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524 Imaging technical aspects 75±31 ml, p<0.01, respectively). (3) The %LV particles in patients with vortex was higher than that in patients without vortex (14% vs. 2%, medians, p<0.01). The %LV particles from right PVs was also higher than that from left PVs in patients with vortex (22% vs. 5%, p<0.01), whereas it did not differ in patients without vortex (2% vs. 0%, p=ns). Conclusions: 4D-Flow MRI can visualize the intra-LA vortex formation and flow dynamics from PVs to LV. The vortex formation may be dependent on the LV and LA volume, and may affect the flow dynamic from PVs to LV. The blood flow from left PVs seems to be more stagnant within LA than that from right PVs. P2940 | BEDSIDE Stress-induced myocardial ischemia modifies phase analysis indices obtained from Tc-99m sestamibi gated single photon emission computed tomography myocardial perfusion imaging J.F. Casuscelli, E.N. Aramayo G, M. Daicz, C.M. Cortes, M. Embon. Hospital Universitario Fundacion Favaloro, Ciudad Autonoma de Buenos Aires, Argentina Purpose: Phase analysis of gated myocardial perfusion single photon emission computed tomography (GSPECT) images allows the assessment of left ventricle (LV) mechanical synchrony. The aim of our study was to determine whether stress-induced ischemia modifies the two most commonly used phase analysis synchrony parameters: Histogram bandwidth (HB) and Standard deviation (SD) obtained from Tc 99m sestamibi of GSPECT images and to evaluate the correlation between these indices and different amounts of ischemia. Methods: We included 92 consecutive ischemic patients defined by SDS≥2 who underwent a two-day stress-rest protocol Tc99 sestamibi GSPECT between August 2011 and July 2012 and we compared them to a group of 22 normal subjects defined as asymptomatic, without known coronary artery disease, with low pretest of coronary artery disease, and normal ECG, stress test, left ventricular function and perfusion (SSS: 0), who followed the same GSPECT protocol. Patients with left bundle branch block, ventricular pacing and fixed perfusion defects were excluded. Phase analysis indices HB and SD were obtained from stress and rest images in both groups. We obtained the change (stress minus rest) of SD and HB indices for each patient. The ischemic group was divided into moderate-tosevere ischemia (SDS≥5), and severe ischemia (SDS≥8). Results: The ischemic group had a mean age of 63±10 years, 47 were men, 21 had moderate-to-severe ischemia and 10 severe ischemia. Ischemic patients showed higher stress SD and HB values than normal subjects (SD 15.65 vs 11.76, p=0.0002 and HB 47.74 vs 38.04, p=0.002 respectively) and larger amounts of ischemia showed higher values: moderate to severe ischemia (SD 20.08 vs 11.76, p<0.001 and HB 59.61 vs 38.04 p=0.001 respectively) and severe ischemia (SD 19 vs 11.76, p<0.0001 and HB 60.4 vs 38, p<0.0001 respectively). Changes in SD and HB were significatively higher in ischemic patients than in normal subjects (SD -0.19 vs -0.58, p<0.0001; HB 1.27 vs -0.95, p=0.0002 respectively). These differences were even higher in moderate to severe ischemia (SD 2.49 vs -0.58, p=0,0002; HB 4.76 vs -0.95, p<0.0001) and severe ischemia (SD 2.42 vs -0.58, p=0,0001; HB 12.5 vs -0.95, p<0.0001). Conclusion: In our population left ventricular mechanical synchrony indices obtained by phase analysis of Tc99sestamibi GSPECT imaging, HD and SD are altered in the presence of myocardial ischemia. Larger amounts of ischemia are related to higher dyssynchrony values of the phase-derived indices HB and SD. P2941 | BEDSIDE Evaluation of knowledge-based reconstruction for magnetic resonance volumetry of the right ventricle in tetralogy of fallot E.C.A. Nyns, A. Dragulescu, S.J. Yoo, L. Grosse-Wortmann. Labatt Family Heart Center, Hospital for Sick Children and University of Toronto, Toronto, Canada Purpose: Evaluating right ventricular (RV) volumes and function is important in the clinical management of patients after tetralogy of Fallot (TOF) repair. Currently, cardiac magnetic resonance (CMR) using Simpson’s method is the gold standard for RV quantitative assessment. However, this method is time consuming and not without sources of error. Knowledge-based reconstruction (KBR) is a new imaging tool for RV volumetry and has been recently validated on echocardiography. The aim of this study was to assess the feasibility, accuracy, and Projection of the 3D model on a 2D image labor intensity of KBR on CMR datasets in a group of repaired TOF patients by comparison with measurements obtained by Simpson’s method. Methods: Thirty five patients (mean age 14±3 years) after TOF repair were studied using KBR and Simpson’s method. Parameters analyzed were RV enddiastolic volume (EDV), end-systolic volume (ESV), ejection fraction (EF) and post-processing time. All measurements were compared with the standard Simpson’s method. Intraobserver, interobserver and intermethod variability was assessed using Pearson’s correlation analysis, coefficients of variation and BlandAltman analysis. Results: KBR was feasible and highly accurate as compared to Simpson’s method. Intra- and intermethod variability for KBR measurements showed good agreements. When compared with Simpson’s method, volumetry using KBR was faster (10.9±2.0 vs. 7.1±2.4 minutes, P<.001, respectively). Conclusion: In repaired TOF patients, KBR is a feasible, accurate and reproducible method for measuring RV volumes and function. In addition, the postprocessing time of RV volumetry using KBR was significantly shorter when compared with Simpson’s method. P2942 | BEDSIDE Comparison of myocardial perfusion and function with the severity of coronary artery disease between 201Tl and 99mTc-agent using a cadmium-zinc-telluride camera S. Hida, T. Chikamori, H. Tanaka, Y. Igarashi, C. Shiba, Y. Usui, T. Hatano, A. Yamashina. Tokyo Medical University, Tokyo, Japan Background: Although cadmium-zinc-telluride (CZT) camera system (Discovery NM 530c) have recently been introduced in myocardial perfusion imaging (MPI), no study has shown whether myocardial perfusion analysis using CZT camera is affected by the type of radiotracer or the severity of coronary artery disease (CAD). Methods: The study group comprised 164 consecutive patients who underwent both stress MPI and coronary angiography within 3 months. Standard dose 1-day 99mTc-radiotracer (370/740MBq) protocol was performed in 74 patients with a 5-min scan time for stress, a 3-min for at rest, while 201Tl (111MBq) protocol was performed in 90 patients with a 5-min for stress, a 10-min for at rest. Myocardial perfusion was assessed visually using a 17-segment model, and the changes in LV volume and function with stress were analyzed using a QGS software. Highrisk CAD was defined as a Duke CAD Prognostic Index of ≥42 and non-high-risk CAD was defined as those of <42. Results: Average of Duke CAD prognostic index in patients who underwent 99mTc scans was similar to those who had 201Tl scan, either in the high-risk CAD (64.1±7.8 vs 65.3±11.2) or in the non-high-risk CAD (21.3±15.1 vs 20.9±16.1). Summed difference score was less with 99mTc MPI than with 201Tl MPI either in patients with high-risk (4.8±4.4 vs 10.6±6.2; p=0.004) or with non-high-risk CAD (3.1±4.4 vs 6.0±4.9; p=0.001). LV functional analysis demonstrated that post-stress changes were greater with 99mTc MPI than with 201Tl MPI in endsystolic volume (7.9±2.8ml vs 3.2±9.1ml; p<0.03 for high-risk CAD, 3.9±6.5ml vs 0.9±5.8ml; p=0.01, for non-high-risk CAD, respectively) and ejection fraction (-6.9±3.3% vs -1.2±6.6%; p=0.001, for high-risk CAD, -2.8±4.8% vs 0.0±5.3%; p=0.003, for non-high-risk CAD, respectively). In patients with 99mTc MPI, poststress changes such as ESV and EF were greater in those with high-risk than in non-high risk CAD (p=0.001 for ESV and p<0.005 for EF) whereas post-stress changes were similar between those with high-risk and non-high risk CAD in patients who had 201Tl MPI. Conclusions: These results suggested that although 99mTc MPI using the CZT camera system may underestimate the extent and severity of myocardial ischemia with 201Tl MPI, 99mTc is superior to 201Tl MPI in the functional analysis to reveal post-ischemic stunning. P2943 | BEDSIDE Non-contrast angiography of renal artery in 3T magnetic resonance in patients with refractory arterial hypertension before renal denervation U. Speiser, L. Schmiedel, C. Henke, A. Abas, S. Jellinghaus, V. Sandfort, A. Traenkner, H. Schroetter, R.H. Strasser. Dresden University of Technology, Heart Center, University Hospital, Germany, Dresden, Germany Introduction: Catheter-based renal sympathic denervation is a technique for treatment of resistant arterial hypertension. Planning this procedure magnetic resonance (MR) is a non-invasive method without any radiation to reliably image the anatomical conditions like diameters, possible stenosis or abnormalities of renal arteries. Impaired renal function (GFR<30 ml/min) is a known contraindication for gadolinium based contrast agent due to the risk of nephrogenic systemic fibrosis. To address the question if imaging of the anatomy of renal arteries in 3T MR may be feasible and reliable without using contrast agent the present prospective study was performed. Methods: 34 Patients with resistant hypertension (taking four antihypertensive drugs including diuretics and long term blood pressure measurement larger than 135/85mmHg) for whom renal denervation was planned were included prospectively. In 3T magnetic resonance 3D conventional contrast MR angiography (CMRA) was performed after antecubital injection of gadopentetat-dimeglumin during Imaging technical aspects breath-hold. Additionally, an inflow inversion recovery steady state free precession sequence (Inhance) was used for non-contrast MR angiography (NCMRA). Diameters of renal artery were assessed 20 mm from aortic ostium. Furthermore, the aortic diameter was measured at height of renal artery orifice. Results: 34 patients (66±8 years) were included in both conventional contrast and non-contrast MR angiography and presented a total of 76 main and accessory renal arteries. In CMRA mean renal artery diameter was 6.2±1.8 mm, in NCMRA mean renal artery was determined with 6.0±2.0 mm. Mean aortic diameters were identified with 20.4±3.2 in CMRA and with 20.1±2.8 in NCMRA. Measurements of renal artery by NCMRA closely correlate to renal artery diameters assigned by CMRA (r=0.97). Furthermore, detection of aortic diameters showed also good correlation between both MRA (r=0.92). Bland-Altman-analysis did not present any signs of under- and overestimation of both measurement methods. Conclusion: At 3T CMR determination of renal artery and aortic diameter at the orifice of the renal arteries is possible by non-contrast MR angiography as well as by 3D contrast MR angiography. Both methods provide reliable estimates of the diameter of the vessel without relevant under- or overestimation. Non-contrast MR angiography should be regarded as a powerful completely non-invasive tool to image renal arteries without the need to use potentially nephrotoxic contrast media. 525 by CMR in four different ways: 1) Phase-contrast (PC) on the pulmonary artery (PA) as PA systolic volume*heart rate (HR); 2) PC on the aorta as aortic systolic volume*HR; RV Sympson method as [RV end-diastolic volume – RV end-sistolic volume]* HR; and 4) Left ventricular (LV) Sympson method as [LV end-diastolic volume – LV end-sistolic volume]*HR. Accuracy was assessed using intraclass correlation coefficient for absolute agreement and Bland-Altman analysis. Results: Intraclass correlation coefficients for CMR measurements using RHCquantified CO as the gold standard were: 0.94 (95% CI 0.90-0.96) for PC on the PA; 0.87 (95% CI 0.69-0.94) for PC on the aorta; 0.90 (95% CI 0.84-0.94) for RV Sympson method; and 0.89 (95% CI 0.82-0.93) for LV Sympson method. According to Bland-Altman analysis, mean bias and limits of agreement were respectively: -0.13 (-1.45,1.18); -0.47 (-2.02, 1.08); -0.20 (-1.80, 1.40); and -0.23 (-1.78, 1.31). Concordance between the different CMR methods was excellent (Figure). P2944 | BEDSIDE Sonographic position monitoring of central venous catheters by microbubble-injection in real time: development of a new procedure M. Campo Dell Orto 1 , S. Schellknecht 2 , F.H. Seeger 2 , C. Hamm 1 , R. Breitkreutz 3 . 1 Kerckhoff Clinic Bad Nauheim, Bad Nauheim, Germany; 2 University of Frankfurt, Frankfurt, Germany; 3 Hospital of the City of Frankfurt (Hoechst), Frankfurt, Germany Background: Central venous catheter placement requires immediate confirmation of its orthotopic position in the central vena cava to avoid arterial or paravasal infusions which could potentially harm the patient. The correct position is usually verified by chest x-ray or ECG. Echocardiography might offer a fast and safe alternative. This study aimed at developing a new non-invasive, ultrasound-based procedure to determine the orthotopic position of Central Venous Catheters (CVC) position by sonographic detection of injected Microbubbles (MB) Methods: With approval of the local ethics committee 95 patients with 98 CVC and 5 peripheral catheters were examined. The appearance of MB in the right heart can be observed after injection of agitated saline in the subcostal fourchamber view. MB are hyperechogenic and dissolve later. The time from injection at the catheter to the appearance in the RV can be recorded by M-Mode registration allowing an exact measurement independent of user interaction and reaction. To determine positioning, time of appearance of MB was recorded. The transit time was correlated with radiologically confirmed catheter positions. A self assessment of the procedures practicability was performed on a linear anologue scale (0-100%). Results: We report a total of 95 Patients (65.0±18 years, 57% male). The jugular vein was used in 85 and the subclavian vein in 13 cases. The main diagnoses requiring catheter placement were pneumonia (n=49), aortic valve reconstruction (n=9), myocardial infarction (n=6), heart failure (n=6), gastrointestinal bleeding (n=6) or others (n=9). In 95 patients with radiologically confirmed orthotopic position MB appeared in the right heart in less than one second after injection with a reliability of 100%. In 3 patients, quantitatively measured appearance of MB was even below 0.5 seconds. In 5 patients with peripheral venous catheters MB were observed later than 2 sec after injection and in one patient with a heterotopic CVC within 1-2 seconds after injection. Duration of the procedure was 146 (111) seconds (mean, (SD)). Physician’s impression of practicalness was 91% (linear analogue self assessment). Conclusion: Ultrasound-based real-time position monitoring of CVC by this new description of the MB-injection technique has the potential to serve as an alternative to X-ray or other methods. Appearance of MBs in less than one second can be assumed to predict orthotopic position with high accuracy. Appearance of MB in more than two seconds indicates malpositioning. Transit times between one and two seconds require additional X-ray confirmation. P2945 | BENCH Accuracy of magnetic resonance for noninvasive cardiac output quantification in postcapillary pulmonary hypertension A. Garcia-Alvarez, L. Fernandez-Friera, D. Pereda, R. Fernandez-Jimenez, M. Nuno-Ayala, J.M. Garcia-Ruiz, G. Guzman, G. Pizarro, V. Fuster, B. Ibanez. Centro Nacional de Investigaciones Cardiovasculares Carlos III, Madrid, Spain Purpose: Right ventricular (RV) failure is the main prognostic factor in pulmonary hypertension (PH). Our aim was to evaluate the precision of different noninvasive approaches to calculate cardiac output (CO) by cardiac magnetic resonance (CMR) in an experimental model of chronic postcapillary PH. Methods: Postcapillary PH (N=13) was generated by banding of the inferior pulmonary vein in piglets. Animals were followed for 4 months. Two animals died at 2 and 3 moths due to severe PH. At baseline and every 4 weeks, animals underwent RHC and immediate 3T CMR (N=62 pairs of measurements). CO was assessed by RHC using a Swan-Ganz catheter (thermodilution method). CO was measured Concordance among different CO measures Conclusion: CMR accurately quantifies CO noninvasively in postcapillary PH. Phase-contrast on the PA seems the best CMR method. P2946 | BENCH LAA closure monitoring by trans-esophageal echocardiography using ICE probe J. Ternacle, N. Lellouche, R. Gallet, P. Gueret, J.-L. Dubois-Randes, E. Teiger, P. Lim. AP-HP - University Hospital Henri Mondor, Department of Cardiology, Creteil, France Background: Intracardiac echocardiography probe can be used trough esophageal route (ICE-TEE) to monitor transeptal puncture and evaluate left atrial appendage (LAA) without requiring general sedation. The purpose of the study is to evaluate the accuracy and the safety of ICE-TEE during Amplatzer Cardiac Plug (ACP) implantation. Methods: The study included 16 consecutive patients (75±7 years) in atrial fibrillation with high risk of embolism (CHAD-Vasc=5±1.4) that required LAA closure by ACP because of severe bleeding complications occurring under vitamin K antagonist (HAS-BLED=4±0.9). Standard TEE was performed the day before the device implantation for LAA sizing and excluding thrombosis. During the procedure, ICE-TEE was used under local anesthesia to determine ACP diameter (ACP diameter=1.2*LAA diameter by ICE-TEE) and monitor ACP positioning. LAA size by ICE-TEE was compared to the size obtained by fluoroscopy and standard TEE and ACP lobe size after device implantation by ICE-TEE to cardiac computed tomography (CT). Results: LAA maximal diameter by ICE-TEE did not differ from TEE (21±3 mm vs. 20±3 mm, r=0.9, P<0.001), while fluoroscopy measurement was lower (19±3 mm, P<0.05 vs. ICE-TEE and P=0.08 vs. TEE). ACP was successfully implanted in 13 patients after one device, 2 patients after 2 devices and one failed because of a complex LAA anatomy. As expected ACP diameter implanted was 1.2±0.04 (mean=25±3mm, ≤26mm in 10/16 patients) greater than LAA size measured by ICE-TEE. ACP size by ICE-TEE at the end of the procedure was similar to cardiac CT measurement (23±7 mm vs. 23±4mm, R=0.98, p<0.001). Finally, the procedure (mean duration=62±27 minutes, X-ray exposure=78±51 gray/m2 ) was safely conducted in all without pericardial effusion and prosthesis migration. Conclusions: ICE-TEE probe through esophageal route may be used for the sizing and the monitoring of ACP device implantation. Compared to standard TEE, ICE-TEE does not required general sedation.