Executive Summary - Public Health Profiles - PHE



Heart failure prevalence models for small populations:Technical Document produced for Public Health EnglandMartin Cowie, Saba Mian, Jessica Morris, Roger Newson, Michael Soljak, Bowen SuDepartment Primary Care & Public HealthSchool of Public HealthContents TOC \o "1-3" \h \z \u 1Executive Summary PAGEREF _Toc474152582 \h 42Background PAGEREF _Toc474152583 \h 52.1HF Risk Factors PAGEREF _Toc474152584 \h 52.1.1CHD and MI PAGEREF _Toc474152585 \h 62.1.2Hypertension PAGEREF _Toc474152586 \h 62.1.3Smoking PAGEREF _Toc474152587 \h 62.1.4Atrial Fibrillation PAGEREF _Toc474152588 \h 72.1.5Diabetes PAGEREF _Toc474152589 \h 72.1.6Age PAGEREF _Toc474152590 \h 72.1.7Congenital Heart Disease PAGEREF _Toc474152591 \h 72.1.8BMI PAGEREF _Toc474152592 \h 72.1.9Ethnicity PAGEREF _Toc474152593 \h 72.1.10Gender PAGEREF _Toc474152594 \h 82.1.11Alcohol Consumption PAGEREF _Toc474152595 \h 82.1.12Sleep Apnoea PAGEREF _Toc474152596 \h 82.2HF incidence and prevalence PAGEREF _Toc474152597 \h 132.2.1Quality & Outcomes Framework Data PAGEREF _Toc474152598 \h 143Methods PAGEREF _Toc474152599 \h 153.1HF prevalence from UK primary care and hospital data: Clinical Practice Research Datalink & Hospital Episode Statistics PAGEREF _Toc474152600 \h 153.1.1What is the Clinical Practice Research Datalink? PAGEREF _Toc474152601 \h 153.1.2Identification of HF cases and code lists for CPRD and HES doctor diagnosed cases PAGEREF _Toc474152602 \h 153.1.3Additional HF cases from clinical algorithm PAGEREF _Toc474152603 \h 173.1.4Additional HF cases from drugs algorithm PAGEREF _Toc474152604 \h 183.1.5CPRD risk factors PAGEREF _Toc474152605 \h 203.1.6CPRD HF Control group PAGEREF _Toc474152606 \h 203.1.7CPRD descriptive analyses PAGEREF _Toc474152607 \h 203.1.8CPRD prevalence and incidence PAGEREF _Toc474152608 \h 203.1.91.1.1 CPRD regression modelling PAGEREF _Toc474152609 \h 213.1.10Interactions PAGEREF _Toc474152610 \h 213.1.11Internal validation PAGEREF _Toc474152611 \h 213.1.12Local prevalence estimates PAGEREF _Toc474152612 \h 213.2Validation of local estimates PAGEREF _Toc474152613 \h 253.2.1Internal validation PAGEREF _Toc474152614 \h 253.2.2External validation PAGEREF _Toc474152615 \h 254Results PAGEREF _Toc474152616 \h 284.1HF prevalence from CPRD PAGEREF _Toc474152617 \h 284.1.1Baseline characteristics of CPRD respondents PAGEREF _Toc474152618 \h 284.1.2Missing values PAGEREF _Toc474152619 \h 294.1.3CPRD prevalence and incidence PAGEREF _Toc474152620 \h 294.1.4Logistic regression modelling PAGEREF _Toc474152621 \h 334.2External validation – Bland Altman plots PAGEREF _Toc474152622 \h 345References PAGEREF _Toc474152623 \h 36HF prevalence model Technical DocumentExecutive SummaryApproximately 1 to 2% of the UK population is affected with HF, with prevalence rates expected to increase over the next decade.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5EYXZpZXM8L0F1dGhvcj48WWVhcj4yMDAxPC9ZZWFyPjxS

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ADDIN EN.CITE.DATA [3 ,4] A recent survival analysis carried out using UK primary care records from The Health Improvement Network between 1998 and 2012 showed no improvement in survival over this period.[10] However early treatment can reduce significant mortality and morbidity associated with HF.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5UaXRsZXI8L0F1dGhvcj48WWVhcj4yMDA4PC9ZZWFyPjxS

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ADDIN EN.CITE.DATA [3]We used linked Clinical Practice Research Datalink (CPRD) primary care electronic health records (EHRs) and Hospital Episode Statistics (HES) data as a robust data source for the identification of HF prevalence in patients who have been in contact with the health system. A comprehensive list of Medcodes, Prodcodes and ICD-10 codes was compiled for the identification of the CPRD and HES doctor diagnosed HF cases, and for the undiagnosed (but diagnosable) clinical and drugs algorithm HF cases. We used the literature review described in the Background to extract CPRD data on risk factors. We fitted uni-variate then multivariate logistic regression models for HF as described in previous publications, to produce odds ratios (ORs) and regression coefficients. Derived ORs (or regression coefficients) are used to estimate prevalence in small population subgroups. Having estimated the regression model parameters, we used these for out-of-sample prediction of HF prevalence. We also carried out internal and external validation.We identified 224,265 HF cases from CPRD GP diagnoses. We found 14,097 additional HES diagnosed HF cases, 32,846 additional drugs algorithm probable HF cases, and no additional clinical algorithm probable HF cases. The prevalence of HF is estimated at around 0.74% for doctor-diagnosed HF, rising if algorithm cases are included as above. Between 2000-2015 incidence rates have halved and we have also shown a decrease in HF admission rates over this period. For the local estimates, Bland-Altman plots for the practice-level QOF and estimated prevalence for HF showed higher modelled prevalence compared with QOF registered prevalence. Scatter plots of practice-level model-estimated and QOF prevalence of diagnosed HF showed GP-diagnosed prevalence is lower than CPRD prevalence.BackgroundHeart failure (HF) is a chronic disease in which cardiac structure or function is abnormal, resulting in the inability of the heart to deliver oxygen at a rate that is necessary for metabolising tissues, regardless of normal filling pressures.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5EaWNrc3RlaW48L0F1dGhvcj48WWVhcj4yMDA4PC9ZZWFy

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ADDIN EN.CITE.DATA [3 ,4] In the USA, the estimated annual cost of HF in 2010 is estimated to be $39.2 billion or ~2% of the total US health-care budget. Evaluations from different European countries indicate a similar share of HF-related costs in relation to overall health-care expenditure. ADDIN EN.CITE <EndNote><Cite><Author>Braunschweig</Author><Year>2011</Year><RecNum>206</RecNum><DisplayText>[7]</DisplayText><record><rec-number>206</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1358938737">206</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Braunschweig, Frieder</author><author>Cowie, Martin R.</author><author>Auricchio, Angelo</author></authors></contributors><titles><title>What are the costs of heart failure?</title><secondary-title>Europace</secondary-title></titles><periodical><full-title>Europace</full-title></periodical><pages>ii13-ii17</pages><volume>13</volume><number>suppl 2</number><dates><year>2011</year><pub-dates><date>May 1, 2011</date></pub-dates></dates><urls><related-urls><url>;[7] The overall global economic cost of HF in 2012 was estimated at $108 billion per annum. ADDIN EN.CITE <EndNote><Cite><Author>Cook</Author><Year>2014</Year><RecNum>344</RecNum><DisplayText>[8]</DisplayText><record><rec-number>344</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1486023755">344</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Cook, Christopher</author><author>Cole, Graham</author><author>Asaris, Perviz</author><author>Jabbour, Richard</author><author>Francis, Darrel</author></authors></contributors><titles><title>49?The Annual Global Economic Burden of Heart Failure</title><secondary-title>Heart</secondary-title></titles><periodical><full-title>Heart</full-title></periodical><pages>A28-A29</pages><volume>100</volume><number>Suppl 3</number><dates><year>2014</year><pub-dates><date>June 1, 2014</date></pub-dates></dates><urls><related-urls><url>;[8]Treatment can reduce significant mortality and morbidity associated with HF.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5UaXRsZXI8L0F1dGhvcj48WWVhcj4yMDA4PC9ZZWFyPjxS

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ADDIN EN.CITE.DATA [3] However, almost half of HF patients die within five years of being diagnosed. ADDIN EN.CITE <EndNote><Cite><Author>Roger</Author><Year>2004</Year><RecNum>162</RecNum><DisplayText>[9]</DisplayText><record><rec-number>162</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1358869434">162</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Roger, Véronique L.</author><author>Weston, Susan a</author><author>Redfield, Margaret M.</author><author>Hellermann-Homan, Jens P.</author><author>Killian, Jill</author><author>Yawn, Barbara P.</author><author>Jacobsen, Steven J.</author></authors></contributors><titles><title>Trends in heart failure incidence and survival in a community-based population</title><secondary-title>JAMA : the journal of the American Medical Association</secondary-title></titles><periodical><full-title>JAMA : the journal of the American Medical Association</full-title></periodical><pages>344-50</pages><volume>292</volume><number>3</number><keywords><keyword>Age Factors</keyword><keyword>Aged</keyword><keyword>Female</keyword><keyword>Heart Failure</keyword><keyword>Heart Failure: diagnosis</keyword><keyword>Heart Failure: epidemiology</keyword><keyword>Heart Failure: mortality</keyword><keyword>Humans</keyword><keyword>Incidence</keyword><keyword>Male</keyword><keyword>Middle Aged</keyword><keyword>Minnesota</keyword><keyword>Minnesota: epidemiology</keyword><keyword>Poisson Distribution</keyword><keyword>Proportional Hazards Models</keyword><keyword>Risk</keyword><keyword>Sex Factors</keyword><keyword>Survival Analysis</keyword></keywords><dates><year>2004</year></dates><urls><related-urls><url> Support/Mendeley Desktop/Downloaded/Roger et al. - 2004 - Trends in heart failure incidence and survival in a community-based population.pdf</url></pdf-urls></urls><electronic-resource-num>10.1001/jama.292.3.344</electronic-resource-num></record></Cite></EndNote>[9] A recent survival analysis carried out using UK primary care records from The Health Improvement Network (THIN) between 1998 and 2012 showed no improvement in survival over this period. ADDIN EN.CITE <EndNote><Cite><Author>Taylor</Author><Year>2017</Year><RecNum>342</RecNum><DisplayText>[10]</DisplayText><record><rec-number>342</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1485854052">342</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Taylor, Clare J</author><author>Ryan, Ronan</author><author>Nichols, Linda</author><author>Gale, Nicola</author><author>Hobbs, Richard</author><author>Marshall, Tom </author></authors></contributors><titles><title>Survival following a diagnosis of heart failure in primary care</title><secondary-title>Family Practice</secondary-title></titles><periodical><full-title>Family Practice</full-title></periodical><pages>8</pages><section>1</section><dates><year>2017</year></dates><urls><related-urls><url>;[10] Therefore, HF represents a major public health burden which is growing, but unlike coronary heart disease (CHD), this is not because of improved survival.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5BdmVyeTwvQXV0aG9yPjxZZWFyPjIwMTI8L1llYXI+PFJl

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ADDIN EN.CITE.DATA [11] Because HF is a medical diagnosis that patients may not report, using data from a single national survey such as the Health Survey for England would not provide a suitable basis for a HF prevalence model. However, linked Clinical Practice Research Datalink (CPRD) primary care electronic health records (EHRs) and Hospital Episode Statistics (HES) data should form a robust data source for the identification of HF patients who have been in contact with the health system. We therefore used these as primary data sources for prevalence modelling, with an adjustment if needed from published population surveys or from the National Heart Failure Audit, ADDIN EN.CITE <EndNote><Cite><Author>Mitchell</Author><Year>2015</Year><RecNum>364</RecNum><DisplayText>[12]</DisplayText><record><rec-number>364</rec-number><foreign-keys><key app="EN" db-id="2d9sfv0rhp02eteepzbv9vp4zezt00xrfxrp" timestamp="1450105503">364</key></foreign-keys><ref-type name="Report">27</ref-type><contributors><authors><author>Mitchell, Polly</author><author>Marle, Damian</author><author>Donkor, Akosua</author><author>Shote, Aminat</author><author>McDonagh, Theresa</author><author>et al,</author></authors></contributors><titles><title>National Heart Failure Audit Report 2013-14</title></titles><dates><year>2015</year></dates><pub-location>London</pub-location><publisher>NICOR (National Institute for Cardiovascular Outcomes Research)</publisher><urls><related-urls><url>;[12] data from which PCPH already holds. HF Risk FactorsMany studies have investigated the relationship between HF and risk factors such as history of CHD, hypertension, hypercholesterolemia, obesity, smoking, and arrhythmias.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Hb3R0ZGllbmVyPC9BdXRob3I+PFllYXI+MjAwMDwvWWVh

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ADDIN EN.CITE.DATA [15-17] HFR risk prediction equations developed from UK primary care EHRs include age, body mass index (BMI), systolic blood pressure (BP), cholesterol/high density lipoprotein (HDL) ratio, HbA1c, material deprivation, ethnicity, smoking, duration and type of diabetes, atrial fibrillation (AF), cardiovascular disease (CVD), and chronic kidney disease (CKD). ADDIN EN.CITE <EndNote><Cite><Author>Hippisley-Cox</Author><Year>2015</Year><RecNum>328</RecNum><DisplayText>[18]</DisplayText><record><rec-number>328</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1460451158">328</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Hippisley-Cox, J.</author><author>Coupland, C.</author></authors></contributors><auth-address>Division of Primary Care, University Park, Nottingham, UK.</auth-address><titles><title>Development and validation of risk prediction equations to estimate future risk of heart failure in patients with diabetes: a prospective cohort study</title><secondary-title>BMJ Open</secondary-title><alt-title>BMJ open</alt-title></titles><periodical><full-title>BMJ Open</full-title></periodical><alt-periodical><full-title>BMJ Open</full-title></alt-periodical><pages>e008503</pages><volume>5</volume><number>9</number><edition>2015/09/12</edition><keywords><keyword>Epidemiology</keyword><keyword>Preventive medicine</keyword><keyword>Primary care</keyword></keywords><dates><year>2015</year></dates><accession-num>26353872</accession-num><urls><related-urls><url>;[18] Myocardial infarction (MI) has been found to be a precursor of HF and death, and is the most occurring event during post-MI patient management.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5DbGVyZm9uZDwvQXV0aG9yPjxZZWFyPjIwMTU8L1llYXI+

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ADDIN EN.CITE.DATA [19] We conducted a non-systematic literature search to validate these predictors. HF risk factors we confirmed are shown in the following table, with associated references ( REF _Ref346798903 \h \* MERGEFORMAT Table 1).Table 1: HF risk factor list Risk factorReferencesMIPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5DbGVyZm9uZDwvQXV0aG9yPjxZZWFyPjIwMTU8L1llYXI+

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ADDIN EN.CITE.DATA [26], ADDIN EN.CITE <EndNote><Cite><Author>Britton</Author><Year>2009</Year><RecNum>289</RecNum><DisplayText>[29]</DisplayText><record><rec-number>289</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1458555150">289</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Britton, K. A.</author><author>Gaziano, J. M.</author><author>Djousse, L.</author></authors></contributors><auth-address>Department of Medicine, Brigham and Women&apos;s Hospital and Harvard Medical School, Boston, MA 02115, USA. kfinnerty@post.harvard.edu</auth-address><titles><title>Normal systolic blood pressure and risk of heart failure in US male physicians</title><secondary-title>Eur J Heart Fail</secondary-title><alt-title>European journal of heart failure</alt-title></titles><alt-periodical><full-title>European Journal of Heart Failure</full-title></alt-periodical><pages>1129-34</pages><volume>11</volume><number>12</number><edition>2009/10/29</edition><keywords><keyword>*Blood Pressure</keyword><keyword>Heart Failure/*physiopathology</keyword><keyword>Humans</keyword><keyword>Male</keyword><keyword>Middle Aged</keyword><keyword>*Physicians</keyword><keyword>Risk Factors</keyword><keyword>Systole</keyword></keywords><dates><year>2009</year><pub-dates><date>Dec</date></pub-dates></dates><isbn>1388-9842</isbn><accession-num>19861382</accession-num><urls><related-urls><url>;[29], PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5aYW5jaGV0dGk8L0F1dGhvcj48WWVhcj4yMDE1PC9ZZWFy

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ADDIN EN.CITE.DATA [34] Body Mass Index (BMI)PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5BdmVyeTwvQXV0aG9yPjxZZWFyPjIwMTI8L1llYXI+PFJl

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ADDIN EN.CITE.DATA [11]Alcohol ADDIN EN.CITE <EndNote><Cite><Author>Wannamethee</Author><Year>2016</Year><RecNum>249</RecNum><DisplayText>[38]</DisplayText><record><rec-number>249</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1458038040">249</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Wannamethee, S. G.</author><author>Shaper, A. G.</author><author>Papacosta, O.</author><author>Lennon, L.</author><author>Welsh, P.</author><author>Whincup, P. H.</author></authors></contributors><auth-address>Department of Primary Care and Population Health, University College London, London, UK.&#xD;Institute of Cardiovascular &amp; Medical Sciences, BHF Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.&#xD;Division of Population Health Sciences and Education, Population Health Research Centre, St George&apos;s University of London, London, UK.</auth-address><titles><title>Lung function and airway obstruction: associations with circulating markers of cardiac function and incident heart failure in older men-the British Regional Heart Study</title><secondary-title>Thorax</secondary-title><alt-title>Thorax</alt-title></titles><periodical><full-title>Thorax</full-title><abbr-1>Thorax</abbr-1></periodical><alt-periodical><full-title>Thorax</full-title><abbr-1>Thorax</abbr-1></alt-periodical><dates><year>2016</year><pub-dates><date>Jan 25</date></pub-dates></dates><isbn>1468-3296 (Electronic)&#xD;0040-6376 (Linking)</isbn><accession-num>26811343</accession-num><urls><related-urls><url>;[38] & ADDIN EN.CITE <EndNote><Cite><Author>Larsson</Author><Year>2015</Year><RecNum>320</RecNum><DisplayText>[39]</DisplayText><record><rec-number>320</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1459521044">320</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Larsson, S. C.</author><author>Orsini, N.</author><author>Wolk, A.</author></authors></contributors><auth-address>Unit of Nutritional Epidemiology, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.</auth-address><titles><title>Alcohol consumption and risk of heart failure: a dose-response meta-analysis of prospective studies</title><secondary-title>Eur J Heart Fail</secondary-title><alt-title>European journal of heart failure</alt-title></titles><alt-periodical><full-title>European Journal of Heart Failure</full-title></alt-periodical><pages>367-73</pages><volume>17</volume><number>4</number><edition>2015/01/20</edition><keywords><keyword>Adult</keyword><keyword>Aged</keyword><keyword>Aged, 80 and over</keyword><keyword>Alcohol Drinking/adverse effects/*epidemiology</keyword><keyword>Female</keyword><keyword>Heart Failure/*epidemiology/etiology</keyword><keyword>Humans</keyword><keyword>Male</keyword><keyword>Middle Aged</keyword><keyword>Prospective Studies</keyword><keyword>Risk Factors</keyword><keyword>Young Adult</keyword><keyword>Alcohol consumption</keyword><keyword>Heart failure</keyword><keyword>Meta-analysis</keyword></keywords><dates><year>2015</year><pub-dates><date>Apr</date></pub-dates></dates><isbn>1388-9842</isbn><accession-num>25598021</accession-num><urls><related-urls><url>;[39] Sleep apnoeaPEVuZE5vdGU+PENpdGU+PEF1dGhvcj5ManVuZ2dyZW48L0F1dGhvcj48WWVhcj4yMDE2PC9ZZWFy

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ADDIN EN.CITE.DATA [28]CHD and MIIn developed countries, CHD is the leading cause of HF.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5HaGVvcmdoaWFkZTwvQXV0aG9yPjxZZWFyPjIwMDY8L1ll

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ADDIN EN.CITE.DATA [23] Chronic HF is the terminal stage of several cardiovascular diseases and cardiac dysfunction syndrome.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5MaXU8L0F1dGhvcj48WWVhcj4yMDE1PC9ZZWFyPjxSZWNO

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ADDIN EN.CITE.DATA [24] There has been an increase in the prevalence and incidence of HF in the past 25 years, which may be due to an improvement in the survival of patients after acute MI.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5HaGVvcmdoaWFkZTwvQXV0aG9yPjxZZWFyPjIwMDY8L1ll

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ADDIN EN.CITE.DATA [23] MI is the main clinical intermediate between CHD and HF PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5MYWxhPC9BdXRob3I+PFllYXI+MjAxNDwvWWVhcj48UmVj

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ADDIN EN.CITE.DATA [27]. The occurrence of HF post MI depends on the location and size of the infarct, the severity of artery disease and the development of ischemic mitral regurgitation.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5MYWxhPC9BdXRob3I+PFllYXI+MjAxNDwvWWVhcj48UmVj

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ADDIN EN.CITE.DATA [27] In a population-based study, of 1,915 patients with a previous MI, 41% developed HF over a seven year follow-up period.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5IZWxsZXJtYW5uPC9BdXRob3I+PFllYXI+MjAwNTwvWWVh

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ADDIN EN.CITE.DATA [20] HypertensionStudies have shown that the risk of HF is significantly reduced in hypertensive patients with a reduction in (systolic) BP. A wide range of anti-hypertensive drugs such as angiotensin-converting enzyme inhibitors (ACEi) and angiotensin receptor blockers (ARB) lower the risks of major cardiovascular events in hypertensive people.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5UdXJuYnVsbDwvQXV0aG9yPjxZZWFyPjIwMDM8L1llYXI+

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ADDIN EN.CITE.DATA [26]. Out of 76,017 patients, 622 patients were admitted to hospital for HF. These 622 patients were matched to 3,110 controls. The mean age of the patients and controls was 67 years and 54% of the patients were men. A 34% (95% CI 17%-48%) reduction in the risk of hospitalisation due to HF was observed with high adherence to antihypertensive medication. Turbull et al (2007) found a significant 27% reduction in the risk of HF with ACEi treatment and a 12% reduction with ARB treatment for each 5mmHg reduction in blood pressure PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5UdXJuYnVsbDwvQXV0aG9yPjxZZWFyPjIwMDc8L1llYXI+

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ADDIN EN.CITE.DATA [31]. In an meta-analysis of 20 blood pressure controlling randomised controlled trials (RCTs), Zanchetti et al (2015) found a 46% (95% CI 36-55%) reduction in the risk of HF in hypertensive patients PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5aYW5jaGV0dGk8L0F1dGhvcj48WWVhcj4yMDE1PC9ZZWFy

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ADDIN EN.CITE.DATA [32]. The adjusted hazard ratio for HF associated with hypertension was 1.27 (95% CI 1.18-1.36). A study using data from the Physicians Health Study I (PHS I), a randomised, double-blind, placebo-controlled trial, found a significant relationship between systolic blood pressure (SBP) and the risk of HF ADDIN EN.CITE <EndNote><Cite><Author>Britton</Author><Year>2009</Year><RecNum>289</RecNum><DisplayText>[29]</DisplayText><record><rec-number>289</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1458555150">289</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Britton, K. A.</author><author>Gaziano, J. M.</author><author>Djousse, L.</author></authors></contributors><auth-address>Department of Medicine, Brigham and Women&apos;s Hospital and Harvard Medical School, Boston, MA 02115, USA. kfinnerty@post.harvard.edu</auth-address><titles><title>Normal systolic blood pressure and risk of heart failure in US male physicians</title><secondary-title>Eur J Heart Fail</secondary-title><alt-title>European journal of heart failure</alt-title></titles><alt-periodical><full-title>European Journal of Heart Failure</full-title></alt-periodical><pages>1129-34</pages><volume>11</volume><number>12</number><edition>2009/10/29</edition><keywords><keyword>*Blood Pressure</keyword><keyword>Heart Failure/*physiopathology</keyword><keyword>Humans</keyword><keyword>Male</keyword><keyword>Middle Aged</keyword><keyword>*Physicians</keyword><keyword>Risk Factors</keyword><keyword>Systole</keyword></keywords><dates><year>2009</year><pub-dates><date>Dec</date></pub-dates></dates><isbn>1388-9842</isbn><accession-num>19861382</accession-num><urls><related-urls><url>;[29]. Participants with untreated hypertensive SBP of 140-149 and >150mmHg, were at a 1.44 (95% CI 1.12-1.88, p <0.001) and 1.47 (95% CI 1.01-2.14, p <0.001), respectively, greater risk of HF in comparison to normotensive participants. Participants with treated hypertensive SBP of <140, 140-149 and ≥150mmHg, were at a 2.33 (95% CI 1.83-2.95, p <0.001), 1.98 (95% CI 1.51-2.60, p <0.001) and 2.77 (95% CI 2.06-3.73, p <0.001) respectively, greater risk of HF compared to normotensive participants. SmokingAhmed et al (2015) found a significant effect of smoking on the risk of HF PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5BaG1lZDwvQXV0aG9yPjxZZWFyPjIwMTU8L1llYXI+PFJl

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ADDIN EN.CITE.DATA [37]. Current smokers (n=629) were at a higher risk of HF compared to never smokers (n=2556) (adjusted HR 1.49, 95% CI 1.23 to 1.81, p<0.001). Former smokers (n=312) with a ≥32 pack year history were also associated with a significantly increased risk of HF compared to never smokers (adjusted HR 1.45, 95% CI 1.15 to 1.83, p=0.002). However, there was no significant relationship between former smokers with a ≤31 pack year history and HF risk. Gopal et al (2012) found that over a 9.4 year follow-up period of 2,125 participants from the Health, Aging, and Body Composition Study, 231 participants developed HF.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Hb3BhbDwvQXV0aG9yPjxZZWFyPjIwMTI8L1llYXI+PFJl

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ADDIN EN.CITE.DATA [36] The study found that non-smokers had a HF incidence of 11.4 events per 1,000 person-years, former smokers had a HF incidence of 15.2 events per 1,000 person-years and current smokers had a HF incidence of 21.9 events per 1,000 person-years. Adjusted hazard ratios showed that current smokers (n=221) had a significantly greater risk of HF compared to never smokers (n=1165) (adjusted HR 1.73, 95% CI 1.15 to 2.59, p= 0.008). However, the adjusted hazard ratios did not show a strong association between former smoking (n=739) and risk of HF versus never smoking. Atrial Fibrillation Atrial fibrillation and congestive HF often occur together and each condition can predispose to the other PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5IZWlzdDwvQXV0aG9yPjxZZWFyPjIwMDY8L1llYXI+PFJl

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ADDIN EN.CITE.DATA [42]. DiabetesType 2 diabetes has been identified as a risk factor for HF. ADDIN EN.CITE <EndNote><Cite><Author>Mosterd</Author><Year>2007</Year><RecNum>302</RecNum><DisplayText>[43]</DisplayText><record><rec-number>302</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1458654950">302</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Mosterd, A.</author><author>Hoes, A. W.</author></authors></contributors><auth-address>Department of Cardiology, Meander Medical Centre, Amersfoort, The Netherlands. a.mosterd@meandermc.nl</auth-address><titles><title>Clinical epidemiology of heart failure</title><secondary-title>Heart</secondary-title><alt-title>Heart (British Cardiac Society)</alt-title></titles><periodical><full-title>Heart</full-title></periodical><alt-periodical><full-title>Heart (British Cardiac Society)</full-title></alt-periodical><pages>1137-46</pages><volume>93</volume><number>9</number><edition>2007/08/19</edition><keywords><keyword>Cause of Death</keyword><keyword>Epidemiologic Methods</keyword><keyword>Female</keyword><keyword>Heart Failure/diagnosis/*epidemiology/etiology/prevention &amp; control</keyword><keyword>Hospitalization/statistics &amp; numerical data</keyword><keyword>Humans</keyword><keyword>Male</keyword><keyword>Prognosis</keyword></keywords><dates><year>2007</year><pub-dates><date>Sep</date></pub-dates></dates><isbn>1355-6037</isbn><accession-num>17699180</accession-num><urls><related-urls><url>;[43] HF is often a cause of disability and mortality in patients with type 2 diabetes mellitus, PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5XYW5nPC9BdXRob3I+PFllYXI+MjAxNTwvWWVhcj48UmVj

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ADDIN EN.CITE.DATA [34]. Resengren et al (2015) found a strong positive association between type I diabetes and HF PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Sb3NlbmdyZW48L0F1dGhvcj48WWVhcj4yMDE1PC9ZZWFy

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ADDIN EN.CITE.DATA [33]. A four-fold increased risk of HF was observed in diabetic patients compared with population-based controls (HR 4.69, 95% CI 3.64 to 6.04, p< 0.001). Although most studies investigating HF risk in patients with diabetes have a sample of older patients with type 2 diabetes, a recent nationwide study of 33,402 people with type 1 diabetes in Sweden found a four-times greater risk of being admitted to hospital for HF compared to those without type 1 diabetes.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Sb3NlbmdyZW48L0F1dGhvcj48WWVhcj4yMDE1PC9ZZWFy

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ADDIN EN.CITE.DATA [26] Over a median follow-up of 11.2 years in the Multi-Ethnic Study of Atherosclerosis (MESA), 111 subjects out of 6,781 participants developed HF with preserved ejection fraction (HFpEF).PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5TaWx2ZXJtYW48L0F1dGhvcj48WWVhcj4yMDE2PC9ZZWFy

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ADDIN EN.CITE.DATA [28] Age was found to be a significant risk factor for HFpEF, with increasing age (per SD) the risk increased by 2.27 (95% CI, 1.72-3.01, p<0.001). Congenital Heart DiseasePatients with congenital heart disease are increasingly reaching adulthood with the improvements in paediatric cardiology and cardiac surgery, improving the survival rates significantly.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5ab21lcjwvQXV0aG9yPjxZZWFyPjIwMTM8L1llYXI+PFJl

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ADDIN EN.CITE.DATA [45] Nevertheless, patients with congenital heart disease face complications in adulthood such as arrhythmias, endocarditis and HF. ADDIN EN.CITE <EndNote><Cite><Author>Verheugt</Author><Year>2008</Year><RecNum>310</RecNum><DisplayText>[46]</DisplayText><record><rec-number>310</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1459255678">310</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Verheugt, C. L.</author><author>Uiterwaal, C. S.</author><author>Grobbee, D. E.</author><author>Mulder, B. J.</author></authors></contributors><auth-address>Department of Cardiology, Academic Medical Centre, Amsterdam, The Netherlands.</auth-address><titles><title>Long-term prognosis of congenital heart defects: a systematic review</title><secondary-title>Int J Cardiol</secondary-title><alt-title>International journal of cardiology</alt-title></titles><periodical><full-title>Int J Cardiol</full-title><abbr-1>International journal of cardiology</abbr-1></periodical><alt-periodical><full-title>Int J Cardiol</full-title><abbr-1>International journal of cardiology</abbr-1></alt-periodical><pages>25-32</pages><volume>131</volume><number>1</number><edition>2008/08/09</edition><keywords><keyword>Clinical Trials as Topic/methods/trends</keyword><keyword>Follow-Up Studies</keyword><keyword>Heart Defects, Congenital/*diagnosis/*mortality</keyword><keyword>Humans</keyword><keyword>Prognosis</keyword><keyword>Survival Rate/trends</keyword><keyword>Time</keyword></keywords><dates><year>2008</year><pub-dates><date>Dec 17</date></pub-dates></dates><isbn>0167-5273</isbn><accession-num>18687485</accession-num><urls><related-urls><url>;[46] A cohort study of 10,808 patients with congenital heart disease, with a follow-up time of 21 years, 274 (2.5%) patients were admitted for HF.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5ab21lcjwvQXV0aG9yPjxZZWFyPjIwMTM8L1llYXI+PFJl

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ADDIN EN.CITE.DATA [45] A study using the 2007 Nationwide Inpatient Sample found patients with adult congenital heart disease (ACHD) with ventricular septal defect had 1.54 times greater odds of developing HF (95% CI, 1.31-1.81) compared to those without ventricular septal defect.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Sb2RyaWd1ZXo8L0F1dGhvcj48WWVhcj4yMDEzPC9ZZWFy

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ADDIN EN.CITE.DATA [25] The prevalence of congenital heart disease was <1% in the UK during 2000 to 2005, ADDIN EN.CITE <EndNote><Cite><Author>Dolk</Author><Year>2011</Year><RecNum>316</RecNum><DisplayText>[47]</DisplayText><record><rec-number>316</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1460723692">316</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Dolk, H.</author><author>Loane, M.</author><author>Garne, E.</author></authors></contributors><auth-address>Professor of Epidemiology and Health Services Research, University of Ulster, Co Antrim, Northern Ireland, UK. h.dolk@ulster.ac.uk</auth-address><titles><title>Congenital heart defects in Europe: prevalence and perinatal mortality, 2000 to 2005</title><secondary-title>Circulation</secondary-title><alt-title>Circulation</alt-title></titles><periodical><full-title>Circulation</full-title></periodical><alt-periodical><full-title>Circulation</full-title></alt-periodical><pages>841-9</pages><volume>123</volume><number>8</number><edition>2011/02/16</edition><keywords><keyword>Europe/epidemiology</keyword><keyword>Heart Defects, Congenital/*epidemiology/*mortality</keyword><keyword>Humans</keyword><keyword>Infant, Newborn</keyword><keyword>Perinatal Mortality/*trends</keyword><keyword>Prevalence</keyword><keyword>Registries</keyword><keyword>Retrospective Studies</keyword><keyword>Survival Rate</keyword></keywords><dates><year>2011</year><pub-dates><date>Mar 1</date></pub-dates></dates><isbn>0009-7322</isbn><accession-num>21321151</accession-num><urls><related-urls><url>;[47] therefore congenital heart disease will not make a large contribution to population prevalence of HF, and so it has not been included as a risk factor in the model. BMI In a population-based cohort study of Danish male recruits (n = 12,850), 107 individuals were diagnosed with congestive HF. The 36-year risk of HF was 2.49 times greater in overweight individuals (95% CI, 1.56-3.99) and 4.52 times greater in obese individuals (95% CI 1.96-10.43) compared to those of normal weight (BMI 18.5 – 24.9kg/m2).PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5TY2htaWR0PC9BdXRob3I+PFllYXI+MjAxNDwvWWVhcj48

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ADDIN EN.CITE.DATA [28] Black participants in the study were at a lower risk of HFpEF compared to White participants (95% CI, 0.26-0.82, p=0.009). However, there was no significant difference in the risk of HFpEF in Chinese and Hispanic participants compared to White participants. In their individual predictive risk model for HF using UK primary care EHRs, Hippisley-Cox et al included risk factors for age, BMI, systolic blood pressure, cholesterol/ high-density lipoprotein (HDL) ratio, glycosylated haemoglobin (HbA1c), material deprivation, ethnicity, smoking, diabetes duration, type of diabetes, atrial fibrillation, CVD, CKD, and family history of premature CHD. ADDIN EN.CITE <EndNote><Cite><Author>Hippisley-Cox</Author><Year>2015</Year><RecNum>328</RecNum><DisplayText>[18]</DisplayText><record><rec-number>328</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1460451158">328</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Hippisley-Cox, J.</author><author>Coupland, C.</author></authors></contributors><auth-address>Division of Primary Care, University Park, Nottingham, UK.</auth-address><titles><title>Development and validation of risk prediction equations to estimate future risk of heart failure in patients with diabetes: a prospective cohort study</title><secondary-title>BMJ Open</secondary-title><alt-title>BMJ open</alt-title></titles><periodical><full-title>BMJ Open</full-title></periodical><alt-periodical><full-title>BMJ Open</full-title></alt-periodical><pages>e008503</pages><volume>5</volume><number>9</number><edition>2015/09/12</edition><keywords><keyword>Epidemiology</keyword><keyword>Preventive medicine</keyword><keyword>Primary care</keyword></keywords><dates><year>2015</year></dates><accession-num>26353872</accession-num><urls><related-urls><url>;[18]GenderIn the MESA study, no significant difference was observed in the risk of developing HF between males and females. However, a study investigating the gender difference in the incidence and risk of new-onset heart HF in subjects from the Renal and Vascular Endstage Disease (PREVEND) study, found females were less likely to have new-onset of HF with reduce ejection fraction (HFrEF) (subhazard ratio = 0.47, 95 % CI 0.29–0.76, p = 0.002) compared to males. PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5NZXllcjwvQXV0aG9yPjxZZWFyPjIwMTU8L1llYXI+PFJl

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ADDIN EN.CITE.DATA [48] However, women were more likely to have new-onset of HFpEF (subhazard ratio = 2.16, 95 % CI 1.21–3.83, p = 0.009) compared to males. Alcohol ConsumptionIn a prospective study of 3,530 males (60-79 years of age) without previous diagnosis of HF or MI, 198 HF cases were identified over the follow-up period of 11 years. ADDIN EN.CITE <EndNote><Cite><Author>Wannamethee</Author><Year>2015</Year><RecNum>315</RecNum><DisplayText>[49]</DisplayText><record><rec-number>315</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1459344575">315</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Wannamethee, S. G.</author><author>Whincup, P. H.</author><author>Lennon, L.</author><author>Papacosta, O.</author><author>Shaper, A. G.</author></authors></contributors><auth-address>Department of Primary Care and Population Health , University College London , London , UK.&#xD;Department of Population Health Sciences and Education , St George&apos;s, University of London , London , UK.</auth-address><titles><title>Alcohol consumption and risk of incident heart failure in older men: a prospective cohort study</title><secondary-title>Open Heart</secondary-title><alt-title>Open heart</alt-title></titles><periodical><full-title>Open Heart</full-title><abbr-1>Open heart</abbr-1></periodical><alt-periodical><full-title>Open Heart</full-title><abbr-1>Open heart</abbr-1></alt-periodical><pages>e000266</pages><volume>2</volume><number>1</number><edition>2015/08/21</edition><keywords><keyword>Heart failure</keyword></keywords><dates><year>2015</year></dates><isbn>2053-3624</isbn><accession-num>26290689</accession-num><urls><related-urls><url>;[49] Male subjects drinking 35 drinks or more per week were at a 1.9 times greater risk of HF compared non-drinkers (95% CI, 1.02-3.54). Sleep ApnoeaIn a population-based cohort study, Sleep and Health in Women, obstructive sleep apnoea symptoms such as snoring and excessive daytime sleepiness (EDS) were significantly associated with increased risk of HF. PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5ManVuZ2dyZW48L0F1dGhvcj48WWVhcj4yMDE2PC9ZZWFy

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ADDIN EN.CITE.DATA [31]Intentional BP-lowering trials in hypertensive patientsStandardized RR PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5aYW5jaGV0dGk8L0F1dGhvcj48WWVhcj4yMDE1PC9ZZWFy

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M.</author><author>Djousse, L.</author></authors></contributors><auth-address>Department of Medicine, Brigham and Women&apos;s Hospital and Harvard Medical School, Boston, MA 02115, USA. kfinnerty@post.harvard.edu</auth-address><titles><title>Normal systolic blood pressure and risk of heart failure in US male physicians</title><secondary-title>Eur J Heart Fail</secondary-title><alt-title>European journal of heart failure</alt-title></titles><alt-periodical><full-title>European Journal of Heart Failure</full-title></alt-periodical><pages>1129-34</pages><volume>11</volume><number>12</number><edition>2009/10/29</edition><keywords><keyword>*Blood Pressure</keyword><keyword>Heart Failure/*physiopathology</keyword><keyword>Humans</keyword><keyword>Male</keyword><keyword>Middle Aged</keyword><keyword>*Physicians</keyword><keyword>Risk Factors</keyword><keyword>Systole</keyword></keywords><dates><year>2009</year><pub-dates><date>Dec</date></pub-dates></dates><isbn>1388-9842</isbn><accession-num>19861382</accession-num><urls><related-urls><url>;[29]1.00Reference120-129HR Adjusted for age, smoking, BMI, alcohol consumption, history of diabetes, history of atrial fibrillation, physical activity, egg intake, aspirin arm, and breakfast cereal intake ADDIN EN.CITE <EndNote><Cite><Author>Britton</Author><Year>2009</Year><RecNum>289</RecNum><DisplayText>[29]</DisplayText><record><rec-number>289</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1458555150">289</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Britton, K. 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M.</author><author>Djousse, L.</author></authors></contributors><auth-address>Department of Medicine, Brigham and Women&apos;s Hospital and Harvard Medical School, Boston, MA 02115, USA. kfinnerty@post.harvard.edu</auth-address><titles><title>Normal systolic blood pressure and risk of heart failure in US male physicians</title><secondary-title>Eur J Heart Fail</secondary-title><alt-title>European journal of heart failure</alt-title></titles><alt-periodical><full-title>European Journal of Heart Failure</full-title></alt-periodical><pages>1129-34</pages><volume>11</volume><number>12</number><edition>2009/10/29</edition><keywords><keyword>*Blood Pressure</keyword><keyword>Heart Failure/*physiopathology</keyword><keyword>Humans</keyword><keyword>Male</keyword><keyword>Middle Aged</keyword><keyword>*Physicians</keyword><keyword>Risk Factors</keyword><keyword>Systole</keyword></keywords><dates><year>2009</year><pub-dates><date>Dec</date></pub-dates></dates><isbn>1388-9842</isbn><accession-num>19861382</accession-num><urls><related-urls><url>;[29]1.35[1.09-1.68]Risk factorHypertensive, Untreated140-149HR Adjusted for age, smoking, BMI, alcohol consumption, history of diabetes, history of atrial fibrillation, physical activity, egg intake, aspirin arm, and breakfast cereal intake ADDIN EN.CITE <EndNote><Cite><Author>Britton</Author><Year>2009</Year><RecNum>289</RecNum><DisplayText>[29]</DisplayText><record><rec-number>289</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1458555150">289</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Britton, K. 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M.</author><author>Djousse, L.</author></authors></contributors><auth-address>Department of Medicine, Brigham and Women&apos;s Hospital and Harvard Medical School, Boston, MA 02115, USA. kfinnerty@post.harvard.edu</auth-address><titles><title>Normal systolic blood pressure and risk of heart failure in US male physicians</title><secondary-title>Eur J Heart Fail</secondary-title><alt-title>European journal of heart failure</alt-title></titles><alt-periodical><full-title>European Journal of Heart Failure</full-title></alt-periodical><pages>1129-34</pages><volume>11</volume><number>12</number><edition>2009/10/29</edition><keywords><keyword>*Blood Pressure</keyword><keyword>Heart Failure/*physiopathology</keyword><keyword>Humans</keyword><keyword>Male</keyword><keyword>Middle Aged</keyword><keyword>*Physicians</keyword><keyword>Risk Factors</keyword><keyword>Systole</keyword></keywords><dates><year>2009</year><pub-dates><date>Dec</date></pub-dates></dates><isbn>1388-9842</isbn><accession-num>19861382</accession-num><urls><related-urls><url>;[29]1.98[1.51-2.60]Risk factor≥150HR Adjusted for age, smoking, BMI, alcohol consumption, history of diabetes, history of atrial fibrillation, physical activity, egg intake, aspirin arm, and breakfast cereal intake ADDIN EN.CITE <EndNote><Cite><Author>Britton</Author><Year>2009</Year><RecNum>289</RecNum><DisplayText>[29]</DisplayText><record><rec-number>289</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1458555150">289</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Britton, K. 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M.</author><author>Djousse, L.</author></authors></contributors><auth-address>Department of Medicine, Brigham and Women&apos;s Hospital and Harvard Medical School, Boston, MA 02115, USA. kfinnerty@post.harvard.edu</auth-address><titles><title>Normal systolic blood pressure and risk of heart failure in US male physicians</title><secondary-title>Eur J Heart Fail</secondary-title><alt-title>European journal of heart failure</alt-title></titles><alt-periodical><full-title>European Journal of Heart Failure</full-title></alt-periodical><pages>1129-34</pages><volume>11</volume><number>12</number><edition>2009/10/29</edition><keywords><keyword>*Blood Pressure</keyword><keyword>Heart Failure/*physiopathology</keyword><keyword>Humans</keyword><keyword>Male</keyword><keyword>Middle Aged</keyword><keyword>*Physicians</keyword><keyword>Risk Factors</keyword><keyword>Systole</keyword></keywords><dates><year>2009</year><pub-dates><date>Dec</date></pub-dates></dates><isbn>1388-9842</isbn><accession-num>19861382</accession-num><urls><related-urls><url>;[29]2.77[2.06-3.73]Risk factorMIInfarct size Crude OR PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5DbGVyZm9uZDwvQXV0aG9yPjxZZWFyPjIwMTU8L1llYXI+

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ADDIN EN.CITE.DATA [34]1.43[1.14-1.79]Risk factorHbA1c per 1% increasePooled HR Adjusted for age, gender, BMI, hypertension, smoking status, and cholesterol PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5XYW5nPC9BdXRob3I+PFllYXI+MjAxNTwvWWVhcj48UmVj

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RW5kTm90ZT5=

ADDIN EN.CITE.DATA [34]1.27[1.10-1.47]Risk factorMI (first-time) with covariates:Age at admission (divided into 10 year bands)HR Adjusted for gender, age, comorbidity and year of admission, invasive procedures and cardiovascular medications PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5HamVzaW5nPC9BdXRob3I+PFllYXI+MjAxNDwvWWVhcj48

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ADDIN EN.CITE.DATA [21]1.000.94[0.93-0.96]ReferenceRisk factorDiabetes (Type I/II)HR Adjusted for gender, age, comorbidity and year of admission, invasive procedures and cardiovascular medications PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5HamVzaW5nPC9BdXRob3I+PFllYXI+MjAxNDwvWWVhcj48

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ADDIN EN.CITE.DATA [25]1.54[1.31-1.81]Risk factorTetralogy of FallotCrude OR PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Sb2RyaWd1ZXo8L0F1dGhvcj48WWVhcj4yMDEzPC9ZZWFy

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ADDIN EN.CITE.DATA [25]2.31[1.26-4.24]Risk factorBMI (kg/m2)Underweight (BMI<18.5)HR Adjusted for years of education and body height PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5TY2htaWR0PC9BdXRob3I+PFllYXI+MjAxNDwvWWVhcj48

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ADDIN EN.CITE.DATA [35]1.14[0.46-2.82]NSNormal (BMI 18.5-24.9)HR Adjusted for years of education and body height PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5TY2htaWR0PC9BdXRob3I+PFllYXI+MjAxNDwvWWVhcj48

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ADDIN EN.CITE.DATA [40]2.19[1.14-4.18]Risk factorHF incidence and prevalenceSeferovic et al (2013) conducted a real-life contemporary analysis on the incidence and prevalence of HF in 33 countries using data from HF National Societies (HFNS) representatives in October 2011 PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5TZWZlcm92aWM8L0F1dGhvcj48WWVhcj4yMDEzPC9ZZWFy

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ADDIN EN.CITE.DATA [50]CountryCountry PopulationNo of inhabitants ≥65 years, %Incidence, 1000/yearPrevalence, %Belgium11 076 84718NA2-3Czech Republic10 446 15715NA1.5Denmark5 566 856161.21France63 460 768163.32.2Germany81 471 834208.8NAGreece10 787 69019NA2-10Hungary9 905 5961631.6Ireland4 581 2691242Israel7 411 00010NA1.5Italy59 464 6442013.5Lithuania3 349 872161.412.98Norway4 937 30515NA1-2Portugal10 707 92417NA4.4Romania21 524 0421544.2Russia143 115 70614NA7Serbia7 379 339173.12.3Slovakia5 410 37112NA2Slovenia2 058 03216NA1-2Spain45 989 01618NA5 (in >45 years)Sweden9 276 50918NA2Switzerland7 991 60016NA2UK61 524 87216NA1-2The British Heart Foundation Cardiovascular Disease Statistics Report (2014) estimated the prevalence of HF (see REF _Ref449449747 \h Table 4 below) based on records from a sample of general practices across the UK using data from the Clinical Practice Research Datalink (CPRD). ADDIN EN.CITE <EndNote><Cite><Author>Nick Townsend</Author><Year>2014</Year><RecNum>315</RecNum><DisplayText>[51]</DisplayText><record><rec-number>315</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1460718580">315</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Nick Townsend, Julianne Williams, Prachi Bhatnagar, Kremlin Wickramasinghe</author><author>and Mike Rayner.</author></authors></contributors><auth-address>Nuffield Department of Population Health, University of Oxford</auth-address><titles><title>Cardiovascular disease statistics</title><secondary-title>British Heart Foundation</secondary-title></titles><periodical><full-title>British Heart Foundation</full-title></periodical><dates><year>2014</year></dates><urls><related-urls><url>;[51] This report only presented data on doctor-diagnosed HF. All estimates for the different age groups are age-standardised to the European Standard Population. This table is adapted from reference ADDIN EN.CITE <EndNote><Cite><Author>Nick Townsend</Author><Year>2014</Year><RecNum>315</RecNum><DisplayText>[51]</DisplayText><record><rec-number>315</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1460718580">315</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Nick Townsend, Julianne Williams, Prachi Bhatnagar, Kremlin Wickramasinghe</author><author>and Mike Rayner.</author></authors></contributors><auth-address>Nuffield Department of Population Health, University of Oxford</auth-address><titles><title>Cardiovascular disease statistics</title><secondary-title>British Heart Foundation</secondary-title></titles><periodical><full-title>British Heart Foundation</full-title></periodical><dates><year>2014</year></dates><urls><related-urls><url>;[51], which is based on data from the CPRD GOLD database, 2014.Table 4: prevalence estimates for HF in England, Scotland, Wales, Northern Ireland and United Kingdom, 2013, by gender and age ADDIN EN.CITE <EndNote><Cite><Author>Nick Townsend</Author><Year>2014</Year><RecNum>315</RecNum><DisplayText>[51]</DisplayText><record><rec-number>315</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1460718580">315</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Nick Townsend, Julianne Williams, Prachi Bhatnagar, Kremlin Wickramasinghe</author><author>and Mike Rayner.</author></authors></contributors><auth-address>Nuffield Department of Population Health, University of Oxford</auth-address><titles><title>Cardiovascular disease statistics</title><secondary-title>British Heart Foundation</secondary-title></titles><periodical><full-title>British Heart Foundation</full-title></periodical><dates><year>2014</year></dates><urls><related-urls><url>;[51]EnglandScotlandWalesNorthern IrelandUnited Kingdom(%)(%)(%)(%)(%)Men (age/years)0-440.050.060.070.060.0545-540.310.400.400.200.3355-641.041.421.420.971.1265-742.733.723.392.972.9275+7.648.728.258.487.84All ages1.171.441.371.251.22Women (age/years)0-440.030.060.050.020.0445-540.150.180.180.120.1555-640.430.550.520.540.4565-741.221.561.801.341.3275+5.805.976.376.225.89All ages0.740.820.870.790.76No. of cases in sampleMen16,6182,9422,63875622,954Women13,3822,0942,08963618,201Total no. of cases in sample30,0005,0364,7271,39241,155Quality & Outcomes Framework DataGiven that REF _Ref449449747 \h Table 4 uses GP diagnoses from a fairly representative sample, it should show similar prevalence to data obtained from the Quality & Outcomes Framework of the GP contract. The 2014-15 prevalence in England was 0.72% and in 2015-16 it was 0.76%, somewhat lower than CPRD. However coding may be somewhat better in CPRD practices than UK practices in general.MethodsHF prevalence from UK primary care and hospital data: Clinical Practice Research Datalink & Hospital Episode StatisticsWhat is the Clinical Practice Research Datalink?The Clinical Practice Research Datalink (CPRD) is an ongoing primary care database of longitudinal anonymised electronic health records (EHRs) from general practitioners, with coverage of over 11.3 million patients from 674 practices in the UK. With 4.4 million active (alive, currently registered) patients meeting quality criteria, approximately 6.9% of the UK population are included and patients are broadly representative of the UK general population in terms of age, sex and ethnicity. The distribution of CPRD practices is shown in REF _Ref473991408 \h Figure 1 below. Figure 1: Distribution of the 674 CPRD practices by region in England, Wales, Scotland and Northern IrelandIdentification of HF cases and code lists for CPRD and HES doctor diagnosed cases REF _Ref473991527 \h Table 5 contains the list of Medcodes and Read Codes that were used to identify the CPRD doctor diagnosed cases, and REF _Ref474148003 \h Table 6 shows the ICD-10 codes that were used for the identification of HES doctor diagnosed HF cases. Data was extracted from CPRD () to analyse the prevalence of HF. HF cases were identified in four ways:CPRD doctor diagnosed casesHospital Episode Statistics (HES) inpatient doctor diagnosed casescases that were inferred using records of symptoms, signs and test results that were not explicitly doctor diagnosed, using a clinical algorithm based on the most recent NICE and ESC guidelines, andpatients who had been prescribed HF drugs and had clinical HF signs but were not doctor diagnosed, using a drugs algorithm.A comprehensive list of Medcodes, Prodcodes and ICD-10 codes was compiled for the identification of the CPRD and HES doctor diagnosed HF cases, and for the undiagnosed (but diagnosable) clinical and drugs algorithm HF cases. The clinical and drugs algorithms were developed based on the criteria found in the NICE and European Society of Cardiology (ESC) Guidelines.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Qb25pa293c2tpPC9BdXRob3I+PFllYXI+MjAxNjwvWWVh

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ADDIN EN.CITE.DATA [6 ,52] The Medcodes used for CPRD HF diagnoses are shown in REF _Ref473991527 \h Table 5. These include all QOF HF diagnostic Read codes, plus other codes which reliably indicate a previous diagnosis e.g. “preferred place of care for next exacerbation heart failure”.Table 5: Medcodes that were used for the identification of CPRD doctor diagnosed HF casesRead TermMedcodeRead CodeICD-10 CodeH/O: heart failure1505814A6.00I50.9H/O: heart failure in last year4691214AM.00I50.9Heart failure confirmed 99131O1..00I50.9Echocardiogram shows left ventricular systolic dysfunction11284585f.00I50.1Echocardiogram shows left ventricular diastolic dysfunction11351585g.00I50.1Heart failure self-management plan agreed106198661M500I50.9Congestive heart failure monitoring12366662T.00I50.0Heart failure annual review30779662W.00I50.9New York Heart Association classification - class I18853662f.00I50.9New York Heart Association classification - class II13189662g.00I50.9New York Heart Association classification - class III19066662h.00I50.9New York Heart Association classification - class IV51214662i.00I50.9Heart failure 6 month review83502662p.00I50.9Education about deteriorating heart failure105002679W100I50.9Cardiac failure therapy245038B29.00I50.9Heart failure care plan discussed with patient329458CL3.00I50.9Has heart failure management plan1037328CMK.00I50.9Heart failure clinical pathway1060088CMW800I50.9Preferred place of care for next exacerbation heart failure1055428CeC.00I50.9Admit heart failure emergency328988H2S.00I50.9Heart failure follow-up178518HBE.00I50.9Referral to heart failure exercise programme706198HHz.00I50.9Seen in heart failure clinic126279N0k.00I50.9Seen by community heart failure nurse190029N2p.00I50.9Referred by heart failure nurse specialist690629N6T.00I50.9Malignant hypertensive heart disease with CCF72668G210100I11.0Benign hypertensive heart disease with CCF52127G211100I11.0Hypertensive heart disease NOS with CCF62718G21z100I11.0Hypertensive heart & renal disease with (congestive) heart failure21837G232.00I13.0Hypertensive heart & renal disease + both (congestive) heart and renal failure57987G234.00I13.2Heart failure2062G58..00I50.9Cardiac failure1223G58..11I50.9Congestive heart failure398G580.00I50.0Congestive cardiac failure2906G580.11I50.0Right heart failure10079G580.12I50.0Right ventricular failure10154G580.13I50.0Biventricular failure9524G580.14I50.9Acute congestive heart failure23707G580000I50.0Chronic congestive heart failure32671G580100I50.0Decompensated cardiac failure27884G580200I50.9Compensated cardiac failure11424G580300I50.9Congestive heart failure due to valvular disease94870G580400I50.0Left ventricular failure884G581.00I50.1Impaired left ventricular function5942G581.13I50.1Acute left ventricular failure5255G581000I50.1Acute heart failure27964G582.00I50.9Heart failure with normal ejection fraction101138G583.00I50.9HFNEF – heart failure with normal ejection fraction101137G583.11I50.9Heart failure with preserved ejection fraction106897G583.12I50.9Right ventricular failure104275G584.00I50.0Heart failure NOS4024G58z.00I50.9Cardiac failure NOS17278G58z.12I50.9Post cardiac operation heart failure NOS96799G5y4z00I50.9Left ventricular systolic dysfunction8966G5yy900I50.1Left ventricular diastolic dysfunction12550G5yyA00I50.1Heart failure as a complication of care66306SP11111I50.9 REF _Ref474148003 \h \* MERGEFORMAT Table 6 shows the ICD-10 codes that were used for the identification of HES doctor diagnosed HF cases.Table 6: ICD-10 codes that were used for the identification of HES doctor diagnosed HF casesICD-10 CodeDiagnosisI50.0Congestive Heart FailureI50.1Left ventricular failureI50.9Heart failure, unspecified I11.0Hypertensive heart disease with (congestive) heart failureI13.0Hypertensive heart and renal disease with (congestive) heart failureI13.2Hypertensive heart and renal disease with both (congestive) heart failure and renal failureAdditional HF cases from clinical algorithmIn order to identify additional undiagnosed (but diagnosable) HF cases, the NICE Acute and Chronic HF Guidelines and the 2016 ESC HF Guidelines were used to develop two algorithms– a clinical algorithm and a drugs algorithm. The clinical algorithm combines information about specific symptoms and signs of HF with data from natriuretic peptide test results and ECG and echocardiogram results in order to identify additional probable HF cases. The flowchart of the clinical algorithm that was developed is shown below in REF _Ref473991815 \h Figure 2: clinical algorithm flowchart.Figure 2: clinical algorithm flowchart14439900Develop the Clinical algorithmDevelop the Clinical algorithm1369060391160323850574040Keep cases who have not had echocardiogram(N=162,731)00Keep cases who have not had echocardiogram(N=162,731)1372235948690013716004032250022860007556537623756159503286125101600Keep abnormal echocardiogram cases00Keep abnormal echocardiogram cases190500102870clinical algorithm – keep cases fulfilling criteria00clinical algorithm – keep cases fulfilling criteria27622566040History of myocardial infarction, orthopnoea, paroxysmal nocturnal dyspnoeaORSigns of elevated JVP, displaced apex beatORAbnormal ECG00History of myocardial infarction, orthopnoea, paroxysmal nocturnal dyspnoeaORSigns of elevated JVP, displaced apex beatORAbnormal ECG3771900571500330517550800Exclude HF cases with HES or CPRD diagnosis 00Exclude HF cases with HES or CPRD diagnosis 115125530480ANDAND61214076200NT-proBNP ≥125 pg/mLOr BNP ≥35 pg/mLNT-proBNP ≥125 pg/mLOr BNP ≥35 pg/mL376237569850141922514351003209925170815Additional abnormal echocardiogram probable HF cases00Additional abnormal echocardiogram probable HF cases209550153035Clinical algorithm probable HF cases00Clinical algorithm probable HF cases1400175685800952580010Exclude HF cases with HES or CPRD diagnosis00Exclude HF cases with HES or CPRD diagnosis3733800133350140970015621000167640Additional clinical algorithm probable HF cases0Additional clinical algorithm probable HF cases141605081280057150121920Probable HF cases0Probable HF casesAccording to the 2016 ESC Guidelines, ADDIN EN.CITE <EndNote><Cite><Author>Ponikowski</Author><Year>2016</Year><RecNum>343</RecNum><DisplayText>[6]</DisplayText><record><rec-number>343</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1485854644">343</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Ponikowski, Piotr</author><author>Voors, Adriaan A.</author><author>Anker, Stefan D.</author><author>Bueno, Héctor</author><author>Cleland, John G. F.</author><author>et al,</author></authors></contributors><titles><title>2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failureThe Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC) </title><secondary-title>European Heart Journal</secondary-title></titles><periodical><full-title>European Heart Journal</full-title></periodical><pages>2129-2200</pages><volume>37</volume><number>27</number><dates><year>2016</year></dates><isbn>0195-668X</isbn><urls><related-urls><url>;[6] echocardiography is the single most valuable test in diagnosing HF because structural abnormality, systolic dysfunction, diastolic dysfunction, or a combination of these factors are required to be recognised in patients who have resting and/or exertional symptoms of HF, to conclude a definitive HF diagnosis. 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ADDIN EN.CITE.DATA [53]. Plasma concentration of natriuretic peptides can be used as an initial diagnostic HF test, especially when echocardiography is unavailable. Patients who have natriuretic peptide levels below the cut off points can be ruled out as HF patients. The 2016 ESC Guidelines stated that NTproBNP levels of ≥125pg/mL or BNP levels of ≥35pg/mL could be used as an indication of HF. Additional HF cases from drugs algorithmBeta blockers have been found to reduce morbidity and mortality in patients with HF with reduced left ventricular ejection fraction. ADDIN EN.CITE <EndNote><Cite><Author>Kotecha</Author><Year>2016</Year><RecNum>334</RecNum><DisplayText>[54]</DisplayText><record><rec-number>334</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1461764270">334</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Kotecha, Dipak</author><author>Manzano, Luis</author><author>Krum, Henry</author><author>Rosano, Giuseppe</author><author>Holmes, Jane</author><author>Altman, Douglas G</author><author>Collins, Peter D</author><author>Packer, Milton</author><author>Wikstrand, John</author><author>Coats, Andrew J S</author><author>Cleland, John G F</author><author>Kirchhof, Paulus</author><author>von Lueder, Thomas G</author><author>Rigby, Alan S</author><author>Andersson, Bert</author><author>Lip, Gregory YH</author><author>van Veldhuisen, Dirk J</author><author>Shibata, Marcelo C</author><author>Wedel, Hans</author><author>B?hm, Michael</author><author>Flather, Marcus D</author></authors></contributors><titles><title>Effect of age and sex on efficacy and tolerability of β blockers in patients with heart failure with reduced ejection fraction: individual patient data meta-analysis</title><secondary-title>BMJ</secondary-title></titles><periodical><full-title>BMJ</full-title></periodical><volume>353</volume><dates><year>2016</year><pub-dates><date>2016-04-20 12:05:40</date></pub-dates></dates><urls><related-urls><url>;[54] However, present guidelines make no differentiation in treatment based on age or sex. There is a greater likelihood of patients being female, with increasing age. In many RCTs, there is a moderately low number older patients, which has resulted in an uncertainty regarding the optimum management of HFrEF in older patients. ADDIN EN.CITE <EndNote><Cite><Author>Kotecha</Author><Year>2016</Year><RecNum>334</RecNum><DisplayText>[54]</DisplayText><record><rec-number>334</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1461764270">334</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Kotecha, Dipak</author><author>Manzano, Luis</author><author>Krum, Henry</author><author>Rosano, Giuseppe</author><author>Holmes, Jane</author><author>Altman, Douglas G</author><author>Collins, Peter D</author><author>Packer, Milton</author><author>Wikstrand, John</author><author>Coats, Andrew J S</author><author>Cleland, John G F</author><author>Kirchhof, Paulus</author><author>von Lueder, Thomas G</author><author>Rigby, Alan S</author><author>Andersson, Bert</author><author>Lip, Gregory YH</author><author>van Veldhuisen, Dirk J</author><author>Shibata, Marcelo C</author><author>Wedel, Hans</author><author>B?hm, Michael</author><author>Flather, Marcus D</author></authors></contributors><titles><title>Effect of age and sex on efficacy and tolerability of β blockers in patients with heart failure with reduced ejection fraction: individual patient data meta-analysis</title><secondary-title>BMJ</secondary-title></titles><periodical><full-title>BMJ</full-title></periodical><volume>353</volume><dates><year>2016</year><pub-dates><date>2016-04-20 12:05:40</date></pub-dates></dates><urls><related-urls><url>;[54] Kotecha et al (2016) found that beta-blockers reduced mortality hazard rations significantly and the number of hospital admissions associated with HF in all sex and age subgroups. ADDIN EN.CITE <EndNote><Cite><Author>Hoes</Author><Year>2016</Year><RecNum>335</RecNum><DisplayText>[55]</DisplayText><record><rec-number>335</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1461764348">335</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Hoes, Arno W</author></authors></contributors><titles><title>β blockers for heart failure</title><secondary-title>BMJ</secondary-title></titles><periodical><full-title>BMJ</full-title></periodical><volume>353</volume><dates><year>2016</year><pub-dates><date>2016-04-20 13:59:06</date></pub-dates></dates><urls><related-urls><url>;[55] Drug prescriptions are an additional potential source of diagnostic data. NICE recommends giving both angiotensin-converting enzyme inhibitors (ACEIs) and beta-blockers (BBs) to all patients with heart failure, and in those patients who remain symptomatic an aldosterone antagonist, or an angiotensin II receptor antagonist (ARB), or hydralazine in combination with nitrate if the patient is of African or Caribbean origin. However, we will exclude patients on these drugs with a diagnosis of hypertension of coronary heart disease (CHD), and will explore methods of discriminating heart failure based on NICE’s recommended prescribing pattern. At this stage it appears that a combination of ACEI/ARB + BB licensed for HF (carvedilol, bisoprolol or nebivolol) is likely to be systolic heart failure, and this is even more likely if spironolactone or eplerenone are also prescribed. It is difficult to identify a group that would have these three classes of drug that would not have systolic heart failure. The drugs algorithm we developed combined drug information with HF signs and symptoms and abnormal ECG results, in order to identify possible HF cases which were not recorded in HES or CPRD as doctor-diagnosed cases. The flowchart of the drugs algorithm that was developed is shown below in Figure 3.Figure 3: drugs algorithm Flowchart3708400Develop the Drugs algorithmDevelop the Drugs algorithm1203960248285425452647315Exclude Hypertension and CHD cases0Exclude Hypertension and CHD cases425453123565Drugs algorithm probable HF cases0Drugs algorithm probable HF cases1301753604895Exclude HF cases with HES or CPRD or clinical algorithm diagnosisExclude HF cases with HES or CPRD or clinical algorithm diagnosis1968504223385Additional drugs algorithm probable HF casesAdditional drugs algorithm probable HF cases1250950458914512522204003040125222033902651252220291401512522202437765left102870drugs algorithm – keep cases fulfilling criteria00drugs algorithm – keep cases fulfilling criteria952508255History of myocardial infarction, orthopnoea, paroxysmal nocturnal dyspnoeaORSigns of elevated JVP, displaced apex beatORAbnormal ECG00History of myocardial infarction, orthopnoea, paroxysmal nocturnal dyspnoeaORSigns of elevated JVP, displaced apex beatORAbnormal ECG971550127634AND0AND94615145415Patients prescribed ACEi/Angiotensin II receptor antagonists/Beta-blocker/potassium sparing diuretics in CPRD?Patients prescribed ACEi/Angiotensin II receptor antagonists/Beta-blocker/potassium sparing diuretics in CPRD?429233105548Probable HF casesProbable HF casesCPRD risk factorsWe used the literature review described in the Background to extract CPRD data on risk factors. There were two main reasons why some risk factors from the literature were not used in the final model. Firstly, the data was not available in CPRD. For example, data on educational level, occupational class and socioeconomic status is very poorly recorded. The occupational classification for which Read codes are available is from a 1986 Office for National Statistics classification so is outdated. CPRD links most patients’ data to Index of Multiple Deprivation (IMD) data based on postcode. Secondly, to produce local estimates we use “joint distributions”- cross tabulations which distribute data on each risk factor across the data for all other risk factors- of local risk factor data to which we apply the CPRD prevalence estimates for the same distributions. Hence we can only use in the final regression model variables which are also available locally. This may cause model performance to deteriorate. We evaluated the extent of this by comparing Receiver Operating Characteristic (ROC) curves for the two models. Although, the literature review highlights a significant association between congenital heart disease and HF, congenital heart disease was not included as a risk factor in the final model. This is mainly due to the prevalence of congenital heart in the UK being less than 1% during 2000 to 2005. ADDIN EN.CITE <EndNote><Cite><Author>Dolk</Author><Year>2011</Year><RecNum>316</RecNum><DisplayText>[47]</DisplayText><record><rec-number>316</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1460723692">316</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Dolk, H.</author><author>Loane, M.</author><author>Garne, E.</author></authors></contributors><auth-address>Professor of Epidemiology and Health Services Research, University of Ulster, Co Antrim, Northern Ireland, UK. h.dolk@ulster.ac.uk</auth-address><titles><title>Congenital heart defects in Europe: prevalence and perinatal mortality, 2000 to 2005</title><secondary-title>Circulation</secondary-title><alt-title>Circulation</alt-title></titles><periodical><full-title>Circulation</full-title></periodical><alt-periodical><full-title>Circulation</full-title></alt-periodical><pages>841-9</pages><volume>123</volume><number>8</number><edition>2011/02/16</edition><keywords><keyword>Europe/epidemiology</keyword><keyword>Heart Defects, Congenital/*epidemiology/*mortality</keyword><keyword>Humans</keyword><keyword>Infant, Newborn</keyword><keyword>Perinatal Mortality/*trends</keyword><keyword>Prevalence</keyword><keyword>Registries</keyword><keyword>Retrospective Studies</keyword><keyword>Survival Rate</keyword></keywords><dates><year>2011</year><pub-dates><date>Mar 1</date></pub-dates></dates><isbn>0009-7322</isbn><accession-num>21321151</accession-num><urls><related-urls><url>;[47] Therefore, as the prevalence is low, congenital heart disease may not be a significant risk factor for HF in the UK. Risk factor data were extracted by a defined Read code lists, and by extracting additional data using the ‘adid’, ‘enttype’ and ‘data’ variables in the CPRD Additional datasets. Read code lists were created by searching for relevant Read version 2 5-byte codes using either CPRD’s own code browser or using the “NHS browser” maintained by the Health & Social Care information Centre (HSCIC). We used the NHS browser and CPRD browser to create code lists for ethnicity, BMI, smoking, alcohol consumption, CHD, hypertension, diabetes, sleep apnoea and atrial fibrillation by searching relevant read terms or and selecting the appropriate medcodes. The smoking, alcohol and BMI data extracted using medcodes was combined with information found in the CPRD additional datasets, and the most recent recording for each patient was selected using the ‘eventdate’ variable.CPRD HF Control groupDue to time constraints, a 1:10 random sample was taken from the CPRD cohort for the control group, rather than using the entire CPRD cohort. The sample was extracted with approximately 1.05 million CPRD patients. Any patients below the age of 16 were excluded from the sample with only those 16 years of age and above remaining in the control group. Patients above the age of 105 years were also excluded.CPRD descriptive analysesWe performed a number of descriptive analyses on the patient-level dataset including demographics, risk factor breakdowns and categories.CPRD prevalence and incidenceThe overall and age and gender-specific prevalence and incidence of HF was estimated using denominator data from CPRD. (For sensitivity analysis, the primary-care data from CPRD was combined with secondary-care data from the linked HES data). Patients were identified by Read code and the most suitable ICD-10 classification. Period prevalence was calculated for 2016 using the number of patients that are alive and registered within an up-to-standard (UTS) practice on the beginning of the year point (January 2016) as the denominator. Annual incidence was estimated with regards to the average annual incidence of HF observed since at the beginning of the year.1.1.1CPRD regression modellingWe fitted uni-variate then multivariate logistic regression models for HF as described in previous publications, to produce odds ratios (ORs) and regression coefficients. ADDIN EN.CITE <EndNote><Cite><Author>Nacul</Author><Year>2011</Year><RecNum>346</RecNum><DisplayText>[56]</DisplayText><record><rec-number>346</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1486345940">346</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Nacul, Luis</author><author>Soljak, Michael</author><author>Samarasundera, Edgar</author><author>Hopkinson, Nicholas S</author><author>Lacerda, Eliana</author><author>Indulkar, Tejal</author><author>Flowers, Julian</author><author>Walford, Hannah</author><author>Majeed, Azeem</author></authors></contributors><titles><title>COPD in England: a comparison of expected, model-based prevalence and observed prevalence from general practice data</title><secondary-title>Journal of Public Health</secondary-title></titles><periodical><full-title>Journal of Public Health</full-title></periodical><pages>108-116</pages><volume>33</volume><number>1</number><dates><year>2011</year><pub-dates><date>March 1, 2011</date></pub-dates></dates><urls><related-urls><url>;[56] A range of multivariate regression models were fitted in order to obtain the best performing. We included one additional variable at a time to observe the effects.InteractionsThere is an interaction between the effects of two exposures if the effect of one exposure varies according to the level of the other exposure. ADDIN EN.CITE <EndNote><Cite><Author>Kirkwood</Author><Year>2003</Year><RecNum>1604</RecNum><DisplayText>[57]</DisplayText><record><rec-number>1604</rec-number><foreign-keys><key app="EN" db-id="ed9w09wsu5rwdwe5xscpxsf85twd99faret0" timestamp="1392388479">1604</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author>Kirkwood, B R</author><author>Sterne, J A C</author></authors><secondary-authors><author>Moore K</author></secondary-authors></contributors><titles><title>Regression modelling</title><secondary-title>Medical Statistics</secondary-title></titles><pages>339-342</pages><section>Deciding which exposure variables to include in a regression model</section><dates><year>2003</year></dates><pub-location>USA</pub-location><publisher>Blackwell Publishing company</publisher><urls></urls></record></Cite></EndNote>[57] For example, there might be an interaction between the HF risk factors of education level and social class. An alternative term for interaction ifs effect modification. In this example, we can think of this as educational level modifying the effect of social class. The most flexible approach to examine interactions is to use regression models, but when using Mantel-Haenszel methods to control for confounding an alternative is to use a χ2 test for effect modification, commonly called a test of heterogeneity. Interaction, effect modification and heterogeneity are three different ways of describing the same thing. Log likelihoods are compared in the two models excluding and including the interaction parameters to test the null hypothesis that there is no interaction between selected variables.We tested for interactions between CPRD predictor variables for risk factors. Interactions were tested between age and gender; BMI and smoking status; BMI and economic activity; economic activity and education; age and education; age and socioeconomic status; age and smoking status; age and economic status; age and BMI.Internal validationWe fitted a range of multivariate logistic regression models for in order to obtain the best performing. We included one additional variable at a time to observe the effects. In order to obtain the most parsimonious models we then applied stepwise backward and forward variable selection using the stepwise command in Stata. Finally, we internally validated the models by generating receiver operating characteristic (ROC) curves, by using the predict regression post-estimation command to generate for each CPRD patient the probability of having HF using the derived odds ratios (ORs), and by using these probabilities to examine sensitivity and specificity. The variables included in the final model are also determined by the availability of local data to match with the model variables. Hence variable selection has to be a compromise between the best model which can be produced from CPRD data and the local variable available.All statistical analysis was carried out in StataSE14.Local prevalence estimates Derived ORs (or regression coefficients) are used to estimate prevalence in small population subgroups. Local population breakdowns for each risk factor are used, where these are available. ICL has a wide range of small population risk factor prevalence breakdowns, including age, sex, deprivation, smoking, ethnicity, cardiovascular diseases and other disease conditions. The local model uses locally available data. The “local” model includes only those variables that are available at local population level i.e. age, sex, socioeconomic status, BMI, smoking status, depression and other disease conditions. The steps in applying the prevalence estimates are as follows and in the equations below:?Use the regression coefficients to generate log odds (since they are from a logistic regression model) for each risk factor subcategory?Generate a similar table of odds by exponentiation?Generate a similar table of prevalence in each risk factor subcategory using the epidemiologic formula?Produce a matching table of small population subcategories. If there are no corresponding local data with a sufficiently granular breakdown e.g. ethnicity by age by sex, this requires deciding how each risk factor should be attributed across other risk factor categories, with evenly as the default. For example, we used the national age/sex/ethnicity breakdown from the Census and age/smoking breakdowns from the HSfE to attribute this data at small population levels. The actual breakdown will be somewhat different and needs to be borne in mind as another source of potential error.?Multiply the population cells by the corresponding prevalence to estimate the number of people in each cell with the diseaseIn mathematical notation:Predicted log odds of prevalence = b0 + b1x1i + b2x2 i + b3x3 i + b4x4 Iwhere b0 = regression constant, b1, b2, b3, b4= other regression coefficientsx 1 i, x2 i, x3 i, x4 i = value of risk factors for individual i(NB since all the variables are binary variables, x =1 if specified risk factor is present, x=0 if it is absent). Predicted log odds of prevalence for a community of n individuals is derived by averaging over the values for all individuals included in the community:Predicted log odds of prevalence in community of n individuals:= 1/n ∑i=1n (b0 + b1x1i + b2x2 i + b3x3 i + b4x4 i)= b0 + b1p1 + b2p2 + b3p3 + b4pp4where p1 , p2, p3, p4=proportion of individuals in the community with characteristic x1 , x2 , x3 , x4 . (i.e. proportion with x.=1 rather than x.=0 as in the remainder).The predicted prevalence for an individual is derived from their predictive log odds using:prevalence = exp(log odds)/[1+exp(log odds)]= exp(b0 + b1x1i + b2x2 i + b3x3 i + b4x4 i)/[1+ exp(b0 + b1x1i + b2x2 i + b3x3 i + b4x4 i)]Predicted prevalence in community of n individuals:= 1/n ∑i=1n{exp(b0 +b1x1i +b2x2 i +b3x3 i +b4x4 i)/[1+ exp(b0 +b1x1i +b2x2 i +b3x3 i +b4x4 i)]}Unfortunately, the equation above does not simplify to a linear combination of the predictor variables (in the way the mean log odds does). The average/overall prevalence is not the same as the prevalence for a person with “average” risk factors. So, for instance, it cannot be found by taking exp(log odds)/[1+ exp(log odds)] of the average log odds. There is no linear relationship with the regression coefficients, and with proportions of population with specified risk factors.In order to find a synthetic estimate of prevalence, ideally we need to know the joint distributions of the included risk factors in the relevant population (the population on which are synthetic estimates are required). Ideally, we would know how many people in the population have each specific combination of risk factors. In practice, it might be good enough to know the distribution of some risk factors individually, rather than in combination. For instance, we might know what proportion of the population are smokers, and what proportion are ex-smokers, but not how many smokers we have by age and sex. In this situation, we have assumed that the same proportion of all ages and both genders are smokers and ex-smokers. Even if this is not exactly correct, then the synthetic estimate of prevalence may still be a reasonably accurate estimate (assuming that the smoking distribution does not vary too much by age, sex and other included risk factors). This is considered a good enough approach, and the best possible based on the information currently available in many cases.We have developed two methods for producing small population estimates and associated CIs in Stata software. One uses a bootstrapping method to produce repeated samples (Method 1), the other (Method 2) uses inverse probability weights. Both methods produce CIs for the estimates, which are derived from the variance in the logistic model, not the local populations. It would have been useful to compare the results of both methods, but because of the short timeframe for this project we only used Method 2: Logistic regression and inverse probability weights.Method 1: bootstrapping procedure to produce repeated samplesThe detailed methods of the Stata code we developed and used is included in Annex 1: synthetic estimation using Stata. In summary, within Stata, a new set of variables is created, one for each combination of these risk factors pertinent to the logistic regression model for the chosen disease. With our dataset set up in this way, we can now use Stata’s “predict” command to give us the predicted log odds. Then we find the weighted average of these, averaged across all possible combinations of risk factors, using the weights calculated as above (stored in variable named xyz). The weighted average can be found using the “collapse” command as follows, which results in one line of data per practice or MLSOA (using the population identifier as the by variable) in Stata.We calculated in Stata CIs for prevalence estimates using a “bootstrap” procedure. There is uncertainty in these synthetic estimates of prevalence based on the imprecision not in the more usual sample of people from the population (since the estimates are not a sample but are externally applied), but in the estimated coefficients from the logistic regression equations. A bootstrap procedure can be used to construct confidence intervals on these synthetic estimates of prevalence, based on the imprecision in these logistic regression coefficients.The philosophy underlying the bootstrap procedure is to consider that the people included in the data set used to derive the logistic regression equation represent the whole population of possible people. However, the whole population is effectively considered to contain thousands of copies of each of these people. Bootstrap samples are taken randomly from our initial populations (the subsets of the CPRD population that has complete data on appropriate risk factors). Logistic regression of the same risk factors can then be applied to this boot strap sample, i.e. we rerun the logistic regression that gave us our chosen predictive model. However, we get slightly different regression coefficients, because of the modified sample. Prevalence estimates are then derived for each combination of risk factors, based on these new regression equations.This process is repeated 1,000 times, to find 1,000 different boot strap samples, by random sampling processes, and to then fit logistic regression equations on each. The prevalence estimates are calculated for each combination of risk factors, for each of these 1,000 boot strap samples. For each small population, a synthetic estimate is calculated for each boot strap sample, by appropriately weighting the prevalence estimates on each combination of risk factors (with the same weights as described above which reflect the anticipated prevalence of each combination of risk factors in the population). From these 1,000 synthetic estimates of prevalence of each population, a 95% confidence interval is calculated as the 2.5th to 97.5th centiles. Given that the estimates are distributed normally, these are taken to be mean +/- 1.96 SD (taking mean and SD of the 1,000 boot strap synthetic prevalence estimates for each specified region).Method 2: Logistic regression and inverse probability weightsInverse probability weighting methods are used to standardise from a sampled population to a target population. They are usually defined as a function of a panel of one or more sampling-probability predictor variables. For each combination of the predictor variables, the sampling probability weight is the ratio of the frequency of that combination in the target population to the frequency of that combination in the sampled population. Inverse probability weighting is therefore a generalization of direct standardization. In Stata, it is implemented by using a pweight qualifier on an estimation command. This normally implies the use of a Huber variance formula to generate the confidence limits.In a population case-control study, our sampled population is an exhaustive list of disease cases, plus a random sample of controls without the disease, with a known sampling fraction. The sampling probability weights are inversely proportional to the sampling fraction for each sub-population. For cases, the sampling probability weight is 1. And, for controls, the sampling probability weight is the reciprocal of the sampling fraction. (So, if the sampling fraction is 1/8, then controls are weighted upwards by a factor of 8.) These sampling-probability weights are used in logistic regression models. Predicted disease probabilities from these models will then be unbiased, if the model is correctly specified.Similarly to Method 1 we estimated population parameters for logistic regression models. The risk factors in the model fell into two classes, namely always-present risk factors and sometimes-missing risk factors. The always-present risk factors were gender (Male or Female), age group (18-44, 45-64, 65-74 and 75+), ethnicity (White, Mixed, Black, Asian or Other, imputed to White if not known). The sometimes-missing risk factors were practice index of multiple deprivation (IMD) quintile (1, 2, 3, 4 or 5), smoking status (Non-smoker, Ex-smoker or Smoker), alcohol units per week category (None, (0,14], (14,42] or >42), and body mass index in kilos/square metre (BMI) category ((0, 18.5], (18.5,25], (25,30] or >30).We fitted the logistic regression model, using Huber variances and sampling-probability weights. The parameters were a baseline odds for each of the 2x4=8 combinations of gender and age group, an odds ratio for each ethnicity except White, an odds ratio for each IMD quintile except the first, an odds ratio for each smoking status except Non-smoker, an odds ratio for each alcohol consumption category except Zero units, and an odds ratio for each BMI category except (18.5,25] kilos per square metre. The sampling-probability weights used were equal to the products of two sets of component sampling-probability weights. The first set of component weights standardised by case status from the case-control study sample to the denominator population from which the cases and controls were sampled, and were equal to 1 for HF cases (assumed to be sampled exhaustively from the cases in the CPRD denominator population), and equal in the controls to the reciprocal of the sampling fraction of the controls as a fraction of the non-cases in the CPRD denominator population (equal to 27.211693).We also use inverse probability weights to correct for missing values as an easy-to-use alternative to multiple imputation. We then define the inverse probability weights using a completeness-propensity score. We have a panel of variables V1…VK that are always present (such as age and gender), and a panel of variables U1…UJ that are sometimes missing. Let C (for completeness) be the binary indicator variable indicating that all the variables U1…UJ are present. We then use a logistic regression model, regressing C with respect to the always-complete variables V1…VK. The completeness-propensity score is defined as the predicted completeness probability for each individual, under that regression model. The inverse-probability weight, for each individual with a complete set of data U1…UJ, is then the reciprocal of that individual’s completeness-propensity score. Therefore, individuals with a high probability of having complete data (like elderly females) are weighted downwards. And individuals with a low probability of completeness (like young males) are weighted upwards. These inverse-probability weights can then be used in further regression models, such as a logistic regression model to predict disease.Therefore, the second set of component weights were computed to standardise the sample of cases and controls with all risk factors present to the total sample of cases and controls by gender, age group and ethnicity, and were derived as inverse probabilities of presence of the full set of risk factors (completeness) from a logistic regression model with completeness as the outcome, fitted to the cases and controls, using the first set of sampling-probability weights to standardise by case status, and whose parameters were a baseline odds for each of the 8 combinations of gender and age group and an odds ratio for each non-white ethnic category. The product weights therefore were computed to standardise the odds and odds ratios from the sample of cases and controls with all risk factors present (272,369 subjects out of a total of 101,870 cases and 440,293 sampled controls) to the total denominator population of subjects aged at or above 18 years, with or without HF, on their birthdays in 2015 (13,864,783 subjects). We also fitted logistic regression models of HF status with respect to the 8 combinations of gender and age only, using only the first set of sampling probability weights to standardise by HF status, in order to estimate odds (and thereby prevalence) of HF for each combination of gender and age group in the CPRD population at large.Having estimated the regression model parameters, we used these for out-of-sample prediction of HF prevalence, using the margprev add-on Stata package PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5OZXdzb248L0F1dGhvcj48WWVhcj4yMDEzPC9ZZWFyPjxS

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ADDIN EN.CITE.DATA [58 ,59]. These predicted prevalence estimates were for the sub-populations of patients for 7,692 practices, for 204 clinical care groups (CCGs), and for 6,755 MSOAs, for which information was available on the marginal frequencies of the seven risk factors in the model. We computed estimated prevalence assuming that, within each sub-population, the seven risk factors were mutually statistically independent, implying that we could give each possible combination of the seven risk factors a sampling-probability weight proportional to the product of the proportions of subjects with each of the appropriate risk-factor values. Therefore, for each subpopulation, we had 2x4x5x5x3x4x4=9600 combinations of risk factor values, with proportions of subjects calculated assuming statistical independence, and estimated the expected subpopulation prevalence of HF accordingly. The assumption of statistical independence of risk factors is probably not literally true, but might be expected to give prevalence estimates that are not vastly in error if the effects of the risk factors are not too non-additive. We have not internally or externally validated this method yet.We have used method 2, logistic regression and inverse probability weights for other models because of the large number of variables in most of the models. This required us to produce Stata datasets of local risk factor data which have one observation for every permutation of all the risk factors for every practice, which generated very large files (up to 60 GB). We were able to process these using Stata/MP, the fastest and largest version of Stata. On dual-core chips, Stata/MP runs 40% faster overall and 72% faster on time-consuming estimation commands. It can handle a maximum number of 32,767 variables and 20 billion observations. Some of the datasets we used included over one billion observations.Processing was carried out on a multicore server. It would not have been possible to run the bootstrapping procedure to produce repeated samples which requires fitting a logistic model 1,000 times for each practice.In order to find the estimated prevalence for each population, it is necessary to calculate the synthetic prevalence of risk factors for each possible combination of risk factor (as included in the chosen disease-specific logistic regression model). The estimated prevalence for a population is then the weighted average of the prevalence estimates for each combination of risk factors, according to the estimated number of people with each risk factor combination in the population (the population on which synthetic estimates are sought).These calculations can be carried out in Excel (using VBA code to link prevalence and risk factor spreadsheets with formulae in a workbook) or in Stata software to produce confidence intervals as well as the estimates. We used both methods as a means of validating the synthetic estimation step. The detailed methods of the Stata code we developed and used is included in Annex 1: synthetic estimation using Stata. In summary, within Stata, a new set of variables is created, one for each combination of these risk factors pertinent to the logistic regression model for the chosen disease. With our dataset set up in this way, we can now use Stata’s “predict” command to give us the predicted log odds. Then we find the weighted average of these, averaged across all possible combinations of risk factors, using the weights calculated as above (stored in variable named xyz). The weighted average can be found using the “collapse” command as follows, which results in one line of data per practice or MLSOA (using the population identifier as the by variable) in Stata.Validation of local estimatesInternal validationIn addition to the internal and external validation of the regression models, local estimates can also be validated by aggregating them to the lowest geography available in the raw data and comparing them, a form of internal validation. We have over time increased the number of variables used in the local models as more local data has become available. However as more variables are added we need to take account of the joint effects of multiple risk factors, i.e. it assumes they operate independently. Estimation of the joint effects of multiple risk factors is complex for several reasons. In particular, some of the effects of more distal risk factors are mediated through intermediate factors. We have acknowledged this by creating specific joint distributions for variables where this is known e.g. age and educational level, as older age groups are less likely to have tertiary education.External validationThere are Quality & Outcomes Framework (QOF) disease registers ADDIN EN.CITE <EndNote><Cite><Author>NHS Employers</Author><Year>2013</Year><RecNum>665</RecNum><DisplayText>[60]</DisplayText><record><rec-number>665</rec-number><foreign-keys><key app="EN" db-id="9s9dpv5rcvasxned5zb5tsfrawwe9d9z9ere" timestamp="1467558524">665</key></foreign-keys><ref-type name="Government Document">46</ref-type><contributors><authors><author>NHS Employers,</author></authors><secondary-authors><author>Health</author></secondary-authors></contributors><titles><title>Quality and Outcomes Framework guidance for GMS contract 2013/14</title></titles><dates><year>2013</year></dates><pub-location>Online</pub-location><publisher>NHS Employers</publisher><urls><related-urls><url>;[60] for all the prevalence models we produced for PHE. We have experience in comparing QOF-registered prevalence and estimated prevalence right down to practice level using spatial analyses. ADDIN EN.CITE <EndNote><Cite><Author>Soljak</Author><Year>2011</Year><RecNum>45</RecNum><DisplayText>[61]</DisplayText><record><rec-number>45</rec-number><foreign-keys><key app="EN" db-id="2d9sfv0rhp02eteepzbv9vp4zezt00xrfxrp" timestamp="1301924619">45</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Soljak, Michael</author><author>Samarasundera, Edgar</author><author>Indulkar, Tejal</author><author>Walford, Hannah</author><author>Majeed, Azeem</author></authors></contributors><titles><title>Variations in cardiovascular disease under-diagnosis in England: national cross-sectional spatial analysis</title><secondary-title>BMC Cardiovascular Disorders</secondary-title></titles><periodical><full-title>BMC Cardiovascular Disorders</full-title></periodical><pages>12</pages><volume>11</volume><number>1</number><dates><year>2011</year></dates><isbn>1471-2261</isbn><accession-num>doi:10.1186/1471-2261-11-12</accession-num><urls><related-urls><url>;[61] Local estimates can also be validated against the corresponding QOF register for each geography using Bland-Altman plots. This method uses graphical methods to investigate the assumptions of the method and also gives confidence intervals. ADDIN EN.CITE <EndNote><Cite><Author>Bland</Author><Year>1999</Year><RecNum>666</RecNum><DisplayText>[62]</DisplayText><record><rec-number>666</rec-number><foreign-keys><key app="EN" db-id="9s9dpv5rcvasxned5zb5tsfrawwe9d9z9ere" timestamp="1467559305">666</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Bland, J Martin</author><author>Altman, Douglas G</author></authors></contributors><titles><title>Measuring agreement in method comparison studies</title><secondary-title>Statistical Methods in Medical Research</secondary-title></titles><periodical><full-title>Statistical Methods in Medical Research</full-title></periodical><pages>135-160</pages><volume>8</volume><number>2</number><dates><year>1999</year><pub-dates><date>April 1, 1999</date></pub-dates></dates><urls><related-urls><url>;[62] It aims to quantify the agreement between and clinical importance of two methods of clinical measurement using the differences between observations made using the two methods on the same subjects. The 95% limits of agreement, estimated by mean difference 1.96 standard deviation of the differences, provide an interval within which 95% of differences between measurements by the two methods are expected to lie. The second method is based on errors-in-variables regression in a classical (X,Y) plot and focuses on confidence intervals, whereby two methods are considered equivalent when providing similar measures notwithstanding the random measurement errors. ADDIN EN.CITE <EndNote><Cite><Author>Ludbrook</Author><Year>2010</Year><RecNum>667</RecNum><DisplayText>[63]</DisplayText><record><rec-number>667</rec-number><foreign-keys><key app="EN" db-id="9s9dpv5rcvasxned5zb5tsfrawwe9d9z9ere" timestamp="1467559519">667</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Ludbrook, John</author></authors></contributors><titles><title>Linear regression analysis for comparing two measurers or methods of measurement: But which regression?</title><secondary-title>Clinical and Experimental Pharmacology and Physiology</secondary-title></titles><periodical><full-title>Clinical and Experimental Pharmacology and Physiology</full-title></periodical><pages>692-699</pages><volume>37</volume><number>7</number><keywords><keyword>Altman–Bland</keyword><keyword>bias</keyword><keyword>calibration</keyword><keyword>confidence interval</keyword><keyword>loss function</keyword><keyword>non-parametric methods</keyword><keyword>outlying values</keyword></keywords><dates><year>2010</year></dates><publisher>Blackwell Publishing Ltd</publisher><isbn>1440-1681</isbn><urls><related-urls><url>;[63] A recent update reconciles these two methodologies and shows their similarities and differences using both real data and simulations. ADDIN EN.CITE <EndNote><Cite><Author>Francq</Author><Year>2016</Year><RecNum>669</RecNum><DisplayText>[64]</DisplayText><record><rec-number>669</rec-number><foreign-keys><key app="EN" db-id="9s9dpv5rcvasxned5zb5tsfrawwe9d9z9ere" timestamp="1467560344">669</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Francq, Bernard G.</author><author>Govaerts, Bernadette</author></authors></contributors><titles><title>How to regress and predict in a Bland–Altman plot? Review and contribution based on tolerance intervals and correlated-errors-in-variables models</title><secondary-title>Statistics in Medicine</secondary-title></titles><periodical><full-title>Statistics in Medicine</full-title></periodical><pages>2328-2358</pages><volume>35</volume><number>14</number><keywords><keyword>Bland–Altman</keyword><keyword>agreement</keyword><keyword>prediction</keyword><keyword>tolerance interval</keyword><keyword>method comparison studies</keyword><keyword>correlated-errors-in-variables regressions</keyword><keyword>bivariate least square</keyword></keywords><dates><year>2016</year></dates><isbn>1097-0258</isbn><urls><related-urls><url>;[64]The flowchart in REF _Ref474151038 \h Figure 2 shows the four methods we used to identify HF diagnoses and likely/probable HF diagnoses based on clinical and prescribing data. Figure 4: Flow chart for analysis of HF prevalence (Final Numbers)23945850Medcode extraction of records from CPRD database(N=507,429,744)Medcode extraction of records from CPRD database(N=507,429,744)3074670513715Number of patients(N=224,265)Number of patients(N=224,265)372300587820507687310521335Number of patients(N=1,794,085)Number of patients(N=1,794,085)71100950Prodcode extraction of records from CPRD database(N=977,922,246)Prodcode extraction of records from CPRD database(N=977,922,246)8416290370205841629088582505372100114617545440601834515034956751459865Keep cases who have not had echocardiogram(N=162,731)00Keep cases who have not had echocardiogram(N=162,731)58420508000Linked HES data (N=78,565)Linked HES data (N=78,565)355601375410Extract ICD-10 codes relevant to the diagnosis of HFExtract ICD-10 codes relevant to the diagnosis of HF62007752812415Exclude HF cases with HES or CPRD diagnosis (N=8,251)00Exclude HF cases with HES or CPRD diagnosis (N=8,251)61626751669415Keep abnormal echocardiogram cases(N=8,251)00Keep abnormal echocardiogram cases(N=8,251)8428990965835right1164590drugs algorithm – keep cases fulfilling criteria00drugs algorithm – keep cases fulfilling criteria7595870717550Develop the Drugs algorithmDevelop the Drugs algorithm73196451412875History of myocardial infarction, orthopnoea, paroxysmal nocturnal dyspnoeaORSigns of elevated JVP, displaced apex beatORAbnormal ECGHistory of myocardial infarction, orthopnoea, paroxysmal nocturnal dyspnoeaORSigns of elevated JVP, displaced apex beatORAbnormal ECG81959452327275ANDAND73196452549525Patients prescribed ACEi/Angiotensin II receptor antagonists/Beta-blocker/potassium sparing diuretics in CPRD?Patients prescribed ACEi/Angiotensin II receptor antagonists/Beta-blocker/potassium sparing diuretics in CPRD?72675753364865Exclude Hypertension and CHD cases (N=165,329)0Exclude Hypertension and CHD cases (N=165,329)847725031553158477250363156572675753841115Drugs algorithm probable HF cases (N=44,209)0Drugs algorithm probable HF cases (N=44,209)847725041078158477250472059073552054322445Exclude HF cases with HES or CPRD or clinical algorithm diagnosis (N=11,363)Exclude HF cases with HES or CPRD or clinical algorithm diagnosis (N=11,363)74218804940935Additional drugs algorithm probable HF cases (N=32,846)Additional drugs algorithm probable HF cases (N=32,846)8475980530669521126452439035Identify doctor diagnosed CPRD HF cases(N=244,235)Identify doctor diagnosed CPRD HF cases(N=244,235)2609850315150520948653420110Exclude HF cases who have a HES diagnosis(N=62,595)Exclude HF cases who have a HES diagnosis(N=62,595)2604770411480020758154362450Additional CPRD diagnosed HF cases(N=181,640)Additional CPRD diagnosed HF cases(N=181,640)66675005035550066865501288415066865502307590066770253612515062388754107815Additional abnormal echocardiogram probable HF cases (N=0)00Additional abnormal echocardiogram probable HF cases (N=0)31718255060315Additional clinical algorithm probable HF cases (N=0)0Additional clinical algorithm probable HF cases (N=0)31813504641215Exclude HF cases with HES or CPRD diagnosis (N=10,249)00Exclude HF cases with HES or CPRD diagnosis (N=10,249)4645025531558502619375671830021850351358900Extract medcodes relevant to the diagnosis of HFExtract medcodes relevant to the diagnosis of HF259969050107852614295219456011188703641725Identify doctor diagnosed HES AND CPRD HF cases(N=62,595)Identify doctor diagnosed HES AND CPRD HF cases(N=62,595)949960277558501518285278638015227304738370203202426335Identify doctor diagnosed HES HF cases(N=76,692)Identify doctor diagnosed HES HF cases(N=76,692)03361055Exclude HF cases who have a CPRD HF diagnosis(N=62,595)Exclude HF cases who have a CPRD HF diagnosis(N=62,595)04408170Additional HES diagnosed HF cases(N=14,097)Additional HES diagnosed HF cases(N=14,097)4533905052060467995415734550609531038805060952178050506095107124537230052667033813754212590Clinical algorithm probable HF cases (N=10,249)00Clinical algorithm probable HF cases (N=10,249)34639252317750History of myocardial infarction, orthopnoea, paroxysmal nocturnal dyspnoeaORSigns of elevated JVP, displaced apex beatORAbnormal ECGHistory of myocardial infarction, orthopnoea, paroxysmal nocturnal dyspnoeaORSigns of elevated JVP, displaced apex beatORAbnormal ECG43230803227705ANDAND37839653443605NT-proBNP ≥125 pg/mLOr BNP ≥35 pg/mLNT-proBNP ≥125 pg/mLOr BNP ≥35 pg/mL33623252012316clinical algorithm – keep cases fulfilling criteria00clinical algorithm – keep cases fulfilling criteria46545504038600465899544704004662170490156505531485Probable HF cases (N=291,178)Probable HF cases (N=291,178)454088512769854543425128905000548195565786004615815885825Develop the Clinical algorithmDevelop the Clinical algorithm260921565976500ResultsHF prevalence from CPRDBaseline characteristics of CPRD respondents REF _Ref473650383 \h Table 7 compares the baseline characteristics of HF cases and controls. Cases are older than the control sample, and, partly because of this, more likely to have co-morbidities.Table 7. Characteristics of CPRD respondentsControlsHF casesTotalTotal numbers1,045,427288,3051,333,732Age group16-44458,019 (43.81%)3,388 (1.18%)461,407 (34.60%)45-64332,545 (31.81%)33,446 (11.60%)365,991 (27.44%)65-74110,040 (10.53%)53,656 (18.61%)163,696 (12.27%)Over 75144,823 (13.85%)197,815 (68.61%)342,638 (25.69%)Gender Male 476,605 (45.59%)145,533 (50.48%)622,138 (46.65%)Female 568,822 (54.41%)142,772 (49.52%)711,594 (53.35%)EthnicityWhite897,344(85.84%)253,016(87.76%)1,150,360(86.25%)Black 13,380(1.28%)1,417(0.49%)14,797(1.11%)Asian25,561(2.45%)2,807(0.97%)28,368(2.13%)Mixed 102,945(9.85%)30,502(10.58%)133,447(10.01%)Other 6,197(0.59%)563(0.20%)6,760(0.51%)BMI<18.4 underweight51,347 (6.32%)8,766 (3.92%)60,113 (5.80%)18.5 – 24 normal371,472 (45.69%)71,774 (32.12%)443,246 (42.77%)25 – 29 overweight240,715 (29.61%)75,084 (33.60%)315,799 (30.47%)>30 obese 149,472 (18.39%)67,823 (30.35%)217,295 (20.97%)SmokingNon- smoker522,810 (56.38%)131,413 (48.47%)654,223 (54.59%)Ex-smoker162,203 (17.49%)101,177 (37.32%)263,380 (21.98%)Current smoker242,333 (48.47%)38,519 (14.21%)280,852 (23.43%)CHD (excluding MI)No 1,018,062 (97.38%)220,296 (76.41%)1,238,358 (92.85%)Yes27,365 (2.62%)68,009 (23.59%)95,374 (7.15%)HypertensionNo 901,794 (86.26%)141,983 (49.25%)1,043,777 (78.26%)Yes143,633 (13.74%)146,322 (50.75%)289,955 (21.74%)DiabetesNo929,129 (88.88%)215,593 (74.78%)1,144,722 (85.83%)Type 1 or Type II116,298 (11.12%)72,712 (25.22%)189,010 (14.17%)Atrial FibrillationNo 1,027,363 (98.27%)209,999 (72.84%)1,237,361 (92.77%)Yes18,064 (1.73%)78,306 (27.16%)96,370 (7.23%)Alcohol Intake (Units/Week)Non-drinker99,349 (14.90%)44,842 (20.27%)144,191 (16.23%)(0, 14]387,247 (58.06%)121,448 (54.91%)508,695 (57.27%)(14, 42]156,602 (23.48%)48,199 (21.79%)204,801 (23.06%)>4223,791 (3.57%)6,687 (3.02%)30,478 (3.43%)Missing values REF _Ref473650812 \h Table 8 shows the number and percentage of missing values in total and stratified per year. The biggest percentage of missing values was found in the variable self-reported physical activity, where recording in primary care is still low, followed by BMI. With these two exceptions, all other variables missed less than 1.5% of their observations. Missing values from the variable origin where recoded to be considered within the category “white”, while physical activity and smoking status were finally excluded from both models. The remaining missing values where inferred for analysis using multiple imputation.Table SEQ Table \* ARABIC 8: Missing values in the final population.Risk or Protective factor 2014Frequency%*BMI 297,27922.29%Smoking135,27710.14%Alcohol Consumption Status 445,56733.41%CPRD prevalence and incidencePrevalence and incidence of HF in the CPRD data were calculated for doctor-diagnosed and for algorithm-diagnosed HF (or high risk of HF, not shown here) using the two diagnostic and two algorithm-based methods. Prevalence was inferred from cumulative incidence, with HF cases removed only at death.The prevalence of HF for the years 1959-2015 is shown in REF _Ref444448049 \h Table 9. The prevalence of HF is estimated at around 0.74% for doctor-diagnosed HF, rising if algorithm cases are included. The incidence of HF for the years 2000-2015 is also shown in REF _Ref444448049 \h Table 9. Table 9. Prevalence and incidence of doctor-diagnosed HF in the CPRD data: 1959-2015.YearPrevalence of doctor diagnosed HF (cases per million)Incidence of doctor diagnosed HF (cases per million)195943.032.10196045.894.35196149.154.82196250.943.69196354.325.29196457.985.62196567.1511.33196672.457.53196778.678.39196886.3910.041969100.2916.361970123.7326.441971137.6017.711972156.4123.041973183.1731.651974215.1537.471975243.7235.041976276.6740.971977316.6949.241978365.7959.401979420.8767.561980507.80102.031981576.5486.781982675.47119.051983777.14124.781984897.06145.9619851065.64198.4819861258.59228.7919871475.51260.1419881830.44411.1419892362.92644.3419903127.21988.4719913781.121014.0619924254.40919.5119934726.09963.5219945241.431033.6319955595.01926.0419965936.69908.9219976175.78863.1219986396.61885.2219996627.69892.0720006864.90925.6320017091.87910.3420027251.80878.0220037346.56809.4120047378.48726.3120057343.19639.7420067272.31561.7420077194.47524.0020087154.91520.9920097175.63523.4020107210.58512.2420117258.00498.2520127305.28495.7420137358.98460.4620147409.44417.3520157444.42353.95 REF _Ref444490779 \h Table 10 shows the prevalence rates of doctor-diagnosed HF 2000-2015 in males by age at diagnosis, and REF _Ref474229357 \h Table 11 shows the corresponding data for females. The prevalence and incidence rates of algorithm cases (not shown here) as a percentage of doctor diagnosed cases decreases with increasing age. This could be consistent with the algorithm- diagnosed cases being an at-risk or undiagnosed group who are later confirmed as having HF.Table 10: prevalence rates of doctor-diagnosed HF 2000-2015 in males by age at diagnosisYear16-4445-6465-7475+All ages2000694.55068.58775.518200.032738.52001740.05266.09015.519618.534640.02002801.55468.59314.020709.036293.02003850.55700.09416.021701.537668.02004924.05943.59532.022430.538830.02005991.56063.09421.523120.039596.020061040.56170.59366.523660.540238.020071088.06266.09251.524116.040721.520081129.06358.59186.524713.041387.020091155.06374.09162.525631.542323.020101177.06474.09223.026442.543316.520111193.06542.09296.527310.044341.520121216.56563.59362.528231.545374.020131226.06509.59417.529299.546452.520141200.06459.09427.530263.047349.520151173.56375.59371.531300.048220.5Table 11: prevalence rates of doctor-diagnosed HF 2000-2015 in females by age at diagnosisYear16-4445-6465-7475+All ages2000674.02584.56917.53265242828.02001709.52633.06857.534458.044658.02002735.52634.56839.035801.546010.52003759.52651.06674.536826.046911.02004810.02665.06405.537426.047306.52005821.52600.56078.537783.047283.52006842.02639.05765.037675.046921.02007857.02619.55513.037584.046573.52008868.02608.05321.537627.046424.52009898.02620.05158.038017.046693.02010919.02662.55005.038447.547034.02011930.02706.54881.538956.047474.02012932.02752.04799.039379.047862.02013919.52742.04749.039862.048272.52014903.52743.54656.540535.548839.02015901.02727.04561.541179.049368.5 REF _Ref474229574 \h Table 12 shows the incidence rates of doctor-diagnosed HF between 2000-2015 in males by age at diagnosis, and REF _Ref444490804 \h Table 13 shows the corresponding data for females. Incidence rates have halved and we have also shown a decrease in HF admission rates over this period. ADDIN EN.CITE <EndNote><Cite><Author>Brettell</Author><Year>2013</Year><RecNum>229</RecNum><DisplayText>[65]</DisplayText><record><rec-number>229</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1374483281">229</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Brettell, Rachel</author><author>Soljak, Michael</author><author>Cecil, Elizabeth</author><author>Cowie, Martin R.</author><author>Tuppin, Philippe</author><author>Majeed, Azeem</author></authors></contributors><titles><title>Reducing heart failure admission rates in England 2004–2011 are not related to changes in primary care quality: national observational study</title><secondary-title>European Journal of Heart Failure</secondary-title></titles><periodical><full-title>European Journal of Heart Failure</full-title></periodical><dates><year>2013</year><pub-dates><date>July 11, 2013</date></pub-dates></dates><urls><related-urls><url>;[65] Some of this decrease may have been driven by decreases in CHD incidence. Most published national studies of trends in CHD incidence are from Scandinavian registry data. Mannsverk et al showed a steady downwards trend in CHD incidence in Sweden over time in both males and females from 1994 to 2010. ADDIN EN.CITE <EndNote><Cite><Author>Mannsverk</Author><Year>2015</Year><RecNum>348</RecNum><DisplayText>[66]</DisplayText><record><rec-number>348</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1486421106">348</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Mannsverk, Jan</author><author>Wilsgaard, Tom</author><author>Mathiesen, Ellisiv B.</author><author>L?chen, Maja-Lisa</author><author>Rasmussen, Knut</author><author>Thelle, Dag S.</author><author>Nj?lstad, Inger</author><author>Hopstock, Laila Arnesdatter</author><author>B?naa, Kaare Harald</author></authors></contributors><titles><title>Trends in Modifiable Risk Factors are Associated With Declining Incidence of Hospitalized and Non-Hospitalized Acute Coronary Heart Disease in a Population</title><secondary-title>Circulation</secondary-title></titles><periodical><full-title>Circulation</full-title></periodical><dates><year>2015</year></dates><urls></urls><electronic-resource-num>10.1161/circulationaha.115.016960</electronic-resource-num></record></Cite></EndNote>[66] The age-and sex-adjusted incidence of total coronary heart disease decreased by 3% (95% CI 2.0% to 4.0%, P<0.001) each year. This decline was driven by decreases in out-hospital sudden death and hospitalized ST-elevation myocardial infarction. In Denmark, age-standardised incidence rates declined significantly from 2000 to 2009 for both sexes (females 445 to 340/100,000, males 822 to 678/100,000), reflecting a reduction in the annual number of new cases from 19.345 to 16.757. ADDIN EN.CITE <EndNote><Cite><Author>Koch</Author><Year>2013</Year><RecNum>349</RecNum><DisplayText>[67]</DisplayText><record><rec-number>349</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1486455731">349</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Koch, Mette B.</author><author>Davidsen, Michael</author><author>Andersen, Lisbeth V.</author><author>Juel, Knud</author><author>Jensen, Gorm B.</author></authors></contributors><titles><title>Increasing prevalence despite decreasing incidence of ischaemic heart disease and myocardial infarction. A national register based perspective in Denmark, 1980–2009</title><secondary-title>European Journal of Preventive Cardiology</secondary-title></titles><periodical><full-title>European Journal of Preventive Cardiology</full-title></periodical><pages>189-195</pages><volume>22</volume><number>2</number><dates><year>2013</year><pub-dates><date>2015/02/01</date></pub-dates></dates><publisher>SAGE Publications</publisher><isbn>2047-4873</isbn><urls><related-urls><url>;[67]Table 12: incidence rates of doctor-diagnosed HF 2000-2015 in males by age at diagnosisYear16-4445-6465-7475+All ages200071.5940.51447.023844843.0200184.5954.01398.02456.54893.02002107954.51426.523904878.02003117.0982.512522277.04628.52004127.5991.51335.52037.54492.02005125.5912.51057.51906.04001.52006108.5848.510051631.53593.52007119.0824.5944.51552.03440.02008110.0825.09491631.03515.02009107.5783.58831754.03528.02010116.5831.0950.51651.53549.52011105.5790.5906.51659.53462.02012103.5822.5868.51708.53503.02013100.5734.0850.51689.03374.0201479.0623.0771.51512.52986.0201575.5564.5650.51278.52569.0Table 13. incidence rates of doctor-diagnosed HF 2000-2015 in females by age at diagnosis16-4445-6465-7475+All ages200032.0439.01117.03758.05346.0200157.5457.51083.53687.55286.0200245.0419.51037.03585.55087.0200345.0419.5898.53327.04690.0200478.0400.0786.52722.53987.0200539.0313.0697.02518.53567.5200656.5359.0605.52118.03139.0200757.5293.5599.51967.52918.0200851.5313.0589.51925.02879.0200973.0322.5550.52019.02965.0201066.0320.5549.51933.02869.0201159.0325.0524.51932.52841.0201259.0349.0535.01881.02824.0201345.0290.0503.51714.52553.0201442.5279.5464.51645.52432.0201553.5239.5393.01385.02071.0Logistic regression modellingTo reduce data volumes, the HF data we used for regression modelling is a case-control design, which required us to correct for sampling fraction. Missing ethnicity values were replaced by White. ADDIN EN.CITE <EndNote><Cite><Author>Hippisley-Cox</Author><Year>2015</Year><RecNum>328</RecNum><DisplayText>[18]</DisplayText><record><rec-number>328</rec-number><foreign-keys><key app="EN" db-id="0svrewrstr2fs4e5ddvvpr0o9stzf0efzwdf" timestamp="1460451158">328</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author>Hippisley-Cox, J.</author><author>Coupland, C.</author></authors></contributors><auth-address>Division of Primary Care, University Park, Nottingham, UK.</auth-address><titles><title>Development and validation of risk prediction equations to estimate future risk of heart failure in patients with diabetes: a prospective cohort study</title><secondary-title>BMJ Open</secondary-title><alt-title>BMJ open</alt-title></titles><periodical><full-title>BMJ Open</full-title></periodical><alt-periodical><full-title>BMJ Open</full-title></alt-periodical><pages>e008503</pages><volume>5</volume><number>9</number><edition>2015/09/12</edition><keywords><keyword>Epidemiology</keyword><keyword>Preventive medicine</keyword><keyword>Primary care</keyword></keywords><dates><year>2015</year></dates><accession-num>26353872</accession-num><urls><related-urls><url>;[18] Risk factors with low or minimal missingness were age, gender, ethnicity (see assumption above), CHD, diabetes, atrial fibrillation, and hypertension. The sometimes or often missing risk factors are BMI, smoking, and alcohol consumption. For these predictor variables the missing values were replaced by the inverse probability weight method.The logistic regression model was fitted by using the product weights generated from the sampling probability weights multipliers, using the inverse probability weights method. REF _Ref474267323 \h Table 14 shows the multiple logistic regression model for the combined GP +HES diagnosis HF outcome, which was then utilised for the local prevalence estimates.Table 14: multiple logistic regression model for the combined HF outcome GP+HES HF outcome plus probable casesRisk factorsORsP value95% CIsGender#AgegroupMale#16-440.0007871<0.001[0.0007 - 0.0008]Male#45-640.0071812<0.001[0.0069 - 0.0074]Male#65-740.0227965<0.001[0.0221 - 0.0235]Male#75+0.0498207<0.001[0.0485 - 0.0512]Female#16-440.0005963<0.001[0.0005 - 0.0006]Female#45-640.0050637<0.001[0.0049 - 0.0052]Female#65-740.0189998<0.001[0.0184 - 0.0196]Female#75+0.0499102<0.001[0.0487 - 0.0511]BMI<18.51.313427<0.001[1.2578 - 1.3715](18.5, 25]1.00(25, 30]1.061192<0.001[1.0422 - 1.0804]>301.63105<0.001[1.5982 - 1.6645]SmokingNon-smoker1.00Smoker0.97123790.006[0.9511 - 0.9917]Ex-smoker1.409611<0.001[1.3853 - 1.4342]Alcohol consumptionNon-drinker1.00(0, 14] units/week0.922642<0.001[0.9040 - 0.9416](14, 42] units/week0.8956903<0.001[0.8743 - 0.9175]>42 units/week1.0696780.006[1.0193 - 1.1225]EthnicityWhite1.00Black1.205105<0.001[1.0940 - 1.3274]Asian1.220812<0.001[1.1260 - 1.3235]Mixed1.185719<0.001[1.1572 - 1.2148]Other1.0375490.634[0.8915 - 1.2074]CHD01.00Case2.658932<0.001[2.5996 - 2.7196]Hypertension01.00Case1.447945<0.001[1.4242 - 1.4720]Diabetes01.00Case 1.414926<0.001[1.3883 - 1.4420]Atrial Fibrillation01.00Case5.220019<0.001[5.0962 - 5.3467]External validation – Bland Altman plotsWe externally validated the model-estimated prevalence by carrying out a disagreement analysis between model-estimated and QOF prevalence (%) of HF in practices. We estimated three principal components of disagreement (discordance as measured by Kendall's tau-a, bias as measured by median difference, and calibration as measured by the Theil-Sen median slope). Kendall's tau-a between mean prevalence and prevalence difference of heart failure at practice level is 0.254 (95% CIs (0.239 – 0.270, p<0.001), showing that prevalence means and model-QOF differences are 25.4 percent more likely to be concordant than to be discordant. REF _Ref462831026 \h Table 15 shows the percentile differences between practice-level model-estimated and QOF prevalence of heart failure. Table 15: Percentile differences between model-estimated and QOF prevalence of heart failurePercentPercentile(95% CI)0-2.3(-2.3, -2.3)250.4(0.4, 0.4)500.6(0.6, 0.6)750.9(0.9, 0.9)10015.9(5.9, 5.9)The best way to display the data is to plot the difference between the measurements by the two methods for each subject against their mean, using Bland-Altman plots. REF _Ref462831045 \h Figure 3 shows the Bland-Altman plot for the practice-level QOF and estimated prevalence for HF with higher modelled prevalence compared with QOF registered prevalence. REF _Ref472608610 \h Figure 4 is a scatter plot of practice-level model-estimated and QOF prevalence of diagnosed HF. In both cases, GP-diagnosed prevalence is lower than CPRD prevalence as defined above.Figure 3: Bland-Altman plot for practice-level model-estimated and QOF prevalence of heart failureFigure 4: Scatter plot of practice -level model-estimated and QOF prevalence of diagnosed heart failureReferences ADDIN EN.REFLIST 1. Davies M, Hobbs F, Davis R, Kenkre J, Roalfe AK, Hare R, Wosornu D, Lancashire RJ. Prevalence of left-ventricular systolic dysfunction and heart failure in the Echocardiographic Heart of England Screening study: a population based study. Lancet 2001;358(9280):439-44. Link: . Bhatnagar P, Wickramasinghe K, Williams J, Rayner M, Townsend N. 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