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      Microbiology in minimally invasive autopsy: best techniques to detect infection. ESGFOR (ESCMID study group of forensic and post-mortem microbiology) guidelines

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          Abstract

          This manuscript aims to: 1) provide specific guidelines on PMM techniques in the setting of minimally invasive autopsy (MIA), both for pathologists collecting samples and for microbiologists advising pathologists and interpreting the results and 2) introduce standardization in PMM sampling at MIA. Post-mortem microbiology (PMM) is crucial to identify the causative organism in deaths due to infection. MIA including the use of post-mortem (PM) computed tomography (CT) and PM magnetic resonance imaging (MRI), is increasingly carried out as a complement or replacement for the traditional PM. In this setting, mirroring the traditional autopsy, PMM aims to: detect infectious organisms causing sudden unexpected deaths; confirm clinically suspected but unproven infection; evaluate the efficacy of antimicrobial therapy; identify emergent pathogens; and recognize medical diagnostic errors. Meaningful interpretation of PMM results requires careful evaluation in the context of the clinical history, macroscopic and microscopic findings. These guidelines were developed by a multidisciplinary team with experts in various fields of microbiology and pathology on behalf of the ESGFOR (ESCMID – European Society of Clinical Microbiology and Infectious Diseases - Study Group of Forensic and Post-mortem Microbiology, in collaboration with the ESP -European Society of Pathology-) based on a literature search and the author’s expertise. Microbiological sampling methods for MIA are presented for various scenarios: adults, children, developed and developing countries. Concordance between MIA and conventional invasive autopsy is substantial for children and adults and moderate for neonates and maternal deaths. Networking and closer collaboration among microbiologists and pathologists is vital to maximize the yield of PMM in MIA.

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          Most cited references69

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          Characteristics of pediatric SARS-CoV-2 infection and potential evidence for persistent fecal viral shedding

          We report epidemiological and clinical investigations on ten pediatric SARS-CoV-2 infection cases confirmed by real-time reverse transcription PCR assay of SARS-CoV-2 RNA. Symptoms in these cases were nonspecific and no children required respiratory support or intensive care. Chest X-rays lacked definite signs of pneumonia, a defining feature of the infection in adult cases. Notably, eight children persistently tested positive on rectal swabs even after nasopharyngeal testing was negative, raising the possibility of fecal–oral transmission.
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            Relation Between Chest CT Findings and Clinical Conditions of Coronavirus Disease (COVID-19) Pneumonia: A Multicenter Study

            OBJECTIVE. The increasing number of cases of confirmed coronavirus disease (COVID-19) in China is striking. The purpose of this study was to investigate the relation between chest CT findings and the clinical conditions of COVID-19 pneumonia. MATERIALS AND METHODS. Data on 101 cases of COVID-19 pneumonia were retrospectively collected from four institutions in Hunan, China. Basic clinical characteristics and detailed imaging features were evaluated and compared between two groups on the basis of clinical status: nonemergency (mild or common disease) and emergency (severe or fatal disease). RESULTS. Patients 21-50 years old accounted for most (70.2%) of the cohort, and five (5.0%) patients had disease associated with a family outbreak. Most patients (78.2%) had fever as the onset symptom. Most patients with COVID-19 pneumonia had typical imaging features, such as ground-glass opacities (GGO) (87 [86.1%]) or mixed GGO and consolidation (65 [64.4%]), vascular enlargement in the lesion (72 [71.3%]), and traction bronchiectasis (53 [52.5%]). Lesions present on CT images were more likely to have a peripheral distribution (88 [87.1%]) and bilateral involvement (83 [82.2%]) and be lower lung predominant (55 [54.5%]) and multifocal (55 [54.5%]). Patients in the emergency group were older than those in the non-emergency group. Architectural distortion, traction bronchiectasis, and CT involvement score aided in evaluation of the severity and extent of the disease. CONCLUSION. Patients with confirmed COVID-19 pneumonia have typical imaging features that can be helpful in early screening of highly suspected cases and in evaluation of the severity and extent of disease. Most patients with COVID-19 pneumonia have GGO or mixed GGO and consolidation and vascular enlargement in the lesion. Lesions are more likely to have peripheral distribution and bilateral involvement and be lower lung predominant and multifocal. CT involvement score can help in evaluation of the severity and extent of the disease.
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              Autopsy in suspected COVID-19 cases

              The severe acute respiratory syndrome (SARS)-coronavirus-2 (CoV-2) outbreak in Wuhan, China, has now spread to many countries across the world including the UK with over 3000 deaths as of early March 2020. This will inevitably lead to an increase in the number of suspected coronavirus disease 2019 (COVID-19)-related deaths at autopsy. The Royal College of Pathologists has responded to this concern with the release of guidelines on autopsy practice relating to COVID-19. The following article is a summary and interpretation of these guidelines. It includes a description of hazard group 3 organisms to which SARS-CoV-2 has been assigned, a brief description of what is currently known about the pathological and autopsy findings in COVID-19, a summary of the recommendations for conducting autopsies in suspected COVID-19 cases and the techniques for making the diagnosis at autopsy. It concludes by considering the clinicopathological correlation and notification of such cases.
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                Author and article information

                Contributors
                amparo.fernandezrodriguez@justicia.es
                Journal
                Forensic Sci Med Pathol
                Forensic Sci Med Pathol
                Forensic Science, Medicine, and Pathology
                Springer US (New York )
                1547-769X
                1556-2891
                19 January 2021
                : 1-14
                Affiliations
                [1 ]GRID grid.410569.f, ISNI 0000 0004 0626 3338, Clinical Laboratory, Sint-Niklaas, and Infection Control Department, , AZ Nikolaas, University Hospitals Leuven, ; Moerlandstraat 1Herestraat 49, 91003000 Leuven, Belgium
                [2 ]GRID grid.413991.7, ISNI 0000 0004 0641 6082, FT. Histopathology Department. Western Bank, , Sheffield Children’s Hospital NHS, ; Sheffield, S10 2TH UK
                [3 ]The Medico-Legal Centre, Watery Street, Sheffield, UK
                [4 ]GRID grid.434607.2, ISNI 0000 0004 1763 3517, ISGlobal, Barcelona Centre for International Health Research (CRESIB), ; Barcelona, Spain
                [5 ]GRID grid.410458.c, ISNI 0000 0000 9635 9413, Department of Microbiology, , Hospital Clínic, Universitat de Barcelona, ; Barcelona, Spain
                [6 ]GRID grid.410458.c, ISNI 0000 0000 9635 9413, Department of Pathology, , Hospital Clínic, Universitat de Barcelona, ; Barcelona, Spain
                [7 ]GRID grid.11835.3e, ISNI 0000 0004 1936 9262, Department of Oncology and Metabolism, Department of Radiology, , Academic Unit of Child Health, Sheffield Children’s NHS FT, University of Sheffield, ; Sheffield, UK
                [8 ]GRID grid.419242.8, ISNI 0000 0004 0448 3476, Microbiology Laboratory, Biology Department, , Instituto Nacional de Toxicología y Ciencias Forenses, Las Rozas de Madrid, ; Madrid, Spain
                Author information
                http://orcid.org/0000-0003-0439-0205
                http://orcid.org/0000-0001-5534-444X
                http://orcid.org/0000-0001-8991-5036
                http://orcid.org/0000-0002-2992-3226
                Article
                337
                10.1007/s12024-020-00337-x
                7814172
                33464531
                bddb43de-4993-427c-863e-8b28f2fbdc90
                © Springer Science+Business Media, LLC, part of Springer Nature 2021

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 2 November 2020
                Categories
                Review

                Forensic science
                traditional autopsy,forensic sampling,infection,forensic microbiology,minimally invasive autopsy,post-mortem microbiology

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