Local Ultrasound-Facilitated Thrombolysis in High-Risk Pulmonary Embolism: First Dutch Experience
verfasst von:
Maria A. de Winter, Einar A. Hart, Daniel A. F. van den Heuvel, Adriaan Moelker, Rutger J. Lely, Karin A. H. Kaasjager, Pieter R. Stella, Steven A. J. Chamuleau, Adriaan O. Kraaijeveld, Mathilde Nijkeuter
To provide insight into the current use and results of ultrasound-facilitated catheter-directed thrombolysis (USAT) in patients with high-risk pulmonary embolism (PE).
Introduction
Systemic thrombolysis is an effective treatment for hemodynamically unstable, high-risk PE, but is associated with bleeding complications. USAT is thought to reduce bleeding and is therefore advocated in patients with high-risk PE and contraindications for systemic thrombolysis.
Methods
We conducted a retrospective cohort study of all patients who underwent USAT for high-risk PE in the Netherlands from 2010 to 2017. Characteristics and outcomes were analyzed. Primary outcomes were major (including intracranial and fatal) bleeding and all-cause mortality after 1 month. Secondary outcomes were all-cause mortality and recurrent venous thromboembolism within 3 months.
Results
33 patients underwent USAT for high-risk PE. Major bleeding occurred in 12 patients (36%, 95% CI 22–53), including 1 intracranial and 3 fatal bleeding. All-cause mortality after 1 month was 48% (16/33, 95% CI 31–66). All-cause mortality after 3 months was 50% (16/32, 95% CI 34–66), recurrent venous thromboembolism occurred in 1 patient (1/32, 3%, 95% CI 1–16).
Conclusions
This study was the first to describe characteristics and outcomes after USAT in a study population of patients with high-risk PE only, an understudied population. Although USAT is considered a relatively safe treatment option, our results illustrate that at least caution is needed in critically ill patients with high-risk PE. Further research in patients with high-risk PE is warranted to guide patient selection.
Hinweise
This paper (poster) was presented at the 64th Annual Scientific and Standardization Committee (SSC) meeting of the International Society on Thrombosis and Haemostasis in Dublin, Ireland on July 19, 2018.
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
AZN
St. Antonius Hospital, Nieuwegein
CI
Confidence interval
CTPA
Computed tomographic pulmonary angiography
DOAC
Direct oral anticoagulant
ECMO
Extracorporeal membrane oxygenation
EKOS
EkoSonic Endovascular system (EKOS Corporation; Bothell, WA, USA)
EMC
Erasmus Medical Center Rotterdam
ISTH
International Society on Thrombosis and Haemostasis
Pulmonary embolism (PE) is a common cardiovascular disease that can result in significant morbidity and death. PE patients with hemodynamic shock or hypotension are classified as high-risk, those with right ventricular (RV) dysfunction and/or myocardial injury as intermediate-risk and patients without those signs as low risk of mortality [1]. In the high-risk group, comprising 5% of all PE patients, an in-hospital mortality of 25–65% is found, depending on clinical presentation and timely availability of treatment [1‐3]. Systemic thrombolysis (ST) is standard of care in high-risk patients [1‐4]. It has been shown to restore pulmonary perfusion more rapidly compared to standard anticoagulation alone, thereby improving RV function and reducing mortality [5‐8]. However, systemic thrombolysis carries a 20% risk of major bleeding, including a 2–3% risk of intracranial hemorrhage [1, 4, 9, 10]. Consequently, risk factors for bleeding are considered (relative) contraindications for this treatment [8, 11]. Currently, in patients with high-risk PE in whom ST is contraindicated or has failed, surgical embolectomy or ultrasound-assisted catheter-directed thrombolysis (USAT) is advised [1]. USAT, using the EkoSonic Endovascular system (EKOS Corporation; Bothell, WA, USA) is currently the most studied catheter-based technique using a lower dose of thrombolytic agent. With this catheter, ultrasound is used to drive the thrombolytic agent directly into plasminogen receptor sites within the thrombus and separate fibrin strands more efficiently [12, 13]. Previous studies on USAT and other local thrombolytic interventions for PE did show a reduction of pulmonary artery pressure and improved echocardiographic parameters, with a favorable safety profile [14‐27]. However, these studies had a short follow-up and lacked clinically relevant outcomes, such as major bleeding. More importantly, study populations were relatively small and involved mainly intermediate-risk patients. Whereas most evidence regarding efficacy and safety of USAT originates from data on intermediate-risk patients, its main indication is for high-risk PE. In previous literature, patients with high-risk PE were either not or scarcely included. Ideally, a randomized controlled trial comparing ST and USAT would be undertaken to identify the best strategy for patients with high-risk PE. However, these patients are by definition hemodynamically unstable and often require immediate life-saving therapy that cannot be postponed by asking informed consent. Therefore, we need to assess the effect of this strategy using data from case series and registries. Currently, USAT is only advised in high-risk patients in whom ST is contraindicated or has failed [1]. However, evidence supporting this strategy is scarce.
The aim of this retrospective study was to provide insight into the use and outcomes of USAT in patients with high-risk PE treated according to current guidelines.
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Materials and Methods
Study Design and Setting
This retrospective cohort study was conducted at all hospitals performing USAT in the Netherlands, including three academic hospitals (University Medical Center Utrecht, Utrecht, the Netherlands, Erasmus Medical Center, Rotterdam, the Netherlands and VU University Medical Center, Amsterdam, the Netherlands) and one tertiary referral center for cardiovascular and pulmonary disease (St. Antonius hospital, Nieuwegein, the Netherlands).
Selection of Participants
We included all patients that underwent USAT for PE in the Netherlands since its introduction in 2010 until July 2017. Patients were identified from a database maintained by interventional cardiologists performing USAT, by searching radiology reports on ‘thrombectomy, ‘fibrinolysis’, ‘pulmonary arteries’, ‘thoracic arteries’ and ‘EKOS’ and by using software implemented in the local electronic medical record. Demographic data and clinical information were extracted from medical records.
Definitions
PE was, according to guidelines, diagnosed with computed tomographic pulmonary angiography (CTPA) or, when considered unsafe, a high clinical suspicion with or without RV dysfunction on echocardiography [1]. High-risk PE was defined as PE with hemodynamic shock or hypotension (systolic blood pressure < 100 mmHg or a decline of > 40 mmHg) [1]. Shock is defined as hypotension or other signs of reduced tissue perfusion (altered mental state, oliguria, clammy and pale skin, hyperlactatemia) [1]. Intermediate-risk PE was defined as PE with RV dysfunction and/or elevated cardiac biomarkers [1]. The presence of RV dysfunction (dilated, enlarged or decompensated right ventricle, right heart strain, RV failure or dysfunction) was extracted from echocardiography and CTPA reports. Bleeding risk factors are based on American College of Chest Physicians and European Society of Cardiology guidelines [1, 28]. Major bleeding risk factors include recent hemorrhagic stroke, surgery, trauma, head injury, gastrointestinal bleeding, central nervous system malignancies and active bleeding. Minor bleeding risk factors are recent transient ischemic attack, current therapeutic anticoagulation, pregnancy, traumatic resuscitation, refractory hypertension, end stage liver disease, infectious endocarditis and active stomach ulcer.
Intervention
According to guidelines, ST is administered in high-risk PE patients without major contraindications (abovementioned major risk factors) [1]. USAT is considered in patients with high-risk PE and contraindications for ST whose condition is otherwise stable enough to be transported to the catheterization laboratory. Local practice varies regarding combination with other therapies, including extracorporeal membrane oxygenation (ECMO), thrombus aspiration and ST.
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USAT was performed by interventional cardiologists (Utrecht) or radiologists (Nieuwegein, Rotterdam, Amsterdam). Venous access was obtained via the femoral or internal jugular vein. The catheters are placed under fluoroscopic guidance according to CTPA images. Before inserting the EKOS-catheters, a pulmonary angiogram was performed. In case of bilateral PE, two EKOS-catheters were placed through the thrombus in the pulmonary artery under fluoroscopy, one on each side, and 12 mg of Alteplase was administered per catheter for 12 h. In case of unilateral PE, one EKOS-catheter was placed, and 24 mg of Alteplase was locally administered for 24 h. Echocardiography is frequently performed after catheter removal to assess the effect of USAT on RV dysfunction. Moreover, the patient’s clinical condition is monitored closely. In case of insufficient clinical and echocardiographic improvement, repeat CTPA is often performed to aid further clinical decisions regarding additional therapies. Heparin was administered according to predefined protocols. In one hospital (Utrecht), an intravenous bolus of heparin of 5000 IE or 80 IE per kilogram body weight is administered before USAT, and continuous infusion is started after USAT with a target activated Partial Thromboplastin Time (aPTT) of 2–2.5. In the other hospitals (Nieuwegein, Rotterdam, Amsterdam) heparin is administered concomitantly, based on a target level of 2.5–3, and continued afterwards. If no bleeding had occurred within 24–48 h after thrombolysis, standard anticoagulation therapy consisting of direct oral anticoagulants (DOAC), low molecular weight heparin (LMWH) or a vitamin K antagonist (VKA) was started.
Outcome Assessment
Primary outcomes were all-cause mortality during the first month of follow-up as well as major bleeding, including intracranial hemorrhage and fatal bleeding, as defined by the International Society on Thrombosis and Haemostasis (ISTH) [28]. Secondary outcomes were all-cause mortality and recurrent VTE after 3 months of follow-up, objectively confirmed by CTPA, perfusion-scintigraphy, pulmonary angiography, compression ultrasound or phlebography [1]. All outcomes were evaluated using clinical information as noted in patient files.
Analysis
Baseline characteristics and outcomes are reported as percentages or median with interquartile range (IQR) as variables were non-normally distributed. Patients treated with USAT and other therapies or USAT only were compared using two-sided Chi square and Fisher’s exact tests. All statistical analyses were performed with SPSS version 21 (SPSS Inc., Chicago, Illinois, USA). p values < 0.05 were considered significant.
Results
Characteristics of Study Subjects
We identified 35 patients with high-risk PE that underwent treatment with USAT in the Netherlands (Fig. 1). Two patients were lost to follow-up. Baseline characteristics are shown in Table 1. Before proceeding to therapy, definitive diagnosis was obtained by CTPA in 26/33, and by echocardiography in 5/33 patients. In two patients, PE was suspected on clinical grounds or high pulmonary artery pressures during coronary angiography, and later confirmed by CTPA and pulmonary angiography, respectively. USAT was performed bilaterally in 30/33 patients. Average dose of thrombolytic agent used during USAT in 25 patients treated with Alteplase was 26 mg (SD 11). Three patients received a different thrombolytic agent. USAT was discontinued earlier because of bleeding (n = 2) or in case of death during treatment (n = 3). In these patients, average dose of Alteplase is unknown.
Fig. 1
Flowchart of the included patients. AZN St. Antonius Hospital Nieuwegein, EMC Erasmus Medical Center Rotterdam, UMCU University Medical Center Utrecht, USAT ultrasound-facilitated, catheter-directed local thrombolysis, VUMC VU University Medical Center Amsterdam
Table 1
Baseline characteristics
n (% of 33)
Demographic data
Age (median years (IQR))
63 (51–71)
Female (%)
17 (52)
Patient related factors
History of VTE
8 (25)a
Active malignancy
8 (24)
Therapeutic anticoagulation (VKA, DOAC)
2 (6)
Clinical status
Hypotension (SBP < 100 mmHg)
18 (62)b
Shock
31 (93)a
RV dysfunction
30 (97)c
Resuscitation
20 (61)
Mechanical ventilation
16 (49)a
Major bleeding risk factors
1 risk factor
13 (39)
2 or more risk factors
1 (3)
Minor bleeding risk factors
1 risk factor
6 (18)
2 or more risk factors
1 (3)
Indication for USAT
Contraindications for ST
23 (70)
Insufficient clinical improvement after ST
6 (18)
Unknown
4 (12)
DOAC direct oral anticoagulants, IQR interquartile range, SBP systolic blood pressure, USAT ultrasound-facilitated, catheter-directed local thrombolysis, ST systemic thrombolysis, VKA vitamin K antagonist
an = 32; bn = 29; cn = 31
×
Outcomes
Table 2 shows primary and secondary outcomes. Twelve patients (36%, 95% CI 22–53) suffered from major bleeding, as specified in Table 3. Three patients died from bleeding (3/33, 9%). One of these patients presented with both high-risk PE and ischemic stroke, which was subject to hemorrhagic transformation after USAT. Two other patients with fatal bleeding both experienced traumatic resuscitation resulting in multiple rib fractures and died from hypovolemic shock after severe thoracic bleeding and bleeding from access sites.
Table 2
Outcomes
n (% of 33)
95% CI
Primary outcomes (after 1month)
Major bleeding
12 (36)
22–53
All-cause mortality
16 (49)
31–66
Secondary outcomes (after 3months)
All-cause mortality
16 (50)a
34–66
Recurrence of VTE
1 (3)a
1–16
Other outcomes
Hospital length of stay (median days (IQR))
17 (10–30)b
CI Confidence interval, IQR interquartile range, VTE venous thrombo-embolism
an = 32; bAssessed in all patients surviving the first month of follow-up
Table 3
Major bleeding
Major bleeding (as defined by the ISTH23)
n
Access site hematoma
4
Intrathoracic bleeding (hemothorax or chest wall after traumatic resuscitation or surgery)
4
Intraabdominal hematoma
3
Mucosal bleeding (nasal)
2
Bleeding from ECMO cannula site
1
Hematoma on lower arm, causing compartment syndrome
1
Hemorrhagic transformation of ischemic stroke
1
Total number of major bleeding episodes in 12 patients with major bleeding
16
ECMO extracorporeal membrane oxygenation, ISTH International Society on Thrombosis and Haemostasis, USAT ultrasound-facilitated, catheter-directed local thrombolysis, VKA vitamin K antagonist, VTE venous thrombo-embolism
Thirteen patients (39%, 95% CI 25–56) died from causes other than bleeding, of whom four did not respond to USAT and one died from recurrent PE. Irreversible brain damage, organ failure, heparin-induced thrombocytopenia, sepsis and glioblastoma led to the death of the other patients. No other episodes of recurrent VTE were observed.
USAT and Additional Therapies
Table 4 illustrates treatment and outcomes of fourteen patients that received additional therapy. Thrombus aspiration was performed concomitant with USAT in four patients. In the other cases, when the initial treatment of either ST or USAT led to insufficient improvement, other strategies were opted for.
Table 4
Additional therapies in USAT patients
Patient
ST
Thrombus aspiration
VCF
ECMO
Major bleeding
Mortality
1
Full dose
–
Yes
–
–
Yes
2
–
Yes
Yes
–
–
–
3
Full dose
Yes
–
Yes
–
Yes
4
Low dose
Yes
–
–
Yes
Yes
5
Loading dose
Yes
–
–
–
Yes
6
Full dose
Yes
–
–
Yes
–
7
–
Yes
–
Yes
–
–
8
–
Yes
–
–
Yes
–
9
–
Yes
–
–
–
–
10
Lower dose
–
–
–
–
Yes
11
Lower dose
–
–
–
–
Yes
12
Lower dose
–
–
Yes
–
–
13
Lower dose
–
–
–
–
–
14
Full dose
–
–
Yes
Yes
Yes
Total
10
8
2
4
ECMO extracorporeal membrane oxygenation, ST systemic thrombolysis, USAT ultrasound-facilitated, catheter-directed local thrombolysis, VCF vena cava filter
Of fourteen patients treated with USAT in combination with ST or thrombus aspiration, four patients suffered from major bleeding (29%, 95% CI 12–55), including one fatal. In total, seven patients died (50%, 95% CI 27–73). Similarly, in the group of patients treated with USAT only (n = 19, of whom two with ECMO support), major bleeding occurred in 42% (95% CI 23–64), whereas death occurred in 47% (95% CI 27–28). A somewhat higher mortality was seen in patients treated with both USAT and ST (n = 10) compared to patients treated with USAT with or without thrombus aspiration (n = 23) (70 vs. 39%, p = 0.14). The incidence of major bleeding was similar between those groups (30 vs. 39%, p = 0.71).
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Discussion
The aim of this study was to provide insight into current use and outcomes of USAT for high-risk PE in the Netherlands. We observed a very high rate of major bleeding and a high mortality rate. According to guidelines, USAT is to be considered in patients with high-risk PE and relative contraindications to ST. Our results indeed indicate a critically ill high-risk population, reflecting a real-world clinical setting. This case series adds important data on the characteristics and outcomes of this understudied patient population.
In our study population, major bleeding occurred in 36%, of which a quarter fatal. Several reasons can be identified for this higher incidence compared to ± 10% major bleeding in previous literature. Our study population involved patients with high-risk PE only, as opposed to 12–22% with high-risk PE in other studies [15, 16, 18, 19, 24, 25]. Furthermore, our findings are based on real-world data and reflect how current guidelines are put into practice. This means that our study population involves a large proportion of patients with contraindications to ST (in particular recent surgery or traumatic resuscitation) or whose condition did not improve despite ST. Finally, a high percentage in our cohort had major bleeding risk factors. All patients suffering from fatal bleeding after USAT had at least one minor or major risk factor. This restates that, especially in the presence of major risk factors, USAT carries a serious risk of major bleeding [4, 7].
A higher all-cause mortality was observed in our population compared to other studies [18, 19, 24, 25]. This could, similarly, reflect our study population of high-risk patients only, whose risk of death is almost ten times that of those with intermediate-risk PE [1, 4]. However, a recent meta-analysis on catheter-directed therapies for PE found an all-cause mortality of 13% in a separately analyzed group of 186 patients with massive (high-risk) PE [16]. This could be explained by differences in indication for USAT and patient selection. Our population consisted of those at highest risk among high-risk patients, a subgroup presumably not included in previous literature. A higher mortality was observed in patients who received USAT and ST concurrently. The incidences of major and fatal bleeding were similar, which may be explained by severe PE or comorbidities, as ST was administered in case of persistent or recurrent hemodynamic instability after USAT or vice versa, indicating a severely high-risk situation.
The population of patients with high-risk PE is very heterogeneous, ranging from mildly hypotensive, conscious patients to patients in cardiac arrest in which everything must be brought into play. Current guidelines aimed at high-risk PE patients should apply to both, while actual clinical management clearly differs between patients. Treatment decisions can be particularly difficult, since time is limited and both PE and bleeding can be life-threatening. A multidisciplinary approach to discuss available options (ST, USAT, other catheter-directed or surgical options) is important. The present study affirms that, although USAT is thought to be associated with a lower incidence of bleeding, this type of thrombolysis still carries an important risk of bleeding and mortality. Further research involving patients with high-risk PE is warranted to clarify which patients will benefit most from USAT.
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The main strength of the present study is the inclusion of all patients treated with USAT for high-risk PE in the Netherlands, with little loss to follow-up. Our study is the first case series of high-risk patients treated with USAT for PE. This illustrates how guidelines for high-risk PE are put to practice. Therefore, our results are generalizable to all hospitals treating patients according to current guidelines. In a setting of severe disease such as high-risk PE, results from case series are especially important to provide points of departure to guide patient selection.
Some limitations need to be addressed. First, our study population was small and heterogeneous. As only a small proportion of patients with PE has an indication for USAT, it is infrequently performed, which may limit individual experience. Treatment indications were heterogeneous, as decisions were made by the treating team of physicians. Other potential threats to internal validity are predominantly due to the retrospective design. Information bias could be introduced as data is extracted from medical records. Especially in acute situations, information on baseline characteristics might have been underreported. Moreover, even though hemodynamic stability was clearly defined, misclassification could still have occurred.
Conclusion
Although guidelines advocate the use of USAT in those with high-risk PE and contraindications for thrombolytic treatment, especially in this population it is associated with a very high incidence of major bleeding and mortality. As the first case series of solely high-risk PE patients treated with USAT, this study adds important data on outcomes of this understudied population. Our results illustrate that at least caution is warranted in critically ill patients with high-risk PE when considering USAT. Further research in high-risk patients is essential to establish the place of USAT as treatment of PE.
Compliance with Ethical Standards
Conflict of interest
AK reports to have received speakers fee from BTG. The other authors declare that they have no conflict of interest.
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Consent for Publication
For this type of study consent for publication is not required.
Ethical Approval
For this type of study formal consent is not required. This study was not subject to the Dutch Medical Research Involving Human Subjects Act and was approved by the Medical Research Ethics Committee before data acquisition.
Informed Consent
For this type of study informed consent is not required.
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Local Ultrasound-Facilitated Thrombolysis in High-Risk Pulmonary Embolism: First Dutch Experience
verfasst von
Maria A. de Winter Einar A. Hart Daniel A. F. van den Heuvel Adriaan Moelker Rutger J. Lely Karin A. H. Kaasjager Pieter R. Stella Steven A. J. Chamuleau Adriaan O. Kraaijeveld Mathilde Nijkeuter
