- 1Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Institute of Biomedical Science, Fudan University, Shanghai, China
- 2Department of Cardiovascular Medicine, East Hospital, Tongji University School of Medicine, Shanghai, China
Background: Cardiac troponin T (cTNT) has been widely used in detecting cardiac damage. Elevated cTNT level has been reported to be associated with increased mortality in multiple cardiac conditions. It is not uncommon to observe an increased level of cTNT in patients after left atrial appendage occlusion (LAAO). The objective of the study is to study the incidence, significance, and factors associated with cTNT elevation after LAAO.
Methods: We prospectively included patients who underwent LAAO from January 2019 to July 2020 in Fudan Zhongshan Hospital. Patients were divided into those with elevated cTNT after procedure and those with normal postprocedure cTNT. All individuals were followed up for 1 year. The primary outcome is major adverse cardiovascular events, which include myocardial infarction, heart failure, cardiac death, and stroke. The second outcome is periprocedure complication, including chest pain, tachycardia, cardiac tamponade, change of electrocardiograph, and atrial thrombus.
Results: A total of 190 patients were enrolled. Of the patients, 85.3% had elevated cTNT after LAAO, while 14.7% of them did not. Exposure time, dosage of contrast, types of devices, shapes, and sizes of LAA could contribute to elevated postprocedure cTNT. We found that patients with a Watchman device were more likely to have elevated postprocedure cTNT than those with a Lambre device (89.2 vs. 76.7%, p = 0.029). LAAO shapes were associated with cTNT levels in patients with a Watchman device, while the diameter of the outer disc and LAA depth mattered for the Lambre device. There was no significant difference in the primary and second outcome between the two groups (p-value: 0.619, 0.674).
Conclusion: LAAO was found to be commonly accompanied with cTNT elevation, which might not to be related to the complications and adverse cardiac outcomes within 1 year of follow-up. Moreover, eGFR at baseline, exposure time, dosage of contrast, types of LAAO device, and LAA morphology could contribute to cTNT elevation.
Introduction
Cardiac troponin T (cTNTs) are part of the cardiac contractile mechanism of the cardiac muscle, and they are highly sensitive in detecting minimal myocardial injury (1). Higher cTNT levels can be found in various conditions, such as percutaneous coronary intervention (PCI) (2, 3), coronary artery bypass grafting (CABG) (1, 4, 5), radiofrequency catheter ablation (RFA) (6–8), automatic implantable cardioverter defibrillator (ICD) (9, 10), pacemaker lead insertion (11), and have been shown to be associated with worse clinical outcomes (1, 12, 13).
However, different procedures affect levels of cTNT differently. For cardiac procedures like PCI and CABG, elevated cTNT levels after procedure is associated with worse clinical outcomes (2–5); however, for other cardiac procedures, increased postprocedure cTNT levels do not necessarily affect adverse clinical outcomes (8). It remains controversial whether increased cTNT values after cardiac procedure affect long-term adverse events.
Left atrial appendage occlusion (LAAO) has emerged as a new strategy to prevent stroke in patients with atrial fibrillation (AF) (14, 15). It is applied in AF patients who have relative contraindication to oral anticoagulants (16). For LAAO, little remains unknown about the changes of cTNT and its effect on clinical outcomes after LAAO procedure.
The objective of the study is to study the incidence, significance, and factors associated with cTNT elevation after LAAO.
Methods
Our study is a single-center, prospective study. Postoperative cTNT refers to cTNT 12–24 h after LAAO.
Study Population
Patients who underwent LAAO from January 2019 to July 2020 in Fudan Zhongshan Hospital were consecutively selected. Based on the cTNT levels, eligible patients were separated into elevated cTNT group and normal cTNT group. We further divided patients into two groups based on the LAAO devices: Watchman (Boston Scientific, Plymouth, MN, USA) and Lambre [Lifetech Scientific (Shenzhen) Co. Ltd., Shenzhen, China]. Within each group, we compared the LAA sizes and shapes.
Baseline characteristics of the patients included age, male, hypertension, diabetes, hyperlipidemia, history of cerebrovascular disease, coronary heart disease, structural heart disease, heart failure, history of radiofrequency ablation, history of malignant tumor, preprocedure cTNT, hemoglobin (HB), white blood cell (WBC), endogenous glomerular filtration rate (eGFR), and left ventricular ejection fraction (LVEF). The intraoperative information included types of left atrial appendage, morphological characteristics of the left atrium, and diameter and depth of the left atrial appendage.
The study was approved by the Institutional Review Board of Zhongshan Hospital, Fudan University, Shanghai, China.
Clinical Outcomes and Definitions
The primary endpoint of this study is 1-year major adverse cardiovascular events, including myocardial infarction, heart failure, cardiac death, and stroke. The secondary endpoint is the perioperative adverse events, including chest pain, tachycardia, cardiac tamponade, change in electrocardiograph, and atrial thrombus. According to our hospital lab protocol, elevated cTNT is defined as the level of cTNT ≥0.03 μg/L, and normal cTNT is defined as cTNT <0.03 μg/L. Mild-elevated cTNT is defined as post-cTNT higher than 0.03 but lower than 0.09 μg/L. Severe-elevated post-cTNT is defined as ≥0.09 μ g/L. Myocardial infarction is defined by an elevation of cTn values >5 times of the 99th percentile URL in patients with normal baseline values. Patients with elevated preprocedural cTn values, in whom the preprocedural cTn level is stable (≤ 20% variation) or falling, must meet the criteria for a >5- or >10-fold increase and manifest a change from the baseline value of >20%. In addition, patients have at least one of the following: (1) new ischemic ECG changes (this criterion is related to type 4a MI only), (2) development of new pathological Q waves, (3) imaging evidence of loss of viable myocardium that is presumed to be new and in a pattern consistent with an ischemic etiology, and (4) angiographic findings consistent with a procedural flow-limiting complication such as coronary dissection, occlusion of a major epicardial artery or graft, side-branch occlusion thrombus, disruption of collateral flow, or distal embolization.
Statistical Analysis
We used t-test and chi-square test to compare variables between the positive cTNT group and the negative cTNT group. ANOVA analysis was used for the pairwise comparison among the three group. A time-to-event model was used to analyze the primary endpoint between the two groups. Log rank test was done to compare the significance of the Kaplan–Meier curve. All statistical analyses were performed using Stata 23.0 (Stata Corp, 2015).
Results
A total of 190 patients were enrolled in the study. About 85.3% of the patients were in the group of elevated cTNT, while 14.7% of them were in the group of normal cTNT, among which 55.8% had a mild increase and 29.5% had a severe increase in cTNT (Figure 1). The median and quartile range of postprocedure cTNT was 0.037 μg/L (0.064–0.108 μg/L).
Figure 1. Postprocedure cardiac troponin T (cTNT). Mild-elevated cTNT is defined as post-cTNT higher than 0.03 but lower than 0.09 μg/L. Severe-elevated post-cTNT is defined as ≥0.09 μ g/L. The median and quartile range of postprocedure cTNT was 0.037 μg/L (0.064–0.108 μg/L).
Baseline Characteristics
The baseline characteristics between the normal cTNT and elevated cTNT groups are presented in Table 1. Compared with the normal cTNT group, patients in the elevated cTNT group have lower GFR levels (72.28 ± 18.84 vs. 86.79 ± 12.64, p = 0.017). More patients in the elevated cTNT group have hypertension (67.3 vs. 46.4%, p = 0.053) and history of atrial fibrillation ablation (14.5 vs. 3.6%, p = 0.135), although there was no significant difference.
Table 1. Baseline characteristics between the normal cardiac troponin T (cTNT) and elevated cTNT groups.
Other characteristics like age, sex, history of hyperlipidemia, coronary artery disease, and heart failure are distributed evenly between the two groups.
Intraoperative Information Between the Normal Cardiac Troponin T and the Elevated Cardiac Troponin T Group
We further analyzed the characteristics of the LAAO procedure between the two groups. The procedure length had no significant difference in the different cTNT group [60.0 (57.5–73.8) vs. 60.0 (50.0–70.0), p = 0.923]. It is worth noting that the longer exposure time was in the higher cTNT [11.0 (10.0–17.2) vs. 18.4 (13.6–25.5), p < 0.01], which was the same as the dosage of contrast [277 (194–360) vs. 406.0 (342.5–590.0), p < 0.01]. More patients implanted with the Watchman device had elevated cTNT than patients implanted with the Lambre device (89.2 vs. 76.7%, p = 0.029). Times for changing LAAO devices, morphological characteristics of the left atrium, length and depth of atrial atrium, and heart rate had no statistical difference between the two groups (Table 2).
Watchman Device and Lambre Device
In the patients receiving the Watchman device, we found that shapes of LAA were associated with elevated cTNT, among which chicken wing type was more likely to have a higher cTNT level (100 vs. 0%). We found no difference in the size of Watchman, compression ratio, size of atrial atrium, and residual regurgitation between the two groups (Table 3).
For the patients receiving the Lambre device, a larger diameter of the outer disc of the device (35.04 ± 4.04 vs. 36.86 ± 1.88, p = 0.001) and deeper LAAs (31.31 ± 3.88 vs. 31.96 ± 8.01, p = 0.027) were more prevalent in the elevated cTNT group. Different shapes of the left atrium were distributed equally in the different cTNT groups (Table 4).
Follow-Up Results
Regarding peri-procedural complications, there is no significant difference between the elevated cTNT group and the normal cTNT group, regardless of which device was used (Table 5). There was also no difference in the incidence of 1-year cardiovascular events between the two groups (p-value: 0.619) (Figure 2).
Discussion
Our study found that 85.3% (162/190) of LAAO patients had elevated cTNT after the procedure. This elevation might not be related to the complications of left atrial appendage occlusion and cardiac outcomes within 1 year of follow-up. Furthermore, eGFR at baseline, exposure time, dosage of contrast, type of LAAO device, and LAA morphology were found to be independently associated with cTNT elevation after the procedure. Our study is the first we know to explore the incidence, significance, and risk factors of elevated cTNT for patients after LAAO.
In our study, longer exposure time and higher dose of contrast were associated with higher levels of cTNT, indicating that the cTNT elevation in LAAO was probably related to the procedure itself, since patients with elevated cTNT had no evidence of chest pain, and hemodynamic or respiratory distress afterward (17). The cause of cTNT elevation in our study was likely by the implantation of a LAAO device, which was supported by the positive association between exposure time and cTNT elevation since longer exposure time often suggests more complexity of the procedure and more times of attempts to place a LAAO device, leading to more myocardial damage. However, the longer procedure time was not associated with higher cTNT levels in our study, and the reasons may be that procedure time have more confounding factors such as the puncture time, the skill of the operator, the team coordination, and so on.
What is more, the types of LAAO device affected the level of cTNT. The post-cTNT in the Watchman group was higher than that of the Lambre group. Like other intra-cardiac procedures, LAAO could cause potential cardiac damage by anchoring in the myocardium, decompression of the device, and mechanical compression of the LAA (18). For the Watchman device, certain shapes of LAA correlates with the higher level of cTNT. However, for the Lambre device, the diameter of the outer disc of the device and the length of the left atrial appendage are associated with higher levels of cTNT. The reasons for those results were listed as follows. First, designs of the device could affect postprocedure cTNT levels. For example, the design of the transport system, release mechanism, and the way of the device binding to the left atrial appendage may explain the level of post-cTNT after LAAO. The Watchman has a barb, which is fixed in the left atrial appendage by relying on the barb, which will inevitably cause myocardial injury. In addition, it needs to be pulled before releasing the occlusion, and if the position is not proper, it will need to be adjusted repeatedly, which may increase the injury of the operation; The Lambre occluder is a disc occluder, which will not directly damage the myocardium in most cases, but repeated extrusion or friction may cause damage (18). Second, morphology of LAAs could affect postprocedure cTNT level. The shape of LAA mainly affects postprocedure cTNT in patients receiving the Watchman device. With regard to the Lambre device group, patients who had larger disc diameter and deeper LAA are more likely to have positive postprocedure cTNT. It is likely because the Watchman device requires more for the left atrial morphology, while the Lambre device does not (18–21). The Watchman device becomes spherical after expansion, and when the atrial shape does not match the shape of the Watchman device, myocardial injury is likely to occur, which has been mentioned before. On the contrary, the Lambre device is highly adaptable to different LAA morphologies because of its disc occluder. It can be quite useful in patients with difficulty anatomies (21). The Lambre device is embedded in the atrial wall by hook and parachute, so the requirement of atrial morphology is not as high as that of the Watchman, but the outer disk size and atrial diameter of the Lambre device are accountable for the degree of myocardial injury.
In our study, patients with lower eGFR were also found to be related to higher incidence of cTNT elevation after the procedure. Renal dysfunction is one of the major reasons for cTNT elevation except for acute myocardial infarction (22). cTNT elevation is common among patients with renal failure, indicating that cTNT was cleared by the kidneys (23). In addition, cTNT elevations in these patients could be due to increased cTNT release linked to cardiac stress, called the cardiorenal syndrome (24). Martens et al. found that eGFR was independently associated with cTNT levels, even when eGFR levels do not fulfill the CKD criteria (25). Our results were consistent with a previous study that eGFR was associated with cTNT elevation after LAAO in the condition that the means of eGFR of the two groups do not meet the eGFR criteria.
cTNT elevation has been associated with poor prognosis in many conditions (26, 27). However, the mild and transient elevation of cTNT in our study did not contribute to the poor prognosis, indicating that the increase in cTNT is mostly transient myocardial injury caused by occluder implantation, which does not affect cardiac ejection function and ventricular survival area. Our results were consistent with previous studies (28, 29). Similarly, all patients in our study were followed up for 1 year, and the cTNT elevation had no relation to the complications of the procedure or cardiac outcomes. Thus, it is demonstrated that cTNT elevation after LAAO was not associated with adverse clinical events and complications within 1 year follow-up in this relatively large cohort.
Limitations
The limitations of our analyses are listed as follows: First, the sample of this study is a little small, which decreases the reliability level of the conclusion. Second, our study is a single-center study, which may result in selection bias. Third, we were unable to rule out the influence of differing skill levels of different operators involved in the procedure on cTNT elevation.
Conclusion
LAAO was found to be commonly accompanied with cTNT elevation, which might not to be related to the complications and adverse cardiac outcomes within 1 year of follow-up. Moreover, eGFR at baseline, exposure time, dosage of contrast, types of LAAO device, and LAA morphology could contribute to cTNT elevation.
Data Availability Statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics Statement
The studies involving human participants were reviewed and approved by Institutional Review Board of Zhongshan Hospital, Fudan University. The patients/participants provided their written informed consent to participate in this study. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.
Author Contributions
XiaW, XC, YY, DZ, and QC conceptualized and designed the study. QC and DZ provided administrative support. XiaW and QC analyzed and interpreted the data. XiaW, YY, and QC wrote the manuscript. All authors gave the final approval of the manuscript and provided the study materials or patients and collected and assembled the data.
Funding
This study was supported by the National Natural Science Foundation of China (82000267, 81870197, 81500191, 81900260, and 8180020174) and The Health Science and Technology Project of Shanghai Pudong New Area Health Commission (PW2019A-13).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher's Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Acknowledgments
We thanks a lot for the support of Pro. Yunzeng Zou.
References
1. Thygesen K, Alpert JS, Jaffe AS, Chaitman BR, Bax JJ, Morrow DA, et al. Fourth universal definition of myocardial infarction. J Am Coll Cardiol. (2018) 72:2231–64. doi: 10.1161/CIR.0000000000000617
2. Zeitouni M, Silvain J, Guedeney P, Kerneis M, Yan Y, Overtchouk P, et al. Periprocedural myocardial infarction and injury in elective coronary stenting. Eur Heart J. (2018) 39:1100–9. doi: 10.1093/eurheartj/ehx799
3. Harada Y, Koskinas KC, Ndrepepa G, Raber L, Braun S, Zanchin T, et al. Postprocedural high-sensitivity troponin T and prognosis in patients with non-ST-segment elevation myocardial infarction treated with early percutaneous coronary intervention. Cardiovasc Revasc Med. (2018) 19:480–6. doi: 10.1016/j.carrev.2017.11.010
4. Gahl B, Gober V, Odutayo A, Tevaearai Stahel HT, da Costa BR, Jakob SM, et al. Prognostic value of early postoperative troponin T in patients undergoing coronary artery bypass grafting. J Am Heart Assoc. (2018) 7:e007743. doi: 10.1161/JAHA.117.007743
5. Machado MN, Rodrigues FB, Grigolo IH, Sabbag ATR, Silva OLJ, Maia LN, et al. Early prognostic value of high-sensitivity troponin t after coronary artery bypass grafting. Thorac Cardiovasc Surg. (2019) 67:467–74. doi: 10.1055/s-0038-1675640
6. Reichlin T, Lockwood SJ, Conrad MJ, Nof E, Michaud GF, John RM, et al. Early release of high-sensitive cardiac troponin during complex catheter ablation for ventricular tachycardia and atrial fibrillation. J Interv Card Electrophysiol. (2016) 47:69–74. doi: 10.1007/s10840-016-0125-6
7. Kozinski M, Krintus M, Kubica J, Sypniewska G. High-sensitivity cardiac troponin assays: from improved analytical performance to enhanced risk stratification. Crit Rev Clin Lab Sci. (2017) 54:143–72. doi: 10.1080/10408363.2017.1285268
8. Yoshida K, Yui Y, Kimata A, Koda N, Kato J, Baba M, et al. Troponin elevation after radiofrequency catheter ablation of atrial fibrillation: relevance to AF substrate, procedural outcomes, and reverse structural remodeling. Heart Rhythm. (2014) 11:1336–42. doi: 10.1016/j.hrthm.2014.04.015
9. Vasatova M, Pudil R, Tichy M, Buchler T, Horacek JM, Haman L, et al. High-sensitivity troponin T as a marker of myocardial injury after radiofrequency catheter ablation. Ann Clin Biochem. (2011) 48:38–40. doi: 10.1258/acb.2010.009280
10. Furniss G, Shi B, Jimenez A, Harding SA, Larsen PD. Cardiac troponin levels following implantable cardioverter defibrillation implantation and testing. Europace. (2015) 17:262–6. doi: 10.1093/europace/euu306
11. Brewster J, Sexton T, Dhaliwal G, Charnigo R, Morales G, Parrott K, et al. Acute effects of implantable cardioverter-defibrillator shocks on biomarkers of myocardial injury, apoptosis, heart failure, and systemic inflammation. Pacing Clin Electrophysiol. (2017) 40:344–52. doi: 10.1111/pace.13037
12. Welsh P, Preiss D, Hayward C, Shah ASV, McAllister D, Briggs A, et al. Cardiac troponin t and troponin i in the general population. Circulation. (2019) 139:2754–64. doi: 10.1161/CIRCULATIONAHA.118.038529
13. Willeit P, Evans JDW, Tschiderer L, Boachie C, Jukema JW, Ford I, et al. High-sensitivity cardiac troponin concentration and risk of first-ever cardiovascular outcomes in 154,052 participants. J Am Coll Cardiol. (2017) 70:558–68. doi: 10.1016/j.jacc.2017.05.062
14. Holmes DR, Turi ZG, Doshi SK, Sievert H, Buchbinder M, Mullin CM, et al. Percutaneous closure of the left atrial appendage versus warfarin therapy for prevention of stroke in patients with atrial fibrillation: a randomised non-inferiority trial. Lancet. (2009) 374:534–42. doi: 10.1016/S0140-6736(09)61343-X
15. Reddy VY, Doshi SK, Sievert H, Buchbinder M, Neuzil P, Huber K, et al. Percutaneous left atrial appendage closure for stroke prophylaxis in patients with atrial fibrillation: 2.3-year follow-up of the PROTECT AF (Watchman left atrial appendage system for embolic protection in patients with atrial fibrillation) trial. Circulation. (2013) 127:720–9. doi: 10.1161/CIRCULATIONAHA.112.114389
16. Yves-Laurent Bayard HO, Neuzil P, Thuesen L, Pichler L, Rowland E, Ramondo A, et al. PLAATO (Percutaneous Left Atrial Appendage Transcatheter Occlusion) for prevention of cardioembolic stroke in non-anticoagulation eligible atrial fibrillation patients: results from the European PLAATO study. EuroIntervention. (2010) 6:220–6. doi: 10.4244/EIJV6I2A35
17. Franck Maziere SB, Medimagh S, Arthaud M, Bennaceur M, Riou B, Ray P. Comparison of troponin I and N-terminal-pro B-type natriuretic peptide for risk stratification in patients with pulmonary embolism. Eur J Emerg Med. (2007) 14:207–11. doi: 10.1097/MEJ.0b013e3280bef891
18. Chen S, Chun KRJ, Bordignon S, Weise FK, Nagase T, Perrotta L, et al. Left atrial appendage occlusion using LAmbre Amulet and Watchman in atrial fibrillation. J Cardiol. (2019) 73:299–306. doi: 10.1016/j.jjcc.2018.10.010
19. Chen S, Schmidt B, Bordignon S, Bologna F, Nagase T, Tsianakas N, et al. Feasibility of percutaneous left atrial appendage closure using a novel LAmbre occluder in patients with atrial fibrillation: Initial results from a prospective cohort registry study. J Cardiovasc Electrophysiol. (2018) 29:291–7. doi: 10.1111/jce.13385
20. Fountain RB, Holmes DR, Chandrasekaran K, Packer D, Asirvatham S, Van Tassel R, et al. The PROTECT AF (WATCHMAN left atrial appendage system for embolic PROTECTion in patients with atrial fibrillation) trial. Am Heart J. (2006) 151:956–61. doi: 10.1016/j.ahj.2006.02.005
21. Lam YY. A new left atrial appendage occluder (Lifetech LAmbre Device) for stroke prevention in atrial fibrillation. Cardiovasc Revasc Med. (2013) 14:134–6. doi: 10.1016/j.carrev.2013.04.003
22. Roffi M, Patrono C, Collet JP, Mueller C, Valgimigli M, Andreotti F, et al. 2015 ESC Guidelines for the management of acute coronary syndromes in patients presenting without persistent ST-segment elevation: task force for the management of acute coronary syndromes in patients presenting without persistent ST-segment elevation of the European Society of Cardiology (ESC). Eur Heart J. (2016) 37:267–315. doi: 10.1093/eurheartj/ehv320
23. deFilippi C, Kelley W, Duh SH, Hise M, Christenson RH. Interpreting cardiac troponin results from high-sensitivity assays in chronic kidney disease without acute coronary syndrome. Clin Chem. (2012) 58:1342–51. doi: 10.1373/clinchem.2012.185322
24. Palazzuoli A, Ronco C, Maisel A. Clinical relevance of biomarkers in heart failure and cardiorenal syndrome: the role of natriuretic peptides and troponin. Heart Fail Rev. (2014) 19:267–84. doi: 10.1007/s10741-013-9391-x
25. Martens RJ, Honney K, Kooman JP, Stehouwer CD, Tan FE, BekersO, et al. Estimated glomerular filtration rate and albuminuria are associated with biomarkers of cardiac injury in a population based cohort study: the Maastricht Study. Clin Chem. (2017) 63:887–97. doi: 10.1373/clinchem.2016.266031
26. Mannu GS, Honney K, Spooner R, Clark AB, Bettencourt-Silva JH, Zaman MJ, et al. Incidentally raised cardiac troponin I has a worse prognosis in older patients compared to those with normal cardiac troponin I and patients with acute coronary syndrome: a cohort study. Gerontology. (2016) 62:581–7. doi: 10.1159/000444083
27. Thielmann M, Massoudy P, Neuhauser M, Knipp S, Kamler M, Piotrowski J, et al. Prognostic value of preoperative cardiac troponin I in patients with non-ST-segment elevation acute coronary syndromes undergoing coronary artery bypass surgery. Chest. (2005) 128:3526–36. doi: 10.1016/S0012-3692(15)52926-7
28. Boersma LV, Schmidt B, Betts TR, Sievert H, Tamburino C, Teiger E, et al. Implant success and safety of left atrial appendage closure with the WATCHMAN device: peri-procedural outcomes from the EWOLUTION registry. Eur Heart J. (2016) 37:2465–74. doi: 10.1093/eurheartj/ehv730
Keywords: cardiac troponin T, left atrial appendage occlusion, adverse events, Watchman® -device, LAmbre device
Citation: Wang X, Chen X, Ye Y, Peng J, Lin J, Deng X, Lin L, You J, Wang X, Zhou D, Chen Q and Ge J (2021) Troponin T Elevation After Percutaneous Left Atrial Appendage Occlusion. Front. Cardiovasc. Med. 8:721224. doi: 10.3389/fcvm.2021.721224
Received: 06 June 2021; Accepted: 31 August 2021;
Published: 01 October 2021.
Edited by:
Micha Tobias Maeder, Kantonsspital St. Gallen, SwitzerlandReviewed by:
Cristina Aurigemma, Catholic University of the Sacred Heart, ItalyJean-Bernard Masson, University of Montreal Hospital Centre (CRCHUM), Canada
Copyright © 2021 Wang, Chen, Ye, Peng, Lin, Deng, Lin, You, Wang, Zhou, Chen and Ge. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Qingxing Chen, Y2hlbi5xaW5neGluZyYjeDAwMDQwO3pzLWhvc3BpdGFsLnNoLmNu; Daxin Zhou, emhvdS5kYXhpbiYjeDAwMDQwO3pzLWhvc3BpdGFsLnNoLmNu
†These authors have contributed equally to this work