16 results on '"Carstensen, HG"'
Search Results
2. Poster session 2: Thursday 4 December 2014, 08:30-12:30Location: Poster area
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Domingos, J, Augustine, D, Leeson, P, Noble, J, Doan, HL, Boubrit, L, Cheikh-Khalifa, R, Laveau, F, Djebbar, M, Pousset, F, Isnard, R, Hammoudi, N, Lisi, M, Cameli, M, Di Tommaso, C, Curci, V, Reccia, R, Maccherini, M, Henein, MY, Mondillo, S, Leitman, M, Vered, Z, Rashid, H, Yalcin, MU, Gurses, KM, Kocyigit, D, Evranos, B, Yorgun, H, Sahiner, L, Kaya, B, Aytemir, K, Ozer, N, Bertella, E, Petulla', M, Baggiano, A, Mushtaq, S, Russo, E, Gripari, P, Innocenti, E, Andreini, D, Tondo, C, Pontone, G, Necas, J, Kovalova, S, Hristova, K, Shiue, I, Bogdanva, V, Teixido Tura, G, Sanchez, V, Rodriguez-Palomares, J, Gutierrez, L, Gonzalez-Alujas, T, Garcia-Dorado, D, Forteza, A, Evangelista, A, Timoteo, AT, Aguiar Rosa, S, Cruz Ferreira, R, Campbell, R, Carrick, D, Mccombe, C, Tzemos, N, Berry, C, Sonecki, P, Noda, M, Setoguchi, M, Ikenouchi, T, Nakamura, T, Yamamoto, Y, Murakami, T, Katou, Y, Usui, M, Ichikawa, K, Isobe, M, Kwon, B, Roh, J, Kim, H, Ihm, S, Barron, AJ, Francis, D, Mayet, J, Wensel, R, Kosiuk, J, Dinov, B, Bollmann, A, Hindricks, G, Breithardt, O, Rio, P, Moura Branco, L, Galrinho, A, Cacela, D, Pinto Teixeira, P, Afonso Nogueira, M, Pereira-Da-Silva, T, Abreu, J, Teresa Timoteo, A, Pavlyukova, E, Tereshenkova, E, Karpov, R, Piatkowski, R, Kochanowski, J, Opolski, G, Barbier, P, Mirea, O, Guglielmo, M, Savioli, G, Cefalu, C, Pudil, R, Horakova, L, Rozloznik, M, Balestra, C, Rimbas, R, Enescu, O, Calin, S, Vinereanu, D, Karsenty, C, Hascoet, S, Hadeed, K, Semet, F, Dulac, Y, Alacoque, X, Leobon, B, Acar, P, Dharma, S, Sukmawan, R, Soesanto, A, Vebiona, K, Firdaus, I, Danny, S, Driessen, MM, Sieswerda, G, Post, M, Snijder, R, Van Dijk, A, Leiner, T, Meijboom, F, Chrysohoou, C, Tsitsinakis, G, Tsiachris, D, Aggelis, A, Herouvim, E, Vogiatzis, I, Pitsavos, C, Koulouris, G, Stefanadis, C, Erdei, T, Edwards, J, Braim, D, Yousef, Z, Fraser, A, Avenatti, E, Magnino, C, Omede', P, Presutti, D, Moretti, C, Iannaccone, A, Ravera, A, Gaita, F, Milan, A, Veglio, F, Scali, M, Simioniuc, A, Fusini, L, Dini, F, Okura, H, Murata, E, Kataoka, T, Mikaelpoor, A, Ojaghi Haghighi, S, Alizadeasl, A, Sharifi-Zarchi, A, Zaroui, A, Ben Halima, M, Mourali, M, Mechmeche, R, Rodriguez Palomares, JF, Maldonado, G, Garcia, G, Otaegui, I, Garcia Del Blanco, B, Teixido, G, Gonzalez Alujas, M, Garcia Dorado, D, Godinho, AR, Correia, A, Rangel, I, Rocha, A, Rodrigues, J, Araujo, V, Almeida, P, Macedo, F, Maciel, M, Rekik, B, Mghaieth, F, Aloui, H, Boudiche, S, Jomaa, M, Ayari, J, Tabebi, N, Farhati, A, Mourali, S, Dekleva, M, Markovic-Nikolic, N, Zivkovic, M, Stankovic, A, Boljevic, D, Korac, N, Beleslin, B, Arandjelovic, A, Ostojic, M, Galli, E, Guirette, Y, Auffret, V, Daudin, M, Fournet, M, Mabo, P, Donal, E, Chin, CW, Luo, E, Hwan, J, White, A, Newby, D, Dweck, M, Carstensen, HG, Larsen, LH, Hassager, C, Kofoed, KF, Jensen, JS, Mogelvang, R, Kowalczyk, M, Debska, M, Kolesnik, A, Dangel, J, Kawalec, W, Migliore, R, Adaniya, M, Barranco, M, Miramont, G, Gonzalez, S, Tamagusuku, H, Davidsen, ES, Kuiper, KK, Matre, K, Gerdts, E, Igual Munoz, B, Maceira Gonzalez, A, Erdociain Perales, M, Estornell Erill, J, Valera Martinez, F, Miro Palau, V, Piquer Gil, M, Sepulveda Sanchez, P, Cervera Zamora, A, Montero Argudo, A, Placido, R, Silva Marques, J, Magalhaes, A, Guimaraes, T, Nobre E Menezes, M, Goncalves, S, Ramalho, A, Robalo Martins, S, Almeida, A, Nunes Diogo, A, Abid, L, Ben Kahla, S, Charfeddine, S, Abid, D, Kammoun, S, Tounsi, A, Hammami, R, Triki, F, Akrout, M, Mallek, S, Hentati, M, Sirbu, CF, Berrebi, A, Huber, A, Folliguet, T, Yang, LT, Shih, J, Liu, Y, Li, Y, Tsai, L, Luo, C, Tsai, W, Babukov, R, Bartosh, F, Bazilev, V, Muraru, D, Cavalli, G, Addetia, K, Miglioranza, M, Veronesi, F, Mihaila, S, Tadic, M, Cucchini, U, Badano, L, Lang, R, Miyazaki, S, Slavich, M, Miyazaki, T, Figini, F, Lativ, A, Chieffo, A, Montrfano, M, Alfieri, O, Colombo, A, Agricola, E, Liu, D, Hu, K, Herrmann, S, Stoerk, S, Kramer, B, Ertl, G, Bijnens, B, Weidemann, F, Brand, M, Butz, T, Tzikas, S, Van Bracht, M, Roeing, J, Wennemann, R, Christ, M, Grett, M, Trappe, HJ, Scherzer, S, Geroldinger, A, Krenn, L, Roth, C, Gangl, C, Maurer, G, Rosenhek, R, Neunteufl, T, Binder, T, Bergler-Klein, J, Martins, E, Pinho, T, Leite, S, Azevedo, O, Belo, A, Campelo, M, Amorim, S, Rocha-Goncalves, F, Goncalves, L, Silva-Cardoso, J, Ahn, H, Kim, K, Jeon, H, Youn, H, Haland, T, Saberniak, J, Leren, I, Edvardsen, T, Haugaa, K, Ziolkowska, L, Boruc, A, Turska-Kmiec, A, Zubrzycka, M, Monivas Palomero, V, Mingo Santos, S, Goirigolzarri Artaza, J, Rodriguez Gonzalez, E, Rivero Arribas, B, Castro Urda, V, Dominguez Rodriguez, F, Mitroi, C, Gracia Lunar, I, Fernadez Lozano, I, Palecek, T, Masek, M, Kuchynka, P, Fikrle, M, Spicka, I, Rysava, R, Linhart, A, Hasselberg, N, Borgquist, R, Platonov, P, Ancona, R, Comenale Pinto, S, Caso, P, Coopola, M, Arenga, F, Rapisarda, O, D'onofrio, A, Sellitto, V, Calabro, R, Rosca, M, Popescu, B, Calin, A, Mateescu, A, Beladan, C, Jalba, M, Rusu, E, Zilisteanu, D, Ginghina, C, Pressman, G, Cepeda-Valery, B, Romero-Corral, A, Moldovan, R, Saenz, A, Orban, M, Samuel, S, Fijalkowski, M, Fijalkowska, M, Gilis-Siek, N, Blaut, K, Galaska, R, Sworczak, K, Gruchala, M, Nowak, R, Ikonomidis, I, Triantafyllidi, H, Trivilou, P, Tzortzis, S, Papadopoulos, C, Pavlidis, G, Paraskevaidis, I, Lekakis, J, Padiyath, A, Li, L, Xiao, Y, Danford, D, Kutty, S, Kaymaz, C, Aktemur, T, Poci, N, Ozturk, S, Akbal, O, Yilmaz, F, Tokgoz Demircan, H, Kirca, N, Tanboga, I, Ozdemir, N, Greiner, S, Jud, A, Aurich, M, Hess, A, Hilbel, T, Hardt, S, Katus, H, D'ascenzi, F, Alvino, F, Focardi, M, Solari, M, Bonifazi, M, Konopka, M, Krol, W, Klusiewicz, A, Burkhard, K, Chwalbinska, J, Pokrywka, A, Dluzniewski, M, Braksator, W, King, GJ, Coen, K, Gannon, S, Fahy, N, Kindler, H, Clarke, J, Iliuta, L, Rac-Albu, M, Cortez-Dias, N, Francisco, A, Silva, G, Kyu, K, Kong, W, Songco, G, Galupo, M, Castro, M, Shin Hnin, W, Ronald Lee, C, Poh, K, Milazzo, V, Di Stefano, C, Tosello, F, Leone, D, Sabia, L, Sobrero, G, Maule, S, Jamiel, AM, Ahmed, AM, Farah, I, Al-Mallah, MH, Petroni, R, Magnano, R, Bencivenga, S, Di Mauro, M, Petroni, S, Altorio, S, Romano, S, Penco, M, Kumor, M, Lipczynska, M, Klisiewicz, A, Wojcik, A, Konka, M, Kozuch, K, Szymanski, P, Hoffman, P, Rimbas, M, Reynaud, A, Lund, L, Persson, H, Hage, C, Oger, E, Linde, C, Daubert, J, Maria Oliveira Lima, M, Costa, H, Gomes Da Silva, M, Noman Alencar, M, Carmo Pereira Nunes, M, Costa Rocha, M, Siala, A, Ozawa, K, Funabashi, N, Takaoka, H, Kobayashi, Y, Matsumura, Y, Wada, M, Hirakawa, D, Yasuoka, Y, Morimoto, N, Takeuchi, H, Kitaoka, H, Sugiura, T, Lakkas, L, Naka, K, Ntounousi, E, Gkirdis, I, Koutlas, V, Bechlioulis, A, Pappas, K, Katsouras, C, Siamopoulos, K, Michalis, L, Evangelou, D, Kalaitzidis, R, Tzeltzes, G, Nakas, G, Generati, G, Bandera, F, Pellegrino, M, Labate, V, Alfonzetti, E, Guazzi, M, Zagatina, A, Zhuravskaya, N, Al-Mallah, M, Alsaileek, A, Qureshi, W, Peyre, M, Amadieu, R, Yamanaka, Y, Sotomi, Y, Iwakura, K, Inoue, K, Toyoshima, Y, Tanaka, K, Oka, T, Tanaka, N, Orihara, Y, Fujii, K, Soulat-Dufour, L, Lang, S, Boyer-Chatenet, L, Van Der Vynckt, C, Ederhy, S, Adavane, S, Haddour, N, Boccara, F, Cohen, A, Huitema, M, Boerman, S, Vorselaars, V, Grutters, J, Gopal, AS, Saha, S, Toole, R, Kiotsekoglou, A, Cao, J, Reichek, N, Meyer, CG, Altiok, E, Al Ateah, G, Lehrke, M, Becker, M, Lotfi, S, Autschbach, R, Marx, N, Hoffmann, R, Frick, M, Nemes, A, Sepp, R, Kalapos, A, Domsik, P, Forster, T, Caro Codon, J, Blazquez Bermejo, Z, Lopez Fernandez, T, Valbuena Lopez, SC, Iniesta Manjavacas, AM, De Torres Alba, F, Dominguez Melcon, F, Pena Conde, L, Moreno Yanguela, M, Lopez-Sendon, JL, Lengyel, C, Orosz, A, Varkonyi, T, Rendon, J, Saldarriaga, CI, Duarte, N, Foldeak, D, Borbenyi, Z, Hamdy, A, Fereig, H, Nabih, M, Abdel-Aziz, A, Ali, A, Broyd, C, Wielandts, JY, De Buck, S, Michielsen, K, Louw, R, Garweg, C, Nuyts, J, Ector, J, Maes, F, Heidbuchel, H, Gillis, K, Bala, G, Tierens, S, Cosyns, B, Maurovich-Horvat, P, Horvath, T, Jermendy, A, Celeng, C, Panajotu, A, Bartykowszki, A, Karolyi, M, Tarnoki, A, Jermendy, G, and Merkely, B
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medicine.medical_specialty ,biology ,Early Repolarization Pattern ,business.industry ,Athletes ,Physical therapy ,medicine ,Radiology, Nuclear Medicine and imaging ,General Medicine ,Cardiology and Cardiovascular Medicine ,business ,biology.organism_classification - Published
- 2014
3. Poster Session 5The imaging examination and quality assessmentP1064The natural course of heart failure with preserved ejection fraction (HFpEF) - insights from an exploratory echocardiographic registryP1065Epicardial fat and effectiveness of catheter radiofrequency ablation in patients with atrial fibrillation and metabolic syndromeP1066Systematic disinfection of echocardiographic probe after each examination to reduce the persistence of pathogens as a potential source of nosocomial infectionsP1067Left atrial mechanical function assessed by two-dimensional echocardiography in hypertensive patientsP1068Real live applications of three-dimensional echocardiographic quantification of the left ventricular volumes and function using an automated adaptive analytics algorithmP10693D echocardiographic left ventricular dyssynchrony indices in end stage kidney disease: associations and outcomesP1070Relative contribution of right ventricular longitudinal shortening and radial displacement to global pump function in healthy volunteersP1071ECHO-parameters, associated with short-term mortality and long-term complications in patients with pulmonary embolism of high and intermediate riskP1072Increased epicardial fat is an independent marker of heart failure with preserved ejection fraction.P1073Influence of optimized beta-blocker therapy on diastolic dysfunction determined echocardiographically in heart failure patientsP1074Early diastolic mitral flow velocity/ annular velocity ratio is a sensitive marker of elevated filling pressure in left ventricular dyssynchronyP1075Left ventricular diastolic function in STEMI patients receiving early and late reperfusion by percutaneous coronary intervention P1076Could anatomical and functional features predict cerebrovascular events in patients with patent foramen ovale?P1077Efficacy of endarterectomy of the left anterior descending artery: evaluation by adenosine echocardiography?P1078Left ventricular diastolic dysfunction after acute myocardial infarction with preserved ejection fraction is related to lower exercise capacityP1079Potentially predictors of ventricular arrhythmia during six months follow up in STEMI patientsP1080Association between left atrial dilatation and invasive haemodynamics at rest and during exercise in asymptimatic aortic stenosisP1081Cardiac amyloidosis and aortic stenosis - the convergence of two aging processes and its association with outcomesP1082Prognostic impact of initial left ventricular dysfunction and mean gradient after transcatheter aortic valve implantationP1083Distribution and prognostic significance of left ventricular global longitudinal strain in asymptomatic significant aortic stenosis: an individual participant data meta-analysisP1084Discrepancies between echocardiographic and invasive assessment of aortic stenosis in multimorbid elderly patientsP1085Echocardiographic determinants and outcome of patients with low-gradient moderate and severe aortic valve stenosis: implications for aortic valve replacementP1086Atrial deformation correlated with functional capacity in mitral stenosisP1087Net atrioventricular compliance can predict reduction of pulmonary artery pressure after percutaneous mitral balloon commissurotomy
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Koschutnik, M., primary, Ionin, VA., primary, Boeckstaens, S., primary, Zakhama, L., primary, Hinojar, R., primary, Chiu, D Y Y, primary, Kovacs, A., primary, Kochmareva, EA., primary, Saliba, E., primary, Stanojevic, D., primary, Aalen, J., primary, Chen, XH., primary, Zito, C., primary, Demerouti, E., primary, Smarz, K., primary, Krljanac, G., primary, Christensen, NL., primary, Cavalcante, JL., primary, Pal, M., primary, Magne, J., primary, Giannakopoulos, G., primary, Liu, D., primary, Chien, CY., primary, Moustafa, TAMER, primary, Schwaiger, M., additional, Zotter-Tufaro, C., additional, Aschauer, S., additional, Duca, F., additional, Kammerlander, A., additional, Bonderman, D., additional, Mascherbauer, J., additional, Zaslavskaya, EL., additional, Soboleva, AV., additional, Listopad, OV., additional, Malikov, KN., additional, Baranova, EI., additional, Shlyakhto, EV., additional, Van Der Hoogstraete, M., additional, Coltel, N., additional, De Laet, N., additional, Beernaerts, C., additional, Desmet, K., additional, Gillis, K., additional, Droogmans, S., additional, Cosyns, B., additional, Antit, S., additional, Herbegue, B., additional, Slama, I., additional, Belaouer, A., additional, Chenik, S., additional, Boussabah, E., additional, Thameur, M., additional, Masmoudi, M., additional, Benyoussef, S., additional, Fernandez-Golfin, C., additional, Gonzalez-Gomez, A., additional, Casas, E., additional, Garcia Martin, A., additional, Pardo, A., additional, Del Val, D., additional, Ruiz, S., additional, Moya, JL., additional, Barrios, V., additional, Jimenez Nacher, JJ., additional, Zamorano, JL., additional, Kalra, PA., additional, Green, D., additional, Hughes, J., additional, Sinha, S., additional, Abidin, N., additional, Muraru, D., additional, Lakatos, BK., additional, Surkova, E., additional, Peluso, D., additional, Toser, Z., additional, Tokodi, M., additional, Merkely, B., additional, Badano, LP., additional, Volkova, AL., additional, Rusina, VA., additional, Kokorin, VA., additional, Gordeev, IG., additional, Baudet, M., additional, Chartrand Lefebvre, C., additional, Chen-Tournoux, A., additional, Hodzic, A., additional, Tournoux, F., additional, Apostolovic, S., additional, Jankovic-Tomasevic, R., additional, Djordjevic-Radojkovic, D., additional, Salinger-Martinovic, S., additional, Kostic, T., additional, Tahirovic, E., additional, Dungen, HD., additional, Andersen, OS., additional, Gude, E., additional, Andreassen, A., additional, Aalen, OO., additional, Larsen, CK., additional, Remme, EW., additional, Smiseth, OA., additional, Xu, HG., additional, Liu, FC., additional, Zha, DG., additional, Cui, K., additional, Zhang, AD., additional, Trio, O., additional, Soraci, E., additional, Cusma Piccione, M., additional, D'amico, G., additional, Ioppolo, A., additional, Alibani, L., additional, Falanga, G., additional, Todaro, MC., additional, Oreto, L., additional, Nucifora, G., additional, Vizzari, G., additional, Pizzino, F., additional, Di Bella, G., additional, Carerj, S., additional, Boutsikou, M., additional, Perreas, K., additional, Katselis, CH., additional, Samanidis, G., additional, Antoniou, TH., additional, Karatasakis, G., additional, Zaborska, B., additional, Jaxa-Chamiec, T., additional, Maciejewski, P., additional, Bartoszewicz, Z., additional, Budaj, A., additional, Trifunovic, D., additional, Asanin, M., additional, Savic, L., additional, Matovic, D., additional, Petrovic, M., additional, Zlatic, N., additional, Mrdovic, I., additional, Dahl, JS., additional, Carter-Storch, R., additional, Bakkestroem, R., additional, Soendergaard, E., additional, Videbaek, L., additional, Moeller, JE., additional, Rijal, S., additional, Abdelkarim, I., additional, Althouse, AD., additional, Sharbaugh, MS., additional, Fridman, Y., additional, Han, W., additional, Soman, P., additional, Forman, DE., additional, Schindler, JT., additional, Gleason, TG., additional, Lee, JE., additional, Schelbert, EB., additional, Dekany, G., additional, Mandzak, A., additional, Chaurasia, AK., additional, Gyovai, J., additional, Hegedus, N., additional, Piroth, ZS., additional, Szabo, GY., additional, Fontos, G., additional, Andreka, P., additional, Popescu, BA., additional, Carstensen, HG., additional, Dahl, J., additional, Desai, M., additional, Kearney, L., additional, Marwick, T., additional, Sato, K., additional, Takeuchi, M., additional, Zito, C., additional, Mohty, D., additional, Lancellotti, P., additional, Habib, G., additional, Noble, S., additional, Frei, A., additional, Mueller, H., additional, Hu, K., additional, Liebner, E., additional, Weidemann, F., additional, Herrmann, S., additional, Ertl, G., additional, Voelker, W., additional, Gorski, A., additional, Leyh, R., additional, Stoerk, S., additional, Nordbeck, P., additional, Tsai, WC., additional, Moustafa, TAMER, additional, and Aldydamony, MOHAMD, additional
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- 2016
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4. Oral Abstract sessions * 2 D strain in aortic stenosis: clinical impact: 13/12/2013, 14:00-15:30 * Location: Bursa
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Carstensen, HG, Larsen, LH, Hassager, C, Kofoed, KF, Kristensen, CB, Jensen, JS, Mogelvang, R, Dulgheru, R, Magne, J, Kou, S, Machado, C, Henri, C, Voilliot, D, Laaraibi, S, Pierard, L, Lancellotti, P, Sato, K, Seo, Y, Ishizu, T, Takeuchi, M, Izumo, M, Suzuki, K, Yamashita, E, Miyake, F, Otsuji, Y, Aonuma, K, Rao, C M, Benedetto, FA, Luca, F, Van Garsse, L, Parise, O, Benedetto, D, Aguglia, D, Maessen, JG, Gensini, G F, Gelsomino, S, Knebel, F, Spethmann, S, Baldenhofer, G, Sanad, W, Stangl, V, Laule, M, Dreger, H, Mueller, E, Baumann, G, and Stangl, K
- Abstract
Purpose: Longitudinal function has shown to be a sensitive marker in aortic stenosis, but studies have focused on global measures. We set out to compare global and regional longitudinal function, using both color tissue Doppler imaging (TDI) and 2-dimensional speckle tracking echocardiography (2STE), in relation to severity in moderate-severe aortic stenosis (AS). Methods: We prospectively studied 246 patients with moderate-severe AS with conventional and advanced transthoracic echocardiography. Patients were divided into three groups according to severity: Asymptomatic patients with no indication of aortic valve replacement (AVR) (Controls, n=105), patients with clinical indication of AVR but preserved left ventricular ejection fraction (LVEF) ≥ 50% (AVREF≥50%, n=72), and patients with reduced LVEF < 50% and indication of AVR (AVREF<50%, n=69). Results: Compared to controls AVREF<50%, had decreased longitudinal function (Longitudinal Displacement (LD) 7.6 mm (± 2.2) vs. 10.5 mm (± 1.6); p < 0.001 and Global Longitudinal Strain (GLS) -11.4% (±2.7) vs. -15.6% (±2.7); p < 0.001 as well as significantly higher left ventricular mass index (LVMI) and reduced circumferential and radial function. Interestingly, when comparing AVREF≥50%, to controls there were neither significant differences regarding conventional measures of systolic function or structure, nor with regard to circumferential or radial function by 2STE. Conversely, longitudinal function was significantly reduced: LD: 8.8 mm (± 1.9) vs. 10.5 mm (1.6); p < 0.001 and GLS: -13.8% (±3.9) vs. -15.6% (±2.7); p < 0.01. Furthermore, regional analysis revealed a pattern of reduced basal regional longitudinal strain (RLS) with relatively normal apical RLS in AVREF≥50%, compared to controls: basal segments; -11.3% (±4.4) vs. -14.8% (±3.2); p < 0.001;, apical segments; -16.5% (±6.3) vs. -16.2% (±4.3); p=0.763. By contrast, AVREF<50%, displayed impaired RLS in both basal, midventricular and apical segments. In contrast to GLS, basal RLS remained a significant predictor of indication of AVR when adjusting for age, gender, heart rate, AVA, LAVI, E/e`, TAPSE, and LVMI: basal RLS pr. %: OR 1.20 (95% CI 1.06-1.37; p =0.005) and even in the subgroup with preserved LVEF: basal RLS pr.%: OR 1.23 (95% CI 1.06-1.43; p=0.008). Conclusion: Longitudinal function is associated with severity in moderate-severe AS and begins to decrease before significant changes in conventional measures of structure and systolic function emerges. Compared to GLS reduced basal RLS is an earlier marker and stronger predictor of increasing severity in AS.
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- 2013
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5. Development and validation of the ASGARD risk score for safe monitoring in asymptomatic nonsevere aortic stenosis.
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Hadziselimovic E, Greve AM, Sajadieh A, Olsen MH, Nienaber CA, Ray SG, Rossebø AB, Wachtell K, Dominguez H, Valeur N, Carstensen HG, and Nielsen OW
- Abstract
Aims: Current guidelines recommend serial echocardiography at minimum 1-2 year intervals for monitoring patients with nonsevere aortic valve stenosis (AS), which is costly and often clinically inconsequential.We aimed to develop and test whether the biomarker-based ASGARD risk score (Aortic Valve Stenosis Guarded by Amplified Risk Determination) can guide the timing of echocardiograms in asymptomatic patients with nonsevere AS., Methods: The development cohort comprised 1,093 of 1,589 (69%) asymptomatic patients with mild-to-moderate AS who remained event-free one year after inclusion into the SEAS trial. Cox regression landmark analyses with a 2-year follow-up identified the model (ASGARD) with the lowest Akaike information criterion for association to AS-related composite outcome (heart failure hospitalization, aortic valve replacement, or cardiovascular death). Fine-Gray analyses provided cumulative event rates by ASGARD score quartiles. The ASGARD score was internally validated in the remaining 496 patients (31%) from the SEAS-cohort and externally in 71 asymptomatic outpatients with nonsevere AS from six Copenhagen hospitals., Results: The ASGARD score comprises updated measurements of heart rate and age- and sex-adjusted N-terminal pro-brain natriuretic peptide upon transaortic maximal velocity (Vmax) from the previous year. The ASGARD score had high predictive accuracy across all cohorts (external validation: area under the curve: 0.74 [95% CI, 0.62-0.86]), and similar to an updated Vmax measurement. An ASGARD score ≤50% was associated with AS-related event rates ≤5% for a minimum of 15 months., Conclusion: The ASGARD score could provide a personalized and safe surveillance alternative to routinely planned echocardiograms, so physicians can prioritize echocardiograms for high-risk patients., (© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.)
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- 2024
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6. Chronotropic incompetence demonstrated with cardiopulmonary exercise test.
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Lønnee MF, Carstensen HG, and Jensen MR
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- Male, Humans, Aged, Heart, Dyspnea diagnosis, Dyspnea etiology, Exercise Test, Pacemaker, Artificial
- Abstract
In his case report, a 74-year-old physically fit man was evaluated repeatedly for several years in the cardiology department due to dyspnoea on exertion (DOE). Several standard cardiac and pulmonary tests were performed but did not provide sufficient cause for the DOE. Lastly, the patient was evaluated with a cardiopulmonary exercise test (CPET) with simultaneous in- and expiratory gas sampling. The test revealed a low aerobic capacity due to chronotropic incompetence (CI), thus explaining the DOE. Subsequently, the patient was treated with a rate-responsive pacemaker. CPET-is an ideal test for diagnosing CI., (Published under Open Access CC-BY-NC-BD 4.0. https://creativecommons.org/licenses/by-nc-nd/4.0/.)
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- 2024
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7. The left atrial appendage closure by surgery-2 (LAACS-2) trial protocol rationale and design of a randomized multicenter trial investigating if left atrial appendage closure prevents stroke in patients undergoing open-heart surgery irrespective of preoperative atrial fibrillation status and stroke risk.
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Madsen CL, Park-Hansen J, Irmukhamedov A, Carranza CL, Rafiq S, Rodriguez-Lecoq R, Palmer-Camino N, Modrau IS, Hansson EC, Jeppsson A, Hadad R, Moya-Mitjans A, Greve AM, Christensen R, Carstensen HG, Høst NB, Dixen U, Torp-Pedersen C, Køber L, Gögenur I, Truelsen TC, Kruuse C, Sajadieh A, and Domínguez H
- Subjects
- Humans, Treatment Outcome, Randomized Controlled Trials as Topic, Multicenter Studies as Topic, Atrial Fibrillation complications, Atrial Fibrillation surgery, Atrial Fibrillation diagnosis, Atrial Appendage surgery, Stroke epidemiology, Stroke etiology, Stroke prevention & control, Cardiac Surgical Procedures methods
- Abstract
Background: Current recommendations regarding the use of surgical left atrial appendage (LAA) closure to prevent thromboembolisms lack high-level evidence. Patients undergoing open-heart surgery often have several cardiovascular risk factors and a high occurrence of postoperative atrial fibrillation (AF)-with a high recurrence rate-and are thus at a high risk of stroke. Therefore, we hypothesized that concomitant LAA closure during open-heart surgery will reduce mid-term risk of stroke independently of preoperative AF status and CHA
2 DS2 -VASc score., Methods: This protocol describes a randomized multicenter trial. Consecutive participants ≥18 years scheduled for first-time planned open-heart surgery from cardiac surgery centers in Denmark, Spain, and Sweden are included. Both patients with a previous diagnosis of paroxysmal or chronic AF, as well as those without AF, are eligible to participate, irrespective of their CHA2 DS2 -VASc score. Patients already planned for ablation or LAA closure during surgery, with current endocarditis, or where follow-up is not possible are considered noneligible. Patients are stratified by site, surgery type, and preoperative or planned oral anticoagulation treatment. Subsequently, patients are randomized 1:1 to either concomitant LAA closure or standard care (ie, open LAA). The primary outcome is stroke, including transient ischemic attack, as assigned by 2 independent neurologists blinded to the treatment allocation. To recognize a 60% relative risk reduction of the primary outcome with LAA closure, 1,500 patients are randomized and followed for 2 years (significance level of 0.05 and power of 90%)., Conclusions: The LAACS-2 trial is likely to impact the LAA closure approach in most patients undergoing open-heart surgery., Trial Registration: NCT03724318., Competing Interests: Disclosures All authors declare that they have no affiliations with or involvement in any organization or entity with any financial or nonfinancial interest in the subject matter or materials discussed in this manuscript., (Copyright © 2023 Elsevier Inc. All rights reserved.)- Published
- 2023
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8. Distribution and Prognostic Significance of Left Ventricular Global Longitudinal Strain in Asymptomatic Significant Aortic Stenosis: An Individual Participant Data Meta-Analysis.
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Magne J, Cosyns B, Popescu BA, Carstensen HG, Dahl J, Desai MY, Kearney L, Lancellotti P, Marwick TH, Sato K, Takeuchi M, Zito C, Casalta AC, Mohty D, Piérard L, Habib G, and Donal E
- Subjects
- Aged, Aged, 80 and over, Aortic Valve Stenosis mortality, Aortic Valve Stenosis physiopathology, Aortic Valve Stenosis therapy, Asymptomatic Diseases, Female, Heart Ventricles physiopathology, Humans, Male, Middle Aged, Predictive Value of Tests, Prognosis, Risk Assessment, Risk Factors, Stress, Mechanical, Aortic Valve Stenosis diagnostic imaging, Echocardiography, Heart Ventricles diagnostic imaging, Myocardial Contraction, Stroke Volume, Ventricular Function, Left
- Abstract
Objectives: In this individual participant data meta-analysis on left ventricular global longitudinal strain (LVGLS), our objective was to: 1) describe its distribution; 2) identify the most predictive cutoff values; and 3) assess its impact on mortality in asymptomatic patients with significant aortic stenosis (AS) and preserved left ventricular ejection fraction (LVEF)., Background: The evidence supporting the prognostic role of LVGLS in asymptomatic patients with AS has been obtained from several relatively small studies., Methods: A literature search was performed for studies published between 2005 and 2017 without language restriction according to the following criteria: "aortic stenosis" AND "longitudinal strain." The corresponding authors of selected studies were contacted and invited to share their data that we computerized in a specific database. The primary endpoint was all-cause mortality., Results: Among the 10 studies included, 1,067 asymptomatic patients with significant AS and LVEF >50% were analyzed. The median of LVGLS was 16.2% (from 5.6% to 30.1%). There were 91 deaths reported during follow-up with median of 1.8 (0.9 to 2.8) years, resulting in a pooled crude mortality rate of 8.5%. The LVGLS performed well in the prediction of death (area under the curve: 0.68). The best cutoff value identified was LVGLS of 14.7% (sensitivity, 60%; specificity, 70%). Using random effects model, the risk of death for patients with LVGLS <14.7% is multiplied by >2.5 (hazard ratio: 2.62; 95% confidence interval: 1.66 to 4.13; p < 0.0001), without significant heterogeneity between studies (I
2 = 18.3%; p = 0.275). The relationship between LVGLS and mortality remained significant in patients with LVEF ≥60% (p = 0.001)., Conclusions: This individual participant data meta-analysis demonstrates that in asymptomatic patients with significant AS and normal LVEF, impaired LVGLS is associated with reduced survival. These data emphasize the potential usefulness of LVGLS for risk stratification and management of these patients., (Copyright © 2018 American College of Cardiology Foundation. All rights reserved.)- Published
- 2019
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9. Prognostic implications of left ventricular asymmetry in patients with asymptomatic aortic valve stenosis.
- Author
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Sigvardsen PE, Larsen LH, Carstensen HG, Sørgaard M, Hindsø L, Hassager C, Køber L, Møgelvang R, and Kofoed KF
- Subjects
- Aged, Aged, 80 and over, Aortic Valve Stenosis physiopathology, Asymptomatic Diseases, Cause of Death, Cohort Studies, Comorbidity, Denmark, Echocardiography methods, Female, Hospitals, University, Humans, Hypertrophy, Left Ventricular physiopathology, Male, Middle Aged, Monitoring, Physiologic, Multidetector Computed Tomography methods, Multivariate Analysis, Predictive Value of Tests, Prognosis, Proportional Hazards Models, Prospective Studies, Risk Assessment, Survival Analysis, Aortic Valve Stenosis diagnostic imaging, Aortic Valve Stenosis epidemiology, Hypertrophy, Left Ventricular diagnostic imaging, Hypertrophy, Left Ventricular epidemiology
- Abstract
Aims: Left ventricular (LV) regional hypertrophy in the form of LV asymmetry is a common finding in patients with aortic valve stenosis. The aim of this study was to test the hypothesis that LV asymmetry predicts future symptomatic status and indication for aortic valve replacement (AVR) in patients with asymptomatic aortic valve stenosis., Methods and Results: In total, 114 patients with asymptomatic aortic valve stenosis (peak velocity > 2.5 m/s assessed by echocardiographic screening and LV ejection fraction > 50%) were enrolled in the study. LV asymmetry and LV geometry was assessed by multi-detector computed tomography according to previous definitions. Follow-up was conducted using electronic health records. Event-free survival was assessed using Cox proportional hazards models. Patients were followed for a median of 2.2 years (interquartile range 1.6-3.6). Indication for AVR occurred in 46 patients (40%). Patients with LV asymmetry had more than 3 times the risk of AVR (hazard ratio: 3.16; 95% CI: 1.77-5.66; P < 0.001) compared with patients with no LV asymmetry. Multivariate Cox analysis revealed that LV asymmetry was a predictor of future need of AVR (hazard ratio: 3.10; 95% CI: 1.44-6.65; P = 0.004), independent of LV geometry, jet velocity, valvular calcification, and pro-BNP., Conclusions: LV asymmetry is an independent predictor of future need for AVR in patients with asymptomatic aortic valve stenosis. It has incremental prognostic value to LV geometry and may provide a useful method of risk stratification., (Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2017. For permissions, please email: journals.permissions@oup.com.)
- Published
- 2018
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10. Six-minute walking test and long term prognosis in patients with asymptomatic aortic valve stenosis.
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Sigvardsen PE, Larsen LH, Carstensen HG, Kühl JT, Møgelvang R, Hassager C, Køber L, and Kofoed KF
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- Aged, Aged, 80 and over, Aortic Valve Stenosis mortality, Female, Follow-Up Studies, Humans, Male, Middle Aged, Prognosis, Prospective Studies, Risk Factors, Time Factors, Walking Speed physiology, Aortic Valve Stenosis diagnostic imaging, Aortic Valve Stenosis physiopathology, Asymptomatic Diseases, Walking physiology, Walking trends
- Abstract
Background: Management of asymptomatic patients with aortic valve stenosis is challenging due to the elusive relationship between symptomatic status and hemodynamic parameters in addition to the occurrence of cardiovascular death. The 6-minute walking test (6MWT) reflects overall hemodynamic function and could contribute to risk assessment in such patients., Methods and Results: One hundred sixteen asymptomatic patients (peak velocity>2.5m/s and left ventricular ejection fraction >50% assessed by echocardiographic screening; 85 males; aged 72±8years) underwent clinical workup, transthoracic echocardiography and a 6MWT. The mean distance covered by patients able to perform the 6MWT (n=107) was 422±90m. Patients were grouped in tertiles according to distance covered in the 6MWT: Short, intermediate and long distance patients. During a median follow-up of 5.5years (IQR 4.5-6.3), 29 (25%) patients died, 10 (9%) from cardiovascular causes. Multivariate analysis revealed that short distance patients (≤390m) were at higher risk of all-cause mortality (HR: 2.44; 95% CI: 1.05-5.67; p=0.04) and cardiovascular mortality (HR: 6.12; 95% CI: 1.18-31.83; p=0.03). For every 100m covered, the risk of all-cause mortality decreased by 35% (HR: 0.65; 95% CI: 0.43-0.99; p=0.04). Long distance patients (>465m) did not experience cardiovascular deaths during follow-up., Conclusions: In asymptomatic patients with aortic valve stenosis, the 6MWT is an independent predictor of all-cause and cardiovascular mortality. It is of incremental value to the echocardiographic evaluation, suggesting that the 6MWT might be useful to guide clinical follow-up intervals and treatment strategy., (Copyright © 2017 Elsevier B.V. All rights reserved.)
- Published
- 2017
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11. Basal longitudinal strain predicts future aortic valve replacement in asymptomatic patients with aortic stenosis.
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Carstensen HG, Larsen LH, Hassager C, Kofoed KF, Jensen JS, and Mogelvang R
- Subjects
- Aged, Aortic Valve Stenosis surgery, Asymptomatic Diseases, Biomechanical Phenomena, Coronary Angiography, Echocardiography, Female, Follow-Up Studies, Heart Valve Prosthesis Implantation, Humans, Male, Multidetector Computed Tomography, Predictive Value of Tests, Prognosis, Prospective Studies, Risk Factors, Sensitivity and Specificity, Stress, Mechanical, Aortic Valve Stenosis diagnostic imaging, Aortic Valve Stenosis physiopathology
- Abstract
Aims: To evaluate the prognostic value of global longitudinal strain (GLS) and basal longitudinal strain (BLS) with the knowledge of coexisting coronary pathology evaluated by multi-detector computed tomography (MDCT) coronary angiography., Background: GLS and BLS are both sensitive markers of myocardial dysfunction and predictors of outcome in asymptomatic aortic stenosis. Aortic stenosis and ischaemic heart disease share risk factors and longitudinal function can be severely reduced in both conditions, why some of the previous findings of impaired regional longitudinal function in asymptomatic aortic stenosis could in fact be explained by silent ischaemic heart disease., Methods and Results: Prospective follow-up of 104 asymptomatic patients with moderate-severe aortic stenosis defined as an aortic valve area <1.5 cm(2). Patients underwent a thorough clinical work-up, advanced echocardiographic analysis and coronary angiography by MDCT. The combined endpoint was indication for aortic valve replacement (AVR) and sudden cardiac death. During a median follow-up of 2.3 years (interquartile range 1.7-3.6) 43 patients (41%) met the endpoint of indication for AVR. The basal (13.4 ± 3.1% vs. 15.7 ± 3.1%) and mid-ventricular segments (14.9 ± 2.7% vs. 16.2 ± 2.9%) were significantly reduced, but with sparing of the apical segments, in patients who later underwent AVR. In various multivariable Cox regression models, including only BLS, but not GLS, remained an independent predictor of AVR., Conclusion: In contrast to GLS, reduced BLS is a significant predictor of future AVR in asymptomatic patients with aortic stenosis, independently of clinical characteristics, conventional echocardiographic measures, and coronary pathology., (Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2015. For permissions please email: journals.permissions@oup.com.)
- Published
- 2016
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12. Prognostic value of multi-detector computed tomography in asymptomatic aortic valve stenosis.
- Author
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Larsen LH, Kofoed KF, Carstensen HG, Dalsgaard M, Ersbøll MK, Køber L, and Hassager C
- Subjects
- Aged, Aortic Valve diagnostic imaging, Aortic Valve Stenosis complications, Aortic Valve Stenosis etiology, Asymptomatic Diseases, Calcinosis complications, Diagnosis, Differential, Female, Follow-Up Studies, Humans, Male, Predictive Value of Tests, Prognosis, Retrospective Studies, Severity of Illness Index, Time Factors, Aortic Valve pathology, Aortic Valve Stenosis diagnostic imaging, Calcinosis diagnostic imaging, Multidetector Computed Tomography methods
- Abstract
Background: Multi-Detector Computed Tomography (MDCT) is a high-resolution imaging technique with potential additive value in the evaluation of patients with aortic valve stenosis (AS). We aimed to assess the prognostic value of MDCT in asymptomatic patients with AS compared to conventional transthoracic echocardiography (TTE)., Methods: 116 patients with asymptomatic AS (Vmax>2.5m/s assessed by clinical screening TTE, LVEF>50%) were examined with TTE (Vivid e9) and MDCT (Aquilion 320) on the same day. The treating physician was blinded for research protocol defined imaging results. Outcome was defined as indication for aortic valve replacement (AVR) determined by the treating physician or sudden cardiac death., Results: The mean age was 72 (8) years, 27% were women, mean AVA by TTE was 1.01 (0.30) cm(2). Median follow up time was 27 (IQR 19-44) months. Forty seven patients (41%) developed indication for AVR. No patients suffered a sudden cardiac death. AVA and aortic valve calcification were significant univariable predictors of AVR when measured by both TTE and MDCT, whereas left ventricular mass was only significant measured by MDCT. Significant coronary artery disease by MDCT tended to predict future indication for AVR, but this did not reach statistical significance (HR: 1.79 (95% CI 0.96-3.44), p=0.08)., Conclusion: MDCT derived AVA can be of use as an alternative to TTE derived AVA in patients with asymptomatic AS to predict future clinical indication for AVR., (Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.)
- Published
- 2016
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13. Tissue Velocities and Myocardial Deformation in Asymptomatic and Symptomatic Aortic Stenosis.
- Author
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Carstensen HG, Larsen LH, Hassager C, Kofoed KF, Dalsgaard M, Kristensen CB, Jensen JS, and Mogelvang R
- Subjects
- Aged, Aged, 80 and over, Aortic Valve Stenosis complications, Elastic Modulus, Female, Humans, Image Interpretation, Computer-Assisted methods, Male, Middle Aged, Reproducibility of Results, Sensitivity and Specificity, Stress, Mechanical, Stroke Volume, Ventricular Dysfunction, Left etiology, Aortic Valve Stenosis diagnostic imaging, Aortic Valve Stenosis physiopathology, Echocardiography methods, Ventricular Dysfunction, Left diagnostic imaging, Ventricular Dysfunction, Left physiopathology
- Abstract
Background: Assessment of myocardial longitudinal function has proved to be a sensitive marker of deteriorating myocardial function in aortic stenosis, demonstrated by both color Doppler tissue imaging and recently by two-dimensional speckle-tracking echocardiography. The aim of this study was to compare velocity (color Doppler tissue imaging) and deformation (two-dimensional speckle-tracking echocardiography) in relation to global and regional longitudinal function in asymptomatic and severe symptomatic aortic stenosis., Methods: In a cross-sectional design, 231 patients with aortic stenosis were divided into four groups: asymptomatic moderate aortic stenosis (aortic valve area, 1.0-1.5 cm(2); n = 38), asymptomatic severe aortic stenosis (aortic valve area < 1.0 cm(2); n = 66), and symptomatic severe aortic stenosis with preserved (n = 68) and reduced (<50%) left ventricular ejection fraction (n = 59)., Results: Among all global (peak systolic s', diastolic e' and a', longitudinal displacement, and global longitudinal strain and strain rate) and regional longitudinal (basal, middle, and apical longitudinal strain and strain rate) parameters, only diastolic e', longitudinal displacement, and basal longitudinal strain (BLS) remained significantly associated with symptomatic status, independent of age, gender, heart rate, aortic valve area, stroke volume index, left ventricular mass index, left atrial volume index, and tricuspid annular systolic plane excursion. Furthermore, in a model with the aforementioned parameters, including e', longitudinal displacement, and BLS, only BLS remained significantly associated with symptomatic status in the entire study population (BLS per one-unit decrease: odds ratio, 1.23; 95% CI, 1.04-1.46; P = .017). Furthermore, patients with BLS < 13% were more likely to be symptomatic (odds ratio, 4.97; 95% CI, 2.6-9.4; P < .001), and no patients with asymptomatic severe aortic stenosis with BLS ≥ 13% were admitted with myocardial infarction or heart failure during follow-up of 1,462 days., Conclusions: Among the many echocardiographic measures of longitudinal velocity and deformation, BLS has the strongest association with symptomatic status in aortic stenosis, and BLS < 13% is related to adverse outcomes in severe asymptomatic aortic stenosis., (Copyright © 2015 American Society of Echocardiography. Published by Elsevier Inc. All rights reserved.)
- Published
- 2015
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14. Association of ischemic heart disease to global and regional longitudinal strain in asymptomatic aortic stenosis.
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Carstensen HG, Larsen LH, Hassager C, Kofoed KF, Jensen JS, and Mogelvang R
- Subjects
- Aged, Aged, 80 and over, Aortic Valve Stenosis diagnosis, Aortic Valve Stenosis epidemiology, Asymptomatic Diseases, Coronary Angiography methods, Coronary Artery Disease diagnosis, Coronary Artery Disease epidemiology, Coronary Stenosis diagnosis, Coronary Stenosis epidemiology, Denmark epidemiology, Echocardiography, Doppler, Female, Humans, Male, Middle Aged, Multidetector Computed Tomography, Multimodal Imaging, Predictive Value of Tests, Prevalence, Prospective Studies, Risk Factors, Severity of Illness Index, Stress, Mechanical, Ventricular Dysfunction, Left diagnosis, Ventricular Dysfunction, Left epidemiology, Aortic Valve Stenosis physiopathology, Coronary Artery Disease physiopathology, Coronary Stenosis physiopathology, Myocardial Contraction, Ventricular Dysfunction, Left physiopathology, Ventricular Function, Left
- Abstract
Longitudinal deformation has been shown to deteriorate with progressive aortic stenosis as well as ischemic heart disease. Despite that both conditions share risk factors and are often coexisting, studies have not assessed the influence on longitudinal deformation for both conditions simultaneously. Thus the purpose of this study was to evaluate the association between subclinical ischemic heart disease and global and regional longitudinal strain in asymptomatic patients with significant aortic stenosis. Prevalent patients with a diagnosis of aortic stenosis at six hospitals in the Greater Copenhagen area were screened for inclusion. A total of 104 asymptomatic patients with moderate-severe aortic stenosis (aortic valve area ≤1.5 cm(2)) fulfilled study criteria and underwent advanced echocardiographic analysis and coronary angiography by multi-detector computed tomography. Angiography revealed coronary stenosis >50% in 31% (n = 32). All regional longitudinal strain measures (apical, mid and basal longitudinal strain) were significant predictors of significant coronary stenosis (>70% stenosis), but only apical and mid longitudinal strain were significant predictors in multivariable analyses independent of aortic valve area, stroke volume index, pro-BNP, valvulo-arterial impedance, body mass index and heart rate. In linear regression models with both aortic valve area and significant coronary stenosis, apical (p < 0.001) and mid (p < 0.01) longitudinal strain were associated to significant coronary stenosis but not aortic valve area. Conversely, basal longitudinal strain was significantly associated to aortic valve area (p = 0.001), but not to significant coronary stenosis. Subclinical coronary artery disease is frequent in moderate and severe aortic stenosis, and should be suspected when regional longitudinal dysfunction is predominant in the apical and mid ventricular segments.
- Published
- 2015
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15. Aortic valve area assessed with 320-detector computed tomography: comparison with transthoracic echocardiography.
- Author
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Larsen LH, Kofoed KF, Carstensen HG, Mejdahl MR, Andersen MJ, Kjaergaard J, Nielsen OW, Køber L, Møgelvang R, and Hassager C
- Subjects
- Aged, Aged, 80 and over, Aortic Valve surgery, Aortic Valve Stenosis diagnostic imaging, Aortic Valve Stenosis surgery, Calcinosis diagnostic imaging, Calcinosis surgery, Female, Humans, Male, Middle Aged, Predictive Value of Tests, Radiographic Image Interpretation, Computer-Assisted, Severity of Illness Index, Aortic Valve diagnostic imaging, Aortic Valve pathology, Aortic Valve Stenosis diagnosis, Calcinosis diagnosis, Echocardiography, Doppler, Multidetector Computed Tomography
- Abstract
To evaluate the diagnostic accuracy of aortic valve area (AVA) assessment with 320-detector Computed Tomography (MDCT) compared to transthoracic echocardiography (TTE) in a population with mild to severe aortic valve stenosis. AVA was estimated in 169 patients by planimetry on MDCT images (AVA(MDCT)) and by the continuity equation with TTE (AVA(TTE)). To generate a reference AVA (AVA(REF)) we used the stroke volume from MDCT divided by the velocity time integral from CW Doppler by TTE (according to the continuity equation: stroke volume in LVOT = stroke volume passing the aortic valve). AVA(REF) was used as the reference to compare both measures against, since it bypasses the assumption of LVOT being circular in the continuity equation and the potential placement error of PW Doppler in the LVOT. The mean (±SD) age of the patients was 71 (±9) years, 113 (67%) were males. Mean AVA(TTE) was 0.93 (±0.33) cm(2), mean AVA(MDCT) was 0.99 (±0.36) cm(2) and mean AVA(REF) was 1.00 (±0.39) cm(2). The mean difference between AVA(TTE) and AVA(MDCT) was -0.06 cm(2), p = 0.001, mean difference between AVA(TTE) and AVA(REF) was -0.06 cm(2), p < 0.001, and mean difference between AVA(MDCT) and AVA(REF) was -0.01 cm(2), p = 0.60. Calcification of the aortic valve quantified by Agatston score, significantly decreased the correlation between AVA(MDCT) and AVA(REF), (r low Agatston = 0.90, r high Agatston = 0.57). MDCT measured AVA is slightly larger than AVA measured by TTE (0.06 cm(2)). The accuracy and precision errors on AVA measurements are comparable for MDCT and TTE. Valvular calcification may primarily affect the accuracy of AVA(MDCT).
- Published
- 2014
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16. Atrial fibrillation in aortic stenosis--echocardiographic assessment and prognostic importance.
- Author
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Burup Kristensen C, Jensen JS, Sogaard P, Carstensen HG, and Mogelvang R
- Subjects
- Aged, Aged, 80 and over, Aortic Valve Stenosis complications, Aortic Valve Stenosis mortality, Atrial Fibrillation complications, Atrial Fibrillation physiopathology, Blood Flow Velocity, Case-Control Studies, Female, Heart Rate, Humans, Male, Prognosis, Risk Factors, Stroke Volume, Survival Rate, Ultrasonography, Aortic Valve Stenosis diagnostic imaging, Atrial Fibrillation diagnostic imaging
- Abstract
Background: Atrial fibrillation (AFib) exists more frequently in patients with aortic stenosis (AS) than in patients without, and AFib may be a sign of progressive deterioration of AS. Echocardiographic assessment of AS in sinus rhythm is well documented, however, little is known about AFib in AS since such patients often are excluded from clinical echocardiographic trials., Aim: The purpose of this study was to assess the prognostic importance of AFib in AS., Methods: The study was designed as a single-center case-control study. Patients with AS and AFib were enrolled as cases (n = 103) and subsequently matched to controls (103 patients with AS but sinus rhythm). Cases and controls were matched according to age, gender and severity of AS. Primary outcome was all cause mortality and follow-up was 100% complete., Results: Compared to controls the group with AFib had lower mean ejection fraction (42% vs. 49%; p < 0.001) and stroke volume (47 mL vs. 55 mL; p = 0.004), but higher heart rate (81 bpm vs. 68 bpm; p < 0.001) and no significant difference with regard to cardiac output (3.8 L vs. 4.0 L; p = 0.29). Accordingly, aortic jet velocity and gradients were significantly lower in AFib compared to controls but there were no differences (p = 0.38) in aortic valve area calculated by the continuity equation. During a median follow-up of 2.3 years (IQR: 1.2-3.6), 70 (34%) patients with AS died: 42 patients with AFib and 28 patients with sinus rhythm (p < 0.02). After adjusting for echocardiographic significant differences, AFib remained an independent predictor of mortality (HR 2.72 (95% CI: 1.12-6.61), p < 0.03). There was no significant interaction (p = 0.62) between AFib and AS on the risk of mortality, indicating that AFib predicted bad outcome regardless of the severity of AS., Conclusions: AFib is an independent risk factor in patients with AS and the prognostic impact of AFib seems to be the same despite the severity of AS.
- Published
- 2012
- Full Text
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