Statement of Principles concerning sensorineural hearing loss No. 5 of 2011

Administered by Department of Veterans' Affairs

Legislation au F2010L03252 Not in force Legislative Instrument

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REPATRIATION MEDICAL AUTHORITY

 

INSTRUMENT NO. 5 of 2011

 

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. 29 of 2001, determined under subsection 196B(2) of the VEA concerning sensorineural hearing loss.

 

2.             The Authority is of the view that there is sound medical-scientific evidence that indicates that sensorineural hearing loss and death from sensorineural hearing loss 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. 5 of 2011 concerning sensorineural hearing loss.  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;

 warlike service under the MRCA;

 non-warlike service under the MRCA,

 

before it can be said that a reasonable hypothesis has been raised connecting sensorineural hearing loss or death from sensorineural hearing loss, with the circumstances of that service.

 

5.             This Instrument results from an investigation notified by the Authority in the Government Notices Gazette of 25 June 2008 concerning sensorineural hearing loss 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 'sensorineural hearing loss' in clause 3;
  • revising factors 6(a) & 6(dd) concerning 'peak sound pressure level at the tympanic membrane';
  • revising factors 6(b) & 6(ee) concerning 'sound pressure level at the tympanic membrane as an 8-hour time-weighted average';
  • revising factors 6(c) & 6(ff) concerning 'otitic barotrauma or decompression sickness';
  • revising factors 6(d) & 6(gg) concerning 'a course of treatment with a drug or a drug from a class of drugs';
  • revising factors 6(e) & 6(hh) concerning 'a specified ototopical medication';
  • new factors 6(f) & 6(ii) concerning 'taking aspirin, paracetamol or a nonsteroidal anti-inflammatory drug';
  • revising factors 6(g) & 6(jj) concerning 'suppurative labyrinthitis';
  • revising factors 6(h) & 6(kk) concerning 'chronic suppurative otitis media';
  • revising factors 6(i) & 6(ll) concerning 'acute viral infection';
  • revising factors 6(j) & 6(mm) concerning 'meningitis';
  • revising factors 6(k) & 6(nn) concerning 'neurosyphilis';
  • revising factors 6(l) & 6(oo) concerning 'tuberculosis';
  • new factors 6(m) & 6(pp) concerning 'diphtheria';
  • revising factors 6(n) & 6(qq) concerning 'leprosy';
  • revising factors 6(o) & 6(rr) concerning 'Meniere's disease';
  • revising factors 6(p) & 6(ss) concerning 'Paget's disease of bone';
  • revising factors 6(q) & 6(tt) concerning 'a specified autoimmune disorder';
  • new factors 6(r) & 6(uu) concerning 'multiple sclerosis';
  • new factors 6(s) & 6(vv) concerning 'diabetes mellitus';
  • revising factors 6(t) & 6(ww) concerning 'a hyperviscosity syndrome';
  • revising factors 6(u) & 6(xx) concerning 'a lesion interrupting the supply of blood to the cochlea';
  • revising factors 6(v) & 6(yy) concerning 'structural injury or physiological disruption to the inner ear or the auditory nerve';
  • revising factors 6(w) & 6(zz) concerning 'a neoplasm that involves the auditory nerve';
  • new factors 6(y) & 6(bbb) concerning 'inhaling, ingesting or having cutaneous contact with a specified organic solvent';
  • new factors 6(z) & 6(ccc) concerning 'inhaling, ingesting or having cutaneous contact with lead or emissions containing lead';
  • new factors 6(aa) & 6(ddd) concerning 'smoking cigarettes or the equivalent thereof in other tobacco products';
  • new factors 6(bb) & 6(eee) concerning 'consuming alcohol';
  • new factors 6(cc) & 6(fff) concerning 'being vaccinated with the measles-mumps vaccine';
  • new definitions of 'a drug or a drug from a class of drugs from the specified list', 'a hyperviscosity syndrome', 'a specified autoimmune disorder', 'a specified ototopical medication', 'a specified organic solvent', 'alcohol', 'antineoplastic agents as specified', 'dB(A)', 'dB(C)', 'meningitis', 'neurosyphilis' and 'pack-years of cigarettes, or the equivalent thereof in other tobacco products' in clause 9;
  • revising definitions of 'chronic suppurative otitis media', 'relevant service' and 'specified list of viruses' in clause 9;
  • deleting definitions of 'adequate ear protection', 'an ototoxic drug from the specified list', 'bacterial meningitis', 'hyperviscosity syndrome', 'ICD-10-AM code', 'impulsive noise', 'Meniere's disease', 'neoplasm affecting the auditory apparatus', 'Paget's disease of the skull', 'perilymph fistula', 'systemic immune mediated disorder' and 'tuberculosis involving the temporal bone'; 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 sensorineural hearing loss in the Government Notices Gazette of 25 June 2008, 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 was received for consideration by the Authority during the investigation.

 

9.             The determining of this Instrument finalises the investigation in relation to sensorineural hearing loss as advertised in the Government Notices Gazette of 25 June 2008.

 

10.         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 Secretariat

GPO Box 1014

BRISBANE    QLD    4001

Overview

The Repatriation Medical Authority Instrument No. 5 of 2011, issued under the Veterans' Entitlements Act 1986 and the Military Rehabilitation and Compensation Act 2004, addresses the issue of sensorineural hearing loss by establishing a new Statement of Principles to replace the previously revoked Instrument No. 29 of 2001. This instrument was enacted to ensure that there is sound medical-scientific evidence linking sensorineural hearing loss to specific types of service, thus enabling veterans and service personnel to make informed claims regarding their entitlements. The Repatriation Medical Authority, acting under the authority vested in it by the relevant Acts, determined this Statement of Principles following an investigation notified in the Government Notices Gazette on 25 June 2008. The policy objective behind this instrument is to provide clear and updated criteria for the acceptance of liability for claims related to sensorineural hearing loss, facilitating a more accurate and evidence-based assessment process.

Scope and Application

The Repatriation Medical Authority Instrument No. 5 of 2011, concerning sensorineural hearing loss, is a significant legislative development under the Veterans' Entitlements Act 1986 and the Military Rehabilitation and Compensation Act 2004. It applies to veterans, service personnel, and their dependents who have sustained sensorineural hearing loss as a result of specific types of service, including operational, peacekeeping, hazardous, warlike, and non-warlike service. The Instrument outlines the conditions and circumstances that must be met to establish a connection between sensorineural hearing loss or death from such loss and the service rendered. It effectively replaces a previously revoked instrument and sets out revised factors and definitions to reflect the latest medical-scientific evidence. The Instrument is applicable nationally and is determined by the Repatriation Medical Authority for the purposes of both the Veterans' Entitlements Act and the Military Rehabilitation and Compensation Act. It excludes any claims related to services conducted before 1 July 2004, which are governed by different legislative provisions.

Key Provisions

The Repatriation Medical Authority (the Authority) under subsection 196B(8) of the Veterans' Entitlements Act 1986 (VEA) has revoked Instrument No. 29 of 2001, concerning sensorineural hearing loss, and issued Instrument No. 5 of 2011 as a replacement. This new instrument outlines the Statement of Principles for sensorineural hearing loss, which replaces the previous one. The determination of these principles is in accordance with subsection 196B(2) of the VEA, and is based on sound medical-scientific evidence indicating a link between sensorineural hearing loss, death from sensorineural hearing loss, and certain types of military service. The Statement of Principles sets out specific factors that must exist and be related to the service rendered by a person for a reasonable hypothesis to be raised connecting sensorineural hearing loss or death from sensorineural hearing loss with the circumstances of that service. These factors pertain to operational service, peacekeeping service, hazardous service under the VEA, warlike service, and non-warlike service under the Military Rehabilitation and Compensation Act 2004 (MRCA). The new instrument adopts a revised format and includes updates to definitions, factors, and other elements to reflect the latest medical-scientific evidence. The obligations imposed by the Act on the parties and entities it governs include adherence to the Statement of Principles for determining claims for compensation related to sensorineural hearing loss. The Military Rehabilitation and Compensation Commission must use these principles when deciding claims under section 319 of the MRCA for service injuries, diseases, or deaths that occurred on or after 1 July 2004. Claimants must demonstrate that the factors outlined in the Statement of Principles apply to their specific circumstances of service to substantiate their claims. Breaches of the obligations and requirements set out in the Act can lead to civil or criminal consequences, though the specific penalties are not detailed in the provided text. In general, non-compliance with legislative requirements can result in penalties as prescribed by the relevant statutes, including fines and, in severe cases, imprisonment. The exact penalties would depend on the nature and severity of the breach, and would be determined in accordance with the provisions of the VEA and the MRCA.

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