WORK will soon begin on new guidelines to better support GPs to manage cardiovascular disease (CVD) risk in their patients, as new research shows that CVD risk management in primary care is “sub-optimal”.
Professor Garry Jennings, Chief Medical Advisor to the Heart Foundation, said the introduction of a guideline alone could not support change in CVD risk management in primary care.
“A guideline is just part of the picture,” he said. “And [CVD risk] needs to be addressed across the full continuum of primary care practice from the patient coming in the door to living their life out in the community.
“There is a project beginning now to update the absolute risk guideline with a whole lot of developments that have occurred since the 2012 version. We have more data from larger cohorts which could refine the algorisms used to calculate risk and the availability of a whole lot of other tests which can influence – upwards or downwards – the risk assessment.”
Professor Jennings said that this would be just part of the solution.
“A new guideline won’t necessarily mean the health services are set up in a way which encourages people to have their risk identified and have it properly managed,” he said. “It comes down to GPs being incentivised by the system to manage the whole person over their lifetime, rather than just individual episodes of care.”
The new research, published in the MJA, has found significant room for improvement in the implementation of CVD preventive care guidelines in general practice.
“Adopting the absolute risk assessment approach has not improved adherence to management guidelines, similar to the experience in Europe, Canada, and the United Kingdom,” the researchers wrote.
The researchers examined the implementation of the 2012 guidelines – based on absolute CVD risk estimates – by analysing electronic medical record data of more than 100 000 patients from 95 practices across four states and territories.
They found that about 10% of patients had established CVD and almost 13% had clinically high risk conditions. In 29 645 (29%) patients, electronic medical record documentation of data required for calculating CVD risk was inadequate.
“Among patients with established CVD, 6038 (56.8%) had been prescribed the guideline-recommended treatments; blood pressure targets had been achieved by 4114 patients (38.7%) and [low-density lipoprotein cholesterol] targets by 5645 (53.1%),” the researchers wrote.
“Among the 15 743 patients at high CVD risk, 6486 (41.2%) were prescribed recommended treatments; 8988 (57.1%) had achieved blood pressure targets and 5714 (36.3%) LDL-C targets.”
Blood pressure targets were defined as less than 140/90 mmHg for patients at high CVD risk and less than 130/80 mmHg for people with established CVD or diabetes, while cholesterol targets were low-density lipoprotein cholesterol levels of less than 2.0 mmol/L.
Guideline-recommended treatment was defined as the prescribing of blood pressure- and lipid-lowering medications for patients at high CVD risk, and the prescribing of antiplatelet or anticoagulant medications for patients with established CVD.
Lead researcher Associate Professor Charlotte Hespe, a Sydney GP and Head of General Practice and General Practice Research at the University of Notre Dame, said the findings highlighted the flaws in the current volume-based GP funding model.
“How do we incentivise practitioners to be able to do certain areas of preventive health care that really do make a difference?” she asked, noting that CVD provides a good example of the benefits of preventive care.
“We know that a small implementation of change will make a significant difference in the number of people who are affected by CVD both morbidity and mortality.”
Associate Professor Hespe said the introduction of Medical Benefits Scheme item numbers in 2019 for Heart Health Checks was “just another volume-based carrot” that was unlikely to improve real-world management of cardiovascular risk in primary care.
“As a GP, I don’t just look at the heart, I look at everything, and in 30 minutes I can do a far more comprehensive and value-based offering that is more than just focused on cardiac health,” she told InSight+.
A better initiative to improve CVD risk management, Associate Professor Hespe said, was a shift to value-based care, such as voluntary patient enrolment. A federal government voluntary patient enrolment initiative, that was set for introduction in July of 2020, has been put on ice as a result of the COVID-19 pandemic.
“CVD prevention falls in beautifully to that model because you can make sure that you get cholesterol tested in people from the age they should be being tested, you can have a much more holistic view of patient care,” she said, noting that she hoped such initiatives would be implemented as part of the Primary Health Care 10-Year Plan, which was under development.
Professor Mark Morgan, Chair of the Royal Australian College of GPs’ Expert Committee for Quality Care, said voluntary patient enrolment would enable GPs to take a population health approach to managing cardiovascular risk.
“If GPs knew who their patients were through a system of voluntary enrolment, or some other equivalent way, [they] could identify the people who are potentially under-treated, and actively know that they have an opportunity to approach those people and have shared decision making about treatment according to the guidelines,” said Professor Morgan, who is also Professor of General Practice at Bond University.
Professor Morgan said the introduction last year of the Quality Improvement Practice Incentives Program could, “at a basic level”, support practices to identify patients who may be at high risk of cardiovascular disease.
“There are 10 measures in total that are being collected and that is meant to assist practices, with the support of the Primary Health Network, to engage in quality improvement activities,” he said, adding that this program was still in its early days and was a “light touch”.
He also pointed to the Gold Coast Primary Health Network’s development of a real-time tool to flag patients at high risk of cardiovascular disease.
Professor Morgan, who was part of the development team, said the Primary Sense tool (here, and here) could provide a report to practices flagging patients who were at high risk of cardiovascular disease but had not been prescribed either of the two classes of recommended medications.
Professor Morgan also pointed to Heart Health Checks and the RACGP Red Book, which was currently being updated, as other tools that would support GPs to improve the identification and management of cardiovascular risk in their patients.
The RACGP has also made a submission to the federal government to help inform the upcoming development of a National Preventive Health Strategy.
Associate Professor Hespe said in addition to financial incentives for providing more holistic care for patients, Primary Health Networks could also support GP practices to better use medical records to guide care and prevention.
“As a GP I am taught very well to be a doctor for the patient in front of me; I am not taught so well about how to manage my population, nor have I been taught terribly well about how to use my electronic records,” she said.
How does an ACRA benefit all individuals if they don’t have a regular doctor or even feel the need to see one? I love the concept of prevention of CVD by identifying (via screening) for risk-factors yet when a person usually see’s a GP its for a reason. How does an ACRA target minority groups at greater risk of developing CVD if they don’t see a GP? And how does the ACRA score encourage an individual to keep in contact with a GP especially in rural/Remote Australia? ACRA appears to be a valuable tool but it needs to be part of a more holistic approach, targeting the portion of the population who do not visit GP’s, until it is possibly too late? It’s all and well to offer GP’s some type of financial incentive to perform an ACRA but it’s a completely different matter to aptly apply the results to the benefit of individual patients and the wider population.
As a patient, I would like to see a reminder poster in every treatment room, for patients and doctors to see, as to how to measure blood pressure properly and accurately, for instance, as published by the British Hypertension Society.
I still have to find such a doctor. The last time my blood pressure was measured was with me sitting on the examination table, OMRON unit on the examination table, arms and legs dangling down, cuff put on over a pullover, and the doctor talking to me about my risk of some kind of cancer. Doctors use the same cuff for skinny to overweight to obese patients. Surely, cuffs put on over clothing, especially thicker clothing, arm size of the patient as well as any current pain, may make a difference.
Also, I would like to know what the absolute risk reduction by the treatment is, especially in older patients whose risk of dying increases with advancing age anyhow. Doctors are not clairvoyants and it is very unfortunate that after all these years of treatment with medication the only way is to treat everyone deemed at risk and so expose them to medication side-effects and risk of dying, especially of the elderly, as a result of falls – and old age.
Sometimes I wonder whether the target to get the figures, being BP or pathology, into the right range is more important than the general well-being of the patient, especially of older to elderly patients.
In my experience as a GP RN, I find it takes a whole of practice response to bring the right patients to be in front of the GP, to have their CV risk performed. The whole practice needs to understand why we need to find these patients. Once receptionists are included in the training, they are more likely to encourage patients to have a heart health check. Get them some brochures from Heart Foundation to give to patients 45-74. Get the nurses to find the patients who haven’t had their BP checks/ lipids performed to invite these patients into the practice. Give the GPs their list of patients with High risk CV disease, are they being managed appropriately? Use your clinical audit tool to find those that haven’t the required data and invite them. Make sure everyone in the practice has a role. Reach out to patients with FaceBook education, emails, SMS, notice boards in waiting room. Report on your data at every meeting ( ie QIPIP- CVD measurement data). This is too much work for one individual GP- we need to work together to improve our systems.
Any guidelines should take into account the age of the patient. For those over 70 and particularly over 75 the algorithms will generally show patients at high risk, but the evidence of intervention with no demonstrable CVD is not established, particularly in use of statins.
In this age group I think the clinician has to use their judgement based on the individuals particular circumstances.
As a patient I have never seen a GP offer me a CVD absolute risk score using the Heath Foundation algorithm or one from a similar body and they do not offer me a Coronary Calcium Score (no contrast media) unless I ask for it. The GPs I have seen are fine to measure my BP and order pathology. So I have asked to be referred to Cardiologist (with know prevention skills) to initiate my CVD prevention.