Int J Med Sci 2026; 23(5):1588-1594. doi:10.7150/ijms.130315 This issue Cite

Research Paper

Changes of the QRS-T angle in Patients Undergoing Transcatheter Aortic Valve Implantation

Scharbanu Amirie1,2, Behnam Zadeh1,2, Oliver Bruder1,2, Thomas Schmitz1,2, Karl Toischer4, Christoph Julian Jensen3,4 Corresponding address

1. Department of Cardiology and Angiology, Contilia Heart and Vascular Center, Elisabeth-Krankenhaus Essen, Essen, Germany.
2. Ruhr University Bochum, Bochum, Germany.
3. B. Braun Ambulantes Herzzentrum Kassel, Kassel, Germany.
4. Department of Cardiology and Pulmonology, University Medical Center Goettingen, Goettingen, Germany.

Received 2025-12-21; Accepted 2026-3-4; Published 2026-3-17

Citation:
Amirie S, Zadeh B, Bruder O, Schmitz T, Toischer K, Jensen CJ. Changes of the QRS-T angle in Patients Undergoing Transcatheter Aortic Valve Implantation. Int J Med Sci 2026; 23(5):1588-1594. doi:10.7150/ijms.130315. https://www.medsci.org/v23p1588.htm
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Abstract

Graphic abstract

Objective: This study aimed to investigate changes in the frontal QRST angle in patients who underwent transcatheter aortic valve implantation (TAVI).

Background: The QRS-T angle is a prognostic marker in several clinical settings. The impact of TAVI on the QRS-T angle, especially in the long term, has not been investigated thus far.

Methods: A total of 104 patients undergoing transcatheter aortic valve replacement due to severe aortic stenosis underwent a standardized digital 12-lead ECG for the calculation of the QRS-T angle before and 24 h after the intervention, as well as 30 days after the intervention.

Results: There was a significant and dynamic change in the QRS-T angle during the TAVI procedure. An initial increase in the number of patients with a wider QRS-T angle (>90°) was notable immediately after valve replacement. After 30 days, there was a significant decrease in the number of patients with a wide QRS T-angle.

Conclusion: The QRS-T angle widens early after transcatheter aortic valve replacement and improves below the baseline during a 3 months follow-up. This could be related to the cardiac

ischemic stress during valve intervention. In contrast, QRS-T angle narrowing during follow-up might reflect the normalization of left ventricular hemodynamics and prognostic improvement.

Keywords: QRS-T angle, aortic valve stenosis, transcatheter aortic valve replacement

Introduction

Aortic valve stenosis (AVS) is the most common valvular heart disease in Europe and North America that requires surgical or catheter intervention [1, 2, 3]. Prognosis is poor in untreated severe aortic stenosis as soon as symptoms (angina, dyspnea, syncope) develop [4,5,6]. Surgical aortic valve replacement (SAVR) has been shown to improve symptoms and survival and restore life expectancy to that of the general population [7,9]. However, advanced age and comorbidities leave many patients untreated [8]. During the last decade, transcatheter aortic valve implantation (TAVI) has become an established alternative to surgery in elderly patients with high or intermediate surgical risks [10,11].

Individual risk assessment and joint decision-making (heart team approach) are crucial for adequate treatment in patients with AVS. Apart from imaging, a simple derived parameter from routine ECG would be extremely helpful in risk stratification of patients following TAVI. The frontal QRS-T angle, which represents the balance of depolarization to repolarization and, thus, electrical instability, is a promising risk marker [12]. The QRS-T angle has a strong prognostic impact in various clinical settings [14-17], and a poor prognosis in patients with a wide QRS-T angle undergoing SAVR has been recently demonstrated [13]. In a previous study, we identified a correlation between the extent of myocardial damage caused by ST-elevation myocardial infarction (STEMI), as quantified by late gadolinium enhancement (LGE) on cardiac magnetic resonance imaging (MRI), and a larger QRS-T angle (≥ 90°) [18]. In addition, the extent of myocardial fibrosis in patients with hypertrophic cardiomyopathy is associated with a wide QRS-T angle and can therefore be considered a prognostic predictor of mortality [19].

The serial changes in the QRS-T angle and the impact of valve intervention on the QRS-T angle have not yet been investigated.

This study aimed to examine the long-term changes in the frontal QRST-angle in patients undergoing transcatheter aortic valve replacement.

Methods

In this retrospective trial, patients who underwent transcatheter aortic valve replacement (from January 2014 to December 2014) for symptomatic severe aortic valve stenosis at the Department of Cardiology and Angiology of the Elisabeth Hospital Essen were enrolled. In general, the indications for TAVI followed the current guidelines, and individual decisions were based on the heart team approach for every patient [20]. Demographic, imaging, and procedural data were recorded. Routine 12-lead digital ECG was obtained 24 h before, 24 h after TAVI, and at 1-month follow-up. The 12-lead digital ECGs using a Schiller Cardiovit AT 102 plus® were recorded at a speed of 50 mm/s with 10 mm/mV for the limb and precordial leads. The computerized values of the QRS and T-wave axes were automatically provided by the Schiller AT 102 plus® software. The frontal QRS-T angle was calculated as the absolute difference between the frontal QRS- and frontal T-wave axes and expressed as absolute values (Oehler). Due to the retrospective nature of this study informed consent was waived by the ethics committee.

Statistical analysis

Continuous variables are presented as mean ± standard deviation and were compared using two-way ANOVA. Categorical variables are presented as numbers and percentages and were compared using the chi-square test. Differences between groups were analyzed using a two-way ANOVA. All variables with a univariate p-value <0.05 were included in the final multivariate model. The results of the binary logistic regression model are presented in the same way as the variables in the univariate analysis. All reported p-values were two-sided, and a p-value <0.05 was considered statistically significant. All statistical analyses were performed using IBM SPSS Statistics version 26.0 (IBM Corp., Armonk, N.Y., USA).

Results

A total of 104 patients (82.5±6.19 years, 57,69% female) with symptomatic high-degree aortic valve stenosis (mean maximum velocity 4.19±0.68, mean transvalvular gradient 44.21±13.64, mean aortic valve area 0.74±0.20) underwent transcatheter aortic valve replacement. The median ejection fraction was 52.27 ± 11.73. The rate of syncope prior to TAVI was 14%. The mean (± SD) log. EuroSCORE was 22.38±11.29. (Table 1).

a.) QRS T angle pre TAVI:

Patients with a QRS-T angle ≥90° (n=36; mean angle 130.44° ± 28.70°) at baseline experienced episodes of syncope with significantly greater frequency (p=0.0022) than those with a QRS-T angle < 90° (n=68). Furthermore, patients with a QRS-T angle < 90° showed a higher rate of pulmonary disease (p=0.02) and cancer (p=0.04). (Table 2).

b.) QRS T angle post TAVI

Immediate results post TAVI showed a higher number of patients with a wide QRS-T angle ≥90° (n=48; mean angle 133.81° ± 30.95°) and significantly lower max grades of 64.85 ± 24.03 in comparison to 56 patients with a lower QRS T angle <90° (max grad 75.47 ± 22.97; p=0,0256). The left ventricular mass (Devereux) was significantly lower in patients with a QRS-T angle ≥90° (219.90 ± 53.01; p=0.0498). (Table 3).

c.) One-month follow-up data:

The one-month follow-up (30 days) data indicated a decrease in the patient rate with a high QRS-T angle (n=22) compared to pre-TAVI and a 24-hour analysis post TAVI. The incidence of cancer and pulmonary diseases remained significantly higher in the group of patients with a lower QRS-T angle (< 90°; 0.0097 pulmonary disease; cancer 0.0432). (Table 4).

Discussion

Our study shows that the QRS-T angle, an easily accessible risk marker computed with every routine surface ECG, widens early after transcatheter aortic valve replacement, reflecting global ischemic stress during valve intervention, and improves below baseline during follow-up, which in turn reflects the long-term effects of normalization of left ventricular hemodynamics and prognostic improvement (Figure 1).

 Table 1 

Demographic, imaging, angiographic and QRS-T angle data at baseline

n = 104
Gender w (%)57.7
Age (years)82.5 + 6.2
BMI (kg/m²)26.8 + 4.8
CAD (%)52.9
1 vessel11.5
2 vessels7.7
3 vessels33.7
In %
prev MI 5.8
prev CABG 22.1
prev PCI 26.9
In %
Diabetes31.7
Hypertension98.1
Hypercholesterolemia68.3
Smoker6.7
Family history5.8
Ckd28.9
Carotid disease14.4
Periph. Disease18.3
Af9.6
Pulmonary disease24.1
Cancer9.6
Log Euroscore-I in %22.4 + 11.3
Syncope in %14.4
CCS (I-IV)1.1 + 0.9
NYHA (I-IV)3.0 + 0.6
QRS-T angle in degree °
pre TAVI72.8 + 49.5
post TAVI90.1 + 49.6
FU TAVI58.9 + 47.4
Lab results
Creatinine (mg/dl)1.2 + 0.7
Hb (g/dl)12.0 + 1.6
TnT (ng/l)0.1 + 0.1
Creatinine post (mg/dl)1.3 + 0.8
Hb post (g/dl)9.8 + 1.5
TnT max post (ng/l)0.2 + 0.2
EF pre in %52.2 + 11.7
Left atrial diameter (mm)43.3 + 6.0
Left ventricular enddiastolic diameter (mm)48.1 + 8.0
Max V (m/s)4.2 + 0.7
Max grad (mmHg)71.0 + 24.0
Pmean pre (mmHg)44.2 + 13.6
AVA pre (cm²)0.7 + 0.20
EF post in %53.0 + 9.4
Velocity (m/s)2.2 + 0.6
Pmean post (mmHg)12.3 + 5.3
Pmax post (mmHg)23.3 + 9.1
Valve dimensions (mm)26.5 + 2.1
Access transfemoral (%)99.0
Balloon size in mm22.1 + 4.8
P-P Gradient pre (mmHg)45.5 + 19.6
P-P Gradient post (mmHg)6.2 + 5.2
 Table 2 

QSR-T angle and clinical data at baseline stratified by QRS-T angle.

QRS-T ≥ 90 pre TAVIQRST < 90 pre TAVIp value
(n=36)(n=68)
Gender w (%)64.055.90.28
Age (years)83.2 ± 5.482.4 ± 6,50.22
BMI (kg/m²)27.1 ± 4.1226.5 ± 5.00.25
CAD (%)47.2255.90.20
1 vessel5.614.7
2 vessels11.15.9
3 vessels30.635.3
In %
prev MI8.34.40.21
prev CABG19.423.50.32
prev PCI22.227.90.27
In %
Diabetes41.726.50.13
Hypertension100.097.10.15
Hypercholesterolemia77.863.20.06
Smoker2.88.80.12
Family history5.65.90.47
Ckd27.827.90.49
Carotid disease11.116.10.24
Periph disease16.720.60.31
Af5.610.30.13
Pulmonary disease11.129.40.0269
Cancer2.813.2
Log Euroscore in %22.5 ± 13.622.4 ± 9.80.48
Syncope in %27.87.40.0022
CCS (I-IV)1.3 ± 0.81.0 ± 1.00.16
NYHA (I-IV)3.0 ± 0.72.9 ± 0.60.50
QRS-T angle °130.4 ± 28.741.7 ± 23.8< 0.001
Crea base (mg/dl)1.2 ± 0.71.2 ± 0.80.50
Hb base (g/dl)12.0 ± 1.412.1 ± 1.70.36
TnT base (ng/l)0.02 ± 0.020.1 ± 0.20.38
crea post (mg/dl)1.3 ± 1.01.2 ± 0.80.28
Hb post (g/dl)9.7 ± 1.39.9 ± 1.60.31
TnT max post (ng/l)0.3 ± 0.20.2 ± 0.10.0178
EF base in %51.4 ± 11.652.4 ± 9.90.38
Left atrial diameter (mm)42.4 ± 5.442.8 ± 6.20.28
Left enddiastolic diameter (mm)43.1 ± 5.847.6 ± 7.80.41
Max V (m/s)4.3 ± 0.64.2 ± 0.70.32
Max grad (mmHg)71.1 ± 25.871.4 ± 23.00.48
Pmean mmHg base (mmHg)45.1 ± 10.743.9 ± 15.00.35
AVA base (cm²)0.8 ± 0.20.7 ± 0.20.32
EF post (%)52.4 ± 9.952.4 ± 9.10.45
Velocity (m/s)2.3 ± 0.52.3 ± 0.50.19
Pmean post (mmHg)10.9 ± 5.113.2 ± 4.90.15
Pmax post (mmHg)20.9 ± 9.923.7 ± 8.50.16
Valve dimensions (mm)26.9 ± 1.925.4 ± 2.00.0531
Access in %100100
Balloon size (mm)22.4 ± 1.621.8 ± 6.00.44
P-P Gradient pre (mmHg)44.5 ± 14.544.5 ± 21.60.34
P-P Gradient post (mmHg)7.5 ± 4.15.6 ± 5.40.14
 Table 3 

QSR-T angle and clinical data post-intervention stratified by QRS-T angle.

QRS-T ≥ 90 post TAVIQRST < 90 post TAVIp value
(n=48)(n= 56)
Gender w (%)60.454.40.30
Age (years)83.3 ± 6.281.8 ± 6.10.11
BMI (kg/m²)26.8 ± 4.726.5 ± 5.00.47
CAD (%)49.139.70.26
1 vessel5.911.8
2 vessels7.44.4
3 vessels26.525.0
In %
prev MI8.33.50.15
prev CABG25.019.30.26
prev PCI27.929.80.20
In %
Diabetes27.135.10.31
Hypertension97.996.50.46
Hypercholesterolemia77.159.70.04
Smoker6.37.10.42
Family history2.18.80.07
Ckd31.326.30.31
Carotid disease18.810.50.12
Periph disease14.621.10.19
Af10.48.80.30
Pulmonary disease12.533.30.08
Cancer8.310.50.34
Log euroscore21.8 ± 11.622.9 ± 11.00.33
Syncope in %18.810.50.12
Ccs (i-iv)1.2 ± 1.01.1 ± 0.90.22
Nyha (i-iv)2.9 ± 0.73.1 ± 0.60.11
QRS-T angle °133.8 ± 31.052.5 ± 26.3
Lab results
Creatinine pre (mg/dl)1.3 ± 0.71.2 ± 0.80.39
Hb pre (g/dl)12.1 ± 1.512.0 ± 1.70.08
Tnt pre (ng/l)0.1 ± 1.60.04 ± 0.020.18
Creatinine post (mg/dl)1.2 ± 1.51.2 ± 0.90.39
Hb post (g/dl)9.9 ± 1.59.8 ± 1.50.41
Tnt max post (ng/l)0.2 ± 0.20.2 ± 0.10.08
EF pre in %52.6 ± 11.651.7 ± 11.80.39
Left atrial diameter (mm)43.0 ± 5.143.6 ± 6.70.32
Left ventricular enddiastolic diameter (mm)47.6 ± 8.648.5 ± 7.50.29
Max V (m/s)4.1 ± 0.64.3 ± 0.70.06
Max grad (mmhg)64.9 ± 24.075.5 ± 23.00.0256
Pmean mmhg pre (mmhg)43.2 ± 11.544.9 ± 15.20.29
AVA pre (cm²)0.7 ± 0.20.8 ± 0.20.32
EF post (%)54.7 ± 8.951.9 ± 9.50.15
Velocity (m/s)2.2 ± 0.62.2 ± 0.50.49
Pmean post (mmhg)11.8 ± 5.112.5 ± 5.30.34
Pmax post (mmhg)22.1 ± 10.624.0 ± 7.80.25
Valve dimensions (mm)26.5 ± 1.926.4 ± 2.20.41
Access TF in %100100
Balloon size (mm)20.2 ± 7.223.1 ± 1.80.0182
P-P Gradient pre (mmhg)46.4 ± 15.845.1 ± 21.60.40
P-P Gradient post (mmHg)6.0 ± 4.76.3 ± 5.50.42
 Table 4 

QSR-T angle and clinical data at follow-up stratified by QRS-T angle.

QRS-T ≥ 90 FU TAVIQRST < 90 FU TAVIp value
(n = 22)(n = 82)
Gender w (%)45.4661.00.10
Age (years)83.0 ± 5.882.4 ± 6.230.34
BMI (kg/m²)26.3 ± 4.026.9 ± 5.00.27
CAD in %66.650.00.13
1 vessel2.914.7
2 vessels2.98.8
3 vessels14.736.8
In %
Prev MI9.14.90.23
Prev CABG27.320.70.26
Prev PCI40.929.30.15
In %
Diabetes40.929.30.41
Hypertension10097.60.23
Hypercholesterolemia77.365.90.16
Smoker13.64.90.07
Family history07.30.10
Ckd13.632.90.04
Carotid disease4.617.10.07
Periph disease18.218.30.50
Af012.20.40
Pulmonary disease9.128.10.0097
Cancer012.20.0432
Log euroscore (%)21.1 ± 12.422.7 ± 11.00.28
Syncope in %13.614.60.45
Ccs (i-iv)1.1 ± 0.81.2 ± 0.90.46
Nyha (i-iv)3.1 ± 0.23.0 ± 0.70.30
QRS-T angle °133.2 ± 27.438.7 ± 27.4< 0.001
Lab results
Creatinine pre (mg/dl)1.1 ± 0.31.3 ± 0.80.16
Hb pre (g/dl)12.5 ± 1.311.9 ± 1.70.10
Tnt pre (ng/l)0.03 ± 0.010.1 ± 0.10.27
Crea post (mg/dl)1.1 ± 0.458.5 ± 31.50.15
Hb post (g/dl)10.1 ± 1.89.8 ± 1.40.29
Tnt max post (ng/l)0.2 ± 0.20.2 ± 0.20.39
EF pre in %53.0 ± 11.352.1 ± 11.90.38
Left atrial diameter (mm)43.3 ± 7.443.3 ± 5.50.50
Left ventricular enddiastolic diameter (mm)47.7 ± 7.048.2 ± 8.30.40
Max V (m/s)4.2 ± 0.74.0 ± 0.70.48
Max grad (mmhg)71.6 ± 21.270.8 ± 24.70.45
Pmean pre (mmhg) 44.0 ± 9.044.3 ± 14.50.47
AVA pre (cm²)0.8 ± 0.20.7 ± 0.20.48
EF post (%)53.0 ± 7.252.9 ± 9.70.49
Velocity (m/s)2.2 ± 0.62.2 ± 0.60.46
Pmean post (mmhg)13.6 ± 5.912.0 ± 5.10.22
Pmax post (mmhg)24.2 ± 7.623.1 ± 9.40.38
Valve dimensions (mm)27.1 ± 2.222.0 ± 5.10.0404
Access TF in %100100
Balloon size (mm)22.7 ± 1.522.0 ± 5.10.37
P-P Gradient Pre (mmHg)43.1 ± 16.646.0 ± 20.10.35
P-P Gradient Post (mmHg)7.6 ± 6.96.0 ± 4.80.21
 Figure 1 

Changes in the QRS-T angle over time. Before, immediately, and 1 month after TAVI. Values are displayed as mean QRST angles in degrees.

Int J Med Sci Image

The QRS-T angle is a marker of electrical instability and poor prognosis. However, evidence of its potential role in patients with aortic valve stenosis is limited. In 34 patients with hemodynamically assessed aortic valve stenosis, the spatial QRS-T angle was correlated with the peak systolic and mean transvalvular gradients. A QRS-T angle above 90°was diagnostic of severe aortic valve stenosis (mean transvalvular gradient of ≥ 50 mmHg) [20]. In 372 patients undergoing SAVR, Erturk et al. found that in-hospital and long-term mortality were significantly higher in patients with a wide QRS-T angle above 90° [13]. An electrical risk score, including the frontal QRS-T angle, was associated with poor prognosis in patients with severe aortic valve stenosis following TAVI [21].

Only a few studies have focused on changes in the QRS-T angle. Widening of the QRS-T angle during follow-up was independently associated with mortality in 2,929 patients with heart failure [22]. In 152 of 455 patients from the Defibrillators in Nonischemic Cardiomyopathy Treatment Evaluation (DEFINITE) trial with serial ECG follow-ups, changes in the QRS-T angle over time were associated with changes in left ventricular function [23]. Perez-Alday et al. demonstrated dynamic changes of the prediction of sudden cardiac death by a combination of ECG markers (global electrical heterogeneity index) including the QRS-T angle from 15,716 patients of the Atherosclerosis Risk In Community study [17].

Our study highlights the dynamic changes in the QRS-T angle during the catheter-based treatment of severe aortic stenosis. Changes in the QRS-T angle (narrowing) following successful therapeutic interventions have been demonstrated in patients undergoing thrombolysis for pulmonary artery embolism [25], thrombolysis for ST-segment elevation myocardial infarction [26], percutaneous coronary intervention in patients with chronic total occlusion [27], and improvements in left ventricular function following renal transplantation [28]. These findings underscore the sensitivity of the QRS-T angle to alterations in myocardial electrical activity and structural remodeling after intervention.

During TAVI, patients experience extreme hemodynamic fluctuations that impose significant stress on the myocardium and cardiovascular system. These hemodynamic changes trigger a cascade of physiological responses, including myocardial remodeling, characterized by alterations in myocardial fibrosis, cellular architecture, and electrophysiological properties. The left ventricle, which is directly impacted by the relief of valvular obstruction, undergoes substantial electrical remodeling, as reflected in the shifting QRS-T angle values. This remodeling encompasses changes in depolarization and repolarization patterns due to modifications of myocardial conduction pathways and repolarization heterogeneity. Consequently, the QRS-T angle serves not only as a marker of electrical instability but also reflects the underlying structural and functional myocardial recovery. Importantly, the observed QRS-T angle dynamics during and after catheter-based aortic valve implantation suggest that this parameter can be leveraged as a model to investigate the complex interplay between myocardial structural changes, such as fibrosis progression or regression, and electrical remodeling in severe aortic stenosis. Understanding this interplay is crucial because myocardial fibrosis influences both mechanical function and arrhythmogenic potential.

This research has several limitations that need to be recognized. Firstly, the sample size was quite small, which might restrict the applicability of the results to a wider population. Furthermore, the study's retrospective nature limits the ability to determine causal links and could introduce selection bias. The follow-up period was also relatively brief, which hampers the evaluation of long-term changes in QRS-T angle dynamics and their clinical significance. Moreover, the lack of prognostic data, such as patient outcomes related to arrhythmia occurrence or survival, limits the capacity to associate QRS-T angle changes with significant clinical endpoints. These limitations underscore the necessity for prospective studies with longer follow-up durations and thorough outcome monitoring to better understand the prognostic importance of QRS-T angle variations after catheter-based aortic valve implantation.

Given the unique pathophysiological environment created by TAVI, with its abrupt hemodynamic shifts and subsequent myocardial adaptation, this patient population provides a valuable opportunity to study disease progression and recovery using noninvasive ECG markers, such as the QRS-T angle. Future research focusing on correlating QRS-T angle changes with advanced imaging modalities that assess myocardial fibrosis and function could yield deeper insights into the mechanisms of electrical and structural remodeling.

Moreover, integrating cutting-edge computational approaches, such as deep learning algorithms applied to large-scale patient data, could enhance the predictive accuracy and clinical utility of QRS-T angle monitoring [29]. Such advancements may facilitate personalized risk stratification and optimize post-TAVI management by identifying patients at a higher risk for adverse remodeling or arrhythmic events.

In summary, the QRS-T angle emerges as a promising, easily accessible biomarker that reflects the dynamic myocardial and electrical remodeling processes occurring during and after catheter-based aortic valve replacement, offering significant potential for both clinical monitoring and mechanistic research in patients with severe aortic stenosis.

AI Usage Statement

Generative AI was used in the creation of the graphical abstract figure.

Competing Interests

The authors have declared that no competing interest exists.

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Author contact

Corresponding address Corresponding author: Christoph Jensen, MD, Associate Professor of Medicine, Department of Cardiology and Pneumology, University Medical Center Göttingen, Robert Koch Strasse 40, Göttingen, Germany; Email: Chris.jensenuni-goettingen.de.


Citation styles

APA
Amirie, S., Zadeh, B., Bruder, O., Schmitz, T., Toischer, K., Jensen, C.J. (2026). Changes of the QRS-T angle in Patients Undergoing Transcatheter Aortic Valve Implantation. International Journal of Medical Sciences, 23(5), 1588-1594. https://doi.org/10.7150/ijms.130315.

ACS
Amirie, S.; Zadeh, B.; Bruder, O.; Schmitz, T.; Toischer, K.; Jensen, C.J. Changes of the QRS-T angle in Patients Undergoing Transcatheter Aortic Valve Implantation. Int. J. Med. Sci. 2026, 23 (5), 1588-1594. DOI: 10.7150/ijms.130315.

NLM
Amirie S, Zadeh B, Bruder O, Schmitz T, Toischer K, Jensen CJ. Changes of the QRS-T angle in Patients Undergoing Transcatheter Aortic Valve Implantation. Int J Med Sci 2026; 23(5):1588-1594. doi:10.7150/ijms.130315. https://www.medsci.org/v23p1588.htm

CSE
Amirie S, Zadeh B, Bruder O, Schmitz T, Toischer K, Jensen CJ. 2026. Changes of the QRS-T angle in Patients Undergoing Transcatheter Aortic Valve Implantation. Int J Med Sci. 23(5):1588-1594.

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