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Coronary Occlusion

Coronary Occlusion is the partial or complete blockage of one or more coronary arteries, resulting in reduced blood flow to the heart muscle.
This condition can lead to myocardial infarction, angina, and other serious cardiovascular complications.
Effective research and treatment approaches are critical for addressing this significant health concern.
PubCompare.ai offers powerful tools to optimize Coronary Occlusion research, enhancing reproducibility, accuracy, and workflow efficiency.
Easily locate relevant protocols from literature, preprints, and patents, and leverage AI-driven comparisons to identify the best protocols and products.
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Most cited protocols related to «Coronary Occlusion»

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Publication 2008
Angina Pectoris Asymptomatic Diseases Biological Markers Blood Vessel Brain Brain Metastases Cardiovascular System Cerebral Ventriculography Cerebrovascular Accident Chest Pain Clinical Reasoning Compassion Fatigue Congenital Abnormality Coronary Artery Disease Coronary Occlusion Diagnosis Dyspnea Echocardiography Edema Exercise Tests Heart Heart Ventricle Hospitalization Infection Interviewers Left Ventricular Diastolic Dysfunction Myocardial Infarction Myocardial Ischemia Neoplasms Outpatients Patients Physical Examination Physicians Pulmonary Edema Radiography, Thoracic Traumatic Brain Injury Wounds and Injuries
The conditioned medium was prepared by growing the transformed MSCs in a chemically defined serum free culture medium for three days as previously described [33 (link)]. The concentrated conditioned medium was processed by HPLC fractionation to obtain the exosomes as mentioned above. The exosomes were tested in a mouse model of MI/R injury. Myocardial ischemia was induced by 30 minutes left coronary artery (LCA) occlusion and subsequent reperfusion. Five minutes before reperfusion, mice were intravenously infused with 200 μl saline solution of 0.3 μg exosome protein purified from culture medium conditioned by MYC-MSCs. Control animals were infused with 200 μl saline. After 24 hours reperfusion, infarct size (IS) as a percentage of the area at risk (AAR) was assessed using Evans' blue dye injection and TTC staining as described previously [27 (link)]. All animal experiments were performed in accordance with the national guidelines on animal care and with prior approval by the Animal Experimentation Committee of Utrecht University.
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Publication 2011
Animals Coronary Occlusion Culture Media Culture Media, Conditioned Evans Blue Exosomes Fractionation, Chemical High-Performance Liquid Chromatographies Infarction Injuries Mus Myocardial Ischemia Proteins Reperfusion Saline Solution Serum
The ACh‐provocation test was performed as described previously in the indication and procedure of the VSA Guideline by the Japanese Circulation Society.22 (link) Coronary spasm was defined as total or subtotal obstruction within the borders of 1 isolated coronary segment as defined by the American Heart Association23 (link) (focal spasm) or severe diffuse vasoconstriction (90% stenosis defined by the American Heart Association23 (link) [76% to 90% narrowing of the luminal diameter]) observed in ≥2 adjacent coronary segments (diffuse spasm) of epicardial coronary arteries associated with transient myocardial ischemia, as evidenced by ischemic ST‐segment changes on the ECG. In the present study, we divided the patients positive for ACh‐provocation test into 2 groups based on the pattern of coronary artery spasm on coronary angiography during ACh‐provocation test: those with focal and those with nonfocal (diffuse) spasm patterns. Figure 1 shows coronary angiographic findings of representative cases of focal and diffuse spasm patterns. Patients who developed ACh‐induced focal spasm with or without diffuse spasm in other coronary segments were included into the focal spasm group (Figure 1A through 1C), whereas patients who had only ACh‐induced diffuse spasm were included in the diffuse spasm group (Figure 1D through 1F). In this study, ischemic ST‐segment changes were defined as ST‐segment elevation (>0.1 mV), ST‐segment depression (>0.1 mV) from baseline level occurring at 60 to 80 ms after J point in at least 2 contiguous leads on the 12‐lead ECG, or appearance of a new negative U wave on the ECG. Multivessel spasm was defined as ACh‐induced spasm of ≥2 major epicardial arteries. Myocardial lactate production was evidenced by comparing serum lactate concentrations at the root of the aorta and coronary sinus, sampled during myocardial ischemia induced by ACh‐provocation.
Publication 2013
Aortic Root Arteries Artery, Coronary Coronary Angiography Coronary Arteriosclerosis Coronary Artery Vasospasm Coronary Occlusion Electrocardiography, 12-Lead Heart Japanese Lactate Myocardium Patients Phenobarbital Serum Sinus, Coronary Spasm Stenosis Transients Vasoconstriction
All animal studies were approved by the animal protocol review committee at Baylor College of Medicine. Smad3 −/− mice 17 (link),16 (link) and wildtype (WT) C57/BL/6 controls underwent reperfused myocardial infarction experiments using a closed-chest model of coronary occlusion/reperfusion. 18 (link)
Sections from paraffin-embedded hearts were immunolabeled with anti-Ki-67 and anti-α-SMA antibodies to allow identification of proliferating myofibroblasts. Identification of apoptotic cells was performed using fluorescent In situ Cell Death Detection Kit (Roche). 19 (link) The collagen content in infarcted hearts network was assessed using picrosirius red staining and a hydroxyproline assay. Single cell suspensions were prepared from infarcted hearts after 72h of reperfusion and underwent flow cytometric analysis of α-SMA and collagen I expression.
In order to investigate the role of Smad3 signaling in fibroblast phenotype and function, mouse fibroblasts from WT and Smad3 −/− hearts were isolated by enzymatic digestion. Growth factor-stimulated cells were used for collagen lattice contraction assay, transwell migration assay, 19 (link) cell proliferation assay, 19 (link) immunofluorescence, flow cytometry, RNA and protein extraction. Real time PCR was used to assess expression of extracellular matrix proteins. α-SMA expression in infarcted hearts and isolated cells was assessed using established western blotting protocols. 16 (link)
Publication 2010
Animals Anti-Antibodies Apoptosis Biological Assay Cell Death Cell Migration Assays Cell Proliferation Cells Chest Collagen Collagen Type I Coronary Occlusion Dental Occlusion Digestion Enzymes Extracellular Matrix Proteins Fibroblasts Flow Cytometry Growth Factor Heart Hydroxyproline Immunofluorescence Mus Myocardial Reperfusion Myofibroblasts Paraffin Embedding Pharmaceutical Preparations Phenotype Proteins Real-Time Polymerase Chain Reaction Reperfusion SMAD3 protein, human
Please see detailed Methods in the Online Supplement which provide expanded details of in vivo I/R and hemodynamic measurements, heart tissue preparation and nuclear fractionation, TUNEL, DNA laddering, CaMKII and NF-κB activity assays, immunofluorescence staining and affymetrix gene array analysis. Generation of global CaMKIIδ KO mice was described previously23 (link). Cardiac specific CaMKIIδ KO mice were generated by crossing heterozygous floxed CaMKIIδ mice23 (link) with MLC 2v-Cre mice28 (link) as detailed in the Online Supplement. Myocardial I/R was induced by left anterior descending (LAD) coronary artery occlusion for 1 hr followed by reperfusion for various times up to 24 hrs. All animal studies were performed in accordance with the NIH Guide for the Care and Use of Laboratory Animals and approved by the Institutional Animal Care and Use Committee of UCSD.
Publication 2013
Animals Animals, Laboratory Biological Assay Calmodulin-Dependent Protein Kinase II Coronary Occlusion Dietary Supplements Fractionation, Chemical Genes Heart Hemodynamics Heterozygote Immunofluorescence In Situ Nick-End Labeling Institutional Animal Care and Use Committees Mice, Laboratory Myocardium RELA protein, human Reperfusion Tissues

Most recents protocols related to «Coronary Occlusion»

It is a preliminary report with a quasi-experimental design, and with a pre-test and post-test approach to compare the effect of PCI in CTO patients. Forty subjects were recruited from January through June 2019. The inclusion criteria in this study were: 1) coronary heart disease (CHD) patients who showed CTO on coronary angiography that involved only one coronary artery branch occlusion; 2) patients who were willing to sign the informed consent of the study to undergo elective PCI; 3) patients who did not have heart failure abnormalities; 4) age between 40 and 70 years; 5) not in the acute phase of myocardial infarction; 6) not having abnormalities on the 12-lead electrocardiography (ECG) (signs of acute ischemia in the form of ST-elevation or ST depression); 7) left ventricular ejection fraction (LVEF) > 50%; 8) angiography with critical stenosis > 90%; and 9) normal valvular function. Based on the included samples, patients who were: 1) with multi-vessel disease; 2) with stage V renal failure requiring regular hemodialysis; 3) with malignancy; 4) with conditions that do not allow elective PCI intervention; and 5) with diastolic dysfunction (> grade 1) on echocardiography, should be excluded from the study sample.
Publication 2023
Angiography Congenital Abnormality Congenital Heart Defects Coronary Angiography Coronary Arteriosclerosis Coronary Occlusion Diastole Echocardiography Electrocardiography, 12-Lead Hemodialysis Ischemia Kidney Failure Malignant Neoplasms Myocardial Infarction Patients Stenosis Vascular Diseases Ventricular Ejection Fraction
After anesthesia of the animal using a combination of ketamine and xylazine, the surgical site on the animal’s chest was disinfected with 70% alcohol. After keeping the animal fixed on the operating desk, using an otoscope number 3 and a green angiocatheter, the animal was intubated and connected to a ventilator (inter med Bear) (inhaul to exhalation ratio of 1 to 2 and 80–90 breaths per minute with a volume of 8 ml). In the space between the third and fourth ribs, the chest was cut to a length of 10 mm. With this incision, the LAD vessel was identified as a bright red pulsating spike that flows in the middle of the heart wall from under the left atrium to the apex of the heart. The LAD vessel was closed with the help of 0.6 mm polypropylene suture 1–2 mm below the level of the tip of the left atrium and was completely closed by tying two knots at this point. Left ventricular anterior wall infarction was confirmed by sudden myocardial coloration (discoloration). An increase in ST was also observed after ligation. Then, the chest, muscle layers, and skin were sewn in three layers using 0.5 proline suture and the animal's skin was sutured with 0.3 proline suture. When the rats regained consciousness, they were removed from the ventilator. After 48 h, the rats were anesthetized again and with echo vivid7 probe 10 s (MHz), an echo was performed to determine MI. In addition, cefazolin and tramadol as antibiotics and analgesics were injected twice a day, 1 day before surgery and 3 days after surgery. Rats in the MI group underwent all surgeries without occlusion of the left coronary artery. Also, Ct group rats did not receive any intervention and were kept only in the laboratory.
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Publication 2023
Analgesics Anesthesia Animals Anterior Wall Myocardial Infarction Antibiotics, Antitubercular Atrium, Left Bears Bladder Detrusor Muscle Blood Vessel Cefazolin Chest Consciousness Coronary Occlusion ECHO protocol Ethanol Exhaling Heart Ketamine Left Ventricles Ligation Myocardium Operative Surgical Procedures Otoscopes Polypropylenes Proline Rattus norvegicus Ribs Skin Sutures Thoracic Surgical Procedures Tramadol Xylazine
We started a CTO program in our institution in May 2007 with a low case volume during its initial stages increasing trend in patient recruitment with at least 50 procedures a year since 2013. Five workshops over 5 consecutive years with experienced operators were organized in our center as part of training in CTO-PCI and in order to improve local operators’ experience. We had a dedicated operator in our institution for CTOs, although a few procedures were performed by a second operator in the first 100 block of cases. A CTO was defined as the presence of a coronary artery segment obstruction greater than 3 months standing with Thrombolysis in Myocardial Infarction (TIMI) grade 0 flow [10 (link)]. All data were prospectively introduced into a database including all potential angiographic variables previously related to the difficulty of the procedural success such as ostial location for example [11 (link)]. Since the publication of the J-CTO score by Morino et al. [7 (link)] in 2011 derived from Multicenter CTO Registry in Japan [12 (link)] those variables related to the wire crossing time through a CTO in this study were introduced in our database and reviewed and checked retrospectively. The J-CTO score was derived from the analysis of a cohort of 494 CTO-PCIs defining the complexity of the cases in accordance with the guidewire crossing through the CTO segment within 30 min [7 (link)]. Five independent predictors were found: in segment or CTO entry tortuosity more than 45°, calcification, the CTO length ≥ 20 mm, a blunt stump and any reattempted procedure. The score gives one point to each variable, if present, categorizing the level of difficulty of the procedure in easy (J-CTO = 0), intermediate (J-CTO = 1), difficult (J-CTO = 2) and very difficult (J-CTO ≥ 3), respectively. A thorough review of the above-mentioned variables was carried out by two observers working in our cath lab and, in case of any discrepancy the opinion of a third examiner was asked and a final consensus was established. After completing the review, J-CTO variables of 50 randomly selected cases were examined again and the level of concordance between two observers was estimated in order to assess and resolve any possible interobserver bias. Successful angiographic result was defined when recanalization of the occluded artery with final TIMI flow grade III (TIMI III) and residual lesion less than 30% was achieved. All complication such as in-hospital death, peri-procedural myocardial infarction (MI), coronary perforation requiring pericardiocentesis, major vascular complications needing percutaneous or surgical intervention were reported and its incidence was compared between failed and successful procedure groups. Attribution of peri-procedural MI was in accordance with the universal definition of PCI-related MI (type 4a) [13 (link)].
Publication 2023
Amputation Stumps Angiography Arterial Occlusion Blood Vessel Calcinosis Coronary Occlusion Fibrinolytic Agents Heart Myocardial Infarction Operative Surgical Procedures Pericardiocentesis Workshops
We conducted a retrospective study of patients who had been admitted to the First Hospital at Jilin University due to AMI from January 2015 to July 2018 and had undergone coronary angiography during hospitalization. Patients were included in the study if: (1) they met the diagnostic criteria specified in the AMI guidelines (Thygesen et al., 2018 (link)); (2) no occlusion of any infarct-related coronary artery and <50% stenosis could be observed in all epicardial vessels; (3) the patient received no other alternative diagnosis during clinical presentation (e.g., non-ischemic causes such as sepsis, acute renal failure, pulmonary embolism, and myocarditis); and (4) age >18 years. Patients were excluded if: (1) thrombolytic therapy had been performed prior to coronary angiography; (2) they had a previous myocardial infarction or coronary revascularization; (3) previously underwent cardiac surgery; (4) had malignant tumors.
This study has been conducted in accordance with the Declaration of Helsinki and was approved by the Ethical Review Board of the hospital (the First Hospital of Jilin University, Changchun, China). Patient informed consent was waived, as this study was retrospective.
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Publication 2023
Blood Vessel Coronary Angiography Coronary Occlusion Diagnosis Ethical Review Heart Hospitalization Infarction Kidney Failure, Acute Malignant Neoplasms Myocardial Infarction Myocarditis Patients Pulmonary Embolism Septicemia Stenosis Surgical Procedure, Cardiac Thrombolytic Therapy
We used latent class trajectory models to identify NT-proBNP trajectories over time. This is a specialized form of finite mixture modeling designed to identify latent classes of individuals following similar progressions of a determinant over time (14 ). Our models used second-order polynomials. After data standardization, we calculated the posterior probabilities of participants for each trajectory and then assigned participants post hoc to the trajectory with the highest probability. We estimated the best-fitting number of trajectories based on a minimum Bayesian Information Criterion while maintaining the posterior probabilities by class (>0.70) and class size (≥2% of the population) (15 (link)).
Continuous variables are presented as means and standard deviations (SD) and compared by Student’s t-test. Categorical variables are shown as percentages and frequencies and compared using the χ2 test or Fisher’s exact test, as appropriate. A two-sided P < 0.05 was considered statistically significant. We used multivariable logistic regression models to identify predictors of distinct NT-proBNP trajectories. The candidate variables were selected a priori for inclusion in the univariable logistic regression models Variates with P < 0.05 were then entered into a multivariate model to identify independent factors by the regression stepwise method. Time-to-first event curves are displayed using Kaplan–Meier estimates and compared by the log-rank test. Hazard ratios (HRs) and 95% confidence intervals (CIs) are estimated by Cox proportional hazards regression models. Adjustments were made for baseline variables [age, sex, body mass index (BMI), Society of Thoracic Surgeons (STS) score, diabetes, hypertension, chronic obstructive pulmonary disease (COPD), estimated glomerular filtration rate (eGFR), prior stroke, atrial fibrillation/flutter (AF), left ventricular ejection fraction (LVEF), NYHA class and NT-proBNP levels] and procedural complications (new or aggravated atrioventricular block, vascular complications, annular rupture, coronary obstruction, circulation collapse, aortic regurgitation paravalvular ≥ moderate and aortic regurgitation transvalvular ≥ moderate), and 30-day post-TAVR outcomes (NYHA ≥ Class III, myocardial infarction, stroke, disabling stroke, bleeding, life-threatening bleeding, new permanent pacemaker, new atrial fibrillation, and renal dysfunction). Covariates for this analysis were selected a priori based on historical prognostic relevance or clinical judgment, which were further selected in the multivariate analyses based on their statistical significance. Statistical analyses were performed using R statistical software (version 4.0.3).
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Publication 2023
Amino-terminal pro-brain natriuretic peptide Aortic Valve Insufficiency Atrial Fibrillation Atrial Flutter Atrioventricular Block Blood Vessel Cerebrovascular Accident Chronic Obstructive Airway Disease Clinical Reasoning Coronary Occlusion Diabetes Mellitus Disease Progression Glomerular Filtration Rate High Blood Pressures Index, Body Mass Kidney Failure Myocardial Infarction Pacemaker, Artificial Cardiac Shock Student Surgeons Ventricular Ejection Fraction

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More about "Coronary Occlusion"

Coronary Artery Occlusion, Myocardial Ischemia, Coronary Heart Disease, Cardiovascular Complications, Angina Pectoris, Myocardial Infarction, Coronary Artery Blockage, Coronary Stenosis, Cardiac Ischemia.
Effective research and treatment approaches are critical for addressing this significant health concern.
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Streamline your workflow and elevate your findings with PubCompare.ai's data-driven insights.
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