Autopsy-Based Pulmonary and Vascular Pathology: Pulmonary Endotheliitis and Multi-Organ Involvement in COVID-19 Associated Deaths

Abstract

Background

Findings from autopsies have provided evidence on systemic microvascular damage as one of the underlying mechanisms of Coronavirus disease 2019 (CO­VID-19). The aim of this study was to correlate autopsy-based cause of death in SARS-CoV-2, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) positive patients with chest imaging and severity grade of pulmonary and systemic morphological vascular pathology.

Methods

Fifteen SARS-CoV-2 positive autopsies with clinically distinct presentations (age 22–89 years) were retrospectively analyzed with focus on vascular, thromboembolic, and ischemic changes in pulmonary and in extrapulmonary sites. Eight patients died due to COVID-19 associated respiratory failure with diffuse alveolar damage in various stages and/or multi-organ failure, whereas other reasons such as cardiac decompensation, complication of malignant tumors, or septic shock were the cause of death in 7 further patients. The severity of gross and histopathological changes was semi-quantitatively scored as 0 (absent), 1 (mild), and 3 (severe). Severity scores between the 2 groups were correlated with selected clinical parameters, initial chest imaging, autopsy-based cause of death, and compared using Pearson χ² and Mann-Whitney U tests.

Results

Severe pulmonary endotheliitis (p = 0.031, p = 0.029) and multi-organ involvement (p = 0.026, p = 0.006) correlated significantly with COVID-19 associated death. Pulmonary microthrombi showed limited statistical correlation, while tissue necrosis, gross pulmonary embolism, and bacterial superinfection did not differentiate the 2 study groups. Chest imaging at hospital admission did not differ either.

Conclusions

Extensive pulmonary endotheliitis and multi-organ involvement are characteristic autopsy features in fatal CO­VID-19 associated deaths. Thromboembolic and ischemic events and bacterial superinfections occur frequently in SARS-CoV-2 infection independently of outcome.

Introduction

Coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus is a challenge for health-care systems and for affected patients worldwide [1]. Hypoxic respiratory failure is the leading cause of death in patients with severe CO­VID-19 disease as is also seen in other respiratory viral infections. The general histological correlate of acute respiratory distress syndrome (ARDS) is diffuse alveolar damage (DAD) characterized by intra-alveolar hyaline membrane formation, edema, and hemorrhage in the acute stage, followed by fibroblast proliferation in the organizing stage. DAD is a nonspecific finding with a long list of potential etiologies, including other viral diseases, like influenza and SARS-CoV [2, 3, 4]. However, severe COVID-19 is associated with early pronounced gas exchange disturbance and particularly severe hypoxemic respiratory failure compared to the degree of radiographic abnormalities and more severe multi-organ failure compared to, for example, influenza, particularly in patients with vascular risk factors [2, 4, 5, 6].

Among the distinctive attributes of COVID-19 are associated microvascular changes and thrombosis [2, 7]. Endothelial cells not only play an important role in the pathogenesis of ARDS but also in the pathogenesis of multi-organ failure. This is thought to be due to vascular inflammation (endotheliitis) and mediating inflammatory cell infiltration as well as apoptotic bodies found in different organ systems [7, 8]. This systemic endotheliitis with evidence of modulation of vessel barrier integrity, promoting a pro-coagulative state could thus explain the disproportional hypoxemia in relation to radiological changes and complications seen in different organs in patients with COVID-19 [9]. Quantitative RT-PCR results for SARS-CoV-2 also demonstrated that SARS-CoV-2 has organotropism beyond the respiratory tract, including the heart, the brain, skin, subcutaneous tissue, neuromuscular system, the kidneys, the intestine, and the liver [5, 6, 10, 11, 12, 13, 14, 15]. Recent terms such as cardio-COVID-19 define the increased risk for cardiac injury, such as arrhythmias, fulminant myocarditis, while neuromuscular-COVID-19 refers to a broad spectrum of associated neuromuscular disorders, hyposmia, anosmia, etc [10, 11, 12].

Risk factors for a severe disease course of COVID-19, such as old age, obesity, hypertension, and diabetes mellitus are all risk factors for pre-existing vascular dysfunction with altered endothelial metabolism, and therefore might explain the worse outcome in these patient groups [16]. Since the outbreak of the pandemics, several further parameters including tissue-based factors have been identified in association with severe disease course in COVID-19 [5, 6, 13, 17, 18, 19]. Complement activation and increased neutrophilic infiltration of pulmonary capillaries and extracellular spaces (so called NETosis) have been described in autopsy studies and have been associated with an explosive inflammatory response and a poor prognosis in COVID-19 [17, 19, 20]. The interaction between viral-induced endothelial necrosis, excessive cytokine production (“cytokine storm”), and a systemic viral vasculopathy syndrome have been described in several autopsy-based studies [5, 13, 18, 20]. A recent meta-analysis on published COVID-19 autopsies conclude that DAD is the most common pulmonary mortality cause and that a broad spectrum of ischemic necrosis, endotheliitis, and thromboembolism characterize extrapulmonary COVID-19 disease [6]. Different from other respiratory pandemics, such as in SARS-CoV-1, the extensive thromboembolic events and multifocal endotheliitis is more often seen in COVID-19 [6]. Damaged endothelial cell activation and increased plasma von Willebrand factor antigen have been described as the key drivers in severe COVID-19 disease along with associated coagulopathy [21, 22, 23]. Whether a sum of the aforementioned factors or any single parameter alone may contribute to poor prognosis or can predict lethal outcome in COVID-19 is a challenging question to address in individual patients.

The aim of this study was to correlate autopsy-based cause of death in SARS-CoV-2 positive autopsies with selected clinical parameters and with the severity grade of pulmonary and systemic morphological vascular pathology. We addressed the questions (a) whether SARS-CoV-2 infection has any distinct morphological vascular pattern depending on the autopsy-based cause of death, (b) if pulmonary thromboembolic events and bacterial superinfection have an impact on COVID-19-associated death, (c) how the involvement of extrapulmonary sites affects fatal outcome, and (d) if some clinical parameter may correlate with morphological findings or cause of death identified at autopsy. In order to answer these questions, we analyzed 15 SARS-CoV-2 positive autopsies with 2 distinct clinical late phase disease patterns: 8 patients deceased due to CO­VID-19 associated respiratory or multi-organ failure and 7 patients died due to other reasons based on autopsy results.

Material and Methods

Postmortem examinations on 15 SARS-CoV-2 positive deceased patients were performed at the Institute of Pathology and Molecular Pathology of the University Hospital Zurich, Switzerland, according to standard procedures in a biosafety level 3 isolation room.

The diagnosis of SARS-CoV-2 infection was confirmed by real-time reverse transcriptase-polymerase chain reaction testing (rRT-PCR) on nasopharyngeal swabs prior to and during hospitalization in 14 of 15 patients. In 1 patient (patient 2), postmortem formalin-fixed and paraffin-embedded (FFPE) lung tissue was positive for SARS-CoV-2 using rRT-PCR in the Reference Infectious Pathology of Switzerland in the Institute of Pathology Cantonal Hospital Liestal Switzerland using the methodology as described earlier [5]. In all patients, a complete autopsy was performed including macroscopic organ assessment and histological analysis of a predefined organ list. The organs of the central nervous systems were examined in the Institute of Neuropathology, University Hospital Zurich (in collaboration with KF).

For histological diagnosis, tissue sections from FFPE tissues (2 μm) from all organs (fixed in 4% paraformaldehyde) were stained with hematoxylin and eosin (H&E) according to standard techniques. The diagnoses and histopathological features in this study were carried out on gross examination and using routine H&E stains on tissue sections. Fibrin thrombi were confirmed with fibrin stains (modified Picro-Mallory stain). A large subset of cases underwent further immunohistochemistry analyzes and were characterized by a panel of lympho- and hematopoietic and further markers (such as CD3, CD4, CD45, CD68, and ACE2). Selected lung, kidney, and heart samples were tested for the presence of viral particles and viral-like particles using FFPE or frozen snap tissues for immunofluorescence (in collaboration with XZ) and glutaraldehyde fixed samples for electron microscopy (in collaboration with FS) as described earlier [5, 24, 25]. Postmortal swabs and FFPE samples of selected organs in a subset of autopsies were tested for SARS-CoV-2 by rRT-PCR as described above.

Patient Cohort

Altogether, 15 autopsies with SARS-CoV-2 infection were included in this study. The first autopsy was performed in March 2020 and the autopsy of the last included subject was performed in January 2021. Ten patients were male and 5 patients were female. Age at the time of the autopsy ranged between 22 and 89 years (median 72.9 years). All 15 patients were hospitalized (2–40 days, median 16.6 days). Five patients were not mechanically ventilated (do not intubate order) and 10 patients were intubated (intubation time ranged between 1 and 24 days [median 11.5 days]). Cardiovascular risk factors were present in all 15 patients: hypertension in 10 of 15 patients (67%), diabetes mellitus in 2 of 15 patients (13%), and smoking in 6 of 15 patients (40%), in 3 of 15 patients, there was no information on smoking from patient history. Obesity defined as body mass index >30 kg/m² was present in 6 of 15 patients (40%). Comorbidities included COPD (2 of 15), pulmonary hypertension (2 of 15), chronic interstitial lung disease (3 of 15), asthma (1 of 15), coronary artery disease (4 of 15), hypertensive heart disease (2 of 15), atrial fibrillation (7 of 15), chronic renal failure (7 of 15), current malignant tumor (3 of 15), recurrence-free malignant tumor (3 of 15), solid organ transplantation (2 of 15), autoimmune disorder (1 of 15), hematological disease (2 of 15), and depression (3 of 15). Clinical data are shown Table 1.

Table 1.

Clinical parameters in both groups with SARS-CoV-2 infection (patients 1–8 died from severe COVID-19, patients 9–15 died due other causes)

Clinical characteristics	Patient
	1°	2°	3°	4°	5+	6+	7+	8+	9	10	11	12	13	14	15
Age, years	70	77	58	79	56	61	79	72	22	69	67	87	58	89	78
Sex	M	F	F	M	M	M	M	M	M	F	M	F	F	M	M
BMI, kg/m2	22.7	24.5	37	33.7	34.2	30.9	22.6	23.1	27.8	31.1	27.5	35	27.2	19.8	27.7
Days in hospital until death	8	9	18	7	19	20	18	40	1	32	11	5	23	2	28
Days intubated	8	0	17	0	15	1	0	20	1	0	10	4	15	0	24
Cardiovascular risk factors
Hypertension	Yes	Yes	Yes	Yes	No	No	Yes	Yes	No	Yes	No	Yes	Yes	Yes	Yes
Diabetes	No	No	Yes	No	No	No	No	No	No	No	No	No	Yes	No	No
Smoking (packs per year)	Yes*	0	N/A	Yes*	0	0	60	7.5	Yes*	0	N/A	N/A	0	0	Yes*
Obesity1	No	No	Yes	Yes	Yes	Yes	No	No	No	Yes	No	Yes	No	No	No
Comorbidities
COPD	No	No	No	No	No	No	Yes	No	No	No	Yes	No	No	No	No
Pulmonary hypertension	No	No	No	Yes	No	No	No	No	No	No	No	Yes	No	No	No
Interstitial lung disease	No	No	No	Yes	No	No	No	No	No	No	No	No	Yes	No	Yes
Asthma	No	No	No	No	No	No	No	No	Yes	No	No	No	No	No	No
Coronary artery disease	Yes	No	No	No	No	No	Yes	No	No	No	No	No	No	Yes	Yes
Hypertension cardiopathy	No	No	Yes	No	No	No	Yes	No	No	No	No	No	No	No	No
Atrial fibrillation	Yes	No	No	Yes	Yes	Yes	Yes	Yes	No	No	No	Yes	No	No	No
Chronic renal failure	Yes	No	No	Yes	Yes	No	No	Yes	No	Yes	No	No	No	Yes	Yes
Malignant solid tumor (current)	No	No	No	No	No	No	No	No	No	Yes	Yes	No	No	Yes	No
Malignant solid tumor (recurrence free)	No	Yes	No	No	Yes	No	Yes	No	No	No	No	No	No	No	No
Solid organ transplantation	Yes	No	No	No	Yes	No	No	No	No	No	No	No	No	No	No
Autoimmune disease	No	No	No	No	No	No	No	No	No	No	No	No	Yes	No	No
Hematological disorder	No	No	No	Yes	No	Yes	No	No	No	No	No	No	No	No	No
Depression	No	Yes	No	No	No	No	No	Yes	No	No	No	No	Yes	No	No
Severity of disease
SOFA (mean)	12	N/A	12.3	N/A	11.5	10.5	N/A	10.9	17	N/A	12	11.5	7.4	N/A	8.75
SOFA (max)	14	N/A	19	N/A	16	15	N/A	18	17	N/A	12	12	11	N/A	11
SOFA (delta)2	2	N/A	11	N/A	7	9	N/A	12	0	N/A	5	1	−3	N/A	8

Patients 9–15 died due to other causes. N/A, not assessed; SOFA, Sequential Organ Failure Assessment; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; COVID-19, coronavirus disease 2019; BMI, body mass index.

¹Obesity was defined as BMI >30.

²Difference of SOFA score upon admission and last registered score.

^°Patient of the first COVID-19 wave − death due to COVID-19.

⁺Patient of second COVID-19 wave − death due to COVID-19.

^*Current/former smoker − pack years not assessed.

Statistical Analyses

Statistical analysis was performed using IBM SPSS Statistics for Windows, Version 26.0. IBM Corp., Armonk, NY, USA. The Mann-Whitney U test and Pearson R test were used for comparison of morphological findings in autopsy tissue between groups. p value <0.05 was regarded as statistically significant. Parameters being statistically significant with both tests were weighted as biologically relevant. Graphics were plotted using GraphPadPrism (version 9.0).

Scoring of Autopsy Findings and Definition of Groups

Definition of Severity Scores

Macro- and histopathological scoring: Various parameters were scored according to the severity of histological appearance and/or gross findings. Score 0: absent (not apparent on H&E section and/or not evident with ancillary immunohistochemistry). Low intensity as score 1 (discrete and modest changes were pooled in 1 low intensity score 1): discrete (score 1) and modest (score 2) presence of macro -und histopathological feature only in small anatomical compartments and in focal (only 1 anatomical region) or only in scattered (in max. 2 anatomical compartments per organ) distribution. Ancillary tests were used if not apparent on H&E staining. Score 3: diffuse expression of the feature involving multiple (>2 foci per organ) anatomical compartments.

Multi-organ involvement and necrosis scoring: 1 score point was allocated to each organ showing histological signs of endotheliitis or necrosis, respectively. The sum of all affected organs was taken as the final score.

Definition of Biological Groups

To test the hypothesis “correlation of morphological autopsy findings with clinical course/severity/cause of death in SARS-Cov-2 positive deceased patients”, autopsy cases were assigned to 1 of 2 groups. Group 1: “Death due to COVID-19” were patients with fatal course of COVID-19 disease − hospitalized due to COVID-19 and autopsy-based cause of death was due to respiratory or cardio-respiratory failure with diffuse alveolar damage. Group 2: “Death due to other causes” were SARS-CoV-2 positive patients, with or without clinical symptoms of COVID-19 and death defined at autopsy due to other causes such as underlying disease, for example, malignancy or hematological disorder (Table 2).

Table 2.

Cause of death based on overall findings at autopsy

Patient	Cause of death	Death due to COVID-19
1°	Respiratory failure with diffuse alveolar damage	Yes
2°	Respiratory failure with diffuse alveolar damage	Yes
3°	Respiratory failure with diffuse alveolar damage	Yes
4°	Respiratory failure with diffuse alveolar damage	Yes
5	Respiratory failure with diffuse alveolar damage	Yes
6	Respiratory failure with diffuse alveolar damage	Yes
7	Respiratory failure with diffuse alveolar damage	Yes
8	Respiratory failure with diffuse alveolar damage	Yes
9	Acute myocardial infarction	No
10	Complication, metastatic colorectal cancer	No
11	Complication, metastatic non-small cell lung cancer	No
12	Cardiac decompensation and pulmonary hypertension	No
13	Cardio-respiratory insufficiency due to chronic interstitial lung disease	No
14	Complication, metastatic malignant melanoma	No
15	Septic shock and pulmonary aspergillosis	No

COVID-19, coronavirus disease 2019. Patients of first COVID-19 wave.

Results

Postmortem Pulmonary Findings

Gross Findings

Macroscopic examination of the lungs was in line with full ARDS in 8 cases (Nr 1–8, 100% of the group) and showed a broad panel of gross lesions in 7 further cases. There were bilateral diffuse or focal, partially confluent large pale to yellowish hemorrhagic zones of consolidation and edema (shown in Fig. 1d, h). Macroscopic pulmonary infarction was evident in 6 of 15 cases (40%), macroscopic thromboembolism in 5 of 15 cases (30%).

Fig. 1.

Histological vascular and gross pulmonary vascular findings in SARS-CoV-2 positive autopsies. Images demonstrate severe grade of vascular changes (larger involved areas and high number of foci) (a–d), images show mild grade morphological changes (smaller or only scattered areas involved) (e–h). Numerous (a) and only scattered (e) lymphocytes beneath the endothelium. Multiple middle- and small-sized (b and c) and only scattered small-sized peripheral (f, g) fibrin and leucocytic thrombi. Large multiple areas (d) and only small foci (h) of pulmonary hemorrhagic infarction and consolidation. a−g: H & E stain. b (inset): modified Picro-Mallory stain. H&E, hematoxylin and eosin; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2.

Histological Findings

Microscopic examination of the lungs revealed signs of DAD in different stages in 8 patients (53%) who died from COVID-19. Bronchopneumonia was identified in 8 of 15 cases (53%). Endotheliitis of small and medium-sized pulmonary vessels was seen in all but 1 patient (14 of 15, 93%) (Fig. 1a, e). Fibrin thrombi were evident in 7 of 15 cases (47%) (Fig. 1b, f) and leucocytic vessel occlusion (“leucocytic thrombi”) in 9 of 15 cases (60%) (Fig. 1c, g). Thrombotic vessel occlusions were noted within a few small pulmonary artery branches as often seen in DAD but also in small to medium-sized vessels and in areas not affected by DAD.

The extension of pulmonary endotheliitis significantly correlated with autopsy-based cause of death due to COVID-19 (R-test p = 0.031, U test p = 0.029) (Fig. 2a, 3a). Individual severity scores of macro and microscopic pathology findings are shown in Table 3.

Fig. 2.

Correlation between severity scores of macroscopic and histopathological findings and autopsy-based cause of death in SARS-CoV-2 positive autopsies. Axe Y demonstrates mean score per gross or histopathological pulmonary findings (a) and of organ involvement (b). Axe X shows the distribution of autopsy findings in terms of cause of death identified at the autopsy. The extension of pulmonary endotheliitis and the evidence of multi-organ involvement correlated significantly with COVID-19 associated cause of death. Individual scores are shown in Table 3. Statistical correlation between scores and autopsy-based cause of death is shown in Table 4. SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; COVID-19, coronavirus disease 2019; CT, computed tomography.

Fig. 3.

a The extension of pulmonary endotheliitis (R-test p = 0.031, U test p = 0.029) and b) the evidence of multi-organ involvement (R-test p = 0.026, U test p = 0.006) correlated significantly with CO­VID-19 associated cause of death (Pearson χ² and Mann-Whitney tests). COVID-19, coronavirus disease 2019.

Table 3.

Scores of histological and gross macroscopic findings at autopsy

Histological scoring	Patients
	1°	2°	3°	4°	5+	6+	7+	8+	9	10	11	12	13	14	15
Lung1
Endotheliitis2	3	3	3	1	3	1	3	1	0	1	1	1	1	1	1
Fibrin thrombi2	1	1	1	1	3	0	1	0	0	0	1	0	0	0	0
Leucocytic thrombi2	3	1	1	0	3	0	1	0	0	0	3	1	1	1	0
Infarction	1	0	0	0	3	3	3	3	0	0	0	0	0	1	0
Bronchopneumonia2	0	0	0	0	1	0	1	3	3	0	3	0	1	3	3
Macroscopic thrombi	0	0	0	0	1	3	3	3	1	0	0	0	0	0	0
Heart1
Endotheliitis2	1	1	1	1	3	0	3	1	1	1	1	0	1	1	0
Fibrin thrombi2	1	0	1	1	3	0	3	0	0	0	0	0	0	0	0
Leucocytic thrombi2	0	0	3	0	3	0	3	0	0	0	1	1	1	1	0
All organ systems
Involved organs	5	2	4	3	2	3	3	4	2	2	2	1	2	2	1
Endotheliitis in different organs2, 3	9	2	8	5	6	3	9	3	2	2	2	1	2	2	1
Necrosis in different organs	3	0	2	1	3	1	4	0	1	1	2	2	2	2	1

Patients 9–15 died due to other causes. COVID-19, coronavirus disease 2019.

¹Pooled low intensity score 1 versus high intensity score 3.

²Microscopic evaluation only.

³Sum score of all affected organs.

^°Patients of the first COVID-19 wave, death due to COVID-19.

⁺Patients of second COVID-19 wave, death due to COVID-19.

Viral RNA was evident in 30–80% of selected organs in 10 of 15 autopsies, being the highest in lung samples and showing a lower but similar distribution in the extrapulmonary organs (see online suppl. Fig. 1; see www.karger.com/doi/10.1159/000518914 for all online suppl. material). There was no statistically significant difference in RNA positive samples between the 2 study groups (χ² test, p = 0.991, not significant at p < 0.05).

Chest CT Morphology

Chest computed tomography (CT) at initial hospital admission showed a different extent of bilateral pulmonary ground-glass opacities and consolidations in both autopsy groups. Severe or mild vascular damage at autopsy did not correlate with the extent of pulmonary ground-glass opacities, which was evidenced in patients who died due to COVID-19 and those who succumbed to other underlying causes (Fig. 4a-d).

Fig. 4.

Chest CT morphology in SARS-CoV-2 infected and deceased patients at initial hospital admission. CT images show no correlation to different extent of histopathological and gross vascular changes at the autopsy and are not associated with clinical course. Images (a, c) show diffuse bilateral pulmonary consolidations (with severe and mild histopathological changes, respectively). Image (b) displays focal consolidations at severe histopathological findings at autopsy. Image (d) shows diffuse bilateral pulmonary consolidations at only mild histopathological changes at autopsy. SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; COVID-19, coronavirus disease 2019; CT, computed tomography.

Vascular Postmortem Findings in Further Organ Involvement

Heart

Endotheliitis was a frequent finding in the small intramyocardial and subepicardial vessels present in all but 2 cases (13/15). Fibrin thrombi were less frequent (5 of 15 cases, 30%) and leucocytic thrombi in 7 of 15 cases (47%).

Kidney

Acute tubular necrosis was a frequent finding seen in 13 of 15 patients (87%). In contrast to the lungs and the heart, the kidneys demonstrated only very mild endotheliitis with few infiltrating cells in 2 of 15 patients (13%).

Liver

Patchy centrilobular hepatocyte necrosis and confluent necrosis associated with fibrin thrombi in the respective vessels were found in those patients with multi-organ failure (in 8 of 15 cases [53%]).

Small Intestine

Small intestine necrosis was present in 4 of 15 patients (27%), leading in the setting of multi-organ failure to death in all 4 patients. Identical histomorphological changes were seen in all cases, with microangiopathic chances of the submucosal vessels consisting of fibrin thrombi, endotheliitis, and apoptotic endothelial cells. Individual severity scores of pathology findings are shown in Table 3.

Association between cause of death based on autopsy findings and vascular manifestations of COVID-19

Severe pulmonary endotheliitis (R-test p = 0.031, U test p = 0.029) and multi-organ involvement of CO­VID-19 (R-test p = 0.026, U test p = 0.006) correlated significantly with COVID-19 associated death (Fig. 2, 3; Table 4). Histological evidence of small fibrin thrombi was more frequent in COVID-19 associated death (U test p = 0.040), while tissue necrosis, gross thromboemboli, and bacterial superinfection did not differentiate the 2 study groups. Chest imaging at hospital admission did not differ either and lacked correlation to any pathological factors analyzed. We did not find any statistically relevant interaction between clinical SOFA scores, the use of ventilation and morphological parameters at the autopsy.

Table 4.

Summary of statistical comparison between cause of death (2 groups) and autopsy findings as well as SOFA score in SARS-CoV-2 positive autopsies

Clinical course of disease
	SOFA (mean)		SOFA (max)		SOFA (delta)
Pearson χ2	0.540		0.189		0.358
Mann-Whitney	0.841		0.056		0.247

Pulmonary autopsy findings
	pulmonary endotheliitis	pulmonary fibrin thrombi	pulmonary leucocytic thrombi	pulmonary infarction	broncho-pneumonia	gross pulmonary embolism
Pearson χ2	0.031	0.060	0.875	0.084	0.186	0.182
Mann-Whitney	0.029	0.040	0.779	0.072	0.152	0.336

Multi-organ autopsy findings
	multi-organ endotheliitis		overall endotheliitis severity	multi-organ necrosis		overall necrosis severity
Pearson χ2	0.026		0.113	0.138		0.374
Mann-Whitney	0.006		0.001	0.955		1.000

p values <0.05 are considered as statistically significant. SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; SOFA, Sequential Organ Failure Assessment.

Discussion

In this study, we retrospectively analyzed the correlation between morphological vascular findings, autopsy-based cause of death and clinical parameters (such as SOFA score) and chest imaging in 15 COVID-19 autopsies with a different clinical course. We could show in our cohort that severe grade pulmonary endotheliitis, multi-organ involvement of endotheliitis, and tissue necrosis significantly correlate with COVID-19 associated death. Vascular changes were less prevalent in COVID-19 positive patients dying from other causes. Pulmonary infarction, bronchopneumonia, grossly visible pulmonary embolism, and frequent neutrophilic thrombi were common pathological findings in the autopsies. However, disease severity and cause of death did not correlate with these additional findings. Neither the initial chest CT imaging nor clinical disease severity parameters such as SOFA score or duration of ventilation correlated with autopsy findings or morphological cause of death. According to our knowledge, this autopsy-based study is the first to address the relationship between the magnitude and site involvement of morphological vascular changes, clinical parameters, and autopsy-based cause of death in COVID-19 autopsies.

The correlation between morphological pathological autopsy findings and imaging modalities especially chest CT at initial presentation or hospitalization have been the subject of several previous studies [8, 22, 26, 27, 28, 29]. In a previous autopsy-based study, the typical ground-glass opacities on imaging harbored a high correlation to a broad spectrum of pulmonary autopsy findings; however, all these patients died due to COVID-19 so a correlation to the cause of death in SARS-CoV-2 positive autopsies was not possible [27]. In our autopsy series, 7 SARS-CoV-2 positive patients died due to other causes than COVID-19 although a direct comparison between initial CT images and the magnitude of histopathological and gross autopsy findings or RNA viral evidence in selected organs did not show any association. These findings were seen in all patients, independent of the use of mechanical ventilation in our cohort, and are similar to those described in COVID-19 autopsy series from other centers as well as in influenza pneumonia and findings during the 2002–2003 SARS (SARS-CoV-1) pandemic [4, 27, 30, 31, 32].

The correlation between clinical parameters (such as SOFA scores or neutrophilic activation) to disease course has been observed in previous studies indicating the possibility to monitor disease severity [17, 19]. In our series, the relationship between dynamic SOFA scores and the degree of histopathological and gross vascular autopsy findings did not prove to be significant and we could not identify any morphological factors in our autopsy series harboring a link to clinical SOFA scores. Interestingly, none of the SOFA scores (mean, maximal, and delta) could be correlated to COVID-19 associated cause of death in our series, possibly pointing to the biological role and relevance of global immunological SARS-CoV-2 induced host response independently of morphological disease extension. However, the extent of endotheliitis has been described to be associated with critical illness and fatal COVID-19 disease, which further strengthens our data [21].

The extent of endothelial damage described in this study is most prominent in the lung, while extrapulmonary manifestations are less evident. Endothelial cell injury at the blood-gas barrier may explain the observed high alveolo-arterial gradient with pronounced hypoxemia both in spontaneous breathing patients with less severe dyspnea than expected and in the early phase of mechanical ventilation with severe hypoxemia but initially only mildly reduced lung compliance than ARDS of other origins [1, 8, 17, 19, 22, 23, 33, 34]. Corroborating with these clinical, tissue, and autopsy-based previous observations, our study data support the preferential role of the magnitude in pathological vascular alterations especially in pulmonary vascular involvement and the role of morphological multi-organ involvement in COVID-19 [17, 19, 21, 22].

The vascular pattern described in this study may explain the adverse outcome of COVID-19 in patients with pre-existing endothelial dysfunction, and thus less capacity to restore the injured vasculature and inhibit microthrombosis. In line with the observed association of the extent of systemic microvascular damage with clinical signs of organ failure in this study, circulating markers of endotheliopathy were associated with mortality in a plasma profiling study in a small sample of COVID-19 patients.

Endothelial tropism and endothelial cell apoptosis have been observed in case of infection with other respiratory viruses, for example, influenza A infection or SARS-CoV-1 have been suggested as underlying mechanism of, for example, encephalopathy in influenza infection [35, 36]. In an autopsy-based meta-analysis, SARS-CoV-1, Influenza A, and SARS-CoV-2 infections share the high prevalence of DAD as the main pulmonary pathology; however, extrapulmonary findings are different especially in terms of multifocal pulmonary and extrapulmonary thrombosis and multifocal endotheliitis pointing to higher frequency of multi-organ involvement at COVID-19 [2, 5, 6]. It is however at current time not possible to answer the question whether the multi-organ involvement triggers the endotheliitis or contrariwise or whether both factors represent 2 biologically distinct mechanisms in COVID-19. If the endothelium of the blood-gas barrier is damaged or dysfunctional, both diffusion impairment and ventilation-perfusion mismatch will further increase and aggravate hypoxemia [8, 23, 26, 28]. Therefore, treatment strategies that reduce ventilation-perfusion mismatch might be particularly important (e.g., prone positioning). The effect of substances active on the pulmonary endothelium needs to be systematically studied. Secondary preventive measures in patients with pre-existing endothelial dysfunction who seem to be prone to a severe course of COVID-19 might be of epidemiological interest [17, 19, 22, 33]. Therapeutic implications of the described vascular damage, such as anticoagulation are established, however, which other interventions might be helpful against the procoagulant state in case of microvascular damage are still subject to debate [17, 19, 22]. Whether survivors of severe COVID-19 will suffer from long-term vascular damage (e.g., pulmonary hypertension or COVID-19-promoted atherosclerosis) and other consequences of microvascular damage-associated multi-organ failure should be systematically studied during a long-term follow-up.

Limitations of the Study

The small sample size (n = 15 autopsies) and the variable clinical presentations (such as diverging time-frame between first diagnosis and death, different postmortem time to autopsy and individual pre- and in-hospital treatment) likely explain why morphological vascular findings and viral RNA evidence in available selected tissues are discordant in this study. Discrepant results between virus detection and clinical outcome have been described in previous studies and were linked to numerous co-factors such as the presence of viral load in vivo, the disease phase and treatment modalities [5, 13, 18, 37]. Higher viral load resulting from direct viral attack is consequently mostly measured in pulmonary vessels, while extrapulmonary sites (e.g., kidney, skin, brain, heart, etc.) harbor rather a low viral load due to docking pseudovirions (spikes and neurocapsid SARS-CoV-2 elements [5, 14, 18, 30, 37]).

Conclusions

In conclusion, our autopsy-based data show that a distinct histopathological pattern in terms of extensive pulmonary endotheliitis and manifestation of systemic multi-organ vascular and tissue damage correlates with COVID-19 associated death and differs in SARS-CoV-2 positive patients dying due to other causes. Pulmonary infarction, bronchopneumonia, grossly visible pulmonary embolism and increased neutrophilic thrombi were common pathological findings in autopsies of SARS-CoV-2 positive patients independent of disease severity or the cause of death. Clinical parameters such as initial chest CT imaging, SOFA score, duration of ventilation, or tissue-based viral RNA evidence did not correlate with autopsy findings or with morphological cause of death. The vascular pattern in fatal COVID-19 described here is another piece of the puzzle to support treatment strategies focusing on the endothelium, inflammatory response, and on avoidance of thrombi.

Statement of Ethics

Consent to perform the autopsy was given in all cases and the Institutional Review Board (Department of Pathology and Molecular Pathology of the University Hospital Zurich, Switzerland) approved the study (PN626). Ethical aspects in research on autopsy tissue of deceased patients, postmortem diagnostic and molecular analyses were completed in accordance with the Swiss Federal Research Regulations (BASEC2020-1316).

Conflict of Interest Statement

The authors have no financial or other conflict of interests to reveal.

Funding Sources

No external funding was necessary for this study.

Author Contributions

M.H.: designed the study, performed several autopsies, collected samples, analyzed immunohistochemical and morphological data, and drafted the manuscript. E.I.S.: designed the manuscript, interpreted, collected clinical information and correlation, and drafted the manuscript P.S.: interpreted clinical information and correlation and critically revised the manuscript. K.F.: performed central nervous system autopsies, interpreted data on cerebral pathology, and critically revised the manuscript. F.S.: interpreted ultrastructural findings in routine autopsy service and critically revised the manuscript. X.Z.: provided antibodies for fluorescence labeled immunohistochemistry, interpreted results on immunofluorescence in routine autopsy service, and critically revised the manuscript. S.H.: coordinated necessary additional stains and immunostains in autopsy diagnostic procedure and critically revised the manuscript. H.M.: designed the study, interpreted clinical and pathological data, and critically revised the manuscript. Z.V.: designed the study, supervised the autopsies, analyzed all gross and histopathological autopsy findings, interpreted clinical and pathological data, and drafted the manuscript.

Data Availability Statement

Individual participant data that underlie the results reported in this article will only be available after de-identification upon justified request addressed to the corresponding author.

Supplementary Material

Supplementary data

Supplementary data