Browsing by Author "Petrović, Milovan (16234216100)"
Now showing 1 - 7 of 7
- Results Per Page
- Sort Options
- Some of the metrics are blocked by yourconsent settings
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 An analysis of published cases of cutting balloon use in spontaneous coronary artery dissection(2023) ;Maričić, Bojan (57207569284) ;Perišić, Zoran (21834957000) ;Kostić, Tomislav (26023450500) ;Božinović, Nenad (56614042000) ;Petrović, Milovan (16234216100) ;Čanković, Milenko (57204401342) ;Mehmedbegović, Zlatko (55778381000) ;Juričić, Stefan (57203033137) ;Vasilev, Vladimir (57224717435) ;Dakić, Sonja (55358323700) ;Perišić, Jelena (58713206400) ;Milošević, Jelena (59793378300) ;Bojanović, Mihajlo (57193237478) ;Nikolić, Miroslav (57194436285) ;Maričić, Tijana (57202990526)Apostolović, Svetlana (13610076800)Introduction: SCAD involves a sudden tear or separation within the layers of the coronary artery wall, resulting in blood flow obstruction and subsequent myocardial ischemia. Materials and methods: A comprehensive literature search was conducted to identify relevant published cases of cutting balloon use in patients diagnosed with spontaneous coronary artery dissection. Electronic databases including PubMed, MEDLINE, Embase, Cochrane Library and Google Scholar were systematically searched from inception until the present using terms “cutting balloon,” “SCAD,” “acute coronary syndrome,” “intramural hematoma,” and “angioplasty.” Results: A total of 32 published cases of cutting balloon use in spontaneous coronary artery dissection were analyzed in this study. The majority of the patients included in the analysis were female without prior history of cardiovascular disease. The median age of the SCAD population was approximately 46 years. The most frequently affected artery in SCAD cases was the Left Anterior Descending artery. Intravascular ultrasound was utilized more frequently than other modalities of adjunctive imaging techniques. The most frequent complication was the distal propagation of hematoma. Despite the successful dilation achieved with the cutting balloon, in some cases stenting was required to provide additional support. Conclusion: The results of this analysis demonstrate that cutting balloon use in SCAD cases yields favorable outcomes. 2023 Maričić, Perišić, Kostić, Božinović, Petrović, Čanković, Mehmedbegović, Juričić, Vasilev, Dakić, Perišić, Milošević, Bojanović, Nikolić, Maričić and Apostolović. - Some of the metrics are blocked by yourconsent settings
Publication Characteristics and Outcomes of Patients with Acute Coronary Syndrome and COVID-19(2022) ;Milovančev, Aleksandra (57217948632) ;Petrović, Milovan (16234216100) ;Popadić, Višeslav (57223264452) ;Miljković, Tatjana (57204991851) ;Klašnja, Slobodan (57222576460) ;Djuran, Predrag (57223255944) ;Ilić, Aleksandra (57383582400) ;Kovačević, Mila (56781110100) ;Milosavljević, Anastazija Stojšić (6505915662) ;Brajković, Milica (56115773900) ;Crnokrak, Bogdan (57208706438) ;Memon, Lidija (13007465900) ;Milojević, Ana (57473639100) ;Todorović, Zoran (7004371236) ;Čanković, Milenko (57204401342) ;Šarkanović, Mirka Lukić (55615043800) ;Bjelić, Snežana (57546653200) ;Tadić, Snežana (57194334307) ;Redžek, Aleksandar (6508302832)Zdravković, Marija (24924016800)Acute coronary syndrome (ACS) in patients with COVID-19 is triggered by various mechanisms and can significantly affect the patient’s further treatment and prognosis. The study aimed to investigate the characteristics, major complications, and predictors of mortality in COVID-19 patients with ACS. All consecutive patients hospitalized from 5 July 2020 to 5 May 2021 for ACS with confirmed SARS-Co-2 were prospectively enrolled and tracked for mortality until 5 June 2021. Data from the electronic records for age and diagnosis, matched non-COVID-19 and COVID-19 ACS group, were extracted and compared. Overall, 83 COVID-19 ACS patients, when compared to 166 non-COVID ACS patients, had significantly more prevalent comorbidities, unfavorable clinical characteristics on admission (acute heart failure 21.7% vs. 6.6%, p < 0.01) and higher rates of major complications, 33.7% vs. 16.8%, p < 0.01, and intrahospital 30-day mortality, 6.7% vs. 26.5%, p < 0.01. The strongest predictors of mortality were aortic regurgitation, HR 9.98, 95% CI 1.88; 52.98, p < 0.01, serum creatinine levels, HR 1.03, 95% CI 1.01; 1.04, p < 0.01, and respiratory failure therapy, HR 13.05, 95% CI 3.62; 47.01, p < 0.01. Concomitant ACS and COVID-19 is linked to underlying comorbidi-ties, adverse presenting features, and poor outcomes. Urgent strategies are needed to improve the outcomes of these patients. © 2022 by the authors. Licensee MDPI, Basel, Switzerland. - 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 Relationship between azithromycin and cardiovascular outcomes in unvaccinated patients with covid-19 and preexisting cardiovascular disease(2023) ;Bergami, Maria (57204641344) ;Manfrini, Olivia (6505860414) ;Nava, Stefano (7005445868) ;Caramori, Gaetano (7003847659) ;Yoon, Jinsung (57192154835) ;Badimon, Lina (7102141956) ;Cenko, Edina (55651505300) ;David, Antonio (7402606823) ;Demiri, Ilir (55481504100) ;Dorobantu, Maria (6604055561) ;Fabin, Natalia (57218175196) ;Gheorghe-Fronea, Oana (57204444889) ;Jankovic, Radmilo (15831502700) ;Kedev, Sasko (23970691700) ;Ladjevic, Nebojsa (16233432900) ;Lasica, Ratko (14631892300) ;Loncar, Goran (55427750700) ;Mancuso, Giuseppe (7004330020) ;Mendieta, Guiomar (56248226000) ;Miličić, Davor (56503365500) ;Mjehović, Petra (58266126900) ;Pašalić, Marijan (36010787900) ;Petrović, Milovan (16234216100) ;Poposka, Lidija (23498648800) ;Scarpone, Marialuisa (57204641989) ;Stefanovic, Milena (57216929189) ;Van Der Schaar, Mihaela (35605361700) ;Vasiljevic, Zorana (6602641182) ;Vavlukis, Marija (14038383200) ;Pittao, Maria Laura Vega (57194336728) ;Vukomanovic, Vladan (57144261800) ;Zdravkovic, Marija (24924016800)Bugiardini, Raffaele (26541113500)BACKGROUND: Empiric antimicrobial therapy with azithromycin is highly used in patients admitted to the hospital with COVID-19, despite prior research suggesting that azithromycin may be associated with increased risk of cardiovascular events. METHODS AND RESULTS: This study was conducted using data from the ISACS-COVID- 19 (International Survey of Acute Coronavirus Syndromes-COVID- 19) registry. Patients with a confirmed diagnosis of SARS-CoV- 2 infection were eligible for inclusion. The study included 793 patients exposed to azithromycin within 24 hours from hospital admission and 2141 patients who received only standard care. The primary exposure was cardiovascular disease (CVD). Main outcome measures were 30-day mortality and acute heart failure (AHF). Among 2934 patients, 1066 (36.4%) had preexisting CVD. A total of 617 (21.0%) died, and 253 (8.6%) had AHF. Azithromycin therapy was consistently associated with an increased risk of AHF in patients with preexisting CVD (risk ratio [RR], 1.48 [95% CI, 1.06–2.06]). Receiving azithromycin versus standard care was not significantly associated with death (RR, 0.94 [95% CI, 0.69–1.28]). By contrast, we found significantly reduced odds of death (RR, 0.57 [95% CI, 0.42–0.79]) and no significant increase in AHF (RR, 1.23 [95% CI, 0.75–2.04]) in patients without prior CVD. The relative risks of death from the 2 subgroups were significantly different from each other (Pinteraction=0.01). Statistically significant association was observed between AHF and death (odds ratio, 2.28 [95% CI, 1.34–3.90]). CONCLUSIONS: These findings suggest that azithromycin use in patients with COVID-19 and prior history of CVD is significantly associated with an increased risk of AHF and all-cause 30-day mortality. REGISTRATION: URL: Https://www.clini caltr ials.gov; Unique identifier: NCT05188612. © 2023 The Authors. - Some of the metrics are blocked by yourconsent settings
Publication Results of the trycort: Cohort study of add-on antihypertensives for treatment of resistant hypertension(2023) ;Janković, Slobodan M. (7101906319) ;Stojković, Siniša (6603759580) ;Petrović, Milovan (16234216100) ;Kostić, Tomislav (26023450500) ;Zdravković, Marija (24924016800) ;Radovanović, Slavica (24492602300) ;Cvjetan, Radosava (56866434200) ;Ratković, Nenad (6506233469) ;Rihor, Branislav (57190662754) ;Spiroski, Dejan (57190161724) ;Stanković, Aleksandar (57208351458) ;Andelković, Branko (58300622000)Gocić Petrović, Renata (58300359900)Although true treatment resistant hypertension is relatively rare (about 7.3% of all patients with hypertension), optimal control of blood pressure is not achieved in every other patient due to suboptimal treatment or nonadherence. The aim of this study was to compare effectiveness, safety and tolerability of various add-on treatment options in adult patients with treatment resistant hypertension The study was designed as multi-center, prospective observational cohort study, which compared effectiveness and safety of various add-on treatment options in adult patients with treatment resistant hypertension. Both office and home blood pressure measures were recorded at baseline and then every month for 6 visits. The study cohort was composed of 515 patients (268 females and 247 males), with average age of 64.7 ± 10.8 years. The patients were switched from initial add-on therapy to more effective ones at each study visit. The blood pressure measured both at office and home below 140/90 mm Hg was achieved in 80% of patients with add-on spironolactone, while 88% of patients taking this drug also achieved decrease of systolic blood pressure for more than 10 mm Hg from baseline, and diastolic blood pressure for more than 5 mm Hg from baseline. Effectiveness of centrally acting antihypertensives as add-on therapy was inferior, achieving the study endpoints in <70% of patients. Adverse drug reactions were reported in 9 patients (1.7%), none of them serious. Incidence rate of hyperkalemia with spironolactone was 0.44%, and gynecomastia was found in 1 patient (0.22%). In conclusion, the most effective and safe add-on therapy of resistant hypertension were spironolactone alone and combination of spironolactone and a centrally acting antihypertensive drug. © 2023 Lippincott Williams and Wilkins. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication Sex differences and disparities in cardiovascular outcomes of COVID-19(2023) ;Bugiardini, Raffaele (26541113500) ;Nava, Stefano (7005445868) ;Caramori, Gaetano (7003847659) ;Yoon, Jinsung (57192154835) ;Badimon, Lina (7102141956) ;Bergami, Maria (57204641344) ;Cenko, Edina (55651505300) ;David, Antonio (7402606823) ;Demiri, Ilir (55481504100) ;Dorobantu, Maria (6604055561) ;Fronea, Oana (57219160643) ;Jankovic, Radmilo (15831502700) ;Kedev, Sasko (23970691700) ;Ladjevic, Nebojsa (16233432900) ;Lasica, Ratko (14631892300) ;Loncar, Goran (55427750700) ;Mancuso, Giuseppe (7004330020) ;Mendieta, Guiomar (56248226000) ;Miličić, Davor (56503365500) ;Mjehović, Petra (58266126900) ;Pašalić, Marijan (36010787900) ;Petrović, Milovan (16234216100) ;Poposka, Lidija (23498648800) ;Scarpone, Marialuisa (57204641989) ;Stefanovic, Milena (57216929189) ;van der Schaar, Mihaela (35605361700) ;Vasiljevic, Zorana (6602641182) ;Vavlukis, Marija (14038383200) ;Pittao, Maria Laura Vega (57194336728) ;Vukomanovic, Vladan (57144261800) ;Zdravkovic, Marija (24924016800)Manfrini, Olivia (6505860414)Aims Previous analyses on sex differences in case fatality rates at population-level data had limited adjustment for key patient clinical characteristics thought to be associated with coronavirus disease 2019 (COVID-19) outcomes. We aimed to estimate the risk of specific organ dysfunctions and mortality in women and men. Methods This retrospective cross-sectional study included 17 hospitals within 5 European countries participating in the International Survey and results of Acute Coronavirus Syndromes COVID-19 (NCT05188612). Participants were individuals hospitalized with positive severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) from March 2020 to February 2022. Risk-adjusted ratios (RRs) of in-hospital mortality, acute respiratory failure (ARF), acute heart failure (AHF), and acute kidney injury (AKI) were calculated for women vs. men. Estimates were evaluated by inverse probability weighting and logistic regression models. The overall care cohort included 4499 patients with COVID-19-associated hospitalizations. Of these, 1524 (33.9%) were admitted to intensive care unit (ICU), and 1117 (24.8%) died during hospitalization. Compared with men, women were less likely to be admitted to ICU [RR: 0.80; 95% confidence interval (CI): 0.71–0.91]. In general wards (GWs) and ICU cohorts, the adjusted women-to-men RRs for in-hospital mortality were of 1.13 (95% CI: 0.90–1.42) and 0.86 (95% CI: 0.70–1.05; pinteraction = 0.04). Development of AHF, AKI, and ARF was associated with increased mortality risk (odds ratios: 2.27, 95% CI: 1.73–2.98; 3.85, 95% CI: 3.21–4.63; and 3.95, 95% CI: 3.04–5.14, respectively). The adjusted RRs for AKI and ARF were comparable among women and men regardless of intensity of care. In contrast, female sex was associated with higher odds for AHF in GW, but not in ICU (RRs: 1.25; 95% CI: 0.94–1.67 vs. 0.83; 95% CI: 0.59–1.16, pinteraction = 0.04). Conclusions Women in GW were at increased risk of AHF and in-hospital mortality for COVID-19 compared with men. For patients receiving ICU care, fatal complications including AHF and mortality appeared to be independent of sex. Equitable access to COVID-19 ICU care is needed to minimize the unfavourable outcome of women presenting with COVID-19-related complications. © The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved.
