Browsing by Author "Stojkovic, Sinisa (6603759580)"
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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 Association of Successful Percutaneous Revascularization of Chronic Total Occlusions with Quality of Life: A Systematic Review and Meta-Analysis(2023) ;Kucukseymen, Selcuk (55846782700) ;Iannaccone, Mario (56641379600) ;Grantham, James A. (36130013900) ;Sapontis, James (55884724900) ;Juricic, Stefan (57203033137) ;Ciardetti, Niccolò (57224183207) ;Mattesini, Alessio (36080934900) ;Stojkovic, Sinisa (6603759580) ;Strauss, Bradley H. (7202247260) ;Wijeysundera, Harindra C. (8875771700) ;Werner, Gerald S. (7202099557) ;D'Ascenzo, Fabrizio (36604133600)Di Mario, Carlo (7101723312)Importance: Chronic total occlusion percutaneous coronary intervention (CTO-PCI) is not usually offered because of skepticism about long-term clinical benefits. Objective: To assess the association of successful CTO-PCI with quality of life by analyzing the relevant domains of the Seattle Angina Questionnaire (SAQ). Data Sources: PubMed, EMBASE, Web of Science, Google Scholar, and Cochrane databases were searched to identify randomized trials and observational studies specifically addressing quality of life domains of SAQ from January 2010 to June 2022. Study Selection: Studies included reporting SAQ metrics such as angina frequency, physical limitation, and quality of life, before and after CTO-PCI. Data Extraction and Synthesis: The present study was performed according to the Cochrane Collaboration and Preferred Reporting Items for Systematic Reviews and Meta-Analyses statements, in which fixed-effect or random-effect models with generic inverse-variance weighting depending on statistical homogeneity were applied. Data were extracted by 3 independent reviewers. Outcomes and Measures: The primary outcome was angina frequency; physical limitation and quality of life were assessed as secondary outcomes. Results: Seven prospective randomized or observational studies (2500 patients) were included, with a mean (SD) participant age of 61.2 (2.1) years. CTO-PCI was associated with significantly improved quality-of-life metrics during a mean (SD) follow-up of 14.8 (16.3) months. In patients with successful procedures, angina episodes became less frequent (mean [SD] difference for SAQ angina frequency of 12.9 [3.1] survey points [95% CI, 7.1-19.8 survey points]; standardized mean difference was 0.54 [95% CI, 0.21-0.92]; P =.002; I2 = 86.4%) and they experienced less physical activity limitation (mean [SD] difference for SAQ physical limitation of 9.7 [6.2] survey points [95% CI, 3.5-16.2 survey points]; standardized mean difference was 0.42 [95% CI, 0.24-0.55]; P <.001; I2 = 20.9%), and greater quality-of-life domain (mean [SD] difference for SAQ quality of life of 14.9 [3.5] survey points [95% CI, 7.7-22.5 survey points]; standardized mean difference was 0.41 [95% CI, 0.25-0.61]; P <.001; I2 = 58.8%) compared with patients with optimal medical therapy or failed procedure. Furthermore, follow-up duration (point estimate, 0.03; 95% CI, 0.01-0.04; P =.01) was associated with a significant decrease in angina frequency in meta-regression analysis. Conclusions and Relevance: In this systematic review and meta-analysis examining quality of life following CTO-PCI, successful procedures were associated with improved quality-of-life parameters compared with patients on optimal medical therapy or after failed CTO-PCI. These findings suggest support for using PCI to treat CTOs in symptomatic patients unresponsive to medical treatment. © 2023 American Medical Association. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication Care of patients with ST-elevation myocardial infarction: an international analysis of quality indicators in the acute coronary syndrome STEMI Registry of the EURObservational Research Programme and ACVC and EAPCI Associations of the European Society of Cardiology in 11 462 patients(2023) ;Ludman, Peter (7004079970) ;Zeymer, Uwe (7005045618) ;Danchin, Nicolas (57205956592) ;Kala, Petr (57203043232) ;Laroche, Cécile (7102361087) ;Sadeghi, Masoumeh (35516248000) ;Caporale, Roberto (56211780000) ;Shaheen, Sameh Mohamed (57194856712) ;Legutko, Jacek (7004544253) ;Iakobishvili, Zaza (6603020069) ;Alhabib, Khalid F. (6504139629) ;Motovska, Zuzana (6602188732) ;Studencan, Martin (24282235800) ;Mimoso, Jorge (24734134200) ;Becker, David (57202123334) ;Alexopoulos, Dimitrios (7006042805) ;Kereseselidze, Zviad (57373068900) ;Stojkovic, Sinisa (6603759580) ;Zelveian, Parounak (6603421475) ;Goda, Artan (23049970100) ;Mirrakhimov, Erkin (57508336100) ;Bajraktari, Gani (12764374400) ;Farhan, Hasan Ali (57191269123) ;Šerpytis, Pranas (9841245500) ;Raungaard, Bent (56480714800) ;Marandi, Toomas (7801654145) ;Moore, Alice May (59437777600) ;Quinn, Martin (35747114300) ;Karjalainen, Pasi Paavo (14825484800) ;Tatu-Chitoiu, Gabriel (6602395161) ;Gale, Chris P. (35837808000) ;Maggioni, Aldo P. (57203255222) ;Weidinger, Franz (7004052581) ;Sinnaeve, Peter (57195541521) ;Ferrari, Roberto (57645210500) ;Karamflov, Kiril (58483829700) ;Lidon, R.-M. (6701629431) ;Kereselidze, Z. (57374318100) ;Al-Farhan, H. (57211693108) ;Erglis, Andrejs (6602259794) ;Kedev, Sasko (23970691700) ;Dudek, D. (57536454400) ;Shlyakhto, Evgeny (57565057200) ;Bunc, Matjaz (7004186534) ;Mourali, Mohamed Sami (15762890600) ;Konte, Marème (55873144400) ;Larras, Florian (57208489221) ;Lefrancq, Elin Folkesson (57206737641) ;Mekhaldi, Souad (57337997300) ;Shuka, N. (55385773000) ;Pavli, E. (57373069200) ;Tafaj, E. (57223031094) ;Gishto, T. (57373428800) ;Dibra, A. (8944233800) ;Duka, A. (57373965800) ;Gjana, A. (58375212500) ;Kristo, A. (58483812200) ;Knuti, G. (57338739100) ;Demiraj, A. (14821761300) ;Dado, E. (56001179800) ;Hasimi, E. (56146820100) ;Simoni, L. (57203805359) ;Siqeca, M. (57373428900) ;Sisakian, H. (22836045900) ;Hayrapetyan, H. (55325175500) ;Markosyan, S. (58577964500) ;Galustyan, L. (57374320500) ;Arustamyan, N. (57373245700) ;Kzhdryan, H. (57202249157) ;Pepoyan, S. (57201079556) ;Zirkik, A. (57374320600) ;Von Lewinski, D. (8632627400) ;Paetzold, S. (57374140600) ;Kienzl, I. (57373245800) ;Matyas, K. (57373429000) ;Neunteuf, T. (58483854200) ;Nikfardjam, M. (57212948156) ;Neuhold, U. (57565870300) ;Mihalcz, A. (25228647900) ;Glaser, F. (58584660800) ;Steinwender, C. (8071190600) ;Reiter, C. (56577745400) ;Grund, M. (26643548100) ;Hrncic, D. (57219913699) ;Hoppe, U. (7101650810) ;Hammerer, M. (6505849068) ;Hinterbuchner, L. (54787770500) ;Hengstenberg, C. (7003528759) ;Delle Karth, G. (6602167683) ;Lang, I. (36913118600) ;Winkler, W. (59815864500) ;Hasun, M. (36241791900) ;Kastner, J. (7102283390) ;Havel, C. (6701499838) ;Derntl, M. (57091432600) ;Oberegger, G. (57373069400) ;Hajos, J. (56073309500) ;Adlbrecht, C. (6506745649) ;Publig, T. (6507147209) ;Leitgeb, M.-C. (59166785300) ;Wilfng, R. (58483845700) ;Jirak, P. (57193091034) ;Ho, C.-Y. (58830751400) ;Puskas, L. (57209852339) ;Schrutka, L. (56255043000) ;Spinar, J. (55941877300) ;Parenica, J. (6507420390) ;Hlinomaz, O. (6603237931) ;Fendrychova, V. (57502124100) ;Semenka, J. (6506867803) ;Sikora, J. (56562583200) ;Sitar, J. (56575525500) ;Groch, L. (55878884700) ;Rezek, M. (12141732500) ;Novak, M. (59436297600) ;Kramarikova, P. (57192061583) ;Stasek, J. (57202568302) ;Dusek, J. (57205921288) ;Zdrahal, P. (6603491417) ;Polasek, R. (6507443652) ;Karasek, J. (23397307100) ;Seiner, J. (57195805079) ;Sukova, N. (57056492700) ;Varvarovsky, I. (6506379676) ;Lazarák, T. (56720410800) ;Novotny, V. (57373966000) ;Matejka, J. (22958308400) ;Rokyta, R. (57204366867) ;Volovar, S. (57202108232) ;Belohlavek, J. (56721057300) ;Siranec, M. (57194680683) ;Kamenik, M. (57219380058) ;Kralik, R. (59428734400) ;Ravkilde, J. (7004165556) ;Jensen, S.E. (7401855023) ;Villadsen, A. (6602480644) ;Villefrance, K. (57373786500) ;Schmidt Skov, C. (57373242600) ;Maeng, M. (20034699800) ;Moeller, K. (57373603500) ;Hasan-Ali, H. (23570614700) ;Ahmed, T.A. (49962936500) ;Hassan, M. (57190743307) ;ElGuindy, A. (56631052000) ;Farouk Ismail, M. (57373961500) ;Ibrahim Abd El-Aal, A. (57373786600) ;El-Sayed Gaafar, A. (57374137500) ;Magdy Hassan, H. (57373425800) ;Ahmed Shafe, M. (58483829800) ;Nabil El-Khouly, M. (57373426000) ;Bendary, A. (56023725400) ;Darwish, M. (57373603600) ;Ahmed, Y. (58227279300) ;Amin, O.A. (58760108000) ;AbdElHakim, A. (57377504400) ;Abosaif, K. (57373242700) ;Kandil, H. (57191414616) ;Galal, M.A.G. (57220855039) ;El Hefny, E.E. (57194164499) ;El-Sayed, M. (58224498900) ;Aly, K. (57217358078) ;Mokarrab, M. (57200316587) ;Osman, M. (7201930343) ;Abdelhamid, M. (57069808700) ;Mantawy, S. (57374137600) ;Ali, M.R. (59607152800) ;Kaky, S.D. (57373065700) ;Khalil, V.A. (57373961800) ;Saraya, M.E.A. (57216944944) ;Talaat, A. (57373961900) ;Nabil, M. (57374137700) ;Mounir, W.M. (57373065800) ;Mahmoud, K. (36995868900) ;Aransa, A. (57373962000) ;Kazamel, G. (57208798243) ;Anwar, S. (57931866000) ;Al-Habbaa, A. (57203137095) ;Abd El Monem, M. (57373962100) ;Ismael, A. (57438280900) ;Amin Abu-Sheaishaa, M. (57374317500) ;Abd Rabou, M.M. (57338446800) ;Hammouda, T.M.A. (57469293400) ;Moaaz, M. (57337999900) ;Elkhashab, K. (8056440800) ;Ragab, T. (57222706923) ;Rashwan, A. (57217355631) ;Rmdan, A. (57374137800) ;AbdelRazek, G. (57216510722) ;Ebeid, H. (57188762683) ;Soliman Ghareeb, H. (57374317600) ;Farag, N. (7003613636) ;Zaki, M. (58252659900) ;Seleem, M. (57202458118) ;Torki, A. (57374317700) ;Youssef, M. (7102126211) ;AlLah Nasser, N.A. (57373962200) ;Rafaat, A. (57217019727) ;Selim, H. (57373962300) ;Makram, M.M. (57373603700) ;Khayyal, M. (57374317800) ;Malasi, K. (57373065900) ;Madkour, A. (59429558300) ;Kolib, M. (57374137900) ;Alkady, H. (57203551364) ;Nagah, H. (56830452000) ;Yossef, M. (57373603800) ;Wafa, A. (55769707200) ;Mahfouz, E. (59864018500) ;Faheem, G. (57373426100) ;Magdy Moris, M. (57373243100) ;Ragab, A. (57373962500) ;Ghazal, M. (59428690900) ;Mabrouk, A. (57191880451) ;Hassan, M. (57945242200) ;El-Masry, M. (57722869000) ;Naseem, M. (56692499400) ;Samir, S. (57190758900) ;Reinmets, J. (57191952126) ;Allvee, M. (57374317900) ;Saar, A. (56938478700) ;Ainla, T. (8986491300) ;Vaide, A. (57374138000) ;Kisseljova, M. (57373426200) ;Pakosta, U. (57373066000) ;Eha, J. (6603445303) ;Lotamois, K. (57373066100) ;Sia, J. (26024825800) ;Myllymaki, J. (57373962800) ;Pinola, T. (57373603900) ;Paana, T. (39362004200) ;Mikkelsson, J. (6701464290) ;Ampio, M. (57374318000) ;Tsivilasvili, J. (57373604000) ;Zurab, P. (57373066200) ;Agladze, R. (24922963900) ;Melia, A. (57934916900) ;Gogoberidze, D. (57373426400) ;Khubua, N. (57373243200) ;Totladze, L. (57373604100) ;Metreveli, I. (57189536738) ;Chikovani, A. (57373604200) ;Eitel, I. (23990196400) ;Pöss, J. (24478787400) ;Werner, M. (57191873955) ;Constantz, A. (57373426500) ;Ahrens, C. (57932426000) ;Tolksdorf, H. (57209853541) ;Klinger, S. (57209852815) ;Sack, S. (7005553344) ;Heer, T. (6602496717) ;Lekakis, J. (7006346875) ;Kanakakis, I. (58040472400) ;Xenogiannis, I. (56895998300) ;Ermidou, K. (57373604300) ;Makris, N. (59837149400) ;Ntalianis, A. (6507604197) ;Katsaros, F. (57373962900) ;Revi, E. (57218681487) ;Kafkala, K. (6504803699) ;Mihelakis, E. (57374138200) ;Diakakis, G. (6507126850) ;Grammatikopoulos, K. (57216345584) ;Voutsinos, D. (57218283834) ;Xanthopoulou, I. (33267995900) ;Mplani, V. (56491292100) ;Foussas, S. (7003453457) ;Papakonstantinou, N. (57743141200) ;Patsourakos, N. (8668187400) ;Dimopoulos, A. (14010828600) ;Derventzis, A. (57373426800) ;Athanasiou, K. (57373066300) ;Vassilikos, V.P. (35599391300) ;Papadopoulos, C. (59791025100) ;Tzikas, S. (24479249700) ;Vogiatzis, I. (6603579064) ;Datsios, A. (57193697680) ;Galitsianos, I. (56200351600) ;Koutsampasopoulos, K. (55638459800) ;Grigoriadis, S. (16743763300) ;Douras, A. (6505937759) ;Baka, N. (24176604100) ;Spathis, S. (57373426900) ;Kyrlidis, T. (57374138300) ;Hatzinikolaou, H. (57373243300) ;Kiss, R.G. (57050400100) ;Becker, D. (57373245600) ;Nowotta, F. (57190882269) ;Tóth, K. (57658395500) ;Szabó, S. (57873705500) ;Lakatos, C. (57889237900) ;Jambrik, Z. (6602837035) ;Ruzsa, J. (56568459200) ;Ruzsa, Z. (16319626500) ;Róna, S. (57195523662) ;Toth, J. (57208053362) ;Vargane Kosik, A. (57373243400) ;Toth, K.S.B. (57189593415) ;Nagy, G.G. (57195331558) ;Ondrejkó, Z. (57373066500) ;Körömi, Z. (59777968600) ;Botos, B. (22033373500) ;Pourmoghadas, M. (57217988754) ;Salehi, A. (55616514200) ;Massoumi, G. (55263199800) ;Soleimani, A. (36683110900) ;Sarrafzadegan, N. (6701751316) ;Roohafza, H. (57200041711) ;Azarm, M. (57218573229) ;Mirmohammadsadeghi, A. (58072397200) ;Rajabi, D. (57195106796) ;Rahmani, Y. (57203025548) ;Siabani, S. (25227131300) ;Najaf, F. (58483829900) ;Hamzeh, B. (58588698900) ;Karim, H. (57932007100) ;Siabani, H. (57221446487) ;Saleh, N. (57536984200) ;Charehjoo, H. (57373243700) ;Zamzam, L. (57374318300) ;Al-Temimi, G. (57373066700) ;Al-Yassin, A. (57221403689) ;Mohammad, A. (57219419685) ;Ridha, A. (59055363800) ;Al-Saedi, G. (57221700369) ;Atabi, N. (57373963200) ;Sabbar, O. (57374318400) ;Mahmood, S. (57221391775) ;Dakhil, Z. (6507164761) ;Yaseen, I.F. (57202706048) ;Almyahi, M. (57217584546) ;Alkenzawi, H. (57374138600) ;Alkinani, T. (57373787000) ;Alyacopy, A. (57374318500) ;Kearney, P. (36004465400) ;Twomey, K. (57222248657) ;Shlomo, N. (56500440700) ;Beigel, R. (9637772600) ;Caldarola, P. (26424559600) ;Rutigliano, D. (35076457400) ;Sublimi Saponetti, L. (6507878290) ;Locuratolo, N. (6604034423) ;Palumbo, V. (55493417000) ;Scherillo, M. (6603863722) ;Formigli, D. (24481322400) ;Canova, P. (56014422900) ;Musumeci, G. (59455627900) ;Roncali, F. (57373604500) ;Metra, M. (7006770735) ;Lombardi, C. (56653133600) ;Visco, E. (57205055773) ;Rossi, L. (36887228800) ;Meloni, L. (7004438387) ;Montisci, R. (6604083040) ;Pippia, V. (55637562100) ;Marchetti, M.F. (56426789500) ;Congia, M. (57195280296) ;Cacace, C. (57204317747) ;Luca, G. (57205245638) ;Boscarelli, G. (57373604600) ;Indolf, C. (58286892900) ;Ambrosio, G. (35411918900) ;Mongiardo, A. (8954957800) ;Spaccarotella, C. (8954957900) ;De Rosa, S. (56346580100) ;Canino, G. (56435764000) ;Critelli, C. (58915591800) ;Chiappetta, D. (57223942595) ;Battista, F. (59111554500) ;Gabrielli, D. (6701761641) ;Marziali, A. (57211423512) ;Bernabò, P. (57126113700) ;Navazio, A. (7801328956) ;Guerri, E. (36131197800) ;Manca, F. (57194762525) ;Gobbi, M. (36788464100) ;Oreto, G. (7006418080) ;Andò, G. (6602852014) ;Carerj, S. (56251394000) ;Saporito, F. (6602789507) ;Cimmino, M. (57220374217) ;Rigo, F. (6701803166) ;Zuin, G. (7004825862) ;Tuccillo, B. (59891824600) ;Scotto di Uccio, F. (8313544900) ;Irace, L. (24355574900) ;Lorenzoni, G. (57200941120) ;Meloni, I. (36761283400) ;Merella, P. (59268790800) ;Polizzi, G.M. (35849077700) ;Pino, R. (8259649300) ;Marzilli, M. (56236523800) ;Morrone, D. (36478990700) ;Caravelli, P. (6602502521) ;Orsini, E. (7003892087) ;Mosa, S. (58483812900) ;Piovaccari, G. (7004522515) ;Santarelli, A. (6603964869) ;Cavazza, C. (35263722500) ;Romeo, F. (59877751200) ;Fedele, F. (7005613763) ;Mancone, M. (8428804100) ;Straito, M. (57210284197) ;Salvi, N. (57206729365) ;Scarparo, P. (57201361232) ;Severino, P. (56098536600) ;Razzini, C. (6506934585) ;Massaro, G. (59866489400) ;Cinque, A. (57413969000) ;Gaudio, C. (7003692781) ;Barillà, F. (7003852030) ;Torromeo, C. (6603203291) ;Porco, L. (57207208198) ;Mei, M. (57932424700) ;Iorio, R. (57207199672) ;Nassiacos, D. (6507314719) ;Barco, B. (57212114046) ;Sinagra, G. (7005062509) ;Falco, L. (57225880630) ;Priolo, L. (57195276755) ;Perkan, A. (6602577488) ;Strana, M. (57373066900) ;Percuku, L. (57204362355) ;Berisha, G. (56166637200) ;Mziu, B. (57373067000) ;Beishenkulov, M. (8255168800) ;Abdurashidova, T. (57200720621) ;Toktosunova, A. (57210626946) ;Kaliev, K. (57200720857) ;Serpytis, R. (56523186800) ;Butkute, E. (57194440633) ;Lizaitis, M. (57310563700) ;Broslavskyte, M. (57373963500) ;Xuereb, R.G. (6505856173) ;Moore, A.M. (57373428600) ;Mercieca Balbi, M. (57193711143) ;Paris, E. (57373067100) ;Buttigieg, L. (57613557100) ;Musial, W. (57197287144) ;Dobrzycki, S. (56228737400) ;Dubicki, A. (57373963600) ;Kazimierczyk, E. (57203958301) ;Tycinska, A. (36465694600) ;Wojakowski, W. (55937490100) ;Kalanska-Lukasik, B. (57209502377) ;Ochala, A. (6602690913) ;Wanha, W. (55505179400) ;Dworowy, S. (42561131300) ;Sielski, J. (14023466000) ;Janion, M. (7006611798) ;Janion-Sadowska, A. (8356987700) ;Wojtasik-Bakalarz, J. (57193826943) ;Bryniarski, L. (6701830118) ;Peruga, J.Z. (6603426226) ;Jonczyk, M. (57209454323) ;Jankowski, L. (55502075700) ;Klecha, A. (6603066899) ;Michalowska, J. (57373963700) ;Brzezinski, M. (57432331200) ;Kozmik, T. (57373244100) ;Kowalczyk, T. (57373067300) ;Adamczuk, J. (58102015200) ;Maliszewski, M. (57221859522) ;Kuziemka, P. (57374318700) ;Plaza, P. (26646974600) ;Jaros, A. (58828282000) ;Pawelec, A. (57226182456) ;Sledz, J. (15840873900) ;Bartus, S. (7006869042) ;Zmuda, W. (59823113400) ;Bogusz, M. (57374318800) ;Wisnicki, M. (57373787200) ;Szastak, G. (15132987600) ;Adamczyk, M. (57373427200) ;Suska, M. (26421832800) ;Czunko, P. (6505989814) ;Opolski, G. (55711952200) ;Kochman, J. (6701766095) ;Tomaniak, M. (55962994800) ;Miernik, S. (57492429300) ;Paczwa, K. (57189032340) ;Witkowski, A. (7005762608) ;Opolski, M.P. (23498767100) ;Staruch, A.D. (55208340000) ;Kalarus, Z. (56266442700) ;Honisz, G. (6506240776) ;Mencel, G. (55872078100) ;Swierad, M. (6505793791) ;Podolecki, T. (26431607700) ;Marques, J. (24314835900) ;Azevedo, P. (16644708600) ;Pereira, M.A. (24734386000) ;Gaspar, A. (7102545870) ;Monteiro, S. (35484706700) ;Goncalves, F. (57216745520) ;Leite, L. (58850017600) ;Manuel Lopes dos Santos, W. (57373963900) ;Amado, J. (16681010100) ;Pereira, D. (59868859900) ;Silva, B. (58542500800) ;Caires, G. (18333282800) ;Neto, M. (57214240740) ;Rodrigues, R. (57189234203) ;Correia, A. (59861674300) ;Freitas, D. (57207509749) ;Lourenco, A. (57374319000) ;Ferreira, F. (55815782400) ;Sousa, F. (57373427300) ;Portugues, J. (56182220900) ;Calvo, L. (56182278800) ;Almeida, F. (57197092454) ;Alves, M. (57930438600) ;Silva, A. (18337135100) ;Caria, R. (6507300449) ;Seixo, F. (11639327700) ;Militaru, C. (56538381800) ;Ionica, E. (57374319100) ;Istratoaie, O. (36631934700) ;Florescu, M. (57337676500) ;Lipnitckaia, E. (57373605300) ;Osipova, O. (56736188500) ;Konstantinov, S. (57204916139) ;Bukatov, V. (57218902434) ;Vinokur, T. (57373427400) ;Egorova, E. (57374319200) ;Nefedova, E. (57713377200) ;Levashov, S. (59808049200) ;Gorbunova, A. (57217198882) ;Redkina, M. (57373067500) ;Karaulovskaya, N. (57373067600) ;Bijieva, F. (57374139200) ;Babich, N. (57374139300) ;Smirnova, O. (57212176553) ;Filyanin, R. (57373605600) ;Eseva, S. (57373605700) ;Kutluev, A. (57373605800) ;Chlopenova, A. (57373244300) ;Shtanko, A. (57216269799) ;Kuppar, E. (57373427500) ;Shaekhmurzina, E. (57373964000) ;Ibragimova, M. (58966924600) ;Mullahmetova, M. (57374319400) ;Chepisova, M. (57373605900) ;Kuzminykh, M. (57373067800) ;Betkaraeva, M. (57373067900) ;Namitokov, A. (57164765500) ;Khasanov, N. (57208351235) ;Baleeva, L. (55875114300) ;Galeeva, Z. (26030344500) ;Magamedkerimova, F. (57205152309) ;Ivantsov, E. (57205153699) ;Tavlueva, E. (49362267500) ;Kochergina, A. (56703365700) ;Sedykh, D. (57205548346) ;Kosmachova, E. (58062704900) ;Skibitskiy, V. (6602594791) ;Porodenko, N. (57373606000) ;Litovka, K. (57373964100) ;Ulbasheva, E. (57373787400) ;Niculina, S. (6603731700) ;Petrova, M. (59830512800) ;Harkov, E. (57208059479) ;Tsybulskaya, N. (57373427600) ;Lobanova, A. (57373244500) ;Chernova, A. (58956836200) ;Kuskaeva, A. (57195771388) ;Kuskaev, A. (23008689200) ;Ruda, M. (57203197155) ;Zateyshchikov, D. (59662814100) ;Gilarov, M. (57373787500) ;Konstantinova, E. (21743146300) ;Koroleva, O. (12787716200) ;Averkova, A. (57194269547) ;Zhukova, N. (59792429000) ;Kalimullin, D. (57373787600) ;Borovkova, N. (56379947600) ;Tokareva, A. (59858604700) ;Buyanova, M. (57217080113) ;Khaisheva, L. (56933797900) ;Pirozhenko, A. (57216917175) ;Novikova, T. (57190751817) ;Yakovlev, A. (57188740055) ;Tyurina, T. (57209734721) ;Lapshin, K. (59142801900) ;Moroshkina, N. (57219947605) ;Kiseleva, M. (58381626700) ;Fedorova, S. (57373787900) ;Krylova, L. (57373788000) ;Duplyakov, D. (6506125408) ;Semenova, Y. (57204637814) ;Rusina, A. (57373244600) ;Ryabov, V. (35806315500) ;Syrkina, A. (14029376500) ;Demianov, S. (57374139400) ;Reitblat, O. (58705733900) ;Artemchuk, A. (57373072800) ;Efremova, E. (57189685446) ;Makeeva, E. (59361637100) ;Menzorov, M. (58843081600) ;Shutov, A. (59066220300) ;Klimova, N. (57373250300) ;Shevchenko, I. (55673863100) ;Elistratova, O. (57374145000) ;Kostyuckova, O. (57373793200) ;Islamov, R. (57521739000) ;Budyak, V. (56615354800) ;Ponomareva, E. (58168304900) ;Ullah Jan, U. (57374325100) ;Alshehri, A.M. (57297279600) ;Sedky, E. (57373072900) ;Alsihati, Z. (57373793300) ;Mimish, L. (6603112594) ;Selem, A. (6506500606) ;Malik, A. (55426916700) ;Majeed, O. (58288739300) ;Altnji, I. (57207486247) ;AlShehri, M. (58150215300) ;Aref, A. (57208865766) ;AlDosary, M. (59822382500) ;Tayel, S. (57373970600) ;Abd AlRahman, M. (57914599300) ;Asfna, K.N. (57945938600) ;Abdin Hussein, G. (57374145100) ;Butt, M. (57209858780) ;Markovic Nikolic, N. (57211527501) ;Obradovic, S. (59872958000) ;Djenic, N. (35848370100) ;Brajovic, M. (57373073000) ;Davidovic, A. (57195997815) ;Romanovic, R. (6602427698) ;Novakovic, V. (57338127600) ;Dekleva, M. (56194369000) ;Spasic, M. (56157463900) ;Dzudovic, B. (55443513300) ;Jovic, Z. (35366610200) ;Cvijanovic, D. (59021809000) ;Veljkovic, S. (57337678100) ;Ivanov, I. (56437224800) ;Cankovic, M. (57204401342) ;Jarakovic, M. (56755398200) ;Kovacevic, M. (56781110100) ;Trajkovic, M. (58483844200) ;Mitov, V. (26533102800) ;Jovic, A. (57514592000) ;Hudec, M. (57517803300) ;Gombasky, M. (57373611600) ;Sumbal, J. (6508152433) ;Bohm, A. (54937646300) ;Baranova, E. (57194789250) ;Kovar, F. (55880601400) ;Samos, M. (55624413700) ;Podoba, J. (7004515175) ;Kurray, P. (7801591370) ;Obona, T. (57373073100) ;Remenarikova, A. (57374325200) ;Kollarik, B. (33067978700) ;Verebova, D. (57373793500) ;Kardosova, G. (57373611700) ;Alusik, D. (57204539855) ;Macakova, J. (55915745500) ;Kozlej, M. (57094235300) ;Bayes-Genis, A. (7004094140) ;Sionis, A. (7801335553) ;Garcia Garcia, C. (56973129900) ;Duran Cambra, A. (56472843300) ;Labata Salvador, C. (55878570700) ;Rueda Sobella, F. (55880836800) ;Sans Rosello, J. (30567638800) ;Vila Perales, M. (57201121384) ;Oliveras Vila, T. (55897703900) ;Ferrer Massot, M. (56411977500) ;Bañeras, J. (56032997900) ;Lekuona, I. (6603393515) ;Zugazabeitia, G. (42962848000) ;Fernandez-Ortiz, A. (7005318939) ;Viana Tejedor, A. (57194744834) ;Ferrera, C. (54913336500) ;Alvarez, V. (58584073900) ;Diaz-Castro, O. (6602563778) ;Agra-Bermejo, R.M. (55490422400) ;Gonzalez-Cambeiro, C. (55736707000) ;Gonzalez-Babarro, E. (9239486500) ;Domingo-Del Valle, J. (54791957600) ;Royuela, N. (6505819416) ;Burgos, V. (6507247636) ;Canteli, A. (54400867000) ;Castrillo, C. (24381891600) ;Cobo, M. (59572007400) ;Ruiz, M. (57191951016) ;Abu-Assi, E. (35733241600)Garcia Acuna, J.M. (7003794919)Aims To use quality indicators to study the management of ST-segment elevation myocardial infarction (STEMI) in different regions. Methods and results Prospective cohort study of STEMI within 24 h of symptom onset (11 462 patients, 196 centres, 26 European Society of Cardiology members, and 3 affiliated countries). The median delay between arrival at a percutaneous cardiovascular intervention (PCI) centre and primary PCI was 40 min (interquartile range 20–74) with 65.8% receiving PCI within guideline recommendation of 60 min. A third of patients (33.2%) required transfer from their initial hospital to one that could perform emergency PCI for whom only 27.2% were treated within the quality indicator recommendation of 120 min. Radial access was used in 56.6% of all primary PCI, but with large geographic variation, from 76.4 to 9.1%. Statins were prescribed at discharge to 98.7% of patients, with little geographic variation. Of patients with a history of heart failure or a documented left ventricular ejection fraction ≤40%, 84.0% were discharged on an angiotensin-converting enzyme inhibitor/angiotensin receptor blocker and 88.7% were discharged on beta-blockers. Conclusion Care for STEMI shows wide geographic variation in the receipt of timely primary PCI, and is in contrast with the more uniform delivery of guideline-recommended pharmacotherapies at time of hospital discharge. © The Author(s) 2022. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication Chronic total occlusion percutaneous coronary intervention in clinical practice: Novel grounds to be EXPLOREd(2018) ;Stojkovic, Sinisa (6603759580)Milasinovic, Dejan (24823024500)[No abstract available] - 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 Contemporary indications for percutaneous revascularization of coronary chronic total occlusions(2019) ;Dobric, Milan (23484928600)Stojkovic, Sinisa (6603759580)Chronic total occlusions (CTO) are frequently encountered during coronary angiography, and are generally regarded as the most challenging coronary lesions for percutaneous coronary intervention (PCI). Despite great technical advancements and greatly improved reported procedural success rates during previous years, data on clinical benefit of these procedures still remain scarce and controversial. Data from observational trials suggested that PCI for CTO could be linked to improvements both in symptoms and hard cardiovascular outcomes, while randomized controlled trials showed symptomatic improvement only, without improvement in patient’s prognosis. This is in parallel with findings for non-CTO PCI in patients with stable angina. Having in mind complexity of these interventions, high costs, greater volume of contrast, and radiation exposure, appropriate patient selection is crucial for optimizing treatment effectiveness. There are few important factors that should be taken into consideration before planning and attempting PCI for CTO. These are: severity of patient’s symptoms despite optimal medical therapy, presence of inducible myocardial ischemia and/or viability in the territory of occluded coronary artery. © The Author(s) 2019. - 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 Erratum: Third generation drug eluting stent (DES) with biodegradable polymer in diabetic patients: 5 years follow-up [Cardiovasc Diabetol. (2017)16, 23] 10.1186/s12933-017-0500-3(2017) ;Wiemer, Marcus (7003827848) ;Stojkovic, Sinisa (6603759580) ;Samol, Alexander (15923652000) ;Dimitriadis, Zisis (37085103100) ;Ruiz-Nodar, Juan M. (6602784974) ;Birkemeyer, Ralf (24167873400) ;Monsegu, Jacques (6701634628) ;Finet, Gérard (16554652600) ;Hildick-Smith, David (8089365300) ;Tresukosol, Damras (7003853497) ;Novo, Enrique Garcia (57220415663) ;Koolen, Jacques J. (7004991760) ;Barbato, Emanuele (58118036500)Danzi, Gian Battista (57209549829)After publication of the original article [1], it came to the authors' attention that there was a typo within the author list. The family name of Sinisa Stojkovic was incorrectly spelled 'Stoikovic'. The author's name appears in its correct form in this erratum. - Some of the metrics are blocked by yourconsent settings
Publication Evaluation and management of patients with coronary chronic total occlusions considered for revascularisation. A clinical consensus statement of the European Association of Percutaneous Cardiovascular Interventions (EAPCI) of the ESC, the European Association of Cardiovascular Imaging (EACVI) of the ESC, and the ESC Working Group on Cardiovascular Surgery(2024) ;Galassi, Alfredo R. (7004438532) ;Vadalà, Giuseppe (57203403924) ;Werner, Gerald S. (7202099557) ;Cosyns, Bernard (57202595662) ;Sianos, Georgios (7003691774) ;Hill, Jonathan (55652210200) ;Dudek, Dariusz (7006649800) ;Picano, Eugenio (7102408994) ;Novo, Giuseppina (56962711700) ;Andreini, Daniele (8342392800) ;Gerber, Bernhard L.M. (7102014010) ;Buechel, Ronny (30267456100) ;Mashayekhi, Kambis (36915264400) ;Thielmann, Mathias (55855120800) ;McEntegart, Margaret (12787521600) ;Vaquerizo, Beatriz (24578251900) ;Di Mario, Carlo (7101723312) ;Stojkovic, Sinisa (6603759580) ;Sandner, Sigrid (6602137763) ;Bonaros, Nikolaos (6602270254)Lüscher, Thomas F. (18935805600)Chronic total occlusions (CTOs) of coronary arteries can be found in the context of chronic or acute coronary syndromes; sometimes they are an incidental finding in those apparently healthy individuals undergoing imaging for preoperative risk assessment. Recently, the invasive management of CTOs has made impressive progress due to sophisticated preinterventional assessment, including advanced non-invasive imaging, the availability of novel and dedicated tools for CTO percutaneous coronary intervention (PCI), and experienced interventionalists working in specialised centres. Thus, it is crucial that referring physicians who see patients with CTO be aware of recent developments and of the initial evaluation requirements for such patients. Besides a careful history and clinical examination, electrocardiograms, exercise tests, and non-invasive imaging modalities are important for selecting the patients most suitable for CTO PCI, while others may be referred to coronary artery bypass graft or optimal medical therapy only. While CTO PCI improves angina and reduces the use of antianginal drugs in patients with symptoms and proven ischaemia, hibernation and/or wall motion abnormalities at baseline or during stress, the effect of CTO PCI on major cardiovascular events is still controversial. This clinical consensus statement specifically focuses on referring physicians, providing a comprehensive algorithm for the preinterventional evaluation of patients with CTO and the current evidence for the clinical effectiveness of the procedure. The proposed care track has been developed by members and with the support of the European Association of Percutaneous Cardiovascular Interventions (EAPCI), the European Association of Cardiovascular Imaging (EACVI), and the European Society of Cardiology (ESC) Working Group on Cardiovascular Surgery. © 2024 Taylor and Francis Inc.. All rights reserved. - 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 clinical outcomes after bioresorbable and permanent polymer drug-eluting stent implantation: Final five-year results of the CENTURY II randomised clinical trial(2018) ;Wijns, William (7006420435) ;Valdes-Chavarri, Mariano (7101845217) ;Richardt, Gert (7006414918) ;Moreno, Raul (6506647911) ;Iniguez-Romo, Andres (7005329352) ;Barbato, Emanuele (58118036500) ;Carrie, Didier (7006798967) ;Ando, Kenji (35399496600) ;Merkely, Béla (7004434435) ;Kornowski, Ran (16947378300) ;Eltchaninoff, Hélène (7005210072) ;Stojkovic, Sinisa (6603759580)Saito, Shigeru (7404854449)Aims: The aim of this study was to establish the long-term safety and efficacy of a sirolimus-eluting stent with bioresorbable polymer (BP-SES; Ultimaster) by comparison with an everolimus-eluting stent with permanent polymer (PP-EES; XIENCE). Methods and results: CENTURY II (Clinical Evaluation of New Terumo Drug-Eluting Coronary Stent System in the Treatment of Patients with Coronary Artery Disease) is a large-scale, prospective, multicentre, randomised single-blind, controlled, non-inferiority trial conducted at 58 study sites globally, including Europe, Japan and Korea, powered to prove non-inferiority for freedom from target lesion failure (TLF: cardiac death, target vessel-related myocardial infarction [MI] and target lesion revascularisation) at nine months. Patients requiring a percutaneous coronary intervention (PCI) were randomised (1:1) to BP-SES (n=551) or PP-EES (n=550). Freedom from TLF at five years was 90.0% in the BP-SES and 91.1% in the PP-EES group (p=0.54). The patient-oriented composite endpoint (all death, any MI, any revascularisation) was 24.1 and 25.6% (p=0.57) with BP-SES and PP-EES, respectively. The very late stent thrombosis rate from one to five years was especially low at 0.2% in both arms. Conclusions: This randomised clinical trial showed that the BP-SES stent was non-inferior to the benchmark PP-EES stent for TLF. Safety and efficacy measures were comparable up to five-year follow-up after PCI. © Europa Digital & Publishing 2018. - 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 One-year performance of thin-strut cobalt chromium sirolimus-eluting stent versus thicker strut stainless steel biolimus-eluting coronary stent: A propensity-matched analysis of two international all-comers registries(2021) ;Vlieger, Selina (57202132865) ;Danzi, Gian B. (57209549829) ;Kauer, Floris (26434782400) ;Oemrawsingh, Rohit M. (24172653000) ;Stojkovic, Sinisa (6603759580) ;Ijsselmuiden, Alexander J.J. (6603297809) ;Routledge, Helen (6601978602) ;Laanmets, Peep (55345333500) ;Roffi, Marco (7004532440) ;Fröbert, Ole (7003840907) ;Baello, Pascual (6508051562) ;Wlodarczak, Adrian (56664531100) ;Puentes, Angel (36157145300) ;Polad, Jawed (8561333000)Hildick-Smith, David (8089365300)Objectives Recent improvements in coronary stent design have focussed on thinner struts, different alloys and architecture, more biocompatible polymers, and shorter drug absorption times. This study evaluates safety and efficacy of a newer generation thin-strut cobalt chromium sirolimus-eluting coronary stent (SES, Ultimaster) in comparison with a second-generation thicker strut stainless steel biolimus-eluting stent (BES, Nobori) in percutaneous coronary intervention (PCI) practice. Methods A propensity score analysis was performed to adjust for differences in baseline characteristics of 8137 SES patients and 2738 BES patients of two PCI registries (e-Ultimaster and NOBORI 2). An independent clinical event committee adjudicated all endpoint-related adverse events. Results The use of SES, as compared with BES was associated with a significantly lower rate of myocardial infarction (MI) (1.2% vs 2.2%; P = 0.0006) and target vessel-related MI (1.1% vs 1.8%; P = 0.002) at 1 year. One-year composite endpoints of all predefined endpoints were lower in patients undergoing SES implantation (target lesion failure: 3.2% vs 4.1%; P = 0.03, target vessel failure: 3.7% vs 5.0%; P = 0.003, patient-oriented composite endpoint 5.7% vs 6.8%; P = 0.03). No significant differences between SES and BES were observed in all-cause death (2.0% vs 1.6%; P = 0.19), cardiac death (1.2% vs 1.2%; P = 0.76) or stent thrombosis (0.6% vs 0.8%; P = 0.43). Conclusions These findings suggest an improved clinical safety and efficacy of a newer generation thin-strut SES as compared with a second-generation thicker strut BES. © 2021 Lippincott Williams and Wilkins. All rights reserved. - 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 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). - Some of the metrics are blocked by yourconsent settings
Publication Reclassification of CTO Crossing Strategies in the ERCTO Registry According to the CTO-ARC Consensus Recommendations(2024) ;Vadalà, Giuseppe (57203403924) ;Mashayekhi, Kambis (36915264400) ;Boukhris, Marouane (55771360100) ;Behnes, Michael (24175917200) ;Pyxaras, Stylianos (24179362300) ;Christiansen, Evald Høj (16149043800) ;Gutiérrez-Chico, Juan Luis (8316785400) ;Maniscalco, Laura (57204080896) ;Stojkovic, Sinisa (6603759580) ;Bozinovic, Nenad Z. (56614042000) ;Boudou, Nicolaus (25644193800) ;Garbo, Roberto (6506467751) ;Werner, Gerald S. (7202099557) ;Avran, Alexander (57191835867) ;Gasparini, Gabriele L. (12775032600) ;La Scala, Eugenio (6508334276) ;Ladwiniec, Andrew (26026356500) ;Sianos, George (7003691774) ;Goktekin, Omer (7003402250) ;Gorgulu, Sevket (56209450200) ;Agostoni, Pierfrancesco (57226223987) ;Rathore, Sudhir (22235271400) ;Ayoub, Mohamed (57055208800) ;Diletti, Roberto (36542096100) ;di Mario, Carlo (7101723312) ;Bulum, Joško (23017736900)Galassi, Alfredo R. (7004438532)Background: The CTO-ARC (Chronic Total Occlusion Academic Research Consortium) recognized that a nonstandardized definition of chronic total occlusion (CTO) percutaneous coronary intervention approaches can bias the complications’ attribution to each crossing strategy. Objectives: The study sought to describe the numbers, efficacy, and safety of each final CTO crossing strategy according to CTO-ARC recommendations. Methods: In this cross-sectional study, data were retrieved from the European Registry of Chronic Total Occlusions between 2021 and 2022. Results: Out of 8,673 patients, antegrade and retrograde approach were performed in 79.2% and 20.8% of cases, respectively. The antegrade approach included antegrade wiring and antegrade dissection and re-entry, both performed with or without retrograde contribution (antegrade wiring without retrograde contribution: n = 5,929 [68.4%]; antegrade wiring with retrograde contribution: n = 446 [5.1%]; antegrade dissection and re-entry without retrograde contribution: n = 353 [4.1%]; antegrade dissection and re-entry with retrograde contribution: n = 137 [1.6%]). The retrograde approach included retrograde wiring (n = 735 [8.4%]) and retrograde dissection and re-entry (n = 1,073 [12.4%]). Alternative antegrade crossing was associated with lower technical success (70% vs 86% vs 93.1%, respectively; P < 0.001) and higher complication rates (4.6% vs 2.9% vs 1%, respectively; P < 0.001) as compared with retrograde and true antegrade crossing. However, alternative antegrade crossing was applied mostly as a rescue strategy (96.1%). Conclusions: The application of CTO-ARC definitions allowed the reclassification of 6.7% of procedures as alternative antegrade crossing with retrograde or antegrade contribution which showed higher MACCE and lower technical success rates, as compared with true antegrade and retrograde crossing. © 2024 The Authors
