Browsing by Author "Vukcevic, Vladan (15741934700)"
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Publication A multicentre, prospective, randomised controlled trial to assess the safety and effectiveness of cooling as an adjunctive therapy to percutaneous intervention in patients with acute myocardial infarction: The COOL AMI EU Pivotal Trial(2021) ;Noc, Marko (7004055753) ;Laanmets, Peep (55345333500) ;Neskovic, Aleksandar N. (35597744900) ;Petrović, Milovan (16234216100) ;Stanetic, Bojan (56624448800) ;Aradi, Daniel (22984252200) ;Kiss, Robert G. (57050400100) ;Ungi, Imre (6602555341) ;Merkely, Béla (7004434435) ;Hudec, Martin (57517803300) ;Blasko, Peter (21233522600) ;Horvath, Ivan (35315794200) ;Davies, John R. (56939639900) ;Vukcevic, Vladan (15741934700) ;Holzer, Michael (15740955800) ;Metzler, Bernhard (56180476500) ;Witkowski, Adam (7005762608) ;Erglis, Andrejs (6602259794) ;Fister, Misa (13105598500) ;Nagy, Gergely (57195331558) ;Bulum, Josko (23017736900) ;Edes, Istvan (7003689191) ;Peruga, Jan Z. (6603426226) ;Średniawa, Beata (57197282694) ;Erlinge, David (7005319185)Keeble, Thomas R. (20334838200)Background: Despite primary PCI (PPCI), ST-elevation myocardial infarction (STEMI) can still result in large infarct size (IS). New technology with rapid intravascular cooling showed positive signals for reduction in IS in anterior STEMI. Aims: We investigated the effectiveness and safety of rapid systemic intravascular hypothermia as an adjunct to PPCI in conscious patients, with anterior STEMI, without cardiac arrest. Methods: Hypothermia was induced using the ZOLL® Proteus™ intravascular cooling system. After randomisation of 111 patients, 58 to hypothermia and 53 to control groups, the study was prematurely discontinued by the sponsor due to inconsistent patient logistics between the groups resulting in significantly longer total ischaemic delay in the hypothermia group (232 vs 188 minutes; p<0.001). Results: There were no differences in angiographic features and PPCI result between the groups. Intravascular temperature at wire crossing was 33.3+0.9°C. Infarct size/left ventricular (IS/LV) mass by cardiac magnetic resonance (CMR) at day 4-6 was 21.3% in the hypothermia group and 20.0% in the control group (p=0.540). Major adverse cardiac events at 30 days increased non-significantly in the hypothermia group (8.6% vs 1.9%; p=0.117) while cardiogenic shock (10.3% vs 0%; p=0.028) and paroxysmal atrial fibrillation (43.1% vs 3.8%; p<0.001) were significantly more frequent in the hypothermia group. Conclusions: The ZOLL Proteus intravascular cooling system reduced temperature to 33.3°C before PPCI in patients with anterior STEMI. Due to inconsistent patient logistics between the groups, this hypothermia protocol resulted in a longer ischaemic delay, did not reduce IS/LV mass and was associated with increased adverse events. © Europa Digital & Publishing 2021. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication Additive prognostic value of the SYNTAX score over GRACE, TIMI, ZWOLLE, CADILLAC and PAMI risk scores in patients with acute ST-segment elevation myocardial infarction treated by primary percutaneous coronary intervention(2013) ;Brkovic, Voin (55602397800) ;Dobric, Milan (23484928600) ;Beleslin, Branko (6701355424) ;Giga, Vojislav (55924460200) ;Vukcevic, Vladan (15741934700) ;Stojkovic, Sinisa (6603759580) ;Stankovic, Goran (59150945500) ;Nedeljkovic, Milan A. (7004488186) ;Orlic, Dejan (7006351319) ;Tomasevic, Miloje (57196948758) ;Stepanovic, Jelena (6603897710)Ostojic, Miodrag (34572650500)This study evaluated additive prognostic value of the SYNTAX score over GRACE, TIMI, ZWOLLE, CADILLAC and PAMI risk scores in patients with STsegment elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (pPCI). All six scores were calculated in 209 consecutive STEMI patients undergoing pPCI. Primary end-point was the major adverse cardiovascular event (MACE-composite of cardiovascular mortality, non-fatal myocardial infarction and stroke); secondary end point was cardiovascular mortality. Patients were stratified according to the SYNTAX score tertiles (≤12; between 12 and 19.5; >19.5). The median follow-up was 20 months. Rates of MACE and cardiovascular mortality were highest in the upper tertile of the SYNTAX score (p<0.001 and p = 0.003, respectively). SYNTAX score was independent multivariable predictor of MACE and cardiovascular mortality when added to GRACE, TIMI, ZWOLLE, and PAMI risk scores. However, the SYNTAX score did not improve the Cox regression models of MACE and cardiovascular mortality when added to the CADILLAC score. The SYNTAX score has predictive value for MACE and cardiovascular mortality in patients with STEMI undergoing primary PCI. Furthermore, SYNTAX score improves prognostic performance of well-established GRACE, TIMI, ZWOLLE and PAMI clinical scores, but not the CADILLAC risk score. Therefore, long-term survival in patients after STEMI depends less on detailed angiographical characterization of coronary lesions, but more on clinical characteristics, myocardial function and basic angiographic findings as provided by the CADILLAC score. - Some of the metrics are blocked by yourconsent settings
Publication Complex angioplasty up to chronic total occlusion(2006) ;Nedeljkovic, Milan A. (7004488186) ;Ostojic, Miodrag C. (34572650500) ;Saito, Shigeru (7404854449) ;Seferovic, Petar M. (6603594879) ;Beleslin, Branko (6701355424) ;Stankovic, Goran (59150945500) ;Stojkovic, Sinisa (6603759580) ;Vukcevic, Vladan (15741934700) ;Saponjski, Jovica (56629875900)Orlic, Dejan (7006351319)[No abstract available] - Some of the metrics are blocked by yourconsent settings
Publication COOL AMI EU pilot trial: A multicentre, prospective, randomised controlled trial to assess cooling as an adjunctive therapy to percutaneous intervention in patients with acute myocardial infarction(2017) ;Noc, Marko (7004055753) ;Erlinge, David (7005319185) ;Neskovic, Aleksandar N. (35597744900) ;Kafedzic, Srdjan (55246101300) ;Merkely, Béla (7004434435) ;Zima, Endre (7003913627) ;Fister, Misa (13105598500) ;Petrović, Milovan (16234216100) ;Čanković, Milenko (57204401342) ;Veress, Gábor (59099028800) ;Laanmets, Peep (55345333500) ;Pern, Teele (57195330004) ;Vukcevic, Vladan (15741934700) ;Dedovic, Vladimir (55959310400) ;Średniawa, Beata (57197282694) ;Światkowski, Andrzej (57204007408) ;Keeble, Thomas R. (20334838200) ;Davies, John R. (56939639900) ;Warenits, Alexandra-Maria (55317914100) ;Olivecrona, Göran (8656313100) ;Peruga, Jan Zbigniew (6603426226) ;Ciszewski, Michal (6602484219) ;Horvath, Ivan (35315794200) ;Edes, Istvan (7003689191) ;Nagy, Gergely Gyorgy (57195331558) ;Aradi, Daniel (22984252200)Holzer, Michael (15740955800)Aims: We aimed to investigate the rapid induction of therapeutic hypothermia using the ZOLL Proteus Intravascular Temperature Management System in patients with anterior ST-elevation myocardial infarction (STEMI) without cardiac arrest. Methods and results: A total of 50 patients were randomised; 22 patients (88%; 95% confidence interval [CI]: 69-97%) in the hypothermia group and 23 patients (92%; 95% CI: 74-99) in the control group completed cardiac magnetic resonance imaging at four to six days and 30-day follow-up. Intravascular temperature at coronary guidewire crossing after 20.5 minutes of endovascular cooling decreased to 33.6°C (range 31.9-35.5°C). There was a 17-minute (95% CI: 4.6-29.8 min) cooling-related delay to reperfusion. In "per protocol" analysis, median infarct size/left ventricular mass was 16.7% in the hypothermia group versus 23.8% in the control group (absolute reduction 7.1%, relative reduction 30%; p=0.31) and median left ventricular ejection fraction (LVEF) was 42% in the hypothermia group and 40% in the control group (absolute reduction 2.4%, relative reduction 6%; p=0.36). Except for self-terminating paroxysmal atrial fibrillation (32% versus 8%; p=0.074), there was no excess of adverse events in the hypothermia group. Conclusions: We rapidly and safely cooled patients with anterior STEMI to 33.6°C at the time of coronary guidewire crossing. This is ≥1.1°C lower than in previous cooling studies. Except for self-terminating atrial fibrillation, there was no excess of adverse events and no clinically important cooling-related delay to reperfusion. A statistically non-significant numerical 7.1% absolute and 30% relative reduction in infarct size warrants a pivotal trial powered for efficacy. © Europa Digital & Publishing 2017. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication Coronary flow velocity reserve using dobutamine test for noninvasive functional assessment of myocardial bridging(2022) ;Aleksandric, Srdjan B. (35274271700) ;Djordjevic-Dikic, Ana D. (57003143600) ;Giga, Vojislav L. (55924460200) ;Tesic, Milorad B. (36197477200) ;Soldatovic, Ivan A. (35389846900) ;Banovic, Marko D. (33467553500) ;Dobric, Milan R. (23484928600) ;Vukcevic, Vladan (15741934700) ;Tomasevic, Miloje V. (57196948758) ;Orlic, Dejan N. (7006351319) ;Boskovic, Nikola (6508290354) ;Jovanovic, Ivana (57223117334) ;Nedeljkovic, Milan A. (7004488186) ;Stankovic, Goran (59150945500) ;Ostojic, Miodrag C. (34572650500)Beleslin, Branko D. (6701355424)Background: It has been shown that coronary flow velocity reserve (CFVR) measurement by transthoracic Doppler echocardiography (TTDE) during dobutamine (DOB) provocation provides a more accurate functional evaluation of myocardial bridging (MB) compared to adenosine. However; the cut-off value of CFVR during DOB for identification of MB associated with myocardial ischemia has not been fully clarified. Purpose: This prospective study aimed to determine the cut-off value of TTDE-CFVR during DOB in patients with isolated-MB, as compared with stress-induced wall motion abnormalities (VMA) during exercise stress-echocardiography (SE) as reference. Methods: Eighty-one symptomatic patients (55 males [68%], mean age 56 ± 10 years; range: 27–74 years) with the existence of isolated-MB on the left anterior descending artery (LAD) and systolic MB-compression ≥50% diameter stenosis (DS) were eligible to participate in the study. Each patient underwent treadmill exercise-SE, invasive coronary angiography, and TTDE-CFVR measurements in the distal segment of LAD during DOB infusion (DOB: 10–40 µg/kg/min). Using quantitative coronary angiography, both minimal luminal diameter (MLD) and percent DS at MB-site at end-systole and end-diastole were determined. Results: Stress-induced myocardial ischemia with the occurrence of WMA was found in 23 patients (28%). CFVR during peak DOB was significantly lower in the SE-positive group compared with the SE-negative group (1.94 ± 0.16 vs. 2.78 ± 0.53; p < 0.001). ROC analyses identified the optimal CFVR cut-off value ≤ 2.1 obtained during high-dose dobutamine (>20 µg/kg/min) for the identification of MB associated with stress-induced WMA, with a sensitivity, specificity, positive and negative predictive value of 96%, 95%, 88%, and 98%, respectively (AUC 0.986; 95% CI: 0.967–1.000; p < 0.001). Multivariate logistic regression analysis revealed that MLD and percent DS, both at end-diastole, were the only independent predictors of ischemic CFVR values ≤2.1 (OR: 0.023; 95% CI: 0.001–0.534; p = 0.019; OR: 1.147; 95% CI: 1.042–1.263; p = 0.005; respectively). Conclusions: Non-invasive CFVR during dobutamine provocation appears to be an additional and important noninvasive tool to determine the functional severity of isolated-MB. A transthoracic CFVR cut-off ≤2.1 measured at a high-dobutamine dose may be adequate for detecting myocardial ischemia in patients with isolated-MB. © 2021 by the authors. Licensee MDPI, Basel, Switzerland. - Some of the metrics are blocked by yourconsent settings
Publication Coronary Microcirculation: The Next Frontier in the Management of STEMI(2023) ;Milasinovic, Dejan (24823024500) ;Nedeljkovic, Olga (56958449900) ;Maksimovic, Ruzica (55921156500) ;Sobic-Saranovic, Dragana (57202567582) ;Dukic, Djordje (57919369500) ;Zobenica, Vladimir (58118595100) ;Jelic, Dario (57201640680) ;Zivkovic, Milorad (55959530600) ;Dedovic, Vladimir (55959310400) ;Stankovic, Sanja (7005216636) ;Asanin, Milika (8603366900)Vukcevic, Vladan (15741934700)Although the widespread adoption of timely invasive reperfusion strategies over the last two decades has significantly improved the prognosis of patients with ST-segment elevation myocardial infarction (STEMI), up to half of patients after angiographically successful primary percutaneous coronary intervention (PCI) still have signs of inadequate reperfusion at the level of coronary microcirculation. This phenomenon, termed coronary microvascular dysfunction (CMD), has been associated with impaired prognosis. The aim of the present review is to describe the collected evidence on the occurrence of CMD following primary PCI, means of assessment and its association with the infarct size and clinical outcomes. Therefore, the practical role of invasive assessment of CMD in the catheterization laboratory, at the end of primary PCI, is emphasized, with an overview of available technologies including thermodilution- and Doppler-based methods, as well as recently developing functional coronary angiography. In this regard, we review the conceptual background and the prognostic value of coronary flow reserve (CFR), index of microcirculatory resistance (IMR), hyperemic microvascular resistance (HMR), pressure at zero flow (PzF) and angiography-derived IMR. Finally, the so-far investigated therapeutic strategies targeting coronary microcirculation after STEMI are revisited. © 2023 by the authors. - Some of the metrics are blocked by yourconsent settings
Publication Effect of remote ischaemic conditioning on clinical outcomes in patients with acute myocardial infarction (CONDI-2/ERIC-PPCI): a single-blind randomised controlled trial(2019) ;Hausenloy, Derek J (6602976997) ;Kharbanda, Rajesh K (57202041603) ;Møller, Ulla Kristine (7006233565) ;Ramlall, Manish (56786381300) ;Aarøe, Jens (6602662728) ;Butler, Robert (7401524941) ;Bulluck, Heerajnarain (53981151600) ;Clayton, Tim (26322352300) ;Dana, Ali (15059843000) ;Dodd, Matthew (57206894090) ;Engstrom, Thomas (7004069840) ;Evans, Richard (57204878565) ;Lassen, Jens Flensted (57189389659) ;Christensen, Erika Frischknecht (7202966096) ;Garcia-Ruiz, José Manuel (35955892300) ;Gorog, Diana A (7003699023) ;Hjort, Jakob (6602379009) ;Houghton, Richard F (57211330538) ;Ibanez, Borja (13907649300) ;Knight, Rosemary (14009998600) ;Lippert, Freddy K (7004650443) ;Lønborg, Jacob T (12240126300) ;Maeng, Michael (20034699800) ;Milasinovic, Dejan (24823024500) ;More, Ranjit (7006807960) ;Nicholas, Jennifer M (25630004900) ;Jensen, Lisette Okkels (7403326527) ;Perkins, Alexander (57201567357) ;Radovanovic, Nebojsa (10139867800) ;Rakhit, Roby D (6603035925) ;Ravkilde, Jan (7004165556) ;Ryding, Alisdair D (16246250300) ;Schmidt, Michael R (7404397924) ;Riddervold, Ingunn Skogstad (56878945000) ;Sørensen, Henrik Toft (36038149900) ;Stankovic, Goran (59150945500) ;Varma, Madhusudhan (57211065395) ;Webb, Ian (25423460600) ;Terkelsen, Christian Juhl (7003830752) ;Greenwood, John P (58588572000) ;Yellon, Derek M (7103223278) ;Bøtker, Hans Erik (56962746200) ;Junker, Anders (7006817075) ;Kaltoft, Anne (6602937543) ;Madsen, Morten (35810648300) ;Christiansen, Evald Høj (16149043800) ;Jakobsen, Lars (7004161225) ;Carstensen, Steen (35858179300) ;Kristensen, Steen Dalby (35334519400) ;Thim, Troels (14822428500) ;Pedersen, Karin Møller (58422519200) ;Korsgaard, Mette Tidemand (57211341374) ;Iversen, Allan (24474730000) ;Jørgensen, Erik (35372961000) ;Joshi, Francis (37052277200) ;Pedersen, Frants (55414868300) ;Tilsted, Hans Henrik (23089464900) ;Alzuhairi, Karam (37013099600) ;Saunamäki, Kari (7005608992) ;Holmvang, Lene (6603670977) ;Ahlehof, Ole (57211339575) ;Sørensen, Rikke (18635010900) ;Helqvist, Steffen (6701361402) ;Mark, Bettina Løjmand (57211329546) ;Villadsen, Anton Boel (6602480644) ;Raungaard, Bent (56480714800) ;Thuesen, Leif (7006326598) ;Christiansen, Martin Kirk (57211341955) ;Freeman, Philip (57213032138) ;Jensen, Svend Eggert (7401855023) ;Skov, Charlotte Schmidt (57015004300) ;Aziz, Ahmed (7103371963) ;Hansen, Henrik Steen (7403334070) ;Ellert, Julia (35175814800) ;Veien, Karsten (24172249100) ;Pedersen, Knud Erik (7201733433) ;Hansen, Knud Nørregård (17342237800) ;Ahlehoff, Ole (25932048400) ;Cappelen, Helle (57191952080) ;Wittrock, Daniel (57211330017) ;Hansen, Poul Anders (55909196000) ;Ankersen, Jens Peter (6507525260) ;Hedegaard, Kim Witting (57211337434) ;Kempel, John (57211338262) ;Kaus, Henning (57211339295) ;Erntgaard, Dennis (57211342211) ;Pedersen, Danny Mejsner (55932322100) ;Giebner, Matthias (36028067400) ;Hansen, Troels Martin Hansen (7401668134) ;Radosavljevic-Radovanovic, Mina (10141617200) ;Prodanovic, Maja (57211335833) ;Savic, Lidija (16507811000) ;Pejic, Marijana (58491942500) ;Matic, Dragan (25959220100) ;Uscumlic, Ana (56807174000) ;Subotic, Ida (57213608856) ;Lasica, Ratko (14631892300) ;Vukcevic, Vladan (15741934700) ;Suárez, Alfonso (57201591949) ;Samaniego, Beatriz (57194448507) ;Morís, César (57221077664) ;Segovia, Eduardo (56680965600) ;Hernández, Ernesto (57197255066) ;Lozano, Iñigo (35448203700) ;Pascual, Isaac (24765156600) ;Vegas-Valle, Jose M. (15052696600) ;Rozado, José (55933459100) ;Rondán, Juan (9737126400) ;Avanzas, Pablo (6603073164) ;del Valle, Raquel (57221975129) ;Padrón, Remigio (56814625000) ;García-Castro, Alfonso (57211338205) ;Arango, Amalia (57211334813) ;Medina-Cameán, Ana B. (56298180900) ;Fente, Ana I. (57211336771) ;Muriel-Velasco, Ana (6504808603) ;Pomar-Amillo, Ángeles (57211330414) ;Roza, César L. (57211336240) ;Martínez-Fernández, César M. (57211335946) ;Buelga-Díaz, Covadonga (57211335767) ;Fernández-Gonzalo, David (57211329736) ;Fernández, Elena (57211331749) ;Díaz-González, Eloy (57211329470) ;Martinez-González, Eugenio (57211331389) ;Iglesias-Llaca, Fernando (18433859100) ;Viribay, Fernando M. (57211335779) ;Fernández-Mallo, Francisco J. (57211337671) ;Hermosa, Francisco J. (57211342503) ;Martínez-Bastida, Ginés (57209663244) ;Goitia-Martín, Javier (57211331283) ;Vega-Fernández, José L. (57211334404) ;Tresguerres, Jose M. (57211338699) ;Rodil-Díaz, Juan A. (57211339335) ;Villar-Fernández, Lara (57211329788) ;Alberdi, Lucía (57682138100) ;Abella-Ovalle, Luis (57211332517) ;de la Roz, Manuel (57211340124) ;Fernández-Carral, Marcos Fernández-Carral (6504756139) ;Naves, María C. (57211340074) ;Peláez, María C. (57211343600) ;Fuentes, María D. (57725086400) ;García-Alonso, María (57211330183) ;Villanueva, María J. (57211340216) ;Vinagrero, María S. (57211340720) ;Vázquez-Suárez, María (57211334602) ;Martínez-Valle, Marta (57211343648) ;Nonide, Marta (57211334019) ;Pozo-López, Mónica (57211337596) ;Bernardo-Alba, Pablo (57211337894) ;Galván-Núñez, Pablo (57189388013) ;Martínez-Pérez, Polácido J. (57211330496) ;Castro, Rafael (56443463500) ;Suárez-Coto, Raquel (57211335463) ;Suárez-Noriega, Raquel (57211343572) ;Guinea, Rocío (57211342607) ;Quintana, Rosa B. (57209238064) ;de Cima, Sara (57195104496) ;Hedrera, Segundo A. (57211341192) ;Laca, Sonia I. (57211332178) ;Llorente-Álvarez, Susana (6506960214) ;Pascual, Susana (57211343312) ;Cimas, Teodorna (57211330630) ;Mathur, Anthony (7201657327) ;McFarlane-Henry, Eleanor (57211336506) ;Leonard, Gerry (59204280600) ;Veerapen, Jessry (57189517525) ;Westwood, Mark (7006465445) ;Colicchia, Martina (57196055412) ;Prossora, Mary (57211340454) ;Andiapen, Mervyn (55695133000) ;Mohiddin, Saidi (6701721053) ;Lenzi, Valentina (57211330027) ;Chong, Jun (57211337944) ;Francis, Rohin (57194779300) ;Pine, Amy (55975487500) ;Jamieson-Leadbitter, Caroline (56497197500) ;Neal, Debbie (57211335494) ;Din, J. (6603118036) ;McLeod, Jane (57130049800) ;Roberts, Josh (57209254763) ;Polokova, Karin (6504339016) ;Longman, Kristel (7801502860) ;Penney, Lucy (57211343136) ;Lakeman, Nicki (57203933005) ;Wells, Nicki (57211337725) ;Hopper, Oliver (57211339149) ;Coward, Paul (57211335527) ;O'Kane, Peter (36658419200) ;Harkins, Ruth (57211332105) ;Guyatt, Samantha (57211333578) ;Kennard, Sarah (57211336780) ;Orr, Sarah (57212859469) ;Horler, Stephanie (57211335145) ;Morris, Steve (59848831900) ;Walvin, Tom (57211337708) ;Snow, Tom (55749613700) ;Cunnington, Michael (24480525500) ;Burd, Amanda (57211341451) ;Gowing, Anne (57211341939) ;Krishnamurthy, Arvindra (55646227400) ;Harland, Charlotte (56286912200) ;Norfolk, Derek (7004128169) ;Johnstone, Donna (57211330306) ;Newman, Hannah (58433341600) ;Reed, Helen (57200047680) ;O'Neill, James (58387268100) ;Greenwood, John (23008007100) ;Cuxton, Josephine (57211343055) ;Corrigan, Julie (57211332784) ;Somers, Kathryn (55932379000) ;Anderson, Michelle (55790712700) ;Burtonwood, Natalie (57211329479) ;Bijsterveld, Petra (42261000700) ;Brogan, Richard (57211338837) ;Ryan, Tony (57211342086) ;Kodoth, Vivek (16203006900) ;Khan, Arif (59642239400) ;Sebastian, Deepti (57211333319) ;Boyle, Georgina (58164430200) ;Shepherd, Lucy (57198118978) ;Hamid, Mahmood (58252754800) ;Farag, Mohamed (56548394600) ;Spinthakis, Nicholas (57195775843) ;Waitrak, Paulina (57211332950) ;De Sousa, Phillipa (57951177500) ;Bhatti, Rishma (57211333376) ;Oliver, Victoria (36442859300) ;Walshe, Siobhan (57211336090) ;Odedra, Toral (57211337230) ;Gue, Ying (57195301818) ;Kanji, Rahim (57202544616) ;Ratcliffe, Amanda (57211342079) ;Merrick, Angela (57211341473) ;Horwood, Carol (57211337392) ;Sarti, Charlotte (57211337063) ;Maart, Clint (55251705900) ;Moore, Donna (57211333549) ;Dockerty, Francesca (58643533700) ;Baucutt, Karen (57211331801) ;Pitcher, Louise (57211336628) ;Ilsley, Mary (57211336542) ;Clarke, Millie (57211337015) ;Germon, Rachel (57211332343) ;Gomes, Sara (59837350300) ;Clare, Thomas (57223134935) ;Nair, Sunil (36993293000) ;Staines, Jocasta (57211329884) ;Nicholson, Susan (57211333046) ;Watkinson, Oliver (6504683022) ;Gallagher, Ian (59812254600) ;Nelthorpe, Faye (57211336755) ;Musselwhite, Janine (56868574200) ;Grosser, Konrad (57188689074) ;Stimson, Leah (57211336845) ;Eaton, Michelle (57211331102) ;Heppell, Richard (6505808880) ;Turney, Sharon (57204664849) ;Horner, Victoria (58254644800) ;Schumacher, Natasha (57205487643) ;Moon, Angela (57204671140) ;Mota, Paula (58584599500) ;O'Donnell, Joshua (57211329975) ;Panicker, Abeesh Sadasiva (57211340362) ;Musa, Anntoniette (57204470454) ;Tapp, Luke (26026430400) ;Krishnamoorthy, Suresh (57211329619) ;Ansell, Valerie (57204475834) ;Ali, Danish (57200836664) ;Hyndman, Samantha (57204472896) ;Banerjee, Prithwish (9434852100) ;Been, Martin (7006307107) ;Mackenzie, Ailie (57211332597) ;McGregor, Andrew (57211337842) ;Hildick-Smith, David (8089365300) ;Champney, Felicity (57200962436) ;Ingoldby, Fiona (57211335624) ;Keate, Kirstie (57211339735) ;Bennett, Lorraine (35847475900) ;Skipper, Nicola (56108237700) ;Gregory, Sally (57211338926) ;Harfield, Scott (57211338856) ;Mudd, Alexandra (57204682139) ;Wragg, Christopher (56009473000) ;Barmby, David (8397579700) ;Grech, Ever (57211953825) ;Hall, Ian (56577404600) ;Middle, Janet (57204249882) ;Barker, Joann (57215597090) ;Fofie, Joyce (57211341763) ;Gunn, Julian (7201609106) ;Housley, Kay (57204671688) ;Cockayne, Laura (57211334758) ;Weatherlley, Louise (57211334279) ;Theodorou, Nana (55798988400) ;Wheeldon, Nigel (7003832828) ;Fati, Pene (57211331784) ;Storey, Robert F. (7101733693) ;Richardson, James (38663332100) ;Iqbal, Javid (58434634100) ;Adam, Zul (57211334336) ;Brett, Sarah (58370323700) ;Agyemang, Michael (57204670999) ;Tawiah, Cecilia (57211335386) ;Hogrefe, Kai (57201409991) ;Raju, Prashanth (58020649000) ;Braybrook, Christine (57204671274) ;Gracey, Jay (12777926800) ;Waldron, Molly (57190486556) ;Holloway, Rachael (57202434669) ;Burunsuzoglu, Senem (57211329422) ;Sidgwick, Sian (57211337741) ;Hetherington, Simon (56543027100) ;Beirnes, Charmaine (57204675588) ;Fernandez, Olga (57211339431) ;Lazar, Nicoleta (57219772830) ;Knighton, Abigail (57322824500) ;Rai, Amrit (57211336252) ;Hoare, Amy (57200966204) ;Breeze, Jonathan (57209856772) ;Martin, Katherine (57195715538) ;Andrews, Michelle (57211339711) ;Patale, Sheetal (57211330967) ;Bennett, Amy (58331157600) ;Smallwood, Andrew (7004343162) ;Radford, Elizabeth (57211337068) ;Cotton, James (7102218822) ;Martins, Joe (57203308130) ;Wallace, Lauren (57211342581) ;Milgate, Sarah (57208408448) ;Munir, Shahzad (36772115700) ;Metherell, Stella (57211329485) ;Cottam, Victoria (57792835300) ;Massey, Ian (57216491051) ;Copestick, Jane (57211339137) ;Delaney, Jane (58352764800) ;Wain, Jill (57204681973) ;Sandhu, Kully (56715268100) ;Emery, Lisa (59573593800) ;Hall, Charlotte (57211335217) ;Bucciarelli-Ducci, Chiara (18534251300) ;Besana, Rissa (57211336458) ;Hussein, Jodie (57211329691) ;Bell, Sheila (57211333545) ;Gill, Abby (57211330891) ;Bales, Emily (57211335047) ;Polwarth, Gary (57192976273) ;East, Clare (57221931285) ;Smith, Ian (16308436900) ;Oliveira, Joana (57211336782) ;Victor, Saji (57223122565) ;Woods, Sarah (57221932761) ;Hoole, Stephen (24176760300) ;Ramos, Angelo (57211337477) ;Sevillano, Annaliza (57204696865) ;Nicholson, Anne (59838082100) ;Solieri, Ashley (57211340389) ;Redman, Emily (57868249200) ;Byrne, Jean (57940570400) ;Joyce, Joan (58424541400) ;Riches, Joanne (57204681714) ;Davies, John (56939639900) ;Allen, Kezia (56254656700) ;Saclot, Louie (57204665161) ;Ocampo, Madelaine (57204663858) ;Vertue, Mark (57204682537) ;Christmas, Natasha (57195546189) ;Koothoor, Raiji (57211332861) ;Gamma, Reto (55998580000) ;Alvares, Wilson (57205490168) ;Pepper, Stacey (59892862900) ;Kobson, Barbara (57211335165) ;Reeve, Christy (57211334194) ;Malik, Iqbal (8874031800) ;Chester, Emma (57211340468) ;Saunders, Heidi (57211335001) ;Mojela, Idah (57211335709) ;Smee, Joanna (57159690400) ;Davies, Justin (24729417300) ;Davies, Nina (59327660500) ;Clifford, Piers (56574780500) ;Dias, Priyanthi (57213869390) ;Kaur, Ramandeep (57211335561) ;Moreira, Silvia (57211334765) ;Ahmad, Yousif (55064203300) ;Tomlinson, Lucy (57211343662) ;Pengelley, Clare (57211334786) ;Bidle, Amanda (57211336847) ;Spence, Sharon (58334086100) ;Al-Lamee, Rasha (35730930200) ;Phuyal, Urmila (57211342990) ;Abbass, Hakam (59783821700) ;Bose, Tuhina (57211338531) ;Elliott, Rebecca (58452054200) ;Foundun, Aboo (57211331924) ;Chung, Alan (57211338971) ;Freestone, Beth (6602146949) ;Lee, Dr Kaeng (57211338371) ;Elshiekh, Dr Mohamed (57211338488) ;Pulikal, George (8650065600) ;Bhatre, Gurbir (57211329905) ;Douglas, James (57951201000) ;Kaeng, Lee (57211339199) ;Pitt, Mike (56216827000) ;Watkins, Richard (57211333631) ;Gill, Simrat (57211872194) ;Hartley, Amy (57045551700) ;Lucking, Andrew (16301995400) ;Moreby, Berni (57208485311) ;Darby, Damaris (59807361300) ;Corps, Ellie (57211330072) ;Parsons, Georgina (57195265789) ;De Mance, Gianluigi (57211334647) ;Fahrai, Gregor (57211343245) ;Turner, Jenny (59891057400) ;Langrish, Jeremy (25932300200) ;Gaughran, Lisa (57196257067) ;Wolyrum, Mathias (57211343391) ;Azkhalil, Mohammed (57211337481) ;Bates, Rachel (57211330761) ;Given, Rachel (57211341416) ;Douthwaite, Rebecca (57211332640) ;Lloyd, Steph (58442759300) ;Neubauer, Stephen (55794522200) ;Barker, Deborah (57220581432) ;Suttling, Anne (57201075548) ;Turner, Charlotte (57221922525) ;Smith, Clare (58466161500) ;Longbottom, Colin (57211337800) ;Ross, David (59776534200) ;Cunliffe, Denise (57211331377) ;Cox, Emily (58712060300) ;Whitehead, Helena (57211330164) ;Hudson, Karen (57211342828) ;Jones, Leslie (57211330206) ;Drew, Martin (57211331205) ;Chant, Nicholas (57211333796) ;Haworth, Peter (24553951400) ;Capel, Robert (57211340984) ;Austin, Rosalynn (57484740000) ;Howe, Serena (57221931611) ;Smith, Trevor (57211330540) ;Hobson, Alex (14066032000) ;Strike, Philip (7006819553) ;Griffiths, Huw (57210391614) ;Anantharam, Brijesh (26657157500) ;Jack, Pearse (57211335718) ;Thornton, Emma (59054871600) ;Hodgson, Adrian (57224649737) ;Jennison, Alan (57211333270) ;McSkeane, Anna (57204249944) ;Smith, Bethany (58595383600) ;Shaw, Caroline (57211336274) ;Leathers, Chris (57203202738) ;Armstrong, Elissa (58362389100) ;Carruthers, Gayle (57211337371) ;Simpson, Holly (57194276150) ;Smith, Jan (59443491100) ;Hodierne, Jeremy (57211332042) ;Kelly, Julie (58420844700) ;Barclay, Justin (8873295400) ;Scott, Kerry (58717327100) ;Gregson, Lisa (57211337139) ;Buchanan, Louise (56041610600) ;McCormick, Louise (57211343505) ;Kelsall, Nicci (57210750450) ;Mcarthy, Rachel (57211342854) ;Taylor, Rebecca (57218326706) ;Thompson, Rebecca (57223121447) ;Shelton, Rhidian (7102100710) ;Moore, Roger (57211329752) ;Tomlinson, Sharon (57211332574) ;Thambi, Sunil (57211337020) ;Cooper, Theresa (59844686900) ;Oakes, Trevor (57211341395) ;Deen, Zakhira (57211341315) ;Relph, Chris (57793115100) ;prentice, Scott (57211341340) ;Hall, Lorna (58711294500) ;Dillon, Angela (57211330875) ;Meadows, Deborah (57211337932) ;Frank, Emma (57211340947) ;Markham-Jones, Helene (57211341717) ;Thomas, Isobel (57207308373) ;Gale, Joanne (59877365700) ;Denman, Joanne (56572515100) ;O'Connor, John (57211339356) ;Hindle, Julia (56398175200) ;Jackson-Lawrence, Karen (57211334314) ;Warner, Karen (57210749799) ;Lee, Kelvin (59864835600) ;Upton, Robert (57211340615) ;Elston, Ruth (57211341995) ;Lee, Sandra (57951181000) ;Venugopal, Vinod (18538897000) ;Finch, Amanda (57195547000) ;Fleming, Catherine (57211338285) ;Whiteside, Charlene (57211341767) ;Pemberton, Chris (7003383566) ;Wilkinson, Conor (57211338790) ;Sebastian, Deepa (57220341513) ;Riedel, Ella (57211335270) ;Giuffrida, Gaia (57211335137) ;Burnett, Gillian (57211341137) ;Spickett, Helen (57195542479) ;Glen, James (58286002700) ;Brown, Janette (59631539100) ;Thornborough, Lauren (57211335762) ;Pedley, Lauren (57794516200) ;Morgan, Maureen (59801341700) ;Waddington, Natalia (57204249808) ;Brennan, Oliver (57211329876) ;Brady, Rebecca (7201469567) ;Preston, Stephen (59876054900) ;Loder, Chris (57193421069) ;Vlad, Ionela (57211342705) ;Laurence, Julia (57205493203) ;Smit, Angelique (57221410136) ;Dimond, Kirsty (57211339253) ;Hayes, Michelle (57211329740) ;Paddy, Loveth (57211336675) ;Crause, Jacolene (57205492718) ;Amed, Nadifa (57211339156) ;Kaur-Babooa, Priya (57211335204) ;Kotecha, Tushar (38661453500) ;Fayed, Hossam (56950600900) ;Pavlidis, Antonis (6603259696) ;Prendergast, Bernard (20135595700) ;Clapp, Brian (23093277600) ;Perara, Divaka (57211339157) ;Atkinson, Emma (57211340246) ;Ellis, Howard (57191856375) ;Wilson, Karen (7403727040) ;Gibson, Kirsty (57211338230) ;Smith, Megan (59622662700) ;Khawaja, Muhammed Zeeshan (35253895800) ;Sanchez-Vidal, Ruth (59603887000) ;Redwood, Simon (7004926172) ;Jones, Sophie (59825489200) ;Tipping, Aoife (57211338163) ;Oommen, Anu (57044459700) ;Hendry, Cara (28367584300) ;Fath-Orboubadi, DR Fazin (57211338469) ;Phillips, Hannah (57211330215) ;Kolakaluri, Laurel (57211334442) ;Sherwood, Martin (57211330893) ;Mackie, Sarah (57471360800) ;Aleti, Shilpa (57211332844) ;Charles, Thabitha (57211343577) ;Roy, Liby (57211334154) ;Henderson, Rob (57065808400) ;Stables, Rod (55384131000) ;Marber, Michael (7005212420) ;Berry, Alan (57211331475) ;Redington, Andrew (7102622991) ;Thygesen, Kristian (7005076421) ;Andersen, Henning Rud (26642940200) ;Berry, Colin (57203056149) ;Copas, Andrew (7003490365) ;Meade, Tom (7102321493) ;Kelbæk, Henning (26643065200) ;Bueno, Hector (57218323754) ;von Weitzel-Mudersbach, Paul (6505494465) ;Andersen, Grethe (55568472700) ;Ludman, Andrew (23667880400) ;Cruden, Nick (6602682960) ;Topic, Dragan (24330141400) ;Mehmedbegovic, Zlatko (55778381000) ;de la Hera Galarza, Jesus Maria (6603245999) ;Robertson, Steven (57190237733) ;Van Dyck, Laura (56149567300) ;Chu, Rebecca (57211084730) ;Astarci, Josenir (57211329484) ;Jamal, Zahra (57200532218) ;Hetherington, Daniel (57211337221)Collier, Lucy (57211331136)Background: Remote ischaemic conditioning with transient ischaemia and reperfusion applied to the arm has been shown to reduce myocardial infarct size in patients with ST-elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PPCI). We investigated whether remote ischaemic conditioning could reduce the incidence of cardiac death and hospitalisation for heart failure at 12 months. Methods: We did an international investigator-initiated, prospective, single-blind, randomised controlled trial (CONDI-2/ERIC-PPCI) at 33 centres across the UK, Denmark, Spain, and Serbia. Patients (age >18 years) with suspected STEMI and who were eligible for PPCI were randomly allocated (1:1, stratified by centre with a permuted block method) to receive standard treatment (including a sham simulated remote ischaemic conditioning intervention at UK sites only) or remote ischaemic conditioning treatment (intermittent ischaemia and reperfusion applied to the arm through four cycles of 5-min inflation and 5-min deflation of an automated cuff device) before PPCI. Investigators responsible for data collection and outcome assessment were masked to treatment allocation. The primary combined endpoint was cardiac death or hospitalisation for heart failure at 12 months in the intention-to-treat population. This trial is registered with ClinicalTrials.gov (NCT02342522) and is completed. Findings: Between Nov 6, 2013, and March 31, 2018, 5401 patients were randomly allocated to either the control group (n=2701) or the remote ischaemic conditioning group (n=2700). After exclusion of patients upon hospital arrival or loss to follow-up, 2569 patients in the control group and 2546 in the intervention group were included in the intention-to-treat analysis. At 12 months post-PPCI, the Kaplan-Meier-estimated frequencies of cardiac death or hospitalisation for heart failure (the primary endpoint) were 220 (8·6%) patients in the control group and 239 (9·4%) in the remote ischaemic conditioning group (hazard ratio 1·10 [95% CI 0·91–1·32], p=0·32 for intervention versus control). No important unexpected adverse events or side effects of remote ischaemic conditioning were observed. Interpretation: Remote ischaemic conditioning does not improve clinical outcomes (cardiac death or hospitalisation for heart failure) at 12 months in patients with STEMI undergoing PPCI. Funding: British Heart Foundation, University College London Hospitals/University College London Biomedical Research Centre, Danish Innovation Foundation, Novo Nordisk Foundation, TrygFonden. © 2019 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license - Some of the metrics are blocked by yourconsent settings
Publication Efficiency, safety, and long-term follow-up of retrograde approach for CTO recanalization: Initial (belgrade) experience with international proctorship(2012) ;Stojkovic, Sinisa (6603759580) ;Sianos, George (7003691774) ;Katoh, Osamu (7006116841) ;Galassi, Alfredo R. (7004438532) ;Beleslin, Branko (6701355424) ;Vukcevic, Vladan (15741934700) ;Nedeljkovic, Milan (7004488186) ;Stankovic, Goran (59150945500) ;Orlic, Dejan (7006351319) ;Dobric, Milan (23484928600) ;Tomasevic, Miloje (57196948758)Ostojic, Miodrag (34572650500)Background: Retrograde approach increases the success rate for percutaneous recanalization of complex chronic total occlusion (CTO) of coronary arteries. Objectives: The purpose of this study was to describe our initial experience of retrograde percutaneous coronary intervention for CTO program, focusing on its safety and feasibility, and long-term clinical follow-up. Methods: The study was a single center retrospective registry which included a total of 40 patients, of 590 CTO treated patients (6.7%), between January 2008 and October 2011, who underwent retrograde approach for CTO recanalization. Results: Mean occlusion duration was 37.8 ± 40.3 months. Overall success recanalization rate was 87.5% (35/40). Septal collaterals were used to access the occlusion in all cases (100%). Retrograde guidewire crossing of collateral channels was successful in 36/40 (90.0%) patients with success rate of CTO recanalization in these patients of 97.2%. Retrograde approach as the primary strategy was applied in 23/40 (57.5%) patients, retrograde approach immediately after antegrade failure attempt was performed in 8/40 (20.0%) patients, and retrograde approach as elective procedure, after previously failed antegrade attempt, was performed in 9/40 (22.5%) patients. The success rate of these strategies was: 87.0% (20/23 patients) for primary, 87.5% (7/8 patients) for retrograde immediately after antegrade failure, and 88.9% (8/9 patients) for retrograde after previous failed antegrade attempt, respectively. Total in-hospital major adverse cardiac events (MACE) rate was 5.0% (2 non-Q-wave myocardial infarctions). The MACE free survival at median follow-up of 20 months was 89% (95% CI: 78-100%). Conclusions: This study has demonstrated that adequate training and international proctorship for this complex and demanding technique is a necessity and prerequisite to achieve high overall success rates, with acceptable complication rates and excellent long-term survival rate. © 2012, Wiley Periodicals, Inc. - Some of the metrics are blocked by yourconsent settings
Publication Immediate Versus Delayed Invasive Intervention for Non-STEMI Patients: The RIDDLE-NSTEMI Study(2016) ;Milosevic, Aleksandra (56622640900) ;Vasiljevic-Pokrajcic, Zorana (6602641182) ;Milasinovic, Dejan (24823024500) ;Marinkovic, Jelena (7004611210) ;Vukcevic, Vladan (15741934700) ;Stefanovic, Branislav (57210079550) ;Asanin, Milika (8603366900) ;Dikic, Miodrag (25959947200) ;Stankovic, Sanja (7005216636)Stankovic, Goran (59150945500)Objectives This study aimed to assess the clinical impact of immediate versus delayed invasive intervention in patients with non-ST-segment myocardial infarction (NSTEMI). Background Previous studies found conflicting results on the effects of earlier invasive intervention in a heterogeneous population of acute coronary syndromes without ST-segment elevation. Methods We randomized 323 NSTEMI patients to an immediate-intervention group (<2 h after randomization, n = 162) and a delayed-intervention group (2 to 72 h, n = 161).The primary endpoint was the occurrence of death or new myocardial infarction (MI) at 30-day follow-up. Results Median time from randomization to angiography was 1.4 h and 61.0 h in the immediate-intervention group and the delayed-intervention group, respectively (p < 0.001). At 30 days, the primary endpoint was achieved less frequently in patients undergoing immediate intervention (4.3% vs. 13%, hazard ratio: 0.32, 95% confidence interval: 0.13 to 0.74; p = 0.008). At 1 year, this difference persisted (6.8% in the immediate-intervention group vs. 18.8% in delayed-intervention group; hazard ratio: 0.34, 95% confidence interval: 0.17 to 0.67; p = 0.002). The observed results were mainly attributable to the occurrence of new MI in the pre-catheterization period (0 deaths + 0 MIs in the immediate-intervention group vs. 1 death + 10 MIs in the delayed-intervention group). The rate of deaths, new MI, or recurrent ischemia was lower in the immediate-intervention group at both 30 days (6.8% vs. 26.7%; p < 0.001) and 1 year (15.4% vs. 33.1%; p < 0.001). Conclusions Immediate invasive strategy in NSTEMI patients is associated with lower rates of death or new MI compared with the delayed invasive strategy at early and midterm follow-up, mainly due to a decrease in the risk of new MI in the pre-catheterization period. (Immediate Versus Delayed Invasive Intervention for Non-STEMI Patients [RIDDLE-NSTEMI]; NCT02419833) © 2016 by the American College of Cardiology Foundation. - Some of the metrics are blocked by yourconsent settings
Publication Improved propensity-score matched long-term clinical outcomes in patients with successful percutaneous coronary interventions of coronary chronic total occlusion(2018) ;Stojkovic, Sinisa (6603759580) ;Juricic, Stefan (57203033137) ;Dobric, Milan (23484928600) ;Nedeljkovic, Milan A. (7004488186) ;Vukcevic, Vladan (15741934700) ;Orlic, Dejan (7006351319) ;Stankovic, Goran (59150945500) ;Tomasevic, Miloje (57196948758) ;Aleksandric, Srdjan (35274271700) ;Dikic, Miodrag (25959947200) ;Tesic, Milorad (36197477200) ;Mehmedbegovic, Zlatko (55778381000) ;Boskovic, Nikola (6508290354) ;Zivkovic, Milorad (55959530600) ;Dedovic, Vladimir (55959310400) ;Milasinovic, Dejan (24823024500) ;Ostojic, Miodrag (34572650500)Beleslin, Branko (6701355424)The objective of the study was to evaluate major adverse cardiovascular events (MACE) after successful versus failed percutaneous coronary intervention for chronic total occlusion (PCI-CTO). Limited data are available on long-term clinical follow-up in the treatment of chronic total occlusion (CTO). Between January 2009 and December 2010 PCI-CTO was attempted in 283 consecutive patients with 289 CTO lesions. Procedural success was 62.3% and clinical follow-up covered 83% (235/283) of the study population with a median follow-up of 66 months (range, 59-74). The total incidence of MACE was 57/235 (24.3%), and was significantly higher in the procedural failure group than in the procedural success group (33/87 (37.9%) versus 24/148 (16.2%), P < 0.001). All-cause mortality was significantly lower in patients with successful PCI-CTO compared to failed PCI-CTO (10.8% versus 20.7%, P < 0.05). Also, the rate of cardiovascular death in the procedural failure group (14.9%) was slightly higher than that in the procedural success group (7.4%, P = 0.066). The rate of TVR was statistically higher in the procedural failure group (P < 0.009). Propensity score-adjusted Cox regression showed that procedural success remained a significant predictor of MACE (adjusted HR 0.402; 95% CI 0.196-0.824; P = 0.013). Our study emphasizes the importance of CTO recanalization in improving long-term outcome including all-cause mortality with a borderline effect on cardiovascular mortality. © 2018, International Heart Journal Association. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication Long-term Follow-up Optical Coherence Tomography Assessment of Primary Percutaneous Coronary Intervention for Unprotected Left Main(2024) ;Mehmedbegovic, Zlatko (55778381000) ;Vukcevic, Vladan (15741934700) ;Stojkovic, Sinisa (6603759580) ;Beleslin, Branko (6701355424) ;Orlic, Dejan (7006351319) ;Tomasevic, Miloje (57196948758) ;Dikic, Miodrag (25959947200) ;Tesic, Milorad (36197477200) ;Milasinovic, Dejan (24823024500) ;Aleksandric, Srdjan (35274271700) ;Dedovic, Vladimir (55959310400) ;Zivkovic, Milorad (55959530600) ;Juricic, Stefan (57203033137) ;Jelic, Dario (57201640680) ;Mladenovic, Djordje (58483820500)Stankovic, Goran (59150945500)Background: Elective unprotected left main (ULM) percutaneous coronary intervention (PCI) has long-term mortality rates comparable to surgical revascularization, thanks to advances in drug-eluting stent (DES) design, improved PCI techniques, and frequent use of intravascular imaging. However, urgent PCI of ULM culprit lesions remains associated with high in-hospital mortality and unfavourable long-term outcomes, including DES restenosis and stent thrombosis (ST). This analysis aimed to examine the long-term outcomes and healing of DES implanted in ULM during primary PCI using high-resolution optical coherence tomography (OCT) imaging. Methods: A total of 15 consecutive patients undergoing long-term OCT follow-up of ULM primary PCI from a high-volume center were included in this analysis. During the index primary PCI all subjects underwent angio-guided DES implantation, and follow-up was uneventful in all but one subject who had a non-target PCI lesion. The primary endpoint was the percentage of covered, uncovered, and malappossed stent struts at long-term follow-up. Secondary endpoints included quantitative and qualitative OCT measurements. For the left main bifurcation, a separate analysis was performed for three different segments: left main (LM), polygon of confluence (POC) and distal main branch (dMB), in all cases. Results: The average follow-up interval until OCT was 1580 ± 1260 days. Despite aorto-ostial stent protrusions in 40% of patients, optimal image quality was achieved in 93.3% of cases. There were higher rates of malapposed (11.4 ± 16.6 vs. 13.1 ± 8.3 vs. 0.3 ± 0.5%; p < 0.001) and lower rates of covered struts (81.7 ± 16.8 vs. 83.7 ± 9.2 vs. 92.4 ± 6.8%; p = 0.041) observed for the LM and POC segment compared to the dMB. Significantly malapposed stent struts (>400 µm) were less likely to be covered at follow-up, than struts with a measured strut to vessel wall distance of <400 µm (15.4 ± 21.6 vs. 24.8 ± 23.9%; p = 0.011). Neoatherosclerosis was observed in 5 (33.3%) and restenotic neointimal hyperplasia (NIH) in 2 (13.3%) patients, requiring PCI in 33.3% of patients. Conclusions: Long-term OCT examination of DES implanted during primary PCI for culprit ULM lesions demonstrated high rates of incomplete strut coverage, late malapposition, and high subclinical DES failure rates. These negative OCT results highlight the need for image optimization strategies during primary PCI to improve DES-related long-term outcomes. © 2024 The Author(s). Published by IMR Press. - Some of the metrics are blocked by yourconsent settings
Publication Mental stress-induced ischemia in patients with coronary artery disease: Echocardiographic characteristics and relation to exercise-induced ischemia(2012) ;Stepanovic, Jelena (6603897710) ;Ostojic, Miodrag (34572650500) ;Beleslin, Branko (6701355424) ;Vukovic, Olivera (14044368800) ;Dikic, Ana Djordjevic (59157923800) ;Giga, Vojislav (55924460200) ;Nedeljkovic, Ivana (55927577700) ;Nedeljkovic, Milan (7004488186) ;Stojkovic, Sinisa (6603759580) ;Vukcevic, Vladan (15741934700) ;Dobric, Milan (23484928600) ;Petrasinovic, Zorica (56057995200) ;Marinkovic, Jelena (7004611210)Lecic-Tosevski, Dusica (6602315043)OBJECTIVE: The aims of this study were to investigate the incidence and parameters associated with myocardial ischemia during mental stress (MS) as measured by echocardiography and to evaluate the relation between MS-induced and exercise-induced myocardial ischemia. METHODS: Study participants were 79 patients (63 men; mean [M] [standard deviation {SD}] age = 52 [8] years) with angiographically confirmed coronary artery disease and previous positive exercise test result. The MS protocol consisted of mental arithmetic and anger recall task. The patients performed a treadmill exercise test 15 to 20 minutes after the MS task. Data of post-MS exercise were compared with previous exercise stress test results. RESULTS: The frequency of echocardiographic abnormalities was 35% in response to the mental arithmetic task, compared with 61% with anger recall and 96% with exercise (p <.001, exercise versus MS). Electrocardiogram abnormalities and chest pain were substantially less common during MS than were echocardiographic abnormalities. Independent predictors of MS-induced myocardial ischemia were: wall motion score index at rest (p =.02), peak systolic blood pressure (p =.005), and increase in rate-pressure product (p =.004) during MS. The duration of exercise stress test was significantly shorter (p <.001) when MS preceded the exercise and in the case of earlier exercise (M [SD] = 4.4 [1.9] versus 6.7 [2.2] minutes for patients positive on MS and 5.7 [1.9] versus 8.0 [2.3] minutes for patients negative on MS). CONCLUSIONS: Echocardiography can be successfully used to document myocardial ischemia induced by MS. MS-induced ischemia was associated with an increase in hemodynamic parameters during MS and worse function of the left ventricle. MS may shorten the duration of subsequent exercise stress testing and can potentiate exercise-induced ischemia in susceptible patients with coronary artery disease. Copyright © 2012 by the American Psychosomatic Society. - Some of the metrics are blocked by yourconsent settings
Publication Mental stress-induced ischemia in patients with coronary artery disease: Echocardiographic characteristics and relation to exercise-induced ischemia(2012) ;Stepanovic, Jelena (6603897710) ;Ostojic, Miodrag (34572650500) ;Beleslin, Branko (6701355424) ;Vukovic, Olivera (14044368800) ;Dikic, Ana Djordjevic (59157923800) ;Giga, Vojislav (55924460200) ;Nedeljkovic, Ivana (55927577700) ;Nedeljkovic, Milan (7004488186) ;Stojkovic, Sinisa (6603759580) ;Vukcevic, Vladan (15741934700) ;Dobric, Milan (23484928600) ;Petrasinovic, Zorica (56057995200) ;Marinkovic, Jelena (7004611210)Lecic-Tosevski, Dusica (6602315043)OBJECTIVE: The aims of this study were to investigate the incidence and parameters associated with myocardial ischemia during mental stress (MS) as measured by echocardiography and to evaluate the relation between MS-induced and exercise-induced myocardial ischemia. METHODS: Study participants were 79 patients (63 men; mean [M] [standard deviation {SD}] age = 52 [8] years) with angiographically confirmed coronary artery disease and previous positive exercise test result. The MS protocol consisted of mental arithmetic and anger recall task. The patients performed a treadmill exercise test 15 to 20 minutes after the MS task. Data of post-MS exercise were compared with previous exercise stress test results. RESULTS: The frequency of echocardiographic abnormalities was 35% in response to the mental arithmetic task, compared with 61% with anger recall and 96% with exercise (p <.001, exercise versus MS). Electrocardiogram abnormalities and chest pain were substantially less common during MS than were echocardiographic abnormalities. Independent predictors of MS-induced myocardial ischemia were: wall motion score index at rest (p =.02), peak systolic blood pressure (p =.005), and increase in rate-pressure product (p =.004) during MS. The duration of exercise stress test was significantly shorter (p <.001) when MS preceded the exercise and in the case of earlier exercise (M [SD] = 4.4 [1.9] versus 6.7 [2.2] minutes for patients positive on MS and 5.7 [1.9] versus 8.0 [2.3] minutes for patients negative on MS). CONCLUSIONS: Echocardiography can be successfully used to document myocardial ischemia induced by MS. MS-induced ischemia was associated with an increase in hemodynamic parameters during MS and worse function of the left ventricle. MS may shorten the duration of subsequent exercise stress testing and can potentiate exercise-induced ischemia in susceptible patients with coronary artery disease. Copyright © 2012 by the American Psychosomatic Society. - Some of the metrics are blocked by yourconsent settings
Publication N-terminal pro-brain natriuretic peptide is related with coronary flow velocity reserve and diastolic dysfunction in patients with asymmetric hypertrophic cardiomyopathy(2017) ;Tesic, Milorad (36197477200) ;Seferovic, Jelena (23486982900) ;Trifunovic, Danijela (9241771000) ;Djordjevic-Dikic, Ana (57003143600) ;Giga, Vojislav (55924460200) ;Jovanovic, Ivana (57223117334) ;Petrovic, Olga (33467955000) ;Marinkovic, Jelena (7004611210) ;Stankovic, Sanja (7005216636) ;Stepanovic, Jelena (6603897710) ;Ristic, Arsen (7003835406) ;Petrovic, Milan (56595474600) ;Mujovic, Nebojsa (16234090000) ;Vujisic-Tesic, Bosiljka (6508177183) ;Beleslin, Branko (6701355424) ;Vukcevic, Vladan (15741934700) ;Stankovic, Goran (59150945500)Seferovic, Petar (6603594879)Background The relations of elevated N-terminal pro-brain natriuretic peptide (NT-pro-BNP) and cardiac ischemia in hypertrophic cardiomyopathy (HCM) patients is uncertain. Therefore we designed the study with the following aims: (1) to analyze plasma concentrations of NT-pro-BNP in various subsets of HCM patients; (2) to reveal the correlations of NT-pro-BNP, myocardial ischemia, and diastolic dysfunction; (3) to assess predictors of the elevated plasma levels of NT-pro-BNP. Methods and results In 61 patients (mean age 48.9 ± 16.3 years; 26 male) with asymmetric HCM plasma levels of NT-pro-BNP were obtained. Standard transthoracic examination, tissue Doppler echocardiography with measurement of transthoracic coronary flow velocity reserve (CFVR) in left anterior descending artery (LAD) was done. Mean natural logarithm value of NT-pro-BNP was 7.11 ± 0.95 pg/ml [median value 1133 (interquartile range 561–2442) pg/ml]. NT-pro-BNP was significantly higher in patients with higher NYHA class, in obstructive HCM, more severe mitral regurgitation, increased left atrial volume index (LAVI), presence of calcified mitral annulus, elevated left ventricular (LV) filling pressure and in decreased CFVR. Levels of NT-pro-BNP significantly correlated with the ratio of E/e′ (r = 0.534, p < 0.001), LV outflow tract gradient (r = 0.503, p = 0.024), LAVI (r = 0.443, p < 0.001), while inversely correlated with CFVR LAD (r = −0.569, p < 0.001). When multivariate analysis was done only CFVR LAD and E/e′ emerged as independent predictors of NT-pro-BNP. Conclusion Plasma levels of NT-pro-BNP were significantly higher in HCM patients with more advanced disease. Elevated NT-pro-BNP not only reflects the diastolic impairment of the LV, but it might also be the result of cardiac ischemia in patients with HCM. © 2017 Japanese College of Cardiology - Some of the metrics are blocked by yourconsent settings
Publication OCT Guidance for Detection and Treatment of Free-Floating Struts Following Ostial LAD Stenting(2021) ;Milasinovic, Dejan (24823024500) ;Tomasevic, Miloje (57196948758) ;Vukcevic, Vladan (15741934700)Stankovic, Goran (59150945500)[No abstract available] - Some of the metrics are blocked by yourconsent settings
Publication Prognostic impact of non-culprit chronic total occlusion over time in patients with ST-elevation myocardial infarction treated with primary percutaneous coronary intervention(2021) ;Milasinovic, Dejan (24823024500) ;Mladenovic, Djordje (58483820500) ;Zaharijev, Stefan (58483845200) ;Mehmedbegovic, Zlatko (55778381000) ;Marinkovic, Jelena (7004611210) ;Jelic, Dario (57201640680) ;Zobenica, Vladimir (58118595100) ;Radomirovic, Marija (58483860800) ;Dedovic, Vladimir (55959310400) ;Pavlovic, Andrija (57204964008) ;Dobric, Milan (23484928600) ;Stojkovic, Sinisa (6603759580) ;Asanin, Milika (8603366900) ;Vukcevic, Vladan (15741934700)Stankovic, Goran (59150945500)Aims: Previous studies indicated that a chronic total occlusion (CTO) in a non-infarct-related artery is linked to higher mortality mainly in the acute setting in patients with ST-elevation myocardial infarction (STEMI). Our aim was to assess the temporal distribution of mortality risk associated with non-culprit CTO over years after STEMI. Methods and results: The study included 8679 STEMI patients treated with primary percutaneous coronary intervention (PCI). Kaplan-Meier cumulative mortality curves for non-culprit CTO vs. no CTO were compared with log-rank test, with landmarks set at 30 days and 1 year. Adjusted Cox regression models were constructed to assess the impact of non-culprit CTO on mortality over different time intervals. Tests for interaction were pre-specified between non-culprit CTO and acute heart failure and left ventricular ejection fraction. The primary outcome variable was all-cause mortality, and the median follow-up was 5 years. Non-culprit CTO was present in 11.6% of patients (n = 1010). Presence of a CTO was associated with increased early [30-day adjusted hazard ratio (HR) 1.91, 95% confidence interval (CI) 1.54-2.36; P < 0.001] and late mortality (5-year adjusted HR 1.66, 95% CI 1.42-1.95; P < 0.001). Landmark analyses revealed an annual two-fold increase in mortality in patients with vs. without a CTO after the first year of follow-up. The observed pattern of mortality increase over time was independent of acute or chronic LV impairment. Conclusions: Non-culprit CTO is independently associated with mortality over 5 years after primary PCI for STEMI, with a constant annual two-fold increase in the risk of death beyond the first year of follow-up. © 2021. - Some of the metrics are blocked by yourconsent settings
Publication Prognostic value of health-related quality of life in elderly patients hospitalized with heart failure(2019) ;Erceg, Predrag (18133470500) ;Despotovic, Nebojsa (6602679190) ;Milosevic, Dragoslav P. (56405221200) ;Soldatovic, Ivan (35389846900) ;Mihajlovic, Gordana (16064492500) ;Vukcevic, Vladan (15741934700) ;Mitrovic, Predrag (14012420700) ;Markovic-Nikolic, Natasa (57211527501) ;Micovic, Milica (57209393153) ;Mitrovic, Dragica (57197019152)Davidovic, Mladen (9940513000)Purpose: Previous research has shown that poor health-related quality of life (HRQOL) is associated with adverse long-term prognosis in patients with heart failure (HF); however, there have been inconsistencies among studies and not all of them confirmed the prognostic value of HRQOL. In addition, few studies involved elderly patients and most focused on all-cause mortality and HF-related hospitalization as outcomes. The aim of our study was to determine whether HRQOL is a predictor and an independent predictor of long-term cardiac mortality, all-cause mortality, and HF-related rehospitalization in elderly patients hospitalized with HF. Patients and methods: This prospective observational study included 200 elderly patients hospitalized with HF in Serbia. HRQOL was measured using the Minnesota Living with Heart Failure questionnaire (MLHFQ). The median follow-up period was 28 months. The primary outcome was cardiac mortality, and all-cause mortality and HF-related rehospitalization were secondary outcomes. Survival analysis was conducted using the Kaplan–Meier method and Cox-proportional hazards regression. Results: Subjects with poor HRQOL (higher than the median MLHFQ score) had a higher probability of cardiac mortality (P=0.029) and HF-related rehospitalization (P=0.001) during long-term follow-up. Poor HRQOL was an independent predictor of cardiac mortality (HR: 2.051, 95% CI: 1.260–3.339, P=0.004), all-cause mortality (HR: 1.620, 95% CI: 1.076–2.438, P=0.021), and HF-related rehospitalization (HR: 2.040, 95% CI: 1.290–3.227, P=0.002). Conclusion: HRQOL is an independent predictor of long-term cardiac mortality in elderly patients hospitalized with HF. It also independently predicts all-cause mortality and HF-related rehospitalization. HRQOL could be used as a complementary clinical predictive tool in this patient population. © 2019 Erceg et al. - Some of the metrics are blocked by yourconsent settings
Publication Prognostic value of transthoracic doppler echocardiography coronary flow velocity reserve in patients with asymmetric hypertrophic cardiomyopathy(2021) ;Tesic, Milorad (36197477200) ;Beleslin, Branko (6701355424) ;Giga, Vojislav (55924460200) ;Jovanovic, Ivana (57223117334) ;Marinkovic, Jelena (7004611210) ;Trifunovic, Danijela (9241771000) ;Petrovic, Olga (33467955000) ;Dobric, Milan (23484928600) ;Aleksandric, Srdjan (35274271700) ;Juricic, Stefan (57203033137) ;Boskovic, Nikola (6508290354) ;Tomasevic, Miloje (57196948758) ;Ristic, Arsen (7003835406) ;Orlic, Dejan (7006351319) ;Stojkovic, Sinisa (6603759580) ;Vukcevic, Vladan (15741934700) ;Stankovic, Goran (59150945500) ;Ostojic, Miodrag (34572650500)Dikic, Ana Djordjevic (59157923800)BACKGROUND: Microvascular dysfunction might be a major determinant of clinical deterioration and outcome in patients with hypertrophic cardiomyopathy (HCM). However, long-term prognostic value of transthoracic Doppler echocardiography (TDE) coronary flow velocity reserve (CFVR) on clinical outcome is uncertain in HCM patients. Therefore, the aim of our study was to assess long-term prognostic value of CFVR on clinical outcome in HCM population. METHODS AND RESULTS: We prospectively included 150 HCM patients (82 women; mean age 48±15 years). Patients’ clinical characteristics, echocardiographic and CFVR findings (both for left anterior descending [LAD] and posterior descending artery [PD]), were assessed in all patients. The primary outcome was a composite of: HCM related death, heart failure requir-ing hospitalization, sustained ventricular tachycardia and ischemic stroke. Patients were stratified into 2 subgroups depend-ing on CFVR LAD value: Group 1 (CFVR LAD>2, [n=87]) and Group 2 (CFVR LAD≤2, [n=63]). During a median follow-up of 88 months, 41/150 (27.3%) patients had adverse cardiac events. In Group 1, there were 8/87 (9.2%), whereas in Group 2 there were 33/63 (52.4%, P<0.001 vs. Group 1) adverse cardiac events. By Kaplan-Meier analysis, patients with preserved CFVR LAD had significantly higher cumulative event-free survival rate compared to patients with impaired CFVR LAD (96.4% and 90.9% versus 66.9% and 40.0%, at 5 and 8 years, respectively: log-rank 37.2, P<0.001). Multivariable analysis identified only CFVR LAD≤2 as an independent predictor for adverse cardiac outcome (HR 6.54; 95% CI 2.83–16.30, P<0.001), while CFVR PD was not significantly associated with outcome. CONCLUSIONS: In patients with HCM, impaired CFVR LAD (≤2) is a strong, independent predictor of adverse cardiac outcome. When the aim of testing is HCM risk stratification and CFVR LAD data are available, the evaluation of CFVR PD is redundant. © 2021 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. - Some of the metrics are blocked by yourconsent settings
Publication Prognostic Value of Transthoracic Doppler Echocardiography Coronary Flow Velocity Reserve in Patients with Nonculprit Stenosis of Intermediate Severity Early after Primary Percutaneous Coronary Intervention(2018) ;Tesic, Milorad (36197477200) ;Djordjevic-Dikic, Ana (57003143600) ;Giga, Vojislav (55924460200) ;Stepanovic, Jelena (6603897710) ;Dobric, Milan (23484928600) ;Jovanovic, Ivana (57223117334) ;Petrovic, Marija (57207720679) ;Mehmedbegovic, Zlatko (55778381000) ;Milasinovic, Dejan (24823024500) ;Dedovic, Vladimir (55959310400) ;Zivkovic, Milorad (55959530600) ;Juricic, Stefan (57203033137) ;Orlic, Dejan (7006351319) ;Stojkovic, Sinisa (6603759580) ;Vukcevic, Vladan (15741934700) ;Stankovic, Goran (59150945500) ;Nedeljkovic, Milan (7004488186) ;Ostojic, Miodrag (34572650500)Beleslin, Branko (6701355424)Background: Treatment of nonculprit coronary stenosis during primary percutaneous coronary intervention in patients with ST-segment elevation myocardial infarction may be beneficial, but the mode and timing of the intervention are still controversial. The aim of this study was to examine the significance and prognostic value of preserved coronary flow velocity reserve (CFVR) in patients with nonculprit intermediate stenosis early after primary percutaneous coronary intervention. Methods: Two hundred thirty patients with remaining intermediate (50%–70%) stenosis of non-infarct-related arteries, in whom CFVR was performed within 7 days after primary percutaneous coronary intervention, were prospectively enrolled. Twenty patients with reduced CFVR and positive results on stress echocardiography or impaired fractional flow reserve underwent revascularization and were not included in further analysis. The final study population of 210 patients (mean age, 58 ± 10 years; 162 men) was divided into two groups on the basis of CFVR: group 1, CFVR > 2 (n = 174), and group 2, CFVR ≤ 2 (n = 36). Cardiac death, nonfatal myocardial infarction, and revascularization of the evaluated vessel were considered adverse events. Results: Mean follow-up duration was 47 ± 16 months. Mean CFVR for the whole group was 2.36 ± 0.40. There were six adverse events (3.4%) related to the nonculprit coronary artery in group 1, including one cardiac death, one ST-segment elevation myocardial infarction, and four revascularizations. In group 2, there were 30 adverse events (83.3%, P <.001 vs group 1), including two cardiac deaths, two ST-segment elevation myocardial infarctions, and 26 revascularizations. Conclusions: In patients with CFVR > 2 of the intermediate nonculprit coronary lesion, deferral of revascularization is safe and associated with excellent long-term clinical outcomes. © 2018 American Society of Echocardiography - Some of the metrics are blocked by yourconsent settings
Publication Prompt and consistent improvement of coronary flow velocity reserve following successful recanalization of the coronary chronic total occlusion in patients with viable myocardium(2020) ;Dobric, Milan (23484928600) ;Beleslin, Branko (6701355424) ;Tesic, Milorad (36197477200) ;Djordjevic Dikic, Ana (57003143600) ;Stojkovic, Sinisa (6603759580) ;Giga, Vojislav (55924460200) ;Tomasevic, Miloje (57196948758) ;Jovanovic, Ivana (57223117334) ;Petrovic, Olga (33467955000) ;Rakocevic, Jelena (55251810400) ;Boskovic, Nikola (6508290354) ;Sobic Saranovic, Dragana (57202567582) ;Stankovic, Goran (59150945500) ;Vukcevic, Vladan (15741934700) ;Orlic, Dejan (7006351319) ;Simic, Dragan (57212512386) ;Nedeljkovic, Milan A. (7004488186) ;Aleksandric, Srdjan (35274271700) ;Juricic, Stefan (57203033137)Ostojic, Miodrag (34572650500)Background: Coronary chronic total occlusion (CTO) is characterized by the presence of collateral blood vessels which can provide additional blood supply to CTO-artery dependent myocardium. Successful CTO recanalization is followed by significant decrease in collateral donor artery blood flow and collateral derecruitment, but data on coronary hemodynamic changes in relation to myocardial function are limited. We assessed changes in coronary flow velocity reserve (CFVR) by echocardiography in collateral donor and recanalized artery following successful opening of coronary CTO. Methods: Our study enrolled 31 patients (60 ± 9 years; 22 male) with CTO and viable myocardium by SPECT scheduled for percutaneous coronary intervention (PCI). Non-invasive CFVR was measured in collateral donor artery before PCI, 24 h and 6 months post-PCI, and 24 h and 6 months in recanalized artery following successful PCI of CTO. Results: Collateral donor artery showed significant increase in CFVR 24 h after CTO recanalization compared to pre-PCI values (2.30 ± 0.49 vs. 2.71 ± 0.45, p = 0.005), which remained unchanged after 6-months (2.68 ± 0.24). Baseline blood flow velocity of the collateral donor artery significantly decreased 24 h post-PCI compared to pre-PCI (0.28 ± 0.06 vs. 0.24 ± 0.04 m/s), and remained similar after 6 months, with no significant difference in maximum hyperemic blood flow velocity pre-PCI, 24 h and 6 months post-PCI. CFVR of the recanalized coronary artery 24 h post-PCI was 2.55 ± 0.35, and remained similar 6 months later (2.62 ± 0.26, p = NS). Conclusions: In patients with viable myocardium, prompt and significant CFVR increase in both recanalized and collateral donor artery, was observed within 24 h after successful recanalization of CTO artery, which maintained constant during the 6 months. © 2020 The Author(s).
