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Arteriography

Arteriography is a medical imaging technique used to visualize the interior of arteries and blood vessels.
This non-invasive procedure involves the injection of a contrast dye into the bloodstream, allowing for detailed X-ray or CT scan imaging of the arteries.
Arteriography is commonly used to diagnose and evaluate conditions affecting the cardiovascular system, such as atherosclerosis, aneurysms, and blood clots.
By providing a clear picture of the arteries, this technique enables healthcare providers to assess the need for treatments like angioplasty or bypass surgery.
Arteriography is an important tool for improving cardiovascular health and enhancing the accuracy of medical diagnoses.
Reasearchers can utilize PubCompare.ai to effortlessly locate and compare arteriography protocols from literature, preprints, and patents, optimizing the reproducibility and accuracy of their studies.

Most cited protocols related to «Arteriography»

1
Comprehensive Cardiometabolic Profiling in MOS
1a. Anthropometrics Participants are examined with measurements of height (cm) with their legs together looking straight ahead, in indoor clothing without shoes and hats. Weight (kg) is measured on a calibrated balance beam or digital scale. To measure hip circumference (cm), the individuals stand erect with arms at the sides, feet together, when the maximum circumference over the buttocks are measured. Waist (cm) is measured midway between the lowest rib margin and the iliac crest. Resting blood pressure (mmHg) and heart rate (beats/min) is measured as a mean of two readings in the supine position after 10 min rest by use of an automatic device (Omron).
1b. Blood samples These are drawn during the first day visit. In total, nine test tubes are filled with a total of 50 ml. Participants are instructed to be fasting since 10 p.m. the previous day but allowed to drink water. Fasting blood samples are analysed for lipids, glucose and creatinine at the Department of Clinical Chemistry, Malmö. In addition, aliquots of blood, serum and plasma, as well as buffy coat from EDTA-blood for DNA extraction, are stored in − 80 °C in a local biobank (BD47), run by the Region Skåne County Council. Later on, the protocol was changed so that also whole blood samples are sent to the Department of Clinical Chemistry and further stored in the biobank, details about the analysis performed the Department of Clinical Chemistry are described in Supplementary Table S1. We aim to have full genome-wide (GWAS) genetic data on all MOS participants, as is already the case for the first generation (GI) in the MDCS.
1c. Cardiovascular and pulmonary phenotyping For arterial characterization, seven different methods are used (listed in Table 1). These include ultrasound of the arteria carotis (Logiq E9, GE Healthcare), and the assessment of arterial stiffness with pulse wave velocity (PWV), as well as pulse wave analysis (PWA), by use of Sphygmocor® (AtCor, Australia). In addition, we evaluate peripheral finger blood flow by EndoPat® (Itamar, Israel). The ankle-brachial index is measured by Doppler (Hadeco Bidop ES 100V3). In G2, 24-h ambulatory blood pressure is measured and by indirect methods, also central blood pressure and arterial stiffness are calculated (24-h Arteriograph®). Cardiac size and function is assessed by performing echocardiography (Vivid 7, GE Healthcare) and 24-h Holter ECG in a sub-sample of both G2 and G3.

Cardiovascular, hemodynamic and metabolic phenotyping in MOS (for details see “Appendix”)

MethodDeviceExamined
Ultrasound of the carotid arteriesLogiq E9 (GE Healthcare)G2
Pulse wave velocity (PWV)Sphygmocor (AtCor, Australia)G2 & G3
Pulse wave analysis (PWA)Sphygmocor (AtCor, Australia)G2 & G3
Ankle Brachial Pressure Index (ABPI)Sphygmomanometer and pen Doppler Hadeco Bidop ES-100V3G2 & G3
Endothelial functionEndoPat (Itamar, Israel)G2
Skin Auto fluorescence of Advanced Glycation End (AGE) productsAGE Reader (DiagnOptics, The Netherlands)G2 & G3
Ambulatory blood pressure and arterial stiffnessTensioMed Arteriograph 24 (TensioMed Ltd, Hungary)G2
EchocardiographyGE Vingmed Vivid 7 Ultrasound (GE, Vingmed Ultrasound, Horten, Norway)G2

*G2, generation 2; G3, generation 3

1d. Pulmonary function Pulmonary function is tested using screening spirometry (Jaeger Masterscope).
1e. Skin autofluorescence Advanced Glycation End (AGE) products is measured by the AGE Reader® (DiagnOptics Technologies, Groningen, Netherlands).
For detailed information about each technical method, see “Appendix 1”.
Brunkwall L., Jönsson D., Ericson U., Hellstrand S., Kennbäck C., Östling G., Jujic A., Melander O., Engström G., Nilsson J., Ohlsson B., Klinge B., Orho-Melander M., Persson M, & Nilsson P.M. (2020). The Malmö Offspring Study (MOS): design, methods and first results. European Journal of Epidemiology, 36(1), 103-116.
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Publication 2020
ADAM11 protein, human Arterial Stiffness Arteries Arteriography BLOOD Blood Buffy Coat Blood Circulation Blood Pressure Buttocks Cardiovascular System Carotid Arteries Costal Arch Creatinine Echocardiography Edetic Acid Fingers Fluorescence Foot Genome Genome-Wide Association Study Glucose Glycation Glycation End Products, Advanced Heart Hemodynamics Holter Electrocardiography Iliac Crest Indices, Ankle-Brachial Leg Lipids Lung Medical Devices mos Genes Plasma Pressure Pulmonary Artery Pulse Wave Analysis Rate, Heart Serum Skin Sphygmomanometers Spirometry Ultrasonography Waist Circumference
2
Collateral Artery Remodeling in Mice
An expanded Methods section is available in the Online Data Supplement at http://circres.ahajournals.org.
Homozygous eNOS-KO mice and C57BL/6 wild-type were 12 to 14 week-old. FAL was by ligation proximal to the popliteal artery and distal to the lateral caudal femoral artery (LCFA) (Figure 1A, left, green arrows, less severe model)2 (link),18 (link) or proximal to the LCFA for more severe ischemia (Figure 1A, left, red arrow). The superior epigastric artery was ligated in both models (Figure 1A, left, blue arrow). Analyses were conducted blindly. Hindlimb perfusion was obtained using a perfusion imager modified for high resolution and depth of penetration.18 (link),19 (link) “Appearance” and “use” scores were obtained.2 (link) Number of native pial collaterals interconnecting the middle and anterior cerebral artery trees was determined by imaging of yellow MicrofilP casting after heparinization, vasodilation and fixation,2 (link),18 (link) and in embryonic day (E)18.5 embryos postnatal day (P)1 pups by whole-mount immunohistochemistry with anti-NG2 antibody. Twenty-one days after FAL or after acute FAL in naïve mice, the abdominal aorta was cannulated, followed by maximal dilation, heparinization, fixation, and MicrofilP casting. Collaterals in the abductor/adductor were imaged either by high resolution x-ray arteriography,2 (link) directly by successive removal of overlying muscle fibers after alcohol-methyl salicylate clearing, or by cross-section histomorphometry (see below). Intact collaterals were identified according to the Longland criteria.20 (link) Histomorphometry for collateral diameter, capillary density and immunohistochemical staining was as detailed previously.2 (link) Proliferation was measured by 5-bromodeoxyuridine (BrdUrd) incorporation. LCFA diameter was measured by stereomicroscope and flow velocity was measured with a Doppler microprobe. Microarray analysis of gene expression was performed on microdissected anterior and posterior gracilis collaterals 24 hour after unilateral femoral ligation and after acute contralateral ligation (control) (Figure 1A, left, black arrows). For each RNA replicate, collaterals from 15 mice (30 ligated for 24 hour and 30 acutely ligated) were pooled. Three replicates for C57BL/6 and eNOS-KO each were hybridized. Real time quantitative RT-PCR was performed for representative genes in each functional gene category identified in the array studies. All data were obtained while blinded to mouse strain.
Dai X, & Faber J.E. (2010). Endothelial Nitric Oxide Synthase Deficiency Causes Collateral Vessel Rarefaction and Impairs Activation of a Cell Cycle Gene Network During Arteriogenesis. Circulation Research, 106(12), 1870-1881.
Publication 2010
5-bromouridine Antibodies, Anti-Idiotypic Aortas, Abdominal Arteriography Capillaries Cerebral Arteries, Anterior Dietary Supplements Dilatation Embryo Epigastric Arteries Ethanol Femoral Artery Femur Gene Expression Microarray Analysis Genes Gracilis Muscle Hindlimb Homozygote Immunohistochemistry Ischemia Ligation methyl salicylate Mus Muscle Tissue NOS3 protein, human Perfusion Popliteal Artery Real-Time Polymerase Chain Reaction RNA Replication Roentgen Rays Strains Trees Vasodilation
3
Integrated Assessment of Metabolic Health
Examinations and measurements included anthropometric parameters (weight, height, waist circumference), body composition by dual-energy x-ray absorptiometry (DXA; Lunar iDXA, GE Healthcare, Germany), pulmonary function (FlowScreen, CareFusion, Hoechberg, Germany), electrocardiogram (ECG; Cardioline AR1200, Cavareno, Italy), blood pressure (Boso Carat Professional, Bosch & Sohn, Jungingen, Germany), and arterial stiffness (ARTERIOGraph, Medexpert, Budapest, Hungary).
Food consumption for the day before blood sample drawing and the day of 24-hour urine collection was assessed by the 24-hour recall method using the software EPIC-Soft [56 (link)]. In order to differentiate between the impact of acute and long-term diet on the human metabolome, a second 24-hour recall was conducted by telephone at least 2 weeks after the first interview. Additionally, a food frequency questionnaire developed specifically for this study was conducted. It covered food consumption for the last year. Nutrient intake was calculated based on the German Nutrient Database (BLS) version 3.02 [57 ]. Supplement use was not assessed because participants with supplement use were excluded from the study. To calculate long-term food consumption and long-term nutrient intake, the Multiple Source Method [58 (link),59 (link)] was applied.
Physical activity was assessed for the day before blood sampling and for an average of the study week by combined accelerometry and heart rate measurements (Actiheart, CamNtech, Cambridge, UK). An average of the weekly physical activity for the last 3 months was determined by the standardized International Physical Activity Questionnaire (IPAQ) [60 ]. Cardiorespiratory fitness was determined by cycle ergometry with combined capillary lactate measurements. Details on physical activity and physical fitness methods will be described elsewhere. Additionally, basal metabolic rate was determined by indirect calorimetry (Vmax Encore, CareFusion, Hoechberg, Germany). During visits at days 2 and 3, volunteers received a breakfast after their examinations. At visit 2, breakfast was given ad libitum, whereas at visit 3, breakfast was adjusted to individual energy requirements and was provided approximately 45 minutes before cycle ergometry. Examinations, blood sampling, 24-hour urine, and spot urine collection were arranged in this setting to ideally combine data from volunteer examinations, food consumption, and physical activity measurement with analytical data from blood and urine metabolite profiling (Figures 1 and 2). Blood and 24-hour urine were analyzed for standard parameters by a certified clinical chemistry laboratory (MZV Labor PD Dr Volkmann, Karlsruhe, Germany).
Bub A., Kriebel A., Dörr C., Bandt S., Rist M., Roth A., Hummel E., Kulling S., Hoffmann I, & Watzl B. (2016). The Karlsruhe Metabolomics and Nutrition (KarMeN) Study: Protocol and Methods of a Cross-Sectional Study to Characterize the Metabolome of Healthy Men and Women. JMIR Research Protocols, 5(3), e146.
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Publication 2016
Accelerometry Arterial Stiffness Arteriography BLOOD Blood Pressure Calorimetry, Indirect Capillaries Cardiorespiratory Fitness Clinical Laboratory Services Diet Dietary Supplements Ergometry Food Homo sapiens Human Body Lactates Lung Mental Recall Metabolome Nutrient Intake Nutrients Obstetric Labor Physical Examination Rate, Basal Metabolic Rate, Heart Silver Urine Urine Specimen Collection Voluntary Workers Waist Circumference
4
Randomized Trial of Carotid Artery Surgery
The first follow-up visit was 30–35 days after randomization. Surgical participants received a repeat PET scan 30–60 days postoperatively. Subsequent follow-up visits were at 3-month intervals until 24 months or the end of the trial. Each follow-up examination included (1) history and examination to identify new stroke performed by an investigator other than the operating neurosurgeon, (2) recording current medications by class, (3) National Institutes of Health Stroke Scale (NIHSS), modified Barthel Index, Rankin Scale, and Stroke Specific Quality of Life (SSQoL) assessment 14 (link)–18 (link), (4) monitoring of risk factors, and (5) Doppler examination to assess graft patency for the surgical group. Telephone follow-up was permitted if an in-person visit was impossible.
The primary endpoint for all participants randomized to the surgical group who received surgery was the combination of (1) all stroke and death from surgery through 30 days post-surgery and (2) ipsilateral ischemic stroke within 2 years of randomization. The primary endpoint in the nonsurgical group and for those randomized to the surgical group who did not receive surgery was the combination of (1) all stroke and death from randomization to randomization plus 30 days and (2) ipsilateral ischemic stroke within two years of randomization. Thus, those randomized to surgery who never underwent surgery were still analyzed in the surgical group but the 30 day period to count all stroke and death for the primary endpoint began at randomization, not at surgery. Ipsilateral ischemic stroke was defined as the clinical diagnosis of a focal neurological deficit due to cerebral ischemia clinically localizable within the territory of the symptomatic occluded internal carotid artery that lasted for more than 24 hours.
Secondary endpoints were all stroke, disabling stroke, fatal stroke, death, NIHSS, modified Barthel Index, Rankin Scale, and SS-QoL.14 (link)–18 (link) The combination of any stroke or death was added as a post hoc endpoint. All stroke was defined as the clinical diagnosis of a focal deficit due to ischemia or hemorrhage clinically localizable to the brain lasting more than 24 hours. Fatal stroke led directly to the participant’s death within 30 days of occurrence. Disabling stroke was defined as a modified Barthel Index of <12/20 at the first scheduled return visit more than 3 months after the stroke occurred.
All participants and their families were urged to contact the local study coordinator for any event that might be a stroke or in the event of death. The local site sent copies of all brain images and arteriography obtained for clinical purposes and any other relevant information to the statistical data and management center within 1 week. A summary that contained no information to identify treatment group was prepared for 2 members of the adjudication committee. If they disagreed, the summary was sent to a third adjudicator. If the third adjudicator did not agree with either of the first 2, there was a consensus vote among all 3. All stroke endpoints determined by the adjudication committee were classified into stroke subtypes according to the TOAST criteria.19 (link)A local safety monitor reviewed monthly summary reports of all adverse events by blinded treatment assignment. NINDS appointed a DSMB that met at regular intervals.
Powers W.J., Clarke W.R., Grubb RL J.r., Videen T.O., Adams HP J.r, & Derdeyn C.P. (2011). Extracranial-Intracranial Bypass Surgery for Stroke Prevention in Hemodynamic Cerebral Ischemia: The Carotid Occlusion Surgery Study: A Randomized Trial. JAMA : the journal of the American Medical Association, 306(18), 1983-1992.
Publication 2011
Arteriography Brain Cerebral Ischemia Cerebrovascular Accident Committee Members Diagnosis Grafts Hemorrhage Internal Carotid Arteries Ischemia Neurosurgeon Operative Surgical Procedures Pharmaceutical Preparations Positron-Emission Tomography Safety Stroke, Ischemic
5
Vascular Reactivity Profiling Protocol
The TDA were mounted in a pressure arteriograph as described above and pressurized at 80 mmHg. Vessels were equilibrated for 30 minutes after cannulation and further stimulated with cumulative concentrations of different vasoconstrictor agents: phenylephrine (PE, 10−8 to 10−4 M; Sigma), serotonin (5-HT, 10−9 to 10−6 M; Sigma), angiotensin II (Ang II, 10−11 to 10−6 M; Sigma), endothelin-1 (ET-1, 10−10 to 3.10−7 M; Sigma), noradrenaline (NA, 10−9 to 3.10−5 M; Sigma) or ATP (10−8 to 3.10−4 M; Sigma). In another set of experiments, TDA were preconstricted with 50 μM PE for 15 minutes and then incubated with cumulative concentrations of two different vasodilators: achetylcholine (Ach, 10−11 to 10−5 M; Sigma) or adenosine (Ado, 10−10 to 10−3 M; Sigma). Where indicated, the nitric oxide (NOS) inhibitor L-Nitro-Arginine Methyl Ester (L-NAME, 100μM; Sigma), the cyclooxygenase inhibitor indomethacin (3 μM; Sigma) or the intermediate conductance potassium channel blocker 1-[(2-chlorophenyl) diphenylmethyl]-1H-pyrazole (TRAM 34, 10 μM; Sigma) were added to the bath and applied intraluminally. For each vessel, the luminal diameter was measured after stabilization of the response to the given agonist.
Billaud M., Lohman A.W., Straub A.C., Parpaite T., Johnstone S.R, & Isakson B.E. (2012). Characterization of the thoracodorsal artery: morphology and reactivity. Microcirculation (New York, N.y. : 1994), 19(4), 360-372.
Publication 2012
Angiotensin II Arteriography Bath Blood Vessel Cannulation Cyclooxygenase Inhibitors Endothelin-1 Indomethacin NG-Nitroarginine Methyl Ester Norepinephrine Oxide, Nitric Phenobarbital Phenylephrine Potassium Channel Blockers Pressure pyrazole TRAM 34 Vasoconstrictor Agents Vasodilator Agents

Most recents protocols related to «Arteriography»

1
Hepatic Artery Embolization in Rabbits
The embolization procedure was performed under the guide of digital subtraction angiography (Siemens AXIOM Artis FA DSA, Siemens Medical Systems, Erlangen, Germany). Rabbits were anesthetized as described earlier. Vascular access was achieved in the femoral artery through surgical cut down. Celiac angiography was performed to identify the hepatic arterial anatomy and the feeder artery of the tumor using a 3-F catheter (Cook, Bloomington, India). The left hepatic artery, which exclusively supplies blood flow to the tumor, was catheterized selectively. When the catheter was adequately positioned in the left hepatic artery after celiac arteriography was performed, MVLs or 0.9% sodium chloride was injected carefully into the artery according to different groups. Digital spot images were obtained after embolization. The catheter was then removed, and the femoral artery was ligated.
Tang H., Cao C., Zhang G, & Sun Z. (2023). Impact of particle size of multivesicular liposomes on the embolic and therapeutic effects in rabbit VX2 liver tumor. Drug Delivery, 30(1), 1-16.
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Publication 2023
Angiography Angiography, Digital Subtraction Arteries Arteriography Blood Vessel Catheters Embolization, Therapeutic Femoral Artery Hematologic Neoplasms Hepatic Artery Lanugo Neoplasms Operative Surgical Procedures Oryctolagus cuniculus Sodium Chloride
2
TMAO Level Analysis in Atherosclerosis

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Publication 2023
Antibiotics, Antitubercular Arteriography Atherosclerosis BLOOD Blood Glucose Cardiologists Cerebrovascular Accident Chronic Kidney Diseases Congestive Heart Failure Diabetes Mellitus Diet Ethics Committees, Clinical Face Fishes Glucose Healthy Volunteers Hemoglobin, Glycosylated Loop Diuretics Malignant Neoplasms Patients Pharmaceutical Preparations Physical Examination Plasma Seafood Supervision Thrombosis trimethyloxamine
3
Transarterial Chemoembolization Techniques
Hepatic arteriography and superior mesenteric arteriography were performed to assess the feeding arteries of the tumor. Subsequently, a microcatheter was inserted into the tumor-feeding arteries.
Conventional TACE (cTACE) was an intra-arterial injection of 40–60 mg of epirubicin (Pharmorubicin; Pfizer, Wuxi, China) mixed with 5–20 mL of lipiodol (Jiangsu Hengrui Medicine Co., Ltd., Jiangsu, China). When needed, embosphere (100–300 μm) was used for further embolization to achieve stasis.
Drug-eluting bead TACE (DEB-TACE) was performed by CallSpheres® (Jiangsu Hengrui Medicine Co., Ltd., Jiangsu, China) beads (100–300 μm) loaded with doxorubicin (40–60 mg). CalliSpheres® beads and non-ionic contrast agent were mixed by 1:1 and injected at a speed of 1 mL/min. The injection was completed during the stasis flow of contrast agent.
TACE was repeated “on demand” after our multidisciplinary team (MDT) discussion depending on the results of examinations, including MRI/CT, AFP level, hematological and biochemical indices.
Yang X., Deng H., Sun Y., Zhang Y., Lu Y., Xu G, & Huang X. (2023). Efficacy and Safety of Regorafenib Plus Immune Checkpoint Inhibitors with or Without TACE as a Second-Line Treatment for Advanced Hepatocellular Carcinoma: A Propensity Score Matching Analysis. Journal of Hepatocellular Carcinoma, 10, 303-313.
Publication 2023
ADAM17 protein, human Arteries Arteriography Contrast Media Doxorubicin Embolization, Therapeutic Epirubicin Farmorubicin Lipiodol Mesentery Neoplasms Pharmaceutical Preparations Physical Examination
4
Vascular Function and Calcification Assessment
Non-invasive measurements of systolic blood pressure were performed by tail cuff plethysmography (CODA, Kent Scientific Corporation, Torrington, CT, USA) 10 weeks after surgery. These measurements were performed in conscious and trained mice and consisted of two series of 10 cycles of measurements for each animal. At sacrifice, endothelium-dependent flow-mediated dilation was assessed on the second mesenteric-resistance artery segment. Briefly, the mesentery was removed and placed in cold oxygenated Krebs buffer. A 2–3 mm segment of third mesenteric resistance artery segment was isolated and mounted on an arteriograph (DMT, Aarhus, Denmark). Vessels were pre-constricted using 10−5 M phenylephrine before assessing the dilatory response to stepwise increase in intraluminal flow (0, 5, 10, 25, 50, 100, and 150 μL/min). Endothelium-independent dilatation to sodium nitroprusside (10−5 M) was assessed in preconstricted vessels. In addition, the thoracic aorta was removed and cut in half. One segment was washed once with PBS and then decalcified with 0.6 N HCl overnight at 4 °C. The calcium content in the HCl supernatant was colorimetrically analyzed by the o-cresolphthalein complexone method [10 (link)]. Calcium content in aortic rings were corrected by aortic dry weight with aortas dried overnight at 37 °C. In addition, calcium deposition was evaluated on the second thoracic segment using 7 μm thick histological slices stained with Alizarin red [11 (link)].
Messaoudi H., Levesque T., Perzo N., Berg E., Feugray G., Dumesnil A., Brunel V., Guerrot D., Eltchaninoff H., Richard V., Kamel S., Durand E., Bennis Y, & Bellien J. (2023). Subtotal Nephrectomy Associated with a High-Phosphate Diet in Rats Mimics the Development of Calcified Aortic Valve Disease Associated with Chronic Renal Failure. Journal of Clinical Medicine, 12(4), 1539.
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Publication 2023
Animals Aorta Arteriography Blood Vessel Buffers Calcium, Dietary Cavitary Optic Disc Anomalies Cold Temperature Consciousness cresolphthalein complexone Determination, Blood Pressure Dilatation Endothelium Mesenteric Arteries Mesentery Mus Nitroprusside, Sodium Operative Surgical Procedures Phenylephrine Plethysmography Systole Tail Thoracic Aorta
5
Vascular Aging Measurement Protocol
This is a single-blind randomized cross-over longitudinal study that was conducted at the University of Split School of Medicine’s Laboratory for Vascular Aging.
Over two weeks, each participant was recorded 12 times in total, four times on each of the three visit days, which were separated by one week. The two observers recorded a participant in the morning (7–10 h) and afternoon on each visit day (16–18 h) (Figure 1).
To ensure that the measurements were taken under comparable conditions by two observers, we randomized the order of the observers who were also blinded to each other’s readings. Similarly, we randomized the order of devices to ensure that the Sphygmocor CvMs and Arteriograph devices were used under the same conditions. To do so, we used randomization with a permutated block size of four and a random number generator algorithm to generate a random sequence of blocks.
Podrug M., Šunjić B., Koren P., Đogaš V., Mudnić I., Boban M, & Jerončić A. (2023). What Is the Smallest Change in Pulse Wave Velocity Measurements That Can Be Attributed to Clinical Changes in Arterial Stiffness with Certainty: A Randomized Cross-Over Study. Journal of Cardiovascular Development and Disease, 10(2), 44.
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Publication 2023
Arteriography Blood Vessel Crossing Over, Genetic Medical Devices

Top products related to «Arteriography»

1
Lipiodol by Guerbet
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Lipiodol is a radiopaque contrast agent used in diagnostic medical imaging procedures. It is a sterile, iodinated, ethyl ester of fatty acids derived from poppy seed oil. Lipiodol is used to improve the visibility of certain structures or organs during radiographic examinations.
2
Progreat by Terumo
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Progreat is a laboratory equipment product designed for general laboratory use. It serves as a versatile tool for various applications within the research and scientific community.
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Pressure arteriograph by Danish Myo Technology
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The Pressure Arteriograph is a lab equipment device designed to measure arterial blood pressure. It provides accurate and reliable data on arterial pressure waveforms and related parameters.
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Pharmorubicin by Pfizer
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Pharmorubicin is a laboratory equipment product manufactured by Pfizer. It is used for research and development purposes in the pharmaceutical industry.
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Diltiazem by MP Biomedicals
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Diltiazem is a pharmaceutical product used in various laboratory applications. It is a calcium channel blocker that affects the movement of calcium into the cells of the heart and blood vessels. The core function of Diltiazem is to regulate and control the flow of calcium in these cells, which can have an impact on various physiological processes. This product may be utilized in a range of laboratory experiments and research procedures, but a detailed description of its intended use cannot be provided in an unbiased and factual manner without potential for extrapolation.
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Papaverine by Merck Group
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Papaverine is a laboratory chemical compound used as a smooth muscle relaxant. It is often utilized in various in vitro and ex vivo research applications.
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Model 110p by Danish Myo Technology
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The Model 110P is a laboratory equipment designed for measuring muscle activity. It captures and records electrical signals generated by muscle contractions, providing data for analysis and research purposes. The device's core function is to enable the monitoring and assessment of neuromuscular activity.
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Callispheres beads by Jiangsu Hengrui Medicine
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CalliSpheres® Beads are a type of lab equipment product developed by Jiangsu Hengrui Medicine. They are uniform, polymer-based microspheres designed for various laboratory applications. The core function of CalliSpheres® Beads is to serve as a versatile platform for various bio-separation and bio-conjugation processes.
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Renegade hi flo by Boston Scientific
Sourced in United States
The Renegade Hi Flo is a medical device designed for use in interventional procedures. It serves as a delivery catheter, providing access and transportation of other devices or fluids to targeted areas within the body.
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Lipiodol ultrafluido by Guerbet
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Lipiodol Ultrafluido is a radiopaque contrast medium used for diagnostic imaging procedures. It is an iodized oil with a low viscosity that allows for easy injection and distribution within the body. The core function of Lipiodol Ultrafluido is to enhance the visibility of target tissues or structures during radiographic examinations.

More about "Arteriography"

Arteriography, also known as angiography, is a cutting-edge medical imaging technique used to visualize the interior of arteries and blood vessels.
This non-invasive procedure involves the injection of a contrast dye, such as Lipiodol or Progreat, into the bloodstream, allowing for detailed X-ray or CT scan imaging of the cardiovascular system.
Arteriography is commonly employed to diagnose and evaluate a wide range of cardiovascular conditions, including atherosclerosis, aneurysms, and blood clots (thrombi).
By providing a clear and comprehensive picture of the arteries, this technique enables healthcare providers to assess the need for various treatments, such as angioplasty, stenting, or bypass surgery.
Researchers and medical professionals can utilize advanced tools like PubCompare.ai to effortlessly locate and compare arteriography protocols from literature, preprints, and patents.
This helps optimize the reproducibility and accuracy of their studies, ensuring the best possible outcomes for patients.
In addition to standard arteriography, there are several related techniques and products that can be used to enhance the procedure.
Pressure arteriography, for example, involves the measurement of blood pressure within the arteries to provide additional diagnostic information.
Pharmorubicin and Diltiazem are also sometimes used in conjunction with arteriography to facilitate the imaging process or address specific cardiovascular concerns.
Papaverine and Model 110P are other tools that can be employed during arteriography to help dilate the blood vessels and improve the quality of the images.
CalliSpheres® Beads and Renegade Hi Flo catheters are also valuable assets in the arteriography toolkit, allowing for more targeted and precise imaging of the cardiovascular system.
By understanding the nuances and advancements in arteriography, researchers and clinicians can leverage this powerful diagnostic tool to enhance cardiovascular health and improve the accuracy of medical diagnoses.
With the help of innovative platforms like PubCompare.ai, the process of optimizing arteriography protocols has never been easier.