Summary
In patients with severe clinical features of COVID-19 infection, the proportion of
patients with acute pulmonary embolus was 23% (95% CI: 15%, 33%) on pulmonary CT angiography.
Introduction
Chest CT plays an important role in optimizing the management of patients with COVID-19
while also eliminating alternate diagnoses or added pathologies, particularly for
acute pulmonary embolism (1). A few studies and isolated clinical cases of COVID-19
pneumonia with coagulopathy and pulmonary embolus have recently been published (2–4).
The main objective of our study was to evaluate pulmonary embolus in association with
COVID-19 infection using pulmonary CT angiography.
Materials and Methods
This retrospective study was approved by our institutional review board. It followed
the ethical guidelines of the declaration of Helsinki. Written informed consent was
waived. Three authors (F.G., J.B., P.C.) had access to the study data. No author has
any conflict of interest to declare in relation to this study.
Patients
The inclusion criteria were consecutive adult patients (≥ 18 years old) with a RT-PCR
diagnosis (NucleoSpin RNA Virus kit, Macherey-Nagel Inc., Bethlehem, PA, USA) of SARS-CoV-2
or a strong clinical suspicion of COVID-19 (fever and/or acute respiratory symptoms,
exposure to an individual with confirmed SARS-CoV-2 infection) who underwent a chest
CT scan between March 15 to April 14, 2020 at a single center. In patients with suspected
or confirmed SARS-CoV-2 infection, chest CT scan was performed when clinical features
of severe disease were present (e.g., requirement for mechanical ventilation [IMV])
or underlying comorbidities). Patients with non-contrast chest CT scans were excluded.
CT Protocol
Our routine protocol for patients with severe clinical features of COVID-19 infection
was multidetector pulmonary CT angiography using 256 slice multi-detector CT (Revolution,
GE Healthcare, Milwaukee, WI) after intravenous injection of 60 ml iodinated contrast
agent (Iomeprol 400 Mg I/mL, Bracco Imaging, Milan, IT) at a flow rate of 4 mL/s,
triggered on the main pulmonary artery. CT scan settings were 120 kVp, 80 x .625 mm,
rotation time .28 s, average tube current 300 mA, pitch .992 and CTDIvol 4.28 mGy.
Imaging Analysis. Chest CT scan pattern of COVID-19 and presence of pulmonary embolus
were independently analyzed by two chest radiologists (J.B. and F.G. with 11 and 6
years of experience) on a PACS workstation (Carestream Health, Rochester, NY). Readers
were blinded to patient status as well as clinical and biological features. In cases
of discordance, a simultaneous reading to reach consensus was achieved.
Statistical Analysis
Comparisons between continuous variables were performed using Student t-test when
distribution was normal. Comparison between categorical variables were performed using
Pearson's chi-squared test or Fisher’s exact test. To determine the clinical factors
associated with pulmonary embolus, we considered the CT extent of lesions, need for
invasive mechanical ventilation, demographics, and the presence of comorbidities as
potential independent variables in a logistic regression model. A P value of less
than .05 indicated a significant difference. All analyses were performed with R version
3.4.4 (R Core Team 2017).
Results
Of 2003 patients diagnosed with COVID-19, 280 patients were hospitalized during the
study period. Of these, 129 of 280 (46%) hospitalized patients underwent CT scan at
an average of 9 ± 5 days after symptom onset. Twenty-nine patients had non-contrast
chest CT due to contraindication to iodinated contrast or non-severe clinical features
and thus were excluded. Finally, 100 patients with COVID-19 infection and severe clinical
features were included were examined with contrast enhanced CT (Figure 1). The mean
age of the included patients was 66 ± 13 years old, with 70 men and 30 women (Table;
Appendix E1 [online]). Of 100 patients meeting inclusion criteria, 23 (23%, [95%CI,
15-33%]) patients had acute pulmonary embolism (Figure 2; Appendix E1 [online]). Patients
with pulmonary embolus were more frequently in the critical care unit than those without
pulmonary embolus (17 (74%) vs 22 (29%) patients, p<.001), required mechanical ventilation
more often (15 (65%) versus 19 (25%) patients, p<.001) and had longer delay from symptom
onset to CT diagnosis of pulmonary embolus (12 ± 6 versus 8 ± 5 days, p<.001), respectively
(Table). In multivariable analysis, requirement for mechanical ventilation (OR = 3.8
IC95% [1.02 - 15], p=.049) remained associated with acute pulmonary embolus.
Figure 1:
Flow chart of the study.
Figure 2:
Pulmonary CT angiography of a 68 year old male. The CT scan was obtained 10 days after
the onset of COVID-19 symptoms and on the day the patient was transferred to the intensive
care unit. Axial CT images (lung windows) (a,b) show peripheral ground-glass opacities
(arrow) associated with areas of consolidation in dependent portions of the lung (arrowheads).
Interlobular reticulations, bronchiectasis (black arrow) and lung architectural distortion
are present. Involvement of the lung volume was estimated to be between 25% and 50%.
Coronal CT reformations (mediastinum windows) (c,d) show bilateral lobar and segmental
pulmonary embolism (black arrows).
Table.
Patient Characteristics
Discussion
Our study points to a high prevalence of acute pulmonary embolism in patients with
COVID-19 (23%, [95%CI, 15-33%]). Pulmonary embolus was diagnosed at mean of 12 days
from symptom onset. Patients with pulmonary embolus were more likely require care
in the critical care unit and to require mechanical ventilation than those without
pulmonary embolus (Table).
Current guidelines (1,5,6) recommend performing non-contrast chest CT to assess the
COVID-19 CT pattern and its extension. However, prior reports suggested coagulopathy
associated with COVID-19 infection [e.g. (2,3)]. Further, these patients have frequent
risk factors for pulmonary embolus (e.g. mechanical ventilation, intensive care unit
admission). Therefore, we routinely performed contrast enhanced CT for COVID-19 patients
with severe clinical features to evaluate the lung parenchyma as well as to evaluate
other complications that may result in respiratory distress.
Our results showed frequent (23%) pulmonary embolus in patients with COVID-19. In
multivariate analysis, pulmonary embolus was associated with invasive mechanical ventilation
and male gender. Interestingly, extent of lesions was not a associated with pulmonary
embolus. We acknowledge the preliminary nature of these findings, including its retrospective
nature and limited sample size. Important clinical markers were not available that
may explain or be associated with pulmonary embolus, including D-dimer (only 22 of
100 patients had D-dimer levels available). Nevertheless, our results suggest that
patients with severe clinical features of COVID-19 may have associated acute pulmonary
embolus. Therefore, the use of contrast enhanced CT rather than routine non-contrast
CT may be considered for these patients.
APPENDIX
Appendix E1, Tables E1-E3, Figures E1-E2 (PDF)