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Author

Lawrence Rajan

Other affiliations: University of Kentucky
Bio: Lawrence Rajan is an academic researcher from HealthPartners. The author has contributed to research in topics: Acute coronary syndrome & Percutaneous coronary intervention. The author has an hindex of 10, co-authored 19 publications receiving 1663 citations. Previous affiliations of Lawrence Rajan include University of Kentucky.

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Journal ArticleDOI
TL;DR: Patients with takotsubo cardiomyopathy had a higher prevalence of neurologic or psychiatric disorders than did those with an acute coronary syndrome and physical triggers, acute neurologics or psychiatric diseases, high troponin levels, and a low ejection fraction on admission were independent predictors for in-hospital complications.
Abstract: BackgroundThe natural history, management, and outcome of takotsubo (stress) cardiomyopathy are incompletely understood. MethodsThe International Takotsubo Registry, a consortium of 26 centers in Europe and the United States, was established to investigate clinical features, prognostic predictors, and outcome of takotsubo cardiomyopathy. Patients were compared with age- and sex-matched patients who had an acute coronary syndrome. ResultsOf 1750 patients with takotsubo cardiomyopathy, 89.8% were women (mean age, 66.8 years). Emotional triggers were not as common as physical triggers (27.7% vs. 36.0%), and 28.5% of patients had no evident trigger. Among patients with takotsubo cardiomyopathy, as compared with an acute coronary syndrome, rates of neurologic or psychiatric disorders were higher (55.8% vs. 25.7%) and the mean left ventricular ejection fraction was markedly lower (40.7±11.2% vs. 51.5±12.3%) (P<0.001 for both comparisons). Rates of severe in-hospital complications including shock and death were ...

1,721 citations

Journal ArticleDOI
Jelena-R. Ghadri1, Ken Kato1, Victoria L. Cammann1, Sebastiano Gili1, Stjepan Jurisic1, Davide Di Vece1, Alessandro Candreva1, Katharina J. Ding1, Jozef Micek1, Konrad A. Szawan1, Beatrice Bacchi1, Rahel Bianchi1, Rena A. Levinson2, Manfred Wischnewsky3, Burkhardt Seifert1, Susanne A. Schlossbauer1, Rodolfo Citro, Eduardo Bossone, Thomas Münzel, Maike Knorr, Susanne Heiner, Fabrizio D'Ascenzo4, Jennifer Franke5, Annahita Sarcon6, L. Christian Napp7, Miłosz Jaguszewski8, Michel Noutsias9, Hugo A. Katus5, Christof Burgdorf, Heribert Schunkert10, Holger Thiele11, Johann Bauersachs7, Carsten Tschöpe12, Burkert Pieske12, Lawrence Rajan13, Guido Michels14, Roman Pfister14, Alessandro Cuneo, Claudius Jacobshagen15, Gerd Hasenfuß15, Mahir Karakas16, Wolfgang Koenig10, Wolfgang Rottbauer17, Samir M. Said18, Ruediger C. Braun-Dullaeus18, Adrian P. Banning19, Florim Cuculi, Richard Kobza, Thomas Fischer20, Tuija Vasankari21, K.E. Juhani Airaksinen21, Grzegorz Opolski22, Rafal Dworakowski13, Philip MacCarthy13, Christoph Kaiser23, Stefan Osswald23, Leonarda Galiuto24, Filippo Crea24, Wolfgang Dichtl, Klaus Empen25, Stephan B. Felix25, Clément Delmas, Olivier Lairez, Ibrahim El-Battrawy26, Ibrahim Akin26, Martin Borggrefe26, John D. Horowitz27, Martin Kozel28, Petr Tousek28, Petr Widimský28, Ekaterina Gilyarova, Alexandra Shilova, Mikhail Gilyarov, David E. Winchester29, Christian Ukena, Jeroen J. Bax30, Abhiram Prasad31, Michael Böhm, Thomas F. Lüscher32, Frank Ruschitzka1, Christian Templin1 
TL;DR: It is demonstrated that TTS can either be benign or a life-threating condition depending on the inciting stress factor, and a new classification based on triggers is proposed, which can serve as a clinical tool to predict short- and long-term outcomes of TTS.

192 citations

Journal ArticleDOI
Sebastiano Gili1, Sebastiano Gili2, Victoria L. Cammann2, Susanne A. Schlossbauer2, Ken Kato2, Fabrizio D'Ascenzo1, Davide Di Vece2, Stjepan Jurisic2, Jozef Micek2, Slayman Obeid2, Beatrice Bacchi2, Konrad A. Szawan2, Flurina Famos2, Annahita Sarcon3, Rena A. Levinson4, Rena A. Levinson2, Katharina J. Ding2, Burkhardt Seifert2, Olivia Lenoir2, Eduardo Bossone, Rodolfo Citro, Jennifer Franke5, L. Christian Napp6, Miłosz Jaguszewski7, Michel Noutsias8, Thomas Münzel, Maike Knorr, Susanne Heiner, Hugo A. Katus5, Christof Burgdorf, Heribert Schunkert9, Holger Thiele10, Johann Bauersachs6, Carsten Tschöpe11, Burkert Pieske11, Lawrence Rajan12, Guido Michels13, Roman Pfister13, Alessandro Cuneo, Claudius Jacobshagen14, Gerd Hasenfuß, Mahir Karakas, Wolfgang Koenig9, Wolfgang Rottbauer15, Samir M. Said16, Ruediger C. Braun-Dullaeus16, Adrian P. Banning17, Florim Cuculi, Richard Kobza, Thomas Fischer18, Tuija Vasankari19, K.E. Juhani Airaksinen19, Grzegorz Opolski20, Rafal Dworakowski12, Philip MacCarthy12, Christoph Kaiser21, Stefan Osswald21, Leonarda Galiuto22, Filippo Crea22, Wolfgang Dichtl, Klaus Empen23, Stephan B. Felix23, Clément Delmas, Olivier Lairez, Ibrahim El-Battrawy24, Ibrahim Akin24, Martin Borggrefe24, Ekaterina Gilyarova, Alexandra Shilova, Mikhail Gilyarov, John D. Horowitz25, Martin Kozel26, Petr Tousek26, Petr Widimský26, David E. Winchester27, Christian Ukena, Fiorenzo Gaita1, Carlo Di Mario, Manfred Wischnewsky28, Jeroen J. Bax29, Abhiram Prasad30, Michael Böhm, Frank Ruschitzka2, Thomas F. Lüscher2, Thomas F. Lüscher31, Jelena R. Ghadri2, Christian Templin2 
TL;DR: Clinical and electrocardiographic parameters independently predicted mortality after cardiac arrest in takotsubo syndrome and cardiac arrest is relatively frequent in TTS and is associated with higher short- and long-term mortality.
Abstract: AIMS We aimed to evaluate the frequency, clinical features, and prognostic implications of cardiac arrest (CA) in takotsubo syndrome (TTS). METHODS AND RESULTS We reviewed the records of patients with CA and known heart rhythm from the International Takotsubo Registry. The main outcomes were 60-day and 5-year mortality. In addition, predictors of mortality and predictors of CA during the acute TTS phase were assessed. Of 2098 patients, 103 patients with CA and known heart rhythm during CA were included. Compared with patients without CA, CA patients were more likely to be younger, male, and have apical TTS, atrial fibrillation (AF), neurologic comorbidities, physical triggers, and longer corrected QT-interval and lower left ventricular ejection fraction on admission. In all, 57.1% of patients with CA at admission had ventricular fibrillation/tachycardia, while 73.7% of patients with CA in the acute phase had asystole/pulseless electrical activity. Patients with CA showed higher 60-day (40.3% vs. 4.0%, P < 0.001) and 5-year mortality (68.9% vs. 16.7%, P < 0.001) than patients without CA. T-wave inversion and intracranial haemorrhage were independently associated with higher 60-day mortality after CA, whereas female gender was associated with lower 60-day mortality. In the acute phase, CA occurred less frequently in females and more frequently in patients with AF, ST-segment elevation, and higher C-reactive protein on admission. CONCLUSIONS Cardiac arrest is relatively frequent in TTS and is associated with higher short- and long-term mortality. Clinical and electrocardiographic parameters independently predicted mortality after CA.

65 citations

Journal ArticleDOI
TL;DR: The International Takotsubo Registry (www.takotubo-registry.com) is an observational, prospective, and retrospective registry established at the University Hospital Zurich in 2011, with the largest TTS database worldwide.
Abstract: The clinical course of takotsubo syndrome (TTS) can be complicated by several life-threatening conditions. In particular, cardiogenic shock (CS) represents one of the leading causes of mortality in the acute phase and occurs in a considerable number of patients with TTS, with an incidence of ≈10%. At present, no established guidelines are available to support specific treatment recommendations,and the conventional therapy for CS leads to uncertain results in TTS cases. The International Takotsubo Registry (www.takotsubo-registry.com) is an observational, prospective, and retrospective registry established at the University Hospital Zurich in 2011, with the largest TTS database worldwide. Patients were included in the registry between 2011 and 2017 based on modified Mayo Clinic Diagnostic criteria. Hospitalization data were recorded through standardized forms on admission or during revision of clinical charts; follow-up data were obtained from medical records, telephone follow-up, or clinical visits. The study population was categorized into 2 groups: patients with TTS with and without CS. The study protocol was reviewed by the respective local ethics committees or investigational review boards at each collaboration site. Where informed consent was required, formal written consent was obtained from patients.

61 citations

Journal ArticleDOI
L. Christian Napp1, Victoria L. Cammann2, Miłosz Jaguszewski3, Konrad A. Szawan2, Manfred Wischnewsky4, Sebastiano Gili, Maike Knorr, Susanne Heiner, Rodolfo Citro, Eduardo Bossone, Fabrizio D'Ascenzo5, Michael Neuhaus, Jennifer Franke6, Ioana Sorici-Barb6, Michel Noutsias7, Christof Burgdorf, Wolfgang Koenig8, Behrouz Kherad9, Annahita Sarcon10, Lawrence Rajan11, Guido Michels12, Roman Pfister12, Alessandro Cuneo, Claudius Jacobshagen13, Mahir Karakas, Alexander Pott14, Philippe Meyer, Jose David Arroja, Adrian P. Banning15, Florim Cuculi, Richard Kobza, Thomas Fischer16, Tuija Vasankari17, K.E. Juhani Airaksinen17, Christian Hauck18, Carla Paolini, Claudio Bilato, Yoichi Imori19, Ken Kato20, Yoshio Kobayashi20, Grzegorz Opolski21, Monika Budnik21, Rafal Dworakowski22, Philip MacCarthy22, Christoph Kaiser23, Stefan Osswald23, Leonarda Galiuto24, Wolfgang Dichtl, Christina Chan25, Paul Bridgman25, Daniel Beug26, Clément Delmas, Olivier Lairez, Ibrahim El-Battrawy27, Ibrahim Akin27, Ekaterina Gilyarova, Alexandra Shilova, Mikhail Gilyarov, John D. Horowitz28, Karolina Polednikova29, Petr Tousek29, Petr Widimský29, David E. Winchester30, Jan Galuszka, Christian Ukena, Gregor Poglajen, Pedro Carrilho-Ferreira31, Carlo Di Mario, Abhiram Prasad32, Charanjit S. Rihal32, P. Christian Schulze33, Matteo Bianco, Filippo Crea24, Martin Borggrefe27, Lars S. Maier18, Fausto J. Pinto31, Ruediger C. Braun-Dullaeus34, Wolfgang Rottbauer14, Hugo A. Katus6, Gerd Hasenfuß13, Carsten Tschöpe9, Burkert Pieske9, Holger Thiele35, Heribert Schunkert8, Michael Böhm, Stephan B. Felix26, Thomas Münzel, Jeroen J. Bax36, Johann Bauersachs1, Eugene Braunwald37, Thomas F. Lüscher2, Thomas F. Lüscher38, Frank Ruschitzka2, Jelena R. Ghadri2, Christian Templin2 
TL;DR: Coronary artery disease frequently coexists in TTS patients, presents with the whole spectrum of coronary pathology including acute coronary occlusion, and is associated with adverse outcome.
Abstract: AIMS Takotsubo syndrome (TTS) is an acute heart failure syndrome, which shares many features with acute coronary syndrome (ACS). Although TTS was initially described with angiographically normal coronary arteries, smaller studies recently indicated a potential coexistence of coronary artery disease (CAD) in TTS patients. This study aimed to determine the coexistence, features, and prognostic role of CAD in a large cohort of patients with TTS. METHODS AND RESULTS Coronary anatomy and CAD were studied in patients diagnosed with TTS. Inclusion criteria were compliance with the International Takotsubo Diagnostic Criteria for TTS, and availability of original coronary angiographies with ventriculography performed during the acute phase. Exclusion criteria were missing views, poor quality of angiography loops, and angiography without ventriculography. A total of 1016 TTS patients were studied. Of those, 23.0% had obstructive CAD, 41.2% had non-obstructive CAD, and 35.7% had angiographically normal coronary arteries. A total of 47 patients (4.6%) underwent percutaneous coronary intervention, and 3 patients had acute and 8 had chronic coronary artery occlusion concomitant with TTS, respectively. The presence of CAD was associated with increased incidence of shock, ventilation, and death from any cause. After adjusting for confounders, the presence of obstructive CAD was associated with mortality at 30 days. Takotsubo syndrome patients with obstructive CAD were at comparable risk for shock and death and nearly at twice the risk for ventilation compared to an age- and sex-matched ACS cohort. CONCLUSIONS Coronary artery disease frequently coexists in TTS patients, presents with the whole spectrum of coronary pathology including acute coronary occlusion, and is associated with adverse outcome. TRIAL REGISTRATION ClinicalTrials.gov number: NCT01947621.

48 citations


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TL;DR: This dissertation aims to provide a history of web exceptionalism from 1989 to 2002, a period chosen in order to explore its roots as well as specific cases up to and including the year in which descriptions of “Web 2.0” began to circulate.
Abstract: Kristian Thygesen∗ (Denmark) Joseph S. Alpert∗ (USA) Allan S. Jaffe (USA) Bernard R. Chaitman (USA) Jeroen J. Bax (The Netherlands) David A. Morrow (USA) Harvey D. White∗ (New Zealand) Hans Mickley (Denmark) Filippo Crea (Italy) Frans Van de Werf (Belgium) Chiara Bucciarelli-Ducci (

3,355 citations

Journal ArticleDOI
TL;DR: From the Department of Medicine, Division of Translational Medicine and Human Genetics, Center for Cytokine Storm Treatment and Laboratory, and the Center for Cellular Immunotherapies and the Parker Institute for Cancer Immunotherapy, University of Pennsylvania, Philadelphia.
Abstract: From the Department of Medicine, Division of Translational Medicine and Human Genetics, Center for Cytokine Storm Treatment and Laboratory (D.C.F.), and the Center for Cellular Immunotherapies and the Parker Institute for Cancer Immunotherapy (C.H.J.), Perelman School of Medicine, University of Pennsylvania, Philadelphia. Address reprint requests to Dr. Fajgenbaum at davidfa@ pennmedicine . upenn . edu or to Dr. June at cjune@ upenn . edu.

1,517 citations

Journal ArticleDOI
TL;DR: The clinical expert consensus document part I summarizes the current state of knowledge on clinical presentation and characteristics of TTS and agrees on controversies surrounding TTS such as nomenclature, different TTS types, role of coronary artery disease, and etiology.
Abstract: Takotsubo syndrome (TTS) is a poorly recognized heart disease that was initially regarded as a benign condition. Recently, it has been shown that TTS may be associated with severe clinical complications including death and that its prevalence is probably underestimated. Since current guidelines on TTS are lacking, it appears timely and important to provide an expert consensus statement on TTS. The clinical expert consensus document part I summarizes the current state of knowledge on clinical presentation and characteristics of TTS and agrees on controversies surrounding TTS such as nomenclature, different TTS types, role of coronary artery disease, and etiology. This consensus also proposes new diagnostic criteria based on current knowledge to improve diagnostic accuracy.

903 citations

Journal ArticleDOI
TL;DR: Novel structured approaches to diagnosis, risk stratification, and management are presented, with new algorithms to aid decision‐making by practising clinicians in the management of complex cases with ongoing symptoms after recovery, recurrent episodes, or spontaneous presentation.
Abstract: Takotsubo syndrome is an acute reversible heart failure syndrome that is increasingly recognized in modern cardiology practice. This Position Statement from the European Society of Cardiology Heart Failure Association provides a comprehensive review of the various clinical and pathophysiological facets of Takotsubo syndrome, including nomenclature, definition, and diagnosis, primary and secondary clinical subtypes, anatomical variants, triggers, epidemiology, pathophysiology, clinical presentation, complications, prognosis, clinical investigations, and treatment approaches. Novel structured approaches to diagnosis, risk stratification, and management are presented, with new algorithms to aid decision-making by practising clinicians. These also cover more complex areas (e.g. uncertain diagnosis and delayed presentation) and the management of complex cases with ongoing symptoms after recovery, recurrent episodes, or spontaneous presentation. The unmet needs and future directions for research in this syndrome are also discussed.

784 citations