Pulmonary and Respiratory Medicine Open Access

Volume 2017; Issue 1
13 Sep 2017

Extensive Pulmonary Embolism with Patent Foramen Ovale: Unique Presentation Highlights Importance of Multidisciplinary Management Strategies

Case Report

Ryan Richard1, Ashley Desmett1, Alexandra Kadl1,2*

1Department of Medicine, University of Virginia, USA
2Department of Pharmacology, University of Virginia, USA

*Corresponding author:Alexandra Kadl, Department of Pharmacology, University of Virginia, USA. Tel: + +1 434-243-4851; E-Mail: AK5SC@hscmail.mcc.virginia.edu.

Received Date: 07June 2017;Accepted Date:16 June 2017; Published Date: 24June, 2017

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Introduction

References

Figures

Tables

Suggested Citation

Introduction

 

Paradoxical embolism occurs when a venous clot enters the arterial circulation through a right to left shunt, most commonly through a patent foramen ovale (PFO). Paradoxical embolism can also be seen with atrial septal defects, ventricular septal defects, and, rarely, with extra cardiac vascular shunts [1]. These events can occasionally be detected as clots in transit on imaging, when clot is visualized in the systemic circulation prior to and during embolization. We have found multiple case reports in which a large clot has been detected traversing the PFO [2-4]. Paradoxical emboli can create dangerous clinical scenarios and surgical intervention is often recommended. We report a case of a 65-year-old female who was admitted to our hospital with a large pulmonary embolism and was found to have a clot in transit through a PFO.

 

Presentation

 

The patient is a 65-year-old female with a history of morbid obesity (BMI of 52), moderate obstructive sleep apnea (non-compliant with prescribed CPAP), and a single episode of provoked deep vein thrombosis 5 years prior to presentation. She was no longer on anticoagulation at the time of presentation. Three months prior to presentation, she underwent transthoracic echocardiogram due to bilateral, symmetric lower extremity edema. This study showed moderate left ventricular hypertrophy and normal right ventricular size.

 

She had been on multiple cross-country trips, including lengthy flights, in the weeks leading to presentation. In July 2016, she presented to the pulmonary clinic for a one week history of progressive, acute dyspnea. On a six-minute walk test, she was only able to walk 50 meters due to severe hip pain and dyspnea. At rest, pulse oximetry was 87-90%, and on exam she was tachycardic with heart rates between 100 and 110, her blood pressure was 138/78. She was transferred to the Emergency Room due to concern for acute pulmonary embolism. Lower extremity ultrasounds showed bilateral deep vein thrombosis. A CT-Pulmonary Angiogram (CTPA) revealed defect, extensive bilateral pulmonary emboli and an atrial septal defect with concern for thrombus extending from the right atrium into the left atrium (see Figure 1 and Figure 2).

 

Hospital Course

 

She was admitted to the Medical Intensive Care Unit and started on anticoagulation with heparin. Subsequent aorticangiogram further demonstrated thrombus extending through the PFO into the descending aorta, and continuing into the bilateral internal iliac arteries and a branch of the right profunda femoral artery (Figure 3). An emergent transthoracic echocardiogram confirmed a clot extending through a PFO and traversing her mitral valve into her left ventricular outflow tract (LVOT) (Figure 4). Her right ventricle was severely dilated with a severely reduced ejection fraction. Her hypoxia worsened, and she developed hemodynamic instability, necessitating the initiation of a norepinephrine infusion (see Table 1). Throughout her admission, there was ongoing collaboration between critical care, vascular medicine, cardiothoracic surgery, and interventional radiology. Given her clinical deterioration and the concern for further systemic embolism and/or stroke with thrombolysis (systemic or catheter-directed), the decision was made to proceed to surgery. Intra-operative transesophageal echocardiography confirmed the clot in transit. She was placed on cardiopulmonary bypass, her atrial septal defect was closed, large amounts of thrombi were removed from both main pulmonary arteries, and a large thrombus was removed from her left atrium. After surgery, the patient was on norepinephrine and milrinone infusions, as well as in haled nitric oxide. She was alert and responding to commands with no focal neurologic deficits, making paradoxical emboli into the cerebral circulation unlikely. The patient was weaned off vasoactive drugs and inhaled nitric oxide within 48h after surgery. She was successfully extubated on post operative day (POD) 8, and discharged home on POD 11. She was discharged on 4L supplemental oxygen.

 

Outpatient Follow-Up

                                                

At her 6-month follow-up visit, she was no longer requiring supplemental oxygen, and showed significant improvement in her 6-minute walk distance to 270 meters. Despite clinical improvement, her echocardiogram continued to show a severely dilated right ventricle with severely reduced right ventricular function. A repeat CTPA at that time showed a decrease in the overall clot burden, but with persistent wedge-shaped infarcts and segmental clots. A subsequent ventilation-perfusion scan and right heart catheterization supported a diagnosis of mild chronic thromboembolic pulmonary hypertension (CTEPH). The patient will be continued on life-long anticoagulation with apixiban for CTEPH. Her age-appropriate cancer screening has been negative thus far. She was referred to Hematology, but no further investigation into clotting disorders has been necessary, given her indication for life-long anticoagulation. She has also been initiated on nightly CPAP for her OSA and is now compliant with therapy.

 

Discussion

 

This case highlights the complex clinical decision-making process involved in the treatment of clots in transit. Studies have shown the incidence of PFOs in the population is around 25-30% on autopsy [5]. These PFOs are most often asymptomatic; however, they can cause a significant right to left shunt when right-sided cardiac pressures exceed left-sided pressures, as seen in a large acute PE. The treatment of a thrombus extending through a PFO remains controversial [6]. Our current treatment options for clinically significant pulmonary embolism now include: anticoagulation, systemic thrombolysis, catheter directed thrombolysis, and mechanical extraction (intravascular vs surgical) [7-9]. Studies have shown the major bleeding risk with thrombolytic therapy to be increased when compared to anticoagulation with heparin alone (9.2 vs 3.4 percent), including an increased risk of intracranial hemorrhage (1.5 vs 0.2 percent) [10]. In patients with a thrombus lodged in the PFO, consensus opinion in the literature states that emergency surgery is indicated [6,11]. This is due in large part to the concern that thrombolytic therapy may cause pieces of clot to dislodge and lead to further systemic embolization and stroke [12]; however, there is a lack of clinical trial data to show whether any other treatment modality would have less risk of embolization. Decisions are based on expert opinion and on the individual patient risk and presentation. This case also highlights the importance of collaboration between specialists to determine the best individualized treatment approach in this complex clinical scenario. In our institution, we have established a PE-alert team that evaluates every patient admitted with sub-massive or massive pulmonary embolism. In our case, there were extensive discussions between multiple specialists regarding the best treatment choice. As shown in Table 1, her PE-severity index was rather low at 85, putting her into a low risk group; while her simplified PE-severity index was 1, putting her into a high-risk group. These severity scores do not consider complications such as a PFO or a thrombus extending into the arterial circulation. In this case, the patient showed worsening right heart failure and respiratory failure requiring vasoactive drugs, as well as an increase in supplemental oxygen. We also discussed the treatment options with the patient and her family. Together, we decided that she was at high risk for stroke with any therapy, but we thought that placing her on cardiopulmonary bypass, removing the left atrial clot, and closing the PFO would be the most beneficial and safest approach. Her excellent neurologic outcome supported our decision. We feel this multi-disciplinary collaborative approach was vital to her positive outcome, and supports the development of PE response teams in academic centers throughout the country.

References

 

  1. Corrin B (1964) Paradoxical Embolism. Br Heart J 26:549-553.
  2. Caes FL, Van Belleghem YV, Missault LH, Coenye KE, Van Nooten GJ (1995) Surgical treatment of impending paradoxical embolism through patent foramen ovale. Ann ThoracSurg 59:1559-1561.
  3. Falk V, Walther T, Krankenberg H, Mohr FW (1997) Trapped thrombus in a patent foramen ovale. ThoracCardiovascSurg 45:90-92.
  4. Meacham RR 3rd, Headley AS, Bronze MS, Lewis JB, Rester MM (1998) Impending paradoxical embolism. Arch Intern Med158:438-448.
  5. Hagen PT, Scholz DG, Edwards WD (1984) Incidence and size of patent foramen ovale during the first 10 decades of life an autopsy study of 965 normal hearts. Mayo Clin Proc 59:17-20.
  6. Mas JL (1996) Diagnosis and management of paradoxical embolism and patent foramen ovale. CurrOpinCardiol11:519-524.
  7. Jaff MR, Mcmurtry MS, Archer SL, Cushman M, Goldenberg N, et al. (2011) Management of Massive and Submassive Pulmonary Embolism, Iliofemoral Deep Vein Thrombosis, and Chronic Thromboembolic Pulmonary Hypertension a Scientific Statement from the American Heart Association. Circulation 123: 1788-1830. 
  8. Konstantinides SV, Torbicki A, Agnelli G, Fitzmaurice D, Galie N, et al. (2014) ESC Guidelines on The Diagnosis and Management of Acute Pulmonary Embolism. European Heart Journal 35: 3033-3073.
  9. Kearon C, Akl EA, Ornelas J,Blaivas A, Jimenez D, et al. (2016) Antithrombotic Therapy for VTE Disease CHEST Guideline and Expert Panel Report. Chest 149: 315-352.
  10. Chatterjee S, Chakraborty A, Weinberg I,Kadakia M, Wilensky RL, et al. (2014) Thrombolysis for pulmonary embolism and risk of all-cause mortality major bleeding and intracranial hemorrhage a meta-analysis. JAMA 311:2414-2421.
  11. Chartier L, Bera J, Delomez M, Asseman P, Beregi JP, et al. (1999) Free floating thrombi in the right heart diagnosis management and prognostic indexes in 38 consecutive patients. Circulation 99:2779-2783.
  12. Digonnet A, Moya-Plana A, Aubert S, Flecher E, Bonnet N, et al. (2007) Acute pulmonary embolism a current surgical approach. Interact CardiovascThoracSurg 6: 27-29.
Figures

 

Figure 1:Axial View of CTPA Showing Clot Burden in the Both Main Pulmonary Arteries.

Figure 2: Axial View Showing Clot in the PFO.

Figure 3: Axial View of CTA Showing Clot Burden in the both Main Pulmonary Arteries (red arrows). There is also Evidence of Clot in the Descending Aorta (Blue Arrow).

 

Figure 4: TTE.Parasternal Long AxisView Showing a Mobile Mass (Red Arrow) in the Left Atrium.

Tables

 

Table 1 : Clinical Parameters at Transfer to the Medical ICU-Highlighting Pitfalls Of Clinical Scoring Systems in Certain Patient Populations.

Suggested Citation

 

Citation: Richard R, Desmett A, Kadl A (2017) Extensive Pulmonary Embolism with Patent Foramen Ovale: Unique Presentation Highlights Importance of Multidisciplinary Management Strategies. J Pulm Respir Med 2017: PROA-J106.

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