102 results on '"Lang, Roberto M."'
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2. Contributors
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Aboulhosn, Jamil A., primary, Abraham, Theodore P., additional, Akoum, Nazem, additional, Appleton, Christopher P., additional, Aurigemma, Gerard P., additional, Bax, Jeroen J., additional, Bhatt, Ami B., additional, Bolger, Ann F., additional, Bosch, Johan G., additional, Brosnan, Maria, additional, Bruce, Charles J., additional, Burchill, Luke J., additional, Capoulade, Romain, additional, Carroll, John D., additional, Celermajer, David S., additional, Chen, Michael A., additional, Cheng, Andrew, additional, Cheng, Richard K., additional, Connolly, Heidi M., additional, Cullen, Michael W., additional, Dahou, Abdellaziz, additional, Deen, Jason F., additional, Delgado, Victoria, additional, Delling, Francesca Nesta, additional, Di Tullio, Marco R., additional, Douglas, Pamela S., additional, Drake, Daniel H., additional, Dumesnil, Jean G., additional, Edvardsen, Thor, additional, Evangelista, Artur, additional, Fleischmann, Kirsten E., additional, Foster, Elyse, additional, Freeman, Rosario V., additional, Gay, Laura Galian, additional, Gerber, Ivor L., additional, Hall, Michael T., additional, Hung, Judy, additional, Iung, Bernard, additional, Jander, Nikolaus, additional, Kim, Michael S., additional, Kim, Yuli Y., additional, Kirkpatrick, James N., additional, Kolias, Theodore J., additional, Krieger, Eric V., additional, Lang, Roberto M., additional, Lewin, Mark, additional, Lin, Jeannette, additional, Linefsky, Jason, additional, Mahjoub, Haïfa, additional, Masri, Sofia Carolina, additional, Mayer, Susan A., additional, Mertens, Luc, additional, Messika-Zetoun, David, additional, Minners, Jan, additional, Naqvi, Tasneem Z., additional, Olson, Aaron, additional, Oxorn, Donald C., additional, Pellikka, Patricia A., additional, Pibarot, Philippe, additional, Playford, David, additional, Prior, David, additional, Prutkin, Jordan M., additional, Quaife, Robert A., additional, Rader, Florian, additional, Raghav, Vrishank, additional, Roldan, Carlos A., additional, Salcedo, Ernersto E., additional, Samad, Zainab, additional, Sanders, Stephen P., additional, Sekiguchi, Hiroshi, additional, Sidebotham, David A., additional, Siegel, Robert J., additional, Silversides, Candice K., additional, Silvestry, Frank E., additional, Siu, Samuel C., additional, Smiseth, Otto A., additional, Stout, Karen, additional, Torp, Hans, additional, Tsang, Wendy, additional, Urena, Marina, additional, Vahanian, Alec, additional, Vaidya, Anjali, additional, Valente, Anne Marie, additional, Wald, Rachel M., additional, Wang, Andrew, additional, Weeks, Sarah G., additional, Weiner, Rory B., additional, Welch, Terrence D., additional, Woo, Anna, additional, Wu, Audrey H., additional, Yeh, Doreen DeFaria, additional, Yoganathan, Ajit P., additional, and Zimmerman, Karen G., additional
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- 2017
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3. Normal Values of Aortic Root Size According to Age, Sex, and Race: Results of the World Alliance of Societies of Echocardiography Study
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Patel, H, Miyoshi, T, Addetia, K, Citro, R, Daimon, M, Gutierrez Fajardo, P, Kasliwal, R, Kirkpatrick, J, Monaghan, M, Muraru, D, Ogunyankin, K, Park, S, Ronderos, R, Sadeghpour, A, Scalia, G, Takeuchi, M, Tsang, W, Tucay, E, Tude Rodrigues, A, Amuthan, V, Zhang, Y, Schreckenberg, M, Blankenhagen, M, Degel, M, Hitschrich, N, Mor-Avi, V, Asch, F, Lang, R, Patel, Hena N, Miyoshi, Tatsuya, Addetia, Karima, Citro, Rodolfo, Daimon, Masao, Gutierrez Fajardo, Pedro, Kasliwal, Ravi R, Kirkpatrick, James N, Monaghan, Mark J, Muraru, Denisa, Ogunyankin, Kofo O, Park, Seung Woo, Ronderos, Ricardo E, Sadeghpour, Anita, Scalia, Gregory M, Takeuchi, Masaaki, Tsang, Wendy, Tucay, Edwin S, Tude Rodrigues, Ana Clara, Amuthan, Vivekanandan, Zhang, Yun, Schreckenberg, Marcus, Blankenhagen, Michael, Degel, Markus, Hitschrich, Niklas, Mor-Avi, Victor, Asch, Federico M, Lang, Roberto M, Patel, H, Miyoshi, T, Addetia, K, Citro, R, Daimon, M, Gutierrez Fajardo, P, Kasliwal, R, Kirkpatrick, J, Monaghan, M, Muraru, D, Ogunyankin, K, Park, S, Ronderos, R, Sadeghpour, A, Scalia, G, Takeuchi, M, Tsang, W, Tucay, E, Tude Rodrigues, A, Amuthan, V, Zhang, Y, Schreckenberg, M, Blankenhagen, M, Degel, M, Hitschrich, N, Mor-Avi, V, Asch, F, Lang, R, Patel, Hena N, Miyoshi, Tatsuya, Addetia, Karima, Citro, Rodolfo, Daimon, Masao, Gutierrez Fajardo, Pedro, Kasliwal, Ravi R, Kirkpatrick, James N, Monaghan, Mark J, Muraru, Denisa, Ogunyankin, Kofo O, Park, Seung Woo, Ronderos, Ricardo E, Sadeghpour, Anita, Scalia, Gregory M, Takeuchi, Masaaki, Tsang, Wendy, Tucay, Edwin S, Tude Rodrigues, Ana Clara, Amuthan, Vivekanandan, Zhang, Yun, Schreckenberg, Marcus, Blankenhagen, Michael, Degel, Markus, Hitschrich, Niklas, Mor-Avi, Victor, Asch, Federico M, and Lang, Roberto M
- Abstract
Background: Accurate measurements of the aortic annulus and root are important for guiding therapeutic decisions regarding the need for aortic surgery. Current echocardiographic guidelines for identification of aortic root dilatation are limited because current normative values were derived predominantly from white individuals in narrow age ranges, and based partially on M-mode measurements. Using data from the World Alliance Societies of Echocardiography study, the authors sought to establish normal ranges of aortic dimensions across sexes, races, and a wide range of ages. Methods: Adult individuals free of heart, lung, and kidney disease were prospectively enrolled from 15 countries, with even distributions among sexes and age groups: young (18–40 years), middle aged (41–65 years) and old (>65 years). Transthoracic two-dimensional echocardiograms of 1,585 subjects (mean age, 47 ± 17 years; 50.4% men; mean body surface area [BSA], 1.77 ± 0.22 m2) were analyzed in a core laboratory following American Society of Echocardiography guidelines. Measurements, indexed separately by BSA and by height, included the aortic annulus, sinuses of Valsalva, and sinotubular junction. Differences among age, sex, and racial groups were evaluated using unpaired two-tailed Student's t tests. Results: All aortic root dimensions were larger in men compared with women. After indexing to BSA, all measured dimensions were significantly larger in women, whereas men continued to show larger dimensions after indexing to height. Of note, the upper limits of normal for all aortic dimensions were lower across all age groups, compared with the guidelines. Aortic dimensions were larger in older age groups in both sexes, a trend that persisted regardless of BSA or height adjustment. Last, differences in aortic dimensions were also observed according to race: Asians had the smallest nonindexed aortic dimensions at all levels. Conclusions: There are significant differences in aortic dimensions acco
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- 2022
4. Preface
- Author
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Lang, Roberto M., primary, Goldstein, Steven A., additional, Kronzon, Itzhak, additional, Khandheria, Bijoy K., additional, and Mor-Avi, Victor, additional
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- 2016
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5. Contributors
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Abbas, Amr E., primary, Abdelmoneim, Sahar S., additional, Abraham, Theodore, additional, Acquatella, Harry, additional, Adams, David B., additional, Addetia, Karima, additional, Afilalo, Jonathan, additional, Agarwal, Vikram, additional, Agmon, Yoram, additional, Ahmed, Mohamed, additional, Alviar, Carlos, additional, Anderson, Bonita, additional, Argulian, Edgar, additional, Asch, Federico M., additional, Aurigemma, Gerard P., additional, Axsom, Kelly, additional, Badano, Luigi P., additional, Balakrishnan, Revathi, additional, Banerji, Sourin, additional, Bangalore, Sripal, additional, Bansal, Manish, additional, Bartel, Thomas, additional, Baumann, Rebecca Lynn, additional, Baumgartner, Helmut, additional, Beigel, Roy, additional, Belcik, J. Todd, additional, Belohlavek, Marek, additional, Benenstein, Ricardo, additional, Berkowitz, Eric, additional, Bhave, Nicole M., additional, Biviano, Angelo, additional, Blank, Nimrod, additional, Bonow, Robert O., additional, Burstow, Darryl J., additional, Byrd, Benjamin, additional, Carerj, Scipione, additional, Carroll, John D., additional, Chadderdon, Scott, additional, Chaliki, Hari P., additional, Chan, Kwan-Leung, additional, Chaudhry, Farooq A., additional, Chidsey, Geoff, additional, Churzidse, Sofia, additional, Coll, Blai, additional, Cui, Vivian W., additional, Cusma-Picconne, Maurizio, additional, Dahou, Abdellaziz, additional, Dal-Bianco, Jacob P., additional, Daneshvar, Daniel A., additional, Daubert, Melissa A., additional, Davidoff, Ravin, additional, DeCara, Jeanne M., additional, Delgado-Montero, Antonia, additional, Dellefave-Castillo, Lisa, additional, Desai, Ankit A., additional, DeSouza, Kavit A., additional, Doherty, Bryan, additional, Donnino, Robert, additional, Douglas, Pamela S., additional, Dudzinski, David M., additional, Dulgheru, Raluca, additional, Dumesnil, Jean G., additional, Elkayam, Uri, additional, Erbel, Raimund, additional, Erenberg, Francine, additional, Evangelista, Arturo A., additional, Feinstein, Steven B., additional, Ferreira, Beatriz, additional, Foster, Elyse, additional, Freed, Benjamin H., additional, Gardin, Julius M., additional, Gill, Edward A., additional, Gillam, Linda, additional, Giovannone, Steven, additional, Goldberger, Mark, additional, Goldstein, Steven A., additional, Gorcsan, John, additional, Gorla, Riccardo, additional, Grapsa, Julia, additional, Grawe, Erin S., additional, Gruner, Christiane, additional, Gupta, Pooja, additional, Gurudevan, Swaminatha, additional, Hahn, Rebecca T., additional, Han, Yuchi, additional, Hellawell, Jennifer L., additional, Hillier, Samuel D., additional, Hoit, Brian D., additional, Humes, Richard, additional, Jagadeesan, Vikrant, additional, Jain, Sonia, additional, Janosi, Alexander, additional, Kahn, Peter A., additional, Kaul, Sanjiv, additional, Khandheria, Bijoy K., additional, Kim, Gene H., additional, Kim, Michael S., additional, Kimura, Bruce J., additional, King, Mary Etta, additional, Kireyev, Dmitry, additional, Kirkpatrick, James N., additional, Klein, Allan L., additional, Kohli, Payal, additional, Korcarz, Claudia E., additional, Kort, Smadar, additional, Kosmala, Wojciech, additional, Koulogiannis, Konstantinos, additional, Koutsogeorgis, Ilias, additional, Kremkau, Frederick W., additional, Krieger, Eric V., additional, Kronzon, Itzhak, additional, Kutnick, Richard T., additional, Lai, Wyman, additional, Lambert, Stephane, additional, Lancellotti, Patrizio, additional, Lang, Roberto M., additional, Lee, Alex Pui-Wai, additional, Lee, Ming Sum, additional, Lerakis, Stamatios, additional, Lessick, Jonathan, additional, Lester, Steven J., additional, Leung, Steve W., additional, LeVen, Florent, additional, Levine, Robert A., additional, Li, Qin, additional, Lima, Fabio, additional, Lindner, Jonathan R., additional, Lopez, Leo, additional, Magne, Julien, additional, Mahjoub, Haifa, additional, Mangion, Judy R., additional, Mankad, Sunil V., additional, Maragiannis, Dimitrios, additional, Marcoff, Leo, additional, Martin, Randolph P., additional, Marwick, Thomas H., additional, Massabuau, Pierre, additional, Mathur, Moses, additional, McCully, Robert, additional, McGee, Edwin C., additional, McNally, Elizabeth, additional, Mehta, Sudhir Ken, additional, Mendelson, Todd, additional, Mikati, Issam A., additional, Modesto, Karen, additional, Monaghan, Mark, additional, Mookadam, Farouk, additional, Moonen, Marie, additional, Mukherjee, Monica, additional, Müller, Silvana, additional, Mulvagh, Sharon L., additional, Muraru, Denisa, additional, Murtagh, Gillian, additional, Nagueh, Sherif F., additional, Naqvi, Tasneem Z., additional, Nathan, Sandeep, additional, Negishi, Kazuaki, additional, Nihoyannopoulos, Petros, additional, Nkomo, Vuyisile T., additional, Oechslin, Erwin, additional, Olson, Joan, additional, Palios, John, additional, Parikh, Gaurav, additional, Patel, Amit R., additional, Patel, Amit V., additional, Patel, Aneet, additional, Patel, Anupa, additional, Paterick, Timothy E., additional, Payvandi, Laila A., additional, Pedrizzetti, Gianni, additional, Pellikka, Patricia A., additional, Perk, Gila, additional, Peters, Ferande, additional, Phelan, Dermot, additional, Pibarot, Philippe, additional, Picard, Michael H., additional, Plana, Juan Carlos, additional, Popovic, Zoran B., additional, Porter, Thomas, additional, Pun, Shawn C., additional, Qasim, Atif N., additional, Quader, Nishath, additional, Quinones, Miguel A., additional, Rahko, Peter S., additional, Rakowski, Harry, additional, Rao, Rajeev V., additional, Reiken, Joseph, additional, Reisner, Shimon A., additional, Retzer, Elizabeth M., additional, Rigolin, Vera H., additional, Roberson, David A., additional, Rodgers, Keith, additional, Roper, Damian, additional, Rosenhek, Raphael, additional, Ross, Eleanor, additional, Roy, R. Raina, additional, Ruberg, Frederick L., additional, Rudski, Lawrence G., additional, Ruiz, Carlos, additional, Salcedo, Ernesto E., additional, Sanborn, Danita M. Yoerger, additional, Sardana, Vrinda, additional, Saric, Muhamed, additional, Schiller, Nelson B., additional, Schinkel, Arend F.L., additional, Schwartzenberg, Shmuel S., additional, Sengupta, Partho P., additional, Shah, Pravin M., additional, Shanewise, Jack S., additional, Shernan, Stanton K., additional, Shih, Jeffrey A., additional, Siegel, Robert J., additional, Siriwardena, Maithri, additional, Siu, Samuel, additional, Solomon, Scott D., additional, Sorrell, Vincent L., additional, Spencer, Kirk T., additional, Spiegel, Denise, additional, John Sutton, Martin St., additional, Stein, James H., additional, Stergiopoulos, Kathleen, additional, Supariwala, Azhar A., additional, Szmitko, Paul E., additional, Tajouri, Tanya H., additional, Takeuchi, Masaaki, additional, Tan, Timothy C., additional, Thomas, James D., additional, Tighe, Dennis A., additional, Todaro, Maria C., additional, Tower-Rader, Albree, additional, Tsang, Michael Y.C., additional, Tsang, Teresa S.M., additional, Tsang, Wendy, additional, Tunick, Paul A., additional, Vignon, Philippe, additional, Wafsy, Meagan M., additional, Wald, Rachel, additional, Ward, R. Parker, additional, Watanabe, Nozomi, additional, Wei, Kevin, additional, Weissman, Neil J., additional, Welsch, Mariko, additional, Wiegers, Susan, additional, Williams, Lynne, additional, Woo, Anna, additional, Wuttichaipradit, Chanwit, additional, Xie, Feng, additional, Yingchoncharoen, Teerapat, additional, Yu, Cheuk-Man, additional, Yu, Zoe, additional, Zhao, Qiong, additional, Zito, Concetta, additional, and Zoghbi, William A., additional
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- 2016
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6. Left ventricular function, morphology, and myocardial tissue characterization in Sickle Cell Disease: a multi-modality imaging study
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Machado Roberto, Feehan Sharon, Trevino Sharon, Artz Nicole, Jamison E, Weinert Lynn, Turner Kristen, Thiruvoipati Thejasvi, Lang Roberto M, Desai Ankit A, Homaa Ahmad, Garcia Joe GN, and Patel Amit R
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Diseases of the circulatory (Cardiovascular) system ,RC666-701 - Published
- 2011
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7. Automated quantification of myocardial perfusion based on segmentation and non-rigid registration of contrast-enhanced cardiac magnetic resonance images
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Mor-Avi Victor, Lang Roberto M, Lamberti Claudio, Walter James, Veronesi Federico, Corsi Cristiana, Tarroni Giacomo, and Patel Amit R
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Diseases of the circulatory (Cardiovascular) system ,RC666-701 - Published
- 2011
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8. Feasibility of regional left ventricular endocardial curvature analysis from cardiac magnetic resonance images
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Caiani Enrico G, Steringer-Macherbauer Regina, Niel Johannes, Lang Roberto M, Maffessanti Francesco, Nesser Hans-Joachim, and Mor-Avi Victor
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Diseases of the circulatory (Cardiovascular) system ,RC666-701 - Published
- 2010
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9. Contributors
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Abraham, Theodore P., primary, Almeida, Ana G., additional, Bortnick, Anna E., additional, Dias, Nuno Cortez, additional, Dimanno, Veronica Lea J., additional, Eskesen, Kristian, additional, Gillam, Linda D., additional, Hahn, Rebecca T., additional, Hung, Judy, additional, Lang, Roberto M., additional, Marwick, Thomas H., additional, Mor-Avi, Victor, additional, Nagueh, Sherif F., additional, Olson, Joan J., additional, Otto, Catherine M., additional, Owens, David S., additional, Passeri, Jonathan J., additional, Pinto, Fausto J., additional, Porter, Thomas, additional, Shiota, Takahiro, additional, Silvestry, Frank E., additional, Watanabe, Nozomi, additional, and Xie, Feng, additional
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- 2012
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10. Transthoracic Three-Dimensional Echocardiography
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Mor-Avi, Victor, primary and Lang, Roberto M., additional
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- 2012
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11. The use of volumetric analysis to improve cardiac magnetic resonance evaluation of left ventricular size and function
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Schummers Georg, Baumann Rolf, Sugeng Lissa, Weinert Lynn, Steringer-Macherbauer Regina, Niel Johannes, Lang Roberto M, Mor-Avi Victor, Patel Amit, and Nesser Hans-Joachim
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Diseases of the circulatory (Cardiovascular) system ,RC666-701 - Published
- 2009
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12. Preface
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Lang, Roberto M., primary, Goldstein, Steven, additional, Kronzon, Itzhak, additional, and Khandheria, Bijoy, additional
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- 2011
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13. Anatomic Features of Corrected Transposition of the Great Arteries
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Chandra, Sonal, primary, Pollard, Heidi, additional, Lang, Roberto M., additional, and Sugeng, Lissa, additional
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- 2011
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14. Nonischemic Mitral Regurgitation in Infective Endocarditis
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Sugeng, Lissa, primary and Lang, Roberto M., additional
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- 2011
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15. Challenges in Aortic Stenosis
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Lodato, Joseph A., primary and Lang, Roberto M., additional
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- 2011
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16. Echocardiographic Evaluation of Atrial Septal Defects
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Borden, William B., primary, Coon, Patrick D., additional, and Lang, Roberto M., additional
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- 2011
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17. Contributors
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Abraham, Theodore P., primary, Acquatella, Harry, additional, Adams, David, additional, Agler, Deborah A., additional, Aichinger, Josef, additional, Ali, Bilal Shaukat, additional, Asirvatham, Samuel J., additional, Bach, David S., additional, Bangalore, Sripal, additional, Bansal, Manish, additional, Baumgartner, Helmut, additional, Bax, Jeroen J., additional, Bierig, S. Michelle, additional, Bleeker, Gabe B., additional, Borden, William B., additional, Burstow, Darryl J., additional, Carerj, Scipione, additional, Chaliki, Hari P., additional, Chan, Kwan-Leung, additional, Chandra, Sonal, additional, Chandrasekaran, Krishnaswamy, additional, Chaowalit, Nithima, additional, Chaudhry, Farooq A., additional, Chung, Namsik, additional, Coon, Patrick D., additional, Curtin, Ronan J., additional, DeCara, Jeanne M., additional, Derumeaux, Geneviève, additional, Dimaano, Veronica Lea J., additional, Dumesnil, Jean G., additional, Ebner, Christian, additional, Eggebrecht, Holger, additional, Erbel, Raimund, additional, Fountain, Rebecca B., additional, Franke, Andreas, additional, Freeman, William K., additional, Garcia, Mario J., additional, García-Fernández, Eulogio, additional, García-Fernandez, Miguel Angel, additional, García-Robles, José Antonio, additional, Goldstein, Steven A., additional, Zamorano Gomez, José Luis, additional, de Diego, José Juan Gómez, additional, Gutierrez-Bernal, Jose Luis, additional, Ha, Jong-Won, additional, Holmes, David R., additional, Horton, Kenneth, additional, Hung, Judy W., additional, Ito, Hiroshi, additional, Jollis, James G., additional, Jost, Christine Attenhofer, additional, Kabicher, Gudrun, additional, Kaul, Sanjiv, additional, Khandheria, Bijoy K., additional, Kirkpatrick, James N., additional, Klein, Allan L., additional, Kort, Smadar, additional, Kronzon, Itzhak, additional, Kurrelmeyer, Karla M., additional, Lang, Roberto M., additional, Lee, Pui, additional, Lennie, Vera, additional, Lester, Steven J., additional, Leung, Dominic Y., additional, Lindner, Jonathan R., additional, Lodato, Joseph A., additional, Lowe, Boris S., additional, Lusk, Joan L., additional, Malouf, Joseph F., additional, Martin, Randolph P., additional, Marwick, Thomas H., additional, Maurer, Gerald, additional, McCarthy, Patrick M., additional, Melgarejo, Ivàn, additional, Michelena, Hector I., additional, Mor-Avi, Victor, additional, Nagueh, Sherif F., additional, Nesser, Hans Joachim, additional, Niel, Johannes, additional, Ommen, Steve R., additional, Pearlman, Alan S., additional, Pellikka, Patricia A., additional, Pérez-David, Esther, additional, Pibarot, Philippe, additional, Picard, Michael H., additional, Pinto, Fausto J., additional, Pollard, Heidi, additional, Polonsky, Tamar S., additional, Porter, Thomas R., additional, Powell, Brian D., additional, Riarte, Jose E., additional, Rigolin, Vera H., additional, Ronderos, Ricardo E., additional, Saric, Muhamed, additional, Sengupta, Partho P., additional, Shah, Dipak P., additional, Shernan, Stanton K., additional, Spencer, Kirk T., additional, Srichai, Monvadi B., additional, Stergiopoulos, Kathleen, additional, Strachan, G. Monet, additional, Sugeng, Lissa, additional, Takeuchi, Masaaki, additional, Thibault, Hélène, additional, Tkalec, Wolfgang, additional, Tunick, Paul A., additional, Umland, Matt M., additional, Vannan, Mani A., additional, Vignon, Philippe, additional, Villarraga, Hector R., additional, Ward, R. Parker, additional, Watanabe, Nozomi, additional, Wei, Kevin, additional, Weissman, Neil J., additional, Winter, Siegmund, additional, Wood, Malissa J., additional, Xie, Feng, additional, Yang, Hyun Suk, additional, Sanborn, Danita M. Yoerger, additional, Zhao, Qiong, additional, Zito, Concetta, additional, and Zoghbi, William A., additional
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- 2011
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18. Use of Contrast to Distinguish Intracardiac Masses From Thrombi
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Kirkpatrick, James N., primary and Lang, Roberto M., additional
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- 2011
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19. Mitral Stenosis
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Kronzon, Itzhak, primary, Saric, Muhamed, additional, and Lang, Roberto M., additional
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- 2011
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20. Vasodilator Stress With Myocardial Contrast Echocardiography
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Mor-Avi, Victor, primary and Lang, Roberto M., additional
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- 2011
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21. Takotsubo Cardiomyopathy
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Shah, Dipak, primary and Lang, Roberto M., additional
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- 2011
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22. Morphologic Basis of Valvular Nonischemic Mitral Regurgitation
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Sugeng, Lissa, primary and Lang, Roberto M., additional
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- 2011
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23. Aortic Valve Masses
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DeCara, Jeanne M., primary and Lang, Roberto M., additional
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- 2011
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24. Pericardial Tamponade
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Ward, R. Parker, primary and Lang, Roberto M., additional
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- 2011
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25. Use of Guidelines to Evaluate Chamber Quantitation
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Coon, Patrick D., primary and Lang, Roberto M., additional
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- 2011
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26. Three-Dimensional Transthoracic and Transesophageal Echocardiography
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Polonsky, Tamar S., primary, Sugeng, Lissa, additional, Mor-Avi, Victor, additional, and Lang, Roberto M., additional
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- 2011
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27. 1097 Automated frame-by-frame endocardial border detection from cardiac magnetic resonance images for quantitative assessment of left ventricular function: validation and clinical feasibility
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Lang Roberto M, Jamison Ernest B, Bardo Dianna ME, Lamberti Claudio, Veronesi Federico, Corsi Cristiana, and Mor-Avi Victor
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Diseases of the circulatory (Cardiovascular) system ,RC666-701 - Published
- 2008
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28. Considerations when measuring myocardial perfusion reserve by cardiovascular magnetic resonance using regadenoson
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Bhave Nicole M, Freed Benjamin H, Yodwut Chattanong, Kolanczyk Denise, Dill Karin, Lang Roberto M, Mor-Avi Victor, and Patel Amit R
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Stress CMR ,Regadenoson ,Vasodilators ,Diseases of the circulatory (Cardiovascular) system ,RC666-701 - Abstract
Abstract Background Adenosine cardiovascular magnetic resonance (CMR) can accurately quantify myocardial perfusion reserve. While regadenoson is increasingly employed due to ease of use, imaging protocols have not been standardized. We sought to determine the optimal regadenoson CMR protocol for quantifying myocardial perfusion reserve index (MPRi) – more specifically, whether regadenoson stress imaging should be performed before or after rest imaging. Methods Twenty healthy subjects underwent CMR perfusion imaging during resting conditions, during regadenoson-induced hyperemia (0.4 mg), and after 15 min of recovery. In 10/20 subjects, recovery was facilitated with aminophylline (125 mg). Myocardial time-intensity curves were used to obtain left ventricular cavity-normalized myocardial up-slopes. MPRi was calculated in two different ways: as the up-slope ratio of stress to rest (MPRi-rest), and the up-slope ratio of stress to recovery (MPRi-recov). Results In all 20 subjects, MPRi-rest was 1.78 ± 0.60. Recovery up-slope did not return to resting levels, regardless of aminophylline use. Among patients not receiving aminophylline, MPRi-recov was 36 ± 16% lower than MPRi-rest (1.13 ± 0.38 vs. 1.82 ± 0.73, P = 0.001). In the 10 patients whose recovery was facilitated with aminophylline, MPRi-recov was 20 ± 24% lower than MPRi-rest (1.40 ± 0.35 vs. 1.73 ± 0.43, P = 0.04), indicating incomplete reversal. In 3 subjects not receiving aminophylline and 4 subjects receiving aminophylline, up-slope at recovery was greater than at stress, suggesting delayed maximal hyperemia. Conclusions MPRi measurements from regadenoson CMR are underestimated if recovery perfusion is used as a substitute for resting perfusion, even when recovery is facilitated with aminophylline. True resting images should be used to allow accurate MPRi quantification. The delayed maximal hyperemia observed in some subjects deserves further study. Trial registration ClinicalTrials.gov NCT00871260
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- 2012
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29. Late gadolinium enhancement cardiovascular magnetic resonance predicts clinical worsening in patients with pulmonary hypertension
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Freed Benjamin H, Gomberg-Maitland Mardi, Chandra Sonal, Mor-Avi Victor, Rich Stuart, Archer Stephen L, Jamison E Bruce, Lang Roberto M, and Patel Amit R
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Diseases of the circulatory (Cardiovascular) system ,RC666-701 - Abstract
Abstract Background Late gadolinium enhancement (LGE) occurs at the right ventricular (RV) insertion point (RVIP) in patients with pulmonary hypertension (PH) and has been shown to correlate with cardiovascular magnetic resonance (CMR) derived RV indices. However, the prognostic role of RVIP-LGE and other CMR-derived parameters of RV function are not well established. Our aim was to evaluate the predictive value of contrast-enhanced CMR in patients with PH. Methods RV size, ejection fraction (RVEF), and the presence of RVIP-LGE were determined in 58 patients with PH referred for CMR. All patients underwent right heart catheterization, exercise testing, and N-terminal pro-brain natriuretic peptide (NT-proBNP) evaluation; results of which were included in the final analysis if performed within 4 months of the CMR study. Patients were followed for the primary endpoint of time to clinical worsening (death, decompensated right ventricular heart failure, initiation of prostacyclin, or lung transplantation). Results Overall, 40/58 (69%) of patients had RVIP-LGE. Patients with RVIP- LGE had larger right ventricular volume index, lower RVEF, and higher mean pulmonary artery pressure (mPAP), all p < 0.05. During the follow-up period of 10.2 ± 6.3 months, 19 patients reached the primary endpoint. In a univariate analysis, RVIP-LGE was a predictor for adverse outcomes (p = 0.026). In a multivariate analysis, CMR-derived RVEF was an independent predictor of clinical worsening (p = 0.036) along with well-established prognostic parameters such as exercise capacity (p = 0.010) and mPAP (p = 0.001). Conclusions The presence of RVIP-LGE in patients with PH is a marker for more advanced disease and poor prognosis. In addition, this study reveals for the first time that CMR-derived RVEF is an independent non-invasive imaging predictor of adverse outcomes in this patient population.
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- 2012
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30. Defining echocardiographic predictors of outcome in cardiac amyloidosis by subtype.
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Singulane C, Sun D, Hu Z, Lee L, Sarswat N, Emami Neyestanak M, Patel AR, Lang RM, and Addetia K
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- Humans, Male, Female, Aged, Prognosis, Echocardiography methods, Amyloid Neuropathies, Familial diagnostic imaging, Amyloid Neuropathies, Familial physiopathology, Amyloid Neuropathies, Familial diagnosis, Amyloid Neuropathies, Familial mortality, Retrospective Studies, Middle Aged, Aged, 80 and over, Risk Factors, Predictive Value of Tests, Ventricular Function, Left physiology, Amyloidosis diagnosis, Amyloidosis physiopathology, Amyloidosis diagnostic imaging, Heart Ventricles diagnostic imaging, Heart Ventricles physiopathology, Survival Rate trends, Cardiomyopathies physiopathology, Cardiomyopathies diagnosis, Cardiomyopathies diagnostic imaging, Immunoglobulin Light-chain Amyloidosis diagnosis, Immunoglobulin Light-chain Amyloidosis physiopathology, Immunoglobulin Light-chain Amyloidosis diagnostic imaging, Immunoglobulin Light-chain Amyloidosis mortality
- Abstract
Background: Current echocardiographic risk factors for prognosis in cardiac amyloidosis (CA) do not distinguish between the two main subtypes: transthyretin cardiomyopathy (TTR) and immunoglobulin light chain cardiomyopathy (AL), each of which require distinct diagnostic and therapeutic approaches. Additionally, only traditional parameters have been studied with little data on advanced techniques. Accordingly, we sought to determine whether differences exist in 2D transthoracic echocardiography (2DE) predictors of survival between the CA subtypes using a comprehensive approach., Methods: 220 patients (72±12 years) with confirmed CA (AL=89, TTR=131) who underwent 2DE at the time of CA diagnosis were enrolled. Left ventricular (LV) dimensions, indexed mass (LVMi), global longitudinal strain (LVGLS), apical-sparing ratio (LVASR), diastology, right ventricular (RV) size and function indices including tricuspid annular systolic excursion (TAPSE), RV free-wall (RVFWS) and global (RVGLS) strain, indexed left (LA) and right atrial volumes (LAVi and RAVi), LA strain (reservoir and booster) and RV systolic pressure (RVSP) were measured. A propensity-score weighted stepwise variable selection Cox proportional hazards model derived from NYHA class and renal impairment status at diagnosis was used to determine the associations between 2DE parameters and mortality specific to CA subtype over a median follow-up of 36-months., Results: After adjusting for age, atrial fibrillation and treatment, parameters associated with survival were RVFWS (p=0.003, HR 1.15, 95% CI[1.053,1.245]) and RVSP (p=0.03, HR 1.03, 95% CI[1.004,1.063]) in AL and LVASR (p=0.007, HR 6.68, 95% CI[1.75,25.492]) and RAVi (p=0.049, HR 1.03, 95% CI[1.000,1.052]) in TTR., Conclusions: Echocardiographic prognosticators for survival are specific to cardiac amyloid subtype. These results potentially provide information critical for clinical decision-making and follow-up in these patients., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Karima Addetia reports financial support was provided by Pfizer Inc. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)
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- 2024
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31. Anomalous right coronary artery from the main pulmonary artery (ARCAPA): Incidental finding in an asymptomatic septuagenarian.
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Prabhu N, Guile B, Tang M, Lee L, Landeras L, Lang RM, Sarswat N, and Addetia K
- Abstract
Anomalous right coronary artery (RCA) from the main pulmonary artery (ARCAPA) is a rare finding. Clinical presentations range from asymptomatic to sudden death. We present the case of ARCAPA in a septuagenarian initially suspected on a screening chest computed tomography (CT) and later confirmed on cardiac CT. A summary of important points related to this entity is also discussed., (© 2023 The Authors. Published by Elsevier Inc. on behalf of University of Washington.)
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- 2023
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32. AI Based CMR Assessment of Biventricular Function: Clinical Significance of Intervendor Variability and Measurement Errors.
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Wang S, Patel H, Miller T, Ameyaw K, Narang A, Chauhan D, Anand S, Anyanwu E, Besser SA, Kawaji K, Liu XP, Lang RM, Mor-Avi V, and Patel AR
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- Artificial Intelligence, Heart Ventricles diagnostic imaging, Humans, Predictive Value of Tests, Stroke Volume, Ventricular Function, Left, Cardiovascular Diseases, Ventricular Function, Right
- Abstract
Objectives: The aim of this study was to determine whether left ventricular ejection fraction (LVEF) and right ventricular ejection fraction (RVEF) and left ventricular mass (LVM) measurements made using 3 fully automated deep learning (DL) algorithms are accurate and interchangeable and can be used to classify ventricular function and risk-stratify patients as accurately as an expert., Background: Artificial intelligence is increasingly used to assess cardiac function and LVM from cardiac magnetic resonance images., Methods: Two hundred patients were identified from a registry of individuals who underwent vasodilator stress cardiac magnetic resonance. LVEF, LVM, and RVEF were determined using 3 fully automated commercial DL algorithms and by a clinical expert (CLIN) using conventional methodology. Additionally, LVEF values were classified according to clinically important ranges: <35%, 35% to 50%, and ≥50%. Both ejection fraction values and classifications made by the DL ejection fraction approaches were compared against CLIN ejection fraction reference. Receiver-operating characteristic curve analysis was performed to evaluate the ability of CLIN and each of the DL classifications to predict major adverse cardiovascular events., Results: Excellent correlations were seen for each DL-LVEF compared with CLIN-LVEF (r = 0.83-0.93). Good correlations were present between DL-LVM and CLIN-LVM (r = 0.75-0.85). Modest correlations were observed between DL-RVEF and CLIN-RVEF (r = 0.59-0.68). A >10% error between CLIN and DL ejection fraction was present in 5% to 18% of cases for the left ventricle and 23% to 43% for the right ventricle. LVEF classification agreed with CLIN-LVEF classification in 86%, 80%, and 85% cases for the 3 DL-LVEF approaches. There were no differences among the 4 approaches in associations with major adverse cardiovascular events for LVEF, LVM, and RVEF., Conclusions: This study revealed good agreement between automated and expert-derived LVEF and similarly strong associations with outcomes, compared with an expert. However, the ability of these automated measurements to accurately classify left ventricular function for treatment decision remains limited. DL-LVM showed good agreement with CLIN-LVM. DL-RVEF approaches need further refinements., Competing Interests: Funding Support and Author Disclosures This project was supported by the National Center for Advancing Translational Sciences of the National Institutes of Health through grant 5UL1TR002389-02, which funds the Institute for Translational Medicine. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. Dr A.R. Patel has received research support from Philips, Arterys, CircleCVI, and Neosoft. Dr H. Patel was funded by a T32 Cardiovascular Sciences Training Grant (5T32HL7381). All authors have reported that they have no relationships relevant to the contents of this paper to disclose., (Copyright © 2022 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.)
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- 2022
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33. Anatomic Description of Tricuspid Apparatus Interference From Implantable Intracardiac Devices.
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Henry M, Abutaleb A, Jeevanandam V, Smith H, Belkin M, Husain A, Pinney S, Ota T, Lang RM, and Addetia K
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- Humans, Predictive Value of Tests, Tricuspid Valve diagnostic imaging, Tricuspid Valve surgery, Defibrillators, Implantable, Tricuspid Valve Insufficiency diagnostic imaging, Tricuspid Valve Insufficiency surgery
- Abstract
Competing Interests: Funding Support and Author Disclosures Dr Jeevanandum has received consulting fees from Abbott. Dr Pinney has received consulting fees from Abbott, CareDX, Medtronic, Procyrion, and Transmedics; and honoraria from Boston Scientific. Dr Lang has served on the speaker and advisory bureau for Philips Medical Imaging. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.
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- 2022
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34. Echocardiographic predictors of new-onset atrial arrhythmias in patients undergoing hematopoietic stem cell transplantation.
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Singh N, Singh A, Besser SA, Lang RM, Mor-Avi V, Kosuri S, Bishop MR, and DeCara JM
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- Arrhythmias, Cardiac diagnostic imaging, Arrhythmias, Cardiac epidemiology, Atrial Function, Left, Heart Atria diagnostic imaging, Humans, Retrospective Studies, Echocardiography, Hematopoietic Stem Cell Transplantation adverse effects
- Abstract
Background: Atrial arrhythmias following hematopoietic stem cell transplantation (HSCT) have been associated with increased length of stay, need for intensive care, and increased mortality within one-year post-transplant. We sought to identify echocardiographic parameters that may predict the development of new atrial arrhythmias post-HSCT., Methods: We performed a retrospective chart review of 753 consecutive patients who underwent HSCT at the University of Chicago from January 2015 through December 2019. Patients with baseline echocardiogram within 6 months prior to transplantation were included. Those with prior transplants, history of atrial arrhythmias, or unavailable echocardiographic images were excluded, resulting in 187 patients included for final analysis. Baseline clinical and demographic variables, as well as echocardiographic parameters, were compared between patients who developed new atrial arrhythmias post-HSCT versus those who did not., Results: Of the 187 patients included for analysis, 25 (13%) developed new atrial arrhythmias, with 13 of these occurring within 30 days of transplantation. Despite no significant difference in left atrial (LA) end-systolic volume between those with and without new arrhythmia following HSCT (OR 1.04; 95% CI 0.91-1.09, p = 0.233), univariable analysis demonstrated that patients who developed atrial arrhythmias had reduced LA function, as reflected by lower LA emptying fraction (OR 0.94; 95% CI 0.91-0.98, p = 0.003) and lower LA reservoir strain (OR 0.95; 95% CI 0.92-0.99, p = 0.009)., Conclusions: Echocardiographic indices of LA function, namely LA emptying fraction and LA reservoir strain, can identify patients at risk for developing new atrial arrhythmias post-HSCT, prior to the development of morphologic changes in the LA., (Copyright © 2021 Elsevier B.V. All rights reserved.)
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- 2021
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35. Quantifying Right Ventricular Fibrosis Burden Using 3D Strain: Can Echo Approximate a Virtual Heart Biopsy?
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Lang RM and Singh A
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- Biopsy, Fibrosis, Humans, Predictive Value of Tests, Heart, Heart Ventricles diagnostic imaging
- Abstract
Competing Interests: Funding Support and Author Disclosures The authors have reported that they have no relationships relevant to the contents of this paper to disclose.
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- 2021
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36. Prospective Evaluation of Transseptal TMVR for Failed Surgical Bioprostheses: MITRAL Trial Valve-in-Valve Arm 1-Year Outcomes.
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Guerrero M, Pursnani A, Narang A, Salinger M, Wang DD, Eleid M, Kodali SK, George I, Satler L, Waksman R, Meduri CU, Rajagopal V, Inglessis I, Palacios I, Reisman M, Eng MH, Russell HM, Pershad A, Fang K, Kar S, Makkar R, Saucedo J, Pearson P, Bokhary U, Kaptzan T, Lewis B, Tommaso C, Krause P, Thaden J, Oh J, Lang RM, Hahn RT, Leon MB, O'Neill WW, Feldman T, and Rihal C
- Subjects
- Aged, Aged, 80 and over, Cardiac Catheterization adverse effects, Female, Humans, Male, Prospective Studies, Prosthesis Design, Treatment Outcome, Bioprosthesis, Heart Valve Prosthesis, Heart Valve Prosthesis Implantation adverse effects, Mitral Valve Annuloplasty
- Abstract
Objectives: The aim of this study was to assess 1-year clinical outcomes among high-risk patients with failed surgical mitral bioprostheses who underwent transseptal mitral valve-in-valve (MViV) with the SAPIEN 3 aortic transcatheter heart valve (THV) in the MITRAL (Mitral Implantation of Transcatheter Valves) trial., Background: The MITRAL trial is the first prospective study evaluating transseptal MViV with the SAPIEN 3 aortic THV in high-risk patients with failed surgical mitral bioprostheses., Methods: High-risk patients with symptomatic moderate to severe or severe mitral regurgitation (MR) or severe mitral stenosis due to failed surgical mitral bioprostheses were prospectively enrolled. The primary safety endpoint was technical success. The primary THV performance endpoint was absence of MR grade ≥2+ or mean mitral valve gradient ≥10 mm Hg (30 days and 1 year). Secondary endpoints included procedural success and all-cause mortality (30 days and 1 year)., Results: Thirty patients were enrolled between July 2016 and October 2017 (median age 77.5 years [interquartile range (IQR): 70.3 to 82.8 years], 63.3% women, median Society of Thoracic Surgeons score 9.4% [IQR: 5.8% to 12.0%], 80% in New York Heart Association functional class III or IV). The technical success rate was 100%. The primary performance endpoint in survivors was achieved in 96.6% (28 of 29) at 30 days and 82.8% (24 of 29) at 1 year. Thirty-day all-cause mortality was 3.3% and was unchanged at 1 year. The only death was due to airway obstruction after swallowing several pills simultaneously 29 days post-MViV. At 1-year follow-up, 89.3% of patients were in New York Heart Association functional class I or II, the median mean mitral valve gradient was 6.6 mm Hg (interquartile range: 5.5 to 8.9 mm Hg), and all patients had MR grade ≤1+., Conclusions: Transseptal MViV in high-risk patients was associated with 100% technical success, low procedural complication rates, and very low mortality at 1 year. The vast majority of patients experienced significant symptom alleviation, and THV performance remained stable at 1 year., Competing Interests: Funding Support and Author Disclosures Dr. Guerrero has received research grant support from Abbott Vascular and Edwards Lifesciences. Dr. Wang has served as a consultant for Edwards Lifesciences and Boston Scientific; has received research grant support from Boston Scientific assigned to her employer, Henry Ford Health; and holds equity in Encompass Technologies. Dr. Kodali has served as a consultant for Admedus, Meril Lifesciences, Abbott Vascular, JenaValve, and Claret Medical; and has ownership interest in Dura Biotech, Thubrikar Aortic Valve, Micro Interventional Devices, and Supira Medical. Dr. George has served as consultant for Cardiomech, VDyne, MitreMedical, and Neptune Medical. Dr. Meduri has served as a consultant for Medtronic and Boston Scientific; and has served on the advisory board for Boston Scientific. Dr. Reisman has served as consultant for Edwards Lifesciences. Dr. Hahn has received speaker fees from Baylis Medical, Edwards Lifesciences, and Medtronic; is a consultant for Abbott Structural, Edwards Lifesciences, Gore & Associates, Medtronic, Navigate, and Philips Healthcare; has received nonfinancial support from 3mensio; holds equity in Navigate; and is the chief scientific officer for the Echocardiography Core Laboratory at the Cardiovascular Research Foundation for multiple industry-sponsored trials, for which she receives no direct industry compensation. Dr. O’Neill has served as a consultant for Abiomed, Boston Scientific, and Edwards Lifesciences. Dr. Feldman is an employee of Edwards Lifesciences. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose., (Copyright © 2021 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.)
- Published
- 2021
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37. Utilization of Inpatient Transthoracic Echocardiography in Response to the 2017 AHA/ACC/HRS Guidelines for Syncope.
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Lee L, Mishra S, Sun D, Besser SA, Mor-Avi V, Lang RM, and Ward RP
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- Echocardiography, Humans, Predictive Value of Tests, Syncope diagnostic imaging, Syncope etiology, American Heart Association, Inpatients
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- 2021
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38. Validation of non-contrast multiple overlapping thin-slab 4D-flow cardiac magnetic resonance imaging.
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Rashedi N, Landeras L, Mor-Avi V, Genovese D, Lai P, Wang H, Kebed K, McClelland I, Brau A, Janich M, Addetia K, Lang RM, and Patel AR
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- Aorta diagnostic imaging, Aorta physiology, Blood Flow Velocity, Female, Humans, Male, Middle Aged, Heart diagnostic imaging, Imaging, Three-Dimensional methods, Magnetic Resonance Imaging
- Abstract
Background: Cardiac magnetic resonance (CMR) flow quantification is typically performed using 2D phase-contrast (PC) imaging of a plane perpendicular to flow. 3D-PC imaging (4D-flow) allows offline quantification anywhere in a thick slab, but is often limited by suboptimal signal, potentially alleviated by contrast enhancement. We developed a non-contrast 4D-flow sequence, which acquires multiple overlapping thin slabs (MOTS) to minimize signal loss, and hypothesized that it could improve image quality, diagnostic accuracy, and aortic flow measurements compared to non-contrast single-slab approach., Methods: We prospectively studied 20 patients referred for transesophageal echocardiography (TEE), who underwent CMR (GE, 3 T). 2D-PC images of the aortic valve and three 4D-flow datasets covering the heart were acquired, including single-slab, pre- and post-contrast, and non-contrast MOTS. Each 4D-flow dataset was interpreted blindly for ≥moderate valve disease and compared to TEE. Flow visualization through each valve was scored (0 to 4), and aortic-valve flow measured on each 4D-flow dataset and compared to 2D-PC reference., Results: Diagnostic quality visualization was achieved with the pre- and post-contrast 4D-flow acquisitions in 25% and 100% valves, respectively (scores 0.9 ± 1.1 and 3.8 ± 0.5), and in 58% with the non-contrast MOTS (1.6 ± 1.1). Accuracy of detection of valve disease was 75%, 92% and 82%, respectively. Aortic flow measurements were possible in 53%, 95% and in 89% patients, respectively. The correlation between pre-contrast single-slab measurements and 2D-PC reference was weak (r = 0.21), but improved with both contrast enhancement (r = 0.71) and with MOTS (r = 0.67)., Conclusions: Although non-contrast MOTS 4D-flow improves valve function visualization and diagnostic accuracy, a significant proportion of valves cannot be accurately assessed. However, aortic flow measurements using non-contrast MOTS is feasible and reaches similar accuracy to that of contrast-enhanced 4D-flow., (Copyright © 2020 Elsevier Inc. All rights reserved.)
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- 2020
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39. Myocardial strain analysis of the right ventricle: comparison of different cardiovascular magnetic resonance and echocardiographic techniques.
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Erley J, Tanacli R, Genovese D, Tapaskar N, Rashedi N, Bucius P, Kawaji K, Karagodin I, Lang RM, Kelle S, Mor-Avi V, and Patel AR
- Subjects
- Adult, Female, Heart Ventricles diagnostic imaging, Heart Ventricles physiopathology, Humans, Male, Middle Aged, Predictive Value of Tests, Reproducibility of Results, Young Adult, Echocardiography methods, Magnetic Resonance Imaging methods, Ventricular Dysfunction, Right diagnostic imaging, Ventricular Dysfunction, Right physiopathology
- Abstract
Background: Right ventricular (RV) strain is a useful predictor of prognosis in various cardiovascular diseases, including those traditionally believed to impact only the left ventricle. We aimed to determine inter-modality and inter-technique agreement in RV longitudinal strain (LS) measurements between currently available cardiovascular magnetic resonance (CMR) and echocardiographic techniques, as well as their reproducibility and the impact of layer-specific strain measurements., Methods: RV-LS was determined in 62 patients using 2D speckle tracking echocardiography (STE, Epsilon) and two CMR techniques: feature tracking (FT) and strain-encoding (SENC), and in 17 healthy subjects using FT and SENC only. Measurements included global and free-wall LS (GLS, FWLS). Inter-technique agreement was assessed using linear regression and Bland-Altman analysis. Reproducibility was quantified using intraclass correlation (ICC) and coefficients of variation (CoV)., Results: We found similar moderate agreement between both CMR techniques and STE in patients: r = 0.57-0.63 for SENC; r = 0.50-0.62 for FT. The correlation between SENC and STE was better for GLS (r = 0.63) than for FWLS (r = 0.57). Conversely, the correlation between FT and STE was higher for FWLS (r = 0.60-0.62) than GLS (r = 0.50-0.54). FT-midmyocardial strain correlated better with SENC and STE than FT-subendocardial strain. The agreement between SENC and FT was fair (r = 0.36-0.41, bias: - 6.4 to - 10.4%) in the entire study group. All techniques except FT showed excellent reproducibility (ICC: 0.62-0.96, CoV: 0.04-0.30)., Conclusions: We found only moderate inter-modality agreement with STE in RV-LS for both FT and SENC and poor agreement when comparing between the CMR techniques. Different modalities and techniques should not be used interchangeably to determine and monitor RV strain.
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- 2020
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40. The Quest to Better Quantitate Tricuspid Regurgitation.
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Lang RM and Addetia K
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- Echocardiography, Humans, Magnetic Resonance Spectroscopy, Predictive Value of Tests, Tricuspid Valve diagnostic imaging, Tricuspid Valve surgery, Tricuspid Valve Insufficiency diagnostic imaging
- Published
- 2020
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41. Regional myocardial strain by cardiac magnetic resonance feature tracking for detection of scar in ischemic heart disease.
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Stathogiannis K, Mor-Avi V, Rashedi N, Lang RM, and Patel AR
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- Aged, Cohort Studies, Contrast Media, Female, Gadolinium DTPA, Heart Ventricles diagnostic imaging, Humans, Linear Models, Magnetic Resonance Spectroscopy, Male, Middle Aged, Myocardium pathology, ROC Curve, Retrospective Studies, Sensitivity and Specificity, Systole, Ventricular Function, Left, Cicatrix diagnostic imaging, Heart diagnostic imaging, Magnetic Resonance Imaging, Cine, Myocardial Infarction diagnostic imaging, Myocardial Ischemia diagnostic imaging
- Abstract
Background: Although cardiac magnetic resonance (CMR) can accurately quantify global left ventricular strain using feature tracking (FT), it has been suggested that FT cannot reliably quantify regional strain. We aimed to determine whether abnormalities in regional strain measured using FT can be detected within areas of myocardial scar and to determine the extent to which the regional strain measurement is impacted by LV ejection fraction (EF)., Methods: We retrospectively studied 96 patients (46 with LVEF ≤ 40%, 50 with LVEF > 40%) with coronary artery disease and a late gadolinium enhancement (LGE) pattern consistent with myocardial infarction, who underwent CMR imaging (1.5T). Regional peak systolic longitudinal and circumferential strains (RLS, RCS) were measured within LGE and non-LGE areas. Linear regression analysis was performed for strain in both areas against LVEF to determine whether the relationship between strain and LGE holds across the LV function spectrum. Receiver-operating curve (ROC) analysis was performed in 33 patients (derivation cohort) to optimize strain cutoff, which was tested in the remaining 63 patients (validation cohort) for its ability to differentiate LGE from non-LGE areas., Results: Both RLS and RCS magnitudes were reduced in LGE areas: RLS = -10.4 ± 6.2% versus -21.0 ± 8.5% (p < 0.001); RCS = -10.4 ± 6.0% versus -18.9 ± 8.6%, respectively (p < 0.001), but there was considerable overlap between LGE and non-LGE areas. Linear regression revealed that it was partially driven by the natural dependence between strain and EF, suggesting that EF-corrected strain cutoff is needed to detect LGE. ROC analysis showed the ability of both RLS and RCS to differentiate LGE from non-LGE areas: area under curve 0.95 and 0.89, respectively. In the validation cohort, optimal cutoffs of RLS/EF = 0.36 and RCS/EF = 0.37 yielded sensitivity, specificity and accuracy 0.74-0.78., Conclusion: Abnormalities in RLS and RCS within areas of myocardial scar can be detected using CMR-FT; however, LVEF must be accounted for., (Copyright © 2020 Elsevier Inc. All rights reserved.)
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- 2020
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42. Machine learning based quantification of ejection and filling parameters by fully automated dynamic measurement of left ventricular volumes from cardiac magnetic resonance images.
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Goyal N, Mor-Avi V, Volpato V, Narang A, Wang S, Salerno M, Lang RM, and Patel AR
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- Adult, Aged, Algorithms, Automation, Endocardium diagnostic imaging, Female, Heart Ventricles physiopathology, Humans, Male, Middle Aged, Prospective Studies, Reproducibility of Results, Software, Heart diagnostic imaging, Heart Ventricles diagnostic imaging, Image Processing, Computer-Assisted methods, Machine Learning, Magnetic Resonance Imaging, Ventricular Function, Left
- Abstract
Background: Although analysis of cardiac magnetic resonance (CMR) images provides accurate and reproducible measurements of left ventricular (LV) volumes, these measurements are usually not performed throughout the cardiac cycle because of lack of tools that would allow such analysis within a reasonable timeframe. A fully-automated machine-learning (ML) algorithm was recently developed to automatically generate LV volume-time curves. Our aim was to validate ejection and filling parameters calculated from these curves using conventional analysis as a reference., Methods: We studied 21 patients undergoing clinical CMR examinations. LV volume-time curves were obtained using the ML-based algorithm (Neosoft), and independently using slice-by-slice, frame-by-frame manual tracing of the endocardial boundaries. Ejection and filling parameters derived from these curves were compared between the two techniques. For each parameter, Bland-Altman bias and limits of agreement (LOA) were expressed in percent of the mean measured value., Results: Time-volume curves were generated using the automated ML analysis within 2.5 ± 0.5 min, considerably faster than the manual analysis (43 ± 14 min per patient, including ~10 slices with 25-32 frames per slice). Time-volume curves were similar between the two techniques in magnitude and shape. Size and function parameters extracted from these curves showed no significant inter-technique differences, reflected by high correlations, small biases (<10%) and mostly reasonably narrow LOA., Conclusion: ML software for dynamic LV volume measurement allows fast and accurate, fully automated analysis of ejection and filling parameters, compared to manual tracing based analysis. The ability to quickly evaluate time-volume curves is important for a more comprehensive evaluation of the patient's cardiac function., Competing Interests: Declaration of competing interest ARP has received research support from Philips Healthcare and Neosoft. Akhil Narang was funded by a T32 Cardiovascular Sciences Training Grant (5T32HL7381) from the National Institutes of Health (USA)., (Copyright © 2019 Elsevier Inc. All rights reserved.)
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- 2020
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43. Quantitative detection of changes in regional wall motion using real time strain-encoded cardiovascular magnetic resonance.
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Kawaji K, Nazir N, Blair JA, Mor-Avi V, Besser S, Matsumoto K, Goes JP, Dabir D, Stoiber L, Kelle S, Zamani SM, Holzhauser L, Lang RM, and Patel AR
- Subjects
- Coronary Angiography methods, Coronary Artery Disease physiopathology, Evaluation Studies as Topic, Female, Heart diagnostic imaging, Heart physiopathology, Humans, Male, Middle Aged, Prospective Studies, Coronary Artery Disease diagnostic imaging, Magnetic Resonance Imaging methods
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- 2020
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44. Myocardial Tissue Characterization With CMR for the Definitive Diagnosis of Infiltrative Cardiomyopathies.
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Kebed KY, Lang RM, and Patel AR
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- Adult, Aged, Biopsy, Cardiomyopathies pathology, Cardiomyopathies therapy, Contrast Media administration & dosage, Humans, Male, Middle Aged, Multimodal Imaging, Predictive Value of Tests, Prognosis, Cardiomyopathies diagnostic imaging, Magnetic Resonance Imaging, Myocardium pathology
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- 2020
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45. Pathoanatomy of Mitral Regurgitation.
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Karagodin I, Singh A, and Lang RM
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- 2020
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46. On-treatment comparison between corrective His bundle pacing and biventricular pacing for cardiac resynchronization: A secondary analysis of the His-SYNC Pilot Trial.
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Upadhyay GA, Vijayaraman P, Nayak HM, Verma N, Dandamudi G, Sharma PS, Saleem M, Mandrola J, Genovese D, Oren JW, Subzposh FA, Aziz Z, Beaser A, Shatz D, Besser S, Lang RM, Trohman RG, Knight BP, and Tung R
- Subjects
- Cardiac Resynchronization Therapy Devices, Female, Heart Ventricles physiopathology, Humans, Male, Middle Aged, Severity of Illness Index, Stroke Volume, Treatment Outcome, Bundle of His physiopathology, Cardiac Resynchronization Therapy adverse effects, Cardiac Resynchronization Therapy methods, Echocardiography methods, Electrocardiography methods, Heart Failure physiopathology, Heart Failure therapy
- Abstract
Background: The His-SYNC pilot trial was the first randomized comparison between His bundle pacing in lieu of a left ventricular lead for cardiac resynchronization therapy (His-CRT) and biventricular pacing (BiV-CRT), but was limited by high rates of crossover., Objective: To evaluate the results of the His-SYNC pilot trial utilizing treatment-received (TR) and per-protocol (PP) analyses., Methods: The His-SYNC pilot was a multicenter, prospective, single-blinded, randomized, controlled trial comparing His-CRT vs BiV-CRT in patients meeting standard indications for CRT (eg, NYHA II-IV patients with QRS >120 ms). Crossovers were required based on prespecified criteria. The primary endpoints analyzed included improvement in QRS duration, left ventricular ejection fraction (LVEF), and freedom from cardiovascular (CV) hospitalization and mortality., Results: Among 41 patients enrolled (aged 64 ± 13 years, 38% female, LVEF 28%, QRS 168 ± 18 ms), 21 were randomized to His-CRT and 20 to BiV-CRT. Crossover occurred in 48% of His-CRT and 26% of BiV-CRT. The most common reason for crossover from His-CRT was inability to correct QRS owing to nonspecific intraventricular conduction delay (n = 5). Patients treated with His-CRT demonstrated greater QRS narrowing compared to BiV (125 ± 22 ms vs 164 ± 25 ms [TR], P < .001;124 ± 19 ms vs 162 ± 24 ms [PP], P < .001). A trend toward higher echocardiographic response was also observed (80 vs 57% [TR], P = .14; 91% vs 54% [PP], P = .078). No significant differences in CV hospitalization or mortality were observed., Conclusions: Patients receiving His-CRT on-treatment demonstrated superior electrical resynchronization and a trend toward higher echocardiographic response than BiV-CRT. Larger prospective studies may be justifiable with refinements in patient selection and implantation techniques to minimize crossovers., (Copyright © 2019 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.)
- Published
- 2019
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47. First Clinical Experience With 3-Dimensional Echocardiographic Transillumination Rendering.
- Author
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Genovese D, Addetia K, Kebed K, Kruse E, Yamat M, Narang A, Patel AR, Badano LP, Muraru D, Gonçalves A, Mor-Avi V, and Lang RM
- Subjects
- Heart Diseases physiopathology, Humans, Image Interpretation, Computer-Assisted, Observer Variation, Predictive Value of Tests, Reproducibility of Results, Echocardiography, Three-Dimensional, Heart Diseases diagnostic imaging, Transillumination
- Published
- 2019
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48. Echocardiography and cardiovascular magnetic resonance based evaluation of myocardial strain and relationship with late gadolinium enhancement.
- Author
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Erley J, Genovese D, Tapaskar N, Alvi N, Rashedi N, Besser SA, Kawaji K, Goyal N, Kelle S, Lang RM, Mor-Avi V, and Patel AR
- Subjects
- Adult, Female, Heart Ventricles physiopathology, Humans, Male, Middle Aged, Multimodal Imaging, Myocardial Ischemia physiopathology, Observer Variation, Predictive Value of Tests, Reproducibility of Results, Retrospective Studies, Stroke Volume, Ventricular Dysfunction, Left physiopathology, Echocardiography, Heart Ventricles diagnostic imaging, Magnetic Resonance Imaging, Cine, Myocardial Contraction, Myocardial Ischemia diagnostic imaging, Ventricular Dysfunction, Left diagnostic imaging, Ventricular Function, Left
- Abstract
Objectives: We sought to: (1) determine the agreement in cardiovascular magnetic resonance (CMR) and speckle tracking echocardiography (STE) derived strain measurements, (2) compare their reproducibility, (3) determine which approach is best related to CMR late gadolinium enhancement (LGE)., Background: While STE-derived strain is routinely used to assess left ventricular (LV) function, CMR strain measurements are not yet standardized. Strain can be measured using dedicated pulse sequences (strain-encoding, SENC), or post-processing of cine images (feature tracking, FT). It is unclear whether these measurements are interchangeable, and whether strain can be used as an alternative to LGE., Methods: Fifty patients underwent 2D echocardiography and 1.5 T CMR. Global longitudinal strain (GLS) was measured by STE (Epsilon), FT (NeoSoft) and SENC (Myocardial Solutions) and circumferential strain (GCS) by FT and SENC., Results: GLS showed good inter-modality agreement (r-values: 0.71-0.75), small biases (< 1%) but considerable limits of agreement (- 7 to 8%). The agreement between the CMR techniques was better for GLS than GCS (r = 0.81 vs 0.67; smaller bias). Repeated measurements showed low intra- and inter-observer variability for both GLS and GCS (intraclass correlations 0.86-0.99; coefficients of variation 3-13%). LGE was present in 22 (44%) of patients. Both SENC- and FT-derived GLS and GCS were associated with LGE, while STE-GLS was not. Irrespective of CMR technique, this association was stronger for GCS (AUC 0.77-0.78) than GLS (AUC 0.67-0.72) and STE-GLS (AUC = 0.58)., Conclusion: There is good inter-technique agreement in strain measurements, which were highly reproducible, irrespective of modality or analysis technique. GCS may better reflect the presence of underlying LGE than GLS.
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- 2019
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49. Cardiac Implantable Electronic Device Lead-Induced Tricuspid Regurgitation.
- Author
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Addetia K, Harb SC, Hahn RT, Kapadia S, and Lang RM
- Subjects
- Cardiac Catheterization, Device Removal, Diuretics therapeutic use, Echocardiography, Heart Valve Prosthesis Implantation, Humans, Prosthesis Design, Risk Factors, Severity of Illness Index, Tricuspid Valve diagnostic imaging, Tricuspid Valve Insufficiency diagnostic imaging, Tricuspid Valve Insufficiency physiopathology, Tricuspid Valve Insufficiency therapy, Defibrillators, Implantable adverse effects, Hemodynamics, Pacemaker, Artificial adverse effects, Tricuspid Valve physiopathology, Tricuspid Valve Insufficiency etiology
- Abstract
With the expanding use of cardiac implantable electronic device (CIEDs) in an ever-aging population, the looming problem of CIED-associated interference with the tricuspid valve is significant. The first pacemaker was implanted in 1958 for severe symptomatic bradycardia. The concept of a device to avert sudden cardiac death (i.e., the defibrillator) was first published in 1970 by Mirowski and Mower. The first reports of CIED-mediated tricuspid valve apparatus interference surfaced in the late 1900s, but it was not until recently that concentrated efforts have been made to better define the scope of CIED-mediated interference with the tricuspid valve apparatus. Because stopping implantation of these devices is not an option, better understanding of their mechanical complications could potentially lead to improvements in device design or epicardial device implantation, as an alternative, in select patients. This review covers existing evidence for CIED-mediated tricuspid regurgitation, discusses potential mechanisms of CIED-mediated interference of the tricuspid valve apparatus, provides an overview of how to diagnose CIED-mediated interference on echocardiography, and discusses management strategies for patients who have CIED-mediated severe tricuspid regurgitation., (Copyright © 2019 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.)
- Published
- 2019
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50. 3-Dimensional Echocardiographic Analysis of the Tricuspid Annulus Provides New Insights Into Tricuspid Valve Geometry and Dynamics.
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Addetia K, Muraru D, Veronesi F, Jenei C, Cavalli G, Besser SA, Mor-Avi V, Lang RM, and Badano LP
- Subjects
- Adult, Body Size, Chicago, Diastole, Female, Healthy Volunteers, Humans, Italy, Male, Middle Aged, Observer Variation, Predictive Value of Tests, Reproducibility of Results, Sex Factors, Systole, Tomography, X-Ray Computed, Echocardiography, Three-Dimensional, Hemodynamics, Tricuspid Valve diagnostic imaging, Tricuspid Valve physiology
- Abstract
Objectives: The authors used transthoracic 3-dimensional transthoracic echocardiography (3DE) to characterize tricuspid annulus (TA) geometry and dynamics in healthy volunteers., Background: Accurate sizing of the TA is essential for planning tricuspid annuloplasty and for implantation of new percutaneous tricuspid devices., Methods: 3DE of the TA from 209 healthy volunteers was analyzed using custom software to measure TA area, perimeter, circularity, and dimensions at end diastole (equals tricuspid valve closure), mid-systole, end systole, and late diastole. TA intercommissural distances were measured at mid-systole. For comparison, TA diameters were measured at the same time points on multiplanar reconstruction of the 3DE datasets and on 2-dimensional transthoracic echocardiography (2DE) apical 4-chamber and right ventricular focused views. In 13 subjects with both 3DE and computed tomography, TA parameters were compared., Results: 3DE TA area, perimeter, and dimensions were largest in late diastole and smallest at mid-systole/end systole. Normal tricuspid valve parameters in end diastole were 8.6 ± 2.0 cm
2 for area; 10.5 ± 1.2 cm for perimeter; 36 ± 4 mm and 30 ± 4 mm for longest and shortest dimensions, respectively; and 0.83 ± 0.10 for circularity. There were no age-related changes in TA parameters. Women had larger indexed TA perimeter and longer long-axis dimensions compared with men. The longest 3DE TA dimension was significantly longer than diameters measured from both 2DE and 3D multiplanar reconstruction. 3DE TA area, perimeter, and dimensions correlated with both right atrial and right ventricular volumes, suggesting that both chambers may be determinants of TA size. TA fractional area change was 35 ± 10%. Fractional changes in both perimeter and dimensions were ≥20%. When compared with computed tomography, 3DE systematically underestimated TA parameters., Conclusions: Gender and body size should be taken into account to identify the reference values of TA dimensions. 2DE underestimates TA dimensions., (Copyright © 2019 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.)- Published
- 2019
- Full Text
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