Functional Centre |
Subdivisions of an organization for the purpose of recording budgeted and actual revenues, expenses, and statistics pertaining to the function or activity being carried out. They are used to capture cost of labour, supplies, and equipment required to do specific functions. |
CHAR 9 |
Valid MOHLTC Functional Centre Only or current valid MOHLTC Functional centre numbers, see Appendix 1.1. |
To be able to align OH-CCO activity data to MOHLTC OHRS reporting standards. |
|
|
Systemic Drug Delivery Event |
Visit Date |
The date that the patient received systemic treatment. This can include:
|
YYYYMMDD |
Valid dates only. |
Foundational to most measures and indicators – ALR, Wait Times, Funding. Used as a proxy for Consult date for Wait Times. 1st Consult date will be used for Wait Time . |
Mandatory |
|
Systemic Drug Delivery Event |
Visit Time |
Time of this activity. |
HHMM |
0000 (midnight) to 2359, as per CIHI NACRS format. Used for ALR to identify multiple visits in the same day. |
|||
Systemic Drug Delivery Event |
CCO Regimen |
A set of anti-cancer and supportive medications given during an active course of systemic chemotherapy that is named and defined in OH-CCO's Provincial Formulary Regimen List. In addition to the Formulary Regimen list, a set of National Clinical Trial (NCT) numbers is available for entry when reporting a clinical trial. |
CHAR 22 |
See Appendix 1.22 for a list of CCO regimen names. In cases where the Regimen is not in the CCO regimen list, an RCC regimen name is acceptable. If submitting a clinical trial regimen, an NCT number should be submitted as listed in Appendix 1.22 (CCO Regimen or NCT number can not be NULL) |
Concordance with evidence-based practice guidelines, funding. |
Mandatory | |
Systemic Drug Delivery Event |
CCO Drug Code |
OH-CCO hybrid of the First data Bank (FDB) drug number and OPIS generated drug numbers. Uniquely identifies the dug product in OPIS database. |
CHAR 10 |
As per OPIS drug tables |
Uniquely identifies a drug in OPIS. Concordance with evidence-based practice guidelines, funding. |
Conditionally Mandatory Note: Mandatory if "DIN" is null |
|
Systemic Drug Delivery Event |
DIN |
Health Canada Drug Identification Number. Uniquely identifies the drug product by its manufacturer, name and strength of active ingredients, route of administration and pharmaceutical dosage form. |
CHAR 8 |
Valid Health Canada DINs. For clinical trial drugs not yet approved by Health Canada, use the value 9999999A for antineoplastic trial drugs or 9999999S for supportive trial drugs. |
Uniquely identifies the drug product, as to its manufacturer, name and strength of active ingredients, route of administration and pharmaceutical dosage form. Used to identify drugs and to link to CCO drug codes for non-OPIS RCCs. |
Conditionally Mandatory Note: Mandatory if "CCO Drug Code" is null |
|
Systemic Drug Delivery Event |
Drug Origin Flag |
Used to indicate whether the drug is from OPIS or First Data Bank (FDB). |
CHAR 1 |
Y=Yes if FDB N= No if not FDB/investigational created by OPIS. Identifies if the drug is supplied by FDB or created as an investigational drug. Used to uniquely identify the drug given. |
Conditionally Mandatory |
||
Systemic Drug Delivery Event |
Body Surface Area |
Patient body surface area, calculated based on their height and weight using the MEDLOG formula, in M2 (Square Meters). |
REAL |
Any positive real number. |
Concordance with evidence-based practice guidelines. |
||
Systemic Drug Delivery Event |
Dose Administered |
Actual drug dose administered during the patient's visit (total amount as opposed to metres squared). |
REAL |
Any non-negative real number. If the dose is zero, OH-CCO assumes the patient arrived at the clinic but was not treated with this drug as planned. |
Used to support cancer system planning and funding. Concordance with evidence-based guidelines and funding. |
||
Systemic Drug Delivery Event |
Measurement Unit |
The international standard units of measurement for dosage. (e.g. mg=milligram) |
CHAR 4 |
See Appendix 1.20 for CCO measurement unit codes. |
Concordance with evidence-based guidelines and funding. |
||
Systemic Drug Delivery Event |
Route |
The administration method for the drug (e.g. IV= intravenous). |
CHAR 3 |
For current valid OPIS route codes and description, see Appendix 1.21. |
Used to categorize drugs for analysis purposes. |
||
Systemic Drug Delivery Event |
Intent of Systemic Treatment |
Intent of systemic treatment as determined by the oncologist at the time of booking the treatment visit. |
CHAR 1 |
C = Curative, P = Palliative, Enter U for Unknown See Appendix 1.19 for definitions of each term.
|
Concordance with evidence-based guidelines and funding. |
|
|
Systemic Drug Delivery Event |
Line of Therapy |
Identifies each line of therapy given to a patient for incurable disease (palliative intent). Refers to a regimen given to control disease. |
Integer |
1 through 99 |
To identify line of therapy in treating disease |
||
Systemic Drug Delivery Event |
Inpatient Flag |
Identifies whether the patient is currently registered as an inpatient at this healthcare facility. |
CHAR 1 |
Y=Yes for inpatient, N=No |
Used to identify activity provided to inpatients. |
||
Systemic Drug Delivery Event |
Arrived But Not Treated |
Identifies those patients who arrive in a suite but are medically unable or unwilling to receive treatment. |
CHAR 1 |
Y = Yes or N = No |
Identifies those patients who arrive in a suite but are medically unable or unwilling to receive treatment. |
||
Systemic Drug Delivery Event |
CMIR Severity |
Identifies level of Cancer Medication Infusion Reaction severity. |
CHAR 1 |
blank-no reaction 0-no reaction 1-Mild transient reaction; infusion interruption not indicated; intervention not indicated 2-Therapy or infusion interruption indicated but responds promptly to symptomatic treatment (e.g., antihistamines, NSAIDS, narcotics, IV fluids); prophylactic medications indicated for <=24 hrs 3-Prolonged (e.g., not rapidly responsive to symptomatic medication and/or brief interruption of infusion); recurrence of symptoms following initial improvement; hospitalization indicated for clinical sequelae 4-Life-threatening consequences; urgent intervention indicated 5-Death |
To determine level of severity for each reported Cancer Medication Infusion Reaction incidence |
Optional for FY 2019/20. Mandatory starting with FY 2020/21. |
|
Systemic Drug Delivery Event |
Registration Date |
Date this patient was first registered at this RCC and/or hospital for this disease |
YYYYMMDD |
Valid dates only. |
Used as a surrogate for date of initial diagnosis when date of initial diagnosis in not available. Additional purpose: Used to derive disease sequence number for sites who do not submit the disease sequence number. Therefore used to link clinic visit activity to patient’s disease. |
Mandatory |
|
Systemic Drug Delivery Event
|
Disease Sequence Number |
The numeric sequence assigned to a primary cancer for a patient at a specific healthcare facility. |
INTEGER |
1 through 99. |
When combined with a patient identifier, disease sequence number uniquely defines a cancer case. Disease Sequence Number must be either entered or left blank on ALL records in ALL entities from a submitting site, and that must remain consistent from month to month. If left blank, OH-CCO will derive a value from the Registration Date. If this is the case, the field must be unique amongst Diseases within the Patient. Used in ALR, Ontario Cancer Registry, Wait Times, Planning, and funding. |
|
|
Systemic Drug Delivery Event |
HCP Number |
Healthcare professional identifier code for the physician or non-physician who is most responsible for the patient or This code is unique to the submitting healthcare facility. |
CHAR 15 |
Numeric only as per CIHI NACRS format. For physicians, this code has historically been the physician’s OHIP billing number in OPIS. |
Uniquely identifies a healthcare professional (physician or non-physician) so patient activity can be linked to a healthcare provider.
|
Mandatory |
|
Systemic Drug Delivery Event |
Patient Postal Code |
Patient’s postal code of their home address on the date of this event. |
CHAR 10 |
Canadian postal codes must be in the format ANANAN (no space), where A is a letter and N is a number. For US zip codes, use either NNNNN or NNNNN-NNNN. CIHI’s two-letter province/state codes are also acceptable if full code not known or for non-Canadian residence. See Appendix B. |
Used for generating prevalence rates by region, registry linking, Planning, Ontario Cancer Registry. |
Mandatory |
NOTE: Please note that the 'Applies to' column has been replaced with 'Completion Requirement' column. Please refer to Appendix 1.40: ALR activity by Reporting Facility for additional details on facility-specific ALR activity data submission requirements.