Background: There are limited data regarding potential triggering factors of pulmonary embolism (PE) in coronavirus disease 2019 (COVID-19) patients and its outcomes in comparison with non-infected PE patients. We aimed to identify the contribution of COVID-19 among patients diagnosed with PE and compare risk factors, laboratory results, and outcomes between COVID-19 PE patients and non-COVID-19 PE patients.
Methods: This was a retrospective study of all PE patients between March 2020 and December 2020. The patients were segmented into two groups based on a COVID-19 nasopharyngeal swab result. Statistical analysis was used to determine the differences in risk factors, laboratory values, and outcomes.
Results: A total of 58 patients were included. Females comprised 44.8% of the total sample. Overall, 16 patients (27.6%) were COVID-19 positive. Being non-Saudi was observed more in PE COVID-19 patients compared with non-COVID-19 patients (43.7% vs 4.8%, P = 0.001). Intensive care unit (ICU) admission occurred in 50% of COVID-19 PE patients.
Conclusion: COVID-19 was associated with 27.6% of the PEs in our hospital. Being male or a foreign resident was observed to be associated with COVID-19 PE. Further studies with larger sample sizes are needed, but these results may help the medical community regarding the increased risk of PE among COVID-19 patients and provide evidence of some potentially predictive factors that can be used to identify COVID-19 in high-risk patients.
A pulmonary embolism (PE) is diagnosed when a blood clot lodges in an artery supplying the lungs, resulting in an interruption of the blood flow to a lung lobe, segment, or part of a segment. PE is becoming a recognized complication of the coronavirus disease 2019 (COVID-19) . There are an increasing number of studies reporting abnormal serum coagulation parameters in COVID-19 patients, mainly in hospitalized and intensive care unit (ICU) patients . The receptor for SARS-CoV-2 (angiotensin-converting enzyme 2) is expressed on the membrane of the vascular muscle and endothelial cells, facilitating the formation of local thrombi . Computed tomography (CT) has played a major role in the diagnosis of COVID-19 since the initial discovery of the disease and has helped to identify those patients with severe complications, including PE [3,4]. A recent retrospective cohort study reported an incidence rate of venothromboembolism (VTE) of 25%, with 10% of patients with COVID-19 dying of a VTE-related event . The clinical relationship between PE and COVID-19 is already known . However, data identifying risk factors for the prediction of PE in COVID-19 are limited. This study aimed to identify the contribution of COVID-19 to the total cases diagnosed with PE and compare risk factors, laboratory results, and outcomes in COVID-19 PE patients and non-COVID-19 PE patients.
Materials & Methods
This study was performed after obtaining approval from the King Saud University Institutional Review Board and was conducted in accordance with international research ethics standards. Patients provided informed consent. Project number: 21/01075/IRB.
Study subjects and settings
We reviewed all CT pulmonary angiogram (CTPA) scan examinations performed at King Saud University Medical City from March 1, 2020, to December 31, 2020. Images were obtained from the picture archiving and communication system database. We included all patients diagnosed with PE and segmented them into a COVID-19 positive group and a COVID-19 negative group based on reverse transcriptase polymerase chain reaction (PCR) results from nasopharyngeal swabs. To eliminate bias in the COVID-19 positive group, the group included two types of patients: (1) patients who came to the hospital with COVID-19 and then developed PE in the hospital; or (2) patients who came with PE and their admission swab turned out to be positive. Patients without a PCR test at admission were excluded (n = 2). All CTPA studies were initially read by radiology consultants, all with experience and not the authors of this study. The radiology reports for these examinations were reviewed to determine the presence or absence of PE. CT studies that were limited by respiratory motion or poor contrast opacification were excluded (n = 3). All patients had received VTE prophylaxis at admission (enoxaparin 40 mg daily, heparin 5000 U every eight hours, or sequential compression devices if anticoagulant prophylaxis was contraindicated). We compared risk factors, laboratory values, and PE outcomes for both groups. Variables included age, sex, nationality, and body mass index (BMI). Presence or history of smoking, deep venous thrombosis (DVT), previous PE, cancer, diabetes, heart failure, surgery within four weeks, hypertension, and a history of oral contraceptive use. Laboratory results included D-dimer levels, C-reactive protein, lactate dehydrogenase, and ferritin levels. Duration of ICU and ward admissions were also included. The outcome was assessed by the need for intubation and death announcement.
The Statistical Package for the Social Sciences for macOS (version 28.0; IBM Corp., Armonk, NY, USA) was used to analyze the results. Continuous variables are presented as the mean with a standard deviation. Categorical variables are presented as percentages. The χ² test of independence was used to determine the significance of the relationship between categorical variables. A Fisher exact test was used when variable frequencies were less than 5. A T-test was used to compare the means of continuous variables. P-values of less than 0.05 were considered significant. The odds ratio (OR) with a 95% confidence interval (CI) was calculated by multivariate analysis using logistic regression was used for COVID-19 positive group predictors.
A total of 58 patients were diagnosed with PE during the study period. All patients were tested for COVID-19. Females comprised (44.8%, n = 26) of the total sample. The average ages of both groups were comparable (Table 1). Patients with a BMI greater than 30 kg/m2 were seen more frequently in the COVID-19 negative group than in the COVID-19 positive group (63.16% vs 36.84%, n = 15 vs 7, respectively).
Prevalence and potential risk factors
Among the 58 PE patients, 16 (27.6%) were found to be COVID-19 positive. Males were more likely to be seen in the COVID-19-positive group than the other groups (87.5% vs 42.9%, n = 14 vs 18, P = 0.006). Non-Saudis were more in the COVID-19 positive group than in the COVID-19 negative group (43.8% vs 4.8%, n = 7 vs 2, P = 0.001). Cancer was less frequently seen in the COVID-19 positive group than in the non-COVID-19 group (6.3% vs 38.1%, n = 1 vs 16, P = 0.017). There was no statistically significant difference in age, smoking, history of heart failure, history of PE, and diabetes or hypertension. Logistic regression analysis revealed a significant association between the presence of COVID-19 positive cases in PE patients and male gender [Beta = 2.41, OR = 11.14 (95% CI 1.15-107.87), P = 0.04], and being non-Saudi [Beta = 2.45, OR = 11.55 (95% CI 1.13-117.7), P = 0.04]. When we further analyzed as to which nationality had the highest incidence of PE, we did not find any significant results (Tables 1-2).
Outcomes and laboratory values
From the time of admission, PE in COVID-19 patients was diagnosed earlier (1.29 ± 0.02 days) than in the COVID-19 negative group. In our population, we found that COVID-19-negative patients are likely to stay (7.58 ± 18.88 days) longer in the hospital when affected by PE in comparison with COVID-19 patients. COVID-19 patients tend to have more chances of ICU admission than COVID-19 negative patients (50% vs 33.3%, n = 8 vs 14, P = 0.246). There was no significant difference in laboratory values between the groups. The death ratio was higher in the PE COVID-19 group compared with the PE non-COVID (Table 3).
The incidence of PE in COVID-19 patients who undergo CTPA is reported to be between 20% and 30% [6,7]. Approximately 20% of COVID-19 patients develop PE . In our study, we found that out of all PEs diagnosed, 27.6% were associated with COVID-19 infection. Our patients presented with symptoms like fever, cough, and shortness of breath, which are symptoms of PE caused by COVID-19 or by other causes [9,10]. In a study performed in our institution in 2011, females were at more risk of PE than their male counterparts with a ratio of 2:1, and that comes in line with the international trends [11,12]. However, when it comes to VTE events in COVID-19 patients, published reports show that the male gender predominates [13,14]. Our results match with prior publications [13,14]. Our results have shown that most of the non-Saudis seen in the PE COVID-19 positive group, from our observation, non-Saudi patients usually present late to the hospital when they are very sick, and this may be the explanation for this finding in our study. According to the Saudi General Authority of Statistics 2016 demographic survey, the socioeconomic status of non-Saudis is lower than Saudis and most of them are less educated . Lower socioeconomic status is known to be associated with higher levels of venous thromboembolism events and worse outcomes, at both population and individual levels [16,17]. Moreover, there is a known disparity in healthcare delivery and hospital outcomes between Saudis and non-Saudis . Prior to the pandemic, non-Saudis were required to pay out of pocket or have health insurance. However, in April 2020, the Saudi health authorities announced that COVID-19 treatment would be free for all citizens and residents. This includes residency violators without any legal consequences . Hypercoagulability, increased blood viscosity, and inflammation are all VTE-provoking mechanisms of smoking . Active smoking was found to be a predictor of mortality in critically ill COVID-19 patients . Badr et al. study identified smoking as a risk factor for PE in COVID-19 patients . The lack of a significant difference between the two groups in our study is mainly because smoking is a known risk factor for PE regardless of COVID-19 status. The low sample size might also play a significant role in that result. Obesity (BMI>30 kg/m2) in COVID-19 patients is known to cause severe manifestations of the disease . Furthermore, obesity is associated with a 2.7-times increased risk of PE when compared with no PE in COVID-19 patients, which explains why we found that 43.8% of COVID-19 group patients were obese . We did not find a significant difference in the length of hospital stay, ICU admission, or the need for intubation between the two groups. Nevertheless, COVID-19-negative patients tended to stay longer in the hospital, and this may be due to the fact that they had more severe comorbidities such as cancer, heart failure, and a history of PE. Our data suggest that COVID-19 patients can develop PE regardless of requiring ICU care (50% did not require ICU care), which is in contrast to Griller et al. and in line with Poyiadji et al. [6,24]. The noticeable changes in blood coagulation during COVID-19 infection have been well documented and include increased values of D-dimer, fibrin or fibrinogen degradation products, and increased fibrinogen and decreased antithrombin values, prothrombin time activity, and thrombin time . A systemic pro-inflammatory cytokine response is the main mediator of thromboembolism events, inducing the expression of procoagulant factors, local inflammation, and hemodynamic alterations . Clinically, both groups had underlying inflammation. As a result, we found no statistically significant difference in laboratory results. The higher mortality rate in our cohort can be explained by the fact that 9 out of the 13 deaths occurred in cancer and heart failure patients. Cancer and heart failure are predictors of mortality in PE patients . Our study results are limited by the retrospective study design and the constraint of a single-health center. Furthermore, the generalizability to other countries and races may not be applicable due to socioeconomic differences.
In conclusion, COVID-19 is diagnosed in 27.6% of PE cases confirmed with CTPA, and this percentage has a dramatic impact on any healthcare system. Being male or non-Saudi was observed to be more common with COVID-19 PE. Non-Saudis were found more in the COVID-19 positive group versus the COVID-19 negative group. The longer length of stay was noted in our group of patients with PE who were COVID-19 negative, while COVID-19 patients required ICU care and mechanical ventilation. We found a mortality rate of one in every four COVID-19 patients in the study. No statistically significant difference was observed in laboratory values or other clinical outcomes. Further studies with larger sample sizes are encouraged to enhance the statistical power.
- Suh YJ, Hong H, Ohana M, et al.: Pulmonary embolism and deep vein thrombosis in COVID-19: a systematic review and meta-analysis. Radiology. 2021, 298:E70-80. 10.1148/radiol.2020203557
- Zhou F, Yu T, Du R, et al.: Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study. Lancet. 2020, 395:1054-62. 10.1016/S0140-6736(20)30566-3
- Agarwal PP, Cinti S, Kazerooni EA: Chest radiographic and CT findings in novel swine-origin influenza A (H1N1) virus (S-OIV) infection. AJR Am J Roentgenol. 2009, 193:1488-93. 10.2214/AJR.09.3599
- Ai T, Yang Z, Hou H, et al.: Correlation of chest CT and RT-PCR testing for Coronavirus disease 2019 (COVID-19) in China: a report of 1014 cases. Radiology. 2020, 296:E32-40. 10.1148/radiol.2020200642
- Klok FA, Kruip MJ, van der Meer NJ, et al.: Incidence of thrombotic complications in critically ill ICU patients with COVID-19. Thromb Res. 2020, 191:145-7. 10.1016/j.thromres.2020.04.013
- Grillet F, Behr J, Calame P, Aubry S, Delabrousse E: Acute pulmonary embolism associated with COVID-19 pneumonia detected with pulmonary CT angiography. Radiology. 2020, 296:E186-8. 10.1148/radiol.2020201544
- Léonard-Lorant I, Delabranche X, Séverac F, et al.: Acute pulmonary embolism in patients with COVID-19 at CT angiography and relationship to d-dimer levels. Radiology. 2020, 296:E189-91. 10.1148/radiol.2020201561
- Liao SC, Shao SC, Chen YT, Chen YC, Hung MJ: Incidence and mortality of pulmonary embolism in COVID-19: a systematic review and meta-analysis. Crit Care. 2020, 24:464. 10.1186/s13054-020-03175-z
- Xie Y, Wang X, Yang P, Zhang S: COVID-19 complicated by acute pulmonary embolism. Radiol Cardiothorac Imaging. 2020, 2:e200067. 10.1148/ryct.2020200067
- Danzi GB, Loffi M, Galeazzi G, Gherbesi E: Acute pulmonary embolism and COVID-19 pneumonia: a random association?. Eur Heart J. 2020, 41:1858. 10.1093/eurheartj/ehaa254
- Algahtani FH, Bayoumi N, Abdelgadir A, Al-Nakshabandi N, Al Aseri Z, Al Ghamdi M, Al Saeed E: Clinical characteristics and risk factors of pulmonary embolism: data from a Saudi tertiary-care center. J Thromb Haemost. 2013, 11:388-90. 10.1111/jth.12083
- Shiraev TP, Omari A, Rushworth RL: Trends in pulmonary embolism morbidity and mortality in Australia. Thromb Res. 2013, 132:19-25. 10.1016/j.thromres.2013.04.032
- Ameri P, Inciardi RM, Di Pasquale M, et al.: Pulmonary embolism in patients with COVID-19: characteristics and outcomes in the Cardio-COVID Italy multicenter study. Clin Res Cardiol. 2021, 110:1020-8. 10.1007/s00392-020-01766-y
- Melazzini F, Colaneri M, Fumoso F, et al.: Venous thromboembolism and COVID-19: a single center experience from an academic tertiary referral hospital of Northern Italy. Intern Emerg Med. 2021, 16:1141-52. 10.1007/s11739-020-02550-6
- Saudi general authority of statistics, demographic survey. (2016). Accessed: August 1, 2021: https://www.stats.gov.sa/sites/default/files/en-demographic-research-2016_2.pdf.
- Wadhera RK, Secemsky EA, Wang Y, Yeh RW, Goldhaber SZ: Association of socioeconomic disadvantage with mortality and readmissions among older adults hospitalized for pulmonary embolism in the United States. J Am Heart Assoc. 2021, 10:e021117. 10.1161/JAHA.121.021117
- Kort D, van Rein N, van der Meer FJ, Vermaas HW, Wiersma N, Cannegieter SC, Lijfering WM: Relationship between neighborhood socioeconomic status and venous thromboembolism: results from a population-based study. J Thromb Haemost. 2017, 15:2352-60. 10.1111/jth.13868
- AlFaleh HF, Al Shamiri MQ, Ullah A, et al.: Disparities in health care delivery and hospital outcomes between non-Saudis and Saudi nationals presenting with acute coronary syndromes in Saudi Arabia. PLoS One. 2015, 10:e0124012. 10.1371/journal.pone.0124012
- Hathout HM, Almutairi AM, Saleh GM, Aldawsari AA, Alanazi KH: Study of COVID-19 mortality in comprehensive rehabilitation centers in Saudi Arabia. Am J Infect Dis Microbiol. 2020, 7:2382120520963039. 10.12691/ajidm-9-1-2
- Vardavas CI, Nikitara K: COVID-19 and smoking: a systematic review of the evidence. Tob Induc Dis. 2020, 18:20. 10.18332/tid/119324
- Alharthy A, Aletreby W, Faqihi F, et al.: Clinical characteristics and predictors of 28-day mortality in 352 critically ill patients with COVID-19: a retrospective study. J Epidemiol Glob Health. 2021, 11:98-104. 10.2991/jegh.k.200928.001
- Badr OI, Alwafi H, Elrefaey WA, Naser AY, Shabrawishi M, Alsairafi Z, Alsaleh FM: Incidence and outcomes of pulmonary embolism among hospitalized COVID-19 patients. Int J Environ Res Public Health. 2021, 18:10.3390/ijerph18147645
- Zheng KI, Gao F, Wang XB, et al.: Letter to the editor: obesity as a risk factor for greater severity of COVID-19 in patients with metabolic associated fatty liver disease. Metabolism. 2020, 108:154244. 10.1016/j.metabol.2020.154244
- Poyiadji N, Cormier P, Patel PY, et al.: Acute pulmonary embolism and COVID-19. Radiology. 2020, 297:E335-8. 10.1148/radiol.2020201955
- Han H, Yang L, Liu R, et al.: Prominent changes in blood coagulation of patients with SARS-CoV-2 infection. Clin Chem Lab Med. 2020, 58:1116-20. 10.1515/cclm-2020-0188
- Laporte S, Mismetti P, Décousus H, Uresandi F, Otero R, Lobo JL, Monreal M: Clinical predictors for fatal pulmonary embolism in 15,520 patients with venous thromboembolism: findings from the Registro Informatizado de la Enfermedad TromboEmbolica venosa (RIETE) Registry. Circulation. 2008, 117:1711-6. 10.1161/CIRCULATIONAHA.107.726232
Contribution of COVID-19 to the Total Cases of Pulmonary Embolism and the Potential Risk Factors: Single Academic Hospital Study
Ethics Statement and Conflict of Interest Disclosures
Human subjects: Consent was obtained or waived by all participants in this study. King Saud University College of Medicine IRB issued approval 21/01075/IRB. Dear Dr. Fawaz Altuwaijri, I am pleased to inform you that your above-mentioned research project submitted to the IRB was reviewed and approved on December 07, 2021 (03 Jumada’I 1443). You are now granted permission to conduct this study given that your study does not disclose the participant’s identity and poses no risk to the patients. As principal investigator, you are required to abide by the rules and regulations of the Kingdom of Saudi Arabia and the research policies and procedures of the KSU IRB. If you make any changes to the protocol during the period of this approval, you must submit a revised protocol for IRB approval prior to implementing the changes. This approval shall remain valid until the expiry date noted above assuming timely and acceptable responses from the IRB’s periodic requests for surveillance and monitoring information. If you wish to have your protocol approved for continuation, please submit a completed request for reapproval of an approved protocol form (KSU-IRB 017E) at least 30 days before the expiry date. Failure to receive approval for continuation before the expiration date will result in automatic suspension of the approval of this protocol on the expiration date. Information collected following suspension is unapproved research and can never be reported or published as research data. Please quote the project number shown above in any future correspondence or follow-ups related to this study. We wish you success in your research and request you to keep the IRB informed about the progress of the study on a regular basis by submitting a Study Progress Report every 6 months and a Final Report when the study has been completed. Thank you. Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.
Cite this article as:
Altuwaijri F, Amshan K, Alanazi A Y, et al. (September 23, 2022) Contribution of COVID-19 to the Total Cases of Pulmonary Embolism and the Potential Risk Factors: Single Academic Hospital Study. Cureus 14(9): e29513. doi:10.7759/cureus.29513
Peer review began: September 07, 2022
Peer review concluded: September 17, 2022
Published: September 23, 2022
© Copyright 2022
Altuwaijri et al. This is an open access article distributed under the terms of the Creative Commons Attribution License CC-BY 4.0., which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.