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Congenital Heart Disease Imaging in Adults

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161. 2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA Guideline for the Prevention, Detection, Evaluation, and Management of High Blood Pressure in Adults: Executive Summary

pressure monitoring EHR electronic health record HF heart failure HF p EF heart failure with preserved ejection fraction HF r EF heart failure with reduced ejection fraction ICH intracerebral hemorrhage JNC Joint National Commission LV left ventricular LVH left ventricular hypertrophy MI myocardial infarction MRI magnetic resonance imaging PAD peripheral artery disease RAS renin-angiotensin system RCT randomized controlled trial SBP systolic blood pressure SIHD stable ischemic heart disease TIA (...) with a doubling in the risk of death from stroke, heart disease, or other vascular disease. In a separate observational study including >1 million adult patients ≥30 years of age, higher SBP and DBP were associated with increased risk of CVD incidence and angina, myocardial infarction (MI), HF, stroke, peripheral artery disease (PAD), and abdominal aortic aneurysm, each evaluated separately. An increased risk of CVD associated with higher SBP and DBP has been reported across a broad age spectrum, from 30

2017 American Heart Association

162. BSR guideline Management of Adults with Primary Sjögren's Syndrome

BSR guideline Management of Adults with Primary Sjögren's Syndrome We use cookies to enhance your experience on our website. By continuing to use our website, you are agreeing to our use of cookies. You can change your cookie settings at any time. British Society for Rheumatology guideline for the management of adults with primary Sjögren’s Syndrome | Rheumatology | Oxford Academic Search Account Menu Menu Navbar Search Filter Mobile Microsite Search Term Close search filter search input (...) Article Navigation Close mobile search navigation Article navigation October 2017 Article Contents Article Navigation The British Society for Rheumatology guideline for the management of adults with primary Sjögren’s Syndrome Elizabeth J. Price 1Department of Rheumatology, Great Western Hospital NHS Foundation Trust, Swindon * Correspondence to: Elizabeth Price, Great Western Hospital NHS Foundation Trust, Swindon, SN3 6BB, UK. E-mail: Search for other works by this author on: Saaeha Rauz

2017 British Society for Rheumatology

163. Guideline for the management of adults with Systemic Lupus Erythematosus

Guideline for the management of adults with Systemic Lupus Erythematosus We use cookies to enhance your experience on our website. By continuing to use our website, you are agreeing to our use of cookies. You can change your cookie settings at any time. British Society for Rheumatology guideline for the management of systemic lupus erythematosus in adults | Rheumatology | Oxford Academic Search Account Menu Menu Navbar Search Filter Mobile Microsite Search Term Close search filter search input (...) Article Navigation Close mobile search navigation Article navigation January 2018 Article Contents Article Navigation The British Society for Rheumatology guideline for the management of systemic lupus erythematosus in adults Caroline Gordon Rheumatology Research Group, Institute of Inflammation and Ageing, College of Medical and Dental Sciences, University of Birmingham,Rheumatology Department, City Hospital, Sandwell and West Birmingham Hospitals NHS Trust,Rheumatology Department, University

2017 British Society for Rheumatology

164. Catheter Interventions in Congenital Heart Disease Without Regular Catheterization Laboratory Equipment: The Chain of Hope Experience in Rwanda. (Abstract)

Catheter Interventions in Congenital Heart Disease Without Regular Catheterization Laboratory Equipment: The Chain of Hope Experience in Rwanda. This report describes the feasibility and safety of cardiac catheterization in a developing country without access to a regular cardiac catheterization laboratory. The equipment used for imaging consisted of a monoplane conventional C-arm X-ray system and a portable ultrasound machine using the usual guidewires and catheters for cardiovascular access (...) . In this study, 30 patients, including 17 children younger than 2 years and 2 adults, underwent catheterization of the following cardiac anomalies: patent ductus arteriosus (20 patients) and pulmonary valve stenosis (9 patients, including 2 patients with critical stenosis and 3 patients with a secundum atrial septal defect). Except for two cases requiring surgery, the patients were treated successfully without complications. They all were discharged from hospital, usually the day after cardiac

2012 Pediatric Cardiology

165. Myocardial Perfusion and Scarring in Congenital Heart Disease

with a physical exam and medical history. Blood and urine samples will be collected. Participants will have a cardiac MRI scan to look at the blood flow to the heart. Participants will also have a heart stress test to measure heart function during exercise. Other imaging studies of the heart may be performed to collect more information on heart function. Condition or disease Congenital Heart Disease Detailed Description: This is a study of the perfusion of the myocardium in adults with specific forms (...) the heart. This damage can be studied with a heart imaging test called a cardiac magnetic resonance imaging (MRI) scan. Researchers want to use this type of scan to look at the blood supply to the heart in people with congenital heart disease. Objectives: - To learn more about the blood supply to the heart in people with congenital heart disease. Eligibility: - Individuals at least 18 years of age who have heart defects caused by congenital heart disease. Design: Participants will be screened

2012 Clinical Trials

166. Management of Cardiovascular Diseases during Pregnancy

and offspring complications 3174 3.3.3 Pregnancy heart team 3176 3.4 Cardiovascular diagnosis in pregnancy 3176 3.4.1 Electrocardiography 3176 3.4.2 Echocardiography 3176 3.4.3 Exercise testing 3177 3.4.4 Ionizing radiation exposure 3177 3.4.5 Chest radiography and computed tomography 3177 3.4.6 Cardiac catheterization 3177 3.4.7 Magnetic resonance imaging 3177 3.5 Genetic testing and counselling 3177 3.5.1 Pre-natal diagnosis 3178 3.6 Foetal assessment 3178 3.6.1 Screening for congenital heart disease 3178 (...) 3.10.4 In vitro fertilization 3181 3.11 Recommendations 3182 4. Congenital heart disease and pulmonary hypertension 3182 4.1 Introduction 3182 4.2 Pulmonary hypertension and Eisenmenger’s syndrome 3183 4.2.1 Pulmonary hypertension 3183 4.2.2 Eisenmenger’s syndrome 3183 4.2.3 Cyanotic heart disease without pulmonary hypertension 3184 4.3 Specific congenital heart defects 3184 4.3.1 Left ventricular outflow tract obstruction 3184 4.3.2 Atrial septal defect 3184 4.3.3 Ventricular septal defect 3184

2018 European Society of Cardiology

167. Bone changes in congenital cyanotic heart disease. Full Text available with Trip Pro

Bone changes in congenital cyanotic heart disease. 5020720 1972 06 28 2018 11 13 0007-0769 34 4 1972 Apr British heart journal Br Heart J Bone changes in congenital cyanotic heart disease. 412-7 Singh H H Parkash A A Saini M M Wahi P L PL eng Journal Article England Br Heart J 0370634 0007-0769 AIM IM Adolescent Adult Ankle diagnostic imaging Arm diagnostic imaging Bone Marrow Bone and Bones diagnostic imaging Child Child, Preschool Female Fibula diagnostic imaging Heart Defects, Congenital (...) complications diagnostic imaging Hematocrit Hemoglobinometry Humans Infant Leukocyte Count Male Osteoarthropathy, Secondary Hypertrophic diagnostic imaging Pelvis diagnostic imaging Polycythemia complications Radiography Reticulocytes Skull diagnostic imaging Spine diagnostic imaging Tibia diagnostic imaging 1972 4 1 1972 4 1 0 1 1972 4 1 0 0 ppublish 5020720 PMC458494 Am J Med. 1955 Jan;18(1):51-65 13218038 Ann Intern Med. 1958 Mar;48(3):660-8 13521593 Acta Haematol. 1958 Apr-May;19(4-5):253-62 13558973

1972 British Heart Journal

168. Diagnosis and Treatment of Lymphatic Plastic Bronchitis in Adults Using Advanced Lymphatic Imaging and Percutaneous Embolization. (Abstract)

with congenital heart disease.To use advanced lymphatic imaging techniques, including dynamic contrast-enhanced magnetic resonance (MR) lymphangiography (DCMRL) and intranodal lymphangiography, to investigate the mechanism of cast formation in adult patients with plastic bronchitis, and to evaluate the therapeutic outcome of percutaneous lymphatic embolization for these patients.Seven adults (male/female = 3/4, mean age = 50 yr) who presented with expectoration of branching bronchial casts were evaluated (...) Diagnosis and Treatment of Lymphatic Plastic Bronchitis in Adults Using Advanced Lymphatic Imaging and Percutaneous Embolization. Plastic bronchitis is a condition characterized by expectoration of branching bronchial casts. Although the mechanism of cast formation in adults with plastic bronchitis remains poorly understood, abnormal pulmonary lymphatic flow resulting in molding of congealing lymphatic fluids in the airway has been documented as a cause of the disease in children

2016 Annals of the American Thoracic Society

169. Evidence-Based Guideline: Evaluation, Diagnosis, and Management of Congenital Muscular Dystrophy

dystroglycanopathies (2 Class II studies e44,e45 and 1 Class III study e46 ). Question 1d. For children with suspected CMD, how accurately does muscle imaging predict the subtype-specific diagnosis? There were 3 Class I articles and 1 Class III article. In the first Class I article, children with suspected neuromuscular disease underwent qualitative muscle ultrasound. Ultrasound distinguished normal from diseased muscle with a sensitivity of 81% and specificity of 96%. A highly characteristic central shadow (...) commonly associated with Walker –Warburg syndrome than previously thought. e25,e86 Some rare CMDs share features of both CMDs and congenital myopathies. These include SEPN1-related myopathy (rigid spine MD/multiminicore disease), integrin a-7 deficiency, lamin-associated CMD, and a CMD with mitochondrial structural abnormalities. Two small Class III studies found associations between SEPN1 mutations and patients with multiminicore myopathy. e87,e88 Another Class III study demonstrated that ITGA7

2013 American Association of Neuromuscular & Electrodiagnostic Medicine

170. Healing Hearts and Mending Minds in Older Adults Living With HIV

Healing Hearts and Mending Minds in Older Adults Living With HIV Healing Hearts and Mending Minds in Older Adults Living With HIV - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Healing Hearts and Mending (...) : Emory University Information provided by (Responsible Party): Drenna Waldrop-Valverde, Emory University Study Details Study Description Go to Brief Summary: The purpose of this study is to see if exercise is helpful for improving memory, concentration thinking abilities, physical function, and quality of life for adults aged 50 to 89 years living with HIV and who have two or more cardiovascular disease risk factors. The study will test two kinds of intervention exercises: one group will walk

2016 Clinical Trials

171. Adult patent ductus arteriosus: An unusual cause of heart failure in an octogenarian female Full Text available with Trip Pro

Adult patent ductus arteriosus: An unusual cause of heart failure in an octogenarian female Patent ductus arteriosus (PDA) is the third most common congenital abnormality in which the arterial duct, which normally closes spontaneously after birth within 24-48 h in full-term infants, remains permanently open. Breathlessness is very common in elderly patients and can be caused by several comorbidities, mostly cardiac and pulmonary diseases. PDA as a cause of heart failure in this patient (...) population is very rare and diagnosis depends on high clinical awareness. Here we present a case diagnosed with multimodality imaging including 3‑dimensional (3D) transthoracic and transesophageal echocardiography and 3D-volume rendering technique (VRT) computed tomography.

2016 Wiener klinische Wochenschrift

172. Diagnosis and Management of Glycogen Stored Diseases type VI and IX a practice resource of ACMG

difficulties and overnight irritability are common. Due to the protean and nonspecific symptoms in GSDs VI and IX, they are almost certainly underdiagnosed. GSD IX has been diagnosed in adults who were being evaluated for hepatic cirrhosis. Unlike GSD I, lactic acid and uric acid concentrations are usually normal, 24 although postprandial lactic acid can be elevated. 25 Clinical variability in GSD VI Glycogen storage disease type VI (GSD VI) has variable severity and can present in infancy/early childhood (...) Diagnosis and Management of Glycogen Stored Diseases type VI and IX a practice resource of ACMG Diagnosis and management of glycogen storage diseases type VI and IX: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG) A full list of authors and affiliations appears at the end of the paper. Disclaimer This practice resource is designed primarily as an educational resource for medical geneticists and other clinicians to help them provide quality medical

2019 American College of Medical Genetics and Genomics

173. AIM Clinical Appropriateness Guidelines for Genetic Testing for Hereditary Cardiac Disease

with an isolated type 2 or 3 Brugada pattern on EKG. In most cases, the primary value of genetic testing for Brugada syndrome is to benefit at-risk family members. Short QT Syndrome Short QT syndrome (SQTS) is a congenital, inherited, primary electric disorder of the heart characterized by abnormally short QT intervals on the surface ECG (<360 ms) and an increased proclivity to develop atrial and/or ventricular tachyarrhythmias (Gussak 2005). SQTS is a genetically heterogeneous disease caused by mutations (...) Dilated cardiomyopathy (DCM) is characterized by enlargement of the left ventricle of the heart and systolic impairment, in the absence of abnormal loading conditions or coronary artery disease sufficient to cause global systolic dysfunction (Haas 2015). The symptoms of DCM are similar to heart failure including shortness of breath, chest pain/tightness, fainting episodes and cardiac arrhythmias. The most serious complication of DCM is sudden, irregular heart rhythms that can be life threatening. Some

2019 AIM Specialty Health

174. Value of Cardiovascular Magnetic Resonance Imaging in Noninvasive Risk Stratification in Tetralogy of Fallot Full Text available with Trip Pro

imaging in noninvasive risk stratification to predict major adverse clinical outcomes.This multicenter study included 575 adult patients with TOF (4.083 patient-years at risk) from a prospective nationwide registry in whom CMR was performed. This study involved 5 tertiary referral centers with a specialized adult congenital heart disease unit. Multivariable Cox hazards regression analysis was performed to determine factors associated with the primary end point. The CMR variables were combined (...) Value of Cardiovascular Magnetic Resonance Imaging in Noninvasive Risk Stratification in Tetralogy of Fallot Adults late after total correction of tetralogy of Fallot (TOF) are at risk for major complications. Cardiovascular magnetic resonance (CMR) imaging is recommended to quantify right ventricular (RV) and left ventricular (LV) function. However, a commonly used risk model by Khairy et al requires invasive investigations and lacks CMR imaging to identify high-risk patients.To implement CMR

2017 JAMA cardiology

175. Lonsurf (trifluridine / tipiracil) - adult patients with metastatic colorectal cancer (CRC)

Lonsurf (trifluridine / tipiracil) - adult patients with metastatic colorectal cancer (CRC) 30 Churchill Place ? Canary Wharf ? London E14 5EU ? United Kingdom An agency of the European Union Telephone +44 (0)20 3660 6000 Facsimile +44 (0)20 3660 5520 Send a question via our website www.ema.europa.eu/contact 25 February 2016 EMA/CHMP/287846/2016 Committee for Medicinal Products for Human Use (CHMP) Assessment report Lonsurf International non-proprietary name: trifluridine / tipiracil Procedure (...) study report CTCAE: Common Terminology Criteria for Adverse Events CV: Coefficient of variation CYP: Cytochrome P450 DCR: Disease control rate DNA: Deoxyribonucleic acid DPD: Dihydropyridine dehydrogenase DR: Duration of response EC: European Commission ECG: Electrocardiogram ECOG: Eastern Cooperative Oncology Group eCRF: Electronic case report form EGFR: Epidermal growth factor receptor EMA: European medicines agency EP: European Pharmacopoeia EU: European Union EMA/CHMP/287846/2016 Page 5/106 FAS

2016 European Medicines Agency - EPARs

176. Evidence-Based Policy Making: Assessment of the American Heart Association?s Strategic Policy Portfolio Full Text available with Trip Pro

of Smoke-Free Workplace Laws guidelines developed with several national partners. Environmental tobacco smoke (ie, secondhand smoke) causes heart disease, cancer, lung disease, and other illnesses in both children and nonsmoking adults. , The direct and indirect healthcare costs associated with diseases caused by secondhand smoke exposure are estimated at $10 billion each year. If recent trends in the reduction in the prevalence of this exposure continue, the health and economic burden of passive (...) an obese adult. This in turn places obese individuals at risk for CVD, including ischemic heart disease and stroke, as well as type 2 diabetes mellitus and obstructive sleep apnea. BMI is a useful measure of obesity and adiposity in the clinical setting. It is easy to compute from measures of height and weight and is commonly used in national surveys such as NHANES. The AHA includes BMI as one of 4 health behaviors to track for the 2020 Strategic Impact Goals. Although not solely as a result of health

2016 American Heart Association

177. Enhancing Literacy in Cardiovascular Genetics: A Scientific Statement From the American Heart Association

are pediatric and adult primary care cardiologists and trainees, pediatric and adult cardiology subspecialists including congenital heart disease specialists, heart failure specialists, electrophysiologists, cardiac interventionalists, preventive cardiologists, stroke specialists, cardiac surgeons, cardiovascular nurses and nurse practitioners, and cardiology-oriented geneticists and genetic counselors. Core Competencies in Cardiovascular Genetics Several studies have identified barriers to genetic (...) /American College of Cardiology “2008 Guidelines for the Management of Adults With Congenital Heart Disease.” Thoracic Aortic Aneurysms Thoracic aortic aneurysms often occur in the setting of genetic syndromes such as Marfan, Loeys-Dietz, Ehlers-Danlos, or Turner syndrome, each of which have specific clinical phenotypes and specific genetic origins. Isolated (nonsyndromic) thoracic aortic aneurysms can also have a genetic basis, and accurate genetic diagnosis can have important implications in clinical

2016 American Heart Association

178. Current Diagnostic and Treatment Strategies for Specific Dilated Cardiomyopathies: A Scientific Statement From the American Heart Association Full Text available with Trip Pro

to a spectrum of heterogeneous myocardial disorders that are characterized by ventricular dilation and depressed myocardial performance in the absence of hypertension, valvular, congenital, or ischemic heart disease. 5 In clinical practice, the pathogenesis of heart failure (HF) has often been placed into 2 categories: ischemic and nonischemic cardiomyopathy. The term nonisch- emic cardiomyopathy has been interchangeably used with DCM. Although this approach might be practical, it fails to recognize (...) that nonischemic cardiomyopa- thy can include cardiomyopathies caused by volume or pressure overload (such as hypertension or valvular heart disease) that are not conventionally accepted under the definition of DCM. 1,5 Again, in general practice and clinical research trials, the term ischemic cardiomyopathy is defined as cardiomyopathy caused by ischemic heart disease. Current use of ischemic cardiomyopathy terminol- ogy implies ventricular dilation and depressed myocardial contractility caused by ischemia

2016 American Heart Association

179. Vascular Graft Infections, Mycotic Aneurysms, and Endovascular Infections: A Scientific Statement From the American Heart Association Full Text available with Trip Pro

. Bolger , Matthew E. Levison , Kathryn A. Taubert , Robert S. Baltimore , and Larry M. Baddour and On behalf of the American Heart Association Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease of the Council on Cardiovascular Disease in the Young; Council on Cardiovascular and Stroke Nursing; Council on Cardiovascular Radiology and Intervention; Council on Cardiovascular Surgery and Anesthesia; Council on Peripheral Vascular Disease; and Stroke Council Originally published 13 Oct 2016 (...) , there is a risk of introducing pathogens into a perigraft area with high-pressure instillation of contrast material. Invasive angiography is rarely useful for the diagnosis of VGI. The choice of an imaging modality is best determined by consultation among experts in vascular surgery, infectious diseases, vascular medicine, and radiology. Extracavitary VGI Even when clinical or microbiological findings strongly suggest a VGI, imaging, most often ultrasonography or CTA, is used to support the diagnosis

2016 American Heart Association

180. Task Force 2: Pediatric Cardiology Fellowship Training in Noninvasive Cardiac Imaging

-dimensional, and speckle tracking to assess global and regional deformation, color Doppler imaging, as well as pulsed and continuous- wave spectral Doppler imaging for flow, hemodynamics, and tissue motion. Cardiac MRI refers to anatomic and functional cardiovascular MRI for assessment of congenital heart disease (CHD) in children and adults, as well as for assessment of acquired forms of heart disease in children. 1.3. Levels of Expertise—Core and Advanced Innovations in the field of echocardiography (...) in February 2015. It was endorsed by the American Society of Echocardiography and approved by the ACC in March 2015. This document is considered current until the SPCTPD revises or withdraws it. 1.2. Background and Scope For over 25 years, noninvasive cardiac imaging has been the mainstay of anatomic and physiological assessment in pedi- atric cardiology and congenital heart disease. An ACC/AAP/ AHA combined task force published pediatric noninvasive car- diac imaging training guidelines in 2005

2015 American Heart Association

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