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      Initial antimicrobial management of sepsis

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          Abstract

          Sepsis is a common consequence of infection, associated with a mortality rate > 25%. Although community-acquired sepsis is more common, hospital-acquired infection is more lethal. The most common site of infection is the lung, followed by abdominal infection, catheter-associated blood steam infection and urinary tract infection. Gram-negative sepsis is more common than gram-positive infection, but sepsis can also be due to fungal and viral pathogens. To reduce mortality, it is necessary to give immediate, empiric, broad-spectrum therapy to those with severe sepsis and/or shock, but this approach can drive antimicrobial overuse and resistance and should be accompanied by a commitment to de-escalation and antimicrobial stewardship. Biomarkers such a procalcitonin can provide decision support for antibiotic use, and may identify patients with a low likelihood of infection, and in some settings, can guide duration of antibiotic therapy. Sepsis can involve drug-resistant pathogens, and this often necessitates consideration of newer antimicrobial agents.

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          Most cited references114

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          Global, regional, and national sepsis incidence and mortality, 1990–2017: analysis for the Global Burden of Disease Study

          Summary Background Sepsis is life-threatening organ dysfunction due to a dysregulated host response to infection. It is considered a major cause of health loss, but data for the global burden of sepsis are limited. As a syndrome caused by underlying infection, sepsis is not part of standard Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) estimates. Accurate estimates are important to inform and monitor health policy interventions, allocation of resources, and clinical treatment initiatives. We estimated the global, regional, and national incidence of sepsis and mortality from this disorder using data from GBD 2017. Methods We used multiple cause-of-death data from 109 million individual death records to calculate mortality related to sepsis among each of the 282 underlying causes of death in GBD 2017. The percentage of sepsis-related deaths by underlying GBD cause in each location worldwide was modelled using mixed-effects linear regression. Sepsis-related mortality for each age group, sex, location, GBD cause, and year (1990–2017) was estimated by applying modelled cause-specific fractions to GBD 2017 cause-of-death estimates. We used data for 8·7 million individual hospital records to calculate in-hospital sepsis-associated case-fatality, stratified by underlying GBD cause. In-hospital sepsis-associated case-fatality was modelled for each location using linear regression, and sepsis incidence was estimated by applying modelled case-fatality to sepsis-related mortality estimates. Findings In 2017, an estimated 48·9 million (95% uncertainty interval [UI] 38·9–62·9) incident cases of sepsis were recorded worldwide and 11·0 million (10·1–12·0) sepsis-related deaths were reported, representing 19·7% (18·2–21·4) of all global deaths. Age-standardised sepsis incidence fell by 37·0% (95% UI 11·8–54·5) and mortality decreased by 52·8% (47·7–57·5) from 1990 to 2017. Sepsis incidence and mortality varied substantially across regions, with the highest burden in sub-Saharan Africa, Oceania, south Asia, east Asia, and southeast Asia. Interpretation Despite declining age-standardised incidence and mortality, sepsis remains a major cause of health loss worldwide and has an especially high health-related burden in sub-Saharan Africa. Funding The Bill & Melinda Gates Foundation, the National Institutes of Health, the University of Pittsburgh, the British Columbia Children's Hospital Foundation, the Wellcome Trust, and the Fleming Fund.
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            Surviving Sepsis Campaign: International Guidelines for Management of Sepsis and Septic Shock: 2016.

            To provide an update to "Surviving Sepsis Campaign Guidelines for Management of Sepsis and Septic Shock: 2012".
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              Diagnosis and Treatment of Adults with Community-acquired Pneumonia. An Official Clinical Practice Guideline of the American Thoracic Society and Infectious Diseases Society of America

              Background: This document provides evidence-based clinical practice guidelines on the management of adult patients with community-acquired pneumonia. Methods: A multidisciplinary panel conducted pragmatic systematic reviews of the relevant research and applied Grading of Recommendations, Assessment, Development, and Evaluation methodology for clinical recommendations. Results: The panel addressed 16 specific areas for recommendations spanning questions of diagnostic testing, determination of site of care, selection of initial empiric antibiotic therapy, and subsequent management decisions. Although some recommendations remain unchanged from the 2007 guideline, the availability of results from new therapeutic trials and epidemiological investigations led to revised recommendations for empiric treatment strategies and additional management decisions. Conclusions: The panel formulated and provided the rationale for recommendations on selected diagnostic and treatment strategies for adult patients with community-acquired pneumonia.
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                Author and article information

                Contributors
                msn9004@med.cornell.edu
                rbaron@bwh.harvard
                lila.bouadma@aphp.fr
                Thierry.Clandra@chuv.ch
                Nick.Daneman@sunnybrook.ca
                Jan.DeWaele@UGent.be
                kollefm@wustl.edu
                j.lipman@uq.edu.au
                Girish.Nair@beaumont.org
                Journal
                Crit Care
                Critical Care
                BioMed Central (London )
                1364-8535
                1466-609X
                26 August 2021
                26 August 2021
                2021
                : 25
                : 307
                Affiliations
                [1 ]GRID grid.413734.6, ISNI 0000 0000 8499 1112, Pulmonary and Critical Care Medicine, , New York Presbyterian/Weill Cornell Medical Center, ; 425 East 61st St, New York, NY 10065 USA
                [2 ]GRID grid.62560.37, ISNI 0000 0004 0378 8294, Harvard Medical School; Division of Pulmonary and Critical Care Medicine, , Brigham and Women’s Hospital, ; Boston, MA 02115 USA
                [3 ]GRID grid.508487.6, ISNI 0000 0004 7885 7602, AP-HP, Bichat Claude Bernard, Medical and Infectious Diseas ICU, , University of Paris, ; Paris, France
                [4 ]Infectious Diseases Service, Department of Medicine, Lusanne University Hospital, University of Lusanne, Lusanne, Switzerland
                [5 ]GRID grid.17063.33, ISNI 0000 0001 2157 2938, Division of Infectious Diseases, Sunnybrook Health Sciences Centre, , University of Toronto, ; Toronto, Canada
                [6 ]GRID grid.5342.0, ISNI 0000 0001 2069 7798, Department of Critical Care Medicine, Surgical Intensive Care Unit, , Ghent University, ; Ghent, Belgium
                [7 ]GRID grid.4367.6, ISNI 0000 0001 2355 7002, Division of Pulmonary and Critical Care Medicine, , Washington University School of Medicine, ; St. Louis, MO USA
                [8 ]GRID grid.1003.2, ISNI 0000 0000 9320 7537, Royal Brisbane and Women’s Hospital and Jamieson Trauma Institute, , The University of Queensland, ; Brisbane, Australia
                [9 ]GRID grid.411165.6, ISNI 0000 0004 0593 8241, Nimes University Hospital, , University of Montpelier, ; Nimes, France
                [10 ]GRID grid.261277.7, ISNI 0000 0001 2219 916X, Oakland University William Beaumont School of Medicine, ; Royal Oak, MI USA
                Author information
                http://orcid.org/0000-0003-0293-386X
                Article
                3736
                10.1186/s13054-021-03736-w
                8390082
                34446092
                96f5453b-cfc0-4c8e-9243-a77dcef2d278
                © The Author(s) 2021

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 16 August 2021
                : 18 August 2021
                Categories
                Review
                Custom metadata
                © The Author(s) 2021

                Emergency medicine & Trauma
                sepsis,antibiotic therapy,antimicrobial therapy,fungal infection,pneumonia,intra-abdominal infection,pharmacokinetics,bacteremia,biomarkers

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