Improving Cancer Outcomes (Screening Reporting) Regulations 2015
Authorised by the Chief Parliamentary Counsel
Authorised Version
i
Improving Cancer Outcomes (Screening Reporting)
Regulations 2015
S.R. No. 106/2015
TABLE OF PROVISIONS
Regulation Page
1 Objectives 1
2 Authorising provision 1
3 Commencement 2
4 Types of cancer screening required to be reported 2
5 Entities required to report cancer screening 2
6 Cancer screening reports 3
Schedule 1—Prescribed information about breast screening 4
Schedule 2—Prescribed information about cervical cancer
screening (pathology laboratory) 5
Schedule 3—Prescribed information about cervical cancer
screening (cervical screening test provider) 7
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Endnotes 8
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Authorised by the Chief Parliamentary Counsel
Authorised Version
1
STATUTORY RULES 2015
S.R. No. 106/2015
Improving Cancer Outcomes Act 2014
Improving Cancer Outcomes (Screening Reporting)
Regulations 2015
The Governor in Council makes the following Regulations:
Dated: 22 September 2015
Responsible Minister:
JILL HENNESSY
Minister for Health
MATTHEW McBEATH
Clerk of the Executive Council
1 Objectives
The objectives of these Regulations are to
prescribe—
(a) the types of cancer screening that are
required to be reported to the Secretary under
the Improving Cancer Outcomes Act 2014;
and
(b) who must report that screening; and
(c) the form of the reports, the time within
which they must be made and the
information to be included in them.
2 Authorising provision
These Regulations are made under section 28 of
the Improving Cancer Outcomes Act 2014.
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Improving Cancer Outcomes (Screening Reporting) Regulations 2015
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3 Commencement
These Regulations come into operation on
1 October 2015.
4 Types of cancer screening required to be reported
For the purposes of section 8(1) of the Improving
Cancer Outcomes Act 2014, the following types
of cancer screening are prescribed—
(a) mammography, mammographic screening
and subsequent radiology, pathology or
clinical testing or procedures undergone in
order to determine whether an individual has
cancer, or a precursor to cancer, of the
breast;
(b) cervical cytology test, human papilloma
virus test and histopathology of the uterine
cervix to determine whether an individual
has cancer, or a precursor to cancer, of the
cervix.
5 Entities required to report cancer screening
For the purposes of section 8(1) of the Improving
Cancer Outcomes Act 2014, the following
persons and organisations are prescribed—
(a) any organisation that conducts cancer
screening of a kind specified in
regulation 4(a) on behalf of Breast Screen
Victoria Inc.;
(b) any pathology laboratory that provides a
report on a cancer screening test undergone
by a person in Victoria in order to determine
whether the person has cervical cancer or a
precursor to cervical cancer;
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Improving Cancer Outcomes (Screening Reporting) Regulations 2015
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(c) any person who administers a cervical
cytology test or a human papilloma virus
test, including a health practitioner within
the meaning of the Health Practitioner
Regulation National Law (Victoria)
Act 2009.
6 Cancer screening reports
For the purposes of section 8(2) of the Improving
Cancer Outcomes Act 2014—
(a) a report of cancer screening is in the
prescribed form if it contains the prescribed
information; and
(b) the prescribed time within which a report of
cancer screening of a type referred to in
regulation 4(b) must be made by a pathology
laboratory referred to in regulation 5(b) is
30 days from the date the report is
completed; and
(c) the prescribed information to be included in
a report is—
(i) for cancer screening of a type referred
to in regulation 4(a), the information set
out in Schedule 1; and
(ii) for cancer screening of a type referred
to in regulation 4(b) conducted by a
pathology laboratory referred to in
regulation 5(b), the information set out
in Schedule 2; and
(iii) for cancer screening of a type referred
to in regulation 4(b) conducted by a
person who administers a cervical
cytology test or a human papilloma
virus test referred to in regulation 5(c),
the information set out in Schedule 3.
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Schedule 1—Prescribed information about breast screening
Improving Cancer Outcomes (Screening Reporting) Regulations 2015
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Schedule 1—Prescribed information about
breast screening
Regulation 6(c)(i)
Name of organisation where the test was undertaken
Patient details:
Individual Health Identifier (if known)
Family name
Given name(s)
Maiden name (if applicable)
Address (home and postal)
Postcode
Contact telephone number (home and mobile)
Email address
Date of birth
Country of birth
Aboriginal or Torres Strait Islander status
Language spoken at home (if known—please specify)
Breast cancer history:
Patient
Patient's family
Symptoms of breast cancer
Type of test
Test result
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Schedule 2—Prescribed information about cervical cancer screening
(pathology laboratory)
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Schedule 2—Prescribed information
about cervical cancer screening
(pathology laboratory)
Regulation 6(c)(ii)
Details of the person ordering the test:
Name of organisation where the test was undertaken
Name of person ordering the test (title, given and family names)
Medicare provider number (if known)
Healthcare Provider Identifier—Individual (if known)
Address
Phone number
Patient details:
Medicare number (if known)
Individual Health Identifier (if known)
Title
Family name
Given name(s)
Maiden name (if applicable)
Address (home and postal)
Postcode
Contact telephone number (home and mobile)
Email address (if known)
Date of birth
Country of birth (if known)
Aboriginal or Torres Strait Islander status (if known)
Language spoken at home (if known—please specify)
Patient Identifier (e.g. UR number)
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Schedule 2—Prescribed information about cervical cancer screening
(pathology laboratory)
Improving Cancer Outcomes (Screening Reporting) Regulations 2015
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Laboratory details:
Laboratory name
Laboratory Registry Identifier
Accession number
Episode type
Test information:
Test type
Date specimen was taken
Result (to be reported in accordance with Schedule 1 of the
"Victorian Cervical Cancer Screening Reporting Guidelines" as
published by the Department of Health and Human Services from
time to time)
Date of report
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Schedule 3—Prescribed information about cervical cancer screening
(cervical screening test provider)
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Schedule 3—Prescribed information about
cervical cancer screening (cervical screening
test provider)
Regulation 6(c)(iii)
Details of the person ordering the test:
Name of organisation where the test was undertaken
Name of person ordering the test (title, given and family names)
Medicare provider number (if known)
Healthcare Provider Identifier—Individual (if known)
Address
Phone number
Patient details:
Medicare number (if known)
Individual Health Identifier (if known)
Title
Family name
Given name(s)
Maiden name (if applicable)
Address (home and postal)
Postcode
Contact telephone number (home and mobile)
Email address (if known)
Date of birth
Country of birth (if known)
Aboriginal or Torres Strait Islander status (if known)
Language spoken at home (if known—please specify)
Patient Identifier (e.g. UR number)
Clinical symptoms (if applicable)
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Endnotes
Improving Cancer Outcomes (Screening Reporting) Regulations 2015
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Endnotes
Table of Applied, Adopted or Incorporated Matter
The following table of applied, adopted or incorporated matter is included in
accordance with the requirements of regulation 5 of the Subordinate Legislation
Regulations 2014.
Statutory rule
provision
Title of applied, adopted or
incorporated document
Matter in
applied,
adopted or
incorporated
document
Schedule 2 "Victorian Cervical Cancer
Screening Reporting
Guidelines" as published by
the Department of Health and
Human Services from time to
time
Schedule 1
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