Individual patient data meta-analysis of beta-blockers in heart failure: rationale and design
© Kotecha et al.; licensee BioMed Central Ltd. 2013
Received: 24 September 2012
Accepted: 3 December 2012
Published: 18 January 2013
The Beta-Blockers in Heart Failure Collaborative Group (BB-HF) was formed to obtain and analyze individual patient data from the major randomized controlled trials of beta-blockers in heart failure. Even though beta-blockers are an established treatment for heart failure, uptake is still sub-optimal. Further, the balance of efficacy and safety remains uncertain for common groups including older persons, women, those with impaired renal function and diabetes. Our aim is to provide clinicians with a thorough and definitive evidence-based assessment of these agents. We have identified 11 large randomized trials of beta-blockers versus placebo in heart failure and plan to meta-analyze the data on an individual patient level. In total, these trials have enrolled 18,630 patients. Uniquely, the BB-HF group has secured access to the individual data for all of these trials, with the participation of key investigators and pharmaceutical companies.
Our principal objectives include deriving an overall estimate of efficacy for all-cause mortality and cardiovascular hospitalization. Importantly, we propose a statistically-robust sub-group assessment according to age, gender, diabetes and other key factors; analyses which are only achievable using an individual patient data meta-analysis. Further, we aim to provide an assessment of economic benefit and develop a risk model for the prognosis of patients with chronic heart failure.
This paper outlines inclusion criteria, search strategies, outcome measures and planned statistical analyses.
Systematic review registration
Clinical trial registration information: http://clinicaltrials.gov/ct2/show/NCT00832442
KeywordsBeta-blockers Heart failure Meta-analysis Design paper
Heart failure (HF) is a major public health problem with both incidence and prevalence rising rapidly along with associated healthcare costs, estimated to be $39.2 billion in the United States and £625 million per year in the UK [1, 2]. HF accounts for around 5% of all hospital admissions and re-admission rates approach 50% over the following 12 months. Prior to the 1990s, beta-blockers were considered to be contraindicated in HF. With an increased understanding of the pathophysiology of HF, the hypothesis developed that beta-blockers may alleviate inappropriate sympathetic drive, reduce heart rate and allow better cardiac filling. A series of small mechanistic studies followed by larger randomized trials have now established beta-blockers as a key evidence-based treatment to reduce mortality and morbidity alongside angiotensin converting enzyme (ACE) inhibitors and aldosterone antagonists. Current European and American guidelines give a class I recommendation for the use of beta-blockers in patients with symptomatic systolic HF [3, 4].
However, survey data have confirmed that the uptake of beta-blockers in HF patients is still sub-optimal. Although the percentage of eligible patients prescribed beta-blockers increased between the first and second Euro Heart Failure surveys, a substantial number of patients remain untreated or receive sub-maximal therapy [5, 6]. Paradoxically, those at the greatest risk of death are less likely to receive evidence-based therapy after a HF hospitalization . The reasons for this are multi-factorial and include a long entrenched belief that starting beta-blockers in HF may make symptoms worse or that beta-blockers should only be commenced in specialized clinics. There has also been concern that the evidence-base is not representative of broader clinical practice and that common patient groups, including older persons, those with impaired renal function and diabetes may not benefit.
Although a number of sub-group and meta-analyses based on published data have been conducted [8, 9], these can only address reported outcomes and are limited statistically. Only an individual patient data (IPD) meta-analysis is able to explore the effects of treatment on important secondary outcomes such as sudden death, NYHA class or ejection fraction and allow reliable pooled sub-group analyses.
The Beta-blockers in Heart Failure Collaborative Group (BB-HF)
The BB-HF group is a collaborative, multinational effort to combine individual data from the major randomized controlled trials (RCTs) investigating the use of beta-blockers in chronic HF. The group consists of the leading investigators of these trials and international experts, with the support of the four pharmaceutical companies that have marketed beta-blockers in HF (AstraZeneca, GlaxoSmithKline, Merck Serono and Menarini). A full list of collaborators is presented in Appendix A. Two meetings of the collaborative group in November 2008 and August 2010 were used to define our objectives, establish inclusion criteria and develop the primary and secondary objectives. A standardized data request form was generated to obtain IPD from each eligible trial (see Additional file 1)
At the time of this publication, individual data on 15,922 participants (representing 10 of the 11 trials) have been received by the coordinating center, the Clinical Trials and Evaluation Unit, Royal Brompton & Harefield NHS Trust/Imperial College London.
Provide a definitive estimate of the overall treatment effect of beta-blockers in HF on key outcomes including all-cause mortality and hospitalization.
Analyze the influence of important pre-randomization patient characteristics on the clinical effects of beta-blockers, including age, diabetes, gender, ejection fraction, renal function, atrial fibrillation and the etiology of HF.
Pool the adverse event and discontinuation data to assess the safety of beta-blockers in HF patients, particularly the rate of bradycardia and hypotension.
Explore the relationship between the effects of beta blockers and key baseline measurements including heart rate, blood pressure and weight.
Perform an exploratory analysis to assess important post-randomization variables, such as change in heart rate, achieved heart rate, change in blood pressure, achieved dose and the prescription of other concomitant therapies, such as ACE inhibitors, angiotensin receptor blockers (ARB), aldosterone antagonists, diuretics and digoxin.
Describe in detail the effect on hospitalization data including recurrent hospitalization, total number of cardiovascular/HF-related hospitalizations and duration of stay according to treatment allocation.
Develop a risk model for patients with HF using key baseline characteristics to allow clinicians to accurately assess prognosis in individual patients.
Examine the potential economic impact of treatment under a variety of circumstances and different subgroups.
Improve statistical methodology for IPD meta-analysis.
Study inclusion criteria
A number of inclusion criteria were adopted to make the project methodologically sound and technically feasible. All RCTs of beta-blockers versus placebo explicitly reporting mortality as a primary or combination outcome will be included but not head-to-head comparisons with another active agent. Trials must include patients with documented symptomatic HF and only unconfounded trials will be accepted (in which one treatment group differed from another only by the beta-blocker therapy of interest). Finally, RCTs would only be included if they recruited more than 300 patients in total and planned follow-up of six months or greater. By concentrating on the larger trials (which have enrolled 95.7% of all RCT participants), the project remains practical while the amount of data missed by not including the smaller trials is minimized.
Search strategy and eligible studies
To ensure a complete assessment of the evidence, published or unpublished RCTs were identified through computer aided searches (for example, Medline and Current Contents), scrutiny of reference lists of trials, trials registries, meeting abstracts, review articles and discussion with members of the collaborative group and with the pharmaceutical manufacturers.
Details of studies proposed for inclusion in meta-analysis
Trial (drug) by year
Withdrawal/ Lost to follow-up
Treatment with BB or CCB; Significant CAD on angiography; Myocarditis; Life-threatening diseases; COPD requiring beta agonists; Drug or alcohol abuse; IDDM; Thyroid disease; SBP <90 mmHg; HR <45
All-cause mortality; Need for transplantation; exercise capacity; NYHA, QoL
12% metoprolol, 16% placebo /
18 months (12 after 1990); additional 3-year data
Age 16 to 75
Hypertrophic/restrictive cardiomyopathy; Untreated valve disease; Awaiting bypass surgery; MI in previous three months; On heart transplantation list; IDDM; Asthma; Creatinine >300 μmol/L; Thyroid disease; Life threatening disease; SBP <100 or >160 mmHg; HR <65
All-cause mortality; Bisoprolol tolerability (based on NYHA and adverse events)
23% bisoprolol, 26% placebo /
Mean 1.9 years
Age 18 to 75; NYHA III or IV
Major CV event/surgery within three months; Uncorrected valve disease; Myocarditis; Uncontrolled ventricular tachycardia/heart block; Clinically important hepatic or renal disease; Conditions limiting exercise or survival; Treatment with BB, CCB or class 1C antiarrhythmic agents; SBP <85 or >160 mmHg; HR <68
All-cause mortality; Hospitalization
5.7% carvedilol, 7.8% placebo /
Median 6.5 months
Symptomatic HF due to CAD
Coronary event/procedure within four weeks; Sick sinus, 2nd or 3rd degree heart block; Treadmill exercise duration <2 or >18 minutes; Myocardial or valvular disease; Treatment with BB, beta agonist or verapamil; IDDM; COPD; hepatic disease; Creatinine >250 μmol/L); Life-threatening disease; SBP <90 or >160 mmHg; HR <50
EF; Exercise duration; NYHA; Death; Hospitalization
20% carvedilol, 14%
Mean 19 months
NYHA II or III
MI/unstable angina within three months; Revascularization within six months; Prior or scheduled heart transplant; Uncontrolled 2nd/3rd degree heart block; Creatinine >300 μmol/L; Reversible COPD; Treatment with BB, CCB or antiarrhythmic drugs other than amiodarone; SBP <100 mmHg or uncontrolled hypertension; HR <60
All-cause mortality; All-cause hospital admissions; CV mortality
15% bisoprolol, 15% placebo /
Mean 1.3 years
NYHA III or IV
MI/unstable angina within 28 days; BB within six weeks, CCB or amiodarone within six months; Planned or performed transplantation or implanted defibrillator; Bypass surgery or percutaneous intervention planned or in last four months; Uncorrected 2nd/3rd degree heart block; Other serious diseases; SBP <100 mmHg; HR <68
All-cause mortality; All-cause mortality plus all-cause hospitalization
14% metoprolol, 15% placebo /
Mean 1 year
Age 40 to 80
Uncorrected valvular disease or reversible cause; Prior or planned cardiac transplant; Primary pulmonary or hepatic disease; Creatinine >247.5 μmol/L; Potassium <3.5 or >5.2 mmol/L; Coronary revascularization, MI; stroke or ventricular arrhythmia within two months; Treatment with BB within two months or alpha-blocker, CCB or class I antiarrhythmic within four weeks; SBP <85 mmHg; HR <68
All-cause mortality; Hospitalization
15% carvedilol, 19% placebo /
Mean 10.4 months
NYHA III or IV
Left ventricular dysfunction post-MI
3 to 21 days post-MI;
Continued requirement of intravenous diuretics; Unstable angina; Unstable IDDM; BB indication other than HF; Inhaled beta agonists or steroids; SBP <90 mmHg or uncontrolled hypertension; HR <60
All-cause mortality; All-cause mortality or CV hospitalization; Sudden death; HF-hospitalization; Non-fatal events
20% carvedilol, 18% placebo /
Mean 1.3 years
Reversible cause of HF or valvular disease; Untreated thyroid disease; Obstructive/hypertrophic cardiomyopathy; Pericardial disease; Amyloidosis; Myocarditis; MI within six months; Candidate for heart transplantation; Revascularization within 60 days; Unstable angina; Life expectancy <3 years; Active liver disease or excess alcohol; Creatinine >265 μmol/L; Other serious diseases; Treatment with BB within 30 days, CCB or beta-agonists within one week, class 1 antiarrhythmic within two weeks or amiodarone within eight weeks; SBP <80 mmHg; HR <50
All-cause mortality; Death from CV causes; Hospitalization; EF; Non-fatal MI; QoL
23% bucindolol, 25% placebo /
Mean 2 years
NYHA III or IV;
Digoxin in all patients pre-1997
Stable HF due to CAD
Women of child-bearing age; Acute CV event within three months; Hospital admission within one month; Unstable angina; Arrhythmias (for example, atrial fibrillation); Uncontrolled hypertension; COPD; Poorly controlled diabetes; Clinically relevant renal or hepatic disease; Treatment with non-dihydropiridine CCB, BB or antiarrhythmic other than amiodarone; SBP <85 mmHg; HR <60
Change in EF (hibernators vs. non-hibernators);
15% carvedilol, 7% placebo /
Mean 6.3 months
Age ≥40 years;
Regional echocardiographic contractile dysfunction;
NYHA I to III
Death or worsening HF.
Uncorrected valvular disease; Current use of BB; Significant hepatic or renal dysfunction; Stroke within three months; Pending coronary revascularization; Other serious medical conditions reducing survival; SBP <90 mmHg; HR <60
All-cause mortality or CV hospitalization; All-cause mortality; All-cause hospitalization; NYHA
27% nebivolol, 25% placebo /
Mean 21 months
HF-hospitalization within 12 months or EF ≤35% within 6 months
Patient characteristics of studies proposed for inclusion in meta-analysis
Trial (drug) by Year
Mean SBP (mmHg)
Mean HR (bpm)
MDC (metoprolol) 1993
CIBIS (bisoprolol) 1994
US-HF (carvedilol) 1996
ANZ (carvedilol) 1997
CIBIS II (bisoprolol) 1999
MERIT-HF (metoprolol XL) 1999
COPERNICUS (carvedilol) 2001
CAPRICORN (carvedilol) 2001
BEST (bucindolol) 2001
CHRISTMAS (carvedilol) 2003
SENIORS (nebivolol) 2005
TOTAL / WEIGHTED MEAN
Primary and secondary outcomes
The primary outcome for BB-HF will be all-cause mortality, including deaths recorded after publication of the trial, where these data are available. The major secondary outcome will be the composite of all-cause mortality and cardiovascular hospitalizations. Secondary mortality outcomes include death due to acute myocardial infarction (MI), stroke, sudden cardiac death and HF-related death. Other secondary outcomes are non-fatal MI, all-cause hospitalization, cardiovascular hospitalization, HF-related hospitalization and the number and duration of hospital admissions. Drug safety outcomes will focus on discontinuation due to hypotension, bradycardia, renal impairment and HF-exacerbation.
Due to the complexity of the statistical analyses, the following section represents the planned principal analyses; some modifications and secondary analyses are likely to emerge during the project. However, a detailed statistical analysis plan will be produced prior to the analysis.
Careful initial evaluation will be performed to ensure completeness of data, and to check consistency of the results of the primary analyses for each trial with published reports. Baseline characteristics of patients will be presented separately for each trial and overall. Continuous variables will be presented as mean and standard deviation (or median and range if not normally distributed). Binary and categorical variables will be presented as frequencies and percentages. All analyses will follow the principle of intention to treat as closely as possible. Specifically, we will include all randomized patients with outcome data.
The primary and major secondary outcome will be analyzed using a stratified Cox regression model , with studies as strata. Further models will include known prognostic factors for this patient population (for example, age, gender, baseline ejection fraction, blood pressure, heart rate, diabetes and renal function). This adjusted analysis will give estimates that are more relevant to individual patients. This is a fixed effect approach and assumes that all trials are estimating a common treatment effect. Standard tests for heterogeneity will be carried out and as a sensitivity analysis a random effects approach will be followed. Hazard ratios and corresponding 95% confidence intervals will be presented, along with the corresponding P-value.
The secondary outcomes will be analyzed in the same manner as the primary outcome.
Subgroup analyses will be used to assess the effect of beta-blockers in the following pre-specified subgroups: age, diabetes, gender, ejection fraction, atrial fibrillation and etiology of HF. The influence of age and ejection fraction on the effects of beta-blockers will be explored as continuous variables and as clinically relevant categories for other variables. A meta-analysis of interaction estimates will be used to assess whether any improvement depends on baseline LV ejection fraction, blood pressure, and the presence or absence of other concomitant cardiovascular therapies, such as ACE inhibitors, angiotensin receptor blockers, diuretics and digoxin.
Multiple imputation for missing data will be used where appropriate as a sensitivity analysis. Dichotomous outcomes will be combined using an inverse variance meta-analysis. Odds ratios and corresponding 95% confidence intervals will be presented, along with the corresponding P-value. To explore the influence of baseline covariates on the primary and major secondary outcomes, we will develop multivariable models using the Cox proportional hazards approach to develop a risk score. In all analyses, continuous variables will be kept continuous, and the nature of their relation to outcome evaluated using fractional polynomials.
As noted above, we also plan to perform sensitivity analyses for the exclusion (separately) of the BEST and CAPRICORN trials. If data from the eligible trials are unobtainable, then analysis using a combination of IPD and aggregate data will be considered .
For the economic analysis, we propose to perform a cost analysis using standard published information to provide a representative spread of health economic scenarios. Costs of care will be derived from simple drivers like hospital length of stay, medications and other treatments and a cost effectiveness analysis will be carried out based on cost per event avoided (for example, death or hospital admission). Modeling of cost effectiveness will be carried out based on specific subgroups, such as age, gender and diabetes, in a number of different healthcare models (for example, socialized care, private care and a mixed health care model), taking account of the different costs of beta-blockers. An overall population-based cost impact analysis will be derived assessing different levels of uptake of beta-blockers in heart failure with a view to estimating the cost savings of improving beta-blocker utilization.
Despite a wealth of information identifying the overall benefits of beta-blockers in HF for morbidity and mortality, prescription rates remain sub-optimal with consequence for both patients and healthcare providers. Current data are limited to those enrolled in the RCTs and lack sufficient statistical power to examine the harm and benefits of treatment in important patient sub-groups. For example, diabetes is present in about 25% of patients enrolled in the larger trials of beta-blockers in HF. The risk of mortality and other complications is higher in diabetics but meta-analysis of published tabular data has suggested that the absolute mortality reduction using beta-blockers may be less in patients with diabetes . We will update this analysis by including data from four additional studies and uniquely, will be able to adjust for baseline covariates which may account for much of the apparent difference in effect.
Perhaps the most important patient factor that affects prescription of evidence-based therapy is age. In most population-based studies the incidence and prevalence of HF increases with age and the average age of prevalent HF is about 75 years. Most of the trials enrolled patients with a mean age of 60 to 65 years; only SENIORS recruited a population of 70 years or older. The proposed meta-analysis will allow a reliable exploration of any interaction on the effect of beta-blockers with age, albeit limited to the populations recruited in the individual studies. Similarly, most of the trials have enrolled patients with systolic dysfunction (entry ejection fraction <40%; see Table 1) and an interaction between baseline ejection fraction and the benefit of beta-blockers may exist .
Women with HF are under-represented in the literature and account for less than a quarter of patients in the trials listed in Table 1. Further, the benefits of beta-blockade in women are inconsistent. In the pooled CIBIS trials, all-cause mortality was similarly reduced in men and women  and in the US-HF study women apparently benefited more from beta-blockade (hazard ratio 0.23, 0.07 to 0.69) than men (0.41, 0.22 to 0.80) . In comparison, the results from BEST, MERIT-HF and COPERNICUS found no significant benefit in women [16, 28, 29]. Gender also has important consequences on evaluation, treatment and prognosis in HF. We know that women with HF have different prognostic indicators than men, such as older age, more hypertension and higher ejection fraction, are less likely to receive guideline therapies, and have longer hospital stays [28, 30, 31].
There are also concerns that beta-blockers may worsen renal function in HF by reducing renal blood flow and glomerular filtration rate. Renal impairment is a common co-morbidity in HF that limits therapy. However, existing (under-powered) data suggest that beta-blockers are effective regardless of baseline renal function [32, 33]. We aim to model the effects of beta-blockers stratified by renal function as a continuous variable, adjusting these effects for other covariates which is impossible in a simple tabular analysis. Other important controversies that can be addressed by this IPD analysis include the effects of beta-blockers in patients with HF and atrial fibrillation [34–36], and the interaction of benefit with heart rate, blood pressure changes and achieved dose [37, 38]. We will also use the data to develop new insights into risk factors for death and hospitalization in HF patients. There are also important safety issues to explore, including the risk of adverse events, such as hypotension and bradycardia.
Finally, although IPD meta-analyses are considerably more resource-intensive and time-consuming than standard tabular approaches, we believe that only IPD can address the unanswered questions about the use of beta-blockers in HF. Extraction of data from published reports has significant limitations; typically outcomes are described as the number of participants that have died on each intervention over a fixed period, yielding an odds ratio. In comparison, IPD allows a full time-to-event analysis addressing each event from the time of randomization. The hazard ratio obtained provides a more appropriate view of survival and accounts for censored patients. As previously described, IPD also permits robust analyses of subgroups and the ability to estimate the interaction between covariates and treatment effect . The combined sample sizes for the major variables of interest are sufficient to provide statistical power and conclusive data on the safety and efficacy of beta-blockers in HF patients.
In summary, this individual patient-data systematic review and meta-analysis will provide a definitive assessment of the role of beta-blockers in heart failure. The aims of the Collaborative Group are to reduce the burden of morbidity and mortality in heart failure patients and provide clinicians and healthcare agencies with clear guidance on which patients will benefit from beta-blocker therapy.
A.1. Appendix: Members of BB-HF Collaborative Group
A.1.1. Steering Committee
Marcus Flather: Norwich Medical School, University of East Anglia, Norwich, UK.Dipak Kotecha: Clinical Trials and Evaluation Unit, Royal Brompton Hospital/Imperial College London, UK and Monash Centre of Cardiovascular Research and Education in Therapeutics, Monash University, Melbourne, VIC, Australia.Henry Krum: Monash Centre of Cardiovascular Research and Education in Therapeutics, Monash University, Melbourne, VIC, Australia.Luis Manzano: Department of Medicine, Universidad de Alcala, Hospital Universitario Ramon y Cajal, Madrid, Spain.
A.1.2. Statistical Team
Nicola Williams: Centre for Statistics in Medicine, University of Oxford, Oxford, UK.Douglas Altman: Centre for Statistics in Medicine, University of Oxford, Oxford, UK.
A.1.3. Collaborative Group
Bert Andersson: Department of Cardiology, Sahlgrenska University Hospital, Göteborg, Sweden.John Cleland: University of Hull, Kingston upon Hull, UK.Andrew Coats: University of East Anglia, Norwich, UK.Mike Domanski: National Heart, Lung and Blood Institute, Bethesda, MD, USA.Guliz Erdem: Clinical Trials & Evaluation Unit, Royal Brompton Hospital/Imperial College London, UK.Marilena Grana: A. Menarini Farmaceutica Internazionale, Firenze, Italy.Per Haglund: AstraZeneca Clinical Information Science, Mölndal, Sweden.Åke Hjalmarson: Sahlgrenska University Hospital; Göteborg, Sweden.Philippe Lechat: Agence Française de Sécurité Sanitaire des Produits de Sante, Saint Denis, France.Alain Leizorovicz: Service de Pharmacologie Clinique, Université de Lyon, Lyon Cedex, France.Mary Ann Lukas: GlaxoSmithKline Cardiovascular and Metabolism Medicine Development Center, Philadelphia, PA, USA.Wilfried Meyer: Merck Serono Global Medical Affairs, Darmstadt, Germany.Milton Packer: UT Southwestern Medical Center, Dallas, TX, USA.Alan Rigby: Academic Cardiology, Castle Hill Hospital, Kingston upon Hull, UK.Giuseppe Rosano: Department of Medical Sciences, IRCCS San Raffaele Pisana, Roma, Italy.Michael Roughton: Clinical Trials and Evaluation Unit, Royal Brompton Hospital/Imperial College London, London, UK.Rosemary Schroyer: GlaxoSmithKline Cardiovascular and Metabolism Medicine Development Center, Philadelphia, PA, USA.Marcelo Shibata: Division of Cardiology, University of Alberta, Edmonton, AB, Canada.Hans Wedel: Nordic School of Public Health, Göteborg, Sweden.John Wikstrand: Wallenberg Laboratory, Göteborg University, Göteborg, Sweden.Thomas von Lueder: Monash Centre of Cardiovascular Research and Education in Therapeutics, Monash University, Melbourne, VIC, Australia.and in memoriam; Philip Poole-Wilson: National Heart and Lung Institute, Imperial College London, London, UK.
Angiotensin converting enzyme
Australia/New Zealand Heart Failure Study
Angiotensin receptor blockers
Beta-Blockers in Heart Failure Collaborative Group
Beta-Blocker Evaluation Survival Trial
Carvedilol Post-Infarct Survival Control in LV Dysfunction Study
Carvedilol Hibernating Reversible Ischaemia Trial: Marker of Success Study
- CIBIS I:
Cardiac Insufficiency Bisoprolol Study
Cardiac Insufficiency Bisoprolol Study II
Carvedilol Prospective Randomized Cumulative Survival Study
Individual Patient Data
Metoprolol in Idiopathic Dilated Cardiomyopathy Study
Metoprolol CR/XL Randomised Intervention Trial in Congestive Heart Failure
New York Heart Association
randomized controlled trials
Study of the Effects of Nebivolol Intervention on Outcomes and Rehospitalisation in Seniors with Heart Failure Study
U.S. Carvedilol Heart Failure Study.
Daphne Babalis: Clinical Trials and Evaluation Unit, Royal Brompton Hospital/Imperial College London, UK.
David Chen: GlaxoSmithKline, Cardiovascular and Metabolism Medicine Development Center, Philadelphia, PA, USA.
The BB-HF project was investigator initiated. The BB-HF collaborative group extends their thanks to the four pharmaceutical companies that have supported this project. Menarini Farmaceutica Internazionale provided an unrestricted research grant to support administrative costs. None of the pharmaceutical groups have any role in data analysis or the drafting of manuscripts. Any additional funding received will be stipulated in future publications.
- Lloyd-Jones D, Adams RJ, Brown TM, Carnethon M, Dai S, De Simone G, Ferguson TB, Ford E, Furie K, Gillespie C, Go A, Greenlund K, Haase N, Hailpern S, Ho PM, Howard V, Kissela B, Kittner S, Lackland D, Lisabeth L, Marelli A, McDermott MM, Meigs J, Mozaffarian D, Mussolino M, Nichol G, Roger VL, Rosamond W, Sacco R, Sorlie P: Heart disease and stroke statistics–2010 update: a report from the American Heart Association. Circulation. 2010, 121: e46-e215.View ArticlePubMedGoogle Scholar
- National Heart Failure Audit: Report for the audit period between April 2009 and March 2010.http://www.ic.nhs.uk/webfiles/publications/002_Audits/NHS_IC_National_Heart_Failure_Audit_2010_04-01-11.pdf,
- Dickstein K, Cohen-Solal A, Filippatos G, McMurray JJ, Ponikowski P, Poole-Wilson PA, Stromberg A, van Veldhuisen DJ, Atar D, Hoes AW, Keren A, Mebazaa A, Nieminen M, Priori SG, Swedberg K, Vahanian A, Camm J, De Caterina R, Dean V, Dickstein K, Filippatos G, Funck-Brentano C, Hellemans I, Kristensen SD, McGregor K, Sechtem U, Silber S, Tendera M, Widimsky P, Zamorano JL: ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure 2008: the Task Force for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2008 of the European Society of Cardiology. Eur Heart J. 2008, 29: 2388-2442. Erratum in: Eur Heart J 2010, 12:416. Dosage error in article text. Eur Heart J 2010, 31:624. Dosage error in article textView ArticlePubMedGoogle Scholar
- Jessup M, Abraham WT, Casey DE, Feldman AM, Francis GS, Ganiats TG, Konstam MA, Mancini DM, Rahko PS, Silver MA, Stevenson LW, Yancy CW: 2009 focused update: ACCF/AHA Guidelines for the Diagnosis and Management of Heart Failure in Adults. Circulation. 2009, 119: 1977-2016.View ArticlePubMedGoogle Scholar
- Komajda M, Follath F, Swedberg K, Cleland J, Aguilar JC, Cohen-Solal A, Dietz R, Gavazzi A, Van Gilst WH, Hobbs R, Korewicki J, Madeira HC, Moiseyev VS, Preda I, Widimsky J, Freemantle N, Eastaugh J, Mason J: The EuroHeart Failure Survey programme – a survey on the quality of care among patients with heart failure in Europe: part 2: treatment. Eur Heart J. 2003, 24: 464-474. 10.1016/S0195-668X(02)00700-5.View ArticlePubMedGoogle Scholar
- Komajda M, Hanon O, Hochadel M, Lopez-Sendon JL, Follath F, Ponikowski P, Harjola V-P, Drexler H, Dickstein K, Tavazzi L, Nieminen M: Contemporary management of octogenarians hospitalized for heart failure in Europe: Euro Heart Failure Survey II. Eur Heart J. 2009, 30: 478-486.View ArticlePubMedGoogle Scholar
- Lee DS, Tu JV, Juurlink DN, Alter DA, Ko DT, Austin PC, Chong A, Stukel TA, Levy D, Laupacis A: Risk-treatment mismatch in the pharmacotherapy of heart failure. JAMA. 2005, 294: 1240-1247. 10.1001/jama.294.10.1240.View ArticlePubMedGoogle Scholar
- Brophy JM, Joseph L, Rouleau JL: Beta-blockers in congestive heart failure. A Bayesian meta-analysis. Ann Intern Med. 2001, 134: 550-560.View ArticlePubMedGoogle Scholar
- Shibata MC, Flather MD, Wang D: Systematic review of the impact of beta blockers on mortality and hospital admissions in heart failure. Eur J Heart Fail. 2001, 3: 351-357. 10.1016/S1388-9842(01)00144-1.View ArticlePubMedGoogle Scholar
- Australia/New Zealand Heart Failure Research Collaborative Group: Randomised, placebo-controlled trial of carvedilol in patients with congestive heart failure due to ischaemic heart disease. Lancet. 1997, 349: 375-380.View ArticleGoogle Scholar
- Beta-Blocker Evaluation of Survival Trial Investigators: A trial of the beta-blocker bucindolol in patients with advanced chronic heart failure. N Engl J Med. 2001, 344: 1659-1667.View ArticleGoogle Scholar
- Dargie HJ: Effect of carvedilol on outcome after myocardial infarction in patients with left-ventricular dysfunction: the CAPRICORN randomised trial. Lancet. 2001, 357: 1385-1390.View ArticlePubMedGoogle Scholar
- Cleland JG, Pennell DJ, Ray SG, Coats AJ, Macfarlane PW, Murray GD, Mule JD, Vered Z, Lahiri A: Myocardial viability as a determinant of the ejection fraction response to carvedilol in patients with heart failure (CHRISTMAS trial): randomised controlled trial. Lancet. 2003, 362: 14-21. 10.1016/S0140-6736(03)13801-9.View ArticlePubMedGoogle Scholar
- CIBIS Investigators and Committees: A randomized trial of beta-blockade in heart failure. The Cardiac Insufficiency Bisoprolol Study (CIBIS). Circulation. 1994, 90: 1765-1773.View ArticleGoogle Scholar
- CIBIS Investigators and Committees: The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial. Lancet. 1999, 353: 9-13.View ArticleGoogle Scholar
- Packer M, Coats AJ, Fowler MB, Katus HA, Krum H, Mohacsi P, Rouleau JL, Tendera M, Castaigne A, Roecker EB, Schultz MK, DeMets DL: Effect of carvedilol on survival in severe chronic heart failure. N Engl J Med. 2001, 344: 1651-1658. 10.1056/NEJM200105313442201.View ArticlePubMedGoogle Scholar
- Waagstein F, Bristow MR, Swedberg K, Camerini F, Fowler MB, Silver MA, Gilbert EM, Johnson MR, Goss FG, Hjalmarson A, Metoprolol in Dilated Cardiomyopathy (MDC) Trial Study Group: Beneficial effects of metoprolol in idiopathic dilated cardiomyopathy. Lancet. 1993, 342: 1441-1446. 10.1016/0140-6736(93)92930-R.View ArticlePubMedGoogle Scholar
- MERIT-HF Study Group: Effect of metoprolol CR/XL in chronic heart failure: Metoprolol CR/XL Randomised Intervention Trial in Congestive Heart Failure (MERIT-HF). Lancet. 1999, 353: 2001-2007.View ArticleGoogle Scholar
- Flather MD, Shibata MC, Coats AJ, Van Veldhuisen DJ, Parkhomenko A, Borbola J, Cohen-Solal A, Dumitrascu D, Ferrari R, Lechat P, Soler-Soler J, Tavazzi L, Spinarova L, Toman J, Bohm M, Anker SD, Thompson SG, Poole-Wilson PA: Randomized trial to determine the effect of nebivolol on mortality and cardiovascular hospital admission in elderly patients with heart failure (SENIORS). Eur Heart J. 2005, 26: 215-225.View ArticlePubMedGoogle Scholar
- Packer M, Bristow MR, Cohn JN, Colucci WS, Fowler MB, Gilbert EM, Shusterman NH, Carvedilol Heart Failure Study Group: The effect of carvedilol on morbidity and mortality in patients with chronic heart failure. U.S. N Engl J Med. 1996, 334: 1349-1355. 10.1056/NEJM199605233342101.View ArticlePubMedGoogle Scholar
- he RESOLVD Investigators: Effects of metoprolol CR in patients with ischemic and dilated cardiomyopathy: the randomized evaluation of strategies for left ventricular dysfunction pilot study. Circulation. 2000, 101: 378-384.View ArticleGoogle Scholar
- Remme WJ, Riegger G, Hildebrandt P, Komajda M, Jaarsma W, Bobbio M, Soler-Soler J, Scherhag A, Lutiger B, Ryden L: The benefits of early combination treatment of carvedilol and an ACE-inhibitor in mild heart failure and left ventricular systolic dysfunction. The carvedilol and ACE-inhibitor remodelling mild heart failure evaluation trial (CARMEN). Cardiovasc Drugs Ther. 2004, 18: 57-66.View ArticlePubMedGoogle Scholar
- Tudur Smith C, Williamson PR: A comparison of methods for fixed effects meta-analysis of individual patient data with time to event outcomes. Clin Trials. 2007, 4: 621-630. 10.1177/1740774507085276.View ArticlePubMedGoogle Scholar
- Riley RD, Lambert PC, Staessen JA, Wang J, Gueyffier F, Thijs L, Boutitie F: Meta-analysis of continuous outcomes combining individual patient data and aggregate data. Stat Med. 2008, 27: 1870-1893. 10.1002/sim.3165.View ArticlePubMedGoogle Scholar
- Haas SJ, Vos T, Gilbert RE, Krum H: Are beta-blockers as efficacious in patients with diabetes mellitus as in patients without diabetes mellitus who have chronic heart failure? A meta-analysis of large-scale clinical trials. Am Heart J. 2003, 146: 848-853. 10.1016/S0002-8703(03)00403-4.View ArticlePubMedGoogle Scholar
- van Veldhuisen DJ, Cohen-Solal A, Bohm M, Anker SD, Babalis D, Roughton M, Coats AJ, Poole-Wilson PA, Flather MD: Beta-blockade with nebivolol in elderly heart failure patients with impaired and preserved left ventricular ejection fraction: data from SENIORS (Study of Effects of Nebivolol Intervention on Outcomes and Rehospitalization in Seniors With Heart Failure). J Am Coll Cardiol. 2009, 53: 2150-2158. 10.1016/j.jacc.2009.02.046.View ArticlePubMedGoogle Scholar
- Leizorovicz A, Lechat P, Cucherat M, Bugnard F: Bisoprolol for the treatment of chronic heart failure: a meta-analysis on individual data of two placebo-controlled studies–CIBIS and CIBIS II Cardiac Insufficiency Bisoprolol Study. Am Heart J. 2002, 143: 301-307. 10.1067/mhj.2002.120768.View ArticlePubMedGoogle Scholar
- Ghali JK, Krause-Steinrauf HJ, Adams KF, Khan SS, Rosenberg YD, Yancy CW, Young JB, Goldman S, Peberdy MA, Lindenfeld J: Gender differences in advanced heart failure: insights from the BEST study. J Am Coll Cardiol. 2003, 42: 2128-2134. 10.1016/j.jacc.2003.05.012.View ArticlePubMedGoogle Scholar
- Ghali JK, Pina IL, Gottlieb SS, Deedwania PC, Wikstrand JC, Group M-HS: Metoprolol CR/XL in female patients with heart failure: analysis of the experience in Metoprolol Extended-Release Randomized Intervention Trial in Heart Failure (MERIT-HF). Circulation. 2002, 105: 1585-1591. 10.1161/01.CIR.0000012546.20194.33.View ArticlePubMedGoogle Scholar
- Baumhakel M, Muller U, Bohm M: Influence of gender of physicians and patients on guideline-recommended treatment of chronic heart failure in a cross-sectional study. Eur J Heart Fail. 2009, 11: 299-303. 10.1093/eurjhf/hfn041.View ArticlePubMedPubMed CentralGoogle Scholar
- Sheppard R, Behlouli H, Richard H, Pilote L: Effect of gender on treatment, resource utilization, and outcomes in congestive heart failure in Quebec. Canada. Am J Cardiol. 2005, 95: 955-959. 10.1016/j.amjcard.2004.12.033.View ArticlePubMedGoogle Scholar
- Cohen-Solal A, Kotecha D, van Veldhuisen DJ, Babalis D, Bohm M, Coats AJ, Roughton M, Poole-Wilson P, Tavazzi L, Flather M: Efficacy and safety of nebivolol in elderly heart failure patients with impaired renal function: insights from the SENIORS trial. Eur J Heart Fail. 2009, 11: 872-880. 10.1093/eurjhf/hfp104.View ArticlePubMedPubMed CentralGoogle Scholar
- Ghali JK, Wikstrand J, Van Veldhuisen DJ, Fagerberg B, Goldstein S, Hjalmarson A, Johansson P, Kjekshus J, Ohlsson L, Samuelsson O, Waagstein F, Wedel H, MERIT-HS Study Group: The influence of renal function on clinical outcome and response to beta-blockade in systolic heart failure: insights from Metoprolol CR/XL Randomized Intervention Trial in Chronic HF (MERIT-HF). J Card Fail. 2009, 15: 310-318. 10.1016/j.cardfail.2008.11.003.View ArticlePubMedGoogle Scholar
- Fauchier L, Grimard C, Pierre B, Nonin E, Gorin L, Rauzy B, Cosnay P, Babuty D, Charbonnier B: Comparison of beta blocker and digoxin alone and in combination for management of patients with atrial fibrillation and heart failure. Am J Cardiol. 2009, 103: 248-254. 10.1016/j.amjcard.2008.09.064.View ArticlePubMedGoogle Scholar
- Lechat P, Hulot JS, Escolano S, Mallet A, Leizorovicz A, Werhlen-Grandjean M, Pochmalicki G, Dargie H: Heart rate and cardiac rhythm relationships with bisoprolol benefit in chronic heart failure in CIBIS II Trial. Circulation. 2001, 103: 1428-1433. 10.1161/01.CIR.103.10.1428.View ArticlePubMedGoogle Scholar
- van Veldhuisen DJ, Aass H, El Allaf D, Dunselman PH, Gullestad L, Halinen M, Kjekshus J, Ohlsson L, Wedel H, Wikstrand J, MERIT-HF Study Group: Presence and development of atrial fibrillation in chronic heart failure. Experiences from the MERIT-HF Study. Eur J Heart Fail. 2006, 8: 539-546. 10.1016/j.ejheart.2006.01.015.View ArticlePubMedGoogle Scholar
- McAlister FA, Wiebe N, Ezekowitz JA, Leung AA, Armstrong PW: Meta-analysis: beta-blocker dose, heart rate reduction, and death in patients with heart failure. Ann Intern Med. 2009, 150: 784-794.View ArticlePubMedGoogle Scholar
- Dobre D, van Veldhuisen DJ, Mordenti G, Vintila M, Haaijer-Ruskamp FM, Coats AJS, Poole-Wilson PA, Flather MD, SENIORS Investigators: Tolerability and dose-related effects of nebivolol in elderly patients with heart failure: data from the Study of the Effects of Nebivolol Intervention on Outcomes and Rehospitalisation in Seniors with Heart Failure (SENIORS) trial. Am Heart J. 2007, 154: 109-115. 10.1016/j.ahj.2007.03.025.View ArticlePubMedGoogle Scholar
- Stewart LA, Tierney JF: To IPD or not to IPD? Advantages and disadvantages of systematic reviews using individual patient data. Eval Health Prof. 2002, 25: 76-97. 10.1177/0163278702025001006.View ArticlePubMedGoogle Scholar
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