Journal articles: 'Congenital Cardiovascular Disease'

1

Kilner, P. "Congenital cardiovascular disease applications." Journal of Biomechanics 39 (January 2006): S288. http://dx.doi.org/10.1016/s0021-9290(06)84113-8.

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Hlavacek, Anthony Marcus. "Imaging of Congenital Cardiovascular Disease." Journal of Thoracic Imaging 25, no. 3 (August 2010): 247–55. http://dx.doi.org/10.1097/rti.0b013e3181cc05e6.

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Hanchard, Neil A., and Heather C. Mefford. "Editorial overview: Congenital cardiovascular disease." Current Opinion in Genetics & Development 77 (December 2022): 102006. http://dx.doi.org/10.1016/j.gde.2022.102006.

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Bank, Estelle R. "MAGNETIC RESONANCE OF CONGENITAL CARDIOVASCULAR DISEASE." Radiologic Clinics of North America 31, no. 3 (May 1993): 553–72. http://dx.doi.org/10.1016/s0033-8389(22)02605-7.

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Sakamoto, Takahiko. "Cardiovascular Surgery for Congenital Heart Disease." Pediatric Cardiology and Cardiac Surgery 31, no. 1-2 (2015): 39–51. http://dx.doi.org/10.9794/jspccs.31.39.

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Bondy, Carolyn A. "Congenital Cardiovascular Disease in Turner Syndrome." Congenital Heart Disease 3, no. 1 (January 18, 2008): 2–15. http://dx.doi.org/10.1111/j.1747-0803.2007.00163.x.

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Wooley, Charles F., and Elizabeth Henson Sparks. "Congenital heart disease, heritable cardiovascular disease, and pregnancy." Progress in Cardiovascular Diseases 35, no. 1 (July 1992): 41–60. http://dx.doi.org/10.1016/0033-0620(92)90034-w.

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Egbe, Alexander C., William R. Miranda, Francisco Lopez-Jimenez, and Heidi M. Connolly. "Atherosclerotic Cardiovascular Disease in Adults With Congenital Heart Disease." JACC: Advances 1, no. 2 (June 2022): 100026. http://dx.doi.org/10.1016/j.jacadv.2022.100026.

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Powell, AndrewJ, and JamesC Nielsen. "Cardiovascular MRI applications in congenital heart disease." Indian Journal of Radiology and Imaging 17, no. 2 (2007): 86. http://dx.doi.org/10.4103/0971-3026.33618.

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Steiner, Robert M., Gautham P. Reddy, and Stephanie Flicker. "Congenital Cardiovascular Disease in the Adult Patient." Journal of Thoracic Imaging 17, no. 1 (January 2002): 1–17. http://dx.doi.org/10.1097/00005382-200201000-00001.

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Teo, L. L. S., and C. P. P. Hia. "Advanced cardiovascular imaging in congenital heart disease." International Journal of Clinical Practice 65 (April 2011): 17–29. http://dx.doi.org/10.1111/j.1742-1241.2010.02622.x.

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Tann, Oliver Richard, Vivek Muthurangu, Carol Young, and Catherine M. Owens. "Cardiovascular CT imaging in congenital heart disease." Progress in Pediatric Cardiology 28, no. 1-2 (January 2010): 21–27. http://dx.doi.org/10.1016/j.ppedcard.2009.10.007.

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Bhatia, Neal K., and Dimitri C. Cassimatis. "AN UNUSUAL CONSTELLATION OF CONGENITAL CARDIOVASCULAR DISEASE." Journal of the American College of Cardiology 65, no. 10 (March 2015): A639. http://dx.doi.org/10.1016/s0735-1097(15)60639-8.

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Sheppard, Mary N. "Cardiovascular examination in congenital heart disease (CHD)." Pathology 46 (2014): S20. http://dx.doi.org/10.1097/01.pat.0000443450.04023.20.

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Muthurangu, Vivek. "Cardiovascular Magnetic Resonance in Congenital Heart Disease." Heart Failure Clinics 17, no. 1 (January 2021): 157–65. http://dx.doi.org/10.1016/j.hfc.2020.08.012.

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Wisheart, J. D. "Congenital aortic disease." Current Opinion in Cardiology 1, no. 5 (September 1986): 646–51. http://dx.doi.org/10.1097/00001573-198609000-00012.

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17

Wilkinson, James L. "Congenital heart disease." International Journal of Cardiology 13, no. 1 (October 1986): 97. http://dx.doi.org/10.1016/0167-5273(86)90090-2.

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Cullen, Seamus, David S. Celermajer, and John E. Deanfield. "Exercise in congenital heart disease." Cardiology in the Young 1, no. 2 (April 1991): 129–35. http://dx.doi.org/10.1017/s104795110000024x.

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SummaryExercise is of both physical and psychological benefit in children with congenital heart disease, leading to improved cardiovascular fitness and better quality of life. In such children, however, capacity for exercise is often impaired, and there is a risk of exercise-induced mortality or morbidity. We have reviewed the abnormal cardiovascular response to exercise in children with congenital heart defects and postoperative residua, and the role of exercise testing and training in their diagnosis and treatment. Some patients should be excluded absolutely from all but mild regular exercise because of known high risk; for example, those with severe aortic or subaortic stenosis. Other patients should be encouraged to participate in sports without any limitation; for example, those with small left-to-right shunts or mild valvar regurgitation. In many patients strict recommendations cannot be made, and one must consider the individual, the lesion and its hemodynamic implications, and the type and level of exercise contemplated. Children with congenital heart disease should be encouraged to participate in exercise and recreational sport within the limits provided by their cardiovascular defect. Understanding the pathophysiology of these defects, and knowledge of the risk of exercise in certain conditions, will allow the physician to make sensible recommendations for participation in exercise by individual patients.

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Pushparajah, Kuberan, Phuoc Duong, Sujeev Mathur, and Sonya V. Babu-Narayan. "EDUCATIONAL SERIES IN CONGENITAL HEART DISEASE: Cardiovascular MRI and CT in congenital heart disease." Echo Research and Practice 6, no. 4 (December 2019): R121—R138. http://dx.doi.org/10.1530/erp-19-0048.

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Cardiac MRI and CT are increasingly used in the diagnosis and management of patients with congenital heart disease as an imaging adjunct to echocardiography. The benefits and limitations of both modalities are highlighted, with a focus on the anatomical, functional and haemodynamic information that can be gained from the different modalities. Deciding on the imaging modality of choice must also take into account patient factors such as age, compliance, the type of congenital heart disease, and previous procedures. Future developments in CT and MRI are also discussed.

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20

Marian, Ali J. "Congenital Heart Disease." Circulation Research 120, no. 6 (March 17, 2017): 895–97. http://dx.doi.org/10.1161/circresaha.117.310830.

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21

Bruneau, Benoit G., and Deepak Srivastava. "Congenital Heart Disease." Circulation Research 114, no. 4 (February 14, 2014): 598–99. http://dx.doi.org/10.1161/circresaha.113.303060.

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Putra Gofur, Nanda Rachmad, Aisyah Rachmadani Putri Gofur, Soesilaningtyas Soesilaningtyas, Rizki Nur Rachman Putra Gofur, Mega Kahdina, and Hernalia Martadila Putri. "Management Congenital Heart Disease Surgery during COVID-19: A Review Article." Cardiology Research and Reports 4, no. 2 (March 11, 2022): 01–03. http://dx.doi.org/10.31579/2692-9759/040.

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Introduction: Congenital heart disease is a form of heart abnormality that has been acquired since the newborn. The clinical course of this disorder varies from mild to severe. In mild forms, there are often no symptoms, and no abnormalities are found on clinical examination. Whereas in severe CHD, symptoms have been visible since birth and require immediate action. Generally, the management of congenital heart disease includes non-surgical management and surgical management. Non-surgical management includes medical management and interventional cardiology. Medical management is generally secondary as a result of complications from heart disease itself or due to other accompanying disorders. In this case, the goal of medical therapy is to relieve symptoms and signs in addition to preparing for surgery. The duration and method of administration of drugs depend on the type of disease at hand. Discussion: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which led to the coronavirus disease 2019 (COVID-19) pandemic, was initially reported in Wuhan, China in December, 2019. The rapid rise in the number of cases worldwide led to hospitals struggling to cope with the sudden influx of patients. This has had a ripple effect on other parts of health care as manpower and supplies needed to be reallocated. Within cardiology, this has led to outpatient appointments and elective surgeries being reduced and/or postponed. COVID-19 appears to have a complicated relationship with cardiovascular system, as studies have suggested cardiovascular diseases increase disease severity and mortality rates in those who are infected. However, the virus has also been shown to cause cardiovascular complications such as acute myocardial injury, heart failure, and arrhythmia. Conclusion: Coronavirus may also cause myocardial injury via the cytokine storm that occurs in response to a possible large immune response during the infection. Cardiac involvement such as right ventricular failure and congestion can either be a result of respiratory distress or direct cardiac injury caused by the virus, as suggested by the raised cardiac troponin I in critical patients compared to non-critical patients.

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23

Giannakoulas, George, and Despoina Ntiloudi. "Acquired cardiovascular disease in adult patients with congenital heart disease." Heart 104, no. 7 (September 4, 2017): 546–47. http://dx.doi.org/10.1136/heartjnl-2017-311997.

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24

Flannery, Laura, Akl Fahed, Gregory Barinsky, Mohamed Youniss, Doreen Defaria Yeh, and Ami Bhatt. "ATHEROSCLEROTIC CARDIOVASCULAR DISEASE RISK IN ADULTS WITH CONGENITAL HEART DISEASE." Journal of the American College of Cardiology 67, no. 13 (April 2016): 899. http://dx.doi.org/10.1016/s0735-1097(16)30900-7.

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25

Shaikh, Rumana M. "Cardiovascular Diseases Prediction Using Machine Learning Algorithms." Turkish Journal of Computer and Mathematics Education (TURCOMAT) 12, no. 6 (April 11, 2021): 1083–88. http://dx.doi.org/10.17762/turcomat.v12i6.2426.

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A broad variety of health conditions are involved in heart disease. Several illnesses and disorders come under the heart disease umbrella. Heart disease forms include: In arrhythmia, abnormality of the heart rhythm. Arteriosclerosis, Hardening of the arteries is atherosclerosis. Via cardiomyopathy, this disorder causes muscles in the heart to harden or grow weak. Defects of the congenital heart, heart abnormalities that are present at birth are congenital heart defects. Disease of the coronary arteries (CAD), the accumulation of plaque in the heart's arteries triggers CAD. It's called ischemic heart disease occasionally. Infections of the heart, bacteria, viruses, or parasites may trigger heart infections. Heart diseases namely arrhythmias, coronary heart disease, heart attacks, cardiomyopathy will be detect using the proposed algorithm in this paper. Here I compared three algorithms namely Restricted Boltzmann Machines, Deep Belief Networks and Convolutional Neural Networks for electrocardiogram (ECG) classification for heart disease.

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26

Link, Kerry M., Stephen P. Loehr, Eric M. Martin, and Nadja M. Lesko. "Congenital heart disease." Coronary Artery Disease 4, no. 4 (April 1993): 340–44. http://dx.doi.org/10.1097/00019501-199304000-00005.

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27

Kaufman, Stephen L. "Intrathoracic interventional vascular techniques in congenital cardiovascular disease." Journal of Thoracic Imaging 2, no. 2 (April 1987): 1–10. http://dx.doi.org/10.1097/00005382-198704000-00004.

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28

Crean, A. "Cardiovascular MR and CT in congenital heart disease." Heart 93, no. 12 (December 12, 2006): 1637–47. http://dx.doi.org/10.1136/hrt.2006.104729.

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29

Bergersen, Lisa, Allen Dale Everett, Jorge Manuel Giroud, Gerard R. Martin, Rodney Cyril George Franklin, Marie Josée Béland, Otto Nils Krogmann, et al. "Report from The International Society for Nomenclature of Paediatric and Congenital Heart Disease: cardiovascular catheterisation for congenital and paediatric cardiac disease (Part 1 – Procedural nomenclature)." Cardiology in the Young 21, no. 3 (February 11, 2011): 252–59. http://dx.doi.org/10.1017/s104795111000185x.

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AbstractInterventional cardiology for paediatric and congenital cardiac disease is a relatively young and rapidly evolving field. As the profession begins to establish multi-institutional databases, a universal system of nomenclature is necessary for the field of interventional cardiology for paediatric and congenital cardiac disease. The purpose of this paper is to present the results of the efforts of The International Society for Nomenclature of Paediatric and Congenital Heart Disease to establish a system of nomenclature for cardiovascular catheterisation for congenital and paediatric cardiac disease, focusing both on procedural nomenclature and on the nomenclature of complications associated with interventional cardiology. This system of nomenclature for cardiovascular catheterisation for congenital and paediatric cardiac disease is a component of The International Paediatric and Congenital Cardiac Code. This manuscript is the first part of a two-part series. Part 1 will cover the procedural nomenclature associated with interventional cardiology as treatment for paediatric and congenital cardiac disease. This procedural nomenclature of The International Paediatric and Congenital Cardiac Code will be used in the IMPACT Registry™ (IMproving Pediatric and Adult Congenital Treatment) of the National Cardiovascular Data Registry®of The American College of Cardiology. Part 2 will cover the nomenclature of complications associated with interventional cardiology as treatment for paediatric and congenital cardiac disease.

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30

Needleman, Matthew, Joseph May, Michael Mulreany, and Lauren Weber. "A NOVEL CONGENITAL CURRICULUM IMPROVES CARDIOVASCULAR FELLOW PERFORMANCE WITH CONGENITAL HEART DISEASE." Journal of the American College of Cardiology 77, no. 18 (May 2021): 3363. http://dx.doi.org/10.1016/s0735-1097(21)04717-3.

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31

Nicol, Edward D., Olivier Manen, Norbert Guettler, Dennis Bron, Eddie D. Davenport, Thomas Syburra, Gary Gray, Joanna d’Arcy, and Rienk Rienks. "Congenital heart disease in aircrew." Heart 105, Suppl 1 (November 13, 2018): s64—s69. http://dx.doi.org/10.1136/heartjnl-2018-313059.

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This article focuses i on the broad aviation medicine considerations that are required to optimally manage aircrew ii with suspected or confirmed congenital heart disease (both pilots and non-pilot aviation professionals). It presents expert consensus opinion and associated recommendations and is part of a series of expert consensus documents covering all aspects of aviation cardiology. This expert opinion was born out of a 3 year collaborative working group between international military aviation cardiologists and aviation medicine specialists, as part of a North Atlantic Treaty Organization (NATO) led initiative to address the occupational ramifications of cardiovascular disease in aircrew (HFM-251) many of whom also work with and advise civil aviation authorities.

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32

Thakkar, Akanksha N., Ponraj Chinnadurai, and C. Huie Lin. "Adult congenital heart disease." Current Opinion in Cardiology 32, no. 5 (September 2017): 467–74. http://dx.doi.org/10.1097/hco.0000000000000429.

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33

Moodie, Douglas S. "Adult congenital heart disease." Current Opinion in Cardiology 9, no. 1 (January 1994): 137. http://dx.doi.org/10.1097/00001573-199401000-00017.

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34

Moodie, Douglas S. "Adult congenital heart disease." Current Opinion in Cardiology 10, no. 1 (January 1995): 92–98. http://dx.doi.org/10.1097/00001573-199501000-00015.

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35

Morphet, John A. M. "Adult congenital heart disease." Canadian Journal of Cardiology 22, no. 2 (February 2006): 157. http://dx.doi.org/10.1016/s0828-282x(06)70260-4.

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36

Levi, Daniel S. "Congenital Heart Disease Intervention." Interventional Cardiology Clinics 8, no. 1 (January 2019): i. http://dx.doi.org/10.1016/s2211-7458(18)30074-9.

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37

Afilalo, Jonathan, Judith Therrien, Louise Pilote, Raluca Ionescu-Ittu, Giuseppe Martucci, and Ariane J. Marelli. "Geriatric Congenital Heart Disease." Journal of the American College of Cardiology 58, no. 14 (September 2011): 1509–15. http://dx.doi.org/10.1016/j.jacc.2011.06.041.

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38

Chun, Hua, Yan Yue, Yibin Wang, Zhaxi Dawa, Pu Zhen, Qu La, Yang Zong, Yi Qu, and Dezhi Mu. "High prevalence of congenital heart disease at high altitudes in Tibet." European Journal of Preventive Cardiology 26, no. 7 (November 12, 2018): 756–59. http://dx.doi.org/10.1177/2047487318812502.

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Background Previous small sample studies suggested that elevated altitudes might be associated with the incidence of cardiovascular diseases. However, it remains uncertain whether high altitudes (over 3000 m above sea level) are related to congenital heart disease. We therefore explored the prevalence of congenital heart disease in a large cohort of students in the world's largest prefecture-level city with the highest altitude. Methods This cross-sectional study included 84,302 student participants (boys 52.12%, girls 47.88%, with an average age of 10.62 ± 3.33 years). Data were extracted from the screening results among different altitude area schools in Nagqu from June 2016 to August 2017. Students were first screened by performing a physical examination consisting of cardiac auscultations and clinical manifestation screenings. An echocardiography was performed to confirm and identify the subtype of congenital heart disease. Results The prevalence of congenital heart disease among students in Nagqu, Tibet, was 5.21‰ (439 cases). The most common congenital heart disease type was patent ductus arteriosus, representing 66.3% of congenital heart diseases diagnosed in this study, followed by atrial septal defect and ventricular septal defect, representing 20.3% and 9.1% of congenital heart diseases, respectively. Students living in higher altitudes were significantly more prone to have congenital heart disease than students in locations with lower altitudes. The prevalence of congenital heart disease in girls was found to be higher than that of boys. Conclusions The correlation between congenital heart disease and increased altitude is noteworthy. This study's results are the first big data epidemiological investigation to confirm that high altitude is a significant environmental risk factor for congenital heart disease, especially patent ductus arteriosus. Furthermore, the results provide additional support to make a diagnostic and treatment plan to prevent congenital heart disease in high altitude areas.

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39

ROSTI, LUCA, ANGELA E. LIN, and ALESSANDRO FRIGIOLA. "Neuroblastoma and Congenital Cardiovascular Malformations." Pediatrics 97, no. 2 (February 1, 1996): 258–61. http://dx.doi.org/10.1542/peds.97.2.258.

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Congenital cardiovascular malformations (CCVM) are frequently associated with noncardiac malformations, often comprising a multiple malformation syndrome, but occurring infrequently in nonsyndromic systemic disease states such as neuroblastoma. As the most common malignancy in the first year of life, neuroblastoma presents as both clinically apparent and clinically unsuspected in situ tumors detected at autopsy. Neuroblastoma's association with CCVMs, especially conotruncal defects, suggests a possible common embryologic role for abnormal neural crest cell migration and development. We provide further documentation of this intriguing, albeit rare, association by reporting a boy with a prenatally detected complex CCVM (univentricular heart and dextro-transposition of the great arteries [d-TGA]) and congenital neuroblastoma.

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40

HUHTA, JAMES C. "Congenital Heart Disease." Echocardiography 8, no. 4 (July 1991): 439–40. http://dx.doi.org/10.1111/j.1540-8175.1991.tb01005.x.

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41

Siu, S. C. "CONGENITAL HEART DISEASE: Heart disease and pregnancy." Heart 85, no. 6 (June 1, 2001): 710–15. http://dx.doi.org/10.1136/heart.85.6.710.

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42

Rodríguez, María M., Jocelyn H. Bruce, Xavier F. Jiménez, Rita L. Romaguera, Eduardo Bancalari, Otto L. García, and Peter L. Ferrer. "Nonimmune Hydrops Fetalis in the Liveborn: Series of 32 Autopsies." Pediatric and Developmental Pathology 8, no. 3 (May 2005): 369–78. http://dx.doi.org/10.1007/s10024-005-8089-z.

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Nonimmune hydrops fetalis (NIHF) or generalized soft tissue edema and cavity effusions may be due to cardiovascular diseases, congenital infections, genitourinary malformations, thoracic masses, placental conditions, chromosomal abnormalities, and idiopathic. We report 32 cases of NIHF from among 429 neonates who underwent autopsies (incidence 7.45%). Sixteen cases (50%) had cardiovascular disease; all were due to low output cardiac failure; 7 had structural congenital heart disease. Three of the children with congenital heart disease also had chromosomal abnormalities: 2 had trisomy 18 and 1 had Noonan syndrome. Among myocardial conditions were five subjects with cardiomyopathies (1 of each of the following types): oncocytic, dilated, endocardial fibroelastosis, cardiac glycogenosis, and carnitine deficiency; 3 had myocarditis, and 1 had cardiac rhabdomyomas. Congenital infections were due to cytomegalovirus in 3 cases, bacteria in 2, and parvovirus in 1. The mechanism of NIHF in these cases might be a combination of decreased myocardial contractility due to myocarditis and fetal anemia. Genitourinary diseases were present in 5 newborns: Two had congenital nephrotic syndrome, 1 had VACTER association, 1 had prune-belly syndrome, and 1 had urogenital sinus malformation. Intrathoracic lesions were found in 2 babies (pulmonary sequestration and diaphragmatic hernia). One twin died of volume overload due to twin transfusion syndrome. Only 2 newborns were classified as idiopathic. Our study shows that cardiovascular diseases that lead to heart failure or impaired venous return are more common in the liveborn (50%), whereas congenital infections are more common in the stillborn with NIHF.

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43

Ramaswamy, Madhavan, Yi-Ting Yeh, Riya Varman, Neil McIntosh, Denise McIntyre, Oleg Fedevych, Sachin Khambadkone, Martin Kostolny, Richard Hewitt, and Nagarajan Muthialu. "Staging of Surgical Procedures in Comorbid Congenital Tracheal Stenosis and Congenital Cardiovascular Disease." Annals of Thoracic Surgery 109, no. 6 (June 2020): 1889–96. http://dx.doi.org/10.1016/j.athoracsur.2020.01.034.

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44

Bashore, Thomas M. "Adult Congenital Heart Disease." Circulation 115, no. 14 (April 10, 2007): 1933–47. http://dx.doi.org/10.1161/circulationaha.105.592345.

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45

Khairy, Paul, and Michael J. Landzberg. "Adult Congenital Heart Disease." Circulation 117, no. 18 (May 6, 2008): 2311–12. http://dx.doi.org/10.1161/circulationaha.108.770594.

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46

Mahoney, Larry T. "Acyanotic Congenital Heart Disease." Cardiology Clinics 11, no. 4 (November 1993): 603–16. http://dx.doi.org/10.1016/s0733-8651(18)30141-3.

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47

Pinsker, Bret, Izza Shahid, Pankaj Kumar, Matthew R. Krasuski, Sarah Goldstein, J. D. Serfas, Muhammad Khan, and Richard Krasuski. "IMPACT OF CARDIOVASCULAR COMORBIDITY ON CONGENITAL HEART DISEASE DEATHS." Journal of the American College of Cardiology 77, no. 18 (May 2021): 507. http://dx.doi.org/10.1016/s0735-1097(21)01866-0.

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48

Perloff, J. K. "Congenital heart disease in adults. A new cardiovascular subspecialty." Circulation 84, no. 5 (November 1991): 1881–90. http://dx.doi.org/10.1161/01.cir.84.5.1881.

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Davis, Andrew M., John Burn, and Tom R. Karl. "‘Malignant’ congenital cardiovascular disease in twins with William's syndrome." Cardiology in the Young 3, no. 4 (October 1993): 435–37. http://dx.doi.org/10.1017/s104795110000189x.

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SummaryTwins of like sex and concordant for William's syndrome are presented. The first twin presented late with aortic arch atresia and has subsequently developed hypertension associated with renal arterial stenosis. The second twin died with myocardial ischemia late after surgery for supravalvar aortic and pulmonary stenosis.

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Schoen, Frederick J. "Introduction to congenital heart disease articles in Cardiovascular Pathology." Cardiovascular Pathology 19, no. 5 (September 2010): 257–58. http://dx.doi.org/10.1016/j.carpath.2010.04.008.

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Journal articles on the topic 'Congenital Cardiovascular Disease'

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