Availability and affordability of medicines and cardiovascular outcomes in 21 high-income, middle-income and low-income countries.

Clara Kayei Chow ; Tu Ngoc Nguyen ORCID logo ; Simone Marschner ; Rafael Diaz ; Omar Rahman ; Alvaro Avezum ; Scott A Lear ; Koon Teo ; Karen E Yeates ; Fernando Lanas ; +22 more... Wei Li ; Bo Hu ; Patricio Lopez-Jaramillo ; Rajeev Gupta ; Rajesh Kumar ORCID logo ; Prem K Mony ; Ahmad Bahonar ; Khalid Yusoff ; Rasha Khatib ; Khawar Kazmi ; Antonio L Dans ; Katarzyna Zatonska ; Khalid F Alhabib ; Iolanthe Marike Kruger ; Annika Rosengren ; Sadi Gulec ; Afzalhussein Yusufali ; Jephat Chifamba ; Sumathy Rangarajan ; Martin McKee ORCID logo ; Salim Yusuf ; PURE Study ; (2020) Availability and affordability of medicines and cardiovascular outcomes in 21 high-income, middle-income and low-income countries. BMJ GLOBAL HEALTH, 5 (11). e002640-e002640. ISSN 2059-7908 DOI: 10.1136/bmjgh-2020-002640
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OBJECTIVES: We aimed to examine the relationship between access to medicine for cardiovascular disease (CVD) and major adverse cardiovascular events (MACEs) among people at high risk of CVD in high-income countries (HICs), upper and lower middle-income countries (UMICs, LMICs) and low-income countries (LICs) participating in the Prospective Urban Rural Epidemiology (PURE) study. METHODS: We defined high CVD risk as the presence of any of the following: hypertension, coronary artery disease, stroke, smoker, diabetes or age >55 years. Availability and affordability of blood pressure lowering drugs, antiplatelets and statins were obtained from pharmacies. Participants were categorised: group 1-all three drug types were available and affordable, group 2-all three drugs were available but not affordable and group 3-all three drugs were not available. We used multivariable Cox proportional hazard models with nested clustering at country and community levels, adjusting for comorbidities, sociodemographic and economic factors. RESULTS: Of 163 466 participants, there were 93 200 with high CVD risk from 21 countries (mean age 54.7, 49% female). Of these, 44.9% were from group 1, 29.4% from group 2 and 25.7% from group 3. Compared with participants from group 1, the risk of MACEs was higher among participants in group 2 (HR 1.19, 95% CI 1.07 to 1.31), and among participants from group 3 (HR 1.25, 95% CI 1.08 to 1.50). CONCLUSION: Lower availability and affordability of essential CVD medicines were associated with higher risk of MACEs and mortality. Improving access to CVD medicines should be a key part of the strategy to lower CVD globally.


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