1. Introduction
The prevalence of aortic valve disease and particularly calcific aortic valve disease is increasing due to the aging population [
1]. Since its introduction by Alain Cribier and colleagues in 2002 [
2], transcatheter aortic valve implantation (TAVI) has become the primary therapeutic strategy for patients with symptomatic severe aortic stenosis who are at higher surgical risk or those older than 75 years [
3], as well as for selected patients with severe aortic regurgitation [
4].
Compared with surgical access such as the transapical approach, transfemoral access was associated with mortality and morbidity benefits that justify its use as a mainstream strategy [
5,
6]. However, despite the advancement of percutaneous closure device technology, access site complications (including bleeding and vascular complications) remain a major concern in transfemoral TAVI [
7,
8]. Vascular access site-related complications and bleeding are also predictors of poor procedural outcomes [
7,
9,
10]. During the procedure, heparin administration is recommended to maintain an activated clotting time (ACT) of 300 s to reduce thromboembolic risk [
11]. Heparin reversal, with protamine sulfate, is associated with reduced major and life-threatening bleeding events in the absence of an increase in thromboembolic events in patients undergoing TAVI [
12]. However, the routine practice across centers is variable and data defining indications and the optimal dosing regimen of protamine after TAVI are still scarce.
Therefore, our retrospective analysis aimed to evaluate the efficacy and safety of low-dose protamine compared to full-dose protamine in preventing bleeding and vascular complications in patients undergoing transfemoral TAVI.
2. Methods
2.1. Study Population and Inclusion Criteria
Between January 2015 and December 2020, patients admitted to the Department of Cardiology of the University Hospital of the RWTH Aachen due to severe aortic valve stenosis or severe aortic valve regurgitation who met the criteria for treatment based on the European Society of Cardiology guidelines on valvular heart disease [
3] were discussed in our biweekly heart team meeting. The heart team includes an interventional cardiologist, an imaging cardiologist, a cardiovascular surgeon, and an anesthesiologist. Patients were evaluated based upon their medical records, including coronary angiography, pulmonary function, duplex Doppler sonography of the carotid arteries, transthoracic echocardiography, and transoesophageal echocardiography if needed. To estimate the cardiac operative risk, logistic EuroScore, STS-score, and Katz index were documented and patients were subsequently evaluated at the bedside by the heart team. Out of a total of 989 patients accepted for TAVI, 92 were excluded from the current analysis due to non-transfemoral approaches (transapical
n = 60, transaortic
n = 29, transsubclavian
n = 2, transaxillary
n = 1). All patients undergoing TAVI via the femoral artery (
n = 897) were included in this retrospective study. Further details including patient disposition are demonstrated in
Figure 1.
2.2. Ethical Approval
The protocol for this study as a retrospective analysis of routinely collected data was approved by the local ethics committee (EK 481/21). The study was performed in accordance with the ethical standards defined by the latest version of the Declaration of Helsinki.
2.3. Transcatheter Aortic Valve Implantation (TAVI)
The procedure was carried out by an interventional cardiologist, a cardiothoracic surgeon, and an anesthesiologist. TAVI procedures in our center are carried out under analgesic sedation. Femoral arterial access was guided by using a preoperative computed tomography angiogram of the pelvic vasculature. According to our standard operating procedure, weight-adapted unfractionated heparin was administered before placement of the TAVI introducer sheath. ACT was measured every 20 min and additional heparin was given to maintain ACT above 300. Closure of the access site was performed using either Prostar, Manta, or ProGlide devices. An additional pressure bandage was applied for 12 h following the intervention. Dual anti-platelet therapy was prescribed for 6 months.
2.4. Heparin Reversal
Heparin reversal took place after vascular closure in all patients. The standard dose was 1 mg protamine for every 100 units of unfractionated heparin that were given in the last 30–60 min. In long procedures, 0.75 of protamine was additionally administered per 100 IU of heparin that were given earlier than 60 min. ACT measurements were done both before and after protamine administration. Indications for low-dose protamine included planned PCI during the index procedure or in the 4 weeks prior to the TAVI. ‘Low dose’ protamine was half the usual calculated dose.
2.5. Post-Interventional Care
After the procedure, patients were monitored for 24 h in the intermediate care unit. Transthoracic echocardiography was performed immediately after TAVI and before discharge from our center. All patients underwent a duplex Doppler sonography of the access site of the femoral artery.
2.6. Study Outcomes and Definitions
The classifications of the vascular access site and access-related complications were based on the standardized definitions for important clinical endpoints in TAVI as proposed by the updated consensus document of the Valve Academic Research Consortium from 2012 (VARC-2 criteria) [
13]. Primary outcomes were in-hospital (pre-discharge) life-threatening bleeding, major bleeding, major vascular complications, or death from any cause, taken individually or as a combined endpoint. Secondary outcomes consisted of minor bleeding, minor vascular complications, stroke, and myocardial infarction.
2.7. Statistical Analysis
Continuous variables are reported as mean ± standard deviation if normally distributed and median (interquartile ratio) if not normally distributed. Normal distribution was assessed by visual histogram inspection as well as with the Kolgomorov–Smirnov test. Dichotomic variables are reported as a proportion (percentage). The comparison of baseline continuous variables was performed with a t-test for normally distributed variables and with a Mann–Whitney test for non-normally distributed variables; distributions of binary variables were compared with a chi-squared test. In order to assess the association of two different protamine doses with interventional outcomes and complications, we performed a univariable logistic analysis; results are expressed as an odds ratio (OR) with a 95%-confidence interval. In order to adjust for possible confounders, we performed multivariable logistic analysis for the prediction of the combined endpoint, including in the model all variables with p < 0.10 in the univariable analysis (EuroScore, COPD, peripheral artery disease, glomerular filtration rate, hemoglobin levels, LDL levels, coronary artery disease, dual antiplatelet therapy) and then performing backward selection.
To exclude the effects of different baseline characteristics between the two study groups, we performed propensity matching based on sex, age (with a tolerance of ±5 years), and dual antiplatelet therapy. We then repeated our analyses in the matched population.
Analysis was performed with SPSS software. Statistical significance was awarded for p < 0.05.
4. Discussion
Transfemoral TAVI has emerged as an optimal therapy for high-risk patients with aortic stenosis and selected patients with aortic insufficiency. Access site-related complications remain the primary driver of post-interventional morbidity and mortality. In addition to closure devices, heparin reversal by protamine sulfate is an option to reduce access site bleeding, although a standardized dosing scheme during TAVI is lacking. Therefore, the aim of our study was to compare the efficacy of two regularly used doses of protamine in a retrospective analysis.
The major finding of our analysis is that full-dose protamine administration (1:1 protamine/heparin ratio) following transfemoral TAVI was associated with a lower incidence of the combined intra-hospital endpoint of all-cause mortality, major and life-threatening bleeding, as well as major vascular complications when compared with a low-dose protamine scheme (0.5:1 protamine/heparin ratio), mainly due to a significantly lower incidence of major and life-threatening bleeding. First, our data show an overall complication rate mostly comparable to major cohorts [
14], especially when outcomes were defined according to VARC-2 criteria [
7]. One of the largest registries of aortic stenosis treatment worldwide, the GARY registry, reported in-hospital mortality, major vascular complications, and major bleeding events in 5.2%, 4.1%, and 26.3% of patients following TAVI [
15]. The rates of in-hospital mortality and major vascular complications were approximately equal to our data (4.1% for both). However, the rate of life-threatening and major bleeding in the GARY registry was considerably higher than that of our analysis (26.3% vs. 5.6%). It is likely that the difference in rates is accounted for by differences in definitions of major bleeding events. However, overall, our study cohort is representative of real-life data from larger registries.
Although the only existing single-center randomized clinical trial (PS TAVI) on protamine sulfate during TAVI, which was limited by its small sample size (
n = 100), provided no evidence for a significant decrease in major and life-threatening bleeding complications among patients who routinely received protamine sulfate as compared to those in the placebo group [
16], the use of protamine after cardiac and vascular interventions is routine practice [
17,
18]. In a meta-analysis of five trials including 6762 patients, protamine was associated with significantly less major bleeding after coronary angioplasty [
19]. There also seems to be no greater rate of stent thrombosis after elective PCI when protamine is used [
20]. A recent study reported protamine usage to lower significant bleeding and major vascular complications after TAVI without increasing the incidence of thromboembolic events [
12]. More robust evidence on the efficacy of routine protamine administration versus selective protamine administration after TAVI is expected when the results of the ongoing ACE PROTAVI randomized double-blind trial are published. Notably, the optimal protamine dose required to prevent major bleeding events after TAVI has not been addressed. Evidence from the field of cardiac surgery suggests that a high dose of protamine sulfate (>1:1) can lead to adverse outcomes with respect to increased bleeding complications due to impaired hemostasis through the downregulation of thrombin generation as well as other side effects of protamine [
21,
22,
23]. On the other hand, a lower dose of protamine (<0.6 mg per 100 IU of heparin) was associated with a reduced need for blood transfusion [
20]. A protamine-heparin ratio between 0.6 to 1 was consequently suggested to provide optimal effects on hemostasis and bleeding during cardiothoracic operations [
22], with a generally proposed dosing regimen of 1 IU per IU of heparin [
24].
Our routine practice of the use of low-dose protamine in patients with recent PCI (0.5:1 protamine/heparin ratio) with the intention of balancing bleeding complications with stent thrombosis offered the opportunity to compare two doses of protamine in a real-world scenario. Patients receiving low-dose protamine experienced a significantly higher rate of the combined intra-hospital endpoint of death, life-threatening major bleeding, and major vascular complications compared with patients receiving full-dose protamine. This was driven by a significantly higher rate of both life-threatening and major bleeding events in the low-dose group, and translated into a higher blood transfusion volume as well as a longer hospital stay.
Whilst it is tempting to speculate that incomplete heparin reversal using the low-dose protamine scheme is insufficient in preventing access site bleeding in patients after TAVI, the conclusion should be tempered by the higher risk profile, as demonstrated by EuroScore and more frequent medication of anti-platelet and anticoagulant agents in those allocated low-dose protamine. In order to control for these baseline differences, we performed propensity matching between both groups, although this was only partially successful given that the primary indication for low-dose protamine was a recent or concurrent coronary intervention. Nevertheless, despite propensity matching, the primary combined endpoint as well as secondary endpoints such as minor bleeding, blood transfusion volume, and the length of hospital stay were still significantly greater in the low-dose group. A multivariable analysis determined that low-dose protamine alongside with EuroScore and baseline hemoglobin predicted the combined endpoint. Even after repeating the same analysis in the matched model, the combined endpoint was predicted only by low-dose protamine and baseline hemoglobin.
With respect to thrombosis, the overall rates of intervention-related stroke and myocardial infarction were extremely low in both study groups. We found no association between stroke rates and the dosage of protamine used. Stent thrombosis was confirmed only in one patient who received low-dose protamine after recent elective PCI, a further two cases of myocardial infarction due to coronary embolism were reported in patients in the full-dose protamine group. Overall, the extremely low rate of thromboembolic complications demonstrates that protamine application, independently of the suggested dosing scheme, seems not to be associated with thrombotic events.