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Cerebral Ventriculography

Cerebral Ventriculography is a radiographic imaging technique used to visualize the cerebral ventricles, the fluid-filled cavities within the brain.
This procedure involves the injection of a contrast agent into the ventricular system, allowing for the detailed assessment of the size, shape, and position of the ventricles.
Cerebral Ventriculography can be used to diagnose a variety of neurological conditions, such as hydrocephalus, tumors, and other structural abnormalities.
The PubCompare.ai platform provides a comprehensive, AI-powered solution for researchers to explore the latest advancements in this field, quickly identify the best protocols and products from literature, pre-prits, and patents, and optimize their research efforts.

Most cited protocols related to «Cerebral Ventriculography»

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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
This prospective study comprised the CMR imaging arm of the Prospective Observational Study of implantable Cardioverter Defibrillators (PROSE-ICD; NCT00733590), which enrolls patients receiving ICD therapy for primary prevention of SCD. Between November 2003 and December 2010, we approached patients with LVEF≤35% (assessed clinically by echocardiography, nuclear, or ventriculography) scheduled for clinically-indicated primary prevention ICD insertion, based on published guidelines,20 (link) at the Johns Hopkins Medical Institutions. Exclusion criteria are listed in the Online Data Supplement. We enrolled 235 patients (30% of eligible patients). The reasons for non-enrollment were refusal to participate in research (78% of those non-enrolled), claustrophobia (7%) and insufficient time to schedule the scan before device implantation (15%).
We included both ischemic and nonischemic cardiomyopathy. Patients were classified as nonischemic if they had no history of myocardial infarction or revascularization and no coronary artery stenoses >50% of ≥2 major epicardial vessels or involving the left main or proximal left anterior descending artery.21 (link) CMR was performed as close in time to ICD insertion as logistically possible (median 3 days). The study protocol was approved by the Johns Hopkins Hospital Institutional Review Board. All patients gave written informed consent.
Publication 2012
Arteries Blood Vessel Cardiomyopathies Cerebral Ventriculography Claustrophobia Coronary Stenosis Dietary Supplements Echocardiography Ethics Committees, Research Implantable Defibrillator Medical Devices Myocardial Infarction Ovum Implantation Patients Primary Prevention Radionuclide Imaging
Eligible patients were 18 years of age or older and had normal sinus rhythm, no contraindication to warfarin therapy, and an LVEF of 35% or less as assessed by quantitative echocardiography (or a wall-motion index of ≤1.2) or as assessed by radionuclide or contrast ventriculography within 3 months before randomization. Patients who had a clear indication for warfarin or aspirin were not eligible. Patients in any New York Heart Association (NYHA) functional class were eligible, but patients in NYHA class I could account for no more than 20% of the total number of patients undergoing randomization. Additional eligibility criteria were a modified Rankin score of 4 or less (on a scale of 0 to 6, with higher scores indicating more severe disability), and planned treatment with a beta-blocker, an angiotensin-converting–enzyme (ACE) inhibitor (or, if the side-effect profile with ACE inhibitors was unacceptable, with an angiotensin-receptor blocker), or hydralazine and nitrates. Patients were ineligible if they had a condition that conferred a high risk of cardiac embolism, such as atrial fibrillation, a mechanical cardiac valve, endocarditis, or an intracardiac mobile or pedunculated thrombus.
Publication 2012
Adrenergic beta-Antagonists Angiotensin-Converting Enzyme Inhibitors Angiotensin Receptor Antagonists Aspirin Atrial Fibrillation Cerebral Ventriculography Disabled Persons Echocardiography Eligibility Determination Embolism Endocarditis Heart Heart Valves Hydralazine Nitrates Patients Radioisotopes Sinuses, Nasal Thrombus Warfarin
Median follow-up time was 4.0 years (interquartile range, 3.1-4.2 years), which resulted in 25 107 person-years of observation. A telephone interviewer contacted each participant every 6 to 9 months to inquire about all interim hospital admissions, cardiovascular outpatient diagnoses, and deaths. Two physicians reviewed each record for independent endpoint classification and assignment of event dates.
The endpoint for this study was symptomatic CHF. End point criteria were (a) CHF diagnosed by a physician and patient receiving medical treatment for CHF; (b) pulmonary edema/congestion seen on a chest radiograph; and (c) dilated ventricle or poor LV systolic function by echocardiography or ventriculography, or evidence of LV diastolic dysfunction by echocardiography. Participants who met only criterion a were considered to meet a “soft” criterion, and participants who met criteria b and c in addition to a physician diagnosis were classified as meeting “hard” criteria for CHF. For this analysis, participants who met either soft or hard criteria were considered as having incident CHF. An MI was diagnosed based on standard criteria consisting of combinations of symptoms, ECG findings, and cardiac biomarker levels.24 (link)
Publication 2008
Biological Markers Cardiovascular System Cerebral Ventriculography Echocardiography Heart Heart Ventricle Interviewers Left Ventricular Diastolic Dysfunction Outpatients Patients Physicians Pulmonary Edema Radiography, Thoracic Systole Vision
Incident hospitalized HF was ascertained yearly in WHI by medical record abstraction of self-report hospitalizations and classified by trained adjudicators using the standardized methodology as previously described.18 (link) Hospitalized HF requiring and/or occurring during hospitalization required physician diagnosis of new-onset or worsened congestive HF on the reported hospital admission and 1 or more of the following 4 criteria: HF diagnosed by physician and receiving medical treatment for HF, symptoms plus documentation in the current medical record of a history of an imaging procedure showing impaired left ventricular (LV) systolic or diastolic LV function, pulmonary edema/congestion on chest x-ray on the current admission, dilated ventricle(s) or “poor” LV or right ventricular (RV) function by echocardiography, radionuclide ventriculography, or other contrast ventriculography, or evidence of LV diastolic dysfunction. This method was found to have an excellent 79% agreement rate (kappa) comparing central adjudicated HF to local adjudication.18 (link)Interim CHD was defined by adjudicated hospitalization for myocardial infarction, PTCA, CABG, or angina after baseline and prior to the HF hospitalization.18 (link)
Publication 2012
Angina Pectoris Cerebral Ventriculography Coronary Artery Bypass Surgery Diastole Echocardiography Heart Ventricle Hospitalization Left Ventricles Left Ventricular Diastolic Dysfunction Left Ventricular Function Medical Imaging Myocardial Infarction Percutaneous Transluminal Coronary Angioplasty Physicians Pulmonary Edema Radiography, Thoracic Radionuclide Ventriculography Systole Ventricular Function, Right

Most recents protocols related to «Cerebral Ventriculography»

A retrospective cohort analysis was used for this study. Ninety-seven patients diagnosed with CAD at the Department of Cardiovascular Medicine in the Affiliated Hospital of Xuzhou Medical University from September 2021 and January 2022 were selected. LVEDP ≥ 16 mmHg (1 mmHg = 0.133 kPa) was defined as increased LV filling pressure [7 (link), 8 (link)]. Based on LVEDP, patients were divided into the HFpEF group (LVEDP ≥ 16 mmHg, 47 cases) and the normal LV diastolic function group (LVEDP < 16 mmHg, 50 cases). The Medical Ethics Committee approved the study of the Affiliated Hospital of Xuzhou Medical University (Number: XYFY2021-KL164-01).
Inclusion criteria: (1) All patients with suspected or known coronary artery disease who have completed echocardiography, planar MUGA and cardiac catheterization 1–3 days after admission and whose diagnosis of CAD was confirmed by coronary arteriography with a subepicardial coronary artery diameter stenosis more than 50% [9 (link)]; (2) sinus rhythm; (3) hemodynamic stability; (4) LVEF ≥ 50% (based on left ventriculography findings) .
Exclusion criteria: pulmonary heart disease (10), congenital heart disease (1), rheumatic heart disease (0), cardiomyopathy and pericardial disease (2), hyperthyroidism (2), arrhythmias (5), severe anemia (0), severe hepatic and renal dysfunction (1), LVESV′ < 20 mL measured by planar MUGA (3) (because assessment of LV volume and function is less accurate in very small volume patients [6 (link), 10 (link)]).
Publication 2023
Anemia Cardiac Arrhythmia Cardiomyopathies Cardiovascular Agents Catheterizations, Cardiac Cerebral Ventriculography Congenital Heart Defects Coronary Angiography Coronary Artery Disease Coronary Stenosis Cor Pulmonale Diagnosis Diastole Echocardiography Ethics Committees Gated Blood-Pool Imaging Hemodynamics Hyperthyroidism Kidney Failure Patients Pericardium Pressure Rheumatic Heart Disease Sinuses, Nasal
Heart catheterization was performed only in patients with a history of typical chest pains during exercise or at rest, signs of ischemia in ECG and/or dynamic changes in cardiac marker levels. In cases, when a ventriculography was performed, LVEDP was measured invasively with a pigtail catheter placed in the left ventricle.
Publication 2023
Catheterizations, Cardiac Catheters Cerebral Ventriculography Chest Pain Heart Ischemia Left Ventricles Patients
Figure 1 shows the flow chart of our study. Among 1398 patients undergoing left ventricular reconstruction (LVR), there were 10 patients with prior myocardial infarction in the absence of obstructive coronary artery on preoperative angiogram. These 10 patients constituted the target population in this study. The operative indication for LVR was the presence of both of the following criteria: (1) there was clear evidence of aneurysmal and akinetic left ventricle according to echocardiography, left ventriculography, or magnetic resonance imaging. (2) patients presented symptoms of heart failure, refractory angina, thromboembolism, a concomitant structural cardiac disease requiring surgery or ventricular arrhythmias which were refractory to medical treatment, implantable cardioverter defibrillator, and endocardial ablation [10 ].

Flow chart of the study

Publication 2023
Aneurysm Angina Pectoris Angiography Artery, Coronary Cardiac Arrhythmia Cerebral Ventriculography concomitant disease Echocardiography Endocardium Heart Heart Diseases Heart Failure Heart Ventricle Implantable Defibrillator Left Ventricles Myocardial Infarction Operative Surgical Procedures Patients Reconstructive Surgical Procedures Surgical Procedure, Cardiac Target Population Thromboembolism
We also investigated associations between serum reactivity to citrullinated protein/peptide antigens and incident heart failure. These events were adjudicated by a committee in MESA, and included both definite and probable heart failure, defined by heart failure symptoms, and by physician diagnosis with medical treatment. Specifically, definite and probable heart failure required clinical symptoms, e.g., shortness of breath, and signs e.g., edema since asymptomatic disease was not an endpoint. Probable heart failure required a physician diagnosis and medical treatment for heart failure. Definite heart failure required pulmonary edema/congestion on chest x-ray and/or dilated ventricle or poor LV function by echocardiography or ventriculography, or evidence of LV diastolic dysfunction [30 (link), 31 (link)].
Publication 2023
Antigens Asymptomatic Diseases Cerebral Ventriculography Congestive Heart Failure Diagnosis Dyspnea Echocardiography Edema Heart Heart Ventricle Left Ventricular Diastolic Dysfunction Peptides Physicians Proteins Pulmonary Edema Radiography, Thoracic Serum Sickness
The procedure was performed under general anesthesia using transesophageal echocardiography (TEE) control. A left ventriculography was performed to assess the anatomy of the defect. The choice of device was always determined according to the TEE dimension of the defect on the right ventricular side with possible modifications related to the dimension on the left ventricular side [5 (link)]. Device implantation was performed using either a retrograde or antegrade approach. In the retrograde approach, no complete arteriovenous loop was required. Regardless of the approach used, TEE was always used to check after deployment but before release, the device position, the amount of residual shunting, and the presence of aortic or tricuspid valve regurgitation. All patients had 24-h continuous/telemetry monitoring after implantation. The patients were discharged from hospital on the following day, after TTE and electrocardiogram (ECG) control, most often without any treatment or sometimes, at the beginning of our experience, under aspirin (3–5 mg/kg once daily for 6 months). In the case of a residual shunt, hemolysis was determined using blood and urine analyses. Endocarditis prophylaxis was recommended for the first 6 months. Routine outpatient follow-up visits were planned at 1 month, 3 to 6 months, and 12 months after implantation, and thereafter annually including TTE and ECG monitoring. On TTE, the residual shunt was graded according to the color jet width and defined as small (1–2 mm), moderate (2–4 mm), or large (>4 mm) [2 (link),5 (link)].
Publication 2023
Aorta Aspirin BLOOD Cerebral Ventriculography Echocardiography, Transesophageal Electrocardiogram Endocarditis General Anesthesia Hemolysis Left Ventricles Medical Devices Outpatients Ovum Implantation Patients Telemetry Tricuspid Valve Insufficiency Urinalysis Ventricles, Right

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More about "Cerebral Ventriculography"

Cerebral Ventriculography is a radiographic imaging technique used to visualize the fluid-filled cavities within the brain, known as the cerebral ventricles.
This procedure involves the injection of a contrast agent into the ventricular system, allowing for a detailed assessment of the size, shape, and position of the ventricles.
Cerebral Ventriculography can be used to diagnose a variety of neurological conditions, such as hydrocephalus, tumors, and other structural abnormalities.
The PubCompare.ai platform provides a comprehensive, AI-powered solution for researchers to explore the latest advancements in this field.
Researchers can quickly identify the best protocols and products from literature, pre-prints, and patents using the platform's advanced search and analysis tools.
This can help optimize research efforts and stay up-to-date with the latest developments in cerebral ventriculography.
In addition to the cerebral ventriculography technique, researchers may also be interested in exploring related imaging technologies, such as digital cardiac imaging software, AIA-CL2400, EPIQ 7, SPC-454D, Cobas 8000, OEC 9800 Plus, and Centaur XPT.
These tools can provide valuable insights and support for researchers working in the field of neurovascular imaging and diagnostics.
Furthermore, researchers may also be interested in exploring related biomarkers and assays, such as the VITROS® troponin I assay and the Human Galectin-1 Quantikine ELISA Kit DGAL10.
These tools can provide additional data and insights to support the diagnosis and monitoring of neurological conditions.
Overall, the PubCompare.ai platform offers a powerful and comprehensive solution for researchers working in the field of cerebral ventriculography and related imaging technologies.
By leveraging the platform's advanced search and analysis capabilities, researchers can optimize their research efforts and stay at the forefront of the latest advancements in this important field of study.