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1.
Cardiovasc Revasc Med ; 53: 28-35, 2023 08.
Article de Anglais | MEDLINE | ID: mdl-36907696

RÉSUMÉ

BACKGROUND: Ultra-thin strut drug-eluting stent (UTS-DES) may improve outcomes after percutaneous coronary intervention (PCI) but have received limited study in chronic total occlusion (CTO) PCI. AIMS: To compare of 1-year incidence of major adverse cardiac events (MACE) between patients who underwent CTO PCI with ultrathin (≤ 75 µm) versus thin (>75 µm) strut DES in the LATAM CTO registry. METHODS: Patients were considered for inclusion only if successful CTO PCI was performed and when only one type of stent strut thickness (ultrathin or thin) was used. A propensity score matching (PSM) was computed to produce similar groups in relation to clinical and procedural characteristics. RESULTS: Between January 2015 and January 2020, 2092 patients underwent CTO PCI, of whom 1466 were included in the present analysis (475 in the ultra-thin and 991 in the thin strut DES). In unadjusted analysis the UTS-DES group had lower rate of MACE (HR: 0.63 95 % CI 0.42 to 0.94, p = 0.04) and repeat revascularizations (HR: 0.50 95 % CI 0.31 to 0.81, p = 0.02) at 1-year follow-up. After adjustment for confounding factors in a Cox regression model there was no difference in 1-year incidence of MACE between groups (HR: 1.15 95 % CI 0.41 to 2.97, p = 0.85). On PSM of 686 patients (343 in each group) the 1-year incidence of MACE (HR 0.68 95 % CI 0.37-1.23; P = 0.22) and individual components of MACE did not differ between groups. CONCLUSIONS: One-year clinical outcomes after CTO PCI were similar with ultrathin and thin strut DES.


Sujet(s)
Occlusion coronarienne , Endoprothèses à élution de substances , Intervention coronarienne percutanée , Humains , Endoprothèses à élution de substances/effets indésirables , Intervention coronarienne percutanée/effets indésirables , Occlusion coronarienne/imagerie diagnostique , Occlusion coronarienne/thérapie , Occlusion coronarienne/étiologie , Résultat thérapeutique , Enregistrements , Maladie chronique , Facteurs de risque
2.
J Am Heart Assoc ; 11(11): e024815, 2022 06 07.
Article de Anglais | MEDLINE | ID: mdl-35656976

RÉSUMÉ

Background Coronary perforation is a life-threatening complication of acute percutaneous coronary intervention (PCI) for chronic total occlusions (CTO), but data on midterm outcomes are limited. Methods and Results Data from LATAM (Latin American)-CTO Registry (57 centers; 9 countries) were analyzed. We assessed the risk of 30-day, 1-year major adverse cardiac events of coronary perforation using time-to-event and weighted composite end point analysis having CTO PCI without perforation as comparators. Additionally, we studied the independent predictors of perforation in these patients. Of 2054 patients who underwent CTO PCI between 2015 and 2018, the median Multicenter CTO Registry in Japan and Prospective Global Registry for the Study of Chronic Total Occlusion Intervention-Chronic total occlusions scores were 2.0 (1.0-3.0) and 1.0 (0.0-2.0), respectively. The perforation rate was 3.7%, of which 55% were Ellis class 1. After 1-year coronary perforation had higher major adverse cardiac events rates (24.9% versus 13.3%; P<0.01). Using weighted composite end point, perforation was associated with increased bleeding and ischemic events at 6 months (P=0.04) and 1 year (P<0.01). We found as independent predictors associated with coronary perforation during CTO PCI: maximum activated clotting time (P<0.01), Multicenter CTO Registry in Japan score ≥2 (P=0.05), antegrade knuckle wire (P=0.04), and right coronary artery CTO PCI (P=0.05). Conclusions Coronary perforation was infrequent and associated with anatomical and procedural complexity, resulting in higher risk of hemorrhagic and ischemic events. Landmark and weighted analysis showed a sustained burden of major events between 6 months and 1 year follow-up.


Sujet(s)
Lésions traumatiques du coeur , Intervention coronarienne percutanée , Maladie chronique , Coronarographie/effets indésirables , Lésions traumatiques du coeur/épidémiologie , Lésions traumatiques du coeur/étiologie , Humains , Amérique latine/épidémiologie , Intervention coronarienne percutanée/effets indésirables , Intervention coronarienne percutanée/méthodes , Études prospectives , Enregistrements , Facteurs de risque , Facteurs temps , Résultat thérapeutique
3.
Catheter Cardiovasc Interv ; 96(5): 1046-1055, 2020 11.
Article de Anglais | MEDLINE | ID: mdl-31990453

RÉSUMÉ

OBJECTIVES: To report clinical, angiographic characteristics, outcomes, and predictors of unsuccessful procedures in patients who underwent chronic total occlusion (CTO) percutaneous coronary interventions (PCI) in Latin America. BACKGROUND: CTO PCI has been increasingly performed worldwide, but there is a lack of information in this region. METHODS: An international multicenter registry was developed to collect data on CTO PCI performed in centers in Latin America. Patient, angiographic, procedural and outcome data were evaluated. Predictors of unsuccessful procedures were assessed by multivariable analysis. RESULTS: We have included data related to 1,040 CTO PCIs performed in seven countries in Latin America (Argentina, Brazil, Chile, Colombia, Ecuador, Mexico, and Puerto Rico). The mean age was 64 ± 10 years, and CTO PCI was performed mainly for angina control (81%) or treatment of a large ischemic area (30%). Overall technical success rate was 82.5%, and it was achieved with antegrade wire escalation in 81%, antegrade dissection/re-entry in 8% and with retrograde techniques in 11% of the successful procedures. Multivariable analysis identified moderate/severe calcification, a blunt proximal cap and a previous attempt as independent predictors of unsuccessful procedures. In-hospital major adverse cardiovascular events (MACE) occurred in 3.1% of the cases, death in 1% and cardiac tamponade in 0.9% CONCLUSIONS: CTO PCI in Latin America has been performed mainly for ischemia relief. Procedures were associated with a success rate above 80% and low incidence of MACE. Predictors of unsuccessful procedures were similar to those previously reported in the literature.


Sujet(s)
Occlusion coronarienne/thérapie , Intervention coronarienne percutanée , Sujet âgé , Maladie chronique , Coronarographie , Occlusion coronarienne/imagerie diagnostique , Occlusion coronarienne/mortalité , Femelle , Mortalité hospitalière , Humains , Amérique latine , Mâle , Adulte d'âge moyen , Infarctus du myocarde/mortalité , Intervention coronarienne percutanée/effets indésirables , Intervention coronarienne percutanée/mortalité , Enregistrements , Appréciation des risques , Facteurs de risque , Accident vasculaire cérébral/mortalité , Facteurs temps , Résultat thérapeutique
4.
Int J Artif Organs ; 40(3): 118-122, 2017 Apr 21.
Article de Anglais | MEDLINE | ID: mdl-28315503

RÉSUMÉ

INTRODUCTION: Roller pumps are widely used in procedures involving cardiopulmonary bypass (CPB) due to their ease of operation and maintenance, safety, and cost. Several studies in the literature have compared the use of roller pumps with centrifugal pumps, but the influence of the roller pump adjustment on hemolysis has been poorly explored. METHODS: Measurements of hemolysis rates were carried out in 86 patients. The pump was adjusted by the dynamic calibration method, which was performed by an auxiliary device, and the patients were grouped according to the pump calibration: Group 1 (n = 20) 75 mmHg; Group 2 (n = 24) 150 mmHg; Group 3 (n = 22) 300 mmHg and Group 4 (n = 21) 450 mmHg. The hemolysis rates were measured at 4 different times during CPB (T0: before the surgical procedure; T1: 5 minutes after the start of CPB; T2: 30 minutes of CPB; and T3: 5 minutes after the CPB procedure). Hemolysis rates were calculated between the time intervals T0-T1, T1-T2, and T0-T3. RESULTS: No difference in hemolysis rates was observed between the groups (p>0.31). During the first 5 minutes of CPB, hemolysis represented 35.5% of the total hemolysis and no significant difference was found between groups (p>0.60). CONCLUSIONS: Calibration of roller pumps by the dynamic method did not influence the hemolysis rates. Additionally, the hemolysis during the first 5 minutes of CPB accounted for ~1/3 of the total hemolysis.


Sujet(s)
Calibrage , Pontage cardiopulmonaire/instrumentation , Coeur-poumon artificiel , Hémolyse , Femelle , Hématocrite , Hémoglobines/analyse , Humains , Mâle , Adulte d'âge moyen , Période périopératoire , Spectrophotométrie
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