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Dive into the research topics where Marc Sintek is active.

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Featured researches published by Marc Sintek.


Heart | 2015

Prognostic utility of novel biomarkers of cardiovascular stress in patients with aortic stenosis undergoing valve replacement

Brian R. Lindman; Jared Breyley; Joel D. Schilling; Anna Vatterott; Alan Zajarias; Hersh S. Maniar; Ralph J. Damiano; Marc R. Moon; Jennifer S. Lawton; Brian F. Gage; Marc Sintek; Alejandro Aquino; Christopher L. Holley; Neil M. Patel; Cassandra Lawler; John M. Lasala; Eric Novak

Objective In heart failure populations without aortic stenosis (AS), the prognostic utility of multiple biomarkers in addition to clinical factors has been demonstrated. We aimed to determine whether multiple biomarkers of cardiovascular stress are associated with mortality in patients with AS undergoing aortic valve replacement (AVR) independent of clinical factors. Methods From a prospective registry of patients with AS, 345 participants who were referred for and treated with AVR (transcatheter (n=183) or surgical (n=162)) were included. Eight biomarkers were measured on blood samples obtained prior to AVR: growth differentiation factor 15 (GDF15), soluble ST2 (sST2), amino-terminal pro-B-type natriuretic peptide (NTproBNP), galectin-3, high-sensitivity cardiac troponin T, myeloperoxidase, high-sensitivity C reactive protein and monocyte chemotactic protein-1. Biomarkers were evaluated based on median value (high vs low) in a Cox proportional hazards model for all-cause mortality and a parsimonious group of biomarkers selected. Mean follow-up was 1.9±1.2 years; 91 patients died. Results Three biomarkers (GDF15, sST2 and NTproBNP) were retained in the model. One-year mortality was 5%, 12%, 18% and 33% for patients with 0 (n=79), 1 (n=96), 2 (n=87) and 3 (n=83) biomarkers elevated, respectively (p<0.001). After adjustment for the Society of Thoracic Surgeons (STS) risk score, a greater number of elevated biomarkers was associated with increased mortality (referent: 0 elevated): 1 elevated (HR 1.47, 95% CI 0.60 to 3.63, p=0.40), 2 elevated (HR 2.89, 95% CI 1.24 to 6.74, p=0.014) and 3 elevated (HR 4.59, 95% CI 1.97 to 10.71, p<0.001). Among patients at intermediate or high surgical risk (STS score ≥4), 1-year and 2-year mortality rates were 34% and 43% for patients with three biomarkers elevated versus 4% and 4% for patients with 0 biomarkers elevated. When added to the STS score, the number of biomarkers elevated provided a category-free net reclassification improvement of 64% at 1 year (p<0.001). The association between a greater number of elevated biomarkers and increased mortality after valve replacement was similar in the transcatheter and surgical AVR populations. Conclusions These findings demonstrate the potential utility of multiple biomarkers to aid in risk stratification of patients with AS. Further studies are needed to evaluate their utility in clinical decision-making in specific AS populations.


Journal of Cardiac Failure | 2015

Intra-Aortic Balloon Counterpulsation in Patients With Chronic Heart Failure and Cardiogenic Shock: Clinical Response and Predictors of Stabilization

Marc Sintek; Mark Gdowski; Brian R. Lindman; Michael E. Nassif; Kory J. Lavine; Eric Novak; Richard G. Bach; Scott C. Silvestry; Douglas L. Mann; Susan M. Joseph

OBJECTIVE The aim of this work was to characterize the clinical response and identify predictors of clinical stabilization after intra-aortic balloon counterpulsation (IABP) support in patients with chronic systolic heart failure in cardiogenic shock before implantation of a left ventricular assist device (LVAD). BACKGROUND Limited data exist regarding the clinical response to IABP in patients with chronic heart failure in cardiogenic shock. METHODS We identified 54 patients supported with IABP before LVAD implantation. Criteria for clinical decompensation after IABP insertion and before LVAD included the need for more advanced temporary support, initiation of mechanical ventilation or dialysis, increase in vasopressors/inotropes, refractory ventricular arrhythmias, or worsening acidosis. The absence of these indicated stabilization. RESULTS Clinical decompensation after IABP occurred in 23 patients (43%). Both patients who decompensated and those who stabilized had similar hemodynamic improvements after IABP support, but patients who decompensated required more vasopressors/inotropes. Clinical decompensation after IABP was associated with worse outcomes after LVAD implantation, including a 3-fold longer intensive care unit stay and 5-fold longer time on mechanical ventilation (P < .01 for both). Although baseline characteristics were similar between groups, right and left ventricular cardiac power indexes (cardiac power index = cardiac index × mean arterial pressure/451) identified patients who were likely to stabilize (area under the receiver operating characteristic curve = 0.82). CONCLUSIONS Among patients with chronic systolic heart failure who develop cardiogenic shock, more than one-half of patients stabilized with IABP support as a bridge to LVAD. Baseline measures of right and left ventricular cardiac power, reflecting work performed for a given flow and pressure, may allow clinicians to identify patients with sufficient contractile reserve who will be likely to stabilize with an IABP versus those who may need more aggressive ventricular support.


Progress in Cardiovascular Diseases | 2014

Patient evaluation and selection for transcatheter aortic valve replacement: the heart team approach.

Marc Sintek; Alan Zajarias

Transcatheter aortic valve replacement (TAVR) has been shown to significantly impact mortality and quality of life in patients with severe aortic stenosis (AS) who are deemed high risk for surgical aortic valve replacement (SAVR). Essential to these outcomes is proper patient selection. The multidisciplinary TAVR heart team was created to provide comprehensive patient evaluation and aid in proper selection. This review with outline the history and components of the heart team, and delineate the teams role in risk and frailty assessment, evaluation of common co-morbidities that impact outcomes, and the complex multi-modality imaging necessary for procedural planning and patient selection. The heart team is critical in determining patient eligibility and benefit and the optimal operative approach for TAVR. The future of structural heart disease will certainly require a team approach, and the TAVR heart team will serve as the successful model.


Current Opinion in Cardiology | 2014

Coronary subclavian steal syndrome.

Marc Sintek; Edward Coverstone; Jasvindar Singh

Purpose of review Coronary subclavian steal syndrome (CSSS) is the reversal of blood flow in an internal mammary artery bypass graft that results in coronary ischemia. CSSS is an uncommon but treatable cause of coronary ischemia. In this review, we highlight the historical background and epidemiology of CSSS, common clinical presentations, diagnosis of CSSS and management strategies for relieving ischemia. We also present a case report to illustrate the complexity of CSSS and percutaneous management using current technology. Recent findings Most commonly, CSSS results from atherosclerotic stenosis of the subclavian artery and occurs in 2.5–4.5% of patients referred for coronary artery bypass grafting (CABG). All patients referred for CABG should have bilateral noninvasive brachial blood pressures checked to screen for the underlying subclavian stenosis. A review of 98 case reports with 128 patients demonstrated a diverse clinical presentation of CSSS, including acute myocardial infarction, unstable angina and acute systolic heart failure. Resolution of CSSS symptoms has been reported with both surgical and percutaneous revascularization. Long-term patency with either revascularization strategy is excellent. Percutaneous revascularization is largely considered the first-line therapy for CSSS and can be safely performed prior to CABG to prevent CSSS. Summary CSSS should be suspected in patients presenting with angina, heart failure or myocardial infarction after CABG. Successful amelioration of CSSS symptoms can be safely and effectively performed via percutaneous revascularization.


Circulation-heart Failure | 2013

Coronary Collaterals Predict Improved Survival and Allograft Function in Patients with Coronary Allograft Vasculopathy

Kory J. Lavine; Marc Sintek; Eric Novak; Gregory A. Ewald; Edward M. Geltman; Susan M. Joseph; John D. Pfeifer; Douglas L. Mann

Background—Despite improvements in the care of patients who have received cardiac transplants, coronary allograft vasculopathy (CAV) remains the most prevalent cause of late allograft failure and cardiac mortality. Few proven therapies are available for this important disease. The presence of coronary collaterals imparts a favorable prognosis in patients with native ischemic heart disease; however, the impact of collaterals in CAV is unknown. Methods and Results—To determine whether the development of coronary collaterals is associated with improved outcomes in patients with CAV, we performed a retrospective analysis of patients followed in the heart transplant program at Barnes Jewish Hospital from 1994 to 2008. The primary end points included all cause mortality and the composite of all cause mortality, retransplantation, and inotrope dependence. We screened 485 patients and identified 59 (12%) subjects with moderate-to-severe CAV. Angiographically visible coronary collaterals were present in 34 (57%) subjects. Kaplan–Meier and Cox multivariable analyses revealed that patients with collaterals had reduced incidence of all cause mortality (hazard ratio, 0.20; P<0.001) and the composite end point (hazard ratio, 0.17; P<0.001). In addition, patients with collaterals had less severe heart failure symptoms as measured by New York Heart Association class. Immunostaining of biopsy specimens revealed that among patients with CAV, the presence of coronary collaterals correlated with increased microvascular density, reduced fibrosis, and decreased left ventricular end-diastolic pressure. Conclusions—Together, these data demonstrate that the presence of coronary collaterals predicts a favorable prognosis in patients with CAV and suggests that interventions aimed at promoting collateral and microvascular growth may serve as effective therapies for this disease.


Heart | 2016

Repeat revascularisation outcomes after percutaneous coronary intervention in patients with rheumatoid arthritis

Marc Sintek; Christopher T. Sparrow; Ted R. Mikuls; Kathyrn J Lindley; Richard G. Bach; Howard I. Kurz; Eric Novak; Jasvindar Singh

Objective To investigate repeat revascularisation outcomes in patients with rheumatoid arthritis(RA) after percutaneous coronary intervention (PCI). Methods We performed a single-centre, retrospective matched cohort study of patients with RA matched to non-RA patients post PCI. Primary endpoints were time to target lesion revascularisation (TLR) and target vessel revascularisation (TVR) analysed by Cox proportional hazard shared frailty models. Results A total of 228 lesions (143 patients) were identified in the RA cohort and matched to 677 control lesions (541 patients). TLR occurred in 33% (n=75) of RA lesions versus 25% (n=166) of control lesions (adjusted HR 1.3; 95% CI 0.97 to 1.8). TVR occurred in 39% (n=89) of RA lesions versus 31% (n=213) of control lesions (adjusted HR 1.15; 95% CI 0.82 to 1.6). There was a significant hazard for TLR (adjusted HR 1.48; 95% CI 1.03 to 2.13) and TVR (adjusted HR 1.55; 95% CI 1.12 to 2.14) when excluding lesions with revascularisation events or follow-up less than 1 year. When stratified by treatment with methotrexate or tumour necrosis factor (TNF) α inhibitors or both at discharge, lesions from patients with RA treated with these agents had similar TVR and TLR as control lesions, whereas lesions from patients with RA not treated with these agents had significantly more TLR and TVR (TLR adjusted HR 1.48; 95% CI 1.08 to 2.03; TVR adjusted HR 1.38; 95% CI 1.04 to 1.84). Conclusions RA predisposes to repeat revascularisation, specifically in patients followed after the 1-year landmark. In the absence of RA treatments including methotrexate and/or TNFα inhibitors, RA is associated with a 50% increased relative risk of repeat revascularisation following PCI. These findings emphasise the adverse effects of chronic inflammation on the durability of PCI and provide further support for aggressive anti-inflammatory treatment in patients with RA.


The Journal of Thoracic and Cardiovascular Surgery | 2018

Observed to Expected 30- Day Mortality as a Benchmark for Transcatheter Aortic Valve Replacement

Matthew C. Henn; Alan Zajarias; Nishath Quader; Marc Sintek; John M. Lasala; Kelly Koogler; Marci S. Damiano; Puja Kachroo; D. Craig Miller; C. Ryan King; Spencer J. Melby; Marc R. Moon; Ralph J. Damiano; Hersh S. Maniar

Objective: The observed‐to‐expected 30‐day mortality ratio (O:E ratio) is a standard metric by which transcatheter aortic valve replacement (TAVR) trials have been evaluated. Early TAVR trials consistently demonstrated O:E ratio less than 0.6 after TAVR when based on the Society for Thoracic Surgery Predicted Risk of Mortality (STS‐PROM) for surgical aortic valve replacement. Recent published results from the Transcatheter Valve Therapy (TVT) Registry have demonstrated O:E ratios of 1.0. We evaluated our own O:E ratios for TAVR to investigate this discordance. Methods: Data were collected prospectively for TAVR patients from 2008 through 2015 (N = 546) and were reviewed retrospectively. The observed mortality and STS‐PROM were calculated to formulate O:E ratios and were compared over a variety of subgroups. Results: Overall, the O:E ratio for 30‐day mortality was 0.4 and significantly less than 1 (P < .001; 95% confidence interval, 0.25‐0.63). The O:E ratio relationship remained less than 0.5 for patients with low (STS‐PROM < 4), moderate (STS‐PROM = 4‐8) and high risk (STS‐PROM > 8). The O:E ratio was significantly higher for transapical patients (O:E ratio = 0.8) when compared with transfemoral patients (O:E ratio = 0.2). Lastly, O:E ratios for both commercial (O:E ratio = 0.5) and research (O:E ratio = 0.3) patients were similar (P = .337), and both were significantly less than 1 (P = .007 and P < .001, respectively). Conclusions: The STS‐PROM consistently overestimated 30‐day mortality after TAVR. Achieving an O:E ratio less than 0.6 may be a realistic goal for all TAVR programs. While an accurate and specific risk calculator for 30‐day mortality after TAVR remains to be established, our data suggest that current TVT results are not acceptable for commercial TAVR and that programs with an O:E ratio greater than 0.6, based on the STS‐PROM, should reevaluate internal processes to improve their results.


Current Treatment Options in Cardiovascular Medicine | 2015

Dynamic Evaluation of Coronary Anomalies Originating from the Opposite Sinus of Valsalva (ACAOS)

Marc Sintek; Jasvindar Singh; Joseph J. Billadello

Opinion statementCoronary anomalies originating from the opposite sinus of Valsalva (ACAOS) are a rare anomaly associated with sudden cardiac death. Dynamic, invasive evaluation using coronary angiography, intravascular ultrasound, and fractional flow reserve can more clearly identify important pathophysiologic variants and guide treatment. This dynamic evaluation can assist the clinician in the appropriate surgical and percutaneous treatment options and aid in patient counseling. Long-term outcomes data regarding treatment and prognosis is still lacking.


Archive | 2018

Coronary Aorto-Ostial Lesion Interventions

Marc Sintek; Jasvindar Singh

Aorto-ostial lesions (AOLs), defined as a significant stenosis within 3 mm of the aortic orifice, are an uncommon but challenging lesion subset to manage. AOLs account for roughly 2.6% of interventions and frequently involve the right coronary artery. Risk factors for target lesion failure include treatment of bypass grafts, prior in-stent restenosis, direct stenting, and narrow postprocedure luminal diameter; all factors that can be influenced by the operator. Intravascular ultrasound (IVUS) is a key tool that provides a means of identifying the optimal landing zone and ensures optimal luminal gain and stent coverage after stent deployment. IVUS is strongly recommended for treatment of all AOLs. Additionally, appropriate lesion preparation with atherectomy or specialty angioplasty balloons is crucial in achieving maximal luminal gain. Although specialized AOL devices and techniques have been developed, the simple algorithm of adequate lesion preparation and heavy use of IVUS provides a robust and broadly applicable approach to AOLs. Successful long-term results can be obtained with AOLs involving the right coronary artery, left main, or the anastomosis of surgical bypass grafts.


Journal of Cardiology Cases | 2018

Acute right ventricular failure and pulseless electrical activity arrest following auto-transfusion of blood

Kolade M. Agboola; John M. Lasala; Marc Sintek; Amit Noheria

Air embolism is a rare but potentially catastrophic complication of interventional procedures. The occurrence of acute right ventricular dysfunction during intraoperative auto-transfusion of blood, presumably related to pulmonary embolism of agitated air microbubbles and microthrombi, is less commonly recognized. We report a case of auto-transfusion complicated by acute right ventricular failure and pulseless electrical activity arrest. Auto-transfusion of recovered blood is a practical solution to reduce need for post-procedure allogenic transfusions. Although such interventions are frequently performed without complications, they do have inherent risks that should be readily acknowledged. This case clearly describes a severe complication and sequelae of auto-transfusion. <Learning objective: Auto-transfusion of recovered blood is commonly performed in surgical and interventional procedures to reduce the need for allogenic transfusion. Despite this benefit, the risks and complications of auto-transfusion can be severe and must be considered. We report a case of intraprocedural auto-transfusion resulting in introduction of air emboli and subsequent cardiac arrest. Additionally, we provide a brief review of air emboli and underlying pathophysiology that leads to cardiovascular decline.>.

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Eric Novak

Washington University in St. Louis

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Alan Zajarias

Washington University in St. Louis

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Jasvindar Singh

Washington University in St. Louis

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John M. Lasala

Washington University in St. Louis

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Brian R. Lindman

Washington University in St. Louis

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Hersh S. Maniar

Washington University in St. Louis

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Kory J. Lavine

Washington University in St. Louis

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Marc R. Moon

Washington University in St. Louis

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Ralph J. Damiano

Washington University in St. Louis

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Susan M. Joseph

Baylor University Medical Center

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