To assess the blood pressure and lipid-lowering efficacy and tolerability of ‘polypills’ used in cardiovascular disease prevention trials.
Systematic review and meta-analysis. Search strategy: The Cochrane Central Register of Controlled Trials, Medline, and PubMed databases were searched for eligible trials. Study inclusion criteria: Randomised controlled trials of at least six weeks duration, which compared a ‘polypill’ (that included at least one anti-hypertensive and one lipid-lowering medication) with a placebo (or one active component). Outcome measures: Change from baseline in systolic and diastolic blood pressures, and total and LDL-cholesterol; discontinuation of study medication and reported adverse effects. Of 44 potentially eligible studies, six trials (including 2,218 patients without previous cardiovascular disease) fulfilled the inclusion criteria. Compared with placebo, ‘polypills’ reduced systolic blood pressure by −9.2 mmHg (95% confidence interval (CI): −13.4, −5.0) diastolic blood pressure by −5.0 mmHg (95%CI: −7.4, −2.6), total cholesterol by −1.22 mmol/L (95%CI: −1.60, −0.84) and LDL-cholesterol by −1.02 mmol/L (95%CI: −1.37, −0.67). However, those taking a ‘polypill’ (vs. placebo or component) were more likely to discontinue medication (20% vs 14%) (Odds ratio: 1.5 (95% CI: 1.2, 1.9)). There was no significant difference in reported adverse effects amongst those on a ‘polypill’ (36% vs. 28%) (OR: 1.3 (95%CI: 0.7, 2.5)). There was high statistical heterogeneity in comparisons for blood pressure and lipid-lowering but use of random-effects and quality-effects models produced very similar results.
Compared with placebo, the ‘polypills’ reduced blood pressure and lipids. Tolerability was lower amongst those on ‘polypills’ than those on placebo or one component, but differences were moderate. Effectiveness trials are needed to help clarify the status of ‘polypills’ in primary care and prevention strategies.
Citation: Elley CR, Gupta AK, Webster R, Selak V, Jun M, et al. (2012) The Efficacy and Tolerability of ‘Polypills’: Meta-Analysis of Randomised Controlled Trials. PLoS ONE 7(12): e52145. doi:10.1371/journal.pone.0052145
Editor: James M. Wright, University of British Columbia, Canada
Received: August 8, 2012; Accepted: November 8, 2012; Published: December 19, 2012
Copyright: © 2012 Elley et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The authors did not receive any extrenal funding for this project. Therefore funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have read the journal's policy and have the following conflicts: AR and RW have received a grant from Dr Reddy's Ltd (DRL) for the SPACE collaboration centre but this is unrelated to the current meta-analysis. DRL also provided a fixed dose combination formulation free of charge for four randomized controlled trials to assess the effectiveness of a “polypill-based strategy.” CRE, VS, AP, ST and AR are investigators or are on the steering committee of at least one of these trials. The George Institute for Global Health is now negotiating a global license for these products, following a decision by DRL not to proceed with taking the products to market because of existing regulatory requirements. DRL has provided travel assistance to meetings on “polypills” for CRE, RW, VS, AP, ST and AR in the past. AKG has received travel assistance to attend a conference from Pfizer. This does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials.
Cardiovascular disease is the leading cause of death worldwide.  On the basis of a substantial body of evidence, cardiovascular guidelines have recommended that those with a past history of cardiovascular disease  or who otherwise have a high risk of disease  follow lifestyle interventions and receive blood pressure lowering  and lipid-lowering medications, ,  and where benefit outweighs risk, aspirin therapy. ,  This combination of therapies substantially reduces risk of future cardiovascular events. , ,  Despite guidelines, high proportions of those at high cardiovascular risk are not prescribed these preventive medications, particularly in low income countries. , ,  Besides relatively low rates of prescribing of recommended medications, long-term adherence to medications is also low, which further compromises the preventive potential of these medications. A 2003 World Health Organisation (WHO) report estimated that less than 50% of those prescribed long-term medications for chronic conditions take their medications regularly.  Each additional cardiovascular medication prescribed tends to be associated with lower adherence.  Adherence also reduces sharply in the first year after commencing medication, although adherence is better if medications are initiated together. ,  The WHO report recommends that interventions to improve adherence should be developed and could improve health outcomes to a greater extent than developing new medications.  Using fixed dose combinations, or ‘polypills’, that combine generic versions of different classes of preventive medications for high risk individuals is one such strategy, as it may simplify the medication regime for both prescriber and patient and reduce cost for health funder and patient. , .
In 2001, a WHO and Wellcome Trust meeting of experts concluded that a fixed-dose combination pill containing aspirin, statin and two blood pressure (BP) lowering agents may improve adherence to treatment as well as substantially reduce the cost of the drugs, particularly for low and middle income countries.  In 2003, Wald and Law claimed that ischemic heart disease could be reduced by 88% and strokes by 80% if all those over 55 years of age were given a ‘polypill’ containing three low-dose blood pressure lowering medications, a statin, low dose aspirin and folic acid.  This controversial approach of ‘medicalising’ the population has been followed by more targeted approaches of ‘polypills’ recommended for high risk individuals only, where effectiveness and cost-effectiveness are likely to be most favourable.  An important aspect of the ‘polypills’ is their affordability, particularly for low-income countries where cardiovascular mortality is increasing. .
Evidence for fixed-dose combination (FDC) medications has been promising, as shown by a meta-analysis of antihypertensive FDCs.  In 2002, the WHO recommended that bioavailability, pharmacokinetics, effects on risk factors and side effects of ‘polypill’ formulations should be assessed by short-term efficacy trials, followed by community-based effectiveness trials and cost-effectiveness evaluations comparing ‘polypills’ to standard practice.  It has taken more than 10 years to progress these aims. Several efficacy trials of ‘polypills’ including at least one antihypertensive and one lipid-lowering medication have been conducted. Some are placebo-controlled while others have active component comparators. This systematic review and meta-analysis aimed to assess the efficacy and tolerability of the ‘polypill’ approach by examining the effects on blood pressure, lipid profiles and discontinuation and side effects of medication.
This was a meta-analysis of published summary data and therefore did not require ethics approval.
Definition of a ‘Polypill’
For the purposes of this review, a ‘polypill’ has been defined as a medication formulation containing at least one blood pressure lowering medication and one lipid-lowering medication (with or without an anti-platelet agent such as aspirin).
Selection of Studies
This meta-analysis included randomised controlled trials of cardiovascular ‘polypills’ that were published in English. Trials of at least six weeks duration were eligible to allow reasonable estimation of clinical effect and likely discontinuation of medication. Trials must have assessed at least one primary outcome of this review, which included systolic and diastolic blood pressure, serum total and LDL-cholesterol and a measure of tolerability, either discontinuation of medication or proportion reporting side effects. The comparator could be placebo or component medications that allowed a placebo comparison for at least one primary outcome.
The Cochrane Central Register of Controlled Trials, Medline, and PubMed databases were searched for eligible trials using the terms in Table S1. The strategy was guided by the Cochrane Systematic Review Handbook.  Reference lists were also searched. A second researcher undertook an independent literature search of Medline, PubMed and Embase (Table S2).
Data were extracted on design, intervention, duration of follow-up, sample size (intervention and control) and follow-up rate. Study population demographic, cardiovascular risk and co-morbidity characteristics were also recorded. Data extraction was undertaken separately by two researchers. Study quality was assessed using the Jadad criteria where a score out of five is given for description and appropriateness of randomisation and blinding, and for description of withdrawals and drop-outs.  The Cochrane criteria for risk of bias were also used to assess study quality.  Change in outcome measures in each group over the trial was recorded. Authors were contacted where data were missing. The number and proportion of study participants who discontinued the study medication during the trial and the proportion of participants with side effects were compared between intervention and control groups.
The weighted mean difference in continuous outcomes was calculated using Cochrane RevMan 5.1 software  and checked by a separate researcher using STATA (v12, StataCorp LP). Means and standard deviations of change of the primary outcome measures were used where reported. Where standard deviations could not be obtained from the published data or from contacting the authors, standard deviations from baseline were used.  Where there was no placebo control, comparators not containing an anti-hypertensive for blood pressure analyses or not containing a lipid-lowering medication for lipid analyses were used. Odds ratios and 95% confidence intervals were calculated for dichotomous variables. Heterogeneity was investigated using Tau2 and I2 statistics. Where substantial statistical heterogeneity was found, random-effects models were used and compared with quality-effects models.  Publication bias was investigated using Begg’s rank correlation and Egger’s regression methods in STATA v12, and funnel plots in RevMan. , ,  Sensitivity analyses were carried out on the basis of duration of follow-up, as it was hypothesized that effect size may reduce if adherence decreased over time.
Of the 44 studies identified by the literature search, six fulfilled the inclusion criteria and were included in the meta-analysis (Figure 1 and Table S1). A search undertaken independently by a second researcher did not identify any additional eligible studies (Figure S1). The characteristics and quality of the eligible studies are included in Table 1.
Figure 1. Polypills Meta-analysis ‘PRISMA’ Flow Diagram.doi:10.1371/journal.pone.0052145.g001
Table 1. Baseline Characteristics and Study Quality of included Randomised Controlled Trials.doi:10.1371/journal.pone.0052145.t001
Characteristics of Studies
The intervention of all trials was a fixed dose combination that contained either one, two or three antihypertensives (including a calcium channel blocker , , a thiazide and ACE inhibitor , , a thiazide, ACE inhibitor and beta-blocker , or a thiazide, angiotensin receptor blocker and a calcium channel blocker ) plus one lipid lowering medication (including atorvastatin (20 mg) , ,  or simvastatin (20 mg ,  or 40 mg )). Three ‘polypills’ also included aspirin (75 mg or 100 mg). , ,  The comparison was either a true placebo , ,  or one cardiovascular component (aspirin , simvastatin  or amlodipine ). All trials were double-blind. Five were parallel designs and one was a cross-over design.  One parallel trial included nine arms of varying numbers of fixed dose components but with no placebo arm.  For this trial only the ‘polycap’ arm and the arms not containing an antihypertensive (‘aspirin arm’ and ‘statin arm’) for blood pressure comparisons and one arm not containing a lipid-lowering agent (‘aspirin arm’) for lipid comparisons were used.  Five studies were of 6–12 weeks and one trial of 12 months duration.  Two other randomised controlled trials of ‘polypills’ were identified but excluded. One study compared low-dose with high-dose polycap components but did not include a placebo arm or reduced number of components that allowed a placebo comparison of blood pressure or serum lipid concentrations.  The other study was an open label trial comparing a ‘polypill’ with usual care. .
Table 1 summarises the study and participant characteristics. A total of 2,218 patients were included in the meta-analysis comparisons. This was made up of 1,116 in a ‘polypill’ group and 1,102 in a comparison group. No participants had previous cardiovascular disease but most had at least one cardiovascular risk factor. Despite this, there were some differences between study populations. Two trials excluded those with diabetes. ,  Mean baseline systolic blood pressure varied from 125 mmHg  to 147 mmHg  in the intervention groups across trials and the proportion of women participants varied from 19%  to 53%.  All trials except two ,  allowed concomitant blood-pressure lowering medication, although levels of use were low.
Effect on Blood Pressure
Results from five trials, where control arms did not contain antihypertensive medication, were combined to assess effects of ‘polypills’ on blood pressure lowering (Figure 2). Compared with placebo, the ‘polypills’ reduced systolic blood pressure by −9.2 mmHg (95% confidence interval (CI): −13.4, −5.0) and diastolic blood pressure by −5.0 mmHg (95%CI: −7.4, −2.6). However, there was evidence of significant heterogeneity of trials (I2 87% and 83%, respectively). A sensitivity analysis including the four shorter trials of 6 to 12 weeks duration and excluding the longer trial of 12 months , found systolic blood pressure reduced by −10.8 mmHg (95%CI: −15.2, −6.3), and diastolic blood pressure by −6.0 mmHg (95%CI: −8.1, −4.0).
Figure 2. Forest Plots of Polypills versus Control for Change in Systolic and Diastolic Blood Pressure.doi:10.1371/journal.pone.0052145.g002
Effect on Lipid Profiles
Results from all trials, where the control did not contain lipid-lowering medication, were combined to assess effects on serum lipids (Figure 3). Compared with placebo, the ‘polypills’ reduced total cholesterol by −1.22 mmol/L (95%CI: −1.60, −0.84) and LDL-cholesterol by −1.02 mmol/L (95%CI: −1.37, −0.67). There was high statistical heterogeneity (I2 = 96%). If the 12 month trial was excluded , total cholesterol reduced by −1.33 mmol/L (95%CI: −1.72, −0.95) and LDL-cholesterol by −1.13 mmol/L (95%CI: −1.47, −0.79).
Figure 3. Forest Plots of Polypills versus Control for Change in Total Cholesterol and LDL-cholesterol.doi:10.1371/journal.pone.0052145.g003
Discontinuation of Study Medication and Side Effects
Those taking ‘polypills’ were more likely to discontinue medication compared with placebo or one component (20% vs 14%) (OR: 1.5 (95%CI: 1.2, 1.9); Figure 4). There was lower heterogeneity (I2 = 21%) than for the estimates of effects on blood pressure or lipids. When only comparisons with placebo were included, , ,  the odds ratio was 1.7 (95%CI: 1.3, 2.3) (24% vs 16%). Amongst the four trials that reported overall side effects , , , , the difference between ‘polypills’ and comparison arms in the proportion experiencing side effects (36% vs 28%) was not statistically significant (OR: 1.3 (95%CI: 0.7, 2.5; I2 = 73%) (Figure 4). The difference approached significance when only placebo-controlled trials were compared (45% vs 33%) (OR: 1.7 (95%CI: 0.97, 2.9)).
Figure 4. Forest Plots of Polypills versus Control for Change in Discontinuation of Study Medication and Side Effects.doi:10.1371/journal.pone.0052145.g004
Study Quality and Potential Bias
Due to the high levels of heterogeneity, quality-effects models were also conducted and compared with the results from random-effects models, using MetaXL in Excel.  Very similar effect estimates were obtained (Figure S2). Overall, included trials were of high quality (Jadad score 4/5 to 5/5), (Table 1). However, there were differences in baseline systolic blood pressure between intervention and control groups in the trials of the Pill Collaborative Group and Malekzadeh et al. (4.0 and 5.5 mmHg, respectively). ,  The latter trial had imbalances in several baseline characteristics suggesting inadequacy of randomisation.  It also had moderately high rates of attrition from both groups but more in the intervention group (31% vs 22%), representing another potential source of bias. Risk of bias in this trial was therefore “uncertain” according to Cochrane criteria (Table S3).  There was no evidence of publication bias in any of the analyses (as evaluated by Begg’s and Egger’s tests and graphical representation using funnel plots (Figure S3)). The PRISMA checklist can be found for this meta-analysis in Table S4.
Summary of Findings
Compared with placebo, the ‘polypills’ reduced systolic blood pressure by −9.2 mmHg, diastolic blood pressure by −5.0 mmHg, total cholesterol by −1.22 mmol/L and LDL-cholesterol by −1.02 mmol/L. Those taking a ‘polypill’ were more likely to discontinue study medication than those taking one component or placebo, although reported adverse effects were not significantly different.
Strengths and Limitations
There was significant clinical and statistical heterogeneity amongst the trials. It may be argued that these studies should not have been combined in a meta-analysis because they contained interventions and controls with different components, and duration of follow-up varied from 6 weeks to 12 months. However, the meta-analysis assesses the use of cardiovascular ‘polypills’ in a variety of settings and populations, typical of real life, where at least one antihypertensive and one lipid-lowering medication have been combined in a fixed dose combination. Therefore, heterogeneity would be expected. Random-effects and quality-effects models found very similar effect sizes.  There are also limitations with using summary level data rather than individual-level data in a meta-analysis.
Compared with the Literature and Implications for Future Practice
This meta-analysis reviewed the current evidence for efficacy and tolerability of cardiovascular ‘polypills’. The ‘polypills’ reduced risk factors compared with placebo; although less than has been estimated previously.  Wald et al estimated that a cardiovascular ‘polypill’ could reduce LDL cholesterol by 1.8 mmol/L and blood pressure by 20/11 mmHg. Actual reductions in risk factors depend on baseline risk factor levels and the number and doses of medications contained within the polypills. Wald’s estimated reduction in LDL cholesterol used a baseline of 4.8 mmol/L.  A 2003 meta-analysis of statin trials provides expected reductions in LDL based on statin and dose , from which expected reductions in LDL can be estimated for each of the trials in this meta-analysis taking into account baseline LDL level (Table 2). The ‘polypills’ in the trials included within this meta-analysis contained between one and three anti-hypertensives with doses of a quarter to twice the standard dose equivalent for each of these components (Table 2). The observed reductions in systolic blood pressure and LDL-cholesterol for the ‘polypills’ were comparable to that expected for two of the trials (Neutel and Wald). Although the observed reduction in systolic blood pressure was comparable to that expected in the PILL collaborative trial, the observed reduction in LDL-cholesterol was only 64% of that expected. The observed reduction in LDL cholesterol in the Grimm trial was 89% of that expected. The observed reduction in systolic blood pressure and LDL-cholesterol were much less than expected in the Malekzadeh and TIPS trials. This discrepancy could be explained by the greater loss to follow up in these trials, which would dilute treatment effect when ‘intention to treat’ analyses are undertaken, a lower adherence rate than reported, concomitant treatment in the control groups or methodological issues. However, it may also be closer to the real change in risk factors likely if used in practice. The trial that found the greatest reductions in blood pressure and lipids was the trial that had few participants drop-out, good adherence, and no concomitant blood pressure and lipid-lowering medication.  Almost all the participants had been taking the component medications prior to the trial, so presumably would be those most likely to tolerate and adhere to a combination ‘polypill’.  For this type of patient, we can expect predicted results. The real test will be in comparing ‘polypills’ to current care.
Table 2. Actual vs Expected Reductions in Systolic Blood Pressure and LDL-cholesterol in Trials of ‘Polypills’.doi:10.1371/journal.pone.0052145.t002
A short 12-week effectiveness trial comparing a ‘polypill’ with current care has been completed, but showed no difference between groups in systolic blood pressure or total cholesterol.  Several longer trials comparing a ‘polypill’ with current care are well underway or soon to be published. , , , ,  The doses and number of components used will obviously influence both effectiveness and tolerability. A recent trial showed that doubling the doses of five ‘polypill’ components resulted in further significant reductions in systolic blood pressure (2.8 mmHg), diastolic blood pressure (1.7 mmHg), total cholesterol (0.19 mmol/L) and LDL-cholesterol (0.17 mmol/L). .
Even if the effectiveness of the ‘polypill’ strategy is found only to be equivalent to current care, cost is likely to be reduced, making preventive therapies more affordable, particularly for low-income countries.  A large part of the burden of chronic disease, particularly cardiovascular disease, is now borne by low-income countries. In 2005, it was estimated that 35 million people would die from non-communicable chronic diseases around the world.  Cardiovascular disease was found to be the leading single cause of death and accounted for 20% of the total disability-adjusted years lost amongst people over 30 years of age globally. Furthermore, 80% of the burden of chronic disease occurs in people under the age of 70 years.  Rates of preventive therapy are lower in low- and middle-income countries than in high-income countries.  Patented medications have made many of the cardiovascular preventive medications prohibitively expensive for these countries, severely limiting access to medications, increasing levels of poverty  and causing impoverishment in households struggling to afford medication.  The use of affordable ‘polypills’ could help address this issue.
A recent review of the cost-effectiveness of interventions for primary prevention of cardiovascular disease found that one of the ‘best value for money’ interventions was a combination of low cost blood pressure lowering medications and a statin, aimed at those at increased CVD risk.  Modelled cost-effectiveness analyses of a ‘polypill’ have also been promising in middle and higher income countries. ,  However, the actual clinical and economic potential of a polypill strategy will require the results of effectiveness trials that compare ‘polypills’ with current care and subsequent cost-utility analyses.
‘Polypills’ meta-analysis flow diagram of a second literature search.
Meta-analyses comparing ‘quality effects’ models with ‘random effects’ or Mantel Haenszel fixed effects models undertaken in Excel.
Funnel plots to assess for publication bias.
Literature search terms and results, conducted by CRE.
Literature search terms and results, conducted by AKG.
Risk of bias of included studies, using the Cochrane collaboration criteria.
We would like to thank the corresponding authors of the studies who contributed extra data and information for this meta-analysis.
Conceived and designed the experiments: CRE AKG RW VS MJ AP AR ST. Performed the experiments: CRE AKG VS. Analyzed the data: CRE AKG VS. Contributed reagents/materials/analysis tools: CRE AKG VS. Wrote the paper: CRE AKG RW VS MJ AP AR ST. Contributed to literature search strategy: RW MJ. Critically appraised analyses:W MJ AP AR ST. Contributed to interpretation of results: RW MJ AP AR ST.
- 1. World Health Organization (2008) The global burden of disease: 2004 update. Geneva: World Health Organization: WHO website. Available: http://www.who.int/healthinfo/global_burden_disease/2004_report_update/en/index.html Accessed: August 2012.
- 2. National Institute for Health and Clinical Excellence (2011) Secondary prevention in primary and secondary care for patients following a myocardial infarction. UK: NHS website. Available: http://publications.nice.org.uk/mi-secondary-prevention-cg48/introduction Accessed: 8th June 2012.
- 3. New Zealand Guidelines Group (2012) New Zealand Primary Care Handbook 2012: Cardiovascular risk assessment and diabetes screening; Cardiovascular risk factor management; Management of type 2 diabetes. NZGG website. Available: http://www.health.govt.nz/publication/new-zealand-primary-care-handbook-2012 Accessed: November 2012.
- 4. Law MR, Morris JK, Wald NJ (2009) Use of blood pressure lowering drugs in the prevention of cardiovascular disease: meta-analysis of 147 randomised trials in the context of expectations from prospective epidemiological studies. BMJ 338: b1665. doi: 10.1136/bmj.b1665
- 5. Law MR, Wald NJ, Rudnicka AR (2003) Quantifying effect of statins on low density lipoprotein cholesterol, ischaemic heart disease, and stroke: systematic review and meta-analysis. BMJ 326: 1423. doi: 10.1136/bmj.326.7404.1423
- 6. Cholesterol Treatment Trialists’ (CTT) Collaborators (2012) The effects of lowering LDL cholesterol with statin therapy in people at low risk of vascular disease: meta-analysis of individual data from 27 randomised trials. Lancet 6736: 60367–60365. doi: 10.1371/journal.pone.0029849
- 7. Antithrombotic Trialists Collaboration (2002) Collaborative meta-analysis of randomised trials of antiplatelet therapy for prevention of death, myocardial infarction, and stroke in high risk patients. BMJ 324: 71–86. doi: 10.1136/bmj.324.7329.71
- 8. U.S. Preventive Services Task Force (2009) Aspirin for the prevention of cardiovascular disease: U.S. Preventive Services Task Force Recommendation Statement. Ann Intern Med 150: 396–404. doi: 10.7326/0003-4819-150-6-200903170-00008
- 9. Yusuf S (2002) Two decades of progress in preventing vascular disease. Lancet 360: 2–3. doi: 10.1016/S0140-6736(02)09358-3
- 10. Murray CJL, Lauer JA, Hutubessy RCW, Niessen L, Tomijima N, et al. (2003) Effectiveness and costs of interventions to lower systolic blood pressure and cholesterol: a global and regional analysis on reduction of cardiovscular-disease risk. Lancet 361: 717–725. doi: 10.1016/S0140-6736(03)12655-4
- 11. Wald N, Law M (2003) A strategy to reduce cardiovascular disease by more than 80%. BMJ 326: 1419–1424. doi: 10.1136/bmj.326.7404.1419
- 12. Elley CR, Kenealy T, Robinson E, Bramley D, Selak V, et al. (2008) Cardiovascular risk management of different ethnic groups with type 2 diabetes in primary care in New Zealand. Diabetes Res Clin Pract 79: 468–473. doi: 10.1016/j.diabres.2007.09.018
- 13. Yusuf S, Islam S, Chow CK, Rangarajan S, Dagenais G, et al. (2011) Use of secondary prevention drugs for cardiovascular disease in the community in high-income, middle-income, and low-income countries (the PURE Study): a prospective epidemiological survey. Lancet 378: 1231–1243. doi: 10.1016/S0140-6736(11)61215-4
- 14. Selak V, Rafter N, Parag V, Tomlin A, Hoorn SV, et al. (2009) Cardiovascular treatment gaps: Closing, but slowly. N Z Med J 122: 41–49.
- 15. World Health Organization (2003) Adherence to Long-term Therapies: Evidence for action WHO website. Available: http://www.who.int/chp/knowledge/publications/adherence_report/en/index.html Accessed: August 2012.
- 16. Kulkarni SP, Alexander KP, Lytle B, Heiss G, Peterson ED (2006) Long-term adherence with cardiovascular drug regimens. Am Heart J 151: 185–191. doi: 10.1016/j.ahj.2005.02.038
- 17. Chapman RH, Benner JS, Petrilla AA, Tierce JC, Collins SR, et al. (2005) Predictors of adherence with antihypertensive and lipid-lowering therapy. Arch Intern Med 165: 1147–1152. doi: 10.1001/archinte.165.10.1147
- 18. Gaziano TA, Opie LH, Weinstein MC (2006) Cardiovascular disease prevention with a multidrug regimen in the developing world: a cost-effectiveness analysis. Lancet 368: 679–686. doi: 10.1016/S0140-6736(06)69252-0
- 19. Lafeber M, Spiering W, Singh K, Guggilla R, Patil V, et al.. (2011) The cardiovascular polypill in high-risk patients. Eur J Prev Cardiol http://cpr.sagepub.com/content/early/2011/10/20/1741826711428066: 1–9; Accessed: August 2012.
- 20. World Health Organization (2002) Secondary prevention of non-communicable disease in low and middle income countries through community-based and health service interventions. World Health Organization - Wellcome Trust meeting report 1–3 August 2001, Geneva. WHO website. Available: http://www.who.int/cardiovascular_diseases/media/en/615.pdf Accessed: November 2012.
- 21. Lonn E, Bosch J, Teo KK, Pais P, Xavier D, et al. (2010) The polypill in the prevention of cardiovascular diseases: key concepts, current status, challenges, and future directions. Circulation 122: 2078–2088. doi: 10.1161/CIRCULATIONAHA.109.873232
- 22. Strong K, Mathers C, Leeder S, Beaglehole R (2005) Preventing chronic diseases: how many lives can we save? Lancet 366: 1578–1582. doi: 10.1016/S0140-6736(05)67341-2
- 23. Gupta AK, Arshad S, Poulter NR (2010) Compliance, safety, and effectiveness of fixed-dose combinations of antihypertensive agents: a meta-analysis. Hypertension 55: 399–407. doi: 10.1161/HYPERTENSIONAHA.109.139816
- 24. Cochrane Collaboration (2011) Cochrane Handbook for Systematic Reviews of Interventions, Version 5.1.0. In: Higgins J, Green S, editors.
- 25. Jadad AR, Moore RA, Carroll D, Jenkinson C, Reynolds DJ, et al. (1996) Assessing the quality of reports of randomized clinical trials: is blinding necessary? Control Clin Trials 17: 1–12. doi: 10.1016/0197-2456(95)00134-4
- 26. Furukawa TA, Barbui C, Cipriani A, Brambilla P, Watanabe N (2006) Imputing missing standard deviations in meta-analyses can provide accurate results. J Clin Epidemiol 59: 7–10. doi: 10.1016/j.jclinepi.2005.06.006
- 27. Doi SAR, Barendregt JJ, Mozurkewich EL (2011) Meta-analysis of heterogeneous clinical trials: an empirical example. Contemp Clin Trials 32: 288–298. doi: 10.1016/j.cct.2010.12.006
- 28. Begg CB, Mazumdar M (1994) Operating characteristics of a rank correlation test for publication bias. Biometrics 50: 1088–1101. doi: 10.2307/2533446
- 29. Egger M, Davey Smith G, Schneider M, Minder C (1997) Bias in meta-analysis detected by a simple, graphical test. BMJ 315: 629–634. doi: 10.1136/bmj.315.7109.629
- 30. Sterne JA, Egger M, Smith GD (2001) Systematic reviews in health care: Investigating and dealing with publication and other biases in meta-analysis. BMJ 323: 101–105. doi: 10.1136/bmj.323.7304.101
- 31. Grimm R, Malik M, Yunis C, Sutradhar S, Kursun A, et al. (2010) Simultaneous treatment to attain blood pressure and lipid goals and reduced CV risk burden using amlodipine/atorvastatin single-pill therapy in treated hypertensive participants in a randomized controlled trial. Vasc Health Risk Manag 6: 261–271. doi: 10.2147/VHRM.S7710
- 32. Neutel JM, Bestermann WH, Dyess EM, Graff A, Kursun A, et al. (2009) The use of a single-pill calcium channel blocker/statin combination in the management of hypertension and dyslipidemia: a randomized, placebo-controlled, multicenter study. J Clin Hypertens 11: 22–30. doi: 10.1111/j.1751-7176.2008.00058.x
- 33. Pill Collaborative Group, Rodgers A, Patel A, Berwanger O, Bots M, et al (2011) An international randomised placebo-controlled trial of a four-component combination pill (“polypill”) in people with raised cardiovascular risk. PLoS ONE 6: e19857. doi: 10.1371/journal.pone.0019857
- 34. Malekzadeh F, Marshall T, Pourshams A, Gharravi M, Aslani A, et al. (2010) A pilot double-blind randomised placebo-controlled trial of the effects of fixed-dose combination therapy (‘polypill’) on cardiovascular risk factors. Int J Clin Pract 64: 1220–1227. doi: 10.1111/j.1742-1241.2010.02412.x
- 35. The Indian Polycap Study (TIPS) (2009) Effects of a polypill (Polycap) on risk factors in middle-aged individuals wihtout cardiovascular disease (TIPS): a phase II, double-blind, randomised trial Lancet. 373: 1341–1351. doi: 10.1111/j.1751-7176.2008.00058.x
- 36. Wald DS, Morris JK, Wald NJ (2012) Randomized polypill crossover trial in people aged 50 and over. PLoS ONE 7: e41297. doi: 10.1371/journal.pone.0041297
- 37. Yusuf S, Pais P, Sigamani A, Xavier D, Afzal R, et al. (2012) Comparison of Risk Factor Reduction and Tolerability of a Full-Dose Polypill (With Potassium) Versus Low-Dose Polypill (Polycap) in Individuals at High Risk of Cardiovascular Diseases: The Second Indian Polycap Study (TIPS-2) Investigators. Circ Cardiovasc Qual Outcomes 5: 463–471. doi: 10.1161/CIRCOUTCOMES.111.963637
- 38. Soliman EZ, Mendis S, Dissanayake WP, Somasundaram NP, Gunaratne PS, et al. (2011) A Polypill for primary prevention of cardiovascular disease: a feasibility study of the World Health Organization. Trials 12: 3. doi: 10.1186/1745-6215-12-3
- 39. Liu H, Patel A, Brown A, Eades S, Hayman N, et al. (2010) Rationale and design of the Kanyini guidelines adherence with the polypill (Kanyini-GAP) study: a randomised controlled trial of a polypill-based strategy amongst indigenous and non indigenous people at high cardiovascular risk. BMC Public Health 10: 458. doi: 10.1186/1471-2458-10-458
- 40. Sanz G, Fuster V, Guzman L, Guglietta A, Arnaiz JA, et al. (2011) The fixed-dose combination drug for secondary cardiovascular prevention project: improving equitable access and adherence to secondary cardiovascular prevention with a fixed-dose combination drug. Study design and objectives. Am Heart J 162: 811–817.e811. doi: 10.1016/j.ahj.2011.08.012
- 41. Selak V, Elley CR, Crengle S, Harwood M, Doughty R, et al. (2011) Improving adherence using combination therapy (IMPACT): Design and protocol of a randomised controlled trial in primary care. Contemp Clin Trials 32: 909–915. doi: 10.1016/j.cct.2011.07.006
- 42. Zamorano J, Erdine S, Lopez AP, Kim JH, Al Khadra A, et al. (2010) Design and rationale of a real-life study to compare treatment strategies for cardiovascular risk factors: the CRUCIAL study. Postgrad Med 122: 7–15. doi: 10.3810/pgm.2010.03.2117
- 43. Thom S, Field J, Poulter N, Patel A, Prabhakaran D, et al.. (2012) Use of a Multidrug Pill In Reducing cardiovascular Events (UMPIRE): rationale and design of a randomised controlled trial of a cardiovascular preventive polypill-based strategy in India and Europe. Eur J Preventive Cardiology.
- 44. Lim SS, Gaziano TA, Gakidou E, Reddy KS, Farzadfar F, et al. (2007) Prevention of cardiovascular disease in high-risk individuals in low-income and middle-income countries: health effects and costs. Lancet 370: 2054–2062. doi: 10.1016/S0140-6736(07)61699-7
- 45. Niens LM, Cameron A, Van de Poel E, Ewen M, Brouwer WBF, et al.. (2010) Quantifying the impoverishing effects of purchasing medicines: a cross-country comparison of the affordability of medicines in the developing world. PLoS Med 7.
- 46. Banerjee A, Hollis A, Pogge T (2010) The Health Impact Fund: incentives for improving access to medicines. Lancet 375: 166–169. doi: 10.1016/S0140-6736(09)61296-4
- 47. Cobiac LJ, Magnus A, Lim S, Barendregt JJ, Carter R, et al. (2012) Which interventions offer best value for money in primary prevention of cardiovascular disease? PLoS ONE 7: e41842. doi: 10.1371/journal.pone.0041842
- 48. Liew D, Park H-J, Ko S-K (2009) Results of a Markov model analysis to assess the cost-effectiveness of a single tablet of fixed-dose amlodipine and atorvastatin for the primary prevention of cardiovascular disease in Korea. Clin Ther 31: 2189–2203; discussion 2150–2181.
- 49. van Gils PF, Over EAB, Hamberg-van Reenen HH, de Wit GA, van den Berg M, et al. (2011) The polypill in the primary prevention of cardiovascular disease: cost-effectiveness in the Dutch population. BMJ Open 1: e000363. doi: 10.1136/bmjopen-2011-000363
- 50. Law MR, Wald NJ, Morris JK, Jordan RE (2003) Value of low dose combination treatment with blood pressure lowering drugs: analysis of 354 randomised trials. BMJ 326: 1427. doi: 10.1136/bmj.326.7404.1427