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        <title>Population Health Metrics - Most accessed articles</title>
        <link>http://www.pophealthmetrics.com</link>
        <description>The most accessed research articles published by Population Health Metrics</description>
        <dc:date>2012-04-24T00:00:00Z</dc:date>
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                                <rdf:li rdf:resource="http://www.pophealthmetrics.com/content/9/1/16" />
                                <rdf:li rdf:resource="http://www.pophealthmetrics.com/content/8/1/29" />
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        <item rdf:about="http://www.pophealthmetrics.com/content/9/1/16">
        <title>Falling behind: life expectancy in US counties from 2000 to 2007 in an international context</title>
        <description>Background:
The United States health care debate has focused on the nation&apos;s uniquely high rates of lack of insurance and poor health outcomes relative to other high-income countries. Large disparities in health outcomes are well-documented in the US, but the most recent assessment of county disparities in mortality is from 1999. It is critical to tracking progress of health reform legislation to have an up-to-date assessment of disparities in life expectancy across counties. US disparities can be seen more clearly in the context of how progress in each county compares to international trends.
Methods:
We use newly released mortality data by age, sex, and county for the US from 2000 to 2007 to compute life tables separately for each sex, for all races combined, for whites, and for blacks. We propose, validate, and apply novel methods to estimate recent life tables for small areas to generate up-to-date estimates. Life expectancy rates and changes in life expectancy for counties are compared to the life expectancies across nations in 2000 and 2007. We calculate the number of calendar years behind each county is in 2000 and 2007 compared to an international life expectancy time series.
Results:
Across US counties, life expectancy in 2007 ranged from 65.9 to 81.1 years for men and 73.5 to 86.0 years for women. When compared against a time series of life expectancy in the 10 nations with the lowest mortality, US counties range from being 15 calendar years ahead to over 50 calendar years behind for men and 16 calendar years ahead to over 50 calendar years behind for women. County life expectancy for black men ranges from 59.4 to 77.2 years, with counties ranging from seven to over 50 calendar years behind the international frontier; for black women, the range is 69.6 to 82.6 years, with counties ranging from eight to over 50 calendar years behind. Between 2000 and 2007, 80% (men) and 91% (women) of American counties fell in standing against this international life expectancy standard.
Conclusions:
The US has extremely large geographic and racial disparities, with some communities having life expectancies already well behind those of the best-performing nations. At the same time, relative performance for most communities continues to drop. Efforts to address these issues will need to tackle the leading preventable causes of death.</description>
        <link>http://www.pophealthmetrics.com/content/9/1/16</link>
                <dc:creator>Sandeep Kulkarni</dc:creator>
                <dc:creator>Alison Levin-Rector</dc:creator>
                <dc:creator>Majid Ezzati</dc:creator>
                <dc:creator>Christopher Murray</dc:creator>
                <dc:source>Population Health Metrics 2011, null:16</dc:source>
        <dc:date>2011-06-15T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1478-7954-9-16</dc:identifier>
                            <dc:title>US life expectancy in a global context</dc:title>
                            <dc:description>As the world&amp;apos;s healthiest nations enjoy increasingly longer life spans, people living in most of the United States &amp;#8211; especially women &amp;#8211; are falling further behind with each decade.</dc:description>
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        <item rdf:about="http://www.pophealthmetrics.com/content/8/1/29">
        <title>Projection of the year 2050 burden of diabetes in the US adult population: dynamic modeling of incidence, mortality, and prediabetes prevalence</title>
        <description>Background:
People with diabetes can suffer from diverse complications that seriously erode quality of life. Diabetes, costing the United States more than $174 billion per year in 2007, is expected to take an increasingly large financial toll in subsequent years. Accurate projections of diabetes burden are essential to policymakers planning for future health care needs and costs.
Methods:
Using data on prediabetes and diabetes prevalence in the United States, forecasted incidence, and current US Census projections of mortality and migration, the authors constructed a series of dynamic models employing systems of difference equations to project the future burden of diabetes among US adults. A three-state model partitions the US population into no diabetes, undiagnosed diabetes, and diagnosed diabetes. A four-state model divides the state of &quot;no diabetes&quot; into high-risk (prediabetes) and low-risk (normal glucose) states. A five-state model incorporates an intervention designed to prevent or delay diabetes in adults at high risk.
Results:
The authors project that annual diagnosed diabetes incidence (new cases) will increase from about 8 cases per 1,000 in 2008 to about 15 in 2050. Assuming low incidence and relatively high diabetes mortality, total diabetes prevalence (diagnosed and undiagnosed cases) is projected to increase from 14% in 2010 to 21% of the US adult population by 2050. However, if recent increases in diabetes incidence continue and diabetes mortality is relatively low, prevalence will increase to 33% by 2050. A middle-ground scenario projects a prevalence of 25% to 28% by 2050. Intervention can reduce, but not eliminate, increases in diabetes prevalence.
Conclusions:
These projected increases are largely attributable to the aging of the US population, increasing numbers of members of higher-risk minority groups in the population, and people with diabetes living longer. Effective strategies will need to be undertaken to moderate the impact of these factors on national diabetes burden. Our analysis suggests that widespread implementation of reasonably effective preventive interventions focused on high-risk subgroups of the population can considerably reduce, but not eliminate, future increases in diabetes prevalence.</description>
        <link>http://www.pophealthmetrics.com/content/8/1/29</link>
                <dc:creator>James Boyle</dc:creator>
                <dc:creator>Theodore Thompson</dc:creator>
                <dc:creator>Edward Gregg</dc:creator>
                <dc:creator>Lawrence Barker</dc:creator>
                <dc:creator>David Williamson</dc:creator>
                <dc:source>Population Health Metrics 2010, null:29</dc:source>
        <dc:date>2010-10-22T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1478-7954-8-29</dc:identifier>
                            <dc:title>Diabetes incidence set to rise </dc:title>
                            <dc:description>Statistics show that diabetes prevalence is set to rise in the US adult population to 33% by 2050 and so implementation of preventative measures needs to be considered.</dc:description>
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        <prism:startingPage>29</prism:startingPage>
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        <item rdf:about="http://www.pophealthmetrics.com/content/10/1/1">
        <title>Modeling causes of death: an integrated approach using CODEm</title>
        <description>Background:
Data on causes of death by age and sex are a critical input into health decision-making. Priority setting in public health should be informed not only by the current magnitude of health problems but by trends in them. However, cause of death data are often not available or are subject to substantial problems of comparability. We propose five general principles for cause of death model development, validation, and reporting.
Methods:
We detail a specific implementation of these principles that is embodied in an analytical tool - the Cause of Death Ensemble model (CODEm) - which explores a large variety of possible models to estimate trends in causes of death. Possible models are identified using a covariate selection algorithm that yields many plausible combinations of covariates, which are then run through four model classes. The model classes include mixed effects linear models and spatial-temporal Gaussian Process Regression models for cause fractions and death rates. All models for each cause of death are then assessed using out-of-sample predictive validity and combined into an ensemble with optimal out-of-sample predictive performance.
Results:
Ensemble models for cause of death estimation outperform any single component model in tests of root mean square error, frequency of predicting correct temporal trends, and achieving 95% coverage of the prediction interval. We present detailed results for CODEm applied to maternal mortality and summary results for several other causes of death, including cardiovascular disease and several cancers.
Conclusions:
CODEm produces better estimates of cause of death trends than previous methods and is less susceptible to bias in model specification. We demonstrate the utility of CODEm for the estimation of several major causes of death.</description>
        <link>http://www.pophealthmetrics.com/content/10/1/1</link>
                <dc:creator>Kyle Foreman</dc:creator>
                <dc:creator>Rafael Lozano</dc:creator>
                <dc:creator>Alan Lopez</dc:creator>
                <dc:creator>Christopher Murray</dc:creator>
                <dc:source>Population Health Metrics 2012, null:1</dc:source>
        <dc:date>2012-01-06T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1478-7954-10-1</dc:identifier>
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        <item rdf:about="http://www.pophealthmetrics.com/content/10/1/7">
        <title>Impact of diabetes mellitus on life expectancy and health-adjusted life expectancy in Canada</title>
        <description>The objectives of this study were to estimate life expectancy (LE) and health-adjusted life expectancy (HALE) for Canadians with and without diabetes and to evaluate the impact of diabetes on population health using administrative and survey data.Mortality data from the Canadian Chronic Disease Surveillance System (2004 to 2006) and Health Utilities Index data from the Canadian Community Health Survey (2000 to 2005) were used. Life table analysis was applied to calculate LE, HALE, and their confidence intervals using the Chiang and the adapted Sullivan methods.LE and HALE were significantly lower among people with diabetes than for people without the disease. LE and HALE for females without diabetes were 85.0 and 73.3 years, respectively (males: 80.2 and 70.9 years). Diabetes was associated with a loss of LE and HALE of 6.0 years and 5.8 years, respectively, for females, and 5.0 years and 5.3 years, respectively, for males, living with diabetes at 55 years of age. The overall gains in LE and HALE after the hypothetical elimination of prevalent diagnosed diabetes cases in the population were 1.4 years and 1.2 years, respectively, for females, and 1.3 years for both LE and HALE for males.The results of the study confirm that diabetes is an important disease burden in Canada impacting the female and male populations differently. The methods can be used to calculate LE and HALE for other chronic conditions, providing useful information for public health researchers and policymakers.KeywordsLife expectancy, health-adjusted life expectancy, diabetes mellitus, health utility index, summary measure of population health</description>
        <link>http://www.pophealthmetrics.com/content/10/1/7</link>
                <dc:creator>Lidia Loukine</dc:creator>
                <dc:creator>Chris Waters</dc:creator>
                <dc:creator>Bernard Choi</dc:creator>
                <dc:creator>Joellyn Ellison</dc:creator>
                <dc:source>Population Health Metrics 2012, null:7</dc:source>
        <dc:date>2012-04-24T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1478-7954-10-7</dc:identifier>
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        <prism:startingPage>7</prism:startingPage>
        <prism:publicationDate>2012-04-24T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.pophealthmetrics.com/content/7/1/16">
        <title>Diabetes prevalence and diagnosis in US states: analysis of health surveys</title>
        <description>Background:
Current US surveillance data provide estimates of diabetes using laboratory tests at the national level as well as self-reported data at the state level. Self-reported diabetes prevalence may be biased because respondents may not be aware of their risk status. Our objective was to estimate the prevalence of diagnosed and undiagnosed diabetes by state.
Methods:
We estimated undiagnosed diabetes prevalence as a function of a set of health system and sociodemographic variables using a logistic regression in the National Health and Nutrition Examination Survey (2003-2006). We applied this relationship to identical variables from the Behavioral Risk Factor Surveillance System (2003-2007) to estimate state-level prevalence of undiagnosed diabetes by age group and sex. We assumed that those who report being diagnosed with diabetes in both surveys are truly diabetic.
Results:
The prevalence of diabetes in the U.S. was 13.7% among men and 11.7% among women &#8805; 30 years. Age-standardized diabetes prevalence was highest in Mississippi, West Virginia, Louisiana, Texas, South Carolina, Alabama, and Georgia (15.8 to 16.6% for men and 12.4 to 14.8% for women). Vermont, Minnesota, Montana, and Colorado had the lowest prevalence (11.0 to 12.2% for men and 7.3 to 8.4% for women). Men in all states had higher diabetes prevalence than women. The absolute prevalence of undiagnosed diabetes, as a percent of total population, was highest in New Mexico, Texas, Florida, and California (3.5 to 3.7 percentage points) and lowest in Montana, Oklahoma, Oregon, Alaska, Vermont, Utah, Washington, and Hawaii (2.1 to 3 percentage points). Among those with no established diabetes diagnosis, being obese, being Hispanic, not having insurance and being &#8805; 60 years old were significantly associated with a higher risk of having undiagnosed diabetes.
Conclusion:
Diabetes prevalence is highest in the Southern and Appalachian states and lowest in the Midwest and the Northeast. Better diabetes diagnosis is needed in a number of states.</description>
        <link>http://www.pophealthmetrics.com/content/7/1/16</link>
                <dc:creator>Goodarz Danaei</dc:creator>
                <dc:creator>Ari Friedman</dc:creator>
                <dc:creator>Shefali Oza</dc:creator>
                <dc:creator>Christopher Murray</dc:creator>
                <dc:creator>Majid Ezzati</dc:creator>
                <dc:source>Population Health Metrics 2009, null:16</dc:source>
        <dc:date>2009-09-25T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1478-7954-7-16</dc:identifier>
                            <dc:title>Improving diabetes diagnosis in US states</dc:title>
                            <dc:description>Prevalence of undiagnosed and total diabetes, determined from analysis of US national blood tests and state survey data, indicate that some states are under diagnosing this condition.</dc:description>
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        <prism:startingPage>16</prism:startingPage>
        <prism:publicationDate>2009-09-25T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.pophealthmetrics.com/content/8/1/17">
        <title>Thermal discomfort with cold extremities in relation to age, gender, and body mass index in a random sample of a Swiss urban population</title>
        <description>Background:
The aim of this epidemiological study was to investigate the relationship of thermal discomfort with cold extremities (TDCE) to age, gender, and body mass index (BMI) in a Swiss urban population.
Methods:
In a random population sample of Basel city, 2,800 subjects aged 20-40 years were asked to complete a questionnaire evaluating the extent of cold extremities. Values of cold extremities were based on questionnaire-derived scores. The correlation of age, gender, and BMI to TDCE was analyzed using multiple regression analysis.
Results:
A total of 1,001 women (72.3% response rate) and 809 men (60% response rate) returned a completed questionnaire. Statistical analyses revealed the following findings: Younger subjects suffered more intensely from cold extremities than the elderly, and women suffered more than men (particularly younger women). Slimmer subjects suffered significantly more often from cold extremities than subjects with higher BMIs.
Conclusions:
Thermal discomfort with cold extremities (a relevant symptom of primary vascular dysregulation) occurs at highest intensity in younger, slimmer women and at lowest intensity in elderly, stouter men.</description>
        <link>http://www.pophealthmetrics.com/content/8/1/17</link>
                <dc:creator>Maneli Mozaffarieh</dc:creator>
                <dc:creator>Paolo Fontana Gasio</dc:creator>
                <dc:creator>Andreas Schotzau</dc:creator>
                <dc:creator>Selim Orgul</dc:creator>
                <dc:creator>Josef Flammer</dc:creator>
                <dc:creator>Kurt Krauchi</dc:creator>
                <dc:source>Population Health Metrics 2010, null:17</dc:source>
        <dc:date>2010-06-04T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1478-7954-8-17</dc:identifier>
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        <prism:startingPage>17</prism:startingPage>
        <prism:publicationDate>2010-06-04T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.pophealthmetrics.com/content/9/1/50">
        <title>Performance of InterVA for assigning causes of death to verbal autopsies: multisite validation study using clinical diagnostic gold standards</title>
        <description>Background:
InterVA is a widely disseminated tool for cause of death attribution using information from verbal autopsies. Several studies have attempted to validate the concordance and accuracy of the tool, but the main limitation of these studies is that they compare cause of death as ascertained through hospital record review or hospital discharge diagnosis with the results of InterVA. This study provides a unique opportunity to assess the performance of InterVA compared to physician-certified verbal autopsies (PCVA) and alternative automated methods for analysis.
Methods:
Using clinical diagnostic gold standards to select 12,542 verbal autopsy cases, we assessed the performance of InterVA on both an individual and population level and compared the results to PCVA, conducting analyses separately for adults, children, and neonates. Following the recommendation of Murray et al., we randomly varied the cause composition over 500 test datasets to understand the performance of the tool in different settings. We also contrasted InterVA with an alternative Bayesian method, Simplified Symptom Pattern (SSP), to understand the strengths and weaknesses of the tool.
Results:
Across all age groups, InterVA performs worse than PCVA, both on an individual and population level. On an individual level, InterVA achieved a chance-corrected concordance of 24.2% for adults, 24.9% for children, and 6.3% for neonates (excluding free text, considering one cause selection). On a population level, InterVA achieved a cause-specific mortality fraction accuracy of 0.546 for adults, 0.504 for children, and 0.404 for neonates. The comparison to SSP revealed four specific characteristics that lead to superior performance of SSP. Increases in chance-corrected concordance are attained by developing cause-by-cause models (2%), using all items as opposed to only the ones that mapped to InterVA items (7%), assigning probabilities to clusters of symptoms (6%), and using empirical as opposed to expert probabilities (up to 8%).
Conclusions:
Given the widespread use of verbal autopsy for understanding the burden of disease and for setting health intervention priorities in areas that lack reliable vital registrations systems, accurate analysis of verbal autopsies is essential. While InterVA is an affordable and available mechanism for assigning causes of death using verbal autopsies, users should be aware of its suboptimal performance relative to other methods.</description>
        <link>http://www.pophealthmetrics.com/content/9/1/50</link>
                <dc:creator>Rafael Lozano</dc:creator>
                <dc:creator>Michael Freeman</dc:creator>
                <dc:creator>Spencer James</dc:creator>
                <dc:creator>Benjamin Campbell</dc:creator>
                <dc:creator>Alan Lopez</dc:creator>
                <dc:creator>Abraham Flaxman</dc:creator>
                <dc:creator>Christopher Murray</dc:creator>
                <dc:creator>the Population Health Metrics Research Consortium (phmrc)</dc:creator>
                <dc:source>Population Health Metrics 2011, null:50</dc:source>
        <dc:date>2011-08-05T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1478-7954-9-50</dc:identifier>
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        <item rdf:about="http://www.pophealthmetrics.com/content/10/1/6">
        <title>Determining the best population-level alcohol consumption model and its impact on estimates of alcohol-attributable harms</title>
        <description>Background:
The goals of our study are to determine the most appropriate model for alcohol consumption as an exposure for burden of disease, to analyze the effect of the chosen alcohol consumption distribution on the estimation of the alcohol Population- Attributable Fractions (PAFs), and to characterize the chosen alcohol consumption distribution by exploring if there is a global relationship within the distribution.
Methods:
To identify the best model, the Log-Normal, Gamma, and Weibull prevalence distributions were examined using data from 41 surveys from Gender, Alcohol and Culture: An International Study (GENACIS) and from the European Comparative Alcohol Study. To assess the effect of these distributions on the estimated alcohol PAFs, we calculated the alcohol PAF for diabetes, breast cancer, and pancreatitis using the three above-named distributions and using the more traditional approach based on categories. The relationship between the mean and the standard deviation from the Gamma distribution was estimated using data from 851 datasets for 66 countries from GENACIS and from the STEPwise approach to Surveillance from the World Health Organization.
Results:
The Log-Normal distribution provided a poor fit for the survey data, with Gamma and Weibull distributions providing better fits. Additionally, our analyses showed that there were no marked differences for the alcohol PAF estimates based on the Gamma or Weibull distributions compared to PAFs based on categorical alcohol consumption estimates. The standard deviation of the alcohol distribution was highly dependent on the mean, with a unit increase in alcohol consumption associated with a unit increase in the mean of 1.258 (95% CI: 1.223 to 1.293) (R2 = 0.9207) for women and 1.171 (95% CI: 1.144 to 1.197) (R2 = 0. 9474) for men.
Conclusions:
Although the Gamma distribution and the Weibull distribution provided similar results, the Gamma distribution is recommended to model alcohol consumption from population surveys due to its fit, flexibility, and the ease with which it can be modified. The results showed that a large degree of variance of the standard deviation of the alcohol consumption Gamma distribution was explained by the mean alcohol consumption, allowing for alcohol consumption to be modeled through a Gamma distribution using only average consumption.</description>
        <link>http://www.pophealthmetrics.com/content/10/1/6</link>
                <dc:creator>Tara Kehoe</dc:creator>
                <dc:creator>Gerrit Gmel</dc:creator>
                <dc:creator>Kevin Shield</dc:creator>
                <dc:creator>Gerhard Gmel</dc:creator>
                <dc:creator>Jurgen Rehm</dc:creator>
                <dc:source>Population Health Metrics 2012, null:6</dc:source>
        <dc:date>2012-04-10T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1478-7954-10-6</dc:identifier>
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        <prism:startingPage>6</prism:startingPage>
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        <item rdf:about="http://www.pophealthmetrics.com/content/7/1/18">
        <title>Further validation of the Multidimensional Fatigue Inventory in a US adult population sample</title>
        <description>Background:
The Multidimensional Fatigue Inventory (MFI-20) was developed in 1995. Since then, it has been widely used in cancer research and cancer-related illnesses but has never been validated in fatiguing illnesses or in a large US population-selected sample. In this study, we sought to examine the reliability and validity of the MFI-20 in the population of the state of Georgia, USA. Further, we assessed whether the MFI-20 could serve as a complementary diagnostic tool in chronically fatigued and unwell populations.
Methods:
The data derive from a cross-sectional population-based study investigating the prevalence of chronic fatigue syndrome (CFS) in Georgia. The study sample was comprised of three diagnostic groups: CFS-like (292), chronically unwell (269), and well (222). Participants completed the MFI-20 along with several other measures of psychosocial functioning, including the Medical Outcomes Survey Short Form-36 (SF-36), the Zung Self-Rating Depression Scale (SDS), and the Spielberger State-Trait Anxiety Inventory (STAI). We assessed the five MFI-20 subscales using several criteria: inter-item correlations, corrected item-total correlations, internal consistency reliability (Cronbach&apos;s alpha coefficients), construct validity, discriminant (known-group) validity, floor/ceiling effects, and convergent validity through correlations with the SF-36, SDS, and STAI instruments.
Results:
Averaged inter-item correlations ranged from 0.38 to 0.61, indicating no item redundancy. Corrected item-total correlations for all MFI-20 subscales were greater than 0.30, and Cronbach&apos;s alpha coefficients achieved an acceptable level of 0.70. No significant floor/ceiling effect was observed. Factor analysis demonstrated factorial complexity. The MFI-20 also distinguished clearly between three diagnostic groups on all subscales. Furthermore, correlations with depression (SDS), anxiety (STAI), and functional impairment (SF-36) demonstrated strong convergent validity.
Conclusions:
This study provides support for the MFI-20 as a valuable tool when used in chronically unwell and well populations. It also suggests that the MFI-20 could serve as a complementary diagnostic tool in fatiguing illnesses, such as CFS.</description>
        <link>http://www.pophealthmetrics.com/content/7/1/18</link>
                <dc:creator>Jin-Mann Lin</dc:creator>
                <dc:creator>Dana Brimmer</dc:creator>
                <dc:creator>Elizabeth Maloney</dc:creator>
                <dc:creator>Ernestina Nyarko</dc:creator>
                <dc:creator>Rhonda BeLue</dc:creator>
                <dc:creator>William Reeves</dc:creator>
                <dc:source>Population Health Metrics 2009, null:18</dc:source>
        <dc:date>2009-12-15T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1478-7954-7-18</dc:identifier>
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        <prism:startingPage>18</prism:startingPage>
        <prism:publicationDate>2009-12-15T00:00:00Z</prism:publicationDate>
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        <title>National and subnational mortality effects of metabolic risk factors and smoking in Iran: a comparative risk assessment </title>
        <description>Background:
Mortality from cardiovascular and other chronic diseases has increased in Iran. Our aim was to estimate the effects of smoking and high systolic blood pressure (SBP), fasting plasma glucose (FPG), total cholesterol (TC), and high body mass index (BMI) on mortality and life expectancy, nationally and subnationally, using representative data and comparable methods.
Methods:
We used data from the Non-Communicable Disease Surveillance Survey to estimate means and standard deviations for the metabolic risk factors, nationally and by region. Lung cancer mortality was used to measure cumulative exposure to smoking. We used data from the death registration system to estimate age-, sex-, and disease-specific numbers of deaths in 2005, adjusted for incompleteness using demographic methods. We used systematic reviews and meta-analyses of epidemiologic studies to obtain the effect of risk factors on disease-specific mortality. We estimated deaths and life expectancy loss attributable to risk factors using the comparative risk assessment framework.
Results:
In 2005, high SBP was responsible for 41,000 (95% uncertainty interval: 38,000, 44,000) deaths in men and 39,000 (36,000, 42,000) deaths in women in Iran. High FPG, BMI, and TC were responsible for about one-third to one-half of deaths attributable to SBP in men and/or women. Smoking was responsible for 9,000 deaths among men and 2,000 among women. If SBP were reduced to optimal levels, life expectancy at birth would increase by 3.2 years (2.6, 3.9) and 4.1 years (3.2, 4.9) in men and women, respectively; the life expectancy gains ranged from 1.1 to 1.8 years for TC, BMI, and FPG. SBP was also responsible for the largest number of deaths in every region, with age-standardized attributable mortality ranging from 257 to 333 deaths per 100,000 adults in different regions.DiscussionManagement of blood pressure through diet, lifestyle, and pharmacological interventions should be a priority in Iran. Interventions for other metabolic risk factors and smoking can also improve population health.</description>
        <link>http://www.pophealthmetrics.com/content/9/1/55</link>
                <dc:creator>Farshad Farzadfar</dc:creator>
                <dc:creator>Goodarz Danaei</dc:creator>
                <dc:creator>Hengameh Namdaritabar</dc:creator>
                <dc:creator>Julie Rajaratnam</dc:creator>
                <dc:creator>Jacob Marcus</dc:creator>
                <dc:creator>Ardeshir Khosravi</dc:creator>
                <dc:creator>Siamak Alikhani</dc:creator>
                <dc:creator>Christopher Murray</dc:creator>
                <dc:creator>Majid Ezzati</dc:creator>
                <dc:source>Population Health Metrics 2011, null:55</dc:source>
        <dc:date>2011-10-11T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1478-7954-9-55</dc:identifier>
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        <prism:startingPage>55</prism:startingPage>
        <prism:publicationDate>2011-10-11T00:00:00Z</prism:publicationDate>
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