TY - JOUR
T1 - Availability and affordability of blood pressure-lowering medicines and the effect on blood pressure control in high-income, middle-income, and low-income countries
T2 - an analysis of the PURE study data
AU - PURE study investigators
AU - Attaei, Marjan W.
AU - Khatib, Rasha
AU - McKee, Martin
AU - Lear, Scott
AU - Dagenais, Gilles
AU - Igumbor, Ehimario U.
AU - AlHabib, Khalid F.
AU - Kaur, Manmeet
AU - Kruger, Lanthe
AU - Teo, Koon
AU - Lanas, Fernando
AU - Yusoff, Khalid
AU - Oguz, Aytekin
AU - Gupta, Rajeev
AU - Yusufali, Afzalhussein M.
AU - Bahonar, Ahmad
AU - Kutty, Raman
AU - Rosengren, Annika
AU - Mohan, Viswanathan
AU - Avezum, Alvaro
AU - Yusuf, Rita
AU - Szuba, Andrzej
AU - Rangarajan, Sumathy
AU - Chow, Clara
AU - Yusuf, Salim
AU - O'Donnell, M.
AU - Mente, A.
AU - Leong, D.
AU - Smyth, A.
AU - Joseph, P.
AU - Islam, S.
AU - Zhang, M.
AU - Hu, W.
AU - Ramasundarahettige, C.
AU - Wong, G.
AU - Dayal, L.
AU - Casanova, A.
AU - Dehghan, M.
AU - Lewis, G.
AU - Aliberti, A.
AU - Reyes, A.
AU - Zaki, A.
AU - Lewis, B.
AU - Zhang, B.
AU - Agapay, D.
AU - Hari, D.
AU - Milazzo, E.
AU - Ramezani, E.
AU - Iqbal, R.
AU - Kazmi, K.
N1 - Funding Information:
The PURE study is an investigator-initiated study that is funded by the Population Health Research Institute, the Canadian Institutes of Health Research, and the Heart and Stroke Foundation of Ontario, and through unrestricted grants from several pharmaceutical companies, with major contributions from AstraZeneca (Canada), Sanofi Aventis (France and Canada), Boehringer Ingelheim (Germany and Canada), Servier, and GlaxoSmithKline, and additional contributions from Novartis and King Pharma and from various national or local organisations in participating countries: Argentina—Fundacion ECLA; Bangladesh—Independent University, Bangladesh, and Mitra and Associates; Brazil—Unilever Health Institute, Brazil; Canada—Public Health Agency of Canada and Champlain Cardiovascular Disease Prevention Network; Chile—Universidad de la Frontera; China—National Center for Cardiovascular Diseases; Colombia—Colciencias (grant number 6566-04-18062); India—Indian Council of Medical Research; Malaysia—Ministry of Science, Technology and Innovation of Malaysia (grant numbers 100-IRDC/BIOTEK 16/6/21 [13/2007] and 07-05-IFN-BPH 010), Ministry of Higher Education of Malaysia (grant number 600-RMI/LRGS/5/3 [2/2011]), Universiti Teknologi MARA, Universiti Kebangsaan Malaysia (UKM-Hejim-Komuniti-15-2010); occupied Palestinian territory—the United Nations Relief and Works Agency for Palestine Refugees in the Near East (UNRWA), occupied Palestinian territory; International Development Research Centre (IDRC), Canada; Philippines—Philippine Council for Health Research & Development (PCHRD); Poland—Polish Ministry of Science and Higher Education (grant number 290/W-PURE/2008/0), Wroclaw Medical University; Saudi Arabia—the Deanship of Scientific Research at King Saud University, Riyadh, Saudi Arabia (research group number: RG -1436-013); South Africa—the North-West University, SANPAD (South Africa and Netherlands Programme for Alternative Development), National Research Foundation, Medical Research Council of South Africa, the South Africa Sugar Association (SASA), Faculty of Community and Health Sciences (UWC); Sweden—AFA Insurance, Swedish Council for Working Life and Social Research, Swedish Research Council for Environment, Agricultural Sciences and Spatial Planning, Swedish Heart and Lung Foundation, Swedish Research Council, grant from the Swedish State under the LäkarUtbildningsAvtalet agreement, grant from the Västra Götaland Region (FOUU), King Gustaf V and Queen Victorias Freemasons Foundation; Turkey—Metabolic Syndrome Society, AstraZeneca, Turkey, Sanofi Aventis, Turkey; United Arab Emirates—Sheikh Hamdan Bin Rashid Al Maktoum Award For Medical Sciences and Dubai Health Authority, Dubai United Arab Emirates. SY is supported by the Mary W Burke endowed chair of the Heart and Stroke Foundation of Ontario.
Publisher Copyright:
© 2017 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY-NC-ND 4.0 license
PY - 2017/9/1
Y1 - 2017/9/1
N2 - Background Hypertension is considered the most important risk factor for cardiovascular diseases, but its control is poor worldwide. We aimed to assess the availability and affordability of blood pressure-lowering medicines, and the association with use of these medicines and blood pressure control in countries at varying levels of economic development. Methods We analysed the availability, costs, and affordability of blood pressure-lowering medicines with data recorded from 626 communities in 20 countries participating in the Prospective Urban Rural Epidemiological (PURE) study. Medicines were considered available if they were present in the local pharmacy when surveyed, and affordable if their combined cost was less than 20% of the households' capacity to pay. We related information about availability and affordability to use of these medicines and blood pressure control with multilevel mixed-effects logistic regression models, and compared results for high-income, upper-middle-income, lower-middle-income, and low-income countries. Data for India are presented separately because it has a large generic pharmaceutical industry and a higher availability of medicines than other countries at the same economic level. Findings The availability of two or more classes of blood pressure-lowering drugs was lower in low-income and middle-income countries (except for India) than in high-income countries. The proportion of communities with four drug classes available was 94% in high-income countries (108 of 115 communities), 76% in India (68 of 90), 71% in upper-middle-income countries (90 of 126), 47% in lower-middle-income countries (107 of 227), and 13% in low-income countries (nine of 68). The proportion of households unable to afford two blood pressure-lowering medicines was 31% in low-income countries (1069 of 3479 households), 9% in middle-income countries (5602 of 65 471), and less than 1% in high-income countries (44 of 10 880). Participants with known hypertension in communities that had all four drug classes available were more likely to use at least one blood pressure-lowering medicine (adjusted odds ratio [OR] 2·23, 95% CI 1·59–3·12); p<0·0001), combination therapy (1·53, 1·13–2·07; p=0·054), and have their blood pressure controlled (2·06, 1·69–2·50; p<0·0001) than were those in communities where blood pressure-lowering medicines were not available. Participants with known hypertension from households able to afford four blood pressure-lowering drug classes were more likely to use at least one blood pressure-lowering medicine (adjusted OR 1·42, 95% CI 1·25–1·62; p<0·0001), combination therapy (1·26, 1·08–1·47; p=0·0038), and have their blood pressure controlled (1·13, 1·00–1·28; p=0·0562) than were those unable to afford the medicines. Interpretation A large proportion of communities in low-income and middle-income countries do not have access to more than one blood pressure-lowering medicine and, when available, they are often not affordable. These factors are associated with poor blood pressure control. Ensuring access to affordable blood pressure-lowering medicines is essential for control of hypertension in low-income and middle-income countries. Funding Population Health Research Institute, the Canadian Institutes of Health Research, Heart and Stroke Foundation of Ontario, Canadian Institutes of Health Research Strategy for Patient Oriented Research through the Ontario SPOR Support Unit, the Ontario Ministry of Health and Long-Term Care, pharmaceutical companies (with major contributions from AstraZeneca [Canada], Sanofi Aventis [France and Canada], Boehringer Ingelheim [Germany amd Canada], Servier, and GlaxoSmithKline), Novartis and King Pharma, and national or local organisations in participating countries.
AB - Background Hypertension is considered the most important risk factor for cardiovascular diseases, but its control is poor worldwide. We aimed to assess the availability and affordability of blood pressure-lowering medicines, and the association with use of these medicines and blood pressure control in countries at varying levels of economic development. Methods We analysed the availability, costs, and affordability of blood pressure-lowering medicines with data recorded from 626 communities in 20 countries participating in the Prospective Urban Rural Epidemiological (PURE) study. Medicines were considered available if they were present in the local pharmacy when surveyed, and affordable if their combined cost was less than 20% of the households' capacity to pay. We related information about availability and affordability to use of these medicines and blood pressure control with multilevel mixed-effects logistic regression models, and compared results for high-income, upper-middle-income, lower-middle-income, and low-income countries. Data for India are presented separately because it has a large generic pharmaceutical industry and a higher availability of medicines than other countries at the same economic level. Findings The availability of two or more classes of blood pressure-lowering drugs was lower in low-income and middle-income countries (except for India) than in high-income countries. The proportion of communities with four drug classes available was 94% in high-income countries (108 of 115 communities), 76% in India (68 of 90), 71% in upper-middle-income countries (90 of 126), 47% in lower-middle-income countries (107 of 227), and 13% in low-income countries (nine of 68). The proportion of households unable to afford two blood pressure-lowering medicines was 31% in low-income countries (1069 of 3479 households), 9% in middle-income countries (5602 of 65 471), and less than 1% in high-income countries (44 of 10 880). Participants with known hypertension in communities that had all four drug classes available were more likely to use at least one blood pressure-lowering medicine (adjusted odds ratio [OR] 2·23, 95% CI 1·59–3·12); p<0·0001), combination therapy (1·53, 1·13–2·07; p=0·054), and have their blood pressure controlled (2·06, 1·69–2·50; p<0·0001) than were those in communities where blood pressure-lowering medicines were not available. Participants with known hypertension from households able to afford four blood pressure-lowering drug classes were more likely to use at least one blood pressure-lowering medicine (adjusted OR 1·42, 95% CI 1·25–1·62; p<0·0001), combination therapy (1·26, 1·08–1·47; p=0·0038), and have their blood pressure controlled (1·13, 1·00–1·28; p=0·0562) than were those unable to afford the medicines. Interpretation A large proportion of communities in low-income and middle-income countries do not have access to more than one blood pressure-lowering medicine and, when available, they are often not affordable. These factors are associated with poor blood pressure control. Ensuring access to affordable blood pressure-lowering medicines is essential for control of hypertension in low-income and middle-income countries. Funding Population Health Research Institute, the Canadian Institutes of Health Research, Heart and Stroke Foundation of Ontario, Canadian Institutes of Health Research Strategy for Patient Oriented Research through the Ontario SPOR Support Unit, the Ontario Ministry of Health and Long-Term Care, pharmaceutical companies (with major contributions from AstraZeneca [Canada], Sanofi Aventis [France and Canada], Boehringer Ingelheim [Germany amd Canada], Servier, and GlaxoSmithKline), Novartis and King Pharma, and national or local organisations in participating countries.
UR - http://www.scopus.com/inward/record.url?scp=85028775982&partnerID=8YFLogxK
U2 - 10.1016/S2468-2667(17)30141-X
DO - 10.1016/S2468-2667(17)30141-X
M3 - Article
C2 - 29253412
AN - SCOPUS:85028775982
SN - 2468-2667
VL - 2
SP - e411-e419
JO - The Lancet Public Health
JF - The Lancet Public Health
IS - 9
ER -