Journal of Medical Cases, ISSN 1923-4155 print, 1923-4163 online, Open Access |
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Case Report
Volume 11, Number 6, June 2020, pages 174-177
Pulmonary Embolism in COVID-19 and the Unanswered Questions
Anchit Bharata, d, Nikita Jainb, Veerpal Singhc
aIndiana University Health Ball Memorial Hospital, Muncie, IN, USA
bChicago Medical School, Rosalind Franklin University of Medicine and Sciences, Mchenry, IL, USA
cNorthwestern Medicine Hospital, Mchenry, IL, USA
dCorresponding Author: Anchit Bharat, Indiana University Health Ball Memorial Hospital, 4201 W University Avenue, Muncie, IN 47303, USA
Manuscript submitted May 4, 2020, accepted May 16, 2020, published online May 28, 2020
Short title: Pulmonary Embolism: COVID-19
doi: https://doi.org/10.14740/jmc3488
Abstract | ▴Top |
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has ravaged the global society as we know it. As almost a dozen pharmaceutical agents go into randomized controlled clinical trials, multiple studies have surfaced trying to associate a hypercoagulable state to coronavirus disease 2019 (COVID-19) patients. We report two COVID-19 cases who presented with occlusive pulmonary embolism (PE) strongly supporting a hypercoagulable state incurred by SARS-CoV-2. This is significant as it is one of the early reports of such an initial presentation of COVID-19 in the USA. Through our report, we invite the medical community to share a perspective about long-term management guidelines for SARS-CoV-2 associated venous thromboembolism (VTE) and prompt future research.
Keywords: SARS-CoV-2; COVID-19; Pulmonary embolism; Venous thromboembolism
Introduction | ▴Top |
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has ravaged the global society as we know it. The medical community is in a desperate need to understand the pathophysiology of coronavirus disease 2019 (COVID-19) (caused by SARS-CoV-2) and explore possible therapeutic strategies in the wake of widespread mortality. At the time of writing this article, globally, 305,395 people have succumbed to this disease with 4,508,435 total infections. As almost a dozen pharmaceutical agents go into randomized controlled clinical trials, multiple studies have surfaced trying to associate a hypercoagulable state to COVID-19 patients [1]. We reference these studies and present two novel COVID-19 cases who presented with pulmonary embolism (PE).
Case Report | ▴Top |
The summary of cases with pertinent patient characteristics, histories, findings and supporting data are presented in Table 1. Until now, there have been only sporadic cases of occlusive PE in COVID-19 patients, coming from China, Italy and the USA. Both our patients presented with dyspnea preceded by a mild flu-like illness and were found to have pulmonary emboli with significant clot burden at initial presentation. There were no significant predisposing risk factors, other than a hypercoagulable state due to COVID-19. The history of prostate carcinoma in patient 2 is unlikely to be contributory as he was in remission, suggested by a normal prostate-specific antigen (PSA). Both patients were treated with heparin products. Patient 1 remains hospitalized with moderate illness (day 4). Patient 2 required 3 days of inpatient stay and was discharged on newer oral anticoagulants (NOACs) with a recommended duration of 3 months. Hypercoagulable workup including factor V Leiden mutation, protein C, protein S, antithrombin III levels, and anti-phospholipid antibody tests was ordered upon outpatient follow-up, which remains pending.
Click to view | Table 1. Pertinent Patient Characteristics, Histories, Laboratory Findings, and Imaging Results |
Discussion | ▴Top |
Initial studies from Greece and France endorse that COVID-19 patients might be at a higher risk of developing venous thromboembolism (VTE), which has been attributed to a hypercoagulable state [1]. The exact putative mechanism of this observation still remains elusive, but the role of antiphospholipid antibodies (APLAs) has been implicated [2]. Interesting autopsy findings from China suggest hyaline thrombi in some microvessels of the alveolar septum on immunohistochemical staining [3]. Our European and Chinese colleagues recommend an early initiation of anticoagulation therapy in selected patients [1, 4]. This has shown to improve prognosis of this group of COVID-19 patients [5]. In summary, all these studies point towards a similar direction, decoding the labyrinth, i.e. pathophysiology of COVID-19 and how anticoagulation therapy might fit in the algorithm. Future randomized controlled studies might help clear this association. In the meantime, low-molecular-weight heparin (LMWH) is being widely used in patients who fit this picture [4, 5]. This brings us to our questions to the medical community: 1) Are NOACs appropriate for these patients? 2) Should we consider these PEs as provoked or unprovoked? 3) What should be the duration of therapy?
Acknowledgments
None to declare.
Financial Disclosure
None to declare.
Conflict of Interest
None to declare.
Informed Consent
Verbal consent for publication of the clinical details was obtained from both patients and all patient identifiable information is anonymized in the manuscript.
Author Contributions
AB and NJ contributed to literature review and manuscript preparation; VS contributed to case information and reviewed manuscript. All authors have read the uploaded manuscript and consented to submission.
Data Availability
The authors declare that data supporting the findings of this study are available within the article. Any further inquiries regarding supporting data availability of this study can be directed to the submitting author.
Abbreviations
SARS-CoV-2: severe acute respiratory syndrome coronavirus 2; COVID-19: coronavirus disease 2019; PE: pulmonary embolism; VTE: venous thromboembolism; APLAs: antiphospholipid antibodies; LMWH: low-molecular-weight heparin; NOAC: newer oral anticoagulant; RT-PCR: reverse-transcriptase polymerase chain reaction; PSA: prostate-specific antigen; HR: heart rate; RR: respiratory rate; HGB: hemoglobin; PLT: platelet; CT: computerized tomography; IV: intravenous
References | ▴Top |
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