75 research outputs found

    Decreasing Mortality in Severe Sepsis and Septic Shock Patients by Implementing a Sepsis Bundle in a Hospital Setting

    Get PDF
    Background The Surviving Sepsis Campaign (SSC) guidelines for the management of severe sepsis (SS) and septic shock (SSh) have been recommended to reduce morbidity and mortality. Materials and Methods A quasi-experimental study was conducted in a medical-surgical ICU. Multiple interventions to optimize SS and SSh shock patients\u27 clinical outcomes were performed by applying sepsis bundles (6- and 24-hour) in May 2006. We compared bundle compliance and patient outcomes before (July 2005-April 2006) and after (May 2006-December 2009) implementation of the interventions. Results A total of 564 SS and SSh patients were identified. Prior to the intervention, compliance with the 6 hour-sepsis resuscitation bundle was only 6%. After the intervention, compliance was as follows: 8.2% from May to December 2006, 9.3% in 2007, 21.1% in 2008 and 13.7% in 2009. For the 24 hour-management bundle, baseline compliance was 15.0%. After the intervention, compliance was 15.1% from May to December 2006, 21.4% in 2007, 27.8% in 2008 and 44.4% in 2009. The in-hospital mortality was 54.0% from July 2005 to April 2006, 41.1% from May to December 2006, 39.3% in 2007, 41.4% in 2008 and 16.2% in 2009. Conclusion These results suggest reducing SS and SSh patient mortality is a complex process that involves multiple performance measures and interventions

    Comparativa y Analisis de Variabilidad Espacial entre las Medidas de Radiacion Solar Terrestres (SIAR) y Satelitales (CMSAF)

    Get PDF
    El objetivo de este trabajo es el análisis comparativo de dos fuentes de irradiación solar para el territorio peninsular español, siguiendo la iniciativa de estudios previos para otras regiones. La primera de estas fuentes corresponde a medidas de irradiación global diaria en el plano horizontal realizadas por los piranómetros de la red de estaciones meteorológicas del Sistema de Información Agroclimática del Regadío (SIAR), perteneciente al Ministerio de Medio Ambiente, Rural y Marino. Esta red está compuesta por más de 360 estaciones ubicadas en once Comunidades Autónomas de la España peninsular. La otra fuente de comparación es un conjunto de imágenes de satélite proporcionadas por la iniciativa denominada ``The Satellite Application Facility on Climate Monitoring'' (CM-SAF)

    Asynchronies during mechanical ventilation are associated with mortality

    Get PDF
    This study aimed to assess the prevalence and time course of asynchronies during mechanical ventilation (MV). Prospective, noninterventional observational study of 50 patients admitted to intensive care unit (ICU) beds equipped with Better Care (TM) software throughout MV. The software distinguished ventilatory modes and detected ineffective inspiratory efforts during expiration (IEE), double-triggering, aborted inspirations, and short and prolonged cycling to compute the asynchrony index (AI) for each hour. We analyzed 7,027 h of MV comprising 8,731,981 breaths. Asynchronies were detected in all patients and in all ventilator modes. The median AI was 3.41 % [IQR 1.95-5.77]; the most common asynchrony overall and in each mode was IEE [2.38 % (IQR 1.36-3.61)]. Asynchronies were less frequent from 12 pm to 6 am [1.69 % (IQR 0.47-4.78)]. In the hours where more than 90 % of breaths were machine-triggered, the median AI decreased, but asynchronies were still present. When we compared patients with AI > 10 vs AI a parts per thousand currency sign 10 %, we found similar reintubation and tracheostomy rates but higher ICU and hospital mortality and a trend toward longer duration of MV in patients with an AI above the cutoff. Asynchronies are common throughout MV, occurring in all MV modes, and more frequently during the daytime. Further studies should determine whether asynchronies are a marker for or a cause of mortality

    Tailoring nanostructured surfaces with plasmonic/magnetic multifunctional response

    Get PDF
    IIn this work, we present an innovative way to functionalize large surfaces combining both plasmonic and magnetic nanoparticles on a substrate, by the growth of bilayers and a subsequent single annealing. In particular, we show here the formation of Au and gamma- Fe₂O₃ nanoparticles using this route. Thermal treatments promote the nanostructuration of the film plus a partial oxidation of Fe to form ferrimagnetic oxides. For this purpose, annealing conditions and the structure of the bilayer must be selected to achieve an optimal nanostructuration, avoiding the full oxidation of Fe to form antiferromagnetic hematite. Published by AIP Publishing

    Stress tolerance mechanisms in Juncus: responses to salinity and drought in three Juncus species adapted to different natural environments

    Full text link
    [EN] Comparative studies on the responses to salinity and drought were carried out in three Juncus species, two halophytes (Juncus maritimus Lam. and Juncus acutus L.) and one more salt-sensitive (Juncus articulatus L.). Salt tolerance in Juncus depends on the inhibition of transport of toxic ions to the aerial part. In the three taxa studied Na+ and Cl accumulated to the same extent in the roots of salt treated plants; however, ion contents were lower in the shoots and correlated with the relative salt sensitivity of the species, with the lowest levels measured in the halophytes. Activation of K+ transport at high salt concentration could also contribute to salt tolerance in the halophytes. Maintenance of cellular osmotic balance is mostly based on the accumulation of sucrose in the three species. Yet, neither the relative salt-induced increase in sugar content nor the absolute concentrations reached can explain the observed differences in salt tolerance. In contrast, proline increased significantly in the presence of salt only in the salt-tolerant J. maritimus and J. acutus, but not in J. articulatus. Similar patterns of osmolyte accumulation were observed in response to water stress, supporting a functional role of proline in stress tolerance mechanisms in JuncusThis work was partly funded by a grant to O.V. from the Spanish Ministry of Science and Innovation (Project CGL2008-00438/BOS), with contribution by the European Regional Development Fund. Mohamad Al Hassan was a recipient of an Erasmus Mundus pre-doctoral scholarship financed by the European Commission (Welcome Consortium)Al Hassan, M.; López Gresa, MP.; Boscaiu Neagu, MT.; Vicente Meana, Ó. (2016). Stress tolerance mechanisms in Juncus: responses to salinity and drought in three Juncus species adapted to different natural environments. FUNCTIONAL PLANT BIOLOGY. 43:949-960. https://doi.org/10.1071/FP16007S94996043Al Hassan, M., Chaura, J., López-Gresa, M. P., Borsai, O., Daniso, E., Donat-Torres, M. P., … Boscaiu, M. (2016). Native-Invasive Plants vs. Halophytes in Mediterranean Salt Marshes: Stress Tolerance Mechanisms in Two Related Species. Frontiers in Plant Science, 7. doi:10.3389/fpls.2016.00473Albert, R., & Popp, M. (1977). Chemical composition of halophytes from the Neusiedler Lake region in Austria. Oecologia, 27(2), 157-170. doi:10.1007/bf00345820Ashraf, M., & Foolad, M. R. (2007). Roles of glycine betaine and proline in improving plant abiotic stress resistance. Environmental and Experimental Botany, 59(2), 206-216. doi:10.1016/j.envexpbot.2005.12.006Bartels, D., & Sunkar, R. (2005). Drought and Salt Tolerance in Plants. Critical Reviews in Plant Sciences, 24(1), 23-58. doi:10.1080/07352680590910410Bates, L. S., Waldren, R. P., & Teare, I. D. (1973). Rapid determination of free proline for water-stress studies. Plant and Soil, 39(1), 205-207. doi:10.1007/bf00018060Boscaiu, M., Ballesteros, G., Naranjo, M. A., Vicente, O., & Boira, H. (2011). Responses to salt stress in Juncus acutus and J. maritimus during seed germination and vegetative plant growth. Plant Biosystems - An International Journal Dealing with all Aspects of Plant Biology, 145(4), 770-777. doi:10.1080/11263504.2011.628446Boscaiu, M., Lull, C., Llinares, J., Vicente, O., & Boira, H. (2012). Proline as a biochemical marker in relation to the ecology of two halophytic Juncus species. Journal of Plant Ecology, 6(2), 177-186. doi:10.1093/jpe/rts017Bose, J., Rodrigo-Moreno, A., & Shabala, S. (2013). ROS homeostasis in halophytes in the context of salinity stress tolerance. Journal of Experimental Botany, 65(5), 1241-1257. doi:10.1093/jxb/ert430Boyer, J. S. (1982). Plant Productivity and Environment. Science, 218(4571), 443-448. doi:10.1126/science.218.4571.443Chen, T. H. H., & Murata, N. (2008). Glycinebetaine: an effective protectant against abiotic stress in plants. Trends in Plant Science, 13(9), 499-505. doi:10.1016/j.tplants.2008.06.007Clarke, L. D., & Hannon, N. J. (1970). The Mangrove Swamp and Salt Marsh Communities of the Sydney District: III. Plant Growth in Relation to Salinity and Waterlogging. The Journal of Ecology, 58(2), 351. doi:10.2307/2258276Drabkova, L., Kirschner, J., & Vlcek, C. (2006). Phylogenetic relationships within Luzula DC. and Juncus L. (Juncaceae): A comparison of phylogenetic signals of trnL-trnF intergenic spacer, trnL intron and rbcL plastome sequence data. Cladistics, 22(2), 132-143. doi:10.1111/j.1096-0031.2006.00095.xDuBois, M., Gilles, K. A., Hamilton, J. K., Rebers, P. A., & Smith, F. (1956). Colorimetric Method for Determination of Sugars and Related Substances. Analytical Chemistry, 28(3), 350-356. doi:10.1021/ac60111a017Espinar, J. L., Garcia, L. V., & Clemente, L. (2005). Seed storage conditions change the germination pattern of clonal growth plants in Mediterranean salt marshes. American Journal of Botany, 92(7), 1094-1101. doi:10.3732/ajb.92.7.1094Espinar, J. L., García, L. V., Figuerola, J., Green, A. J., & Clemente, L. (2006). Effects of salinity and ingestion by ducks on germination patterns of Juncus subulatus seeds. Journal of Arid Environments, 66(2), 376-383. doi:10.1016/j.jaridenv.2005.11.001Fita, A., Rodríguez-Burruezo, A., Boscaiu, M., Prohens, J., & Vicente, O. (2015). Breeding and Domesticating Crops Adapted to Drought and Salinity: A New Paradigm for Increasing Food Production. Frontiers in Plant Science, 6. doi:10.3389/fpls.2015.00978Flowers, T. J., & Colmer, T. D. (2008). Salinity tolerance in halophytes*. New Phytologist, 179(4), 945-963. doi:10.1111/j.1469-8137.2008.02531.xFlowers, T. J., Hajibagheri, M. A., & Clipson, N. J. W. (1986). Halophytes. The Quarterly Review of Biology, 61(3), 313-337. doi:10.1086/415032Flowers, T. J., Munns, R., & Colmer, T. D. (2014). Sodium chloride toxicity and the cellular basis of salt tolerance in halophytes. Annals of Botany, 115(3), 419-431. doi:10.1093/aob/mcu217Gagneul, D., Aïnouche, A., Duhazé, C., Lugan, R., Larher, F. R., & Bouchereau, A. (2007). A Reassessment of the Function of the So-Called Compatible Solutes in the Halophytic Plumbaginaceae Limonium latifolium. Plant Physiology, 144(3), 1598-1611. doi:10.1104/pp.107.099820GIL, R., LULL, C., BOSCAIU, M., BAUTISTA, I., LIDÓN, A., & VICENTE, O. (2011). Soluble Carbohydrates as Osmolytes in Several Halophytes from a Mediterranean Salt Marsh. Notulae Botanicae Horti Agrobotanici Cluj-Napoca, 39(2), 09. doi:10.15835/nbha3927176Gil, R., Boscaiu, M., Lull, C., Bautista, I., Lidón, A., & Vicente, O. (2013). Are soluble carbohydrates ecologically relevant for salt tolerance in halophytes? Functional Plant Biology, 40(9), 805. doi:10.1071/fp12359Gil, R., Bautista, I., Boscaiu, M., Lidon, A., Wankhade, S., Sanchez, H., … Vicente, O. (2014). Responses of five Mediterranean halophytes to seasonal changes in environmental conditions. AoB PLANTS, 6(0), plu049-plu049. doi:10.1093/aobpla/plu049Glenn, E. (1999). Salt Tolerance and Crop Potential of Halophytes. Critical Reviews in Plant Sciences, 18(2), 227-255. doi:10.1016/s0735-2689(99)00388-3GORHAM, J., HUGHES, L., & WYN JONES, R. G. (2006). Chemical composition of salt-marsh plants from Ynys Môn (Anglesey): the concept of physiotypes. Plant, Cell & Environment, 3(5), 309-318. doi:10.1111/1365-3040.ep11581858Grieve, C. M., & Grattan, S. R. (1983). Rapid assay for determination of water soluble quaternary ammonium compounds. Plant and Soil, 70(2), 303-307. doi:10.1007/bf02374789Gupta, B., & Huang, B. (2014). Mechanism of Salinity Tolerance in Plants: Physiological, Biochemical, and Molecular Characterization. International Journal of Genomics, 2014, 1-18. doi:10.1155/2014/701596Hamamoto, S., Horie, T., Hauser, F., Deinlein, U., Schroeder, J. I., & Uozumi, N. (2015). HKT transporters mediate salt stress resistance in plants: from structure and function to the field. Current Opinion in Biotechnology, 32, 113-120. doi:10.1016/j.copbio.2014.11.025Hariadi, Y., Marandon, K., Tian, Y., Jacobsen, S.-E., & Shabala, S. (2010). Ionic and osmotic relations in quinoa (Chenopodium quinoa Willd.) plants grown at various salinity levels. Journal of Experimental Botany, 62(1), 185-193. doi:10.1093/jxb/erq257Jones, E., Simpson, D., Hodkinson, T., Chase, M., & Parnell, J. (2007). The Juncaceae-Cyperaceae Interface: A Combined Plastid Sequence Analysis. Aliso, 23(1), 55-61. doi:10.5642/aliso.20072301.07Kumari, A., Das, P., Parida, A. K., & Agarwal, P. K. (2015). Proteomics, metabolomics, and ionomics perspectives of salinity tolerance in halophytes. Frontiers in Plant Science, 6. doi:10.3389/fpls.2015.00537Munns, R., & Termaat, A. (1986). Whole-Plant Responses to Salinity. Functional Plant Biology, 13(1), 143. doi:10.1071/pp9860143Munns, R., & Tester, M. (2008). Mechanisms of Salinity Tolerance. Annual Review of Plant Biology, 59(1), 651-681. doi:10.1146/annurev.arplant.59.032607.092911Naidoo, G., & Kift, J. (2006). Responses of the saltmarsh rush Juncus kraussii to salinity and waterlogging. Aquatic Botany, 84(3), 217-225. doi:10.1016/j.aquabot.2005.10.002Niu, X., Bressan, R. A., Hasegawa, P. M., & Pardo, J. M. (1995). Ion Homeostasis in NaCl Stress Environments. Plant Physiology, 109(3), 735-742. doi:10.1104/pp.109.3.735Ozgur, R., Uzilday, B., Sekmen, A. H., & Turkan, I. (2013). Reactive oxygen species regulation and antioxidant defence in halophytes. Functional Plant Biology, 40(9), 832. doi:10.1071/fp12389Pang, Q., Chen, S., Dai, S., Chen, Y., Wang, Y., & Yan, X. (2010). Comparative Proteomics of Salt Tolerance inArabidopsis thalianaandThellungiella halophila. Journal of Proteome Research, 9(5), 2584-2599. doi:10.1021/pr100034fPartridge, T. R., & Wilson, J. B. (1987). Salt tolerance of salt marsh plants of Otago, New Zealand. New Zealand Journal of Botany, 25(4), 559-566. doi:10.1080/0028825x.1987.10410086RAVEN, J. A. (1985). TANSLEY REVIEW No. 2. REGULATION OF PH AND GENERATION OF OSMOLARITY IN VASCULAR PLANTS: A COST-BENEFIT ANALYSIS IN RELATION TO EFFICIENCY OF USE OF ENERGY, NITROGEN AND WATER. New Phytologist, 101(1), 25-77. doi:10.1111/j.1469-8137.1985.tb02816.xRodrı́guez-Navarro, A. (2000). Potassium transport in fungi and plants. Biochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1469(1), 1-30. doi:10.1016/s0304-4157(99)00013-1Rozema, J. (1976). An Ecophysiological Study on the Response to Salt of Four Halophytic and Glycophytic Juncus Species. Flora, 165(2), 197-209. doi:10.1016/s0367-2530(17)31845-5Rozema, J. (1991). Growth, water and ion relationships of halophytic monocotyledonae and dicotyledonae; a unified concept. Aquatic Botany, 39(1-2), 17-33. doi:10.1016/0304-3770(91)90019-2Smirnoff, N., & Cumbes, Q. J. (1989). Hydroxyl radical scavenging activity of compatible solutes. Phytochemistry, 28(4), 1057-1060. doi:10.1016/0031-9422(89)80182-7Szabados, L., & Savouré, A. (2010). Proline: a multifunctional amino acid. Trends in Plant Science, 15(2), 89-97. doi:10.1016/j.tplants.2009.11.009Vicente, M. J., Conesa, E., Álvarez-Rogel, J., Franco, J. A., & Martínez-Sánchez, J. J. (2007). Effects of various salts on the germination of three perennial salt marsh species. Aquatic Botany, 87(2), 167-170. doi:10.1016/j.aquabot.2007.04.004Vinocur, B., & Altman, A. (2005). Recent advances in engineering plant tolerance to abiotic stress: achievements and limitations. Current Opinion in Biotechnology, 16(2), 123-132. doi:10.1016/j.copbio.2005.02.001Watson, E. B., & Byrne, R. (2009). Abundance and diversity of tidal marsh plants along the salinity gradient of the San Francisco Estuary: implications for global change ecology. Plant Ecology, 205(1), 113-128. doi:10.1007/s11258-009-9602-7Weimberg, R. (1987). Solute adjustments in leaves of two species of wheat at two different stages of growth in response to salinity. Physiologia Plantarum, 70(3), 381-388. doi:10.1111/j.1399-3054.1987.tb02832.xZhu, J.-K. (2001). Plant salt tolerance. Trends in Plant Science, 6(2), 66-71. doi:10.1016/s1360-1385(00)01838-

    The Changing Landscape for Stroke\ua0Prevention in AF: Findings From the GLORIA-AF Registry Phase 2

    Get PDF
    Background GLORIA-AF (Global Registry on Long-Term Oral Antithrombotic Treatment in Patients with Atrial Fibrillation) is a prospective, global registry program describing antithrombotic treatment patterns in patients with newly diagnosed nonvalvular atrial fibrillation at risk of stroke. Phase 2 began when dabigatran, the first non\u2013vitamin K antagonist oral anticoagulant (NOAC), became available. Objectives This study sought to describe phase 2 baseline data and compare these with the pre-NOAC era collected during phase 1. Methods During phase 2, 15,641 consenting patients were enrolled (November 2011 to December 2014); 15,092 were eligible. This pre-specified cross-sectional analysis describes eligible patients\u2019 baseline characteristics. Atrial fibrillation disease characteristics, medical outcomes, and concomitant diseases and medications were collected. Data were analyzed using descriptive statistics. Results Of the total patients, 45.5% were female; median age was 71 (interquartile range: 64, 78) years. Patients were from Europe (47.1%), North America (22.5%), Asia (20.3%), Latin America (6.0%), and the Middle East/Africa (4.0%). Most had high stroke risk (CHA2DS2-VASc [Congestive heart failure, Hypertension, Age  6575 years, Diabetes mellitus, previous Stroke, Vascular disease, Age 65 to 74 years, Sex category] score  652; 86.1%); 13.9% had moderate risk (CHA2DS2-VASc = 1). Overall, 79.9% received oral anticoagulants, of whom 47.6% received NOAC and 32.3% vitamin K antagonists (VKA); 12.1% received antiplatelet agents; 7.8% received no antithrombotic treatment. For comparison, the proportion of phase 1 patients (of N = 1,063 all eligible) prescribed VKA was 32.8%, acetylsalicylic acid 41.7%, and no therapy 20.2%. In Europe in phase 2, treatment with NOAC was more common than VKA (52.3% and 37.8%, respectively); 6.0% of patients received antiplatelet treatment; and 3.8% received no antithrombotic treatment. In North America, 52.1%, 26.2%, and 14.0% of patients received NOAC, VKA, and antiplatelet drugs, respectively; 7.5% received no antithrombotic treatment. NOAC use was less common in Asia (27.7%), where 27.5% of patients received VKA, 25.0% antiplatelet drugs, and 19.8% no antithrombotic treatment. Conclusions The baseline data from GLORIA-AF phase 2 demonstrate that in newly diagnosed nonvalvular atrial fibrillation patients, NOAC have been highly adopted into practice, becoming more frequently prescribed than VKA in Europe and North America. Worldwide, however, a large proportion of patients remain undertreated, particularly in Asia and North America. (Global Registry on Long-Term Oral Antithrombotic Treatment in Patients With Atrial Fibrillation [GLORIA-AF]; NCT01468701

    Subcortical brain volume, regional cortical thickness, and cortical surface area across disorders: findings from the ENIGMA ADHD, ASD, and OCD Working Groups

    Get PDF
    Objective Attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder (ASD), and obsessive-compulsive disorder (OCD) are common neurodevelopmental disorders that frequently co-occur. We aimed to directly compare all three disorders. The ENIGMA consortium is ideally positioned to investigate structural brain alterations across these disorders. Methods Structural T1-weighted whole-brain MRI of controls (n=5,827) and patients with ADHD (n=2,271), ASD (n=1,777), and OCD (n=2,323) from 151 cohorts worldwide were analyzed using standardized processing protocols. We examined subcortical volume, cortical thickness and surface area differences within a mega-analytical framework, pooling measures extracted from each cohort. Analyses were performed separately for children, adolescents, and adults using linear mixed-effects models adjusting for age, sex and site (and ICV for subcortical and surface area measures). Results We found no shared alterations among all three disorders, while shared alterations between any two disorders did not survive multiple comparisons correction. Children with ADHD compared to those with OCD had smaller hippocampal volumes, possibly influenced by IQ. Children and adolescents with ADHD also had smaller ICV than controls and those with OCD or ASD. Adults with ASD showed thicker frontal cortices compared to adult controls and other clinical groups. No OCD-specific alterations across different age-groups and surface area alterations among all disorders in childhood and adulthood were observed. Conclusion Our findings suggest robust but subtle alterations across different age-groups among ADHD, ASD, and OCD. ADHD-specific ICV and hippocampal alterations in children and adolescents, and ASD-specific cortical thickness alterations in the frontal cortex in adults support previous work emphasizing neurodevelopmental alterations in these disorders

    Measuring the health-related Sustainable Development Goals in 188 countries : a baseline analysis from the Global Burden of Disease Study 2015

    Get PDF
    Background In September, 2015, the UN General Assembly established the Sustainable Development Goals (SDGs). The SDGs specify 17 universal goals, 169 targets, and 230 indicators leading up to 2030. We provide an analysis of 33 health-related SDG indicators based on the Global Burden of Diseases, Injuries, and Risk Factors Study 2015 (GBD 2015). Methods We applied statistical methods to systematically compiled data to estimate the performance of 33 health-related SDG indicators for 188 countries from 1990 to 2015. We rescaled each indicator on a scale from 0 (worst observed value between 1990 and 2015) to 100 (best observed). Indices representing all 33 health-related SDG indicators (health-related SDG index), health-related SDG indicators included in the Millennium Development Goals (MDG index), and health-related indicators not included in the MDGs (non-MDG index) were computed as the geometric mean of the rescaled indicators by SDG target. We used spline regressions to examine the relations between the Socio-demographic Index (SDI, a summary measure based on average income per person, educational attainment, and total fertility rate) and each of the health-related SDG indicators and indices. Findings In 2015, the median health-related SDG index was 59.3 (95% uncertainty interval 56.8-61.8) and varied widely by country, ranging from 85.5 (84.2-86.5) in Iceland to 20.4 (15.4-24.9) in Central African Republic. SDI was a good predictor of the health-related SDG index (r(2) = 0.88) and the MDG index (r(2) = 0.2), whereas the non-MDG index had a weaker relation with SDI (r(2) = 0.79). Between 2000 and 2015, the health-related SDG index improved by a median of 7.9 (IQR 5.0-10.4), and gains on the MDG index (a median change of 10.0 [6.7-13.1]) exceeded that of the non-MDG index (a median change of 5.5 [2.1-8.9]). Since 2000, pronounced progress occurred for indicators such as met need with modern contraception, under-5 mortality, and neonatal mortality, as well as the indicator for universal health coverage tracer interventions. Moderate improvements were found for indicators such as HIV and tuberculosis incidence, minimal changes for hepatitis B incidence took place, and childhood overweight considerably worsened. Interpretation GBD provides an independent, comparable avenue for monitoring progress towards the health-related SDGs. Our analysis not only highlights the importance of income, education, and fertility as drivers of health improvement but also emphasises that investments in these areas alone will not be sufficient. Although considerable progress on the health-related MDG indicators has been made, these gains will need to be sustained and, in many cases, accelerated to achieve the ambitious SDG targets. The minimal improvement in or worsening of health-related indicators beyond the MDGs highlight the need for additional resources to effectively address the expanded scope of the health-related SDGs.Peer reviewe
    corecore