Abstract

BackgroundPulmonary involvement in COVID-19 is characterized pathologically by diffuse alveolar damage (DAD) and thrombosis, leading to the clinical picture of Acute Respiratory Distress Syndrome. The direct action of SARS-CoV-2 in lung cells and the dysregulated immuno-coagulative pathways activated in ARDS influence pulmonary involvement in severe COVID, that might be modulated by disease duration and individual factors. In this study we assessed the proportions of different lung pathology patterns in severe COVID-19 patients along the disease evolution and individual characteristics.MethodsWe analysed lung tissue from 41 COVID-19 patients that died in the period March–June 2020 and were submitted to a minimally invasive autopsy. Eight pulmonary regions were sampled. Pulmonary pathologists analysed the H&E stained slides, performing semiquantitative scores on the following parameters: exudative, intermediate or advanced DAD, bronchopneumonia, alveolar haemorrhage, infarct (%), arteriolar (number) or capillary thrombosis (yes/no). Histopathological data were correlated with demographic-clinical variables and periods of symptoms-hospital stay.ResultsPatient´s age varied from 22 to 88 years (18f/23 m), with hospital admission varying from 0 to 40 days. All patients had different proportions of DAD in their biopsies. Ninety percent of the patients presented pulmonary microthrombosis. The proportion of exudative DAD was higher in the period 0–8 days of hospital admission till death, whereas advanced DAD was higher after 17 days of hospital admission. In the group of patients that died within eight days of hospital admission, elderly patients had less proportion of the exudative pattern and increased proportions of the intermediate patterns. Obese patients had lower proportion of advanced DAD pattern in their biopsies, and lower than patients with overweight. Clustering analysis showed that patterns of vascular lesions (microthrombosis, infarction) clustered together, but not the other patterns. The vascular pattern was not influenced by demographic or clinical parameters, including time of disease progression.ConclusionPatients with severe COVID-19 present different proportions of DAD patterns over time, with advanced DAD being more prevalent after 17 days, which seems to be influenced by age and weight. Vascular involvement is present in a large proportion of patients, occurs early in disease progression, and does not change over time.

Highlights

  • Several autopsy studies have described lung pathology in patients that died due to SARS-CoV-2 infection, showing that most of the patients presented different stagesMauad et al Respir Res (2021) 22:32 of diffuse alveolar damage (DAD) and a high frequency of macro and microvascular thrombosis, leading to the clinical picture of Acute Respiratory Distress Syndrome (ARDS) [1,2,3]

  • The direct action of SARS-CoV-2 in lung cells and the dysregulated immuno-coagulative pathways activated in ARDS may influence patterns and extension of pulmonary involvement in severe COVID-19, that are modulated by disease duration and individual factors

  • We investigated the pathology of severe fatal COVID-19 by implementing a protocol of ultrasound-guided minimally invasive autopsies (MIA/US) which was conceived to reduce the risk of obtaining post-mortem tissue samples in a disease with high contagiousness [3]

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Summary

Introduction

Several autopsy studies have described lung pathology in patients that died due to SARS-CoV-2 infection, showing that most of the patients presented different stagesMauad et al Respir Res (2021) 22:32 of diffuse alveolar damage (DAD) and a high frequency of macro and microvascular thrombosis, leading to the clinical picture of Acute Respiratory Distress Syndrome (ARDS) [1,2,3]. The direct action of SARS-CoV-2 in lung cells and the dysregulated immuno-coagulative pathways activated in ARDS may influence patterns and extension of pulmonary involvement in severe COVID-19, that are modulated by disease duration and individual factors. Polak et al performed a systematic review of 69 COVID-19 autopsies, showing changes compatible with acute DAD, fibroproliferative DAD and vascular pathology in the lungs. Pulmonary involvement in COVID-19 is characterized pathologically by diffuse alveolar damage (DAD) and thrombosis, leading to the clinical picture of Acute Respiratory Distress Syndrome. The direct action of SARSCoV-2 in lung cells and the dysregulated immuno-coagulative pathways activated in ARDS influence pulmonary involvement in severe COVID, that might be modulated by disease duration and individual factors. In this study we assessed the proportions of different lung pathology patterns in severe COVID-19 patients along the disease evolu‐ tion and individual characteristics

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Conclusion

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