Event

Accelerating Australia’s next Cochlear

Accelerating Australia’s next Cochlear

What is the Health 10x secret sauce and how are we enabling Australia’s next generation of innovative health startups?

Health 10x is on a mission to accelerate Australia’s next Cochlear. Health 10x was designed to support startups focused on solving the world’s biggest health challenges. Delivered in partnership by UNSW Founders and The George Institute for Global Health, supported by MTP Connect’s REDI program, Health 10x supports entrepreneurs to build the skills, networks and capital to turn an idea into a global, scalable business. 

By facilitating collaboration between startups, clinicians and academics, our participants are developing health solutions that could improve the lives of millions of people around the world. 

Join us to learn just how we do it and hear from startups including nuroflux and Cardiobionic who are disrupting health systems and challenging the global health landscape.

Keynote speaker: Bruce Neal

Speakers: Pete Ayre (Cardiobionic), Sam van Bohemen (nuroflux)

Facilitator: Dina Titkova (UNSW Founders)


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Event

Seminar: Evidence-based Primary Health Care Systems for Attaining and Sustaining Universal Health Coverage

evidence based PHC seminar

About the seminar

Comprehensive and holistic primary health care (PHC) system is an ally in the achievement of universal health coverage (UHC) and sustainable development goals (SDGs).  

PHC is a broad concept within the realms of public health which has immense potential to alleviate not only the financial distress on individuals but also for governments in pursuit of efficient strategies for better health care and outcomes. It addresses the most significant determinants of health, focusing on person-centric rather than disease-centric approaches. India was one of the first countries to endorse comprehensive PHC in the first national health policy of 1983. The subsequent policies of 2002, 2017 shifted their focus from selective PHC, to the present health policy – Ayushman Bharat 2018 which enshrines the concept of ‘comprehensive approach for the well-being of communities’.   

There is an increasing need for policymakers and implementing agencies to understand what works; and for academia to create robust evidence in alignment with the policymakers’ needs.

Evidence-based primary healthcare policies ensure resiliency, which is vital to improving quality of life, efficient use of resources, and equitably meeting population health needs, especially for those living in remote locations. 

This policy event hosted by The George Institute for Global Health, India which also hosts the Secretariat of the Primary Health Care Research Consortium (PHCRC) will see discussion on the need for using local and contextual evidence for strengthening primary health care to attain and sustain universal health coverage in India. Importantly, it will highlight the importance of political stewardship in creating equitable, resilient, and comprehensive PHC systems.

Speakers

  • Prof Robert Mash

    Chair, Primary Care and Family Medicine Network (Primafamed), Sub-Saharan Africa

  • Dr Rajeev Sadanandan

    CEO, Health Systems Transformation Platform

  • Dr Neha Dumka

    Senior Consultant, NHSRC

  • Prof Sanjiv Kumar

    Chairman and Managing Trustee, Three Domain Health Leadership Foundation

  • Dr Shilpa Karvande

    Research officer, FRCH

  • Dr Krishna Reddy Nallamalla

    Regional Director, ACCESS Health Int

  • Prof Indranil Mukhopadhyay

    Professor, OP Jindal Global University

  • Prof Arnab Mukherji

    Faculty, Indian Institute of Management, Bangaluru

  • Dr Josyula K Lakshmi

    Senior Research Fellow, The George Institute for Global Health, India

  • Moderator: Dr Praveen D

    Program Director, Better Care India The George Institute for Global Health, India

Funding improve outcomes for people with cardiovascular disease

Funding will help improve outcomes for people with cardiovascular disease

Three George Institute researchers have scored finding from the Australian Government’s Medical Research Futures Fund to find new ways of treating high blood pressure and stroke, and preventing brain injury after cardiac arrest.

Will new wearable cuffless devices transform blood pressure control?

Uncontrolled high blood pressure or hypertension is a leading cause of death. Around one in three Australians have the condition and it’s the most common problem managed by General Practitioners (GPs).

If all Australians currently living with high blood pressure were properly treated, as many as 83,000 lives could be saved resulting in a $91.6 billion return. But GPs are hesitant to start or intensify blood pressure treatment after high readings in the clinic due to uncertainty about the reliability of these readings.

All major hypertension guidelines now recommend out-of-office blood pressure measurement, such as home blood pressure monitoring or 24-hour monitoring. The next generation of wrist-worn wearable blood pressure devices without a cuff hold promise as they are calibrated with a cuff and then take hundreds of blood pressure readings in a week without the user being aware. But the Australian marketplace is dominated by devices that are not validated for accuracy.

Professor Alta Schutte will lead the NEXTGEN-BP trial to assess the effectiveness of using a new strategy to manage high blood pressure in primary care. GPs will be guided on medication prescriptions based on hundreds of home blood pressure readings taken from a wrist-worn device, and this will be compared to usual care in around 600 patients over 12 months.

It is hoped that if successful, long-term automated blood pressure readings at home could be rapidly translated into practice, particularly in rural and remote communities, and facilitated through GP telehealth services.

Can machine learning can help guide treatment decisions after a bleed in the brain?

Stroke due to intracerebral haemorrhage (ICH), or spontaneous bleeding into the brain, affects several thousand people in Australia each year. It accounts for greater death and disability than the more common acute ischaemic stroke, caused by a blockage of a blood vessel to the brain. There are fewer proven treatments for ICH, it often affects younger adults, and there are high risks of recurrent serious cardiovascular events.

Clinicians are often faced with making difficult decisions for critically unwell patients with ICH arriving at the hospital. They also need to discuss sensitive topics with family members based on likely outcomes for their loved ones, such as withdrawing active treatment or sending them directly to a nursing home without any rehabilitation.

Although a range of scales or prediction tools have been developed to guide clinicians in managing patients with acute ICH, they have limited use as they are not particularly sensitive, include only a few variables, and are not adaptable to the changing condition of the patient.

Professor Craig Anderson will lead a study using deep learning - a subfield of machine learning - that integrates brain imaging and clinical datasets using a complex structure of algorithms modelled on the human brain to make predictions and help guide treatment decisions for ICH patients.

The funding will help the team develop a prototype device ready to scale up for testing in a large study to determine prediction accuracy and utility in routine clinical practice.

Preventing brain injury from lack of oxygen after cardiac arrest

Over 24,000 Australians will have a cardiac arrest in the community each year. Just over a third will be resuscitated and admitted to hospital, most unconscious and needing treatment in an ICU. Just forty per cent of those admitted to ICU will be discharged alive.

ICU admission costs alone exceed $120,000 for an average 10-day stay. The ongoing community-based costs for those with resulting brain injury is $34,000 per patient each year. Given the devastating mortality, longer term health impact and financial costs involved, treatment strategies that prevent brain injury, improve survival, and reduce costs, are vitally important.

While sedation, temperature and blood pressure control are widely used in intensive care units to improve outcomes in people who have had a cardiac arrest, the optimum targets for these interventions are unknown.

Dr Manoj Saxena will lead the Australian arm of the STEPCARE trial, involving The George Institute for Global Health, Lund University in Sweden, and Helsinki University, Finland. The combined teams will recruit over 3,000 patients to assess the effects of these interventions on survival, functional recovery, brain function, and health-related quality of life after cardiac arrest.

The results are set to inform intensive care policy and practice not only in in Australia but also around the world.

lungs

Preventing heart disease in people suffering from chronic respiratory disease

PACE - Preventing Adverse Cardiac Events in COPD

About the study

Chronic Obstructive Pulmonary Disease (COPD) is the third-leading cause of global health-related disease and deaths. Heart disease is very common in people diagnosed with COPD and is often the cause of health-related sickness and hospitalisations, causing 30 – 50% of deaths. Studies repeatedly show that heart disease is often not diagnosed in persons with COPD, and when it is diagnosed it is often under-treated. People with COPD are also commonly not included in clinical trials of drugs which treat heart disease and heart-related deaths.

Beta (β)-blockers are medications often used to treat heart disease. In this study, we will be investigating whether pro-active treatment with a β-blocker in people with COPD can reduce heart-related events, such as strokes and heart attacks. This is important for people with COPD with either known or unknown underlying heart disease. The study also aims to investigate whether this treatment influences number of respiratory flare ups (exacerbations), hospitalisations, or pharmacological treatment.

Recruitment criteria

  • Diagnosed with COPD
  • Age between 40 to 85 years
  • Had a COPD flare up or exacerbation requiring treatment from their GP or hospital, in the last 2 years, and who can attend for visits and take the study medication over a two year period.

What’s involved?

If eligible for the study, you will be randomly allocated to either take a heart medication or matching placebo medication for a two-year period. You will have to complete some breathing function tests and have an ECG at various time points throughout the study, as well as complete other study assessments. To complete these tests and assessments you will need to attend a respiratory clinic. Over the two years you are in the study, you will be required to visit the respiratory clinic on up to nine separate occasions. In between these visits, the clinic will also contact you via telephone (total of nine phone calls over two years).

online grocery shopping

Understanding how information shapes how people shop for groceries online

Online Grocery Shopping Study

About this study

Australians are increasingly shopping online for their groceries however we don’t have much evidence on the level of influence of information available to consumers online. The aim of this research is to understand how online grocery purchasing choices may change depending on the information being presented online.

Recruitment criteria

  • Aged 18-75
  • Have high blood pressure
  • Diagnosed by your doctor or currently taking a stable dose of blood pressure lowering medications
  • Regularly purchase most of their groceries online from Woolworths and plan to continue for the duration of the study (4 months) or for those who don’t currently shop with Woolworths, you will also be eligible if you switch to shopping at Woolworths for the duration of the study

Would be willing to shop for their groceries online for the study

What’s involved?

Participants will be asked to complete the following research activities if they consent to join this study:

  • Complete your regular grocery shopping online via Woolworths
  • Complete surveys
  • Complete dietary questionnaires
  • Provide at home blood pressure measurements, using a monitor we provide at no cost to you
  • Provide urine samples at a certified Pathology Centre close to you
  • A small selection of participants will be invited to participate in a telephone interview at the end of the study asking you about your thoughts on different elements of the study and suggestions for improvements.

Benefits (gift cards, etc)

You will receive up to $350 worth of Woolworths ‘Essentials/Grocery eGift Card’ grocery vouchers in recognition of your participation. You will also be able to keep the blood pressure monitors provided to you (valued at $179).

Research suggests that high blood pressure is a major cause of heart valve disease

Optimising available treatment for patients with Heart Failure

HFpEF - Polydiuretic Therapy for Heart Failure with Preserved Ejection Fraction

About this study

Heart failure (HF) is a condition where your heart doesn’t pump enough blood for your body’s needs. It is estimated there is approximately 110,000 people diagnosed with HF in Australia affecting approximately 1-2 % of our population. Over half of these people have heart failure with preserved ejection fraction, HFpEF, which has very few treatments proven to help you feel better or stay out of hospital. Polypills containing low dose diuretics have not been extensively studied in patients with HFpEF and this study aims to help improve the treatment for this patient population.

The purpose of this research study is to investigate whether treatment with the polypill (a single pill containing three medications used to treat heart failure, each at low-dose) improves fluid balance, leads to less congestion and fewer side effects when compared with just one of the active medications from the polypill.

Recruitment criteria

Inclusion

  • Adults (≥18 years old) with a diagnosis of heart failure with preserved ejection fraction (EF) which has been present for at least 2 months

Key Exclusions

  • Known contraindication to the study medications.
  • Current acute decompensated HF or hospitalisation due to decompensated HF <4 weeks prior to enrolment.
  • Myocardial infarction, unstable angina, stroke, or transient ischaemic attack (TIA) within 12 weeks prior to enrolment.
  • Symptomatic bradycardia or second or third-degree heart block without a pacemaker.
  • Women who are pregnant, breast feeding or of childbearing potential and are not using and do not plan to continue using medically acceptable form of contraception throughout the study

What’s involved?

  • The HFpEF trial plans to recruit 30 eligible patients across two centres in Sydney, Australia. One will be at the Charles Perkins Centre, Camperdown, and the other at St. Vincent’s Hospital, Darlinghurst.
  • If you are eligible for this study, you will be randomly allocated to either take an active polypill (a single pill containing three medications used to treat heart failure, each at low-dose) or the comparator medicine (just one of the active medications from the polypill) daily, for a total of one month.
  • You will attend a cardiology clinic on a total of 4 occasions across 4 weeks. Blood tests will be performed at each visit, and you will be asked about your adherence to your medication, you will undergo some assessments including the measurement of your BP, HR, and you may have your exercise capacity measured.

Improving the cardiovascular health of patients with chronic kidney disease using blood thinning medication

TRACK - Treatment of cardiovascular disease with low dose Rivaroxaban in Advanced Chronic Kidney Disease

About this study

People with advanced kidney disease or those receiving dialysis often have other diseases related to the heart, brain and blood vessels, known as vascular disease (for example, heart attack, stroke and poor blood circulation). However, few treatments have been proven to prevent these conditions in people with advanced kidney disease. Blood thinners (medicines that prevent blood clots) are frequently used and proven to help other groups of people who are at high risk of vascular disease.

There is little understanding of whether blood thinners provide similar benefits in people with advanced kidney disease. The aim of the TRACK study is to find out whether a low dose of blood thinning medicine can reduce heart and vascular disease better than placebo (a look alike tablet that contains no active medication) in people with advanced kidney disease.

Recruitment criteria

Inclusion:

  • Age ≥18 years,
  • Advanced kidney disease (kidney failure on dialysis, or stage 4 or 5 not receiving dialysis)
  • Increased risk of heart or blood vessel disease:
    • History of coronary artery disease or peripheral artery disease or specific types of stroke, or
    • Diabetes, or
    • Age ≥65 years.

Key Exclusions:

  • Indication for, or contraindication to, anticoagulant therapy
  • High bleeding risk
  • Current treatment with P2Y12 inhibitors/ADP receptor inhibitors (clopidogrel, prasugrel, ticagrelor, cangrelor) or phosphodiesterase inhibitors (dipyridamole), where the treating doctor or patient does not wish to stop these medications
  • Haemoglobin <90 g/L, or platelet count <100 x 109/L,

What’s involved?

  • If eligible for the study, you will receive placebo tablets for approximately 3 weeks. This is to ensure you are able to follow the study medication schedule.
  • If you are able to take the placebo tablets twice a day for 3 weeks, you will be eligible for randomisation. This means that you will be placed into one of two groups (blood thinning medication or placebo) using chance (like tossing a coin).
  • From randomisation, you will be required to take the blood thinning medication or placebo (depending on the group you are placed in) twice a day, for the period of the study. The study will continue for up to about 5 years.
  • Study staff will contact you at 1 month and 3 months after randomisation. From then on, you will be contacted every 3 months. These follow up visits can be done in the clinic or via telephone. Researchers will collect information about your health and whether you have been taking the study medication as prescribed.