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      Intravenous fluid therapy in the perioperative and critical care setting: Executive summary of the International Fluid Academy (IFA)

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          Abstract

          Intravenous fluid administration should be considered as any other pharmacological prescription. There are three main indications: resuscitation, replacement, and maintenance. Moreover, the impact of fluid administration as drug diluent or to preserve catheter patency, i.e., fluid creep, should also be considered. As for antibiotics, intravenous fluid administration should follow the four Ds: drug, dosing, duration, de-escalation. Among crystalloids, balanced solutions limit acid–base alterations and chloride load and should be preferred, as this likely prevents renal dysfunction. Among colloids, albumin, the only available natural colloid, may have beneficial effects. The last decade has seen growing interest in the potential harms related to fluid overloading. In the perioperative setting, appropriate fluid management that maintains adequate organ perfusion while limiting fluid administration should represent the standard of care. Protocols including a restrictive continuous fluid administration alongside bolus administration to achieve hemodynamic targets have been proposed. A similar approach should be considered also for critically ill patients, in whom increased endothelial permeability makes this strategy more relevant. Active de-escalation protocols may be necessary in a later phase. The R.O.S.E. conceptual model (Resuscitation, Optimization, Stabilization, Evacuation) summarizes accurately a dynamic approach to fluid therapy, maximizing benefits and minimizing harms. Even in specific categories of critically ill patients, i.e., with trauma or burns, fluid therapy should be carefully applied, considering the importance of their specific aims; maintaining peripheral oxygen delivery, while avoiding the consequences of fluid overload.

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          The endothelial glycocalyx: composition, functions, and visualization

          This review aims at presenting state-of-the-art knowledge on the composition and functions of the endothelial glycocalyx. The endothelial glycocalyx is a network of membrane-bound proteoglycans and glycoproteins, covering the endothelium luminally. Both endothelium- and plasma-derived soluble molecules integrate into this mesh. Over the past decade, insight has been gained into the role of the glycocalyx in vascular physiology and pathology, including mechanotransduction, hemostasis, signaling, and blood cell–vessel wall interactions. The contribution of the glycocalyx to diabetes, ischemia/reperfusion, and atherosclerosis is also reviewed. Experimental data from the micro- and macrocirculation alludes at a vasculoprotective role for the glycocalyx. Assessing this possible role of the endothelial glycocalyx requires reliable visualization of this delicate layer, which is a great challenge. An overview is given of the various ways in which the endothelial glycocalyx has been visualized up to now, including first data from two-photon microscopic imaging.
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            Guidelines for Perioperative Care in Elective Colorectal Surgery: Enhanced Recovery After Surgery (ERAS®) Society Recommendations: 2018

            This is the fourth updated Enhanced Recovery After Surgery (ERAS®) Society guideline presenting a consensus for optimal perioperative care in colorectal surgery and providing graded recommendations for each ERAS item within the ERAS® protocol.
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              Effects of tranexamic acid on death, vascular occlusive events, and blood transfusion in trauma patients with significant haemorrhage (CRASH-2): a randomised, placebo-controlled trial.

              Tranexamic acid can reduce bleeding in patients undergoing elective surgery. We assessed the effects of early administration of a short course of tranexamic acid on death, vascular occlusive events, and the receipt of blood transfusion in trauma patients. This randomised controlled trial was undertaken in 274 hospitals in 40 countries. 20 211 adult trauma patients with, or at risk of, significant bleeding were randomly assigned within 8 h of injury to either tranexamic acid (loading dose 1 g over 10 min then infusion of 1 g over 8 h) or matching placebo. Randomisation was balanced by centre, with an allocation sequence based on a block size of eight, generated with a computer random number generator. Both participants and study staff (site investigators and trial coordinating centre staff) were masked to treatment allocation. The primary outcome was death in hospital within 4 weeks of injury, and was described with the following categories: bleeding, vascular occlusion (myocardial infarction, stroke and pulmonary embolism), multiorgan failure, head injury, and other. All analyses were by intention to treat. This study is registered as ISRCTN86750102, Clinicaltrials.govNCT00375258, and South African Clinical Trial RegisterDOH-27-0607-1919. 10 096 patients were allocated to tranexamic acid and 10 115 to placebo, of whom 10 060 and 10 067, respectively, were analysed. All-cause mortality was significantly reduced with tranexamic acid (1463 [14.5%] tranexamic acid group vs 1613 [16.0%] placebo group; relative risk 0.91, 95% CI 0.85-0.97; p=0.0035). The risk of death due to bleeding was significantly reduced (489 [4.9%] vs 574 [5.7%]; relative risk 0.85, 95% CI 0.76-0.96; p=0.0077). Tranexamic acid safely reduced the risk of death in bleeding trauma patients in this study. On the basis of these results, tranexamic acid should be considered for use in bleeding trauma patients. UK NIHR Health Technology Assessment programme, Pfizer, BUPA Foundation, and J P Moulton Charitable Foundation. Copyright 2010 Elsevier Ltd. All rights reserved.
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                Author and article information

                Contributors
                manu.malbrain@uzbrussel.be
                thomas.langer@unimib.it
                djillali.annane@aphp.fr
                gattinoniluciano@gmail.com
                p.elbers@amsterdamumc.nl
                r.hahn@telia.com
                inneke.delaet@zna.be
                Andrea.Minini@uzbrussel.be
                avkwong@mac.com
                c.ince@amc.uva.nl
                davidmuckart@gmail.com
                m.mythen@ucl.ac.uk
                pietro.caironi@unito.it
                niels.vanregenmortel@zna.be
                Journal
                Ann Intensive Care
                Ann Intensive Care
                Annals of Intensive Care
                Springer International Publishing (Cham )
                2110-5820
                24 May 2020
                24 May 2020
                2020
                : 10
                : 64
                Affiliations
                [1 ]GRID grid.411326.3, ISNI 0000 0004 0626 3362, Department of Intensive Care Medicine, , University Hospital Brussels (UZB), ; Laarbeeklaan 101, 1090 Jette, Belgium
                [2 ]GRID grid.8767.e, ISNI 0000 0001 2290 8069, Faculty of Medicine and Pharmacy, , Vrije Universiteit Brussel (VUB), ; Laarbeeklaan 103, Jette, 1090 Belgium
                [3 ]International Fluid Academy, Lovenjoel, Belgium
                [4 ]GRID grid.7563.7, ISNI 0000 0001 2174 1754, School of Medicine and Surgery, , Milano-Bicocca University, ; Milan, Italy
                [5 ]Department of Anesthesia and Critical Care, ASST Grande Ospedale Metropolitano Niguarda, Milan, Italy
                [6 ]GRID grid.460789.4, ISNI 0000 0004 4910 6535, General Intensive Care Unit, Raymond Poincaré Hospital (GHU APHP Université Paris Saclay), U1173 Inflammation & Infection, School of Medicine Simone Veil, , UVSQ-University Paris Saclay, ; 104 Boulevard Raymond Poincaré, 92380 Garches, France
                [7 ]GRID grid.7450.6, ISNI 0000 0001 2364 4210, Emergency and Intensive Care Medicine, , University of Göttingen, ; Göttingen, Germany
                [8 ]Department of Intensive Care Medicine, Amsterdam UMC, Location VUmc, Amsterdam, The Netherlands
                [9 ]GRID grid.412154.7, ISNI 0000 0004 0636 5158, Karolinska Institutet at Danderyds Hospital (KIDS), ; Stockholm, Sweden
                [10 ]GRID grid.416667.4, ISNI 0000 0004 0608 3935, Department of Intensive Care Medicine, , Ziekenhuis Netwerk Antwerpen, ZNA Stuivenberg, ; Antwerp, Belgium
                [11 ]GRID grid.46699.34, ISNI 0000 0004 0391 9020, Department of Intensive Care Medicine and Anaesthesia, , King’s College Hospital, ; Denmark Hill, London, UK
                [12 ]GRID grid.5645.2, ISNI 000000040459992X, Department of Intensive Care Medicine, Laboratory of Translational Intensive Care Medicine, Erasmus MC, , University Medical Center Rotterdam, ; Rotterdam, The Netherlands
                [13 ]GRID grid.16463.36, ISNI 0000 0001 0723 4123, Department of Surgery, Nelson R Mandela School of Medicine, , University of KwaZulu-Natal, ; Durban, South Africa
                [14 ]Level I Trauma Unit and Trauma Intensive Care Unit, Inkosi Albert Luthuli Central Hospital, Durban, South Africa
                [15 ]GRID grid.451056.3, ISNI 0000 0001 2116 3923, University College London Hospitals, , National Institute of Health Research Biomedical Research Centre, ; London, UK
                [16 ]GRID grid.415081.9, ISNI 0000 0004 0493 6869, SCDU Anestesia e Rianimazione, , Azienda Ospedaliero-Universitaria S. Luigi Gonzaga, ; Orbassano, Italy
                [17 ]GRID grid.7605.4, ISNI 0000 0001 2336 6580, Dipartimento di Oncologia, , Università degli Studi di Torino, ; Turin, Italy
                [18 ]GRID grid.416667.4, ISNI 0000 0004 0608 3935, Department of Intensive Care Medicine, , Ziekenhuis Netwerk Antwerpen, ZNA Stuivenberg, ; Antwerp, Belgium
                Author information
                http://orcid.org/0000-0002-1816-5255
                Article
                679
                10.1186/s13613-020-00679-3
                7245999
                32449147
                638f1c81-ba54-4dac-be8e-1751694b9594
                © The Author(s) 2020

                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/.

                History
                : 19 February 2020
                : 14 May 2020
                Categories
                Review
                Custom metadata
                © The Author(s) 2020

                Emergency medicine & Trauma
                fluid therapy,intensive care units,resuscitation,maintenance,water–electrolyte balance,goal-directed,crystalloids,acid base,sodium,chloride

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