Search Results for: health information

Complementary Therapies in Cancer Care

Posted on August 25, 2017

“Studies show 77% of cancer patients who incorporate complementary approaches believe it improves their quality of life. 73% state it makes them feel hopeful. 71% say it helps to boost their immune system” (Mao et. al. 2011). In Western Australia Solaris Cancer Care leads the way in providing complementary therapies in cancer care.

Solaris Cancer Care

In July the Cancer Council WA held the ‘Integrative Oncology Symposium: Pathways to Wellness and Survivorship’. The symposium explored new ways to improve symptom control, alleviate patient distress and reduce suffering. The speakers were health professionals and academics who provided their insights into alternative therapies, lessons learnt in the treatment of cancer and patient experience, this included Clinical Professor David Joske founder of Solaris Cancer Care (2001).

“Although excellent resources have long been available to treat cancer medically, it became clear to me that the emotional and supportive care needs of cancer patients and their families were often overlooked.

So Solaris Cancer Care was born – a drop in centre in Sir Charles where cancer patients could receive free support and advice and supervised complementary integrated therapies that would support their mainstream treatment.

It was a radical idea at the time, and still is in some respect. But the idea has continued to grow and over the last 15 years we have opened three additional clinics in Albany, Bunbury and St John of God,” he says (Solaris Cancer Care 2016).

Since its inception Solaris has provided cancer patients with support services and access to complementary integrative therapies. It all started with a comment from a patient, Roy in 1998. Roy said that when he mentioned to one of his treating physicians that he was seeking complementary therapy, they had shut him down. Clinical Prof. Joske said he realised he “needed to get on board with complementary therapy.” By not accepting complementary therapy it had created a barrier between him and his patients so “we weren’t quite rowing in the same direction.”

Solaris Cancer Care Now

Now 100 people per week drop into Solaris, with no medical misadventure. Patients who access the services have a reduction in symptom distress and improved quality of life. Clinical Prof. Joske said during his time treating cancer patients the most valuable lessons he has learnt are from his patients:

  • The power of words and permission to die – What we say to people (and when) matters!
  • A role for complementary medicine – Accept how people cope with cancer.
  • The promise of new biology – cancer is a chronic illness
  • Survivorship

Clinical Prof. Joske closed his presentation with, as Hippocrates said, “Cure sometimes, treat often, comfort always”. For more information about the complementary therapies offered at Solaris Cancer Care go to: solaris care

Lucy Palermo | Marketing & Communications Coordinator | Health Consumers’ Council (WA)

References:

Mao, J, Palmer, C, Healy, K, Desai, K & Amsterdam, J 2011, ‘Complementary and alternative medicine use among cancer survivors: a population-based study’, Journal of Cancer Survivorship: Research and practice, vol. 5, no. 1, pp. 8-17.

Solaris Cancer Care 2017, About Us page, 2016, Solaris Cancer Care. Available from: https://solariscare.org.au/about-us/dr-david-joske/. [28 August 2017]

Mind and Body March 2017 – Ways for consumers to have a voice

Posted on August 13, 2017

In this episode, former staff member Stephanie Newell spoke to Mind and Body Host Cynthia Nixon about  the various ways people can be involved in improving the health system through Health Consumers’ Council (HCC). This included:

  • Reading Group, attending information sessions – e.g. Diversity Dialogues Forums and Focus Groups
  • What being a Consumer Representative means
  • Advocacy – Individual & Systemic
  • What are Consumer Advisory Councils and their country equivalent District Health Advisory Councils?
  • Forthcoming Patient Experience Week events featuring international patient experience community of practice, the Beryl Institute’s CEO Jason Wolf as Keynote speaker
  • Upcoming Orientation to HCC information session

Cultural Diversity

Posted on July 24, 2017

Why do we care about cultural diversity engagement?

At Health Consumers’ Council we believe in inclusion and the best health outcomes for all. WA continues to experience higher than national average population growth through migration and over half of West Australians have one or more parent born overseas. We speak 240 languages across a vast state. Language barriers as well as practices which are not culturally sensitive or inclusive can lead to poor uptake of services and poor health outcomes.

We recognise that the voice of people from Culturally and Linguistically Diverse (CaLD) backgrounds is often left unheard, for example, WA’s Patient Experience in Health Survey specifically excludes people requiring an interpreter. We also have significant concerns about the poor uptake of interpreters in health services and how this impacts on people being able to provide informed consent as patients. Research in the area is also very limited.

What do we do about it?

Health Consumers’ Council is committed to supporting services to assist with effective engagement and care provision to people from diverse cultures. We have developed a range of forums and workshops to assist both health service providers and community members. We are also establishing a panel of CaLD community members who might wish to share lived experience or community perspective in order to improve health services. Click on the links below to find out more.

Information about WA Health System

CaLD Community Workshops and Events

Health Service Provider Workshops and Events

CaLD Community Panel 

 

 

 

Alcohol and Other Drug Consumer & Community Coalition

Posted on July 24, 2017

Background

In 2015, the Health Consumers’ Council was funded to co-ordinate a project to build on the recommendations from the November 2014 Forum, Improving Consumer Involvement in the Alcohol and Other Drug Sector.   An Alcohol and Other Drug Advisory Group (AODAG) comprising government agencies, not for profit organisations and consumers was set up to oversee progress.

The project specifically addressed the following two recommendations:

  1. to develop a common set of principles for engagement
  2. outline best practice engagement strategies for the sector

In 2017 the WA Primary Health Alliance funded HCC to support the ongoing work of the Alcohol and Other Drug Advisory Group (AODAG) to oversee a new project entitled “Improving Consumer Involvement in the Alcohol and Other Drug Sector”.

It was agreed that the term ‘alcohol and other drug consumers’ was inclusive of current users, service users, potential service users, family members and supporters.

The Alcohol and Other Drug Consumer & Community Coalition (AODCCC) was incorporated in June 2018 in response to the need and support for an AOD specific consumer advocacy body. We have recently received funding from the Mental Health Commission in order to progress our establishment and have now released our Mission, Vision and Values.

AODCCC Membership

Membership is open to people who use or who have used alcohol and other drugs, their family members and significant others. A link to an online membership application can be found here and on the Facebook page.  Hard copy applications are available here and can be emailed to info@aodccc.org.

Management Committee

Full details of the current Management Committee are provided on the Australian Charities and Not-for-profit Commission (ACNC) website.

Contact AODCCC

For any information please contact:
Email info@aodccc.org
Phone (08) 6311 8402

Reporting

31st October Report – the first report as per 31st October Mental Health Commission funding deliverables can be found here.

Updates

August update (July activities)

September update (August activities)

October update (September activities)

November update (October activities)

 

Cancer Patient Empowerment

Posted on July 17, 2017

It can be difficult to process the diagnosis of cancer. You are losing control of your body and although you do have choices during the treatment process they are limited. You can’t do the things you used to and you have to accept a new kind of ‘normal’. During this process, it can be difficult to feel empowered as a patient and as a person.

The Path to Patient Empowerment

The path to empowerment includes ‘Surrendering, but only certain elements of your life. It’s not a black and white situation’ says Associate Professor Caroline Bulsara, Notre Dame University. In 2012 Associate Professor Bulsara developed the ‘Patient Empowerment Scale’, for a study to measuring cancer patient empowerment. Using the questionnaire (comprised of 15 scaled questions) she surveyed 210 cancer patients. Through Associate Professor Bulsara’s research into quantifying empowerment she identified these keys to regaining control:

  • Acknowledging what I can and cannot control.
  • Familiarising oneself with the treatment regimen and side effects of treatment.
  • Establish boundaries with family and friends.
  • Learning to recognise what resources and information are and are not relevant.
  • Accepting and adapting to changed lifestyle. (2017, Associate Professor Caroline Bulsara, Notre Dame University)

How Providers Can Support Patient Empowerment

Associate Professor Bulsara identified that patients felt more empowered when all communication was shared with them and well documented. They felt more in control of their condition and had reduced feelings of anxiety. Patients spoke of a sense of empowerment due to their ownership of a paper journal, they called the Patient Held Record (PHR).

However, according to Associate Professor Bulsara more work needs to be done to explore the stages of empowerment during and after active treatment.

You can read more about her research via this link: http://www.ccsenet.org/journal/index.php/cco/article/view/23078

Health Consumers’ Council and Patient Empowerment

It is important to remember that it is your body they are treating. You reap the benefits but also the side effects of that treatment and you may have to live with those side effects for years to come.

Doctors must have your informed consent before you start on any new treatment regime. According to Cordasco, ‘In health care, informed consent refers to the process whereby the patient and the health care practitioner engage in a dialogue about a proposed medical treatment’s nature, consequences, harms, benefits, risks, and alternatives. Informed consent is a fundamental principle of health care’ (Cordasco 2013). This means you have the right to say no and seek a second opinion.

If you are finding it difficult to speak up Health Consumers’ Council can help. We can help you to understand and support your healthcare rights. We can help you find and access health services and assist you in providing feedback about your health experience. This free service is available to anyone in WA. For more information regarding our services and tools to support you click here.

Lucy Palermo | Marketing & Communications Coordinator| Health Consumers’ Council WA

References:

Bulsara, C & Styles, I 2013, ‘Development of a Cancer Related Patient Empowerment Scale Using the Polytomous Rasch Measurement Model’, Cancer and Clinical Oncology, vol. 2, no. 1, pp. 87-102. Available from: Cancer and Clinical Oncology. [13 July 2017]

Cordasco, K 2013, ‘Obtaining Informed Consent from Patients: Brief Update Review’, Making Health Care Safer II: An Updated Critical Analysis of the Evidence for Patient Safety Practices, no. 211. Available from: National Center for Biotechnology Information. [14 July 2017]

Celebrating people who make a difference…

Posted on May 16, 2017

Have you ever encountered a person who absolutely stands out in the way they approach the work they do? There is a noticeable difference in attitude and energy between those who are truly engaged in their role and those who are not… and how difficult must it be to face up every day to something you are not enjoying and you don’t believe in?

This year I have been working with someone who I have never met face to face. We communicate via email and phone and have glimpsed each other once via video conferencing. Why haven’t we met? Because this wonderful person lives in Katanning. Her name is Karen and she has been incredible in her enthusiasm and energy around engaging with people from diverse cultural backgrounds.

Briefly, Katanning is home to people from many different countries, some quite newly arrived while others have become long term residents. It is known as a town that supports cultural diversity and which has been highly successful in doing so. Karen works for the Department of Health in two roles, as a Health Promotion Officer – Culturally and Linguistically Diverse (CaLD) and as a Project Officer, Sexual Health and Blood Borne Virus.

In her role/s Karen has encouraged and supported people from CaLD backgrounds to engage with the health sector with the result that there is now a Multicultural DHAC (District Health Advisory Council) in the Great Southern Region. I suspect this may be the first of its kind in WA and is a fantastic achievement that needs to be celebrated and acknowledged.

Beyond that I would like to say, ‘thank you’ to Karen for the level of interest she has shown in and her support for the work that I do and to acknowledge those things. Also for her willingness to be involved in HCC’s Refugee and Asylum Seeker Health Research Alliance (RAHERA) and her participation in other activities this Program undertakes.

You are really appreciated Karen, thank you. We really value your support.

Footnote: On May 11, I travelled to Katanning and ran information sessions and workshops, also the following day. There I met Karen and she is as dynamic as I suspected!

Click here to read about the work Health Consumers’ Council did with Katanning Senior High School.

Louise Ford | Consumer and Community Engagement Manager

Image Source: https://smallbiztrends.com/2016/11/ways-to-thank-customers.html

How are you improving the Patient Experience? Posters

Posted on May 3, 2017

In 2017 Health Consumers’ Council (WA) invited Hospitals, Health Services & NGO’s to share with other health services, health professionals and consumers how they provide positive patient experiences. They had to answer three simple questions:

  1. Share an initiative that ensures what matters to your patients/consumers is leading to improved patient experience.
  2. What difference has this made?
  3. Share one lesson you have learnt.

The posters were displayed at the Patient Experience Week Community Conversation on April 27, 2017.

If you would like to submit your initiative you can find the forms on this page.

The following services provided information to create the posters below (Click on the links to download a PDF version of the posters):

Bethesda Hospital

Face to Face Bedside Handover Initiative

Bethesda Health Care_Making Consumer Feedback Meaningful

Real Time, Face to Face Consumer Feedback Initiative

 

Cancer Council WA

Cancer Information Hubs Initiative

 

Western Australia Department of Health | Disability Health Network

Disability Health Network

Hospital Stay Guidelines For Hospitals & Disability Service Organisations

 

Western Australia Department of Health | Epidemiology Branch

Patient Evaluation of Health Services (PEHS) Program

Western Australia Department of Health | Patient Safety & Clinical Quality

Patient First Project

Engagement Framework Project

 

East Metropolitan Health Service | Armadale Health Service

Building Collaborative Care with Community Services Project

 

North Metropolitan Health Service

NMHS Disability Liaison Project

 

Osborne Park Hospital | Antepartum Care

Peripartum Satisfaction Tool

 

Princess Margaret Hospital for Children & Curtin University

Calling For Help Program

 

WA Country Health Service | Primary Health & Engagement

Patient Opinion Australia Tool

 

WA Primary Health Alliance | Aboriginal Health

Country Links: Aboriginal Pathways to Care

 

WA Primary Health Alliance | Community Engagement

Patient Opinion Australia Tool

International Mesh Awareness Day – 1st May

Posted on April 30, 2017

Monday 1st May is International Mesh Awareness Day, the start of Mesh Awareness month.  It highlights the complications suffered by women who have had mesh implants to treat stress urinary incontinence and pelvic organ prolapse.

You may have seen a recent episode on The Project which highlighted the little known reality that when a urogynecological mesh implant goes wrong, it can go badly wrong, with life-changing effects for the women affected.  It has taken the recent media activity on the topic for some women to recognise the symptoms in themselves. And despite what Waleed Ally stated in the final moments of the Project episode on the topic, complications can occur quite some time after implanting, and only partial removal options exist for women.

 

The use of mesh is now the subject of a federal Senate Inquiry, which is taking submissions until the 31st May 2017. The Inquiry’s title “Number of women in Australia who have had transvaginal mesh implants and related matters” highlights that we simply don’t know how many women have had these implants, and how many of them have suffered complications.

 

Health Issues Centre Victoria hosted a Facebook Page “Understanding pelvic mesh implants and impacts on women in Australia”. This page is part of a united response by health consumers councils across Australia to ensure women’s voices are at the heart of the Senate Inquiry Submission. It links to an anonymous survey where women and their families are able to provide feedback to inform the joint Submission. The page will be active until the Inquiry Submission deadline of 31st May 2017.

 

Pictured: Caz Chisholm holding both her awards

 

Here in WA, on Thursday 27th April, the Health Consumers’ Council announced our Health Consumer Excellence Awards. The winner of the Health Consumer Award, and the Rosemary Caithness Award to acknowledge outstanding service to health consumers was the same person – Caz Chisholm. Caz is one of the founders of the Australian Pelvic Mesh Support Group, a Facebook page which has grown from 39 members two years ago to just under 600 members in the last week, after the airing of the Project episode. She has spent significant time and energy raising awareness for women about the issue and providing essential peer support. She was also directly responsible for ensuring that the Senate Inquiry was successfully advocated for by Senator Hinch in the first place.

 

For women and families affected by pelvic mesh, we urge you to have your say to ensure the consumer voice is central to the Submission. Check the Having A Say section lower down on this page for the links to the different ways to provide your feedback.

 

Please also note that the health consumers councils across Australia have developed a Consumer Information Sheet which appears below and is also available as a PDF. Please contact us on info@hconc.org.au or 9221 3422 if you have any comments or concerns.

 

Consumer information

For women who have had, or are considering having surgery to treat stress urinary incontinence and pelvic organ prolapse

If you have been diagnosed with pelvic organ prolapse or stress urinary incontinence, the likelihood is that you will be offered surgery once non-surgical options such as physiotherapy have been exhausted.

 

Surgery for these two conditions are usually involves a mesh insertion or implant. It might be called tape or a sling. It is all the same from a consumer perspective and these products are collectively known as mesh. The Therapeutic Goods Advisory Website has an updated list of complications associated with surgery using mesh. https://www.tga.gov.au/alert/urogynaecological-surgical-mesh-complications

 

Mesh implants have been offered to women since the late 1990s. The procedure is considered to be only partially reversible, and some women have travelled to America at their own expense to have mesh removed.

 

Before you consent to any surgical procedure, it is important to ask all the questions you need so you understand what you are consenting to. The Choosing Wisely campaign has created these questions to help you get started. http://www.choosingwisely.org.au/resources/consumers/5-questions-to-ask-your-doctor

 

1.      Do I really need this test or procedure?

Tests may help you and your doctor or other healthcare provider determine the problem and the procedures that may help to treat it.

2.      What are the risks?

Will there be side effects? What are the chances of getting results that aren’t accurate? Could that lead to more testing or another procedure?

3.      Are there simpler, safer options?

Sometimes all you need to do is make lifestyle changes, such as eating healthier foods or exercising more. Another option to ask your doctor about is native tissue repair.

4.      What happens if I don’t do anything?

Ask if your condition might get worse — or better — if you don’t have the test or procedure right away.

Stress urinary incontinence is not a life-threatening condition so consider carefully before undergoing any surgery. Do not consider surgery until all non-surgical options have been exhausted.

5.      What are the costs?

Costs can be financial, emotional or a cost of your time. Where there is a cost to the community, is the cost reasonable or is there a cheaper alternative?

 

What help can I access?

  • There is a Facebook group called the Australian Pelvic Mesh Support Group which can connect you with women who have had these procedures.
  • Shine Lawyers is one of the firms that is currently undertaking class actions in relation to mesh
  • Take this information sheet to your trusted health provider to discuss your current or future options

 

Having A Say

 

Complications associated with use of Pelvic Mesh

These are listed on Australia’s Therapeutic Goods Administration (TGA) website as follows: https://www.tga.gov.au/alert/urogynaecological-surgical-mesh-complications

  • punctures or lacerations of vessels, nerves, structures or organs, including the bladder, urethra or bowel (these may require surgical repair)
  • transitory local irritation at the wound site
  • a ‘foreign body response’ (wound breakdown, extrusion, erosion, exposure, fistula formation and/or inflammation)
  • mesh extrusion, exposure, or erosion into the vagina or other structures or organs
  • as with all foreign bodies, mesh may potentiate an existing infection
  • over-correction (too much tension applied to the tape) may cause temporary or permanent lower urinary tract obstruction
  • acute and/or chronic pain
  • voiding dysfunction
  • pain during intercourse
  • neuromuscular problems including acute and/or chronic pain in the groin, thigh, leg, pelvic and/or abdominal area
  • recurrence of incontinence
  • bleeding including haemorrhage, or haematoma
  • seroma
  • urge incontinence
  • urinary frequency
  • urinary retention
  • adhesion formation
  • atypical vaginal discharge
  • exposed mesh may cause pain or discomfort to the patient’s partner during intercourse
  • mesh migration
  • allergic reaction
  • abscess
  • swelling around the wound site
  • recurrent prolapse
  • contracture
  • scarring
  • excessive contraction or shrinkage of the tissue surrounding the mesh
  • vaginal scarring, tightening and/or shortening
  • constipation/defecation dysfunction
  • granulation tissue formation.

 

Author: Pip Brennan, Executive Director of the Health Consumers’ Council. Consumer Member on the Australian Commission on Safety and Quality in Health Services Reference Committee.

HCC Audio

Posted on March 27, 2017

Meditalk Podcast

Meditalk is a medical podcast for patients – with medical information communicated by medical professionals. Informed patients can make better decisions, this podcast shares local information and knowledge on medial issues affecting us all.

Meditalk | Feb 8 2019, Pip Brennan | Executive Director, Health Consumers’ Council | ‘Making Medical Decisions Best For Me – Choosing Wisely Questions & Informed Consent

Click here to listen to the Feb 2019 episode

Mind & Body – Heritage FM

The team at Health Consumers’ Council feature on the Mind & Body program which airs on Wednesday nights from 6:00pm to 7:00pm on Heritage FM (107.3FM). HCC has a monthly slot with staff members talking about various topics affecting health consumers in WA.

In late 2016, Heritage FM radio presenter Cynthia Keith attended a Consumer Representative Introductory Skills workshop and found it informative and valuable. Impressed by HCC’s work in WA, and the potential and importance of the Consumer Representative, Cynthia created a new radio program ‘Mind and Body’. The pilot episode aired on December 7, featuring Pip Brennan talking about ‘Why it’s important to have consumer perspectives & engagement’.

Mind & Body (Pilot) | Nov 2 2016, Pip Brennan | Executive Director, Health Consumers’ Council | ‘An introduction to Health Consumers’ Council’, Click here to read a summary of the episode

Mind & Body | Dec 7 2016, Pip Brennan | Executive Director, Health Consumers’ Council | ‘Why it’s important to have consumer perspectives & engagement’, Click here to read a summary of the episode

Mind & Body | Jan 4 2017, Pip Brennan | Executive Director, Health Consumers’ Council, Emma Basc, CEO of Women’s Health and Wellbeing Services on ‘Women’s Health‘, Click here to read a summary of the episode

Mind & Body | Feb 1 2017, Louise Ford | Culture and Diversity Manager, Health Consumers’ Council | ‘Healthcare for Culturally & Linguistically Diverse Communities’, Click here to read a summary of the episode.

Unfortunately due to technical issues this episode failed to record.

Mind & Body | Mar 1 2017, Steph Newell | Consumer & Community Engagement Coordinator, Health Consumers’ Council | ‘How you can become involved in improving the health system’, Click here for a summary of the episode.

Mind & Body | Apr 5 2017, Pip Brennan | Executive Director, Health Consumers’ Council | ‘Support services, where can you go for help?‘

You are looking for support… where can you go? You provide the support services…. how do you get the information out? Pip Brennan talks about this and more.

Mind & Body | May 3 2017, Tania Harris | Aboriginal Advocate, Health Consumers’ Council | ‘Advocacy, a day in the life of an Advocate‘, Click here for a summary of the episode.

Mind & Body | Jun 7 2017, Pip Brennan | Executive Director, Health Consumers’ Council | ‘Patient Opinions Matter‘, Click here for a summary of the episode.

Mind & Body | Jul 5 2017, Pip Brennan | Executive Director, Health Consumers’ Council | ‘Aboriginal Health – Closing the Gap‘

Mind & Body | Aug 2 2017, Pip Brennan | Executive Director, Health Consumers’ Council | ‘Sustainable Health Review‘

 

World Tuberculosis Day: Prevention Better Than Cure

Posted on March 24, 2017

World Tuberculosis Day

Today is World Tuberculosis (TB) Day, 2017 is the second year of the “Unite to End TB” campaign. The UN Sustainable Development Goals and the WHO End TB Strategy target is to end TB by 2030. Click here to read more about World Tuberculosis Day and how you can support the “Unite to End TB” and “Leave No One Behind” campaigns.

 

The following article, first published in Health Matters Magazine in 2016, written by Majok Wutchok, (a member of the Sudanese community in Perth) outlines how West Australian Tuberculosis Control Program could be improved from a consumer perspective.

Tuberculosis (TB) is considered the second most deadly disease after HIV/AIDS in developing countries. Every year there is a mass movement of Australian’s travelling overseas on holiday and returning home. A major concern is there isn’t proper health promotion and public health education to protect consumers when they and their relatives return from overseas. Due to the lack of public health education they and their family may not be aware they are coming home infected with a tropical or communicable disease.

 

I recommend the WA Health Department set up a consumer overseas travellers screening task force, to avoid a future catastrophic spread of disease across the state. There is also a need to engage with healthcare providers to empower those infected with Tuberculosis and other communicable diseases and to support and empower their community.

 

Western Australia Tuberculosis Control Program

The current program, ‘Western Australia Tuberculosis Control Program’ is administered by the North Metropolitan Area Health Service (NMAHS). However, the program only endeavours to screen and treat the disease once it has been acquired, it does nothing to educate those at risk on prevention methods. ‘Western Australia Tuberculosis Control Program’ detailed as follows:

 

‘The program manages Tuberculosis in Western Australia and offers a state-wide public health service that operates as a resource centre and clinic. Aspects of the service include:

 

  • Treatment of Active TB: Diagnosis, treatment and case management
  • Surveillance and prevention of TB
  • Active screening of high risk groups
  • Contact tracing
  • Diagnosis and treatment of latent TB infection (preventative therapy)
  • Tuberculin Skin Test (TST), also known as Mantoux testing and BCG vaccinations to selected populations. Training and accreditation can be provided for relevant health professionals.
  • Free Health Service: All services related to the diagnosis, treatment of TB and relevant medications are provided at no charge. (See “Fees and charges related to the diagnosis and management of tuberculosis and leprosy” (Operational Directive OD 0229/09))
  • TB Infection Control
  • Advice on pre-employment screening of Health Care Workers and Tertiary Students
  • Advice on Management of TB risk in health care settings
  • Assistance with contact tracing in health care settings
  • Hansen’s Disease (Leprosy): Outpatient clinic service and consultative advice
  • Consultation: Specialist advice from medical and nursing staff is readily available, including preventative advice, health service education and access to information programs.
  • Policy and Operational Directives: Develop, implement and review policy relevant to TB management and control
  • TB Notification and Enhanced Surveillance data base: Maintenance and reporting on TB epidemiology’

(http://www.health.wa.gov.au/acc/tb/)

 

Prevention is better than Cure

Even in 1918 the thinking regarding Tuberculosis, was ‘Prevention is better than a cure’ (Cobbett, L 1918, British Journal of Tuberculosis, vol. 12, no. 1, pp. 16-19). According to the World Health Organisation (WHO 2014), prevention strategies involve encouraging and conducting research. It has been suggested that integrated intervention programs with consumers and their communities involved can be very beneficial. As opposed to vertical programs which are considered limited, integrated programs are considered far more effective for prevention. However, integrated programs need established communication and consistent health education together with consumers’ participation across all aspects.

 

Engaging Consumers is the key

Regarding primary healthcare and consumers, the involvement of a population group from high-risk consumers is paramount. At the same time public health education and community health promotion are also considered important, and are associated with the continuous use of those preventive measures by the consumer’s communities.

 

In short it is important sustainable prevention measures are taken to educate those at risk, to prevent them catching Tuberculosis and other communicable diseases while travelling, rather than simply screening and treating the disease when it has already been contracted.

 

Majok Wutchok | Consumer Representative | ANUTR | MPH Student

(This article was first published as ‘Consumer Approach Vs Tuberculosis Control in WA’ in HCC Health Matters Magazine 2016 Issue 2)

If you would like assistance partnering with consumers in health, the HCC Consumer & Community Engagement Team can help!

Partnering With Consumers

HCC facilitates on-site workshops that assist health care staff to increase their understanding of effective partnering with consumers in the governance and operational structures of your organisation. Principles of consumer participation within the context of health service accreditation can also be a key component of this bespoke fee for service training. Training can be conducted specifically for board members, executive committee members, management and point of care delivery staff, or with a whole of organisation approach.

Safety And Quality Committees

We can provide new and existing consumer members with information on the elements of quality and why patient safety is a critical area of focus in health care. This fee for service training can be tailored to meet the needs of specific safety and quality committees.

Register Your Interest

Please complete the form here to register your interest in HCC’s workshops.

For Further Information

Please contact the Health Consumers Council Community and Consumer Engagement team on 9221 3422 or email:

Louise Ford: louise.ford@hconc.org.au

Steph Newell: stephanie.newell@hconc.org.au