Antithrombotic therapy in patients undergoing TAVI: an overview of Dutch hospitals
Auteurs:
V. J. Nijenhuis, P. R. Stella, J. Baan, B. R. G. Brueren, P. P. de Jaegere, P. den Heijer, S. H. Hofma, P. Kievit, T. Slagboom, A. F. M. van den Heuvel, F. van der Kley, L. van Garsse, K. G. van Houwelingen, A. W. J. van’t Hof, J. M. ten Berg
To assess current antithrombotic treatment strategies in the Netherlands in patients undergoing transcatheter aortic valve implantation (TAVI).
Methods
For every Dutch hospital performing TAVI (n = 14) an interventional cardiologist experienced in performing TAVI was interviewed concerning heparin, aspirin, thienopyridine and oral anticoagulation treatment in patients undergoing TAVI.
Results
The response rate was 100 %. In every centre, a protocol for antithrombotic treatment after TAVI was available. Aspirin was prescribed in all centres, concomitant clopidogrel was prescribed 13 of the 14 centres. Duration of concomitant clopidogrel was 3 months in over two-thirds of cases. In 2 centres, duration of concomitant clopidogrel was based upon type of prosthesis: 6 months versus 3 months for supra-annular and intra-annular prostheses, respectively.
Conclusions
Leaning on a small basis of evidence and recommendations, the antithrombotic policy for patients undergoing TAVI is highly variable in the Netherlands. As a standardised regimen might further reduce haemorrhagic complications, large randomised clinical trials may help to establish the most appropriate approach.
The online version of this article (doi:10.1007/s12471-013-0496-6) contains supplementary material, which is available to authorized users.
Introduction
Since its introduction in 2002, TAVI has conquered a substantial portion of aortic interventions. It has become standard therapy in inoperable patients [1]. Moreover, in high-risk but operable patients, TAVI has shown to be non-inferior to surgical aortic valve replacement [2]. Due to growing experience, smaller catheters, and new-generation devices, the rate of complications has been reduced. However, the incidence of bleeding and vascular complications remains substantial and has been proven to affect survival [3, 4].
A standardised antithrombotic treatment may reduce the rate of these negative outcomes. However, no large randomised controlled trials have been performed, and current guidelines report only recommendations [5‐7]. The rationale for this survey was to provide insight into the current antithrombotic policy after TAVI. Results could be of value in decision-making on treatment policy for both experienced and inexperienced centres, and provide a basis for further research.
Methods
Setting and data collection
Currently, 14 hospitals in the Netherlands perform TAVI [8]. All centres were approached in the period from February to April 2013. In each hospital, we contacted the interventional cardiologist responsible for TAVI by an introduction e-mail addressing our intention to undertake a national survey. To maximise compliance, the interview was performed by visit (n = 4) or telephone (n = 9). In 1 case, communication was per e-mail. The interview was structured according to the printed survey depicted in the “Supplements”.
Assumptions
In the development of the survey, we assumed antithrombotic treatment could be different per prosthesis or approach. We suspected it to be more dependent on the approach because of the bleeding risk, and designed the survey accordingly. Besides closed questions for plain parameters such as dose and duration, we added two open questions for which we expected diverse answers.
Data analysis
Results are categorical and given as frequencies.
Results
Protocol
A local protocol for antithrombotic treatment in patients undergoing TAVI was available in all centres. In the majority of cases, the protocol was based upon local experience. Regarding the duration of dual antiplatelet therapy (DAPT), centres often followed the recommendations of the respective companies producing prostheses. These include 3 months of DAPT for Edwards SAPIENTM (Edwards Lifesciences, Irvine, USA) and 6 months for Medtronic CoreValveTM (Medtronic, Minneapolis, USA).
Procedure
During the TAVI procedure, all centres used unfractionated heparin (UFH) as anticoagulant. The dose of UFH was according to weight in 3 centres and a standard initial bolus was given in 11 of the 14 centres, mostly 5000 IU (n = 6). Activated clotting time (ACT) was measured in 13 of the 14 centres. Target ACT was >250 s (n = 9), >200 s (n = 2), or >300 s (n = 3).
In patients with an indication for oral anticoagulation (OAC), 3 centres continued OAC periprocedure with an international normalised ratio (INR) aimed at 2.0 or <2.5, whereas 11 of the 14 centres discontinued OAC periprocedure. Of these centres, 1 never performed bridging therapy, 3 always performed bridging therapy, and 7 performed bridging therapy in patients at high thrombotic risk only (e.g. mechanic mitral valve) as illustrated in Fig. 1.
Fig. 1
Periprocedure antithrombotic policy in patients with an indication for oral anticoagulation (OAC)
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Concomitant antiplatelet therapy
In patients without an indication for OAC, all centres prescribed lifelong low-dose aspirin (80–100 mg). When a patient was not preloaded with aspirin, a loading dose (200–600 mg) was given in the week prior to procedure, mostly at day −1 (n = 8). In addition to aspirin, 13 centres routinely prescribed clopidogrel as adjunctive antithrombotic medication. Clopidogrel was loaded in all centres with a loading dose of either 300 (n = 9) or 600 mg (n = 4). All centres prescribed a maintenance dose of 75 mg for a varying duration of 1 (n = 1), 3 (n = 9), and 6 (n = 3) months (Fig. 2).
Fig. 2
Duration of dual antiplatelet therapy (DAPT) after TAVI in patients without an indication for oral anticoagulation (OAC)
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One centre, which only performed transapical procedures, used no additional clopidogrel at all. In total, 4 centres discriminated in the addition of clopidogrel. In 2 centres, discrimination was based upon prosthesis type: SAPIENTM versus CoreValveTM. Whereas 1 centre reduced the loading dose (600 to 300 mg) and the duration (6 to 3 months) after SAPIENTM implantation, the other centre omitted clopidogrel completely after SAPIENTM implantation. In the other 2 centres, discrimination in DAPT was based upon approach: clopidogrel was loaded at day 0 for transfemoral TAVI and at day +1 for transapical TAVI.
In patients with an indication for OAC, concomitant antiplatelet therapy was used in 13 of the 14 centres for all prostheses and approaches. Concomitant antiplatelet therapy either consisted of clopidogrel (n = 9) or aspirin (n = 4) (Fig. 3). A single dose of aspirin in addition to clopidogrel at the time of loading was given in 1 centre. Two centres only used aspirin in addition to OAC when a patient was already loaded, otherwise clopidogrel was administered. Clopidogrel was loaded in all centres with a loading dose of either 300 (n = 5) or 600 mg (n = 4). All centres prescribed a maintenance dose of 75 mg for a varying duration of 1 (n = 1), 3 (n = 6), and 6 (n = 2) months. Considering aspirin, patients received a loading dose at day −1 (n = 1) or day 0 (n = 1) and a maintenance dose for 6 months (n = 1) or lifelong (n = 3).
Fig. 3
Concomitant antiplatelet therapy after TAVI in patients with an indication for oral anticoagulation (OAC)
×
In total, 2 of the 14 centres discriminated in the addition of clopidogrel. In both of these centres, this discrimination was based upon prosthesis type: SAPIENTM versus CoreValveTM. Whereas 1 centre reduced the loading dose (600 to 300 mg) and the duration (6 to 3 months) after SAPIENTM implantation, the other centre omitted clopidogrel completely after SAPIENTM implantation. Centres prescribing aspirin did not discriminate between prosthesis types or approaches.
Bleeding risk
The prescribed antithrombotic regimen was based upon bleeding risk in 7 of the 14 centres. Three centres omitted clopidogrel completely in case of very high bleeding risk or severe thrombocytopenia according to local protocol. One centre reduced the duration of clopidogrel treatment (6 to 3 months) in case of a high bleeding risk. Two centres adjusted the time of commencing and ceasing clopidogrel treatment individually.
DAPT pre-TAVI
When a patient had undergone a recent (≤1 year) PCI and had an absolute indication for DAPT prior to TAVI, all centres continued DAPT. When a patient received a newer thienopyridine (e.g. prasugrel, ticlopidine), the same therapy was continued in 8 centres whereas the thienopyridine was changed to clopidogrel in 2 of the 14 centres. The other 4 centres had no experience with such a scenario.
Triple therapy pre-TAVI
If a patient was receiving triple therapy (i.e. OAC and DAPT) prior to TAVI, only 1 centre continued this. Triple therapy was routinely discontinued in 6 centres or continued for as short as possible (1–2 weeks) in 2 of the 14 centres. Two centres preferred not to continue triple therapy and adjusted medication on an individual basis, whereas 3 centres had no experience with such cases.
If triple therapy was discontinued, aspirin was omitted routinely in 4 centres and clopidogrel in 1 centre. Two centres omitted aspirin only when the patient received triple therapy because of a recent stent and omitted clopidogrel in other cases. OAC was omitted until clopidogrel could be stopped in 1 centre.
New-onset persistent atrial fibrillation
When a patient developed persistent atrial fibrillation (AF) after TAVI during the hospitalisation period and had an indication for OAC, aspirin was replaced by OAC in 9 of the 14 centres. Four centres only replaced aspirin by OAC when the patient received DAPT prior to TAVI because of a recent stent and replaced clopidogrel by OAC in other cases. OAC was added to DAPT in 1 centre.
Discussion
TAVI is an accepted treatment for high-risk patients with severe symptomatic AS and is the first choice of treatment for inoperable patients [1, 2]. Nevertheless, TAVI remains associated with a relatively high number of haemorrhagic and embolic complications [3, 4]. Moreover, little is known about antithrombotic treatment strategies and current guidelines report only recommendations [5‐7] In this survey, we interviewed centres performing TAVI in the Netherlands regarding antithrombotic treatment after TAVI. Although mostly according to one or more recommendations, inter-centre variability of the antithrombotic policy is high.
Haemorrhagic complications are frequent, and major and disabling or life-threatening bleeding after TAVI occurs in approximately 22 % and 16 %, respectively [3]. Regardless of the mechanism, a disabling or life-threatening bleeding is an important predictor of acute and late mortality [9‐13]. More insight into the role of the antithrombotic treatment regimen could provide the most desirable antithrombotic treatment to possibly reduce the rate of disabling or life-threatening bleeding and adverse outcomes [6].
The most prevalent thromboembolic complication is stroke, which occurs in approximately 2.5 % to 4.1 % at 30 days [4, 14‐16]. Most acute strokes are procedure related and of embolic origin, caused by manipulation with large catheters [17]. The incidence of late stroke is approximately 2 % and similar to that observed to other populations of elderly people [11, 18]. Late strokes are more prevalent in patients with classical risk factors such as (new-onset) AF [17, 19]. However, in the PARTNER IB trial, the portion of haemorrhagic stroke after 30 days was higher in the TAVI group than in the medical treatment group [18], emphasising the double-edged sword of antithrombotic treatment in the elderly.
Only the American College of Cardiology Foundation/Society of Thoracic Surgeons (ACCF/AATS/SCAI/STS) Expert Consensus Document on TAVI has mentioned antithrombotic treatment during procedure and recommends UFH with an ACT >300 s [6]. In the PARTNER I trial, UFH was given in an initial bolus of 5000 IU with a target ACT >250 s [1, 2]. In this survey, we found UFH was used in all centres and ACT is routinely measured in 13 of the 14 interviewed centres. The target ACT is >300 in only 3 centres and >250 s in 9 of the 14 centres.
Following TAVI, DAPT consisting of aspirin (lifelong) and clopidogrel (initial period) is currently recommended [5‐7]. However, this is largely based on retrospective registries and 2 cases of severe postprocedural thrombocytopenia in patients treated with clopidogrel without a loading dose in a preliminary first-in-man study with the CoreValveTM [20]. A second rationale for adding clopidogrel to aspirin is supported by the histopathological finding that incorporation of the CoreValveTM prosthesis into the aortic wall by means of endothelialisation is a chronological integration over a period of approximately 3 months [21].
Whereas aspirin (lifelong) is recommended unanimously, recommendations for the duration of clopidogrel vary from 1 to 3 months [7], 1 to 6 months [5] and 3 to 6 months [6]. In this survey, we found aspirin was prescribed in all centres according to recommendations. However, concomitant clopidogrel was prescribed in 13 of the 14 centres. Duration of concomitant clopidogrel therapy was 3 months in over two-thirds of cases. In 2 centres, duration of concomitant clopidogrel was based upon type of prosthesis: 6 months for CoreValveTM versus 3 months for intra-annular prostheses (e.g. SAPIENTM, JenaValveTM). These centres tended to be more careful with CoreValveTM because of the supra-annular design and longer struts, and possible subsequent proneness to more thromboembolic complications, although this has not been described in the literature [4].
In patients with AF or another indication for OAC, the best antithrombotic treatment regimen is unknown. In these patients, a combination of OAC and aspirin or thienopyridine is generally used [5]. We found that in patients with an indication for OAC, 13 of the 14 centres prescribed concomitant antiplatelet therapy. Of these, 9 centres used clopidogrel and 4 centres used aspirin.
Concomitant antiplatelet drugs have shown to increase the risk for major bleeding in patients with AF [22‐24]. A recent Danish registry study shows that in patients with AF and myocardial infarction, the combination of OAC+clopidogrel was comparable with triple therapy [25]. However, in the recent WOEST trial, OAC+clopidogrel was superior to triple therapy in patients with AF undergoing drug-eluting stent placement including a striking decrease in all-cause mortality [26]. In this survey, 1 centre would continue triple therapy when a patient received triple therapy prior to TAVI. When discontinued, 4 centres omitted aspirin in any case and 1 centre omitted clopidogrel in any case. Two centres omitted aspirin only when patients received triple therapy because of a recent stent and omitted clopidogrel in other cases. One centre omitted OAC until clopidogrel could be stopped.
Leaning on a small basis of evidence and recommendations, we found considerable heterogeneity in the antithrombotic treatment practised between TAVI performing centres in the Netherlands. In most TAVI registries, information about antithrombotic treatment is not available. Generalising national antithrombotic policy may homogenise this factor, making clinically important outcomes more comparable in addition to the initiative of VARC-2 [27]. Furthermore, further research is needed to study the effect of antithrombotic therapy on clinical outcomes. We are currently setting up a multicentre randomised controlled clinical trial in the Netherlands, investigating the safety and efficacy of omitting clopidogrel in the first 3 months after TAVI versus aspirin+clopidogrel in patients without an indication for OAC at baseline, and versus OAC+clopidogrel in patients with an indication for OAC at baseline.
Study limitations
This study presents a description of current clinical practice in Dutch hospitals with respect to antithrombotic therapy in patients undergoing TAVI. It does not describe the outcome and complications of these treatment methods and none of the interviews were verified with patient data. Furthermore, this study only describes the current antithrombotic strategy and does not consider possible previous antithrombotic strategies or the experience of centres with the TAVI procedure. Finally, we approached only one cardiologist per centre assuming that cardiologists belonging to a single hospital and organisation apply the same strategies.
Conclusion
Leaning on a small basis of evidence and recommendations, the antithrombotic policy for patients undergoing TAVI is highly variable in the Netherlands. As a standardised regimen might further reduce haemorrhagic complications, large randomised clinical trials may help to establish the most appropriate approach.
Funding
None.
Conflict of interest
None declared.
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Antithrombotic therapy in patients undergoing TAVI: an overview of Dutch hospitals
Auteurs
V. J. Nijenhuis P. R. Stella J. Baan B. R. G. Brueren P. P. de Jaegere P. den Heijer S. H. Hofma P. Kievit T. Slagboom A. F. M. van den Heuvel F. van der Kley L. van Garsse K. G. van Houwelingen A. W. J. van’t Hof J. M. ten Berg
