Statement of Principles concerning atrial fibrillation and atrial flutter No. 50 of 2014

Administered by Department of Veterans' Affairs

Legislation au F2014L00482 Not in force Legislative Instrument

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REPATRIATION MEDICAL AUTHORITY

 

INSTRUMENT NO. 50 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. 20 of 2003 determined under subsection 196B(3) of the VEA concerning atrial fibrillation, and Instrument No. 72 of 2002 determined under subsection 196B(3) of the VEA concerning atrial flutter.

 

2.             The Authority is of the view that on the sound medical-scientific evidence available it is more probable than not that atrial fibrillation and atrial flutter and death from atrial fibrillation and atrial flutter 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. 50 of 2014 concerning atrial fibrillation and atrial flutter.  This Instrument will in effect replace the revoked Statements 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, atrial fibrillation and atrial flutter or death from atrial fibrillation and atrial flutter is connected with the circumstances of that service.

 

5.             This Instrument results from investigations notified by the Authority in the Government Notices Gazette of 18 May 2011 concerning atrial fibrillation and in the Government Notices Gazette of 30 June 2010 concerning atrial flutter, in accordance with section 196G of the VEA.  The investigations 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 Instruments.  Comparing this Instrument and the revoked Instruments, the differences include:

 

  • combining the separate Instruments for atrial fibrillation and atrial flutter into an Instrument entitled 'atrial fibrillation and atrial flutter';
  • adopting the latest revised Instrument format, which commenced in 2005;
  • new definition of 'atrial fibrillation and atrial flutter' in clause 3;
  • revising factor 6(a) concerning 'valvular heart disease';
  • revising factor 6(b) concerning 'ischaemic heart disease';
  • revising factor 6(c) concerning 'myocarditis';
  • revising factor 6(d) concerning 'cardiomyopathy';
  • new factor 6(e) concerning 'familial hypertrophic cardiomyopathy', for clinical onset only;
  • revising factor 6(f) concerning 'cardiac failure';
  • new factors 6(g) & 6(dd) concerning 'hypertension';
  • new factors 6(h) & 6(ee) concerning 'pericarditis';
  • revising factor 6(i) concerning 'hyperthyroidism, thyrotoxicosis, Graves' disease or thyrotoxic goitre';
  • new factors 6(j) & 6(gg) concerning 'subclinical hyperthyroidism';
  • revising factor 6(k) concerning 'alcohol';
  • revising factor 6(l) concerning 'cardiac or thoracic surgery';
  • new factors 6(m) & 6(jj) concerning 'a surgical procedure';
  • revising factor 6(n) concerning 'chronic obstructive pulmonary disease';
  • new factor 6(o) concerning 'physical activity';
  • new factors 6(p) & 6(ll) concerning 'sick sinus syndrome';
  • new factors 6(q) & 6(mm) concerning 'a benign or malignant neoplasm';
  • new factors 6(r) & 6(nn) concerning 'a non-neoplastic mass lesion';
  • new factors 6(s) & 6(oo) concerning 'diabetes mellitus';
  • new factors 6(t) & 6(pp) concerning 'penetrating trauma';
  • new factors 6(u) & 6(qq) concerning 'non-penetrating blow to the chest';
  • new factors 6(v) & 6(rr) concerning 'a spinal cord injury';
  • new factors 6(w) & 6(ss) concerning 'an injury or illness';
  • new factors 6(x) & 6(tt) concerning 'being obese';
  • new factor 6(y) concerning 'valvular heart disease', for clinical worsening;
  • new factor 6(z) concerning 'ischaemic heart disease', for clinical worsening;
  • new factor 6(aa) concerning 'myocarditis', for clinical worsening;
  • new factor 6(bb) concerning 'cardiomyopathy', for clinical worsening;
  • new factor 6(cc) concerning 'cardiac failure', for clinical worsening;
  • new factor 6(ff) concerning 'hyperthyroidism, thyrotoxicosis, Graves' disease or thyrotoxic goitre', for clinical worsening;
  • new factor 6(hh) concerning 'alcohol', for clinical worsening;
  • new factor 6(ii) concerning 'cardiac or thoracic surgery', for clinical worsening;
  • new factor 6(kk) concerning 'chronic obstructive pulmonary disease', for clinical worsening;
  • deleting the factor concerning 'congenital heart disease' as it is now covered by factor 6(e) concerning 'familial hypertrophic cardiomyopathy';
  • deleting the factor concerning 'emphysema' as it is now covered by factors 6(n) & 6(kk) concerning 'chronic obstructive pulmonary disease';
  • deleting the factor concerning 'atrial fibrillation';
  • new definitions of 'alcohol', 'being obese', 'death from atrial fibrillation and atrial flutter', 'ICD-10-AM code', 'MET', 'spinal cord injury', 'subclinical hyperthyroidism' and 'valvular heart disease' in clause 9;
  • revising the definition of 'relevant service' in clause 9;
  • deleting the definitions of 'chronic bronchitis with pulmonary obstruction', 'death from atrial fibrillation', 'death from atrial flutter' and 'hyperthyroidism'; 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 atrial fibrillation in the Government Notices Gazette of 18 May 2011 and its intention to undertake an investigation in relation to atrial flutter in the Government Notices Gazette of 30 June 2010, and circulated a copy of the notices 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.             On 9 January 2014, the Authority wrote to organisations representing veterans, service personnel and their dependants regarding the proposed Instrument and the medical-scientific material considered by the Authority. This letter emphasised the deletion of a factor relating to atrial fibrillation in respect of the clinical onset of atrial flutter. The Authority provided an opportunity to the organisations to make representations in relation to the proposed Instrument prior to its determination. No submissions were received for consideration by the Authority. Minor typographical changes were made to the proposed Instrument following this consultation process.

 

10.         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.

 

11.         The determining of this Instrument finalises the investigations in relation to atrial fibrillation as advertised in the Government Notices Gazette of 18 May 2011 and in relation to atrial flutter as advertised in the Government Notices Gazette of 30 June 2010.

 

12.         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. 50 of 2014

Kind of Injury, Disease or Death: Atrial fibrillation and atrial flutter

 

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 atrial fibrillation or atrial flutter;
  • 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, atrial fibrillation or atrial flutter 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. 20 of 2003 concerning atrial fibrillation and Instrument No. 72 of 2002 concerning atrial flutter; and
  • reflects developments in the available sound medical-scientific evidence concerning atrial fibrillation and atrial flutter which have occurred since those earlier instruments were 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. 50 of 2014 was enacted to address the issue of atrial fibrillation and atrial flutter in the context of veterans' entitlements and military rehabilitation. This instrument, determined under subsection 196B(3) of the Veterans’ Entitlements Act 1986, revokes earlier instruments concerning these conditions and introduces a new Statement of Principles. The Authority determined this Statement based on the latest medical-scientific evidence, concluding that these conditions can be related to particular kinds of service. The enacting body is the Repatriation Medical Authority, acting under the authority granted by the Veterans’ Entitlements Act 1986. The policy objective is to facilitate the assessment and determination of claims for compensation related to service injuries, diseases, or deaths, ensuring that claimants receive appropriate benefits based on sound medical evidence. This instrument ensures that the qualifying conditions for benefits are reasonable, proportionate, and transparent, thereby promoting the human rights of veterans and service personnel, including their right to social security and an adequate standard of living.

Scope and Application

The Repatriation Medical Authority Instrument No. 50 of 2014, determined under the Veterans' Entitlements Act 1986 (VEA) and the Military Rehabilitation and Compensation Act 2004 (MRCA), addresses the connection between atrial fibrillation, atrial flutter, and certain types of military service. This Instrument applies to veterans, service personnel, and their dependents who are eligible for compensation under the VEA and MRCA, specifically in cases where service is connected to these conditions. The Instrument replaces previous Statements of Principles concerning atrial fibrillation and atrial flutter, providing updated medical-scientific evidence to determine the circumstances under which these conditions can be related to service. It outlines specific factors, including types of service and medical conditions, that must exist for a claim to be considered valid. The Instrument also extends its application to claims for compensation that commenced on or after 1 July 2004. Notably, this legislative instrument is compatible with human rights, promoting the rights of veterans and service personnel to social security, adequate living standards, and the highest attainable standard of health.

Key Provisions

The Repatriation Medical Authority Instrument No. 50 of 2014 establishes a new Statement of Principles concerning atrial fibrillation and atrial flutter, as provided for under subsection 196B(3) of the Veterans’ Entitlements Act 1986 (VEA). This Statement of Principles replaces the previously revoked Instruments No. 20 of 2003 and No. 72 of 2002. It sets out the circumstances in which atrial fibrillation, atrial flutter, and death from these conditions can be connected to particular kinds of service. This includes eligible war service, defence service, and peacetime service, as defined under the VEA and the Military Rehabilitation and Compensation Act 2004 (MRCA). The Statement of Principles outlines the factors that must exist for it to be said, on the balance of probabilities, that atrial fibrillation, atrial flutter, or death from these conditions is connected with the service rendered. This includes specific conditions such as valvular heart disease, ischaemic heart disease, and others listed in clause 4 of the explanatory notes. The Instrument also includes new definitions and factors that reflect the latest medical-scientific evidence. The Authority consulted with relevant organisations and invited submissions but did not receive any for consideration. The obligations imposed by this Instrument on parties such as claimants and the Repatriation Commission include adherence to the outlined factors and conditions for claims of atrial fibrillation and atrial flutter related to service. This involves ensuring that the claims are based on the sound medical-scientific evidence as specified in the Statement of Principles. The Authority must also ensure that the process of determining and reviewing claims is transparent and that claimants have access to necessary information and support. There are no specific offences or penalties mentioned in the text for breach of the provisions of this Instrument. However, the determination of claims under the VEA and the MRCA involves legal processes and potential for review by the Veterans' Review Board and the Administrative Appeals Tribunal. Any failure to comply with the specified conditions or provide necessary evidence could result in the rejection of a claim, which might have significant implications for the claimant, including the denial of medical treatment and compensation. This Instrument is designed to improve the medico-scientific quality of outcomes under the VEA and the MRCA, ensuring that benefits are extended to eligible persons in a reasonable, proportionate, and transparent manner. It promotes the human rights of veterans and Defence Force members by facilitating the assessment and determination of social security benefits and compensation related to treatment and rehabilitation.

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