Skip to main content
Journal of Vascular Surgery Cases, Innovations and Techniques logoLink to Journal of Vascular Surgery Cases, Innovations and Techniques
. 2020 Jul 17;6(3):454–459. doi: 10.1016/j.jvscit.2020.06.012

Arterial thrombotic complications in COVID-19 patients

Stef Levolger a,, Reinoud PH Bokkers a, Jan Wille b, Rogier HJ Kropman b, Jean-Paul PM de Vries c
PMCID: PMC7366094  PMID: 32835150

Abstract

The coronavirus disease 2019 (COVID-19), a viral respiratory illness caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has been described to predispose to thrombotic disease in both the venous and arterial circulations. We report four cases of an acute arterial occlusion in COVID-19 patients and literature review on the occurrence of arterial thrombosis in patients with COVID-19. Our findings demonstrate that physicians should be vigilant for signs of thrombotic complications in both hospitalized and new COVID-19 patients.

Keywords: Arterial occlusion, Thrombosis, Ischemia, COVID-19, SARS-CoV-2

Case report

We report four cases of acute arterial occlusive disease or ischemia in patients with the coronavirus disease 2019 (COVID-19) that is caused by the virus designated severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The patients presented at two Dutch hospitals (one university hospital and one large teaching hospital). Since the first presentation of a COVID-19 patient in The Netherlands on February 27 to May 1, there have been 378 reverse transcriptase-polymerase chain reaction-confirmed patients admitted to our two hospitals. Four cases involved an acute arterial occlusion. Medical history, smoking status, laboratory results, and anticoagulation therapy are detailed in Table I.

Table I.

Identified cases of acute arterial occlusive disease or ischemia in patients with COVID-19

Case 1 Case 2 Case 3 Case 4
Medical history None Diabetes mellitus Gout Obstructive sleep apnea, obesity
Smoking Nonsmoker Nonsmoker Smoking cessation 3 years prior Nonsmoker
Laboratory results
 CRP, mg/L 234 100 4.7 339
 Leukocytes, 109/L 8.2 13 7.2 23.6
 Thrombocytes, 109/L 262 458 185 237
 LDH, U/L 868 294 186 421
 aPTT, seconds N/A 34 35 34
 PT, seconds N/A 14 N/A 14.7
 INR N/A N/A 1.1 N/A
 D-dimer, μg/L N/A N/A N/A 28,186
Anticoagulation therapy
 At admission
 Post-therapy Apixaban, 5 mg twice daily Heparin IV Clopidogrel, 75 mg once daily
Nadroparin (Fraxiparine), 2850 IU once daily
Heparin IVa
 At discharge Apixaban, 5 mg twice daily Rivaroxaban, 10 mg once daily Acenocoumarola

aPTT, Activated partial thromboplastin time; CRP, C-reactive protein; INR, international normalized ratio; IV, intravenous; LDH, lactate dehydrogenase; N/A, not available; PT, prothrombin time.

a

In case 4, the patient was treated with heparin intravenously after therapy because of concomitant acute kidney failure, for which continuous venovenous hemofiltration was indicated. Acute atrial fibrillation and subsegmental pulmonary embolisms developed during recovery, for which acenocoumarol was started before discharge to a referral hospital.

The first patient, a 50-year-old healthy man, was admitted because of pneumonia, for which he received supplemental oxygen and chloroquine. Three days after admission, the patient developed acute claudication of the right limb without neurologic deficits. Computed tomography angiography (CTA) showed a short occlusion (3.5 cm) of the right common iliac artery (Fig 1). Surgical embolectomy was not possible because of a high risk for general anesthesia in relation to COVID-19, and thrombolytic therapy was not available because of capacity issues. After 3 days of systemic therapeutic heparin treatment, the patient was discharged home with mild claudication. However, 20 days later, the patient was readmitted with acute ischemia of both legs. CTA showed persistent occlusion of the right common iliac artery. A new thrombus was present at the left tibial-fibular trunk (TTF). The patient subsequently received alteplase for the right common iliac artery and left TTF. Owing to the dislodgment of thrombus to the right TTF and persistent ischemia, infragenual exploration and open thrombectomy were performed, with good clinical outcome.

Fig 1.

Fig 1

A 50-year-old COVID-19-positive man with no medical history developed acute claudication of the right limb without neurologic deficits 3 days after admission. Computed tomography angiography (CTA) showed short occlusion of the right common iliac artery.

The second patient, a nonsmoking 55-year-old man, was referred with a pale pulseless left hand. There was no muscle weakness, with minimal sensory loss of the fingers. CTA was performed and showed a subclavian artery occlusion (Fig 2). One week before, the patient had had a fever without other symptoms. At presentation, the patient had no pulmonary symptoms, fever, or dyspnea. The saturation was 95%. The patient was treated with therapeutic heparin systemically. Because of the absence of fever and hypoxia, no treatment was started for the COVID-19 infection. After 1 day of heparin treatment, distal pulses were still absent, but refill was normalized, and the function of the hand was completely normalized, with no sensory loss. After 2 days, rivaroxaban was started, and the patient was discharged home.

Fig 2.

Fig 2

A 55-year-old COVID-19-positive man with a medical history of diabetes with oral metformin use presented with a pale, pulseless left hand without muscle weakness and minimal sensory loss of the fingers. Acquired computed tomography angiography (CTA) imaging showed subclavian artery occlusion. A, Sagittal view. B, Coronal view. C, Axial view.

The third patient, a 62-year-old man, presented with right-sided hemiparesis. Computed tomography imaging showed dense media with a corresponding perfusion defect as well as M1 occlusion on CTA with subtotal stenosis of the internal carotid artery origin (Fig 3). There was no known history of internal carotid artery stenosis, and CTA showed minimal calcified atherosclerosis. The patient underwent intra-arterial thrombectomy with nearly complete reperfusion, except for some distal cortical emboli. On the second day of admission, the patient developed fever and cough due to COVID-19. Laboratory results were normal. Further symptoms were mild, without the need for supplemental oxygen or other treatment for COVID-19. As of June 9, 2020, the patient is still admitted for neurologic rehabilitation.

Fig 3.

Fig 3

A 62-year-old COVID-19-positive man presented with right-sided hemiparesis. A-C, Cerebral computed tomography showed (A) a left dense media sign, (B) occlusion on computed tomography angiography (CTA), and (C) corresponding perfusion defect. D, Digital subtraction angiography confirmed an M1 occlusion. E, After intra-arterial thrombectomy, cerebral blood flow was restored (Thrombolysis in Cerebral Infarction grade 2C).

The fourth patient, a 58-year-old man, who presented with dyspnea and abdominal pain that had gradually developed within the past 2 weeks. The patient was admitted to the intensive care unit (ICU) for respiratory distress the same day. Gastric retention and abdominal distention were noted during the admission; abdominal portal-venous computed tomography imaging was performed, showing dilated small bowel loops, signs of bowel wall ischemia, an adjacent fluid collection, and splenic and renal infarctions without macrovascular arterial occlusion. Nonsignificant stenosing soft plaque was present in the proximal superior mesenteric artery. Subsequent laparotomy was performed, and a partial small bowel resection was performed for low-flow-associated bowel ischemia. Bowel function recovered. Three weeks after surgery, digital necrosis of both feet was observed clinically. Arterial duplex ultrasound was performed and showed no common femoral artery, profunda femoris artery, superficial femoral artery, or popliteal artery stenosis or occlusion. During recovery, the patient was transferred to a referral hospital. As of June 5, 2020, the patient has not yet been discharged.

Consent has been given by all patients for the publication of the case details and images.

Discussion

The current outbreak of the SARS-CoV-2 is spreading throughout the globe, causing high morbidity and mortality. Preliminary data have reported an increased risk of venous thromboembolism and acute myocardial infarctions, most likely caused by excessive inflammation, platelet activation, endothelial dysfunction, and stasis.1

However, there have also been reports of arterial thrombosis. To investigate the prevalence and incidence of arterial occlusions, we performed a review of the current literature. MEDLINE was searched for peer-reviewed publications on COVID-19 and arterial thromboembolic complications. Four retrospective cohort studies, consisting of a total of 738 patients, and eight case report studies have reported the occurrence of arterial thrombotic events (Table II). In a series of 150 ICU patients referred to four French ICUs reported by Helms et al,2 four arterial occlusions were observed, of which one caused mesenteric ischemia, one limb ischemia, and two cerebral ischemia. von Willebrand factor activity, von Willebrand factor antigen, and factor VIII were considerably increased in all patients, and 50 of 57 tested patients (87.7%) had positive lupus anticoagulant.

Table II.

Studies found in literature review

Study Study design No. Arterial thrombotic events Type
Helms et al2 Multicenter retrospective cohort 150 ICU patients 2 (1.3%)
1 (0.7%)
1 (0.7%)
Ischemic stroke
Mesenteric ischemia
Limb ischemia
Klok et al3 Multicenter retrospective cohort 180 ICU patients 3 (3.7% cumulative incidence) Ischemic stroke
Lodigiani et al4 Single-center retrospective cohort 388 patients 9 (2.5%)
3 ICU, 6 general ward
Ischemic stroke
Bellosta et al5 Single-center retrospective cohort 20 patients 20 Acute limb ischemia
Le Berre et al6 Case report 1 Intra-aortic thrombus
de Barry et al7 Case report 1 Mesenteric thrombosis
Oxley et al8 Case report 5 Large-vessel stroke
Vulliamy et al9 Case report 1 Aorta-iliac and mesenteric
Avula et al10 Case report 4 Ischemic stroke
Giacomelli et al11 Case report 1 Aortic prosthetic graft occlusion
González-Pinto et al12 Case report 1 Large-vessel stroke
Beyrouti et al13 Case report 6 Ischemic stroke

ICU, Intensive care unit.

Furthermore, a single-center cohort study from Bellosta et al5 reported increased incidence of patients presenting with acute limb ischemia in 2020, 16% vs 2% throughout the same calendar period in 2019. Klok et al3 reported that thrombotic complications were observed in 31% of ICU patients in a multicenter cohort of 180 patients admitted to the ICU of three Dutch hospitals. Arterial complications were relatively rare, however, with a cumulative incidence of 3.7%, all of which consisted of ischemic stroke. Similar findings of ischemic stroke occurrence were reported by Lodigiani et al4 in a cohort of 388 patients admitted to an academic hospital in Milan, Italy. Nine patients (2.5%) developed ischemic stroke, of whom three patients were at the moment admitted to the ICU and six were on a general ward.

The eight case reports describe the occurrence of acute arterial occlusions in the aorta and mesenteric and cerebral arteries.6, 7, 8, 9, 10, 11, 12, 13

Complications of COVID-19, including coagulopathy,14,15 may contribute to the development of arterial ischemic events. Elevated D-dimer levels in the setting of COVID-19 have been described in three of the previously described cohort studies.2,4,5 Furthermore, D-dimer levels were elevated in 15 of 17 patients tested in six identified case reports.8, 9, 10, 11, 12, 13 In our centers, D-dimer levels were determined in one patient and found to be significantly elevated. Although an apparent correlation is suggested, possible causality needs to be investigated. Moreover, COVID-19 causes elevated cytokine levels, including but not limited to tumor necrosis factor α, interleukin (IL) 1β, IL-6, and interferon γ.16 Previous research has shown that elevated levels of exogenous tumor necrosis factor α may exacerbate focal ischemic injury in stroke as well as intestinal ischemia in an experimental setting.17, 18, 19 Likewise, IL-1β administration leads to increased infarct size, whereas lack of IL-1β reduces infarct size in experimental focal cerebral ischemia models.20 Guidance for considerations in the preventive and therapeutic use of antithrombotic agents as well as potential drug interactions between antiplatelet agents and investigational therapies for COVID-19 has recently been published.21 Further research is warranted to elucidate this suggested association between COVID-19 and ischemic complications, its possible underlying pathogenesis, and prevention.

Conclusions

Our findings demonstrate that physicians should be vigilant for signs of arterial thrombotic complications in COVID-19 patients.

Footnotes

Author conflict of interest: none.

The editors and reviewers of this article have no relevant financial relationships to disclose per the Journal policy that requires reviewers to decline review of any manuscript for which they may have a conflict of interest.

References

  • 1.Chen S., Huang B., Luo D.J., Li X., Yang F., Zhao Y. [Pregnancy with new coronavirus infection: clinical characteristics and placental pathological analysis of three cases] Zhonghua Bing Li Xue Za Zhi. 2020;49:418–423. doi: 10.3760/cma.j.cn112151-20200225-00138. [DOI] [PubMed] [Google Scholar]
  • 2.Helms J., Tacquard C., Severac F., Leonard-Lorant I., Ohana M., Delabranche X. High risk of thrombosis in patients in severe SARS-CoV-2 infection: a multicenter prospective cohort study. Intensive Care Med. 2020;46:1089–1098. doi: 10.1007/s00134-020-06062-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Klok F.A., Kruip M., van der Meer N.J., Arbous M.S., Gommers D., Kant K.M. Incidence of thrombotic complications in critically ill ICU patients with COVID-19. Thromb Res. 2020;191:145–147. doi: 10.1016/j.thromres.2020.04.013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Lodigiani C., Iapichino G., Carenzo L., Cecconi M., Ferrazzi P., Sebastian T. Venous and arterial thromboembolic complications in COVID-19 patients admitted to an academic hospital in Milan, Italy. Thromb Res. 2020;191:9–14. doi: 10.1016/j.thromres.2020.04.024. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Bellosta R., Luzzani L., Natalini G., Pegorer M.A., Attisani L., Cossu L.G. Acute limb ischemia in patients with COVID-19 pneumonia. J Vasc Surg. 2020 Apr 29 doi: 10.1016/j.jvs.2020.04.483. [Online ahead of print] [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Le Berre A., Marteau V., Emmerich J., Zins M. Concomitant acute aortic thrombosis and pulmonary embolism complicating COVID-19 pneumonia. Diagn Interv Imaging. 2020;101:321–322. doi: 10.1016/j.diii.2020.04.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.de Barry O., Mekki A., Diffre C., Seror M., Hajjam M.E., Carlier R.Y. Arterial and venous abdominal thrombosis in a 79-year-old woman with COVID-19 pneumonia. Radiol Case Rep. 2020;15:1054–1057. doi: 10.1016/j.radcr.2020.04.055. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Oxley T.J., Mocco J., Majidi S., Kellner C.P., Shoirah H., Singh I.P. Large-vessel stroke as a presenting feature of Covid-19 in the young. N Engl J Med. 2020;382:e6. doi: 10.1056/NEJMc2009787. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Vulliamy P., Jacob S., Davenport R.A. Acute aorto-iliac and mesenteric arterial thromboses as presenting features of COVID-19. Br J Haematol. 2020;189:1053–1054. doi: 10.1111/bjh.16760. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Avula A., Nalleballe K., Narula N., Sapozhnikov S., Dandu V., Toom S. COVID-19 presenting as stroke. Brain Behav Immun. 2020;87:115–119. doi: 10.1016/j.bbi.2020.04.077. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Giacomelli E., Dorigo W., Fargion A., Calugi G., Cianchi G., Pratesi C. Acute thrombosis of an aortic prosthetic graft in a patient with severe COVID-19 related pneumonia. Ann Vasc Surg. 2020;66:8–10. doi: 10.1016/j.avsg.2020.04.040. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Gonzalez-Pinto T., Luna-Rodriguez A., Moreno-Estebanez A., Agirre-Beitia G., Rodriguez-Antiguedad A., Ruiz-Lopez M. Emergency room neurology in times of COVID-19: malignant ischemic stroke and SARS-CoV-2 infection. Eur J Neurol. 2020 Apr 30 doi: 10.1111/ene.14286. [Online ahead of print] [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Beyrouti R., Adams M.E., Benjamin L., Cohen H., Farmer S.F., Goh Y.Y. Characteristics of ischaemic stroke associated with COVID-19. J Neurol Neurosurg Psychiatry. 2020 Apr 30 doi: 10.1136/jnnp-2020-323586. [Online ahead of print] [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Zhou F., Yu T., Du R., Fan G., Liu Y., Liu Z. Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study. Lancet. 2020;395:1054–1062. doi: 10.1016/S0140-6736(20)30566-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Zhang Y., Cao W., Xiao M., Li Y.J., Yang Y., Zhao J. [Clinical and coagulation characteristics of 7 patients with critical COVID-2019 pneumonia and acro-ischemia] Zhonghua Xue Ye Xue Za Zhi. 2020;41:E006. doi: 10.3760/cma.j.issn.0253-2727.2020.0006. [DOI] [PubMed] [Google Scholar]
  • 16.Liu B., Li M., Zhou Z., Guan X., Xiang Y. Can we use interleukin-6 (IL-6) blockade for coronavirus disease 2019 (COVID-19)-induced cytokine release syndrome (CRS)? J Autoimmun. 2020;111:102452. doi: 10.1016/j.jaut.2020.102452. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Barone F.C., Arvin B., White R.F., Miller A., Webb C.L., Willette R.N. Tumor necrosis factor-alpha. A mediator of focal ischemic brain injury. Stroke. 1997;28:1233–1244. doi: 10.1161/01.str.28.6.1233. [DOI] [PubMed] [Google Scholar]
  • 18.Souza D.G., Soares A.C., Pinho V., Torloni H., Reis L.F., Teixeira M.M. Increased mortality and inflammation in tumor necrosis factor-stimulated gene-14 transgenic mice after ischemia and reperfusion injury. Am J Pathol. 2002;160:1755–1765. doi: 10.1016/s0002-9440(10)61122-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Souza D.G., Teixeira M.M. The balance between the production of tumor necrosis factor-alpha and interleukin-10 determines tissue injury and lethality during intestinal ischemia and reperfusion. Mem Inst Oswaldo Cruz. 2005;100(Suppl 1):59–66. doi: 10.1590/s0074-02762005000900011. [DOI] [PubMed] [Google Scholar]
  • 20.Kawabori M., Yenari M.A. Inflammatory responses in brain ischemia. Curr Med Chem. 2015;22:1258–1277. doi: 10.2174/0929867322666150209154036. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Bikdeli B., Madhavan M.V., Jimenez D., Chuich T., Dreyfus I., Driggin E. COVID-19 and thrombotic or thromboembolic disease: implications for prevention, antithrombotic therapy, and follow-up. J Am Coll Cardiol. 2020;75:2950–2973. doi: 10.1016/j.jacc.2020.04.031. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Vascular Surgery Cases and Innovative Techniques are provided here courtesy of Elsevier

RESOURCES