TY - JOUR
T1 - Inequalities in the use of secondary prevention of cardiovascular disease by socioeconomic status
T2 - evidence from the PURE observational study
AU - Murphy, Adrianna
AU - Palafox, Benjamin
AU - O'Donnell, Owen
AU - Stuckler, David
AU - Perel, Pablo
AU - AlHabib, Khalid F.
AU - Avezum, Alvaro
AU - Bai, Xiulin
AU - Chifamba, Jephat
AU - Chow, Clara K.
AU - Corsi, Daniel J.
AU - Dagenais, Gilles R.
AU - Dans, Antonio L.
AU - Diaz, Rafael
AU - Erbakan, Ayse N.
AU - Ismail, Noorhassim
AU - Iqbal, Romaina
AU - Kelishadi, Roya
AU - Khatib, Rasha
AU - Lanas, Fernando
AU - Lear, Scott A.
AU - Li, Wei
AU - Liu, Jia
AU - Lopez-Jaramillo, Patricio
AU - Mohan, Viswanathan
AU - Monsef, Nahed
AU - Mony, Prem K.
AU - Puoane, Thandi
AU - Rangarajan, Sumathy
AU - Rosengren, Annika
AU - Schutte, Aletta E.
AU - Sintaha, Mariz
AU - Teo, Koon K.
AU - Wielgosz, Andreas
AU - Yeates, Karen
AU - Yin, Lu
AU - Yusoff, Khalid
AU - Zatońska, Katarzyna
AU - Yusuf, Salim
AU - McKee, Martin
N1 - Funding Information:
AM is funded by a Wellcome Trust Research Fellowship (number 104349/Z/14/Z). BP and MM are supported by a UK Economic and Social Research Council grant (number ES/L014696/1) under its Secondary Data Analysis Initiative scheme. DS is funded by a Wellcome Trust Investigator Award and ERC HRES 313590. KYu is supported by a Ministry of Higher Education Malaysia Research Grant (number 600-RMI/LRGS 5/3 [2/2011]). SY is funded by the Marion Burke Chair of the Heart and Stroke Foundation of Canada. OO'D is supported by a Swiss Agency for Development and Cooperation/National Science Foundation grant (number 400640_160374) under their Programme for Research on Global Issues for Development. The main PURE study and its components are funded by the Population Health Research Institute, the Canadian Institutes of Health Research, 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, King Pharma), and various national or local organisations in participating countries. These include: 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 and Fundacion Oftalmologica de Santander; India: Indian Council of Medical Research; Malaysia: Ministry of Science, Technology and Innovation of Malaysia, grant number 100-IRDC/BIOTEK 16/6/21 (13/2007), grant number 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 UN 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: Saudi Heart Association, 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 (SA and Netherlands Programme for Alternative Development), National Research Foundation, Medical Research Council of South Africa, the South Africa Department of Science and Technology, The South African Sugar Association, Faculty of Community and Health Sciences (UWC); Sweden: AFA Insurance, Swedish Council for Working Life and Social Research, King Gustaf V's and Queen Victoria's Freemasons Foundation, Swedish Heart and Lung Foundation, Swedish Research Council, grant from the Swedish State under (LäkarUtbildningsAvtalet), Agreement, grant from the Västra Götaland Region (FOUU); 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.
Publisher Copyright:
© 2018 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0. license
PY - 2018/3
Y1 - 2018/3
N2 - Background: There is little evidence on the use of secondary prevention medicines for cardiovascular disease by socioeconomic groups in countries at different levels of economic development. Methods: We assessed use of antiplatelet, cholesterol, and blood-pressure-lowering drugs in 8492 individuals with self-reported cardiovascular disease from 21 countries enrolled in the Prospective Urban Rural Epidemiology (PURE) study. Defining one or more drugs as a minimal level of secondary prevention, wealth-related inequality was measured using the Wagstaff concentration index, scaled from −1 (pro-poor) to 1 (pro-rich), standardised by age and sex. Correlations between inequalities and national health-related indicators were estimated. Findings: The proportion of patients with cardiovascular disease on three medications ranged from 0% in South Africa (95% CI 0–1·7), Tanzania (0–3·6), and Zimbabwe (0–5·1), to 49·3% in Canada (44·4–54·3). Proportions receiving at least one drug varied from 2·0% (95% CI 0·5–6·9) in Tanzania to 91·4% (86·6–94·6) in Sweden. There was significant (p<0·05) pro-rich inequality in Saudi Arabia, China, Colombia, India, Pakistan, and Zimbabwe. Pro-poor distributions were observed in Sweden, Brazil, Chile, Poland, and the occupied Palestinian territory. The strongest predictors of inequality were public expenditure on health and overall use of secondary prevention medicines. Interpretation: Use of medication for secondary prevention of cardiovascular disease is alarmingly low. In many countries with the lowest use, pro-rich inequality is greatest. Policies associated with an equal or pro-poor distribution include free medications and community health programmes to support adherence to medications. Funding: Full funding sources listed at the end of the paper (see Acknowledgments).
AB - Background: There is little evidence on the use of secondary prevention medicines for cardiovascular disease by socioeconomic groups in countries at different levels of economic development. Methods: We assessed use of antiplatelet, cholesterol, and blood-pressure-lowering drugs in 8492 individuals with self-reported cardiovascular disease from 21 countries enrolled in the Prospective Urban Rural Epidemiology (PURE) study. Defining one or more drugs as a minimal level of secondary prevention, wealth-related inequality was measured using the Wagstaff concentration index, scaled from −1 (pro-poor) to 1 (pro-rich), standardised by age and sex. Correlations between inequalities and national health-related indicators were estimated. Findings: The proportion of patients with cardiovascular disease on three medications ranged from 0% in South Africa (95% CI 0–1·7), Tanzania (0–3·6), and Zimbabwe (0–5·1), to 49·3% in Canada (44·4–54·3). Proportions receiving at least one drug varied from 2·0% (95% CI 0·5–6·9) in Tanzania to 91·4% (86·6–94·6) in Sweden. There was significant (p<0·05) pro-rich inequality in Saudi Arabia, China, Colombia, India, Pakistan, and Zimbabwe. Pro-poor distributions were observed in Sweden, Brazil, Chile, Poland, and the occupied Palestinian territory. The strongest predictors of inequality were public expenditure on health and overall use of secondary prevention medicines. Interpretation: Use of medication for secondary prevention of cardiovascular disease is alarmingly low. In many countries with the lowest use, pro-rich inequality is greatest. Policies associated with an equal or pro-poor distribution include free medications and community health programmes to support adherence to medications. Funding: Full funding sources listed at the end of the paper (see Acknowledgments).
UR - http://www.scopus.com/inward/record.url?scp=85044636388&partnerID=8YFLogxK
U2 - 10.1016/S2214-109X(18)30031-7
DO - 10.1016/S2214-109X(18)30031-7
M3 - Article
C2 - 29433667
AN - SCOPUS:85044636388
SN - 2214-109X
VL - 6
SP - e292-e301
JO - The Lancet Global Health
JF - The Lancet Global Health
IS - 3
ER -