The European Paediatric Cardiac Code Long List: structure and function — the first revision

2002 ◽  
Vol 12 (S2) ◽  
pp. 9-17 ◽  
Author(s):  
Rodney C. G. Franklin

The Long ListThe Long List is a comprehensive hierarchical system of coding and classification for the diagnosis and treatment of cardiac disease. The list was first published in 2000, as part of the standard coding system recommended by the Association for European Paediatric Cardiology for use across Europe. It embraces the entirety of the diagnosis and therapy of children with congenital and acquired cardiac disease. The Long List, as a whole, was adopted by the Association in 1998. Its development and expansion has been detailed previously. In essence, it grew from a list of 507 purely diagnostic terms published in 1985, through to a 1,777 item, hierarchical 12 tree structure in the Netherlands by 1988, and then to a single hierarchical structure of over 4,300 items in London by 1994. Although originally aimed at the clinician or surgeon treating cardiac disease first appearing in infancy or childhood, during this time it was enlarged to encompass abnormalities first diagnosed in fetal life, as well as cardiac disease first acquired during adult life. The list published in 2000 was composed of 4,777 items. These were made up of 3,906 individual terms, most of whom were mutually exclusive and unambivalent, given the constraints of clinical ambiguities and differing cultures of practice.

2000 ◽  
Vol 10 (S1) ◽  
pp. 27-33 ◽  
Author(s):  
Rodney C. G. Franklin

The Long List is a comprehensive hierarchical system of coding and classification for the diagnosis and treatment of heart disease. Although originally aimed at the clinician or surgeon treating heart disease first appearing in infancy or childhood, it has now been enlarged to encompass abnormalities first diagnosed in fetal life, as well as heart disease first acquired during adult life. There are a total of 3,876 individual terms. For the most part, these are mutually exclusive and unambivalent, given the constraints of clinical ambiguities and differing cultures of practice. In addition, there are 564 qualifier terms. These provide additional detail to individual or multiple items, such as fine anatomical detail, the severity of a lesion, the size of an interposition shunt or conduit, or the material used to close a septal defect. Finally, there are a further 341 duplicate diagnostic or procedural terms included in the List to aid its use, as some terms may have relevance in multiple areas. For example, Hypoplastic left heart syndrome is found under congenital anomalies of the left ventricle as well as in the section dealing with the aortic valve. Thus, altogether the listing consists of 4,781 items. The System is hierarchically arranged, with a major division between diagnostic and therapeutic subhierarchies. The developmental history of the Long List has been published previously, and is detailed earlier in this supplement.


2018 ◽  
pp. 326-334
Author(s):  
L. Samuel Wann

The Stress Echocardiography chapter reviews the opportunities to increase sensitivity and specificity of stress testing for the diagnosis of ischemic heart disease with adjunctive echocardiography with exercise or dobutamine-atropine stress. Baseline imaging prior to stress should include a comprehensive evaluation of cardiac structure and function, including the assessment of valvular disease with Doppler echocardiography. The chapter discusses stress echocardiography protocols; image analysis and reporting; sensitivity, specificity, and accuracy for detection of coronary artery disease; and evaluation of noncoronary cardiac disease. New and developing echocardiographic technology, including ultrasound assessment of myocardial perfusion, real-time 3D echocardiographic, and strain imaging are also discussed.


Circulation ◽  
2015 ◽  
Vol 132 (21) ◽  
pp. 1979-1989 ◽  
Author(s):  
Amil M. Shah ◽  
Brian Claggett ◽  
Aaron R. Folsom ◽  
Pamela L. Lutsey ◽  
Christie M. Ballantyne ◽  
...  

2018 ◽  
Vol 15 (4) ◽  
pp. 290-298 ◽  
Author(s):  
Jianzhu Ma ◽  
Michael Ku Yu ◽  
Samson Fong ◽  
Keiichiro Ono ◽  
Eric Sage ◽  
...  

2017 ◽  
Vol 24 (1) ◽  
pp. 7-21 ◽  
Author(s):  
Anna Klingseisen ◽  
David A. Lyons

Approximately half of the human brain consists of myelinated axons. Central nervous system (CNS) myelin is made by oligodendrocytes and is essential for nervous system formation, health, and function. Once thought simply as a static insulator that facilitated rapid impulse conduction, myelin is now known to be made and remodeled in to adult life. Oligodendrocytes have a remarkable capacity to differentiate by default, but many aspects of their development can be influenced by axons. However, how axons and oligodendrocytes interact and cooperate to regulate myelination in the CNS remains unclear. Here, we review recent advances in our understanding of how such interactions generate the complexity of myelination known to exist in vivo. We highlight intriguing results that indicate that the cross-sectional size of an axon alone may regulate myelination to a surprising degree. We also review new studies, which have highlighted diversity in the myelination of axons of different neuronal subtypes and circuits, and structure-function relationships, which suggest that myelinated axons can be exquisitely fine-tuned to mediate precise conduction needs. We also discuss recent advances in our understanding of how neuronal activity regulates CNS myelination, and aim to provide an integrated overview of how axon-oligodendrocyte interactions sculpt neuronal circuit structure and function.


2018 ◽  
Author(s):  
Christi T Salisbury-Ruf ◽  
Clinton C Bertram ◽  
Aurelia Vergeade ◽  
Daniel S Lark ◽  
Qiong Shi ◽  
...  

ESC CardioMed ◽  
2018 ◽  
pp. 746-748
Author(s):  
Marietta Charakida

In fetal life, the systemic and pulmonary circulations exist in parallel, rather than in series, permitting survival even in the presence of complex congenital heart disease. The fetal heart also differs in terms of its structure and function and has a limited ability to modify cardiac output. Increases in afterload are associated with marked depression in cardiac function. Much has been learnt from fetal cardiac imaging, not only for detection but also for understanding of pathophysiology and transition to the postnatal circulation.


2011 ◽  
Vol 278 (1719) ◽  
pp. 2714-2723 ◽  
Author(s):  
Michael Ibrahim ◽  
Julia Gorelik ◽  
Magdi H. Yacoub ◽  
Cesare M. Terracciano

The transverse tubules (t-tubules) are invaginations of the cell membrane rich in several ion channels and other proteins devoted to the critical task of excitation–contraction coupling in cardiac muscle cells (cardiomyocytes). They are thought to promote the synchronous activation of the whole depth of the cell despite the fact that the signal to contract is relayed across the external membrane. However, recent work has shown that t-tubule structure and function are complex and tightly regulated in healthy cardiomyocytes. In this review, we outline the rapidly accumulating knowledge of its novel roles and discuss the emerging evidence of t-tubule dysfunction in cardiac disease, especially heart failure. Controversy surrounds the t-tubules' regulatory elements, and we draw attention to work that is defining these elements from the genetic and the physiological levels. More generally, this field illustrates the challenges in the dissection of the complex relationship between cellular structure and function.


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