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PROGRAM OF EXPERIENCE<br />

IN THE PALLIATIVE<br />

APPROACH (PEPA)<br />

The Program of Experience in the <strong>Palliative</strong> Approach (PEPA)<br />

is an initiative of the <strong>Australia</strong>n Government Department<br />

of Health and Ageing’s National <strong>Palliative</strong> <strong>Care</strong> Program.<br />

PEPA aims to improve the quality, availability and access to<br />

palliative care for people who are dying and their families.<br />

To achieve this aim, PEPA provides workforce placements<br />

and structured learning experiences to develop the capacity<br />

of health care professionals to deliver a palliative care<br />

approach.<br />

PEPA has been developed and implemented in two parts.<br />

PEPA 1 commenced in 2003 and provides placements for nurses<br />

and allied health professionals from primary health settings<br />

within specialist palliative care services to gain knowledge,<br />

skills and experience in the palliative approach to care. PEPA<br />

2 commenced in 2005 and involves: (a) clinical placements<br />

with specialist palliative care services and structured learning<br />

experiences for GPs and rural and remote medical officers,<br />

and (b) clinical placements for specialist palliative care staff<br />

to develop skills in selected medical specialities.<br />

Over 750 health care practitioners, one-third from rural<br />

settings, have gained knowledge, skills and experience by<br />

completing a PEPA placement.<br />

PEPA is being evaluated using pre and post-placement<br />

participant, employer and palliative care host site surveys.<br />

Interviews are also being conducted with a sample of<br />

participants, employers and host site personnel to collect indepth<br />

descriptive data. To date, respondents to the evaluation<br />

have reported increased confidence in caring for people with<br />

life limiting illness. This enhanced confidence is related to<br />

participants’ perceived improved assessment skills, abilities<br />

to identify and implement interventions and abilities to<br />

communicate with patients, and the formation of links with a<br />

specialist palliative care service if assistance is required. For<br />

example, one participant has commented that:<br />

‘(I am) more confident to discuss issues with the family and<br />

doctor attending to the client…’ and have ‘more contacts<br />

to access necessary information about care and other<br />

resources.’<br />

The formation of links between primary health care providers<br />

and specialist palliative care services is an important<br />

component of PEPA. Participants have indicated that ongoing<br />

contact with the host site has assisted their practice in areas<br />

such as the management of complex clinical and psychosocial<br />

issues. Some host sites have reported that the networks<br />

formed with primary care providers have enhanced referral<br />

pathways and assisted them to gain an insight into the<br />

issues that the primary health providers face. The following<br />

responses from participants provide examples of host site<br />

assistance following the placement:<br />

• We asked the palliative care team to review a resident<br />

who had difficult pain relief problems. They gave us both<br />

support and advice to enhance care delivery.<br />

• Client in end stage motor neurone disease - assistance and<br />

advice regarding management at home now that client<br />

can’t self care anymore (gave advice about) equipment and<br />

carer support.<br />

Other examples provided suggest PEPA is achieving its<br />

goals in terms of enhancing the capacity of primary health<br />

care providers to provide a palliative approach to care. For<br />

example, respondents have reported:<br />

• Open discussions with staff, residents, family and GPs (on)<br />

how to treat residents with life limiting illness. When a<br />

resident had been admitted to hospital we were told that<br />

this person had not long to live. With the assistance of<br />

the palliative care consultant in the hospital and from the<br />

community we were able to have this resident cared for in<br />

her own room and surrounded by the people she loved.<br />

Since the PEPA program we have had two cases like this<br />

and it has been a great experience for the staff, the residents<br />

and the families.<br />

• Improved competence with use of pain relieving medication<br />

– this has also been helpful in managing non-malignant pain<br />

arthritis and osteoporotic fractures. Able to avoid referral to<br />

hospital emergency department.<br />

Further information on PEPA is available at<br />

www.pepaeducation.com<br />

PCA Staff<br />

PCA’s team consists of (left to right): Nicky Reavell, Project<br />

Officer; Catherine Kennedy, National Office Manager; Anna<br />

Picker, Project Officer, Karen Cooper, Project Manager,<br />

Donna Daniell, Acting Executive Director, Cindee<br />

Richardson, Project Manager; Dylan Malloch, Marketing<br />

and Communications Officer; Camilla Rowland, National<br />

Projects Manager; Fiona Couchman, Policy Officer; Stephanie<br />

Bradford, Administrative Assistant.<br />

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