Quadpill for hypertension cuts risk of CVD and stroke by half: Lancet
Hamilton, ON: (Aug. 29, 2021) - A combination therapy of aspirin, statins and at least two blood pressure medications given in fixed doses can slash the risk of fatal cardiovascular disease (CVD) by more than half, says an international study led by Hamilton researchers. The benefits of the polypill are consistent at different blood pressure levels, cholesterol levels and with or without diabetes, but larger benefits may occur in older people.
The strategy involving early treatment with a pill containing four medicine, each at a quarter of their usual doses was shown to be more effective for blood pressure control than the common strategy of starting monotherapy.
The study, published in The Lancet, showed the efficacy, tolerability, and simplicity of a quadpill-based strategy.
The study findings were presented at the world-leading European Society of Cardiology conference, ESC Congress 2021.
High blood pressure is the world's leading killer but poor rates of blood pressure control remain common. Professor Clara Chow, lead and corresponding author and Director of the University of Sydney's Westmead Applied Research Centre, said in a separate Comment in The Lancet this week that control of high blood pressure, known as hypertension, was not ideal anywhere, and in some regions such as Africa, fewer than one in 10 had hypertension under control.
"Statistics on the global burden of high blood pressure this week show that there's been a doubling in the past 30 years of hypertension cases – the leading cause of the world's top killer: heart attack and stroke," Professor Chow said.
This first large-scale, randomized controlled clinical trial of starting this novel combination blood pressure medication brought blood pressure under control in 80 percent of participants in 12 weeks, compared to 60 percent in the control group who nonetheless had access to the best patient care.
Traditionally doctors have started with one drug and then follow up to consider adding or changing treatment – but this strategy is often not successful in practice and blood pressure control rates have remained stubbornly low for decades.
Dr Emily Atkins from The George Institute for Global Health, UNSW Sydney and the University of Sydney said: "In settings with high levels of specialist care and full access to a range of existing blood pressure medicines – like the centers in this trial – the improved reduction in blood pressure with this strategy would be expected to reduce the risk of heart attacks and strokes by about 20 percent. In settings with little or no existing hypertension treatment, the benefits would be much greater."
About the trial
The multi-center, Australian clinical trial of a potential future 'quad pill' dose of four medications, termed Quadruple UltrA-low-dose tReatment for hypErTension (QUARTET), has demonstrated that a single pill containing ultra-low quadruple combination is much more effective than the traditional approach of starting with monotherapy (single drug).
The study funded by the National Health and Medical Research Council enrolled 591 participants with high blood pressure either in no treatment or single therapy across 10 centers in Australia. The primary outcome was the significantly reduced blood pressure, in the group starting on the quadpill, at 12 weeks. These differences were sustained, with blood pressure control still better with the quad pill approach compared to the standard approach at 12 months, and no differences in side effects.
Senior author Professor Anthony Rodgers of The George Institute, UNSW Sydney and Imperial College London, said: "Our trial has overwhelmingly demonstrated the efficacy, tolerability, and safety of this ultra-low-dose combination strategy – a potentially simple and scalable hypertension management strategy to treat hypertension."
Professor Chow said the study built on their previous study comparing a quadpill approach to placebo. "We aimed to test this new quadpill strategy against usual care in Australia; as is often seen in clinical trials, people in the comparison group got much better treatment than average. Nonetheless our new quadpill strategy was much better," she said.
"This was the first study to show the benefits are maintained long-term without any reduction over time. Even though much more add-on blood pressure medicines were used in the comparison group throughout follow-up, they never caught up with the quadpill group."
Changing global practice
Professor Chow said there were still important research questions. "For people who may be having side effects from their current treatments, we would like to know whether a switch to an utra-low-dose combination can improve things," said Professor Chow.
"Also, the WHO Hypertension Guidelines released this week, just like other recent hypertension guidelines in Europe, US and elsewhere, recommend most patients start on two blood pressure drugs rather than one. We need to know how that would compare to a quadpill strategy."
There is also a major research translation challenge ahead: "These kinds of strategies will only make a major impact on global health if they are available and affordable for patients most in need," said Professor Chow.
"When we find treatments that are this effective, simple, and safe we must do our best to get them to those who can benefit most."
Professor Chow said a simple and effective combination quadpill strategy had the potential to impact people's lives worldwide. "High blood pressure is the leading cause of preventable deaths globally – we hope our world-leading findings will be translated swiftly into a product available for the general public," she concluded.
Reference:
The study titled, "Initial treatment with a single pill containing quadruple combination of quarter doses of blood pressure medicines versus standard-dose monotherapy in patients with hypertension (QUARTET): a phase 3, randomised, double-blind, active-controlled trial," is published in The Lancet.
DOI: https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(21)01922-X/fulltext
