164 research outputs found
a systematic analysis for the Global Burden of Disease Study 2013
Background The eastern Mediterranean region is comprised of 22 countries:
Afghanistan, Bahrain, Djibouti, Egypt, Iran, Iraq, Jordan, Kuwait, Lebanon,
Libya, Morocco, Oman, Pakistan, Palestine, Qatar, Saudi Arabia, Somalia,
Sudan, Syria, Tunisia, the United Arab Emirates, and Yemen. Since our Global
Burden of Disease Study 2010 (GBD 2010), the region has faced unrest as a
result of revolutions, wars, and the so-called Arab uprisings. The objective
of this study was to present the burden of diseases, injuries, and risk
factors in the eastern Mediterranean region as of 2013. Methods GBD 2013
includes an annual assessment covering 188 countries from 1990 to 2013. The
study covers 306 diseases and injuries, 1233 sequelae, and 79 risk factors.
Our GBD 2013 analyses included the addition of new data through updated
systematic reviews and through the contribution of unpublished data sources
from collaborators, an updated version of modelling software, and several
improvements in our methods. In this systematic analysis, we use data from GBD
2013 to analyse the burden of disease and injuries in the eastern
Mediterranean region specifically. Findings The leading cause of death in the
region in 2013 was ischaemic heart disease (90·3 deaths per 100 000 people),
which increased by 17·2% since 1990. However, diarrhoeal diseases were the
leading cause of death in Somalia (186·7 deaths per 100 000 people) in 2013,
which decreased by 26·9% since 1990. The leading cause of disability-adjusted
life-years (DALYs) was ischaemic heart disease for males and lower respiratory
infection for females. High blood pressure was the leading risk factor for
DALYs in 2013, with an increase of 83·3% since 1990. Risk factors for DALYs
varied by country. In low-income countries, childhood wasting was the leading
cause of DALYs in Afghanistan, Somalia, and Yemen, whereas unsafe sex was the
leading cause in Djibouti. Non-communicable risk factors were the leading
cause of DALYs in high-income and middle-income countries in the region. DALY
risk factors varied by age, with child and maternal malnutrition affecting the
younger age groups (aged 28 days to 4 years), whereas high bodyweight and
systolic blood pressure affected older people (aged 60–80 years). The
proportion of DALYs attributed to high body-mass index increased from 3·7% to
7·5% between 1990 and 2013. Burden of mental health problems and drug use
increased. Most increases in DALYs, especially from non-communicable diseases,
were due to population growth. The crises in Egypt, Yemen, Libya, and Syria
have resulted in a reduction in life expectancy; life expectancy in Syria
would have been 5 years higher than that recorded for females and 6 years
higher for males had the crisis not occurred. Interpretation Our study shows
that the eastern Mediterranean region is going through a crucial health phase.
The Arab uprisings and the wars that followed, coupled with ageing and
population growth, will have a major impact on the region's health and
resources. The region has historically seen improvements in life expectancy
and other health indicators, even under stress. However, the current situation
will cause deteriorating health conditions for many countries and for many
years and will have an impact on the region and the rest of the world. Based
on our findings, we call for increased investment in health in the region in
addition to reducing the conflicts. Funding Bill & Melinda Gates Foundation
Systemische antibiotische Prophylaxe zur Vorbeugung infektiöser Komplikationen nach maxillofazialer Traumachirurgie: Eine Cochrane systematische Übersichtsarbeit und Metaanalyse
Background: Antibiotics are commonly administrated perioperatively to prevent
postoperative surgical site infection (SSI) of facial fractures treated with open reduction
and internal fixation (ORIF). However, there is no consensus on the optimal duration
and class of prophylactic antibiotics. We investigated the effect of different antibiotic
regimens and examined the efficacy and safety antibiotics for preventing complications
following the surgical reduction of facial fractures.
Methods: In October 2019, we searched the Cochrane Central Register of Controlled
Trials; Ovid MEDLINE; and Ovid EMBASE. We included randomized controlled trials
(RCTs) involving people undergoing ORIF for maxillofacial trauma surgery and
comparing one regimen of antibiotic prophylaxis with any other regimen, placebo or no
antibiotics. The primary outcomes were SSI and systemic infections. Secondary
outcomes were rate of retreatment surgery, adverse events, total treatment costs,
duration of stay in hospital and health-related quality of life. Two assessors examined
the title and abstracts of references identified in the literature search, extracted data
and assessed the risk of bias in included studies.
Main results: We included 14 RCTs in this review that reported the rate of SSI. We
pooled the studies into subgroups based on the prophylaxis regimen. Comparing
intraoperative prophylaxis and postoperative prophylaxis in terms of SSI showed no to
little difference between groups (RR 1.23, 95% CI 0.74 to 2.04; participants = 408;
studies = 5; I2 = 0%; moderate-quality evidence). Also, comparing short-term and longterm postoperative antibiotic prophylaxis showed no to little reduction in the risk of SSI
(RR 0.76, 95% CI 0.39 to 1.47; participants = 570; studies = 7; I2 = 0%; moderatequality evidence) and the risk of adverse events (RR 0.61, 95% CI 0.27 to 1.38;
participants = 295; studies = 4; I2 = 0%, high-quality evidence). There was no difference
in terms of retreatment surgery and systemic infections in both comparisons. Most
studies had an unclear risk of bias prompting us to downgrade the quality of evidence
for outcomes.
Conclusions: There is little or no difference between single-shot intraoperative
prophylaxis or short-term (48 hours) postoperative
prophylaxis in the rate of SSI and adverse events. The studies comparing antibiotic
prophylaxis for facial fractures other than mandibular fractures were scarce. Further
evidence for these fracture sites is neededHintergrund: Antibiotika werden üblicherweise perioperativ verabreicht, um eine
postoperative Infektion der Operationsgebiet von Gesichtsfrakturen zu verhindern,
welche mit einer Reposition und Osteosynthese (ORIF) behandelt wurden. Ein
Konsens über die optimale Dauer und Klasse der prophylaktischen Antibiotika besteht
jedoch nicht. Wir untersuchten die Wirksamkeit und die Sicherheit der perioperativen
antibiotischen Prophylaxe nach der ORIF von Gesichtsfrakturen.
Methoden: Im Oktober 2019 führten wir eine Suche in den folgenden elektronischen
Datenbanken durch: Cochrane Central Register of Controlled Trials, Ovid MEDLINE,
Ovid EMBASE und EBSCO CINAHL. Nur randomisierte kontrollierte Studien (RCTs),
die Patienten mit durch ORIF behandelten maxillofazialen Frakturen rekrutierten,
wurden eingeschlossen. Wir verglichen daraufhin unterschiedlichen Regimen der
Antibiotikaprophylaxe miteinander, mit Placebo oder mit keiner Prophylaxe. Der
primäre Outcome ist die postoperative Infektion. Sekundäre Outcomes waren
systemische Infektionen, Rate der Nachbehandlungsoperationen, unerwünschte
Ereignisse, Gesamtbehandlungskosten, Dauer des Krankenhausaufenthalts und
gesundheitsbezogene Lebensqualität. Zwei Gutachter untersuchten den Titel und die
Abstracts der in der Literaturrecherche identifizierten Referenzen, extrahierten Daten
und bewerteten das Risiko einer Verzerrung in eingeschlossenen Studien.
Hauptergebnisse: Wir haben 14 RCTs eingeschlossen und basierend auf dem
Prophylaxeschema in Untergruppen zusammengefasst.
Der Vergleich der intraoperativen Prophylaxe und der postoperativen Prophylaxe
hinsichtlich der postoperativen Infektion zeigte keinen bis geringen Unterschied
zwischen den Gruppen (RR: 1,23; 95% CI 0,74 bis 2,04; Teilnehmer = 408; Studien =
5; I2 = 0%; mäßiger Evidenzqualität). Der Vergleich der kurz- und langfristigen
postoperativen Antibiotikaprophylaxe zeigte ebenso keine bis geringe Verringerung
des Infektionsrisikos (RR: 0,76; 95% CI 0,39 bis 1,47; Teilnehmer = 570; Studien = 7;
I2 = 0%; mäßige Evidenzqualität) und das Risiko unerwünschter Ereignisse (RR: 0,61;
95% CI 0,27 bis 1,38; Teilnehmer = 295; Studien = 4; I2 = 0%, hochwertige
Evidenzqualität). In beiden Vergleichen gab es keinen Unterschied in Bezug auf
Nachbehandlungsoperationen und systemische Infektionen. Die meisten Studien
hatten ein unklares Verzerrungspotenzial, was uns dazu veranlasste, die Qualität der
Evidenz für die Ergebnisse herabzustufen.
Schlussfolgerungen: Es gibt kaum oder keinen Unterschied zwischen einer intraoperativen Einzelschussprophylaxe oder einer kurzzeitigen (<48 Stunden) oder
langfristigen (> 48 Stunden) postoperativen Prophylaxe in Bezug auf die Rate der
postoperativen Infektionen und unerwünschte Ereignisse. Die Studien zum Vergleich
der Antibiotikaprophylaxe bei anderen Gesichtsfrakturen als Unterkieferfrakturen
waren rar. Weitere Studien für diese Frakturstellen sind erforderlich.vi, 87 Seite
The global burden of injury: Incidence, mortality, disability-adjusted life years and time trends from the global burden of disease study 2013
Background The Global Burden of Diseases (GBD), Injuries, and Risk Factors study used the disabilityadjusted life year (DALY) to quantify the burden of diseases, injuries, and risk factors. This paper provides an overview of injury estimates from the 2013 update of GBD, with detailed information on incidence, mortality, DALYs and rates of change from 1990 to 2013 for 26 causes of injury, globally, by region and by country. Methods Injury mortality was estimated using the extensive GBD mortality database, corrections for illdefined cause of death and the cause of death ensemble modelling tool. Morbidity estimation was based on inpatient and outpatient data sets, 26 cause-of-injury and 47 nature-of-injury categories, and seven follow-up studies with patient-reported long-term outcome measures. Results In 2013, 973 million (uncertainty interval (UI) 942 to 993) people sustained injuries that warranted some type of healthcare and 4.8 million (UI 4.5 to 5.1) people died from injuries. Between 1990 and 2013 the global age-standardised injury DALY rate decreased by 31% (UI 26% to 35%). The rate of decline in DALY rates was significant for 22 cause-of-injury categories, including all the major injuries. Conclusions Injuries continue to be an important cause of morbidity and mortality in the developed and developing world. The decline in rates for almost all injuries is so prominent that it warrants a general statement that the world is becoming a safer place to live in. However, the patterns vary widely by cause, age, sex, region and time and there are still large improvements that need to be made
Global, regional, and national comparative risk assessment of 84 behavioural, environmental and occupational, and metabolic risks or clusters of risks for 195 countries and territories, 1990–2017 : a systematic analysis for the Global Burden of Disease Study 2017
Background: The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2017 comparative risk assessment (CRA) is a comprehensive approach to risk factor quantification that offers a useful tool for synthesising evidence on risks and risk outcome associations. With each annual GBD study, we update the GBD CRA to incorporate improved methods, new risks and risk outcome pairs, and new data on risk exposure levels and risk outcome associations.
Methods: We used the CRA framework developed for previous iterations of GBD to estimate levels and trends in exposure, attributable deaths, and attributable disability-adjusted life-years (DALYs), by age group, sex, year, and location for 84 behavioural, environmental and occupational, and metabolic risks or groups of risks from 1990 to 2017. This study included 476 risk outcome pairs that met the GBD study criteria for convincing or probable evidence of causation. We extracted relative risk and exposure estimates from 46 749 randomised controlled trials, cohort studies, household surveys, census data, satellite data, and other sources. We used statistical models to pool data, adjust for bias, and incorporate covariates. Using the counterfactual scenario of theoretical minimum risk exposure level (TMREL), we estimated the portion of deaths and DALYs that could be attributed to a given risk. We explored the relationship between development and risk exposure by modelling the relationship between the Socio-demographic Index (SDI) and risk-weighted exposure prevalence and estimated expected levels of exposure and risk-attributable burden by SDI. Finally, we explored temporal changes in risk-attributable DALYs by decomposing those changes into six main component drivers of change as follows: (1) population growth; (2) changes in population age structures; (3) changes in exposure to environmental and occupational risks; (4) changes in exposure to behavioural risks; (5) changes in exposure to metabolic risks; and (6) changes due to all other factors, approximated as the risk-deleted death and DALY rates, where the risk-deleted rate is the rate that would be observed had we reduced the exposure levels to the TMREL for all risk factors included in GBD 2017.
Findings: In 2017,34.1 million (95% uncertainty interval [UI] 33.3-35.0) deaths and 121 billion (144-1.28) DALYs were attributable to GBD risk factors. Globally, 61.0% (59.6-62.4) of deaths and 48.3% (46.3-50.2) of DALYs were attributed to the GBD 2017 risk factors. When ranked by risk-attributable DALYs, high systolic blood pressure (SBP) was the leading risk factor, accounting for 10.4 million (9.39-11.5) deaths and 218 million (198-237) DALYs, followed by smoking (7.10 million [6.83-7.37] deaths and 182 million [173-193] DALYs), high fasting plasma glucose (6.53 million [5.23-8.23] deaths and 171 million [144-201] DALYs), high body-mass index (BMI; 4.72 million [2.99-6.70] deaths and 148 million [98.6-202] DALYs), and short gestation for birthweight (1.43 million [1.36-1.51] deaths and 139 million [131-147] DALYs). In total, risk-attributable DALYs declined by 4.9% (3.3-6.5) between 2007 and 2017. In the absence of demographic changes (ie, population growth and ageing), changes in risk exposure and risk-deleted DALYs would have led to a 23.5% decline in DALYs during that period. Conversely, in the absence of changes in risk exposure and risk-deleted DALYs, demographic changes would have led to an 18.6% increase in DALYs during that period. The ratios of observed risk exposure levels to exposure levels expected based on SDI (O/E ratios) increased globally for unsafe drinking water and household air pollution between 1990 and 2017. This result suggests that development is occurring more rapidly than are changes in the underlying risk structure in a population. Conversely, nearly universal declines in O/E ratios for smoking and alcohol use indicate that, for a given SDI, exposure to these risks is declining. In 2017, the leading Level 4 risk factor for age-standardised DALY rates was high SBP in four super-regions: central Europe, eastern Europe, and central Asia; north Africa and Middle East; south Asia; and southeast Asia, east Asia, and Oceania. The leading risk factor in the high-income super-region was smoking, in Latin America and Caribbean was high BMI, and in sub-Saharan Africa was unsafe sex. O/E ratios for unsafe sex in sub-Saharan Africa were notably high, and those for alcohol use in north Africa and the Middle East were notably low.
Interpretation: By quantifying levels and trends in exposures to risk factors and the resulting disease burden, this assessment offers insight into where past policy and programme efforts might have been successful and highlights current priorities for public health action. Decreases in behavioural, environmental, and occupational risks have largely offset the effects of population growth and ageing, in relation to trends in absolute burden. Conversely, the combination of increasing metabolic risks and population ageing will probably continue to drive the increasing trends in non-communicable diseases at the global level, which presents both a public health challenge and opportunity. We see considerable spatiotemporal heterogeneity in levels of risk exposure and risk-attributable burden. Although levels of development underlie some of this heterogeneity, O/E ratios show risks for which countries are overperforming or underperforming relative to their level of development. As such, these ratios provide a benchmarking tool to help to focus local decision making. Our findings reinforce the importance of both risk exposure monitoring and epidemiological research to assess causal connections between risks and health outcomes, and they highlight the usefulness of the GBD study in synthesising data to draw comprehensive and robust conclusions that help to inform good policy and strategic health planning
Global, regional, and national incidence and mortality for HIV, tuberculosis, and malaria during 1990–2013: 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 1·8 million new HIV infections (95% uncertainty interval 1·7 million to 2·1 million), 29·2 million prevalent HIV cases (28·1 to 31·7), and 1·3 million HIV deaths (1·3 to 1·5). At the peak of the epidemic in 2005, HIV caused 1·7 million deaths (1·6 million to 1·9 million). Concentrated epidemics in Latin America and eastern Europe are substantially smaller than previously estimated. Through interventions including PMTCT and ART, 19·1 million life-years (16·6 million to 21·5 million) have been saved, 70·3% (65·4 to 76·1) 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 7·5 million (7·4 million to 7·7 million), prevalence was 11·9 million (11·6 million to 12·2 million), and number of deaths was 1·4 million (1·3 million to 1·5 million) in 2013. In the same year and in only individuals who were HIV-negative, all-form tuberculosis incidence was 7·1 million (6·9 million to 7·3 million), prevalence was 11·2 million (10·8 million to 11·6 million), and number of deaths was 1·3 million (1·2 million to 1·4 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); 64·0% of cases (63·6 to 64·3) and 64·7% of deaths (60·8 to 70·3). Globally, malaria cases and deaths grew rapidly from 1990 reaching a peak of 232 million cases (143 million to 387 million) in 2003 and 1·2 million deaths (1·1 million to 1·4 million) in 2004. Since 2004, child deaths from malaria in sub-Saharan Africa have decreased by 31·5% (15·7 to 44·1). Outside of Africa, malaria mortality has been steadily decreasing since 1990. INTERPRETATION: Our estimates of the number of people living with HIV are 18·7% 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
Burden of musculoskeletal disorders in the Eastern Mediterranean Region, 1990–2013: findings from the Global Burden of Disease Study 2013
Moradi-Lakeh M, Forouzanfar MH, Vollset SE, et al. Burden of musculoskeletal disorders in the Eastern Mediterranean Region, 1990–2013: findings from the Global Burden of Disease Study 2013. Annals of the Rheumatic Diseases. 2017;76(8):annrheumdis-2016-210146
Epidemiology of facial fractures: Incidence, prevalence and years lived with disability estimates from the Global Burden of Disease 2017 study
Background: The Global Burden of Disease Study (GBD) has historically produced estimates of causes of injury such as falls but not the resulting types of injuries that occur. The objective of this study was to estimate the global incidence, prevalence and years lived with disability (YLDs) due to facial fractures and to estimate the leading injurious causes of facial fracture. Methods: We obtained results from GBD 2017. First, the study estimated the incidence from each injury cause (eg, falls), and then the proportion of each cause that would result in facial fracture being the most disabling injury. Incidence, prevalence and YLDs of facial fractures are then calculated across causes. Results: Globally, in 2017, there were 7 538 663 (95% uncertainty interval 6 116 489 to 9 4
Global, regional, and national under-5 mortality, adult mortality, age-specific mortality, and life expectancy, 1970-2016: a systematic analysis for the Global Burden of Disease Study 2016
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Global, regional, and national levels and causes of maternal mortality during 1990–2013: a systematic analysis for the Global Burden of Disease Study 2013
BackgroundThe fifth Millennium Development Goal (MDG 5) established the goal of a 75% reduction in the maternal mortality ratio (MMR; number of maternal deaths per 100,000 livebirths) between 1990 and 2015. We aimed to measure levels and track trends in maternal mortality, the key causes contributing to maternal death, and timing of maternal death with respect to delivery.MethodsWe used robust statistical methods including the Cause of Death Ensemble model (CODEm) to analyse a database of data for 7065 site-years and estimate the number of maternal deaths from all causes in 188 countries between 1990 and 2013. We estimated the number of pregnancy-related deaths caused by HIV on the basis of a systematic review of the relative risk of dying during pregnancy for HIV-positive women compared with HIV-negative women. We also estimated the fraction of these deaths aggravated by pregnancy on the basis of a systematic review. To estimate the numbers of maternal deaths due to nine different causes, we identified 61 sources from a systematic review and 943 site-years of vital registration data. We also did a systematic review of reports about the timing of maternal death, identifying 142 sources to use in our analysis. We developed estimates for each country for 1990-2013 using Bayesian meta-regression. We estimated 95% uncertainty intervals (UIs) for all values.Findings292,982 (95% UI 261,017-327,792) maternal deaths occurred in 2013, compared with 376,034 (343,483-407,574) in 1990. The global annual rate of change in the MMR was -0·3% (-1·1 to 0·6) from 1990 to 2003, and -2·7% (-3·9 to -1·5) from 2003 to 2013, with evidence of continued acceleration. MMRs reduced consistently in south, east, and southeast Asia between 1990 and 2013, but maternal deaths increased in much of sub-Saharan Africa during the 1990s. 2070 (1290-2866) maternal deaths were related to HIV in 2013, 0·4% (0·2-0·6) of the global total. MMR was highest in the oldest age groups in both 1990 and 2013. In 2013, most deaths occurred intrapartum or postpartum. Causes varied by region and between 1990 and 2013. We recorded substantial variation in the MMR by country in 2013, from 956·8 (685·1-1262·8) in South Sudan to 2·4 (1·6-3·6) in Iceland.InterpretationGlobal rates of change suggest that only 16 countries will achieve the MDG 5 target by 2015. Accelerated reductions since the Millennium Declaration in 2000 coincide with increased development assistance for maternal, newborn, and child health. Setting of targets and associated interventions for after 2015 will need careful consideration of regions that are making slow progress, such as west and central Africa.FundingBill & Melinda Gates Foundation
Burden of injury along the development spectrum: associations between the Socio-demographic Index and disability-adjusted life year estimates from the Global Burden of Disease Study 2017
Background The epidemiological transition of non-communicable diseases replacing infectious diseases as the main contributors to disease burden has been well documented in global health literature. Less focus, however, has been given to the relationship between sociodemographic changes and injury. The aim of this study was to examine the association between disability-adjusted life years (DALYs) from injury for 195 countries and territories at different levels along the development spectrum between 1990 and 2017 based on the Global Burden of Disease (GBD) 2017 estimates. Methods Injury mortality was estimated using the GBD mortality database, corrections for garbage coding and CODEm-the cause of death ensemble modelling tool. Morbidity estimation was based on surveys and inpatient and outpatient data sets for 30 cause-of-injury with 47 nature-of-injury categories each. The Socio-demographic Index (SDI) is a composite indicator that includes lagged income per capita, average educational attainment over age 15 years and total fertility rate. results For many causes of injury, age-standardised DALY rates declined with increasing SDI, although road injury, interpersonal violence and self-harm did not follow this pattern. Particularly for self-harm opposing patterns were observed in regions with similar SDI levels. For road injuries, this effect was less pronounced. Conclusions The overall global pattern is that of declining injury burden with increasing SDI. However, not all injuries follow this pattern, which suggests multiple underlying mechanisms influencing injury DALYs. There is a need for a detailed understanding of these patterns to help to inform national and global efforts to address injury-related health outcomes across the development spectrum
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