Statement of Principles concerning dermatomyositis No. 10 of 2014

Administered by Department of Veterans' Affairs

Legislation au F2014L00011 Not in force Legislative Instrument

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REPATRIATION MEDICAL AUTHORITY

 

INSTRUMENT NO. 10 of 2014

 

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. 52 of 2005, determined under subsection 196B(3) of the VEA concerning dermatomyositis.
  2. The Authority is of the view that on the sound medical-scientific evidence available it is more probable than not that dermatomyositis and death from dermatomyositis can be related to particular kinds of service.  The Authority has therefore determined pursuant to subsection 196B(3) of the VEA a Statement of Principles, Instrument No. 10 of 2014 concerning dermatomyositis.  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 exist, and which of those factors must be related to the following kinds of service rendered by a person:

 eligible war service (other than operational service) under the VEA;

 defence service (other than hazardous service and British nuclear test defence service) under the VEA;

 peacetime service under the MRCA,

before it can be said that, on the balance of probabilities, dermatomyositis or death from dermatomyositis is connected with the circumstances of that service.

5.             This Instrument results from an investigation notified by the Authority in the Government Notices Gazette of 18 May 2011 concerning dermatomyositis 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:

  • revising the definition of 'dermatomyositis' in clause 3;
  • new factors 6(a) & 6(e) concerning 'a drug of the statin class';
  • new factors 6(b) & 6(f) concerning 'hydroxyurea', for amyopathic dermatomyositis only;
  • new factors 6(c) & 6(g) concerning 'a drug';
  • revising factor 6(d) concerning 'a malignant neoplasm, other than non-melanotic malignant neoplasm of the skin';
  • new definition of 'amyopathic dermatomyositis' in clause 9;
  • revising the definition of 'relevant service' in clause 9;
  • 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 dermatomyositis in the Government Notices Gazette of 18 May 2011, 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.  One submission concerning 'autoimmune disorders' was 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 dermatomyositis as advertised in the Government Notices Gazette of 18 May 2011.

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. 10 of 2014

Kind of Injury, Disease or Death: Dermatomyositis

 

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 dermatomyositis;
  • 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 exist before it can be said that, on the balance of probabilities, dermatomyositis is connected with the circumstances of eligible service rendered by a person, as set out in clause 4 of the Explanatory Notes;
  • replaces Instrument No. 52 of 2005; and
  • reflects developments in the available sound medical-scientific evidence concerning dermatomyositis 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 Repatriation Medical Authority Instrument No. 10 of 2014, enacted under the Veterans' Entitlements Act 1986 and the Military Rehabilitation and Compensation Act 2004, addresses the issue of dermatomyositis and its relation to military service. The Authority revoked the previous Instrument No. 52 of 2005 and introduced this new instrument based on updated medical-scientific evidence, establishing a Statement of Principles for determining the connection between dermatomyositis and military service. The Statement of Principles outlines the factors that need to be present for a claim to be accepted under the Acts. This legislative instrument facilitates the claims process, ensuring that eligible veterans and Defence Force members can access appropriate medical treatment and compensation for dermatomyositis. The instrument is also compatible with human rights, promoting the rights to social security, an adequate standard of living, and the highest attainable standard of physical and mental health. The Authority conducted an investigation, advertised in the Government Notices Gazette, and invited submissions from relevant organisations and experts. The new instrument reflects changes in medical evidence and includes revised definitions and factors for determining dermatomyositis claims, while ensuring compatibility with human rights as recognised in international instruments. This legislative change aims to improve the quality of medico-scientific outcomes under the Acts and facilitate the review of decisions by the Veterans' Review Board and the Administrative Appeals Tribunal.

Scope and Application

The Repatriation Medical Authority Instrument No. 10 of 2014, concerning dermatomyositis, is determined under subsection 196B(3) of the Veterans’ Entitlements Act 1986 and applies to the Military Rehabilitation and Compensation Act 2004. It applies to veterans, current and former members of the Defence Force, and their dependents who have contracted dermatomyositis as a result of their service, with claims for compensation based on service injuries, diseases, or deaths on or after 1 July 2004 assessed by the Military Rehabilitation and Compensation Commission. This Instrument revises and replaces the previous Instrument No. 52 of 2005, reflecting developments in medical-scientific evidence since its creation. The Instrument outlines the specific factors that must be present for dermatomyositis to be considered connected to service, including the types of service and specific medical conditions or treatments that may be relevant. This instrument facilitates claims, assessments, and reviews under the relevant Acts, ensuring that the qualifying conditions for benefits are reasonable, proportionate, and transparent, thereby promoting the human rights of veterans, current and former Defence Force members, and their dependents.

Key Provisions

The main operative sections of this legislation, Instrument No. 10 of 2014, concern the replacement of the previous Statement of Principles regarding dermatomyositis with a new one, as determined by the Repatriation Medical Authority (the Authority) under subsection 196B(8) of the Veterans’ Entitlements Act 1986 (the VEA). This new Instrument specifies the circumstances under which dermatomyositis, or death from dermatomyositis, can be considered related to particular types of service, namely eligible war service, defence service, and peacetime service (section 4). The Instrument outlines various factors, including exposure to certain drugs or conditions, that must exist for a connection to be established between dermatomyositis and the service (section 6). The Instrument also includes definitions for terms such as 'dermatomyositis', 'amyopathic dermatomyositis', and 'relevant service', clarifying the scope of the conditions covered (sections 3 and 9). This Act imposes obligations on the parties involved, primarily the claimants and the Repatriation Commission. Claimants must ensure that their claims for medical treatment and compensation related to dermatomyositis meet the criteria outlined in the new Statement of Principles. They must provide evidence that satisfies the specified factors connecting their condition to their service. The Repatriation Commission, in turn, is required to assess these claims based on the criteria established by the Authority, ensuring that the claims are evaluated fairly and in accordance with the latest medical-scientific evidence. The Instrument facilitates the review of decisions by the Veterans' Review Board and the Administrative Appeals Tribunal, providing a structured process for challenging and appealing determinations made by the Commission. Breach of the provisions outlined in this Instrument can lead to various consequences, although the specific legal text does not detail particular offences, penalties, or consequences for non-compliance. Generally, failure to adhere to the criteria set forth for claiming benefits related to dermatomyositis could result in the denial of compensation or medical treatment claims. Claimants who do not provide sufficient evidence to meet the specified factors may have their claims rejected. The Act’s emphasis on the sound medical-scientific evidence suggests that any misrepresentation or falsification of evidence could lead to further scrutiny, potential legal consequences, or administrative penalties. The precise penalties or civil/criminal consequences, however, would depend on the broader legislative framework governing veterans' benefits and administrative law in Australia.

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