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      An international RAND/UCLA expert panel to determine the optimal diagnosis and management of burn inhalation injury

      research-article
      1 , 2 , 3 , 4 , 7 , 8 , 5 , 6 , 9 , 10 , 11 , 12 , 13 , 14 , 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 , 23 , 24 , 25 , 26 , 27 , 4 , 28 , 29 , 30 , 31 , 32 , 4 , 7 , 7 , 17 , 7 , 17 , 7 , 17 , 7 , 17 , 1 , 4 , 7 , 33 , 34 , 35 ,
      Critical Care
      BioMed Central
      Burn inhalation injury, Smoke inhalation injury, Burns, Acute lung injury, Acute respiratory distress syndrome, Bronchoscopy, Endotracheal intubation, Mechanical ventilation, Heparin

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          Abstract

          Background

          Burn inhalation injury (BII) is a major cause of burn-related mortality and morbidity. Despite published practice guidelines, no consensus exists for the best strategies regarding diagnosis and management of BII. A modified DELPHI study using the RAND/UCLA (University of California, Los Angeles) Appropriateness Method (RAM) systematically analysed the opinions of an expert panel. Expert opinion was combined with available evidence to determine what constitutes appropriate and inappropriate judgement in the diagnosis and management of BII.

          Methods

          A 15-person multidisciplinary panel comprised anaesthetists, intensivists and plastic surgeons involved in the clinical management of major burn patients adopted a modified Delphi approach using the RAM method. They rated the appropriateness of statements describing diagnostic and management options for BII on a Likert scale. A modified final survey comprising 140 statements was completed, subdivided into history and physical examination (20), investigations (39), airway management (5), systemic toxicity (23), invasive mechanical ventilation (29) and pharmacotherapy (24). Median appropriateness ratings and the disagreement index (DI) were calculated to classify statements as appropriate, uncertain, or inappropriate.

          Results

          Of 140 statements, 74 were rated as appropriate, 40 as uncertain and 26 as inappropriate. Initial intubation with ≥ 8.0 mm endotracheal tubes, lung protective ventilatory strategies, initial bronchoscopic lavage, serial bronchoscopic lavage for severe BII, nebulised heparin and salbutamol administration for moderate-severe BII and N-acetylcysteine for moderate BII were rated appropriate. Non-protective ventilatory strategies, high-frequency oscillatory ventilation, high-frequency percussive ventilation, prophylactic systemic antibiotics and corticosteroids were rated inappropriate. Experts disagreed (DI ≥ 1) on six statements, classified uncertain: the use of flexible fiberoptic bronchoscopy to guide fluid requirements (DI = 1.52), intubation with endotracheal tubes of internal diameter < 8.0 mm (DI = 1.19), use of airway pressure release ventilation modality (DI = 1.19) and nebulised 5000IU heparin, N-acetylcysteine and salbutamol for mild BII (DI = 1.52, 1.70, 1.36, respectively).

          Conclusions

          Burns experts mostly agreed on appropriate and inappropriate diagnostic and management criteria of BII as in published guidance. Uncertainty exists as to the optimal diagnosis and management of differing grades of severity of BII. Future research should investigate the accuracy of bronchoscopic grading of BII, the value of bronchial lavage in differing severity groups and the effectiveness of nebulised therapies in different severities of BII.

          Graphical Abstract

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s13054-023-04718-w.

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          Most cited references39

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          Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome. The Acute Respiratory Distress Syndrome Network.

          Traditional approaches to mechanical ventilation use tidal volumes of 10 to 15 ml per kilogram of body weight and may cause stretch-induced lung injury in patients with acute lung injury and the acute respiratory distress syndrome. We therefore conducted a trial to determine whether ventilation with lower tidal volumes would improve the clinical outcomes in these patients. Patients with acute lung injury and the acute respiratory distress syndrome were enrolled in a multicenter, randomized trial. The trial compared traditional ventilation treatment, which involved an initial tidal volume of 12 ml per kilogram of predicted body weight and an airway pressure measured after a 0.5-second pause at the end of inspiration (plateau pressure) of 50 cm of water or less, with ventilation with a lower tidal volume, which involved an initial tidal volume of 6 ml per kilogram of predicted body weight and a plateau pressure of 30 cm of water or less. The primary outcomes were death before a patient was discharged home and was breathing without assistance and the number of days without ventilator use from day 1 to day 28. The trial was stopped after the enrollment of 861 patients because mortality was lower in the group treated with lower tidal volumes than in the group treated with traditional tidal volumes (31.0 percent vs. 39.8 percent, P=0.007), and the number of days without ventilator use during the first 28 days after randomization was greater in this group (mean [+/-SD], 12+/-11 vs. 10+/-11; P=0.007). The mean tidal volumes on days 1 to 3 were 6.2+/-0.8 and 11.8+/-0.8 ml per kilogram of predicted body weight (P<0.001), respectively, and the mean plateau pressures were 25+/-6 and 33+/-8 cm of water (P<0.001), respectively. In patients with acute lung injury and the acute respiratory distress syndrome, mechanical ventilation with a lower tidal volume than is traditionally used results in decreased mortality and increases the number of days without ventilator use.
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            High-frequency oscillation in early acute respiratory distress syndrome.

            Previous trials suggesting that high-frequency oscillatory ventilation (HFOV) reduced mortality among adults with the acute respiratory distress syndrome (ARDS) were limited by the use of outdated comparator ventilation strategies and small sample sizes. In a multicenter, randomized, controlled trial conducted at 39 intensive care units in five countries, we randomly assigned adults with new-onset, moderate-to-severe ARDS to HFOV targeting lung recruitment or to a control ventilation strategy targeting lung recruitment with the use of low tidal volumes and high positive end-expiratory pressure. The primary outcome was the rate of in-hospital death from any cause. On the recommendation of the data monitoring committee, we stopped the trial after 548 of a planned 1200 patients had undergone randomization. The two study groups were well matched at baseline. The HFOV group underwent HFOV for a median of 3 days (interquartile range, 2 to 8); in addition, 34 of 273 patients (12%) in the control group received HFOV for refractory hypoxemia. In-hospital mortality was 47% in the HFOV group, as compared with 35% in the control group (relative risk of death with HFOV, 1.33; 95% confidence interval, 1.09 to 1.64; P=0.005). This finding was independent of baseline abnormalities in oxygenation or respiratory compliance. Patients in the HFOV group received higher doses of midazolam than did patients in the control group (199 mg per day [interquartile range, 100 to 382] vs. 141 mg per day [interquartile range, 68 to 240], P<0.001), and more patients in the HFOV group than in the control group received neuromuscular blockers (83% vs. 68%, P<0.001). In addition, more patients in the HFOV group received vasoactive drugs (91% vs. 84%, P=0.01) and received them for a longer period than did patients in the control group (5 days vs. 3 days, P=0.01). In adults with moderate-to-severe ARDS, early application of HFOV, as compared with a ventilation strategy of low tidal volume and high positive end-expiratory pressure, does not reduce, and may increase, in-hospital mortality. (Funded by the Canadian Institutes of Health Research; Current Controlled Trials numbers, ISRCTN42992782 and ISRCTN87124254, and ClinicalTrials.gov numbers, NCT00474656 and NCT01506401.).
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              ISBI Practice Guidelines for Burn Care.

              (2016)
              Practice guidelines (PGs) are recommendations for diagnosis and treatment of diseases and injuries, and are designed to define optimal evaluation and management. The first PGs for burn care addressed the issues encountered in developed countries, lacking consideration for circumstances in resource-limited settings (RLS). Thus, the mission of the 2014-2016 committee established by the International Society for Burn Injury (ISBI) was to create PGs for burn care to improve the care of burn patients in both RLS and resource-abundant settings. An important component of this effort is to communicate a consensus opinion on recommendations for burn care for different aspects of burn management. An additional goal is to reduce costs by outlining effective and efficient recommendations for management of medical problems specific to burn care. These recommendations are supported by the best research evidence, as well as by expert opinion. Although our vision was the creation of clinical guidelines that could be applicable in RLS, the ISBI PGs for Burn Care have been written to address the needs of burn specialists everywhere in the world.
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                Author and article information

                Contributors
                suveer.singh@imperial.ac.uk
                Journal
                Crit Care
                Critical Care
                BioMed Central (London )
                1364-8535
                1466-609X
                27 November 2023
                27 November 2023
                2023
                : 27
                : 459
                Affiliations
                [1 ]Faculty of Medicine, Imperial College London, ( https://ror.org/041kmwe10) London, UK
                [2 ]GRID grid.417188.3, ISNI 0000 0001 0012 4167, Department of Anesthesia and Pain Management, , Toronto Western Hospital, University Health Network, ; Toronto, ON Canada
                [3 ]Inserm UMR-S 942, Cardiovascular Markers in Stress Conditions (MASCOT), University of Paris Cité, ( https://ror.org/05f82e368) Paris, France
                [4 ]Department of Intensive Care and Anaesthesia, Chelsea and Westminster Hospital NHS Foundation Trust, ( https://ror.org/02gd18467) London, UK
                [5 ]Department of Surgery and Cancer, Imperial College London, ( https://ror.org/041kmwe10) London, UK
                [6 ]Intensive Care National Audit and Research Centre, ( https://ror.org/057b2ek35) London, UK
                [7 ]Department of Médicine, Critical Care Division, Centre Hospitalier de l’Université de Montréal, ( https://ror.org/0410a8y51) Montréal, Canada
                [8 ]Department of Medicine, Université de Montréal, ( https://ror.org/0161xgx34) Montréal, Canada
                [9 ]Victorian Adult Burns Service, Alfred Health, ( https://ror.org/04scfb908) Melbourne, Australia
                [10 ]Department of Surgery, Central Clinical School, Monash University, ( https://ror.org/02bfwt286) Melbourne, Australia
                [11 ]GRID grid.498924.a, ISNI 0000 0004 0430 9101, University Hospital South Manchester, ; Wythenshawe, UK
                [12 ]Department of Intensive Care, Alfred Health, ( https://ror.org/04scfb908) Melbourne, Australia
                [13 ]Australian and New Zealand Intensive Care Research Centre, Monash University, ( https://ror.org/02bfwt286) Melbourne, Australia
                [14 ]Department of Anaesthesia, Queen Victoria Hospital NHS Foundation Trust, ( https://ror.org/03bs2yy11) East Grinstead, UK
                [15 ]Ross Tilley Burn Center, Department of Surgery, Sunnybrook Health Science Center, ( https://ror.org/03wefcv03) Toronto, ON Canada
                [16 ]Departments of Surgery and Immunology, University of Toronto, ( https://ror.org/03dbr7087) Toronto, ON Canada
                [17 ]Department of Burns, Plastic and Reconstructive Surgery, Chelsea and Westminster Hospital NHS Foundation Trust, ( https://ror.org/02gd18467) London, UK
                [18 ]GRID grid.266102.1, ISNI 0000 0001 2297 6811, Department of Anesthesia and Perioperative Care, Division of Critical Care Medicine, , University of California, ; San Francisco, USA
                [19 ]Investigation Network Initiative-Cardiovascular and Renal Clinical Trialists Network, Nancy, France
                [20 ]Department of Anaesthesia and Burns Intensive Care, St Andrew’s Centre for Burns and Plastic Surgery, Broomfield Hospital, ( https://ror.org/00hn92440) Chelmsford, UK
                [21 ]GRID grid.416409.e, ISNI 0000 0004 0617 8280, Department of Intensive Care Medicine, Multidisciplinary Intensive Care Research Organization (MICRO), , St James Hospital, ; Dublin, Ireland
                [22 ]GRID grid.10403.36, ISNI 0000000091771775, Department of Respiratory Medicine, , Hospital Clinic, IDIBAPS, CIBERes, ; Barcelona, Spain
                [23 ]Universitat Barcelona, ( https://ror.org/021018s57) Barcelona, Spain
                [24 ]GRID grid.8515.9, ISNI 0000 0001 0423 4662, Service of Adult Intensive Care, , Lausanne University Hospital, ; Lausanne, Switzerland
                [25 ]Department of Gastroenterology, University College London Hospitals NHS Foundation Trust, ( https://ror.org/042fqyp44) London, UK
                [26 ]GRID grid.8217.c, ISNI 0000 0004 1936 9705, Trinity College, ; Dublin, Ireland
                [27 ]GRID grid.416409.e, ISNI 0000 0004 0617 8280, Department of Plastic and Reconstructive Surgery, , St James’ Hospital, ; Dublin, Ireland
                [28 ]Burns Unit, Queen Victoria Hospital NHS Foundation Trust, ( https://ror.org/03bs2yy11) East Grinstead, UK
                [29 ]Fiona Stanley Hospital, ( https://ror.org/027p0bm56) Perth, Australia
                [30 ]GRID grid.518128.7, ISNI 0000 0004 0625 8600, Perth Children’s Hospital, ; Perth, Australia
                [31 ]University of Western Australia, ( https://ror.org/047272k79) Perth, Australia
                [32 ]Welsh Centre for Burns and Plastic Surgery, Morriston Hospital, ( https://ror.org/01p830915) Swansea, UK
                [33 ]Department of Research and Development, Chelsea and Westminster Hospital NHS Foundation Trust, ( https://ror.org/02gd18467) London, UK
                [34 ]Academic Department of Anaesthesia, Pain Management and Intensive Care (APMIC), Imperial College London, ( https://ror.org/041kmwe10) London, UK
                [35 ]Royal Brompton Hospital, Guy’s and St Thomas’ Hospitals NHS Foundation Trust, ( https://ror.org/00cv4n034) London, UK
                Author information
                http://orcid.org/0000-0003-3219-8966
                Article
                4718
                10.1186/s13054-023-04718-w
                10680253
                38012797
                b09fba24-afe7-48cd-85b6-d50605d41965
                © The Author(s) 2023

                Open Access This 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
                : 13 September 2023
                : 31 October 2023
                Funding
                Funded by: British Journal of Anaesthesia (BJA)/Royal College of Anaesthetists (RCoA)
                Categories
                Research
                Custom metadata
                © BioMed Central Ltd., part of Springer Nature 2023

                Emergency medicine & Trauma
                burn inhalation injury,smoke inhalation injury,burns,acute lung injury,acute respiratory distress syndrome,bronchoscopy,endotracheal intubation,mechanical ventilation,heparin

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