55 research outputs found
แแแแแฃแแแแแแ แกแแแแแแชแแแ แแแฎแแแ แแแแก แแแ แกแแแแแแก แแแแงแแคแแแแแ (แแแแแแกแแก แแ แ แฃแกแแแแแก แแแแแแแแแ)
Introduction. The organization of an emergency medical service is of great importance for the population of any country. Many factors affect the effective and efficient operation of the service during emergencies, among them: coordinated and timely response, providing adequate medical care in a limited time and making correct decisions, allocation of available resources, motivated human resources. The qualifications, knowledge, skills, psycho-emotional stability and level of satisfaction of medical staff play an important role in these processes. Objectives. The aim of the survey is to study job satisfaction of the emergency medical staff on the example of professionals employed in two cities of Georgia, Tbilisi and Rustavi. Methodology. The survey was conducted in April-June 2020 using a specially designed structured questionnaire. The respondents were employees of the Emergency Medical Service in Tbilisi and Rustavi. Results and discussion. The research revealed many factors that have a negative impact on staff motivation. These factors include staff overwork, overtime, stressful environment, inadequate payment, and more. Most of the staff working in the emergency care system are dissatisfied with the work schedule and system at work, which is reflected in the discrepancy between the workload, responsible stressful work and appreciation.แจแแกแแแแแ. แแแแแฃแแแแแแ แกแแแแแแชแแแ แแแฎแแแ แแแแก แกแแแกแแฎแฃแ แแก แแ แแแแแแแชแแแก แฃแแแแแกแ แแแแจแแแแแแแ แแฅแแก แแแแแกแแแแ แ แฅแแแงแแแก แกแแแแแแแแแแแกแแแแแก. แแแแแฃแแแแแแ แแแแแแแ แแแแแแแก แแ แแก แกแแแกแแฎแฃแ แแก แแคแแฅแขแแแ แแ แแแแแ แแฃแ แคแฃแแฅแชแแแแแ แแแแแ แแแแ แ แคแแฅแขแแ แ แแฎแแแแก แแแแแแแแก: แแแแ แแแแแ แแแฃแแ แแ แแ แแฃแแ แ แแแแแ แแแ, แจแแแฆแฃแแฃแ แแ แแจแ แแแแแฌแงแแแขแแแแแแก แแแฆแแแ แแ แแแแฅแแแขแฃแ แ แกแแแแแแชแแแ แแแฎแแแ แแแแก แแฆแแแฉแแแ, แแ แกแแแฃแแ แ แแกแฃแ แกแแแแก แกแฌแแ แแ แแแแแแแฌแแแแแ, แแแขแแแแ แแแฃแแ แแแแแแแแฃแ แ แ แแกแฃแ แกแ. แแ แแ แแชแแกแแแจแ แแแแจแแแแแแแแ แ แแแก แแกแ แฃแแแแก แกแแแแแแชแแแ แแแ แกแแแแแแก แแแแแแคแแแแชแแ, แชแแแแ, แฃแแแ -แฉแแแแแแ, แคแกแแฅแ-แแแแชแแฃแ แ แกแขแแแแแฃแ แแแ แแ แแแแงแแคแแแแแแก แแแแ. แแแแแแแก แแแแแแ. แแแแแแแก แแแแแแก แฌแแ แแแแแแแแก แแแแแฃแแแแแแ แกแแแแแแชแแแ แแแฎแแแ แแแแกแแแ แกแแแแแแก แแแแงแแคแแแแแแก แแแแแก แจแแกแฌแแแแ แกแแฅแแ แแแแแแก แแ แแแแ แฅแแแแฅแแก, แแแแแแกแแกแ แแ แ แฃแกแแแแแก แแแแแแแแแ. แแแแแแแแแแแ. แแแแแแแแฎแแ แฉแแขแแ แแ 2020 แฌแแแก แแแ แแ-แแแแแกแจแ, แกแแแชแแแแฃแ แแ แจแแแแแแแแ แกแขแ แฃแฅแขแฃแ แแ แแแฃแแ แแแแฎแแแ แแก แแแแแงแแแแแแ. แ แแกแแแแแแแขแแแแ แจแแ แฉแแฃแ แแงแแแแ แแแแแฃแแแแแแ แแแฎแแแ แแแแก แแแแแ แขแแแแแขแแกแ แแ แกแแแแแแแแ แกแแขแฃแแชแแแแแก แแแแ แแแแแชแแแกแ แแ แแแแแฃแแแแแแ แแแฎแแแ แแแแก แชแแแขแ แแแแก แแแแแแจแ แแแแแแ แแแแแแกแกแ แแ แ แฃแกแแแแจแ. แจแแแแแแแ แแ แแแกแแฃแกแแ. แฉแแขแแ แแแฃแแ แแแแแแแก แจแแแแแแ แแแแแแแแแแ แแ แแแแแ แคแแฅแขแแ แ, แ แแแแแแช แแแแแขแแฃแ แแแแแแแแแแก แแฎแแแแก แแแ แกแแแแแแก แแแขแแแแชแแแแ. แแ แคแแฅแขแแ แแแก แจแแ แแก แแฆแกแแแแจแแแแแ แแแ แกแแแแแแก แแแแแซแแแแ แแแแแแแแแแแฃแ แ แกแแแฃแจแแ แกแแแแแแแ, แกแขแ แแกแฃแแ แแแ แแแ, แแ แแกแแแแแ แแกแ แแแแแฆแแฃแ แแแ แแ แกแฎแแ. แแแแแฃแแแแแแ แกแแแแแแชแแแ แแแฎแแแ แแแแก แกแแกแขแแแแจแ แแแแฃแจแแแ แแแ แกแแแแแแก แฃแแแขแแกแแแ แฃแแแแงแแคแแแแ แกแแแกแแฎแฃแ แจแ แแ แกแแแฃแแ แกแแแฃแจแแ แแ แแคแแแแแ แแ แกแแกแขแแแแ, แ แแช แแแแแฎแแขแฃแแแ แกแแแฃแจแแก แแแชแฃแแแแแกแ แแ แกแแแแกแฃแฎแแกแแแแแแ แกแขแ แแกแฃแแ แกแแฅแแแก แจแแฃแกแแแแแแแแ แแแฆแแแฃแ แกแแ แแแแแแกแ (แแแกแแแ แฏแแแ) แแ แแแคแแกแแแแก แจแแ แแก
Survival from five common cancers in Georgia, 2015-2019 (CONCORD).
BACKGROUND: Population-based cancer survival is a key metric of the effectiveness of health systems in managing cancer. Data from population-based cancer registries are essential for producing reliable and robust cancer survival estimates. Georgia established a national population-based cancer registry on 1 January 2015. This is the first analysis of population-based cancer survival from Georgia. METHODS: Data were available from the national cancer registry for 16,359 adults who were diagnosed with a cancer of the stomach, colon, rectum, breast (women) or cervix during 2015-2019. We estimated age-specific and age-standardised net survival at one, two and three years after diagnosis for each cancer, by sex. RESULTS: The data were of extremely high quality, with less than 2% of data excluded from each dataset. For the patients included in analyses, at least 80% of the tumours were microscopically verified. Age-standardised three-year survival from stomach cancer was 30.6%, similar in men and women. For colon cancer, three-year survival was 60.1%, with survival 4% higher for men than for women. Three-year survival from rectal cancer was similar for men and women, at 54.7%. For women diagnosed with breast cancer, three-year survival was 84.4%, but three-year survival from cervical cancer was only 67.2%. CONCLUSION: Establishment of a national cancer registry with obligatory cancer registration has enabled the first examination of population-based cancer survival in Georgia. Maintenance of the registry will facilitate continued surveillance of both cancer incidence and survival in the country
The Burden of Disease due to COVID-19 (BoCO-19): A study protocol for a secondary analysis of surveillance data in Southern and Eastern Europe, and Central Asia
Introduction
The COVID-19 pandemic has had an extensive impact on public health worldwide. However, in many countries burden of disease indicators for COVID-19 have not yet been calculated or used for monitoring. The present study protocol describes an approach developed in the project โThe Burden of Disease due to COVID-19. Towards a harmonization of population health metrics for the surveillance of dynamic outbreaksโ (BoCO-19). The process of data collection and aggregation across 14 different countries and sub-national regions in Southern and Eastern Europe and Central Asia is described, as well as the methodological approaches used.
Materials and methods
The study implemented in BoCO-19 is a secondary data analysis, using information from national surveillance systems as part of mandatory reporting on notifiable diseases. A customized data collection template is used to gather aggregated data on population size as well as COVID-19 cases and deaths. Years of life lost (YLL), as one component of the number of Disability Adjusted Life Years (DALY), are calculated as described in a recently proposed COVID-19 disease model (the โBurden-EUโ model) for the calculation of DALY. All-cause mortality data are collected for excess mortality sensitivity analyses. For the calculation of Years lived with disability (YLD), the Burden-EU model is adapted based on recent evidence. Because Covid-19 cases vary in terms of disease severity, the possibility and suitability of applying a uniform severity distribution of cases across all countries and sub-national regions will be explored. An approach recently developed for the Global Burden of Disease Study, that considers post-acute consequences of COVID-19, is likely to be adopted. Findings will be compared to explore the quality and usability of the existing data, to identify trends across age-groups and sexes and to formulate recommendations concerning potential improvements in data availability and quality.
Discussion
BoCO-19 serves as a collaborative platform in order to build international capacity for the calculation of burden of disease indicators, and to support national experts in the analysis and interpretation of country-specific data, including their strengths and weaknesses. Challenges include inherent differences in data collection and reporting systems between countries, as well as assumptions that have to be made during the calculation process.Peer Reviewe
Global, regional, and national incidence and mortality for HIV, tuberculosis, and malaria during 1990โ2013: a systematic analysis for the Global Burden of Disease Study 2013
BACKGROUND: The Millennium Declaration in 2000 brought special global attention to HIV, tuberculosis, and malaria through the formulation of Millennium Development Goal (MDG) 6. The Global Burden of Disease 2013 study provides a consistent and comprehensive approach to disease estimation for between 1990 and 2013, and an opportunity to assess whether accelerated progress has occured since the Millennium Declaration. METHODS: To estimate incidence and mortality for HIV, we used the UNAIDS Spectrum model appropriately modified based on a systematic review of available studies of mortality with and without antiretroviral therapy (ART). For concentrated epidemics, we calibrated Spectrum models to fit vital registration data corrected for misclassification of HIV deaths. In generalised epidemics, we minimised a loss function to select epidemic curves most consistent with prevalence data and demographic data for all-cause mortality. We analysed counterfactual scenarios for HIV to assess years of life saved through prevention of mother-to-child transmission (PMTCT) and ART. For tuberculosis, we analysed vital registration and verbal autopsy data to estimate mortality using cause of death ensemble modelling. We analysed data for corrected case-notifications, expert opinions on the case-detection rate, prevalence surveys, and estimated cause-specific mortality using Bayesian meta-regression to generate consistent trends in all parameters. We analysed malaria mortality and incidence using an updated cause of death database, a systematic analysis of verbal autopsy validation studies for malaria, and recent studies (2010-13) of incidence, drug resistance, and coverage of insecticide-treated bednets. FINDINGS: Globally in 2013, there were 1ยท8 million new HIV infections (95% uncertainty interval 1ยท7 million to 2ยท1 million), 29ยท2 million prevalent HIV cases (28ยท1 to 31ยท7), and 1ยท3 million HIV deaths (1ยท3 to 1ยท5). At the peak of the epidemic in 2005, HIV caused 1ยท7 million deaths (1ยท6 million to 1ยท9 million). Concentrated epidemics in Latin America and eastern Europe are substantially smaller than previously estimated. Through interventions including PMTCT and ART, 19ยท1 million life-years (16ยท6 million to 21ยท5 million) have been saved, 70ยท3% (65ยท4 to 76ยท1) in developing countries. From 2000 to 2011, the ratio of development assistance for health for HIV to years of life saved through intervention was US$4498 in developing countries. Including in HIV-positive individuals, all-form tuberculosis incidence was 7ยท5 million (7ยท4 million to 7ยท7 million), prevalence was 11ยท9 million (11ยท6 million to 12ยท2 million), and number of deaths was 1ยท4 million (1ยท3 million to 1ยท5 million) in 2013. In the same year and in only individuals who were HIV-negative, all-form tuberculosis incidence was 7ยท1 million (6ยท9 million to 7ยท3 million), prevalence was 11ยท2 million (10ยท8 million to 11ยท6 million), and number of deaths was 1ยท3 million (1ยท2 million to 1ยท4 million). Annualised rates of change (ARC) for incidence, prevalence, and death became negative after 2000. Tuberculosis in HIV-negative individuals disproportionately occurs in men and boys (versus women and girls); 64ยท0% of cases (63ยท6 to 64ยท3) and 64ยท7% of deaths (60ยท8 to 70ยท3). Globally, malaria cases and deaths grew rapidly from 1990 reaching a peak of 232 million cases (143 million to 387 million) in 2003 and 1ยท2 million deaths (1ยท1 million to 1ยท4 million) in 2004. Since 2004, child deaths from malaria in sub-Saharan Africa have decreased by 31ยท5% (15ยท7 to 44ยท1). Outside of Africa, malaria mortality has been steadily decreasing since 1990. INTERPRETATION: Our estimates of the number of people living with HIV are 18ยท7% smaller than UNAIDS's estimates in 2012. The number of people living with malaria is larger than estimated by WHO. The number of people living with HIV, tuberculosis, or malaria have all decreased since 2000. At the global level, upward trends for malaria and HIV deaths have been reversed and declines in tuberculosis deaths have accelerated. 101 countries (74 of which are developing) still have increasing HIV incidence. Substantial progress since the Millennium Declaration is an encouraging sign of the effect of global action. FUNDING: Bill & Melinda Gates Foundation
Global, regional, and national under-5 mortality, adult mortality, age-specific mortality, and life expectancy, 1970โ2016: a systematic analysis for the Global Burden of Disease Study 2016
BACKGROUND: Detailed assessments of mortality patterns, particularly age-specific mortality, represent a crucial input that enables health systems to target interventions to specific populations. Understanding how all-cause mortality has changed with respect to development status can identify exemplars for best practice. To accomplish this, the Global Burden of Diseases, Injuries, and Risk Factors Study 2016 (GBD 2016) estimated age-specific and sex-specific all-cause mortality between 1970 and 2016 for 195 countries and territories and at the subnational level for the five countries with a population greater than 200 million in 2016.
METHODS: We have evaluated how well civil registration systems captured deaths using a set of demographic methods called death distribution methods for adults and from consideration of survey and census data for children younger than 5 years. We generated an overall assessment of completeness of registration of deaths by dividing registered deaths in each location-year by our estimate of all-age deaths generated from our overall estimation process. For 163 locations, including subnational units in countries with a population greater than 200 million with complete vital registration (VR) systems, our estimates were largely driven by the observed data, with corrections for small fluctuations in numbers and estimation for recent years where there were lags in data reporting (lags were variable by location, generally between 1 year and 6 years). For other locations, we took advantage of different data sources available to measure under-5 mortality rates (U5MR) using complete birth histories, summary birth histories, and incomplete VR with adjustments; we measured adult mortality rate (the probability of death in individuals aged 15-60 years) using adjusted incomplete VR, sibling histories, and household death recall. We used the U5MR and adult mortality rate, together with crude death rate due to HIV in the GBD model life table system, to estimate age-specific and sex-specific death rates for each location-year. Using various international databases, we identified fatal discontinuities, which we defined as increases in the death rate of more than one death per million, resulting from conflict and terrorism, natural disasters, major transport or technological accidents, and a subset of epidemic infectious diseases; these were added to estimates in the relevant years. In 47 countries with an identified peak adult prevalence for HIV/AIDS of more than 0ยท5% and where VR systems were less than 65% complete, we informed our estimates of age-sex-specific mortality using the Estimation and Projection Package (EPP)-Spectrum model fitted to national HIV/AIDS prevalence surveys and antenatal clinic serosurveillance systems. We estimated stillbirths, early neonatal, late neonatal, and childhood mortality using both survey and VR data in spatiotemporal Gaussian process regression models. We estimated abridged life tables for all location-years using age-specific death rates. We grouped locations into development quintiles based on the Socio-demographic Index (SDI) and analysed mortality trends by quintile. Using spline regression, we estimated the expected mortality rate for each age-sex group as a function of SDI. We identified countries with higher life expectancy than expected by comparing observed life expectancy to anticipated life expectancy on the basis of development status alone.
FINDINGS: Completeness in the registration of deaths increased from 28% in 1970 to a peak of 45% in 2013; completeness was lower after 2013 because of lags in reporting. Total deaths in children younger than 5 years decreased from 1970 to 2016, and slower decreases occurred at ages 5-24 years. By contrast, numbers of adult deaths increased in each 5-year age bracket above the age of 25 years. The distribution of annualised rates of change in age-specific mortality rate differed over the period 2000 to 2016 compared with earlier decades: increasing annualised rates of change were less frequent, although rising annualised rates of change still occurred in some locations, particularly for adolescent and younger adult age groups. Rates of stillbirths and under-5 mortality both decreased globally from 1970. Evidence for global convergence of death rates was mixed; although the absolute difference between age-standardised death rates narrowed between countries at the lowest and highest levels of SDI, the ratio of these death rates-a measure of relative inequality-increased slightly. There was a strong shift between 1970 and 2016 toward higher life expectancy, most noticeably at higher levels of SDI. Among countries with populations greater than 1 million in 2016, life expectancy at birth was highest for women in Japan, at 86ยท9 years (95% UI 86ยท7-87ยท2), and for men in Singapore, at 81ยท3 years (78ยท8-83ยท7) in 2016. Male life expectancy was generally lower than female life expectancy between 1970 and 2016, an
Global age-sex-specific fertility, mortality, healthy life expectancy (HALE), and population estimates in 204 countries and territories, 1950-2019 : a comprehensive demographic analysis for the Global Burden of Disease Study 2019
Background: Accurate and up-to-date assessment of demographic metrics is crucial for understanding a wide range of social, economic, and public health issues that affect populations worldwide. The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2019 produced updated and comprehensive demographic assessments of the key indicators of fertility, mortality, migration, and population for 204 countries and territories and selected subnational locations from 1950 to 2019.
Methods: 8078 country-years of vital registration and sample registration data, 938 surveys, 349 censuses, and 238 other sources were identified and used to estimate age-specific fertility. Spatiotemporal Gaussian process regression (ST-GPR) was used to generate age-specific fertility rates for 5-year age groups between ages 15 and 49 years. With extensions to age groups 10โ14 and 50โ54 years, the total fertility rate (TFR) was then aggregated using the estimated age-specific fertility between ages 10 and 54 years. 7417 sources were used for under-5 mortality estimation and 7355 for adult mortality. ST-GPR was used to synthesise data sources after correction for known biases. Adult mortality was measured as the probability of death between ages 15 and 60 years based on vital registration, sample registration, and sibling histories, and was also estimated using ST-GPR. HIV-free life tables were then estimated using estimates of under-5 and adult mortality rates using a relational model life table system created for GBD, which closely tracks observed age-specific mortality rates from complete vital registration when available. Independent estimates of HIV-specific mortality generated by an epidemiological analysis of HIV prevalence surveys and antenatal clinic serosurveillance and other sources were incorporated into the estimates in countries with large epidemics. Annual and single-year age estimates of net migration and population for each country and territory were generated using a Bayesian hierarchical cohort component model that analysed estimated age-specific fertility and mortality rates along with 1250 censuses and 747 population registry years. We classified location-years into seven categories on the basis of the natural rate of increase in population (calculated by subtracting the crude death rate from the crude birth rate) and the net migration rate. We computed healthy life expectancy (HALE) using years lived with disability (YLDs) per capita, life tables, and standard demographic methods. Uncertainty was propagated throughout the demographic estimation process, including fertility, mortality, and population, with 1000 draw-level estimates produced for each metric. Findings: The global TFR decreased from 2ยท72 (95% uncertainty interval [UI] 2ยท66โ2ยท79) in 2000 to 2ยท31 (2ยท17โ2ยท46) in 2019. Global annual livebirths increased from 134ยท5 million (131ยท5โ137ยท8) in 2000 to a peak of 139ยท6 million (133ยท0โ146ยท9) in 2016. Global livebirths then declined to 135ยท3 million (127ยท2โ144ยท1) in 2019. Of the 204 countries and territories included in this study, in 2019, 102 had a TFR lower than 2ยท1, which is considered a good approximation of replacement-level fertility. All countries in sub-Saharan Africa had TFRs above replacement level in 2019 and accounted for 27ยท1% (95% UI 26ยท4โ27ยท8) of global livebirths. Global life expectancy at birth increased from 67ยท2 years (95% UI 66ยท8โ67ยท6) in 2000 to 73ยท5 years (72ยท8โ74ยท3) in 2019. The total number of deaths increased from 50ยท7 million (49ยท5โ51ยท9) in 2000 to 56ยท5 million (53ยท7โ59ยท2) in 2019. Under-5 deaths declined from 9ยท6 million (9ยท1โ10ยท3) in 2000 to 5ยท0 million (4ยท3โ6ยท0) in 2019. Global population increased by 25ยท7%, from 6ยท2 billion (6ยท0โ6ยท3) in 2000 to 7ยท7 billion (7ยท5โ8ยท0) in 2019. In 2019, 34 countries had negative natural rates of increase; in 17 of these, the population declined because immigration was not sufficient to counteract the negative rate of decline. Globally, HALE increased from 58ยท6 years (56ยท1โ60ยท8) in 2000 to 63ยท5 years (60ยท8โ66ยท1) in 2019. HALE increased in 202 of 204 countries and territories between 2000 and 2019
Measuring performance on the Healthcare Access and Quality Index for 195 countries and territories and selected subnational locations: A systematic analysis from the Global Burden of Disease Study 2016
Copyright ยฉ 2018 The Author(s). Published by Elsevier Ltd. Background A key component of achieving universal health coverage is ensuring that all populations have access to quality health care. Examining where gains have occurred or progress has faltered across and within countries is crucial to guiding decisions and strategies for future improvement. We used the Global Burden of Diseases, Injuries, and Risk Factors Study 2016 (GBD 2016) to assess personal health-care access and quality with the Healthcare Access and Quality (HAQ) Index for 195 countries and territories, as well as subnational locations in seven countries, from 1990 to 2016. Methods Drawing from established methods and updated estimates from GBD 2016, we used 32 causes from which death should not occur in the presence of effective care to approximate personal health-care access and quality by location and over time. To better isolate potential effects of personal health-care access and quality from underlying risk factor patterns, we risk-standardised cause-specific deaths due to non-cancers by location-year, replacing the local joint exposure of environmental and behavioural risks with the global level of exposure. Supported by the expansion of cancer registry data in GBD 2016, we used mortality-to-incidence ratios for cancers instead of risk-standardised death rates to provide a stronger signal of the effects of personal health care and access on cancer survival. We transformed each cause to a scale of 0-100, with 0 as the first percentile (worst) observed between 1990 and 2016, and 100 as the 99th percentile (best); we set these thresholds at the country level, and then applied them to subnational locations. We applied a principal components analysis to construct the HAQ Index using all scaled cause values, providing an overall score of 0-100 of personal health-care access and quality by location over time. We then compared HAQ Index levels and trends by quintiles on the Socio-demographic Index (SDI), a summary measure of overall development. As derived from the broader GBD study and other data sources, we examined relationships between national HAQ Index scores and potential correlates of performance, such as total health spending per capita. Findings In 2016, HAQ Index performance spanned from a high of 97ยท1 (95% UI 95ยท8-98ยท1) in Iceland, followed by 96ยท6 (94ยท9-97ยท9) in Norway and 96ยท1 (94ยท5-97ยท3) in the Netherlands, to values as low as 18ยท6 (13ยท1-24ยท4) in the Central African Republic, 19ยท0 (14ยท3-23ยท7) in Somalia, and 23ยท4 (20ยท2-26ยท8) in Guinea-Bissau. The pace of progress achieved between 1990 and 2016 varied, with markedly faster improvements occurring between 2000 and 2016 for many countries in sub-Saharan Africa and southeast Asia, whereas several countries in Latin America and elsewhere saw progress stagnate after experiencing considerable advances in the HAQ Index between 1990 and 2000. Striking subnational disparities emerged in personal health-care access and quality, with China and India having particularly large gaps between locations with the highest and lowest scores in 2016. In China, performance ranged from 91ยท5 (89ยท1-93ยท6) in Beijing to 48ยท0 (43ยท4-53ยท2) in Tibet (a 43ยท5-point difference), while India saw a 30ยท8-point disparity, from 64ยท8 (59ยท6-68ยท8) in Goa to 34ยท0 (30ยท3-38ยท1) in Assam. Japan recorded the smallest range in subnational HAQ performance in 2016 (a 4ยท8-point difference), whereas differences between subnational locations with the highest and lowest HAQ Index values were more than two times as high for the USA and three times as high for England. State-level gaps in the HAQ Index in Mexico somewhat narrowed from 1990 to 2016 (from a 20ยท9-point to 17ยท0-point difference), whereas in Brazil, disparities slightly increased across states during this time (a 17ยท2-point to 20ยท4-point difference). Performance on the HAQ Index showed strong linkages to overall development, with high and high-middle SDI countries generally having higher scores and faster gains for non-communicable diseases. Nonetheless, countries across the development spectrum saw substantial gains in some key health service areas from 2000 to 2016, most notably vaccine-preventable diseases. Overall, national performance on the HAQ Index was positively associated with higher levels of total health spending per capita, as well as health systems inputs, but these relationships were quite heterogeneous, particularly among low-to-middle SDI countries. Interpretation GBD 2016 provides a more detailed understanding of past success and current challenges in improving personal health-care access and quality worldwide. Despite substantial gains since 2000, many low-SDI and middle- SDI countries face considerable challenges unless heightened policy action and investments focus on advancing access to and quality of health care across key health services, especially non-communicable diseases. Stagnating or minimal improvements experienced by several low-middle to high-middle SDI countries could reflect the complexities of re-orienting both primary and secondary health-care services beyond the more limited foci of the Millennium Development Goals. Alongside initiatives to strengthen public health programmes, the pursuit of universal health coverage hinges upon improving both access and quality worldwide, and thus requires adopting a more comprehensive view - and subsequent provision - of quality health care for all populations
Measuring performance on the Healthcare Access and Quality Index for 195 countries and territories and selected subnational locations: A systematic analysis from the Global Burden of Disease Study 2016
Background: A key component of achieving universal health coverage is ensuring that all populations have access to quality health care. Examining where gains have occurred or progress has faltered across and within countries is crucial to guiding decisions and strategies for future improvement. We used the Global Burden of Diseases, Injuries, and Risk Factors Study 2016 (GBD 2016) to assess personal health-care access and quality with the Healthcare Access and Quality (HAQ) Index for 195 countries and territories, as well as subnational locations in seven countries, from 1990 to 2016. Methods Drawing from established methods and updated estimates from GBD 2016, we used 32 causes from which death should not occur in the presence of effective care to approximate personal health-care access and quality by location and over time. To better isolate potential effects of personal health-care access and quality from underlying risk factor patterns, we risk-standardised cause-specific deaths due to non-cancers by location-year, replacing the local joint exposure of environmental and behavioural risks with the global level of exposure. Supported by the expansion of cancer registry data in GBD 2016, we used mortality-to-incidence ratios for cancers instead of risk-standardised death rates to provide a stronger signal of the effects of personal health care and access on cancer survival. We transformed each cause to a scale of 0-100, with 0 as the first percentile (worst) observed between 1990 and 2016, and 100 as the 99th percentile (best); we set these thresholds at the country level, and then applied them to subnational locations. We applied a principal components analysis to construct the HAQ Index using all scaled cause values, providing an overall score of 0-100 of personal health-care access and quality by location over time. We then compared HAQ Index levels and trends by quintiles on the Socio-demographic Index (SDI), a summary measure of overall development. As derived from the broader GBD study and other data sources, we examined relationships between national HAQ Index scores and potential correlates of performance, such as total health spending per capita. Findings In 2016, HAQ Index performance spanned from a high of 97\ub71 (95% UI 95\ub78-98\ub71) in Iceland, followed by 96\ub76 (94\ub79-97\ub79) in Norway and 96\ub71 (94\ub75-97\ub73) in the Netherlands, to values as low as 18\ub76 (13\ub71-24\ub74) in the Central African Republic, 19\ub70 (14\ub73-23\ub77) in Somalia, and 23\ub74 (20\ub72-26\ub78) in Guinea-Bissau. The pace of progress achieved between 1990 and 2016 varied, with markedly faster improvements occurring between 2000 and 2016 for many countries in sub-Saharan Africa and southeast Asia, whereas several countries in Latin America and elsewhere saw progress stagnate after experiencing considerable advances in the HAQ Index between 1990 and 2000. Striking subnational disparities emerged in personal health-care access and quality, with China and India having particularly large gaps between locations with the highest and lowest scores in 2016. In China, performance ranged from 91\ub75 (89\ub71-93\ub76) in Beijing to 48\ub70 (43\ub74-53\ub72) in Tibet (a 43\ub75-point difference), while India saw a 30\ub78-point disparity, from 64\ub78 (59\ub76-68\ub78) in Goa to 34\ub70 (30\ub73-38\ub71) in Assam. Japan recorded the smallest range in subnational HAQ performance in 2016 (a 4\ub78-point difference), whereas differences between subnational locations with the highest and lowest HAQ Index values were more than two times as high for the USA and three times as high for England. State-level gaps in the HAQ Index in Mexico somewhat narrowed from 1990 to 2016 (from a 20\ub79-point to 17\ub70-point difference), whereas in Brazil, disparities slightly increased across states during this time (a 17\ub72-point to 20\ub74-point difference). Performance on the HAQ Index showed strong linkages to overall development, with high and high-middle SDI countries generally having higher scores and faster gains for non-communicable diseases. Nonetheless, countries across the development spectrum saw substantial gains in some key health service areas from 2000 to 2016, most notably vaccine-preventable diseases. Overall, national performance on the HAQ Index was positively associated with higher levels of total health spending per capita, as well as health systems inputs, but these relationships were quite heterogeneous, particularly among low-to-middle SDI countries. Interpretation GBD 2016 provides a more detailed understanding of past success and current challenges in improving personal health-care access and quality worldwide. Despite substantial gains since 2000, many low-SDI and middle- SDI countries face considerable challenges unless heightened policy action and investments focus on advancing access to and quality of health care across key health services, especially non-communicable diseases. Stagnating or minimal improvements experienced by several low-middle to high-middle SDI countries could reflect the complexities of re-orienting both primary and secondary health-care services beyond the more limited foci of the Millennium Development Goals. Alongside initiatives to strengthen public health programmes, the pursuit of universal health coverage hinges upon improving both access and quality worldwide, and thus requires adopting a more comprehensive view-and subsequent provision-of quality health care for all populations
Population and fertility by age and sex for 195 countries and territories, 1950โ2017: a systematic analysis for the Global Burden of Disease Study 2017
Background: Population estimates underpin demographic and epidemiological research and are used to track progress on numerous international indicators of health and development. To date, internationally available estimates of population and fertility, although useful, have not been produced with transparent and replicable methods and do not use standardised estimates of mortality. We present single-calendar year and single-year of age estimates of fertility and population by sex with standardised and replicable methods. Methods: We estimated population in 195 locations by single year of age and single calendar year from 1950 to 2017 with standardised and replicable methods. We based the estimates on the demographic balancing equation, with inputs of fertility, mortality, population, and migration data. Fertility data came from 7817 location-years of vital registration data, 429 surveys reporting complete birth histories, and 977 surveys and censuses reporting summary birth histories. We estimated age-specific fertility rates (ASFRs; the annual number of livebirths to women of a specified age group per 1000 women in that age group) by use of spatiotemporal Gaussian process regression and used the ASFRs to estimate total fertility rates (TFRs; the average number of children a woman would bear if she survived through the end of the reproductive age span [age 10โ54 years] and experienced at each age a particular set of ASFRs observed in the year of interest). Because of sparse data, fertility at ages 10โ14 years and 50โ54 years was estimated from data on fertility in women aged 15โ19 years and 45โ49 years, through use of linear regression. Age-specific mortality data came from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2017 estimates. Data on population came from 1257 censuses and 761 population registry location-years and were adjusted for underenumeration and age misreporting with standard demographic methods. Migration was estimated with the GBD Bayesian demographic balancing model, after incorporating information about refugee migration into the model prior. Final population estimates used the cohort-component method of population projection, with inputs of fertility, mortality, and migration data. Population uncertainty was estimated by use of out-of-sample predictive validity testing. With these data, we estimated the trends in population by age and sex and in fertility by age between 1950 and 2017 in 195 countries and territories. Findings: From 1950 to 2017, TFRs decreased by 49\ub74% (95% uncertainty interval [UI] 46\ub74โ52\ub70). The TFR decreased from 4\ub77 livebirths (4\ub75โ4\ub79) to 2\ub74 livebirths (2\ub72โ2\ub75), and the ASFR of mothers aged 10โ19 years decreased from 37 livebirths (34โ40) to 22 livebirths (19โ24) per 1000 women. Despite reductions in the TFR, the global population has been increasing by an average of 83\ub78 million people per year since 1985. The global population increased by 197\ub72% (193\ub73โ200\ub78) since 1950, from 2\ub76 billion (2\ub75โ2\ub76) to 7\ub76 billion (7\ub74โ7\ub79) people in 2017; much of this increase was in the proportion of the global population in south Asia and sub-Saharan Africa. The global annual rate of population growth increased between 1950 and 1964, when it peaked at 2\ub70%; this rate then remained nearly constant until 1970 and then decreased to 1\ub71% in 2017. Population growth rates in the southeast Asia, east Asia, and Oceania GBD super-region decreased from 2\ub75% in 1963 to 0\ub77% in 2017, whereas in sub-Saharan Africa, population growth rates were almost at the highest reported levels ever in 2017, when they were at 2\ub77%. The global average age increased from 26\ub76 years in 1950 to 32\ub71 years in 2017, and the proportion of the population that is of working age (age 15โ64 years) increased from 59\ub79% to 65\ub73%. At the national level, the TFR decreased in all countries and territories between 1950 and 2017; in 2017, TFRs ranged from a low of 1\ub70 livebirths (95% UI 0\ub79โ1\ub72) in Cyprus to a high of 7\ub71 livebirths (6\ub78โ7\ub74) in Niger. The TFR under age 25 years (TFU25; number of livebirths expected by age 25 years for a hypothetical woman who survived the age group and was exposed to current ASFRs) in 2017 ranged from 0\ub708 livebirths (0\ub707โ0\ub709) in South Korea to 2\ub74 livebirths (2\ub72โ2\ub76) in Niger, and the TFR over age 30 years (TFO30; number of livebirths expected for a hypothetical woman ageing from 30 to 54 years who survived the age group and was exposed to current ASFRs) ranged from a low of 0\ub73 livebirths (0\ub73โ0\ub74) in Puerto Rico to a high of 3\ub71 livebirths (3\ub70โ3\ub72) in Niger. TFO30 was higher than TFU25 in 145 countries and territories in 2017. 33 countries had a negative population growth rate from 2010 to 2017, most of which were located in central, eastern, and western Europe, whereas population growth rates of more than 2\ub70% were seen in 33 of 46 countries in sub-Saharan Africa. In 2017, less than 65% of the national population was of working age in 12 of 34 high-income countries, and less than 50% of the national population was of working age in Mali, Chad, and Niger. Interpretation: Population trends create demographic dividends and headwinds (ie, economic benefits and detriments) that affect national economies and determine national planning needs. Although TFRs are decreasing, the global population continues to grow as mortality declines, with diverse patterns at the national level and across age groups. To our knowledge, this is the first study to provide transparent and replicable estimates of population and fertility, which can be used to inform decision making and to monitor progress. Funding: Bill & Melinda Gates Foundation
Population and fertility by age and sex for 195 countries and territories, 1950โ2017: a systematic analysis for the Global Burden of Disease Study 2017
Background:
Population estimates underpin demographic and epidemiological research and are used to track progress on numerous international indicators of health and development. To date, internationally available estimates of population and fertility, although useful, have not been produced with transparent and replicable methods and do not use standardised estimates of mortality. We present single-calendar year and single-year of age estimates of fertility and population by sex with standardised and replicable methods.
Methods:
We estimated population in 195 locations by single year of age and single calendar year from 1950 to 2017 with standardised and replicable methods. We based the estimates on the demographic balancing equation, with inputs of fertility, mortality, population, and migration data. Fertility data came from 7817 location-years of vital registration data, 429 surveys reporting complete birth histories, and 977 surveys and censuses reporting summary birth histories. We estimated age-specific fertility rates (ASFRs; the annual number of livebirths to women of a specified age group per 1000 women in that age group) by use of spatiotemporal Gaussian process regression and used the ASFRs to estimate total fertility rates (TFRs; the average number of children a woman would bear if she survived through the end of the reproductive age span [age 10โ54 years] and experienced at each age a particular set of ASFRs observed in the year of interest). Because of sparse data, fertility at ages 10โ14 years and 50โ54 years was estimated from data on fertility in women aged 15โ19 years and 45โ49 years, through use of linear regression. Age-specific mortality data came from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2017 estimates. Data on population came from 1257 censuses and 761 population registry location-years and were adjusted for underenumeration and age misreporting with standard demographic methods. Migration was estimated with the GBD Bayesian demographic balancing model, after incorporating information about refugee migration into the model prior. Final population estimates used the cohort-component method of population projection, with inputs of fertility, mortality, and migration data. Population uncertainty was estimated by use of out-of-sample predictive validity testing. With these data, we estimated the trends in population by age and sex and in fertility by age between 1950 and 2017 in 195 countries and territories.
Findings:
From 1950 to 2017, TFRs decreased by 49ยท4% (95% uncertainty interval [UI] 46ยท4โ52ยท0). The TFR decreased from 4ยท7 livebirths (4ยท5โ4ยท9) to 2ยท4 livebirths (2ยท2โ2ยท5), and the ASFR of mothers aged 10โ19 years decreased from 37 livebirths (34โ40) to 22 livebirths (19โ24) per 1000 women. Despite reductions in the TFR, the global population has been increasing by an average of 83ยท8 million people per year since 1985. The global population increased by 197ยท2% (193ยท3โ200ยท8) since 1950, from 2ยท6 billion (2ยท5โ2ยท6) to 7ยท6 billion (7ยท4โ7ยท9) people in 2017; much of this increase was in the proportion of the global population in south Asia and sub-Saharan Africa. The global annual rate of population growth increased between 1950 and 1964, when it peaked at 2ยท0%; this rate then remained nearly constant until 1970 and then decreased to 1ยท1% in 2017. Population growth rates in the southeast Asia, east Asia, and Oceania GBD super-region decreased from 2ยท5% in 1963 to 0ยท7% in 2017, whereas in sub-Saharan Africa, population growth rates were almost at the highest reported levels ever in 2017, when they were at 2ยท7%. The global average age increased from 26ยท6 years in 1950 to 32ยท1 years in 2017, and the proportion of the population that is of working age (age 15โ64 years) increased from 59ยท9% to 65ยท3%. At the national level, the TFR decreased in all countries and territories between 1950 and 2017; in 2017, TFRs ranged from a low of 1ยท0 livebirths (95% UI 0ยท9โ1ยท2) in Cyprus to a high of 7ยท1 livebirths (6ยท8โ7ยท4) in Niger. The TFR under age 25 years (TFU25; number of livebirths expected by age 25 years for a hypothetical woman who survived the age group and was exposed to current ASFRs) in 2017 ranged from 0ยท08 livebirths (0ยท07โ0ยท09) in South Korea to 2ยท4 livebirths (2ยท2โ2ยท6) in Niger, and the TFR over age 30 years (TFO30; number of livebirths expected for a hypothetical woman ageing from 30 to 54 years who survived the age group and was exposed to current ASFRs) ranged from a low of 0ยท3 livebirths (0ยท3โ0ยท4) in Puerto Rico to a high of 3ยท1 livebirths (3ยท0โ3ยท2) in Niger. TFO30 was higher than TFU25 in 145 countries and territories in 2017. 33 countries had a negative population growth rate from 2010 to 2017, most of which were located in central, eastern, and western Europe, whereas population growth rates of more than 2ยท0% were seen in 33 of 46 countries in sub-Saharan Africa. In 2017, less than 65% of the national population was of working age in 12 of 34 high-income countries, and less than 50% of the national population was of working age in Mali, Chad, and Niger.
Interpretation:
Population trends create demographic dividends and headwinds (ie, economic benefits and detriments) that affect national economies and determine national planning needs. Although TFRs are decreasing, the global population continues to grow as mortality declines, with diverse patterns at the national level and across age groups. To our knowledge, this is the first study to provide transparent and replicable estimates of population and fertility, which can be used to inform decision making and to monitor progress
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