Statement of Principles concerning porphyria cutanea tarda No. 43 of 2012

Administered by Department of Veterans' Affairs

Legislation au F2012L01357 Not in force Legislative Instrument

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REPATRIATION MEDICAL AUTHORITY

 

INSTRUMENT NO. 43 of 2012

 

VETERANS’ ENTITLEMENTS ACT 1986

MILITARY REHABILITATION AND COMPENSATION ACT 2004

 

EXPLANATORY NOTES FOR TABLING

 

 

  1. The Repatriation Medical Authority (the Authority), under subsection 196B(8) of the Veterans' Entitlements Act 1986 (the VEA), revokes Instrument No. 19 of 2001, determined under subsection 196B(2) of the VEA concerning porphyria cutanea tarda.

 

2.             The Authority is of the view that there is sound medical-scientific evidence that indicates that porphyria cutanea tarda and death from porphyria cutanea tarda can be related to particular kinds of service.  The Authority has therefore determined pursuant to subsection 196B(2) of the VEA a Statement of Principles, Instrument No. 43 of 2012 concerning porphyria cutanea tarda.  This Instrument will in effect replace the revoked Statement of Principles.

 

3.             The provisions of the Military Rehabilitation and Compensation Act 2004 (the MRCA) relating to claims for compensation commenced on 1 July 2004.  Claims under section 319 of the MRCA for acceptance of liability for a service injury sustained, a service disease contracted or service death on or after 1 July 2004 are determined by the Military Rehabilitation and Compensation Commission by reference to Statements of Principles issued by the Authority pursuant to the VEA.

 

4.             The Statement of Principles sets out the factors that must as a minimum exist, and which of those factors must be related to the following kinds of service rendered by a person:

 

 operational service under the VEA;

 peacekeeping service under the VEA;

 hazardous service under the VEA;

 British nuclear test defence service under the VEA;

 warlike service under the MRCA;

 non-warlike service under the MRCA,

 

before it can be said that a reasonable hypothesis has been raised connecting porphyria cutanea tarda or death from porphyria cutanea tarda, with the circumstances of that service.

 

5.             This Instrument results from an investigation notified by the Authority in the Government Notices Gazette of 30 June 2010 concerning porphyria cutanea tarda in accordance with section 196G of the VEA.  The investigation involved an examination of the sound medical-scientific evidence now available to the Authority, including the sound medical-scientific evidence it has previously considered.

 

6.             The contents of this Instrument are in similar terms as the revoked Instrument.  Comparing this Instrument and the revoked Instrument, the differences include:

 

  • adopting the latest revised Instrument format, which commenced in 2005;
  • deleting the ICD code from the Instrument header;
  • revising the definition of 'porphyria cutanea tarda' in clause 3;
  • revising factors 6(a) & 6(o) concerning 'exposure to a halogenated aromatic hydrocarbon as specified';
  • new factors 6(b) & 6(p) concerning 'exposure as specified to a chemical agent contaminated with 2,3,7,8-tetrachlorodibenzo-para-dioxin (TCDD)';
  • new factors 6(c) & 6(q) concerning 'consuming a total of 75 kilograms of alcohol' for males only;
  • new factors 6(d) & 6(r) concerning 'consuming a total of 37 kilograms of alcohol' for females only;
  • new factors 6(e) & 6(s) concerning 'a liver disease from the specified list';
  • revising factors 6(f) & 6(t) concerning 'human immunodeficiency virus';
  • revising factors 6(g)  & 6(u) concerning 'oral oestrogen therapy';
  • new factors 6(h) & 6(v) concerning 'hepatic iron overload';
  • revising factors 6(i) & 6(w) concerning 'haemodialysis or peritoneal dialysis';
  • revising factors 6(j) & 6(x) concerning 'porphyrin-generating hepatocellular tumour';
  • new factors 6(k) & 6(y) concerning 'smoking';
  • new factor 6(l) concerning 'having the affected area of skin exposed to sunlight or ultraviolet light', for clinical onset;
  • new factor 6(m) concerning 'a drug or a drug from a class of drugs from the specified list' for clinical onset;
  • new factors 6(n) & 6(bb) concerning 'being treated with a drug';
  • revising factor 6(z) concerning 'having the affected area of skin exposed to sunlight or ultraviolet light' for clinical worsening;
  • revising factor 6(aa) concerning 'a drug or a drug from a class of drugs from the specified list' for clinical worsening;
  • deleting factors concerning 'hepatic haemosiderosis' and 'haemochromatosis' as they are now covered by factors 6(h) & 6(v) concerning 'hepatic iron overload';
  • deleting factors concerning 'alcohol dependence or alcohol abuse' as they are now covered by factors 6(c), 6(d), 6(q) & 6(r) concerning 'alcohol';
  • new definitions of 'a drug or a drug from a class of drugs from the specified list', 'a halogenated aromatic hydrocarbon from the specified list', 'a liver disease from the specified list', 'a specified chemical agent', 'alcohol', 'cigarettes per day or the equivalent thereof in other tobacco products', 'having exposure as specified to a chemical agent contaminated with 2,3,7,8-tetrachlorodibenzo-para-dioxin (TCDD)', 'having exposure to a halogenated aromatic hydrocarbon as specified' and 'iron overload' in clause 9;
  • revising the definitions of 'ICD-10-AM code' and 'relevant service' in clause 9;
  • deleting the definitions of 'alcohol abuse', 'alcohol dependence', 'being infected with Human Immunodeficiency Virus (HIV)', 'being treated with a drug or class of drugs from the specified list', 'cirrhosis of the liver', 'haemochromatosis', 'halogenated aromatic hydrocarbon' and 'hepatic haemosiderosis'; and
  • specifying a date of effect for the Instrument in clause 11.

 

7.             Further changes to the format of the Instrument reflect the commencement of the MRCA and clarify that pursuant to subsection 196B(3A) of the VEA, the Statement of Principles has been determined for the purposes of both the VEA and the MRCA.

 

8.             Prior to determining this Instrument, the Authority advertised its intention to undertake an investigation in relation to porphyria cutanea tarda in the Government Notices Gazette of 30 June 2010, and circulated a copy of the notice of intention to investigate to a wide range of organisations representing veterans, service personnel and their dependants.  The Authority invited submissions from the Repatriation Commission, organisations and persons referred to in section 196E of the VEA, and any person having expertise in the field.  No submissions were received for consideration by the Authority during the investigation.

 

9.             This instrument is compatible with the Human Rights and Freedoms recognised or declared in the International Instruments listed in Section 3 of the Human Rights (Parliamentary Scrutiny Act 2011). A Statement of Compatibility with Human Rights follows.

 

10.         The determining of this Instrument finalises the investigation in relation to porphyria cutanea tarda as advertised in the Government Notices Gazette of 30 June 2010.

 

11.         A list of references relating to the above condition is available to any person or organisation referred to in subsection 196E(1)(a) to (c) of the VEA.  Any such request must be made in writing to the Repatriation Medical Authority at the following address:

 

The Registrar

Repatriation Medical Authority

GPO Box 1014

BRISBANE    QLD    4001

 


Statement of Compatibility with Human Rights

(Prepared in accordance with Part 3 of the Human Rights (Parliamentary Scrutiny) Act 2011)

 

Instrument No:    Statement of Principles No. 43 of 2012

Kind of Injury, Disease or Death:  Porphyria cutanea tarda

 

This Legislative Instrument is compatible with the human rights and freedoms recognised or declared in the international instruments listed in section 3 of the Human Rights (Parliamentary Scrutiny) Act 2011.

Overview of the Legislative Instrument

1. This Legislative Instrument is determined pursuant to subsection 196B(8) of the Veterans' Entitlements Act 1986 (the VEA) for the purposes of the VEA and the Military Rehabilitation and Compensation Act 2004 (the MRCA).

2. This Legislative Instrument:-

  • facilitates claimants in making, and the Repatriation Commission in assessing, claims under the VEA and the MRCA respectively, by specifying the circumstances in which medical treatment and compensation can be extended to eligible persons who have porphyria cutanea tarda;
  • facilitates the review of such decisions by the Veterans' Review Board and the Administrative Appeals Tribunal;
  • outlines the factors which the current sound medical-scientific evidence indicates must as a minimum exist, before it can be said that a reasonable hypothesis has been raised, connecting porphyria cutanea tarda with the circumstances of eligible service rendered by a person, as set out in clause 4 of the Explanatory Notes;
  • replaces Instrument No. 19 of 2001; and
  • reflects developments in the available sound medical-scientific evidence concerning porphyria cutanea tarda which have occurred since that earlier instrument was determined. 

3. The Instrument is assessed as being a technical instrument which improves the medico-scientific quality of outcomes under the VEA and the MRCA. 

Human Rights Implications

4. This Legislative Instrument does not derogate from any human rights. It promotes the human rights of veterans, current and former Defence Force members as well as other persons such as their dependents, including:

  • the right to social security (Art 9, International Covenant on Economic, Social and Cultural Rights; Art 26, Convention on the Rights of the Child and Art 28, Convention on the Rights of Persons with Disabilities) by helping to ensure that the qualifying conditions for the benefit are 'reasonable, proportionate and transparent'[1];
  • the right to an adequate standard of living (Art 11, ICSECR; Art 27, CRC and Art 28, CRPD) by facilitating the assessment and determination of social security benefits;
  • the right to the enjoyment of the highest attainable standard of physical and mental health (Art 12, ICSECR and Art 25, CRPD), by facilitating the assessment and determination of compensation and benefits in relation to the treatment and rehabilitation of veterans and Defence Force members; and
  • the rights of persons with disabilities by facilitating the determination of claims relating to treatment and rehabilitation (Art 26, CRPD).

Conclusion

This Legislative Instrument is compatible with human rights as it does not derogate from and promotes a number of human rights.

 

Repatriation Medical Authority

 

 

 

 

[1] In General Comment No. 19 (The right to social security), the Committee on Economic, Social and Cultural Rights said (at paragraph 24) this to be one of the elements of ensuring accessibility to social security.

Overview

The Veterans' Entitlements Act 1986 (VEA) and the Military Rehabilitation and Compensation Act 2004 (MRCA) established a framework for providing benefits to veterans and members of the Australian Defence Force. To address the issue of porphyria cutanea tarda, a skin condition related to military service, the Repatriation Medical Authority (the Authority) revoked Instrument No. 19 of 2001 and introduced Instrument No. 43 of 2012 under the VEA. This legislative instrument aims to replace the previous Statement of Principles concerning porphyria cutanea tarda and to specify the circumstances in which medical treatment and compensation can be extended to eligible persons. The Authority determined this Instrument after an investigation and considering the latest medical-scientific evidence, ensuring it aligns with human rights and facilitates claims under the VEA and MRCA. The Authority's approach involved public advertising of the investigation and inviting submissions from relevant organisations and individuals, although no submissions were received. The instrument is compatible with human rights, promoting the rights of veterans and their dependents by ensuring reasonable, proportionate, and transparent benefit conditions. The Repatriation Medical Authority Instrument No. 43 of 2012, enacted under the VEA, was introduced to address the gap in the existing framework concerning porphyria cutanea tarda and its relation to military service. This legislative instrument, determined by the Authority, replaces the previous Statement of Principles and specifies the factors necessary to connect the condition with service circumstances. It ensures the medico-scientific quality of outcomes under the VEA and MRCA and promotes the human rights of veterans and their dependents by facilitating the assessment and determination of benefits. This approach helps ensure that the qualifying conditions for benefits are reasonable, proportionate, and transparent, thereby supporting the right to social security, an adequate standard of living, and the highest attainable standard of physical and mental health.

Scope and Application

The Repatriation Medical Authority Instrument No. 43 of 2012, issued under the Veterans' Entitlements Act 1986 and the Military Rehabilitation and Compensation Act 2004, pertains to claims related to porphyria cutanea tarda, a condition that can be associated with particular types of military service. The Instrument applies to veterans and current or former Defence Force members who may have contracted the condition due to their service. This legislation facilitates the assessment and determination of compensation and benefits for those affected by porphyria cutanea tarda, ensuring that claimants can have their cases assessed based on the latest medical-scientific evidence. The Instrument is designed to replace a previous Statement of Principles and incorporates updated factors and definitions relevant to the condition. It applies to the Commonwealth of Australia and is determined for the purposes of both the Veterans' Entitlements Act and the Military Rehabilitation and Compensation Act. The legislation does not specify any exclusions or exemptions but is instead focused on ensuring that the conditions for receiving benefits are clear, reasonable, and proportionate, thereby promoting the human rights of veterans and Defence Force members, including their rights to social security and health.

Key Provisions

The Repatriation Medical Authority (the Authority), under subsection 196B(8) of the Veterans' Entitlements Act 1986 (the VEA), has determined Instrument No. 43 of 2012 concerning porphyria cutanea tarda, replacing Instrument No. 19 of 2001. This Instrument sets out the Statement of Principles for assessing claims related to porphyria cutanea tarda, specifying the factors that must exist for a reasonable hypothesis to be raised that the condition is related to particular kinds of service (clause 4). The Instrument applies to various types of service, including operational, peacekeeping, hazardous, British nuclear test defence service, warlike, and non-warlike service (clause 4). The determination of this Instrument follows an investigation into porphyria cutanea tarda announced in the Government Notices Gazette on 30 June 2010 and completed under section 196G of the VEA. The Instrument imposes specific obligations on claimants and the Repatriation Commission. Claimants must provide evidence that satisfies the factors outlined in the Instrument to support their claim that porphyria cutanea tarda is related to their service. The Repatriation Commission is required to assess claims based on these specified factors and the sound medical-scientific evidence presented. The Instrument also facilitates the review of decisions by the Veterans' Review Board and the Administrative Appeals Tribunal. Breaches of the requirements set forth in this Instrument could lead to consequences such as the denial of claims for medical treatment and compensation related to porphyria cutanea tarda. While the Instrument itself does not specify penalties for non-compliance, the failure to adhere to the outlined criteria may result in the rejection of a claim. The Repatriation Medical Authority and the Repatriation Commission are tasked with ensuring that claims are assessed in accordance with the Statement of Principles, and any failure to do so could be subject to review and potential corrective action. The Instrument ensures compatibility with human rights by not derogating from any human rights and promoting the rights of veterans, current and former Defence Force members, and their dependents. It supports the right to social security, an adequate standard of living, and the highest attainable standard of physical and mental health by facilitating the assessment and determination of benefits and compensation for treatment and rehabilitation. The Authority's determination of the Instrument is in line with international human rights instruments, promoting accessibility and transparency in the benefits process.

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