Preliminary Pages
Foreword
Polio is a crippling and potentially fatal infectious
disease. During the 20th Century Australia experienced a number of
polio epidemics, affecting many thousands of individuals. International efforts
to eradicate polio have been highly successful, largely due to effective
vaccines developed in the 1950s and 1960s. These efforts led to a 99 per cent decrease
in the number of polio cases worldwide between 1988 and 2010. Australia was officially
declared polio-free by the World Health Organisation in 2000.
Despite the eradication of polio in Australia, the disease
has left a legacy. Many years after contracting the initial infection and
apparently reaching a stable state of recovery, an increasing number of polio
survivors are now developing new symptoms. These symptoms, including muscle
weakness and pain, fatigue and respiratory compromise, characterise the late
effects of polio (LEOP) or post-polio syndrome (PPS). Although it is unclear
just how many polio survivors in Australia are affected, LEOP/PPS is a
potentially debilitating condition. Even so, the level of awareness about
LEOP/PPS among health professionals and the wider community is very low.
In view of this, the Health and Ageing Committee, which I
Chair, expressed interest in learning more about LEOP/PPS and its impact on
polio survivors, their families and carers. Accordingly, on 30 March 2012 the
Committee held a roundtable discussion in Melbourne. Participants at the roundtable
included representatives of Polio Australia and associated state-based
post-polio networks, which between them provide support and advocacy for
Australia’s polio survivors. A number of roundtable participants identified
themselves as polio survivors directly affected by LEOP/PPS. The roundtable
also included representation from health professionals involved with the
treatment and clinical management of LEOP/PPS, as well as a representative of
the Australian Government Department of Health and Ageing. The roundtable
discussions have formed the basis of the Committee’s discussion paper, which I
trust adequately reflects the range and scope of issues considered.
On behalf of the Committee I wish to thank all of the
roundtable participants. The commitment of participants to providing support
and advocacy for polio survivors was evident. In particular the Committee
appreciates the contribution made by those directly affected by LEOP/PPS.
Despite struggling by the end of the day with LEOP/PPS associated fatigue, the
knowledge and experience of this group of individuals provided the Committee
with invaluable insights. The Committee also acknowledges and thanks the
observers who attended the day’s proceedings, including polio survivors, their
family members and carers.
Steve Georganas MP
Chair
Membership of the Committee
Chair
|
Mr Steve Georganas MP
|
|
Deputy
Chair
|
Mr Steve Irons MP
|
|
Members
|
Mr Mark Coulton MP
|
Mr Geoff Lyons MP
|
|
Ms Jill Hall MP
|
Mr Ken Wyatt MP
|
|
Ms Deborah O’Neill MP
|
|
Committee Secretariat
Secretary
|
Dr Alison Clegg
|
Inquiry
Secretary
|
Mr Muzammil Ali
|
Research
Officer
|
Ms Belynda Zolotto
|
Administrative
Officer
|
Ms Fiona McCann
|
List of abbreviations
ABS
|
Australian Bureau of Statistics
|
CPAP
|
Constant Positive Airway Pressure
|
DoHA
|
[Australian Government]
Department of Health and Ageing
|
FaHCSIA
|
[Australian Government]
Department of Families, Housing, Community Services and Indigenous Affairs
|
GPEI
|
Global Polio Eradication
Initiative
|
HWA
|
Health Workforce Australia
|
LEOP
|
Late Effects of Polio
|
MASS
|
[Queensland Government] Mobility
Aids Subsidy Scheme
|
OT
|
Occupational Therapist
|
PCEHR
|
Personally Controlled Electronic
Health Record
|
PPS
|
Post-Polio Syndrome
|
SWEP
|
[Victorian Government] State Wide
Equipment Program
|
PSV
|
Polio Services Victoria
|
WHO
|
World Health Organisation
|
List of recommendations
Recommendation 1
The Committee recommends that the Australian Bureau of
Statistics and/or the Australian Institute of Health and Welfare establish
mechanisms through inclusion of appropriate questions in existing health and/or
disability surveys to estimate and report on the size of the population of
polio survivors living in Australia, and the proportion of that population
experiencing the late effects of polio/post-polio syndrome.
Recommendation 2
The Committee recommends that the relevant National Boards, in
consultation with key stakeholders including peak professional bodies,
medical/health educators and training providers, seek to ensure curricula for
students includes information on the late effects of polio/post-polio syndrome,
to raise awareness of the condition as a possible diagnostic outcome and of
best practice for treatment and management.
Recommendation 3
The Committee recommends that Medicare Locals actively engage
with Polio Australia and the state-based post-polio associations, with state
and territory government departments of health, and with general practitioners
to promote activities which will raise awareness of the late effects of
polio/post-polio syndrome:
among
practicing health professionals through continuing professional development;
and
in
the community through patient education, noting the need to tailor
communication to enhance engagement with specific population groups taking into
account demographic factors such as age and cultural background.