Assessment of CardiOvascular Remodelling following Endovascular aortic repair through imaging and computation: the CORE prospective observational cohort study protocol

Foeke J H Nauta, Arnoud V Kamman, El-Sayed H Ibrahim, Prachi P Agarwal, Bo Yang, Karen Kim, David M Williams, Joost A van Herwaarden, Frans L Moll, Kim A Eagle, Santi Trimarchi, Himanshu J Patel, C Alberto Figueroa, Foeke J H Nauta, Arnoud V Kamman, El-Sayed H Ibrahim, Prachi P Agarwal, Bo Yang, Karen Kim, David M Williams, Joost A van Herwaarden, Frans L Moll, Kim A Eagle, Santi Trimarchi, Himanshu J Patel, C Alberto Figueroa

Abstract

Introduction: Thoracic aortic stent grafts are orders of magnitude stiffer than the native aorta. These devices have been associated with acute hypertension, elevated pulse pressure, cardiac remodelling and reduced coronary perfusion. However, a systematic assessment of such cardiovascular effects of thoracic endovascular aortic repair (TEVAR) is missing. The CardiOvascular Remodelling following Endovascular aortic repair (CORE) study aims to (1) quantify cardiovascular remodelling following TEVAR and compare echocardiography against MRI, the reference method; (2) validate computational modelling of cardiovascular haemodynamics following TEVAR using clinical measurements, and virtually assess the impact of more compliant stent grafts on cardiovascular haemodynamics; and (3) investigate diagnostic accuracy of ECG and serum biomarkers for cardiac remodelling compared to MRI.

Methods and analysis: This is a prospective, nonrandomised, observational cohort study. We will use MRI, CT, echocardiography, intraluminal pressures, ECG, computational modelling and serum biomarkers to assess cardiovascular remodelling in two groups of patients with degenerative thoracic aneurysms or penetrating aortic ulcers: (1) patients managed with TEVAR and (2) control patients managed with medical therapy alone. Power analysis revealed a minimum total sample size of 20 patients (α=0.05, power=0.97) to observe significant left ventricular mass increase following TEVAR after 1 year. Consequently, we will include 12 patients in both groups. Advanced MRI sequences will be used to assess myocardial and aortic strain and distensibility, myocardial perfusion and aortic flow. ECG, echocardiography and serum biomarkers will be collected and compared against the imaging data. Computational models will be constructed from each patient imaging data, analysed and validated. All measurements will be collected at baseline (prior to TEVAR) and 1-year follow-up. The expected study period is 3 years.

Ethics and dissemination: This study has been approved by the University of Michigan IRB. The results will be disseminated through scientific journals and conference presentations.

Trial registration number: NCT02735720.

Keywords: VASCULAR SURGERY.

Conflict of interest statement

Conflicts of Interest: None declared.

Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/.

Figures

Figure 1
Figure 1
Top: MRI Tagging sequence to quantify myocardial strain. SAX and 4CH tagged images at ED and ES. Bottom: Transit time (Δt) between proximal and distal flow waveforms measured with PC MRI sequences is used to evaluate PWV in the aorta. 4CH, four-chamber; ED, end diastole; ES, end systole; SAX, short axis.
Figure 2
Figure 2
Top: Arterial stiffness for a baseline ‘middle-age’ participant, an ‘old-age’ participant showing generalised arterial stiffening and a ‘stent repair’ case with identical stiffness to the baseline except for the ascending aortic segment, in which a stent graft (presented in grey), whose stiffness is 125× higher than the native aortic tissue, was inserted. Bottom: Changes in LV function required to maintain cardiac output following generalised (old age) or stent-induced stiffening. Left: changes in cardiac contractility, as given by a LV elastance function. Right: changes in LV work, estimated by computed pressure–volume loops (unpublished data Lau et al 2016). LV, left ventricle.
Figure 3
Figure 3
Patient population and clinical measurements of our study. BP, blood pressure; HR, heart rate.

References

    1. Perera AH, Rudarakanchana N, Hamady M et al. . New-generation stent grafts for endovascular management of thoracic pseudoaneurysms after aortic coarctation repair. J Vasc Surg 2014;60:330–6. 10.1016/j.jvs.2014.02.050
    1. von Allmen RS, Anjum A, Powell JT. Incidence of descending aortic pathology and evaluation of the impact of thoracic endovascular aortic repair: a population-based study in England and Wales from 1999 to 2010. Eur J Vasc Endovasc Surg 2013;45:154–9. 10.1016/j.ejvs.2012.12.007
    1. Kleinstreuer C, Li Z, Basciano CA et al. . Computational mechanics of Nitinol stent grafts. J Biomech 2008;41:2370–8. 10.1016/j.jbiomech.2008.05.032
    1. Roccabianca S, Figueroa CA, Tellides G et al. . Quantification of regional differences in aortic stiffness in the aging human. J Mech Behav Biomed Mater 2014;29:618–34. 10.1016/j.jmbbm.2013.01.026
    1. Kingwell BA, Waddell TK, Medley TL et al. . Large artery stiffness predicts ischemic threshold in patients with coronary artery disease. J Am Coll Cardiol 2002;40:773–9. 10.1016/S0735-1097(02)02009-0
    1. Redheuil A, Wu CO, Kachenoura N et al. . Proximal aortic distensibility is an independent predictor of all-cause mortality and incident CV events: the MESA study. J Am Coll Cardiol 2014;64:2619–29. 10.1016/j.jacc.2014.09.060
    1. Laurent S, Zanchetti A. New challenges in the disease management of hypertension. J Hypertens Suppl 2001;19:S1.
    1. Dobson G, Flewitt J, Tyberg JV et al. . Endografting of the descending thoracic aorta increases ascending aortic input impedance and attenuates pressure transmission in dogs. Eur J Vasc Endovasc Surg 2006;32:129–35.
    1. Takeda Y, Sakata Y, Ohtani T et al. . Endovascular aortic repair increases vascular stiffness and alters cardiac structure and function. Circ J 2014;78:322–8. 10.1253/circj.CJ-13-0877
    1. Tzilalis VD, Kamvysis D, Panagou P et al. . Increased pulse wave velocity and arterial hypertension in young patients with thoracic aortic endografts. Ann Vasc Surg 2012;26:462–7. 10.1016/j.avsg.2011.06.021
    1. Watanabe H, Ohtsuka S, Kakihana M et al. . Coronary circulation in dogs with an experimental decrease in aortic compliance. J Am Coll Cardiol 1993;21:1497–506. 10.1016/0735-1097(93)90330-4
    1. Alfakih K, Walters K, Jones T et al. . New gender-specific partition values for ECG criteria of left ventricular hypertrophy: recalibration against cardiac MRI. Hypertension 2004;44:175–9. 10.1161/01.HYP.0000135249.66192.30
    1. Devereux RB, Koren MJ, de Simone G et al. . Methods for detection of left ventricular hypertrophy: application to hypertensive heart disease. Eur Heart J 1993;14(Suppl D):8–15. 10.1093/eurheartj/14.suppl_D.8
    1. Courand PY, Gaudebout N, Mouly-Bertin C et al. . Biological, electrical and echocardiographic indices versus cardiac magnetic resonance imaging in diagnosing left ventricular hypertrophy. Hypertens Res 2014;37:444–51. 10.1038/hr.2013.147
    1. Pastormerlo LE, Agazio A, Benelli E et al. . Usefulness of high-sensitive troponin elevation after effort stress to unveil vulnerable myocardium in patients with heart failure. Am J Cardiol 2015;116:567–72. 10.1016/j.amjcard.2015.05.017
    1. Lang RM, Bierig M, Devereux RB et al. . Recommendations for chamber quantification: a report from the American Society of Echocardiography's Guidelines and Standards Committee and the Chamber Quantification Writing Group, developed in conjunction with the European Association of Echocardiography, a branch of the European Society of Cardiology. J Am Soc Echocardiogr 2005;18:1440–63. 10.1016/j.echo.2005.10.005
    1. Dorosz JL, Lezotte DC, Weitzenkamp DA et al. . Performance of 3-dimensional echocardiography in measuring left ventricular volumes and ejection fraction: a systematic review and meta-analysis. J Am Coll Cardiol 2012;59:1799–808. 10.1016/j.jacc.2012.01.037
    1. Grothues F, Smith GC, Moon JC et al. . Comparison of interstudy reproducibility of cardiovascular magnetic resonance with two-dimensional echocardiography in normal subjects and in patients with heart failure or left ventricular hypertrophy. Am J Cardiol 2002;90:29–34. 10.1016/S0002-9149(02)02381-0
    1. Bogaerts J. Clinical Cardiac MRI. Springer-Verlag Berlin Heidelberg 2nd edn 2012.
    1. Ibrahim el SH, Miller AB, White RD. The relationship between aortic stiffness and E/A filling ratio and myocardial strain in the context of left ventricular diastolic dysfunction in heart failure with normal ejection fraction: insights from magnetic resonance imaging. Magn Reson Imaging 2011;29:1222–34. 10.1016/j.mri.2011.08.003
    1. Papanastasiou G, Williams MC, Kershaw LE et al. . Measurement of myocardial blood flow by cardiovascular magnetic resonance perfusion: comparison of distributed parameter and Fermi models with single and dual bolus. J Cardiovasc Magn Reson 2015;17:17 10.1186/s12968-015-0125-1
    1. Mordini FE, Haddad T, Hsu LY et al. . Diagnostic accuracy of stress perfusion CMR in comparison with quantitative coronary angiography: fully quantitative, semiquantitative, and qualitative assessment. JACC Cardiovasc Imaging 2014;7:14–22. 10.1016/j.jcmg.2013.08.014
    1. Ko SM, Hwang HK, Kim SM et al. . Multi-modality imaging for the assessment of myocardial perfusion with emphasis on stress perfusion CT and MR imaging. Int J Cardiovasc Imaging 2015;31(Suppl 1):1–21.
    1. Ibrahim el SH, Johnson KR, Miller AB et al. . Measuring aortic pulse wave velocity using high-field cardiovascular magnetic resonance: comparison of techniques. J Cardiovasc Magn Reson 2010;12:26 10.1186/1532-429X-12-26
    1. Coogan JS, Humphrey JD, Figueroa CA. Computational simulations of hemodynamic changes within thoracic, coronary, and cerebral arteries following early wall remodeling in response to distal aortic coarctation. Biomech Model Mechanobiol 2013;12:79–93. 10.1007/s10237-012-0383-x
    1. FDA. FDA News Release FDA allows marketing of non-invasive device to help evaluate heart blood flow [Internet]. Secondary FDA News Release FDA allows marketing of non-invasive device to help evaluate heart blood flow [Internet] 2014.

Source: PubMed

Подписаться