Contemporary Catheter-Based Treatment Options for Management of Acute Pulmonary Embolism.

INTRODUCTION: Acute pulmonary embolism (PE) remains an important cause of cardiovascular mortality and morbidity in the USA and worldwide. Catheter-based therapies are emerging as a new armamentarium for improving outcomes in these patients. PURPOSE OF REVIEW: The purpose of this review is to familiarize the clinicians with (1) various types of catheter-based modalities available for patients with acute PE, (2) advantages, disadvantages, and appropriate patient selection for the use of these devices, and (3) evidence base and the relevance of such therapies in the COVID-19 pandemic. RECENT
FINDINGS: There are four main types of catheter-based therapies in acute PE: (1) standard catheter-directed thrombolysis (CDT), (2) ultrasound-assisted CDT, (3) pharmacomechanical CDT, and (4) mechanical thrombectomy without thrombolysis. Ultrasound-assisted thrombolysis is the most widely studied modality in this group; however, evidence base for other catheter-based technologies is rapidly emerging.
SUMMARY: Current use of catheter-based therapies is most suitable for patients with intermediate and high-risk acute PE. The adoption of a multidisciplinary approach like the pulmonary embolism response team (PERT) is desirable for appropriate patient selection and possibly/potentially improving patient outcomes. We discuss the current status of these therapies.

Introduction

Acute pulmonary embolism (PE) is the third most common cause of cardiovascular death [1•, 2], and venous thromboembolism (VTE) affects more than 500,000 people in the United States (US) alone annually [2]. In US, it causes approximately 100,000 deaths each year. Majority of deaths caused by acute PE are due to severe pulmonary vascular obstruction. Catheter-based therapies have recently emerged as an important tool in the treatment of PE patients, particularly the high-risk group. In this review, we discuss appropriate patient selection, types, and evidence base for currently available catheter-based technologies and the relevance/utilization of these therapies in the COVID-19 pandemic.

Pathophysiology of acute PE and clinical implications for catheter-based therapies

While percutaneous catheter-based therapies are established as the first-line treatment approaches for thromboembolism in the arterial vasculature such as coronary thrombosis or cerebrovascular embolism, this is not yet true for pulmonary embolism. It is essential to highlight a few pathophysiological differences to fully appreciate the use and limitations of catheter-based therapies for these conditions.

Acute pulmonary embolism often is a result of embolization of thrombi originating in the lower extremity venous circulation which results from stasis and a hypercoagulable state [3] and tends to be occlusive [4]. Adverse hemodynamic consequences of acute pulmonary embolism are related to overall thrombus volume or burden. While small volume thrombi causing acute pulmonary embolism may be subclinical, patients with hemodynamic compromise due to acute PE tend to have a large thrombus volume or burden. These factors have important clinical implications in achieving adequate results with catheter-based therapies. Whereas large thrombus burden is often not amenable for complete resolution with a low dose of thrombolytic agents, adequate mechanical aspiration of thrombi from distal vessels remains also challenging, later being the most important element for reduction of dead space.

Patient selection for catheter-based therapies

Apart from systemic anticoagulation and supportive care, most of the high-risk and selected intermediate-risk patients require advanced therapeutic options targeting the pulmonary artery thrombus to achieve adequate pulmonary vascular reperfusion and reduction in afterload to the right ventricle (RV). Mortality benefit of systemic thrombolysis in patients with hemodynamic instability has been shown in multiple clinical trials and meta-analyses [5, 6] and is recommended as the first-line therapy (grade 2C) for patients with acute unstable PE by the American College of Chest Physicians (ACCP)—2016 guidelines [7]. In the setting of persistent hemodynamic instability (defined as systolic blood pressure < 90 mmHg), the role of catheter-based therapies is limited to patients with high bleeding risk, those who fail systemic thrombolysis, or whose death is imminent before systemic thrombolytic therapy can take effect (grade 2C) [7]. While systemic thrombolysis is the choice of therapy for hemodynamically unstable or high-risk acute PE patients, clinical trials in intermediate-risk acute PE showed significantly higher bleeding rates (extracranial and intracranial hemorrhage rates of 6.3% and 2% respectively in the PEITHO trial), which reduced the overall net benefit of systemic thrombolysis [8].

Catheter-based therapies have emerged as the choice of treatment for patients presenting with intermediate-risk PE in the recent years. Intermediate-risk PE is more common compared to high-risk (massive) acute PE, comprising nearly one third of all patients presenting with acute PE [9]. In addition to that, these patients remain at high risk for severe complications and progression to hemodynamic instability. In the placebo arm of the PEITHO trial [8], patients who were treated with anticoagulation alone, 4.6%, (23/499) patients required rescue treatment with systemic thrombolytic therapy and more than 70% of those patients did not survive in spite of the rescue thrombolysis. In another randomized trial comparing alteplase with placebo in patients with submassive PE, 25% (34/138) of the patients in the placebo arm required escalation of treatment, with 23% (32/138) requiring thrombolytic therapy during hospitalization [10]. In these patients, catheter-based therapies offer a potential clinical benefit without exposing the patients to the risk of high-dose systemic thrombolytic therapy. In the following sections, we discuss specific catheter-based therapies and clinical evidence for use in patients with intermediate-risk acute PE.

Ultrasound-assisted catheter-directed thrombolysis (CDT)

The use of CDT achieves thrombolysis using lower doses of fibrinolytic agents compared to systemic administration of these agents, which often require much higher doses. Due to the lower dose of the fibrinolytic agents, the risk of major or serious bleeding is lower. Although a few catheter devices have received 510(k) FDA approval, ultrasound-facilitated fibrinolysis (EkoSonic, Boston Scientific, Marlborough, MA) is the best-studied catheter in this category [11]. Ultrasound-facilitated thrombolysis relies on the principle of enhancing drug delivery into the thrombus using ultrasound energy [12]. The use of this catheter has been studied in three prospective trials [13, 14, 15•] (Table 1). The SEATTLE II [13] was a single-arm, prospective trial which included 150 patients. These patients underwent ultrasound-facilitated thrombolysis with an infusion of 1 mg/h tPA for 24 h for one device in unilateral PE or 1 mg/h for 12 h (for two devices) for bilateral PEs. The primary outcome in the trial was a change in RV/LV ratio 48 h post-CDT. There was a significant decrease in RV/LV ratio from 1.55 to 1.13 (p < 0.0001) after CDT. There was a significant reduction (29%) of thrombus burden as assessed by the modified Miller score. Another small randomized controlled trial of 59 patients compared ultrasound-accelerated thrombolysis versus heparin-alone infusion [14]. In this trial, CDT was associated with a greater reduction in RV size and RV/LV ratio at 24 h (0.30 versus 0.03 with heparin, p < 0.0001) and 90 days (0.38 versus 0.22 with heparin, p = 0.03). Another trial compared patients who were randomized to various doses of fibrinolytics for shorter durations (4 mg/lung/2 h vs 4 mg/lung/4 h vs 6 mg/lung/6 h vs 12 mg/lung/6 h) [15•]. It showed that lower doses were effective in improving RV size and function; however, the reduction in thrombus burden was poor at lower doses. There was a very clear dose-response relationship of tPA with thrombus burden reduction noted in this trial. We hope more insights will be available from an ongoing prospective registry; KNOCKOUT PE [16] is enrolling 1500 patients undergoing ultrasound-assisted CDT with EkoSonic catheter and plans to study clinical outcomes like mortality and quality of life.

Table 1

Summary of the select evidence base of current and ongoing clinical trials that evaluated catheter-based therapies for the treatment of acute pulmonary embolism

Trial/year	Design/N	Population	Device/intervention	Outcome	Comments
SEATTLE II13—2015	P, SA / 150	Proximal PE symptom ≤14 days, and RV/LV diameter ratio ≥ 0.9	EKOS 24 mg of tissue plasminogen activator (tPA) infusion	Mean RV/LV ratio decreased from 1.55 to 1.13 (p < 0.0001). Mean PA systolic decreased from 51.4 to 36.9 mmHg 1 GUSTO severe bleed 16 GUSTO moderate bleed	No clinical outcomes
ULTIMA14—2014	RCT / 59	acute symptomatic PE and RV to left ventricular dimension (RV/LV) ratio ≥ 1	EKOS 10 h versus heparin	EKOS group, mean RV/LV ratio was reduced 1.28 ➔ 0.99 at 24 h (P < 0.001); heparin group, mean RV/LV ratio 1.20 ➔ 1.17 at 24 h (P = 0.31). At 90 days, there was 1 death (in the heparin group), no major bleeding, 4 minor bleeding episodes (3 in the USAT group and 1 in the heparin group; P = 0.61).	No clinical outcomes
OPTALYSE PE15—2018	RCT / 101	symptomatic, intermediate-risk, acute PE RV-to-LV diameter ratio ≥ 0.9 and proximal PE located in at least 1 main or proximal lobar pulmonary artery	4 tPA infusion strategies (per lung) (4 mg/lung/2 h vs 4 mg/lung/4 h vs 6 mg/lung/6 h vs 12 mg/lung/6 h)	RV/LV diameter ratio were as follows: arm 1 (4 mg/lung/2 h), 0.40 (24%; p = 0.0001); arm 2 (4 mg/lung/4 h), 0.35 (22.6%; p = 0.0001); arm 3 (6 mg/lung/6 h), 0.42 (26.3%; p = 0.0001); and arm 4 (12 mg/lung/6 h), 0.48 (25.5%; p = 0.0001). Improvement in refined modified Miller score was also seen in all groups. Four patients experienced major bleeding (4%).	No clinical efficacy outcomes
SUNSET 20	RCT / 40 per group	Acute PE with RV strain as diagnosed by RV/LV ratio > 1 and elevated cardiac biomarkers; and absence of circulatory shock symptoms ≤14 days and no elevated bleeding risk	EKOS vs standard CDT	1, Primary outcome: clearance of pulmonary thrombus burden; 2, secondary outcomes include resolution of RV strain, improvement in PA pressures; and 3, 12-month improvement in functional capacity, and quality of life measures.	Ongoing trial
KNOCKOUT PE Registry21	O-R / 1500	RV/LV ≥ 1.0 PE symptom duration ≤14 days Troponin elevation	EKOS	1. Change in RV/LV ratio (baseline to 24 h) 2. Persistence of pulmonary hypertension 3. Other urgent interventions for index PE 5. Serious adverse experiences 6. Recurrent symptomatic VTE and bleeding events 7. All-cause mortality 8. Healthcare utilization during hospitalization 9. Quality of life	Ongoing registry
FLARE23	P-SA / 106	Intermediate-risk PE RV/LV ratio ≥ 0.9	FlowTriever	At 48 h post-procedure, average RV/LV ratio reduction was 0.38 (25.1%; p < 0.0001). Four patients (3.8%) experienced 6 major adverse events In patients with elevated mean PA pressure pre-procedure, there was an improvement from a mean of 34.7 ± 7.1 to 31.5 ± 7.7 mmHg post-procedure (p < 0.0001).	No clinical outcomes
EXTRACT PE25	P-SA / 119	Intermediate-risk PE RV/LV ratio > 0.9	Penumbra Indigo	27.3% reduction in RV/LV ratio from baseline.	No clinical outcomes

P = prospective, RCT = randomized controlled trial, O = observational, R = registry, CDT = catheter-directed thrombolysis, VTE = venous thromboembolism, RV = right ventricle, LV = left ventricle PE = pulmonary embolism, EKOS = EkoSonic catheter system

/

/

/

/

/

/

/

Standard catheter-directed thrombolysis (CDT)

Cragg-Mcnamara (Medtronic, Minneapolis, Minnesota), Unifuse (Angiodynamics, Latham, NY), and Fountain (Merritt Inc) catheters are other devices available for CDT. These catheters have multiple side slits, to facilitate the distribution of the fibrinolytic agent within the thrombus [17, 18]. The main advantage of these catheters over the ultrasound facilitated catheter is the lower cost. Comparison of these low-cost catheters with ultrasound facilitated thrombolysis is limited only to retrospective studies. A retrospective study, which included 98 cases, showed a similar degree of reduction in pulmonary artery pressures, RV/LV ratio, or hospital length of stay in both groups [19]. Another retrospective study which included 70 patients showed similar results [20]. SUNSET sPE trial is a randomized trial comparing outcomes in patients undergoing CDT using the EkoSonic catheter versus standard catheter-directed thrombolysis. There was no significant difference in the reduction in the mean obstruction index reduction (21% versus 22%, p = 0.77) or mean thrombus score reduction (post-CDT score 22 ± 7 versus 23 ± 7, p = 0.76) between patients undergoing CDT using the EkoSonic versus the standard catheter device [21].

Mechanical thrombectomy without thrombolysis

The main advantage of mechanical thrombectomy over CDT is potentially the quicker reduction in pulmonary vascular obstruction and the ability to achieve this without using fibrinolytic agents. However, some of these advantages are offset by the need to place large-bore venous access cannulas for some device systems and the risk of distal embolization to normally functioning segments of the pulmonary circulation. Few devices are available in this category. Two important devices in this category that have received FDA clearance include the FlowTriever Retrieval/Aspiration system and the Penumbra Indigo aspiration catheter system.

The FlowTriever Retrieval/Aspiration (Inari Medical, Inc., Irvine, California) catheter is available in three sizes 16F, 20F, and 24F. In addition to the aspiration cannula, this system also has three nitinol mesh disks, which can be deployed beyond the thrombus and then retrieved in the aspiration catheter [22]. The safety and effectiveness of this catheter were tested in the FLARE trial, a prospective, single-arm trial, which enrolled 106 patients with acute intermediate-risk pulmonary embolism and right ventricular strain defined as RV/LV ratio ≥ 0.9. The primary end point was a change in RV/LV ratio. There was a mean RV/LV ratio reduction of 0.38 (p < 0.0001). One patient experienced a major bleeding event and four patients had other major complications (including pulmonary vascular injury in 1 patient, respiratory deterioration requiring emergent intubation in 2 patients, and ventricular fibrillation in 1 patient) during the procedure [23].

Another thrombectomy device, the Penumbra Indigo (Penumbra, Alameda, CA) aspiration catheter, is a continuous aspiration system, which requires an 8 French venous access sheath. The safety and efficacy of this device were evaluated in the EXTRACT PE trial. This trial enrolled 119 patients with intermediate-risk acute PE and showed a significant reduction of mean RV/LV ratio at 48 h. The median ICU length of stay was 1 day and 1.7% of the patients experienced major adverse events at 48 h including one device-related death [24]. While a smaller 8F venous access sheath makes this device less prone to access site–related bleeding complications, it decreases the effectiveness for achieving adequate thrombectomy for some larger-sized proximal clots [25]. Another disadvantage associated with the use of aspiration devices is significant blood loss, often inevitable during aspiration of thrombi from the pulmonary vasculature. The new 12F penumbra device has been recently developed; it uses an intelligent design and performs suction only when in contact with thrombus [26].

In addition to the above devices, some other devices have been used for thrombectomy with mixed results. Angiojet (Boston Scientific, Marlborough, Massachusetts) rheolytic thrombectomy device has been used in patients with high-risk and intermediate-risk acute PE patients. Data from a retrospective study, of 51 patients at a single center, showed that the use of Angiojet was feasible in patients presenting with acute PE [27]. However concerns with bradyarrhythmias, hypotension, and other complications associated with the use of Angiojet led to a black box warning from the FDA for use of this device [25, 28]. The use of other devices such as rotating pigtail catheter with aspiration [29], Aspirex catheter (Straub Medical, Switzerland) [30], or the JETi thrombectomy device (Walk Vascular, Irvine, CA) is mostly limited to case reports or small case series.

Pharmacomechanical catheter-directed thrombolysis

The pharmacomechanical approach to endovascular treatment of acute pulmonary embolism is based on the principle of delivering even lower doses of a fibrinolytic drug with mechanical thrombus fragmentation, to enhance the delivery of the fibrinolytic agent. The approach is commonly employed in the treatment of lower extremity deep venous thrombosis and has been studied in a randomized controlled trial [31]. However, the use of the pharmacomechanical approach in the treatment of acute PE is limited due to the lack of dedicated devices. Angiojet catheter can be used to deliver tPA during thrombectomy, but the use of this device was associated with a high rate of complications in a meta-analysis by Kuo and colleagues [28].

Another currently available catheter is the Bashir Endovascular catheter (BEC, Thrombolex, New Britain, PA) which is based on the principle of pharmacomechanical fragmentation and thrombolysis [32]. This catheter enhances the delivery of tPA by exposing a higher surface area of the thrombus and fibrin-binding sites for both endogenous and exogenous fibrinolytics, thus acting synergistically to enhance thrombus resolution. This catheter insertion requires a 7F venous access sheath. Once deployed within the thrombus, a nitinol reinforced basket at the tip of this catheter expands up to 45 mm, which can then be collapsed and redeployed to increase surface area and binding sites for tPA within the thrombus. The device allows pulse sprays as well as the infusion (Fig. 1). The pulse spray with an expanded basket creates bubbles of tPA that are trapped inside a thrombus and continue to lyse the clot even after the device is removed from the body. The first in human feasibility study included 9 patients who underwent CDT using the BEC [33]. There was significant reduction in RV/LV ratio from 1.52 ± 0.26 to 0.97 ± 0.06 (p = 0.0009; 95% CI = 0.33 to 0.82; 37.0% reduction), and thrombus burden from 25.4 ± 5.3 to 16.0 ± 4.0 (p = 0.0005; 95% CI = 5.5 to 13.4; 37.1% reduction) as measured by the modified Miller index post-CDT compared to baseline. More insights will be available from the RESCUE trial (NCT03927508), a multicenter prospective study which is currently enrolling patients with intermediate-risk acute PE to assess the safety and efficacy of the BEC-directed thrombolysis [32].

Fig. 1

Bashir endovascular catheter device.

Inferior vena cava (IVC) filter for acute PE

Another endovascular therapy to consider in patients with acute PE is the IVC filter. In patients with acute severe PE, but without any contraindications to anticoagulation, there was no benefit of routine use of IVC filter placement in addition to anticoagulation versus anticoagulation alone. The PREPIC-2 trial did not demonstrate any difference in recurrent PE between the two arms [34]. The results of this trial led to the ACCP guideline recommendation against routine use of IVC filter in patients with acute PE, but without any contraindications to anticoagulation use [7, 35].

While IVC filter is commonly used in patients with venous thromboembolism and perceived contraindications to anticoagulation, the benefit of IVC filter on reducing short-term mortality was noted only in patients with active bleeding in a large observational study from California [36]. The use of an IVF filter in patients with acute PE is intended to lower the risk of recurrent PE and further hemodynamic compromise. The evidence base for this particular scenario is mostly limited to observational or retrospective studies and is conflicting [36-38]. A case-control study by Gates and colleagues [37] evaluated the incidence of symptomatic PE in patients with venous thromboembolism and high risk for PE who underwent IVC filter placement due to a perceived contraindication to anticoagulation. There was no difference in the incidence of symptomatic PE between patients with or without IVC filter. Moreover, majority of the patients who were perceived to have contraindication to anticoagulation use received anticoagulant therapy in this study. In the absence of high-quality studies, a recent guideline document from the Society of Interventional Radiology [39] recommends the use of IVC filter placement in patients with acute PE and contraindications to anticoagulation, after careful consideration of risks and benefits of the use of IVF filter.

The use of IVC filter in conjunction with other catheter-based therapies such as thrombolysis or thrombectomy has not been evaluated in any high-quality randomized study. In a study from the national inpatient sample database, out of 7119 patients who underwent CDT for acute PE, nearly one third (34%) underwent IVC filter placement. IVC filter placement did not result in lower in-hospital mortality or bleeding events, but was associated with higher rates of access site hematoma, in-hospital charges, and length of stay [40].

Based on the above evidence, we recommend the use of IVC filter in acute PE patients only in the setting of active bleeding. Routine IVC filter placement in acute PE patients receiving anticoagulation, thrombolysis, or undergoing other catheter-based therapies may not provide additional benefit but may result in higher rates of complications and increased cost of care.

Role of extracorporeal membrane oxygenation (ECMO)

Fatality from acute PE is often the result of severe obstructive circulatory shock. Patients on the extreme end of the spectrum with very high pulmonary vascular thrombus burden remain at risk of imminent cardiac arrest. The term “catastrophic acute PE” can be collectively used to describe patients (1) who have suffered a cardiac arrest with or without (ongoing CPR) return of spontaneous circulation, or those (2) who remain at a very high risk of cardiac arrest such as shock refractory to ionotropic support or those who present with severe refractory hypoxemia.

The use of VA-ECMO in patients with catastrophic PE in conjunction with systemic fibrinolysis remains challenging due to a high rate of access site bleeding complications but is feasible. A retrospective study by Meneveau and colleagues [41] evaluated outcomes in 52 patients receiving ECMO in PE patients. Of these, 37 patients received ECMO support in conjunction with other therapies (fibrinolysis = 20, embolectomy = 17). The incidence of major bleeding was 39% (n = 20). Although the incidence of bleeding was not reported in patients who received concomitant fibrinolytic therapy, it is plausible that this group remains at the highest risk of bleeding from large-bore access cannula placement for ECMO.

The evidence base for use of ECMO followed by catheter-directed thrombolysis is limited mostly to case reports or case series [42]. In a case series, which included 10 patients who required ECMO support for either cardiac arrest (n = 9) or refractory shock (n = 1), adjunctive catheter-based therapies were used in 9 patients and included catheter-directed thrombolysis, thrombectomy, or mechanical thrombus fragmentation or a combination. In this series, the 30-day mortality was 30%. Apart from percutaneous catheter-based therapies, a surgical approach/embolectomy is also feasible in patients on VA-ECMO support [43, 44].

ECMO support for patients with catastrophic PE sometimes may be the only management option available to patients in extremis. Veno-arterial ECMO (VA-ECMO) support in these patients provides hemodynamic stabilization and an opportunity to use interventions aimed at improving pulmonary vascular flow. Some patients may only need ECMO support till anticoagulation improves the pulmonary blood flow.

Adjunctive pharmacotherapy

Although catheter-based therapies have an important role in the management of patients with acute PE, it should always be in the setting of adjunctive pharmacological therapy as tolerated on an individualized basis. In the following section, we discuss adjunctive pharmacotherapy with catheter-based therapies.

Anticoagulation

In patients undergoing CDT, anticoagulation with unfractionated or low molecular weight heparin (bivalirudin or argatroban for those with contraindication to heparin) should be considered universally. Patients who are felt to have contraindications to anticoagulation at initial presentation should be carefully evaluated during follow-up with initiation of anticoagulation when deemed feasible. A study showed that the majority of the patients in whom anticoagulation was perceived to be initially contraindicated were able to safely receive it [37].

For patients undergoing CDT, we recommend the use of low molecular weight heparin (LMWH) over unfractionated heparin (UFH) due to ease of use, predictable pharmacokinetics [45], and early achievement of a therapeutic anticoagulation effect. We recommend using 1 mg/kg body weight of enoxaparin q12h in patients with normal renal function. If UFH is used, we recommend maintaining PTT target 2–2.5 times the upper limit [46]. During the procedure, we recommend maintaining activated clotting time > 200 ms for patients who receive UFH prior to the procedure. For patients with the last dose of LMWH heparin at least 8 h prior to the procedure, intra-procedural anticoagulation can be achieved with UFH to maintain activated clotting time > 200 ms. No additional intra-procedural anticoagulation may be needed for patients with the last dose of LMWH within 8 h of the procedure. Post-procedure, following a brief period of anticoagulation interruption (<1 h) for sheath removal, we recommend resuming therapeutic anticoagulation as soon as possible. In some patients, we may need to remove the sheaths while patients are fully anticoagulated.

Fibrinolytic therapy

Various dose protocols have been used for catheter-directed thrombolysis, depending on the device type. Doses in the range of 8–24 mg of tPA have been used in clinical trials. Recent trials have shown low-dose fibrinolytic dose may be equally effective in improving RV size and hemodynamics [15•]. We recommend lowering PTT target to 50–60 ms during infusion of the fibrinolytic agent in CDT. Once sheaths and catheters for CDT have been removed, we recommend a PTT target of 2–2.5 times the upper limit of normal.

COVID-19-related acute PE and catheter-based therapies

Studies have shown a higher incidence of acute PE in patients with COVID-19 pneumonia [47]. A French study of 107 consecutive patients presenting with COVID-19 pneumonia requiring ICU admission showed a 21% incidence of acute PE, which was much higher when compared to historical controls (6.1%) [48] at the same institute in the pre-COVID era. Similar results were noted in other studies which showed a high incidence of acute PE in COVID-19 pneumonia patients [49-51].

Evidence for the use of catheter-based treatments in patients presenting with COVID-19-related acute PE is limited to case reports, with no studies systematically evaluating the outcomes in this group of patients [52-56]. Furthermore, the use of these devices in case reports is mostly limited to patients with high-risk PE, except in one case report where a patient with intermediate-risk acute PE was treated with thrombectomy using the FlowTriever catheter [54]. Although small in number, patients described in these case reports who received catheter-based treatments had successful outcomes, with improvement in hemodynamic status and oxygenation and successful weaning off from mechanical ventilatory support (Table 2).

Table 2

Summary of available evidence for use of catheter-based therapies in patients with COVID-19-related acute pulmonary embolism

Author	Age/sex	Risk	Adj. therapy	Catheter	tPA/dose	Complications	Outcome
Pendower [52]	64/F	I-H	Deltaperin	EkoS	Alteplase 40 mg—24 h	Self-limiting epistaxis and melena	Weaned off oxygen in 24 h, discharged on day 6
Carlsson* [53]	58/M	H, PEA arrest	Systemic tPA 100 mg	Penumbra		NR	Transferred out of ICU day 14. Alive at day 16
Vyas [54]	32/M	I	UFH	Flowtriever	None	NR	Discharged 3 days later
Qanadli [55]	50s/M	L-I		USAT	30 mg-15 h		Clinical improvement at 24 h with reduction in CT obstruction index from 75% to 28%
Shamsah [56]	42/M	H	UFH VA-ECMO	Not specified	tPA-24 h	No bleeding complications	Discharged to inpatient rehab. Alive at 30 days

*Patient was presumed to have COVID-19 based on imaging and presentation. Swabs were negative for COVID-19, L = low risk, I = intermediate risk, H = high risk, UFH = unfractionated heparin, VA-ECMO=veno-arterial extracorporeal membrane oxygenation, tPA = tissue plasminogen activator, USAT = ultrasound-assisted, CT = computed tomography, ICU = intensive care unit, NR = not reported

Apart from limited evidence of the use of standard catheter-based therapies for COVID-19-related acute PE patients, several other challenges remain. A recent study from New York showed nearly 40% lower Pulmonary Embolism Response Team (PERT) activations during the COVID-19 epidemic from March to April 2020 compared a similar time period a year earlier [57]. This was despite a higher number of acute PE patients treated during the same time period in 2020 at that institute. Despite the lower rate of activation of the PERT team, the recommendations and outcomes were similar to the pre-COVID-19 era in this study. Although the exact reasons for lower utilization of PERT are unclear from this study, it is conjectural that concerns with exposure to staff, higher use of resources, and personal protective equipment may have played a role in this. Another challenge in providing catheter-based therapies to eligible patients with COVID-19-related acute PE is the lack of consensus or clear recommendations from major societies. A recent CHEST guideline/expert panel report from June 2020 for treatment of venous thromboembolism in patients with COVID-19 recommends the use of thrombolytic agent delivery using a peripheral vein over catheter-directed thrombolysis [58]. However, this document neither provides any evidence for this recommendation nor it recommends any clinical situation where the use of catheter-based therapies may be preferred over systemic thrombolysis. It is plausible that this recommendation is mostly related to concerns about staff exposure. With the improvement in personal protective equipment shortages, and significant gain of experience in providing care to COVID-19 patients while minimizing the risk of transmission, it is likely that the use of catheter-based therapies in patients with COVID-19 patients would have the same degree of benefit as in patients with non-COVID-19-related PE particularly by reducing the length of stay.

We hope that further evidence for treatment of these patients will become available from the PERT consortium COVID-19 PE registry [59], which is a nationwide registry currently enrolling patients to assess short-term and long-term outcomes of current treatments in COVID-19 patients with acute PE.

Future directions

Evidence base

Evidence for use of new catheter-based devices is limited to relatively small single-arm studies with no control population. Larger randomized controlled studies are needed to better assess the efficacy of these devices. Most of the clinical trials included surrogate outcomes as the primary study end point. Although parameters like the RV/LV ratio, pulmonary artery pressures, or biomarkers have prognostic implications, more studies are needed to assess more meaningful end points like mortality, quality of life measures, functional capacity, and impact on chronic thromboembolic pulmonary hypertension. Hopefully, the PETRACT study will be funded by NIH and will attempt to answer this question.

Multidisciplinary approach

Another important aspect to a successful implementation of catheter-based therapies and improving outcomes in patients presenting with acute PE patients is the adoption of a multidisciplinary approach (Fig. 2). Studies have shown improved outcomes with an approach of using the PERT concept [60, 61•]. We hope more hospital systems nationwide adopt the PERT model in the future which can further optimize the care of these patients.

Fig. 2

Algorithm for management of patients with acute PE. PERT = pulmonary embolism response team, CDT = catheter-directed thrombolysis, VA-ECMO = veno-arterial extracoporeal membrane oxygenation, RV = right ventricular, PE = pulmonary embolism.

Conclusion

With the improvement in catheter-based technologies and new designs, endovascular modalities have come to the forefront over the last few years and are now considered important therapeutic strategies for patients with intermediate-risk PE and many high-risk acute PE who are ineligible for systemic thrombolysis, where the risk of such therapy outweighs the benefits. While evidence for use of catheter-based therapies is growing, more studies are needed. Implementation of a multidisciplinary or PERT model is likely the best approach to appropriately select patients for these therapies.